Item | Value |
---|---|
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 | 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 | MDYPT others(331): Show |
chr18 | 69848274 | 69952873 |
a0002 | 0/1 | 336 | 106 | 26 | 34 | 29 | 1 | 15 | 17 | CD226_chr18_69848274_69952873 | CD226 | MDYPT others(331): Show |
chr18 | 69848274 | 69952873 |
a0003 | 0/0 | 336 | 12 | 4 | 4 | 2 | 0 | 2 | 1 | CD226_chr18_69848274_69952873 | CD226 | MDYPT others(331): Show |
chr18 | 69848274 | 69952873 |
a0004 | 0/0 | 336 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | MDYPT others(331): Show |
chr18 | 69848274 | 69952873 |
a0005 | 0/0 | 336 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | MDYPT others(331): Show |
chr18 | 69848274 | 69952873 |
a0006 | 0/0 | 336 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | MDYPT others(331): Show |
chr18 | 69848274 | 69952873 |
a0007 | 0/0 | 336 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | MDYPT others(331): Show |
chr18 | 69848274 | 69952873 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1008 | 134 | 55 | 24 | 34 | 3 | 17 | CD226_chr18_69848274_69952873 | CD226 | ATGGA others(1003): Show |
chr18 | 69848274 | 69952873 | ||
a0002c0002 | 0/1 | 1008 | 103 | 24 | 33 | 29 | 1 | 15 | CD226_chr18_69848274_69952873 | CD226 | ATGGA others(1003): Show |
chr18 | 69848274 | 69952873 | ||
a0002c0004 | 0/0 | 1008 | 2 | 1 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | ATGGA others(1003): Show |
chr18 | 69848274 | 69952873 | ||
a0002c0009 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | ATGGA others(1003): Show |
chr18 | 69848274 | 69952873 | ||
a0003c0003 | 0/0 | 1008 | 12 | 4 | 4 | 2 | 0 | 2 | CD226_chr18_69848274_69952873 | CD226 | ATGGA others(1003): Show |
chr18 | 69848274 | 69952873 | ||
a0004c0006 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | ATGGA others(1003): Show |
chr18 | 69848274 | 69952873 | ||
a0005c0005 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | ATGGA others(1003): Show |
chr18 | 69848274 | 69952873 | ||
a0006c0008 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | ATGGA others(1003): Show |
chr18 | 69848274 | 69952873 | ||
a0007c0007 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | ATGGA others(1003): Show |
chr18 | 69848274 | 69952873 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0003 | 0/0 | 12523 | 17 | 0 | 10 | 0 | 1 | 6 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12518): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0004 | 0/0 | 12524 | 16 | 0 | 2 | 12 | 0 | 2 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12519): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0006 | 0/0 | 12525 | 8 | 0 | 0 | 7 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12520): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0008 | 0/0 | 12522 | 7 | 2 | 3 | 0 | 1 | 1 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12517): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0013 | 0/0 | 12524 | 3 | 0 | 0 | 2 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12519): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0014 | 0/0 | 12522 | 3 | 3 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12517): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0015 | 1/0 | 12518 | 3 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12513): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0016 | 0/0 | 12523 | 3 | 1 | 0 | 1 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12518): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0019 | 0/0 | 12524 | 3 | 3 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12519): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0020 | 0/0 | 12504 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12499): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0021 | 0/0 | 12521 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12516): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0022 | 0/0 | 12518 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12513): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0023 | 0/0 | 12524 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12519): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0026 | 0/0 | 12523 | 2 | 0 | 0 | 1 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12518): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0027 | 0/0 | 12522 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12517): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0028 | 0/0 | 12523 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12518): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0029 | 0/0 | 12526 | 2 | 0 | 1 | 0 | 1 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12521): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0032 | 0/0 | 12524 | 2 | 1 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12519): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0033 | 0/0 | 12524 | 2 | 1 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12519): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0034 | 0/0 | 12524 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12519): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0035 | 0/0 | 12523 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12518): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0038 | 0/0 | 12523 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12518): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0039 | 0/0 | 12522 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12517): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0040 | 0/0 | 12518 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12513): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0044 | 0/0 | 12519 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12514): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0045 | 0/0 | 12525 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12520): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0047 | 0/0 | 12526 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12521): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0048 | 0/0 | 12521 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12516): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0049 | 0/0 | 12520 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12515): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0050 | 0/0 | 12520 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12515): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0052 | 0/0 | 12517 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12512): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0053 | 0/0 | 12516 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12511): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0063 | 0/0 | 12521 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12516): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0064 | 0/0 | 12524 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12519): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0065 | 0/0 | 12524 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12519): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0066 | 0/0 | 12522 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12517): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0067 | 0/0 | 12522 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12517): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0068 | 0/0 | 12522 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12517): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0069 | 0/0 | 12523 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12518): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0070 | 0/0 | 12524 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12519): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0071 | 0/0 | 12528 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12523): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0072 | 0/0 | 12526 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12521): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0073 | 0/0 | 12525 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12520): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0074 | 0/0 | 12527 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12522): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0075 | 0/0 | 12523 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12518): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0076 | 0/0 | 12525 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12520): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0078 | 0/0 | 12519 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12514): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0092 | 0/0 | 12524 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12519): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0093 | 0/0 | 12525 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12520): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0094 | 0/0 | 12524 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12519): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0095 | 0/0 | 12525 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12520): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0096 | 0/0 | 12523 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12518): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0097 | 0/0 | 12522 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12517): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0098 | 0/0 | 12523 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12518): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0099 | 0/0 | 12522 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12517): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0100 | 0/0 | 12525 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12520): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0101 | 0/0 | 12524 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12519): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0102 | 0/0 | 12523 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12518): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0103 | 0/0 | 12526 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12521): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0104 | 0/0 | 12526 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12521): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0105 | 0/0 | 12525 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12520): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0106 | 0/0 | 12520 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12515): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0107 | 0/0 | 12519 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12514): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0110 | 0/0 | 12525 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12520): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0111 | 0/0 | 12524 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12519): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0113 | 0/0 | 12525 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12520): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0114 | 0/0 | 12525 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12520): Show |
chr18 | 69848274 | 69952873 |
a0001c0001t0115 | 0/0 | 12526 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12521): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0001 | 0/0 | 12526 | 18 | 1 | 8 | 6 | 0 | 3 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12521): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0002 | 0/0 | 12527 | 17 | 0 | 9 | 2 | 0 | 6 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12522): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0005 | 0/0 | 12522 | 9 | 8 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12517): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0007 | 0/0 | 12525 | 7 | 2 | 2 | 2 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12520): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0009 | 0/0 | 12528 | 5 | 0 | 2 | 2 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12523): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0010 | 0/0 | 12526 | 6 | 0 | 3 | 3 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12521): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0012 | 0/0 | 12523 | 4 | 4 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12518): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0013 | 0/0 | 12524 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12519): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0024 | 0/0 | 12521 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12516): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0025 | 0/0 | 12527 | 2 | 1 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12522): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0030 | 0/0 | 12526 | 2 | 0 | 0 | 2 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12521): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0031 | 0/0 | 12525 | 2 | 0 | 0 | 1 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12520): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0036 | 0/0 | 12524 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12519): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0037 | 0/0 | 12526 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12521): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0041 | 0/0 | 12524 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12519): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0042 | 0/0 | 12525 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12520): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0043 | 0/0 | 12525 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12520): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0046 | 0/0 | 12527 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12522): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0054 | 0/0 | 12523 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12518): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0055 | 0/0 | 12527 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12522): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0056 | 0/0 | 12526 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12521): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0057 | 0/0 | 12526 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12521): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0059 | 0/0 | 12522 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12517): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0060 | 0/0 | 12520 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12515): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0061 | 0/0 | 12522 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12517): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0062 | 0/0 | 12528 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12523): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0079 | 0/0 | 12526 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12521): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0080 | 0/0 | 12529 | 1 | 0 | 0 | 0 | 1 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12524): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0081 | 0/0 | 12529 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12524): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0082 | 0/0 | 12526 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12521): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0083 | 0/0 | 12526 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12521): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0084 | 0/0 | 12522 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12517): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0085 | 0/0 | 12508 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12503): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0086 | 0/1 | 12551 | 1 | 0 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12546): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0087 | 0/0 | 12529 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12524): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0088 | 0/0 | 12527 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12522): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0089 | 0/0 | 12527 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12522): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0090 | 0/0 | 12526 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12521): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0091 | 0/0 | 12526 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12521): Show |
chr18 | 69848274 | 69952873 |
a0002c0002t0112 | 0/0 | 12526 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12521): Show |
chr18 | 69848274 | 69952873 |
a0002c0004t0009 | 0/0 | 12528 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12523): Show |
chr18 | 69848274 | 69952873 |
a0002c0004t0058 | 0/0 | 12526 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12521): Show |
chr18 | 69848274 | 69952873 |
a0002c0009t0108 | 0/0 | 12524 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12519): Show |
chr18 | 69848274 | 69952873 |
a0003c0003t0011 | 0/0 | 12523 | 4 | 3 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12518): Show |
chr18 | 69848274 | 69952873 |
a0003c0003t0017 | 0/0 | 12525 | 3 | 0 | 2 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12520): Show |
chr18 | 69848274 | 69952873 |
a0003c0003t0018 | 0/0 | 12524 | 3 | 1 | 1 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12519): Show |
chr18 | 69848274 | 69952873 |
a0003c0003t0051 | 0/0 | 12524 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12519): Show |
chr18 | 69848274 | 69952873 |
a0003c0003t0077 | 0/0 | 12523 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12518): Show |
chr18 | 69848274 | 69952873 |
a0004c0006t0001 | 0/0 | 12526 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12521): Show |
chr18 | 69848274 | 69952873 |
a0005c0005t0009 | 0/0 | 12528 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12523): Show |
chr18 | 69848274 | 69952873 |
a0006c0008t0109 | 0/0 | 12522 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12517): Show |
chr18 | 69848274 | 69952873 |
a0007c0007t0011 | 0/0 | 12523 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | AGTGA others(12518): Show |
chr18 | 69848274 | 69952873 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0004g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0006g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0006g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0006g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0006g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0006g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0006g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0008g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0008g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0008g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0008g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0008g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0008g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0013g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0013g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0013g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0014g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0014g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0014g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0015g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0015g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0015g0076 | 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 |
a0001c0001t0019g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0019g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0019g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0020g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0020g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0021g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0021g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0022g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0022g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0023g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0023g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0026g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0026g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0027g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0027g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0028g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0028g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0029g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0029g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0032g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0032g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0033g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0033g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0034g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0034g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0035g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0035g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0038g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0039g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0040g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0044g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0045g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0047g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0048g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0049g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0050g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0052g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0053g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0063g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0064g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0065g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0066g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0067g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0068g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0069g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0070g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0071g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0072g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0073g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0074g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0075g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0076g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0078g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0092g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0093g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0094g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0095g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0096g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0097g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0098g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0099g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0100g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0101g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0102g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0103g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0104g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0105g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0106g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0107g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0110g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0111g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0113g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0114g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0115g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0005g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0007g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0007g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0007g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0007g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0007g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0009g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0009g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0009g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0009g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0009g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0010g0149 | 0/0 | 1 | 0 | 1 | 0 | 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 |
a0002c0002t0010g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0010g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0010g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0010g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0012g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0012g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0012g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0012g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0013g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0024g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0024g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0025g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0025g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0030g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0030g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0031g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0031g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0036g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0037g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0041g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0042g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0043g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0046g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0054g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0055g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0056g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0057g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0059g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0060g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0061g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0062g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0079g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0080g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0081g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0082g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0083g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0084g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0085g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0086g0191 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0087g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0088g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0089g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0090g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0091g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0112g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0004t0009g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0004t0058g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0009t0108g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0003c0003t0011g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0003c0003t0011g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0003c0003t0011g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0003c0003t0011g0081 | 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 |
a0003c0003t0018g0165 | 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 |
a0003c0003t0051g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0003c0003t0077g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0004c0006t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0005c0005t0009g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0006c0008t0109g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0007c0007t0011g0024 | 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 | t0029 | g0083 | EUR | GBR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0166 | EUR | GBR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00280 | hp1 | a0002 | c0002 | t0080 | g0154 | EUR | FIN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00280 | hp2 | a0001 | c0001 | t0008 | g0089 | EUR | FIN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00438 | hp1 | a0001 | c0001 | t0006 | g0113 | EAS | CHS | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00438 | hp2 | a0001 | c0001 | t0013 | g0122 | EAS | CHS | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00544 | hp1 | a0002 | c0002 | t0007 | g0039 | EAS | CHS | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00544 | hp2 | a0002 | c0002 | t0057 | g0043 | EAS | CHS | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00597 | hp1 | a0002 | c0002 | t0007 | g0041 | EAS | CHS | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00597 | hp2 | a0001 | c0001 | t0026 | g0092 | EAS | CHS | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0115 | EAS | CHS | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00609 | hp2 | a0001 | c0001 | t0006 | g0116 | EAS | CHS | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00621 | hp1 | a0002 | c0002 | t0085 | g0162 | EAS | CHS | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00621 | hp2 | a0001 | c0001 | t0004 | g0169 | EAS | CHS | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0155 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00639 | hp2 | a0001 | c0001 | t0029 | g0082 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0217 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0211 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00673 | hp1 | a0002 | c0002 | t0013 | g0205 | EAS | CHS | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00673 | hp2 | a0004 | c0006 | t0001 | g0210 | EAS | CHS | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00733 | hp1 | a0002 | c0002 | t0090 | g0200 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00733 | hp2 | a0001 | c0001 | t0003 | 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 | t0002 | g0215 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00738 | hp1 | a0001 | c0001 | t0008 | g0086 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00738 | hp2 | a0002 | c0002 | t0002 | g0126 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01069 | hp1 | a0001 | c0001 | t0099 | g0109 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0213 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0214 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01071 | hp2 | a0002 | c0004 | t0009 | g0136 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01074 | hp1 | a0001 | c0001 | t0008 | g0093 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01074 | hp2 | a0002 | c0002 | t0007 | g0040 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0238 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01081 | hp2 | a0002 | c0002 | t0025 | g0027 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01106 | hp1 | a0002 | c0002 | t0001 | 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 | t0060 | g0015 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0127 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0225 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0195 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01175 | hp1 | a0002 | c0002 | t0089 | g0235 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01175 | hp2 | a0002 | c0002 | t0009 | g0128 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01243 | hp1 | a0001 | c0001 | t0078 | g0135 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01243 | hp2 | a0003 | c0003 | t0051 | g0079 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01255 | hp1 | a0001 | c0001 | t0098 | g0106 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01255 | hp2 | a0002 | c0002 | t0005 | g0065 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0184 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01257 | hp1 | a0002 | c0002 | t0083 | g0119 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01257 | hp2 | a0001 | c0001 | t0097 | g0188 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0187 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01261 | hp1 | a0002 | c0002 | t0062 | g0090 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0152 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01346 | hp1 | a0001 | c0001 | t0103 | g0157 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01346 | hp2 | a0002 | c0002 | t0046 | g0070 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01358 | hp1 | a0001 | c0001 | t0032 | g0108 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0145 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01361 | hp1 | a0002 | c0002 | t0009 | g0193 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01361 | hp2 | a0001 | c0001 | t0033 | g0129 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0174 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01433 | hp2 | a0002 | c0002 | t0002 | g0151 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0156 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0130 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01884 | hp1 | a0002 | c0002 | t0112 | g0255 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01884 | hp2 | a0001 | c0001 | t0076 | g0057 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01891 | hp1 | a0001 | c0001 | t0034 | g0246 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01891 | hp2 | a0003 | c0003 | t0011 | g0074 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01952 | hp1 | a0002 | c0002 | t0042 | g0006 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01952 | hp2 | a0001 | c0001 | t0044 | g0004 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0139 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0175 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0140 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01981 | hp2 | a0002 | c0002 | t0007 | g0088 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0125 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01993 | hp2 | a0002 | c0002 | t0010 | g0150 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02004 | hp1 | a0002 | c0002 | t0010 | g0149 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0105 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02040 | hp1 | a0003 | c0003 | t0011 | g0045 | EAS | KHV | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0206 | EAS | KHV | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02055 | hp1 | a0005 | c0005 | t0009 | g0104 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02055 | hp2 | a0003 | c0003 | t0011 | g0081 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02074 | hp1 | a0001 | c0001 | t0100 | g0168 | EAS | KHV | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02074 | hp2 | a0002 | c0002 | t0081 | g0111 | EAS | KHV | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02129 | hp1 | a0001 | c0001 | t0004 | g0144 | EAS | KHV | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02129 | hp2 | a0001 | c0001 | t0004 | g0143 | EAS | KHV | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02132 | hp1 | a0002 | c0002 | t0010 | g0183 | EAS | KHV | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0171 | EAS | KHV | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02135 | hp1 | a0002 | c0002 | t0009 | g0179 | 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 | t0072 | g0100 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02145 | hp2 | a0001 | c0001 | t0050 | g0096 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02148 | hp1 | a0002 | c0002 | t0010 | g0164 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02148 | hp2 | a0003 | c0003 | t0018 | g0165 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02257 | hp1 | a0003 | c0003 | t0011 | g0078 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02257 | hp2 | a0001 | c0001 | t0028 | g0103 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02258 | hp1 | a0002 | c0004 | t0058 | g0091 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02258 | hp2 | a0001 | c0001 | t0022 | g0099 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02280 | hp1 | a0001 | c0001 | t0068 | g0030 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0142 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02300 | hp1 | a0002 | c0002 | t0002 | g0185 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02300 | hp2 | a0001 | c0001 | t0008 | g0012 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02451 | hp1 | a0001 | c0001 | t0045 | g0009 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02451 | hp2 | a0002 | c0002 | t0056 | g0028 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02523 | hp1 | a0001 | c0001 | t0094 | g0173 | EAS | KHV | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02523 | hp2 | a0002 | c0002 | t0087 | g0177 | EAS | KHV | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02602 | hp1 | a0001 | c0001 | t0003 | 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 | t0074 | g0054 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02615 | hp2 | a0001 | c0001 | t0047 | g0029 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02630 | hp1 | a0001 | c0001 | t0034 | g0247 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02630 | hp2 | a0002 | c0002 | t0005 | g0101 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02647 | hp1 | a0001 | c0001 | t0071 | g0098 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02647 | hp2 | a0001 | c0001 | t0049 | g0046 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0212 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0153 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02717 | hp1 | a0001 | c0001 | t0014 | g0052 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02717 | hp2 | a0002 | c0002 | t0005 | g0072 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02723 | hp1 | a0002 | c0002 | t0012 | g0051 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02723 | hp2 | a0001 | c0001 | t0110 | g0243 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02738 | hp1 | a0002 | c0002 | t0002 | 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 | t0012 | g0053 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02809 | hp2 | a0002 | c0002 | t0012 | g0075 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02886 | hp1 | a0002 | c0002 | t0005 | g0022 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02886 | hp2 | a0001 | c0001 | t0040 | g0008 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02895 | hp1 | a0001 | c0001 | t0111 | g0241 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02895 | hp2 | a0001 | c0001 | t0052 | g0017 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02896 | hp1 | a0002 | c0002 | t0024 | g0050 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02896 | hp2 | a0001 | c0001 | t0019 | g0250 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02897 | hp1 | a0002 | c0002 | t0024 | g0032 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02897 | hp2 | a0001 | c0001 | t0015 | g0016 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02922 | hp1 | a0002 | c0002 | t0007 | g0058 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02922 | hp2 | a0001 | c0001 | t0019 | g0248 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02965 | hp1 | a0001 | c0001 | t0021 | g0073 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02965 | hp2 | a0001 | c0001 | t0021 | g0067 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02976 | hp1 | a0001 | c0001 | t0035 | g0245 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02976 | hp2 | a0001 | c0001 | t0053 | g0033 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03017 | hp1 | a0001 | c0001 | t0102 | g0186 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0196 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03041 | hp1 | a0001 | c0001 | t0063 | g0080 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03041 | hp2 | a0001 | c0001 | t0107 | g0240 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03098 | hp1 | a0001 | c0001 | t0048 | 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 | t0022 | g0069 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03130 | hp2 | a0002 | c0002 | t0005 | g0060 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03139 | hp1 | a0001 | c0001 | t0020 | g0019 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03139 | hp2 | a0001 | c0001 | t0035 | g0244 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03195 | hp1 | a0006 | c0008 | t0109 | g0251 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03195 | hp2 | a0001 | c0001 | t0039 | g0010 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03209 | hp1 | a0001 | c0001 | t0027 | g0025 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03209 | hp2 | a0002 | c0009 | t0108 | g0242 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03225 | hp1 | a0002 | c0002 | t0061 | g0062 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03225 | hp2 | a0001 | c0001 | t0020 | g0023 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0198 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03239 | hp2 | a0001 | c0001 | t0006 | g0123 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03453 | hp1 | a0001 | c0001 | t0014 | g0018 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03453 | hp2 | a0002 | c0002 | t0005 | g0048 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03486 | hp1 | a0001 | c0001 | t0069 | g0047 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03486 | hp2 | a0001 | c0001 | t0073 | g0014 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0167 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0228 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0236 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03492 | hp2 | a0002 | c0002 | t0002 | g0229 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03516 | hp1 | a0002 | c0002 | t0005 | g0031 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03516 | hp2 | a0002 | c0002 | t0005 | g0059 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03540 | hp1 | a0001 | c0001 | t0106 | g0239 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03540 | hp2 | a0001 | c0001 | t0067 | g0071 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03579 | hp1 | a0002 | c0002 | t0054 | g0061 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03579 | hp2 | a0001 | c0001 | t0015 | g0034 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03654 | hp1 | a0001 | c0001 | t0013 | g0160 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0178 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0131 | SAS | STU | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0204 | SAS | STU | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03710 | hp1 | a0002 | c0002 | t0079 | g0190 | 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 | t0031 | g0237 | SAS | BEB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03927 | hp2 | a0002 | c0002 | t0041 | g0011 | SAS | BEB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG04115 | hp1 | a0001 | c0001 | t0064 | g0087 | SAS | STU | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG04115 | hp2 | a0002 | c0002 | t0009 | g0224 | SAS | STU | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0216 | SAS | BEB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG04184 | hp2 | a0001 | c0001 | t0096 | g0197 | SAS | BEB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0163 | SAS | STU | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG04199 | hp2 | a0002 | c0002 | t0082 | g0181 | SAS | STU | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG04204 | hp1 | a0002 | c0002 | t0007 | g0037 | SAS | STU | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG04204 | hp2 | a0001 | c0001 | t0026 | g0042 | SAS | STU | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0159 | SAS | STU | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0180 | SAS | STU | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18522 | hp1 | a0001 | c0001 | t0038 | g0007 | AFR | YRI | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18522 | hp2 | a0002 | c0002 | t0059 | g0035 | AFR | YRI | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | CHB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18747 | hp2 | a0001 | c0001 | t0004 | g0112 | EAS | CHB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18906 | hp1 | a0001 | c0001 | t0023 | g0097 | AFR | YRI | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18906 | hp2 | a0002 | c0002 | t0005 | g0020 | AFR | YRI | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18940 | hp1 | a0002 | c0002 | t0009 | g0146 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18940 | hp2 | a0001 | c0001 | t0092 | g0194 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0161 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0132 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18951 | hp1 | a0002 | c0002 | t0037 | g0002 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18951 | hp2 | a0002 | c0002 | t0036 | g0003 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18952 | hp1 | a0001 | c0001 | t0065 | g0038 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18952 | hp2 | a0002 | c0002 | t0091 | g0133 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18956 | hp1 | a0001 | c0001 | t0006 | g0232 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18956 | hp2 | a0001 | c0001 | t0013 | g0192 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18960 | hp1 | a0002 | c0002 | t0084 | g0138 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18960 | hp2 | a0001 | c0001 | t0104 | g0121 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18962 | hp1 | a0001 | c0001 | t0113 | g0254 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18962 | hp2 | a0001 | c0001 | t0115 | g0253 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18966 | hp1 | a0002 | c0002 | t0010 | g0172 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0189 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18968 | hp1 | a0002 | c0002 | t0043 | g0005 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18971 | hp1 | a0002 | c0002 | t0010 | g0170 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18971 | hp2 | a0003 | c0003 | t0077 | g0137 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18984 | hp1 | a0002 | c0002 | t0088 | g0233 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18984 | hp2 | a0001 | c0001 | t0006 | g0231 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18990 | hp1 | a0001 | c0001 | t0004 | g0114 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18990 | hp2 | a0001 | c0001 | t0114 | g0252 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18995 | hp1 | a0001 | c0001 | t0006 | g0158 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18995 | hp2 | a0001 | c0001 | t0095 | g0209 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19003 | hp1 | a0001 | c0001 | t0006 | g0141 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19003 | hp2 | a0001 | c0001 | t0004 | g0182 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19006 | hp1 | a0001 | c0001 | t0105 | g0208 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19006 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19010 | hp1 | a0002 | c0002 | t0031 | g0148 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19010 | hp2 | a0001 | c0001 | t0093 | g0176 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19060 | hp1 | a0001 | c0001 | t0006 | g0230 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19060 | hp2 | a0002 | c0002 | t0030 | g0227 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19068 | hp2 | a0001 | c0001 | t0004 | g0120 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19090 | hp1 | a0002 | c0002 | t0030 | g0199 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19090 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19240 | hp1 | a0001 | c0001 | t0070 | g0013 | AFR | YRI | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19240 | hp2 | a0001 | c0001 | t0023 | g0066 | AFR | YRI | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA20129 | hp1 | a0001 | c0001 | t0014 | g0021 | AFR | ASW | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA20129 | hp2 | a0001 | c0001 | t0033 | g0134 | AFR | ASW | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA20905 | hp1 | a0001 | c0001 | t0101 | g0202 | SAS | GIH | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA20905 | hp2 | a0001 | c0001 | t0008 | 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 | t0027 | g0068 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02486 | hp1 | a0002 | c0002 | t0025 | g0026 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02486 | hp2 | a0002 | c0002 | t0007 | g0095 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02559 | hp1 | a0001 | c0001 | t0019 | g0249 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02559 | hp2 | a0001 | c0001 | t0075 | g0055 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03471 | hp1 | a0001 | c0001 | t0066 | g0102 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03471 | hp2 | a0007 | c0007 | t0011 | g0024 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG06807 | hp1 | a0001 | c0001 | t0028 | g0064 | AFR | USA | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG06807 | hp2 | a0001 | c0001 | t0008 | g0085 | AFR | USA | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA20300 | hp1 | a0002 | c0002 | t0012 | g0056 | AFR | USA | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA20300 | hp2 | a0001 | c0001 | t0032 | g0107 | AFR | USA | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA21309 | hp1 | a0002 | c0002 | t0055 | g0063 | AFR | LWK | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA21309 | hp2 | a0001 | c0001 | t0008 | g0036 | AFR | LWK | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
homoSapiens | chm13v2 | a0002 | c0002 | t0086 | g0191 | REF | REF | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
homoSapiens | grch38p0 | a0001 | c0001 | t0015 | g0076 | REF | REF | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
view | 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 | a0002 a0004 a0005 |
107 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(104): 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 | a0003 a0007 |
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 | a0004 | 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 | a0005 | 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 |
view | 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 |
view | 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 | a0001c0001t0029 a0001c0001t0074 a0001c0001t0103 |
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 | a0001c0001t0071 a0001c0001t0073 |
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 | 4 | a0001c0001t0006 a0001c0001t0104 a0001c0001t0105 others(1): 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 | a0001c0001t0022 a0001c0001t0040 a0001c0001t0078 |
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 | a0001c0001t0047 | 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 | 14 | a0001c0001t0019 a0001c0001t0023 a0001c0001t0028 others(11): 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 | a0002c0002t0081 | 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 | 4 | a0001c0001t0006 a0001c0001t0104 a0001c0001t0105 others(1): 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 | 110 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(107): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): 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 | a0001c0001t0063 a0006c0008t0109 |
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 | 104 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(101): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): 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 | 40 | a0002c0002t0001 a0002c0002t0002 a0002c0002t0005 others(37): Show |
102 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(99): 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 | 3 | a0001c0001t0006 a0001c0001t0104 a0001c0001t0115 |
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 | a0001c0001t0063 a0006c0008t0109 |
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 | a0001c0001t0035 a0001c0001t0067 |
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 | 66 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(63): 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 | 13 | a0001c0001t0019 a0001c0001t0023 a0001c0001t0028 others(10): 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 | a0001c0001t0094 | 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 | 4 | a0001c0001t0006 a0001c0001t0104 a0001c0001t0105 others(1): 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 | 4 | a0001c0001t0006 a0001c0001t0104 a0001c0001t0105 others(1): 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 | 105 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(102): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): 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 | a0002c0002t0060 | 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 | 4 | a0001c0001t0006 a0001c0001t0104 a0001c0001t0105 others(1): 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 | 4 | a0001c0001t0006 a0001c0001t0104 a0001c0001t0105 others(1): 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 | 2 | a0002c0002t0030 a0002c0002t0057 |
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 | a0001c0001t0063 a0006c0008t0109 |
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 | 66 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(63): 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 | a0001c0001t0048 a0001c0001t0049 a0001c0001t0050 |
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 | a0002c0002t0001 | 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 | 41 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(38): 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 | a0001c0001t0076 | 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 | a0001c0001t0111 | 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 | a0001c0001t0066 | 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 | 4 | a0001c0001t0006 a0001c0001t0104 a0001c0001t0105 others(1): 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 | a0001c0001t0096 | 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 | a0002c0002t0082 | 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 | 110 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(107): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): 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 | 41 | a0002c0002t0001 a0002c0002t0002 a0002c0002t0005 others(38): Show |
104 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(101): 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 | 54 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(51): 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 | a0001c0001t0048 a0001c0001t0049 a0001c0001t0050 |
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 | 1 | a0001c0001t0014 | 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 | a0001c0001t0063 a0006c0008t0109 |
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 | 48 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(45): 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 | 28 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(25): 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 | a0002c0002t0083 | 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 | a0001c0001t0029 a0001c0001t0045 a0001c0001t0071 others(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 | a0002c0002t0084 | 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 | 42 | a0002c0002t0001 a0002c0002t0002 a0002c0002t0005 others(39): Show |
105 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(102): 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 | a0001c0001t0069 | 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 | a0001c0001t0050 | 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 | 46 | a0001c0001t0006 a0001c0001t0104 a0001c0001t0105 others(43): Show |
116 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(113): 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 | a0001c0001t0064 a0001c0001t0065 a0001c0001t0093 others(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 | 6 | a0001c0001t0045 a0001c0001t0073 a0001c0001t0076 others(3): 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 | 8 | a0001c0001t0047 a0001c0001t0072 a0001c0001t0103 others(5): 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 | 15 | a0001c0001t0029 a0002c0002t0001 a0002c0002t0007 others(12): 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 | 7 | a0001c0001t0071 a0001c0001t0074 a0002c0002t0002 others(4): 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 | 6 | a0002c0002t0009 a0002c0002t0037 a0002c0002t0055 others(3): 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 | a0002c0002t0025 a0002c0002t0062 a0002c0002t0080 others(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 | CT | C | 21 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(18): 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 | a0001c0001t0021 a0001c0001t0049 a0001c0001t0050 others(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 | a0002c0002t0085 | 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 | 4 | a0001c0001t0006 a0001c0001t0104 a0001c0001t0105 others(1): 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 | a0001c0001t0068 | 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 | 42 | a0002c0002t0001 a0002c0002t0002 a0002c0002t0005 others(39): Show |
105 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(102): 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 | 110 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(107): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): 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 | a0001c0001t0032 a0001c0001t0098 a0001c0001t0099 |
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 | a0001c0001t0027 | 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 | 4 | a0001c0001t0006 a0001c0001t0104 a0001c0001t0105 others(1): 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 | 42 | a0002c0002t0001 a0002c0002t0002 a0002c0002t0005 others(39): Show |
105 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(102): 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 | 64 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(61): 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 | 38 | a0002c0002t0001 a0002c0002t0002 a0002c0002t0007 others(35): Show |
93 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(90): 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 | 3 | a0001c0001t0006 a0001c0001t0105 a0001c0001t0115 |
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 | a0001c0001t0104 | 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 | 3 | a0001c0001t0006 a0001c0001t0105 a0001c0001t0115 |
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 | 3 | a0001c0001t0006 a0001c0001t0105 a0001c0001t0115 |
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 | 3 | a0001c0001t0006 a0001c0001t0105 a0001c0001t0115 |
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 | 3 | a0001c0001t0006 a0001c0001t0105 a0001c0001t0115 |
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 | a0001c0001t0004 a0001c0001t0026 a0001c0001t0044 others(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 | a0001c0001t0029 a0001c0001t0045 a0001c0001t0071 others(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 | a0002c0002t0085 | 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 | 36 | a0001c0001t0014 a0001c0001t0019 a0001c0001t0021 others(33): 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 | a0001c0001t0029 a0001c0001t0074 a0001c0001t0103 |
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 | 4 | a0001c0001t0006 a0001c0001t0104 a0001c0001t0105 others(1): 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 | a0001c0001t0029 a0001c0001t0074 a0001c0001t0103 |
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 | 42 | a0002c0002t0001 a0002c0002t0002 a0002c0002t0005 others(39): Show |
105 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(102): 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 | a0002c0002t0024 | 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 | a0002c0002t0061 | 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 | 110 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(107): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): 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 | 64 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(61): 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 | 42 | a0002c0002t0001 a0002c0002t0002 a0002c0002t0005 others(39): Show |
105 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(102): 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 | 4 | a0001c0001t0006 a0001c0001t0104 a0001c0001t0105 others(1): 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 | a0001c0001t0029 a0001c0001t0074 a0001c0001t0103 |
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 | a0001c0001t0023 a0001c0001t0034 a0001c0001t0070 |
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 | 27 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(24): 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 | 42 | a0002c0002t0001 a0002c0002t0002 a0002c0002t0005 others(39): Show |
105 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(102): 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 | 110 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(107): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): 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 | 4 | a0001c0001t0006 a0001c0001t0104 a0001c0001t0105 others(1): 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 | 4 | a0001c0001t0006 a0001c0001t0104 a0001c0001t0105 others(1): 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 | a0001c0001t0020 | 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 | a0001c0001t0014 a0001c0001t0047 a0001c0001t0048 others(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 | 8 | a0001c0001t0014 a0001c0001t0021 a0001c0001t0039 others(5): 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 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(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 | a0001c0001t0003 a0001c0001t0092 a0001c0001t0094 |
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 | a0002c0002t0062 | 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 | a0002c0002t0001 a0002c0002t0002 a0002c0002t0009 others(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 |
18 | a0002c0002t0001 a0002c0002t0002 a0002c0002t0007 others(15): Show |
27 | HG00280.hp1 HG00642.hp1 HG00733.hp1 others(24): 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 | a0002c0002t0001 a0002c0002t0002 a0002c0002t0005 others(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 | a0002c0002t0002 a0002c0002t0005 a0002c0002t0007 others(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 | a0002c0002t0002 a0002c0002t0005 a0002c0002t0009 others(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 | a0002c0002t0002 a0002c0002t0054 |
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 | a0002c0002t0001 a0002c0002t0012 a0002c0002t0030 others(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 | a0001c0001t0019 a0001c0001t0023 a0001c0001t0028 others(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 | a0002c0002t0001 a0002c0002t0002 |
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 | a0002c0002t0081 | 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 | a0002c0002t0001 a0002c0002t0002 a0004c0006t0001 |
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 | a0002c0002t0001 a0002c0002t0009 |
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 | a0002c0002t0001 a0002c0002t0031 |
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 | a0002c0002t0001 a0002c0002t0060 |
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 | a0001c0001t0006 a0001c0001t0029 a0001c0001t0045 others(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 | a0001c0001t0014 a0001c0001t0021 a0001c0001t0039 |
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 | a0001c0001t0038 | 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 | a0001c0001t0029 a0001c0001t0074 a0001c0001t0103 |
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 | a0001c0001t0038 | 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 | 7 | a0002c0002t0010 a0002c0002t0037 a0002c0002t0042 others(4): 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 | 93 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(90): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): 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 | 47 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(44): 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 | 4 | a0001c0001t0006 a0001c0001t0104 a0001c0001t0105 others(1): 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 | a0002c0002t0089 a0002c0002t0090 |
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 | a0002c0002t0091 | 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 | 4 | a0001c0001t0006 a0001c0001t0104 a0001c0001t0105 others(1): 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 | a0001c0001t0092 | 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 | 42 | a0002c0002t0001 a0002c0002t0002 a0002c0002t0005 others(39): Show |
105 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(102): 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 | a0001c0001t0045 a0001c0001t0076 |
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 | a0002c0002t0079 | 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 | a0001c0001t0029 a0001c0001t0045 a0001c0001t0071 others(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 | a0002c0002t0062 | 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 | a0002c0002t0043 | 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 | 46 | a0001c0001t0006 a0001c0001t0104 a0001c0001t0105 others(43): Show |
116 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(113): 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 | a0001c0001t0102 | 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 | 4 | a0001c0001t0006 a0001c0001t0104 a0001c0001t0105 others(1): 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 | a0001c0001t0034 | 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 | a0001c0001t0063 a0006c0008t0109 |
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 | a0001c0001t0029 a0001c0001t0045 a0001c0001t0071 others(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 | a0001c0001t0075 | 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 | 45 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(42): 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 | a0001c0001t0045 a0001c0001t0076 |
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 | 4 | a0001c0001t0006 a0001c0001t0104 a0001c0001t0105 others(1): 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 | 58 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(55): Show |
148 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(145): 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 | a0001c0001t0019 a0001c0001t0034 a0001c0001t0035 others(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 | a0001c0001t0038 a0001c0001t0039 a0001c0001t0040 others(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 |
view | 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 | a0001c0001t0093g0176 | 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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | 116 | a0001c0001t0006g0113 a0001c0001t0006g0116 a0001c0001t0006g0123 others(113): Show |
117 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(114): 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 | a0001c0001t0053g0033 | 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 | a0001c0001t0106g0239 | 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 | 105 | a0002c0002t0001g0105 a0002c0002t0001g0115 a0002c0002t0001g0117 others(102): Show |
106 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(103): 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 | a0001c0001t0071g0098 a0001c0001t0072g0100 a0001c0001t0073g0014 |
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 | a0001c0001t0063g0080 a0006c0008t0109g0251 |
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 | a0001c0001t0029g0083 a0001c0001t0074g0054 a0001c0001t0103g0157 |
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 | a0002c0002t0002g0130 | 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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | a0001c0001t0006g0123 | 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 | a0001c0001t0006g0113 a0001c0001t0006g0116 a0001c0001t0006g0141 others(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 | a0001c0001t0105g0208 | 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 | a0001c0001t0006g0113 a0001c0001t0006g0116 a0001c0001t0006g0123 others(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 | a0002c0002t0001g0204 a0002c0002t0005g0020 a0002c0002t0005g0022 others(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 | a0001c0001t0063g0080 | 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 | a0002c0002t0002g0001 a0002c0002t0002g0126 a0002c0002t0002g0130 others(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 | a0001c0001t0029g0082 a0001c0001t0029g0083 a0001c0001t0074g0054 others(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 | a0001c0001t0006g0113 a0001c0001t0006g0116 a0001c0001t0006g0123 others(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 | 215 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(212): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.886-1399C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69865838 | |||||||
chr18:69866018 | GA | G | 177 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(174): Show |
178 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.885+1338delT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69866018 | |||||||
chr18:69866096 | T | C | 55 | a0002c0002t0001g0105 a0002c0002t0001g0131 a0002c0002t0001g0140 others(52): Show |
56 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(53): 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 | a0001c0001t0023g0066 a0001c0001t0023g0097 a0001c0001t0034g0246 others(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 | 115 | a0001c0001t0006g0113 a0001c0001t0006g0116 a0001c0001t0006g0123 others(112): Show |
116 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(113): 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 | a0001c0001t0006g0113 a0001c0001t0006g0116 a0001c0001t0006g0123 others(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 | a0001c0001t0068g0030 | 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 | a0001c0001t0033g0134 | 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 | 118 | a0001c0001t0004g0212 a0001c0001t0006g0113 a0001c0001t0006g0116 others(115): Show |
119 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(116): 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 | a0006c0008t0109g0251 | 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 | a0002c0002t0007g0058 | 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 | a0001c0001t0029g0082 a0001c0001t0029g0083 a0001c0001t0074g0054 others(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 | a0001c0001t0004g0112 a0001c0001t0004g0114 a0001c0001t0004g0120 others(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 | a0001c0001t0038g0007 | 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 | a0001c0001t0045g0009 | 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 | a0006c0008t0109g0251 | 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 | a0001c0001t0107g0240 a0002c0002t0001g0204 a0002c0002t0005g0020 others(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 | a0001c0001t0107g0240 a0002c0002t0001g0204 a0002c0002t0005g0020 others(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 | a0001c0001t0028g0103 a0001c0001t0066g0102 a0003c0003t0011g0045 |
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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | a0001c0001t0070g0013 | 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 | a0001c0001t0107g0240 a0002c0002t0001g0204 a0002c0002t0005g0020 others(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 | a0002c0002t0012g0075 | 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 | a0001c0001t0003g0211 a0001c0001t0006g0113 a0001c0001t0006g0116 others(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 | 102 | a0001c0001t0016g0077 a0001c0001t0033g0129 a0001c0001t0033g0134 others(99): Show |
103 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(100): 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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | a0001c0001t0029g0082 a0001c0001t0029g0083 a0001c0001t0069g0047 others(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 | a0001c0001t0048g0049 a0001c0001t0049g0046 a0001c0001t0050g0096 others(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 | a0001c0001t0028g0103 a0001c0001t0066g0102 |
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 | a0001c0001t0050g0096 a0001c0001t0107g0240 a0002c0002t0001g0204 others(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 | a0001c0001t0006g0123 | 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 | a0003c0003t0017g0221 a0003c0003t0018g0165 a0003c0003t0018g0218 others(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 | 81 | a0001c0001t0102g0186 a0002c0002t0001g0105 a0002c0002t0001g0115 others(78): Show |
82 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(79): 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 | a0001c0001t0035g0244 a0001c0001t0035g0245 a0001c0001t0067g0071 others(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 | a0001c0001t0050g0096 a0001c0001t0107g0240 a0002c0002t0001g0204 others(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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | a0002c0002t0084g0138 | 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 | a0001c0001t0070g0013 | 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 | a0001c0001t0006g0113 a0001c0001t0006g0116 a0001c0001t0006g0123 others(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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0035g0244 a0001c0001t0035g0245 a0001c0001t0067g0071 |
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 | a0006c0008t0109g0251 | 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 | a0001c0001t0035g0244 a0001c0001t0035g0245 |
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 | a0002c0002t0002g0159 a0002c0002t0009g0224 a0002c0002t0083g0119 |
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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | a0001c0001t0035g0244 a0001c0001t0035g0245 a0001c0001t0067g0071 |
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 | a0003c0003t0011g0045 a0003c0003t0011g0074 a0003c0003t0011g0078 others(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 | 81 | a0001c0001t0102g0186 a0002c0002t0001g0105 a0002c0002t0001g0115 others(78): Show |
82 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(79): 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 | a0001c0001t0050g0096 a0001c0001t0107g0240 a0002c0002t0001g0204 others(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 | 70 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(67): Show |
70 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.831-2862dupA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69870272 | |||||||
chr18:69870272 | C | CTT | 9 | a0001c0001t0003g0211 a0001c0001t0008g0093 a0001c0001t0013g0192 others(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 | a0001c0001t0006g0113 a0001c0001t0006g0116 a0001c0001t0006g0123 others(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 | a0001c0001t0021g0067 a0001c0001t0021g0073 a0001c0001t0039g0010 others(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 | a0001c0001t0006g0113 a0001c0001t0006g0116 a0001c0001t0006g0123 others(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 | a0003c0003t0011g0045 a0003c0003t0011g0074 a0003c0003t0011g0078 others(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 | a0002c0009t0108g0242 | 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 | a0001c0001t0003g0187 a0001c0001t0097g0188 |
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 | a0001c0001t0050g0096 a0001c0001t0107g0240 a0002c0002t0001g0204 others(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 | a0001c0001t0048g0049 a0001c0001t0049g0046 a0001c0001t0063g0080 |
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 | a0002c0002t0001g0175 a0002c0002t0002g0174 a0002c0002t0007g0088 others(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 | a0001c0001t0103g0157 | 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 | a0002c0002t0031g0237 | 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 | a0001c0001t0064g0087 | 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 | 241 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(238): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): 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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 |
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 | a0001c0001t0073g0014 | 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 | a0002c0002t0001g0142 | 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 | a0001c0001t0023g0066 a0001c0001t0023g0097 a0001c0001t0034g0246 others(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 | a0002c0002t0001g0105 | 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 | a0002c0002t0001g0105 | 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 | 64 | a0001c0001t0003g0139 a0001c0001t0004g0112 a0001c0001t0004g0114 others(61): Show |
64 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(61): 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 | a0001c0001t0023g0066 a0001c0001t0023g0097 a0001c0001t0034g0246 others(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 | a0001c0001t0003g0124 a0001c0001t0003g0153 a0001c0001t0003g0156 others(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 | a0001c0001t0003g0187 a0001c0001t0003g0216 a0001c0001t0004g0207 others(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 | a0001c0001t0003g0167 a0001c0001t0004g0169 a0001c0001t0019g0248 others(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 | a0001c0001t0003g0198 a0001c0001t0027g0025 a0001c0001t0050g0096 others(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 | a0002c0002t0005g0059 a0002c0002t0012g0056 |
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 | a0001c0001t0074g0054 | 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 | a0002c0002t0010g0149 | 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 | a0002c0002t0001g0222 a0002c0002t0002g0130 a0002c0002t0087g0177 |
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 | a0001c0001t0003g0213 a0001c0001t0026g0042 a0001c0001t0032g0108 others(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 | a0001c0001t0003g0195 a0002c0002t0005g0060 |
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 | a0002c0002t0001g0105 | 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 | a0002c0002t0001g0219 a0002c0002t0002g0215 a0002c0002t0082g0181 |
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 | a0003c0003t0011g0045 a0003c0003t0011g0074 a0003c0003t0011g0078 others(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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 others(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 | a0001c0001t0003g0187 a0001c0001t0097g0188 |
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 | 81 | a0001c0001t0102g0186 a0002c0002t0001g0105 a0002c0002t0001g0115 others(78): Show |
82 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(79): 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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 others(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 | a0003c0003t0011g0045 a0003c0003t0011g0074 a0003c0003t0011g0078 others(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 | a0001c0001t0038g0007 | 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 | a0002c0002t0056g0028 | 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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 others(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 | a0001c0001t0028g0064 a0001c0001t0069g0047 a0001c0001t0110g0243 others(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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | a0001c0001t0045g0009 a0001c0001t0076g0057 |
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 | 241 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(238): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): 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 | a0001c0001t0048g0049 a0001c0001t0049g0046 a0001c0001t0050g0096 others(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 | a0001c0001t0050g0096 a0001c0001t0107g0240 a0002c0002t0001g0204 others(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 | a0002c0002t0001g0140 a0002c0002t0001g0152 a0002c0002t0002g0151 |
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 | a0001c0001t0048g0049 a0001c0001t0049g0046 a0001c0001t0050g0096 others(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 | a0001c0001t0050g0096 a0001c0001t0107g0240 a0002c0002t0001g0204 others(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 | a0001c0001t0050g0096 a0001c0001t0107g0240 a0002c0002t0001g0204 others(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 | a0006c0008t0109g0251 | 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 | a0003c0003t0017g0221 a0003c0003t0018g0165 a0003c0003t0018g0218 others(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 | a0002c0009t0108g0242 | 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 | a0001c0001t0003g0124 a0001c0001t0003g0216 a0001c0001t0008g0086 |
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 | a0001c0001t0048g0049 a0001c0001t0049g0046 a0001c0001t0063g0080 |
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 | 240 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(237): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): 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 | a0002c0002t0046g0070 | 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 | a0001c0001t0003g0225 | 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 | a0003c0003t0011g0045 a0003c0003t0011g0074 a0003c0003t0011g0078 others(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 | a0002c0002t0001g0118 | 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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | a0001c0001t0004g0207 | 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 | a0002c0002t0081g0111 | 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 | a0002c0002t0009g0128 | 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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | a0002c0002t0082g0181 | 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 | a0003c0003t0011g0045 a0003c0003t0011g0074 a0003c0003t0011g0078 others(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 | a0001c0001t0048g0049 a0001c0001t0049g0046 a0001c0001t0063g0080 |
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 | a0006c0008t0109g0251 | 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 | a0001c0001t0035g0244 a0001c0001t0035g0245 a0001c0001t0067g0071 |
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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | a0001c0001t0038g0007 | 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 | a0003c0003t0011g0045 a0003c0003t0011g0074 a0003c0003t0011g0078 others(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 | a0001c0001t0006g0113 a0001c0001t0006g0116 a0001c0001t0006g0123 others(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 | a0002c0002t0084g0138 | 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 | a0001c0001t0068g0030 a0002c0002t0005g0031 |
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 | a0001c0001t0048g0049 a0001c0001t0049g0046 a0001c0001t0063g0080 others(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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | a0001c0001t0006g0113 a0001c0001t0006g0116 a0001c0001t0006g0123 others(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 | a0001c0001t0003g0139 a0001c0001t0003g0163 a0001c0001t0004g0120 others(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 | a0001c0001t0003g0124 a0001c0001t0003g0156 a0001c0001t0003g0166 others(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 | a0001c0001t0003g0153 a0001c0001t0102g0186 a0002c0002t0001g0105 others(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 | a0001c0001t0008g0086 | 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 | a0001c0001t0038g0007 | 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 | a0001c0001t0098g0106 | 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 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(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 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(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 | a0001c0001t0021g0073 a0001c0001t0039g0010 |
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 | a0002c0002t0012g0053 a0002c0002t0059g0035 |
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 | a0002c0002t0007g0039 | 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 | a0002c0002t0079g0190 | 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 | 66 | a0001c0001t0006g0116 a0002c0002t0001g0105 a0002c0002t0001g0117 others(63): Show |
67 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(64): 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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | a0001c0001t0021g0067 a0001c0001t0048g0049 a0001c0001t0049g0046 others(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 | a0001c0001t0023g0066 | 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 | a0001c0001t0004g0132 a0001c0001t0006g0113 a0001c0001t0006g0116 others(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 | a0001c0001t0014g0052 | 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 | a0002c0002t0054g0061 | 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 | a0001c0001t0021g0067 | 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 | a0002c0002t0001g0142 | 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 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(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 | a0001c0001t0004g0132 a0001c0001t0006g0113 a0001c0001t0006g0116 others(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 | a0001c0001t0014g0021 a0001c0001t0029g0082 a0001c0001t0029g0083 others(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 | a0001c0001t0065g0038 | 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 | 75 | a0001c0001t0102g0186 a0002c0002t0001g0105 a0002c0002t0001g0115 others(72): Show |
76 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(73): 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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(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 | a0001c0001t0004g0120 a0001c0001t0004g0182 |
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 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(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 | a0001c0001t0004g0125 a0001c0001t0004g0127 a0001c0001t0004g0169 others(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 | a0002c0002t0060g0015 | 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 | 75 | a0001c0001t0102g0186 a0002c0002t0001g0105 a0002c0002t0001g0115 others(72): Show |
76 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(73): 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 | a0001c0001t0004g0132 a0001c0001t0006g0113 a0001c0001t0006g0116 others(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 | a0006c0008t0109g0251 | 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 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(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 | a0002c0002t0025g0026 a0002c0002t0025g0027 a0002c0002t0056g0028 |
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 | a0001c0001t0033g0134 | 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 | a0002c0002t0001g0117 a0002c0002t0002g0110 |
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 | a0001c0001t0004g0132 a0001c0001t0006g0113 a0001c0001t0006g0116 others(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 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(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 | a0001c0001t0033g0134 | 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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | a0001c0001t0003g0220 | 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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | a0001c0001t0050g0096 a0001c0001t0068g0030 a0001c0001t0107g0240 others(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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | a0002c0002t0010g0183 | 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 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(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 | a0001c0001t0113g0254 | 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 | a0001c0001t0014g0018 a0001c0001t0028g0064 a0001c0001t0110g0243 others(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 | a0002c0002t0012g0075 | 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 | 241 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(238): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): 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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | a0001c0001t0027g0025 a0001c0001t0027g0068 |
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 | a0001c0001t0006g0123 | 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 | a0002c0002t0001g0140 | 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 | a0001c0001t0050g0096 a0001c0001t0068g0030 a0001c0001t0107g0240 others(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 | a0001c0001t0078g0135 | 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 | a0006c0008t0109g0251 | 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 | a0001c0001t0107g0240 a0002c0002t0001g0204 a0002c0002t0041g0011 others(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 | a0001c0001t0050g0096 a0001c0001t0068g0030 a0002c0002t0005g0031 others(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 | a0001c0001t0023g0066 a0001c0001t0023g0097 a0001c0001t0035g0244 others(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 | a0001c0001t0021g0067 a0001c0001t0021g0073 a0001c0001t0034g0246 others(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 | a0001c0001t0004g0132 a0001c0001t0006g0113 a0001c0001t0006g0116 others(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 | a0001c0001t0115g0253 | 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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | a0001c0001t0003g0167 a0001c0001t0004g0212 a0001c0001t0027g0025 others(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 | a0001c0001t0038g0007 a0002c0009t0108g0242 |
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 | |||||||
chr18:69880353 | A | AAAGGAAG others(5): Show |
9 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0195 others(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 | a0001c0001t0032g0107 a0001c0001t0032g0108 a0001c0001t0098g0106 others(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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | a0001c0001t0102g0186 a0002c0002t0001g0105 a0002c0002t0001g0115 others(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 | a0002c0002t0002g0236 | 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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | a0001c0001t0022g0099 a0001c0001t0078g0135 |
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 | a0001c0001t0004g0132 a0001c0001t0006g0113 a0001c0001t0006g0116 others(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 | a0002c0002t0001g0217 a0002c0002t0001g0238 |
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 | a0001c0001t0102g0186 a0002c0002t0002g0155 |
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 | a0001c0001t0014g0052 a0001c0001t0047g0029 |
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 | a0001c0001t0021g0067 a0001c0001t0048g0049 a0001c0001t0049g0046 others(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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | 77 | a0001c0001t0003g0163 a0001c0001t0013g0160 a0001c0001t0016g0077 others(74): Show |
78 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(75): 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 | a0001c0001t0004g0132 a0001c0001t0006g0113 a0001c0001t0006g0116 others(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 | a0001c0001t0050g0096 a0001c0001t0068g0030 a0001c0001t0107g0240 others(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 | 237 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): 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 | a0002c0002t0002g0159 | 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 | a0002c0009t0108g0242 | 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 | 219 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): 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 | a0001c0001t0003g0184 | 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 | 156 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): 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 | a0001c0001t0038g0007 | 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 | a0001c0001t0038g0007 | 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 | 202 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(199): Show |
203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): 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 | a0001c0001t0006g0113 a0001c0001t0006g0116 a0001c0001t0006g0141 others(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 | a0001c0001t0035g0244 a0001c0001t0035g0245 a0001c0001t0067g0071 |
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 | a0001c0001t0014g0021 | 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 | a0002c0002t0030g0227 | 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 | a0002c0002t0030g0199 a0002c0002t0030g0227 a0002c0002t0057g0043 |
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 | a0001c0001t0023g0066 a0001c0001t0023g0097 a0001c0001t0034g0246 others(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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(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 | a0001c0001t0105g0208 | 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 | 237 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): 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 | a0001c0001t0113g0254 | 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 | a0001c0001t0021g0067 | 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 | a0001c0001t0014g0021 | 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 | 159 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(156): Show |
160 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(157): 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 | a0002c0009t0108g0242 | 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 | 146 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(143): Show |
147 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(144): 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 | a0001c0001t0048g0049 a0001c0001t0049g0046 a0001c0001t0063g0080 |
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 | a0001c0001t0008g0036 | 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 | 150 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(147): Show |
151 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(148): 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 | a0001c0001t0014g0021 a0001c0001t0023g0066 a0001c0001t0023g0097 others(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 | a0001c0001t0068g0030 a0002c0002t0005g0031 |
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 | a0001c0001t0021g0067 a0001c0001t0048g0049 a0001c0001t0049g0046 others(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 | 132 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(129): Show |
133 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.728-10397A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69883643 | |||||||
chr18:69883738 | T | A | 223 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(220): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): 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 | a0002c0002t0062g0090 | 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 | 237 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): 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 | a0001c0001t0004g0120 | 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 | a0001c0001t0003g0139 a0001c0001t0003g0153 a0001c0001t0003g0156 others(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 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(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 | a0001c0001t0003g0187 a0001c0001t0097g0188 |
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 | a0001c0001t0050g0096 a0001c0001t0068g0030 a0001c0001t0107g0240 others(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 | a0001c0001t0107g0240 a0002c0002t0007g0095 |
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 | a0001c0001t0003g0216 a0001c0001t0008g0086 |
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 | a0001c0001t0023g0066 a0001c0001t0023g0097 a0001c0001t0034g0246 others(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 | a0002c0002t0007g0039 | 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 | a0002c0002t0046g0070 a0002c0002t0062g0090 |
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 | a0001c0001t0014g0021 a0001c0001t0023g0066 a0001c0001t0023g0097 others(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 | a0001c0001t0008g0089 | 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 | a0002c0009t0108g0242 | 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 | 132 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(129): Show |
133 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(130): 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 | a0002c0002t0007g0041 | 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 | 237 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): 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 | a0001c0001t0023g0066 a0001c0001t0023g0097 a0001c0001t0075g0055 |
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 | a0001c0001t0033g0129 a0001c0001t0033g0134 a0001c0001t0100g0168 |
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 | a0001c0001t0101g0202 | 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 | a0002c0002t0088g0233 | 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 | a0001c0001t0021g0067 a0001c0001t0048g0049 a0001c0001t0049g0046 others(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 | a0002c0002t0007g0039 | 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 | 76 | a0001c0001t0003g0124 a0001c0001t0003g0216 a0001c0001t0008g0086 others(73): Show |
77 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(74): 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 | a0001c0001t0027g0025 a0001c0001t0027g0068 |
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 | a0002c0002t0002g0180 a0002c0004t0009g0136 |
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 | a0002c0002t0024g0032 a0002c0002t0024g0050 |
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 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(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 | a0001c0001t0003g0139 a0001c0001t0003g0220 |
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 | a0001c0001t0076g0057 | 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 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(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 | a0006c0008t0109g0251 | 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 | a0001c0001t0003g0156 | 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 | a0001c0001t0094g0173 | 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 | a0003c0003t0011g0078 a0003c0003t0011g0081 a0003c0003t0051g0079 others(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 | a0001c0001t0021g0067 a0001c0001t0048g0049 a0001c0001t0049g0046 others(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 | a0001c0001t0004g0132 a0001c0001t0006g0113 a0001c0001t0006g0116 others(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 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(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 | 171 | a0001c0001t0003g0124 a0001c0001t0003g0163 a0001c0001t0003g0166 others(168): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): 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 | a0002c0002t0005g0101 | 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 | a0001c0001t0003g0139 a0001c0001t0003g0153 a0001c0001t0003g0156 others(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 | a0001c0001t0014g0021 a0001c0001t0023g0066 a0001c0001t0023g0097 others(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 | 77 | a0001c0001t0003g0124 a0001c0001t0003g0216 a0001c0001t0008g0086 others(74): Show |
78 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(75): 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 | a0002c0002t0088g0233 | 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 | a0002c0002t0059g0035 | 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 | a0001c0001t0023g0066 a0001c0001t0023g0097 a0001c0001t0034g0246 others(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 | a0001c0001t0004g0171 a0001c0001t0004g0189 a0001c0001t0004g0203 others(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 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(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 | 146 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(143): Show |
146 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.727+7284dupA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69888416 | |||||||
chr18:69888416 | C | CTT | 5 | a0002c0002t0002g0001 a0002c0002t0002g0151 a0002c0002t0009g0128 others(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 | a0001c0001t0023g0066 a0001c0001t0023g0097 a0001c0001t0034g0246 others(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 | a0002c0002t0002g0180 | 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 | a0001c0001t0014g0021 | 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 | a0001c0001t0004g0189 | 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 | a0001c0001t0034g0246 a0001c0001t0034g0247 |
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 | a0001c0001t0014g0052 a0001c0001t0047g0029 |
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 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(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 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(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 | 78 | a0001c0001t0003g0124 a0001c0001t0003g0216 a0001c0001t0008g0086 others(75): Show |
79 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(76): 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 | a0001c0001t0072g0100 a0001c0001t0106g0239 a0003c0003t0011g0045 others(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 | 139 | a0001c0001t0003g0139 a0001c0001t0003g0153 a0001c0001t0003g0187 others(136): Show |
140 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.727+6213delT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69889487 | |||||||
chr18:69889487 | TAAA | T | 75 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(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 | a0001c0001t0068g0030 a0002c0002t0005g0031 |
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 | a0001c0001t0045g0009 a0001c0001t0076g0057 |
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 | a0001c0001t0003g0213 a0001c0001t0003g0214 |
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 | a0001c0001t0004g0132 a0001c0001t0006g0113 a0001c0001t0006g0116 others(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 | a0003c0003t0011g0045 a0003c0003t0011g0074 a0003c0003t0011g0078 others(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 | a0001c0001t0033g0134 | 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 | a0001c0001t0023g0066 a0001c0001t0023g0097 a0001c0001t0034g0246 others(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 | a0001c0001t0003g0139 a0001c0001t0003g0153 a0001c0001t0003g0156 others(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 | a0002c0002t0001g0152 a0002c0002t0002g0151 |
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 | a0003c0003t0011g0045 a0003c0003t0011g0074 a0003c0003t0011g0078 others(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 | a0001c0001t0003g0139 a0001c0001t0003g0153 a0001c0001t0003g0156 others(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 | a0002c0002t0012g0051 | 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 | a0001c0001t0003g0139 a0001c0001t0003g0220 |
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 | a0002c0002t0030g0227 | 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 | a0001c0001t0070g0013 | 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 | a0001c0001t0006g0113 a0001c0001t0006g0116 a0001c0001t0006g0141 others(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 | a0001c0001t0021g0067 a0001c0001t0048g0049 a0001c0001t0049g0046 others(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 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(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 | a0001c0001t0003g0139 a0001c0001t0003g0153 a0001c0001t0003g0156 others(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 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(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 | a0001c0001t0026g0092 | 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 | a0001c0001t0110g0243 | 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 | 78 | a0001c0001t0003g0124 a0001c0001t0003g0216 a0001c0001t0008g0086 others(75): Show |
79 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(76): 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 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(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 | 237 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): 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 | a0001c0001t0004g0132 a0001c0001t0006g0113 a0001c0001t0006g0116 others(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 | a0003c0003t0011g0045 a0003c0003t0011g0074 a0003c0003t0011g0078 others(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 | a0001c0001t0014g0052 a0001c0001t0047g0029 |
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 | 219 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): 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 | a0001c0001t0004g0132 a0001c0001t0006g0113 a0001c0001t0006g0116 others(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 | a0002c0002t0079g0190 | 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 | a0001c0001t0006g0141 a0001c0001t0006g0158 |
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 | 237 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): 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 | a0001c0001t0050g0096 a0001c0001t0068g0030 a0001c0001t0107g0240 others(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 | a0001c0001t0048g0049 | 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 | 220 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(217): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): 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 | a0001c0001t0013g0192 a0001c0001t0095g0209 |
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 | 78 | a0001c0001t0003g0124 a0001c0001t0003g0216 a0001c0001t0008g0086 others(75): Show |
79 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(76): 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 | a0002c0002t0112g0255 | 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 | a0006c0008t0109g0251 | 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 | a0001c0001t0070g0013 | 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 | a0002c0002t0012g0053 | 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 | a0001c0001t0008g0012 a0001c0001t0008g0085 a0001c0001t0008g0089 |
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 | a0001c0001t0006g0113 | 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 | a0001c0001t0021g0067 | 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 | a0001c0001t0003g0139 a0001c0001t0003g0153 a0001c0001t0003g0156 others(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 | a0003c0003t0011g0045 a0003c0003t0011g0074 a0003c0003t0011g0078 others(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 | a0001c0001t0074g0054 a0001c0001t0103g0157 a0002c0002t0001g0175 others(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 | a0001c0001t0035g0244 a0001c0001t0035g0245 |
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 | a0001c0001t0014g0052 a0001c0001t0047g0029 |
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 | a0001c0001t0038g0007 | 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 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(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 | 180 | a0001c0001t0003g0124 a0001c0001t0003g0163 a0001c0001t0003g0166 others(177): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): 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 | a0002c0002t0002g0130 | 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 | a0001c0001t0004g0132 a0001c0001t0006g0113 a0001c0001t0006g0116 others(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 | 96 | a0001c0001t0003g0124 a0001c0001t0003g0216 a0001c0001t0008g0086 others(93): Show |
97 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.727+1429C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894272 | |||||||
chr18:69894282 | G | A | 96 | a0001c0001t0003g0124 a0001c0001t0003g0216 a0001c0001t0008g0086 others(93): Show |
97 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(94): 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 | a0001c0001t0003g0139 a0001c0001t0003g0153 a0001c0001t0003g0156 others(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 | 108 | a0001c0001t0003g0124 a0001c0001t0003g0216 a0001c0001t0006g0113 others(105): Show |
109 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(106): 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 | a0001c0001t0027g0025 a0001c0001t0027g0068 a0001c0001t0038g0007 others(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 | a0003c0003t0011g0045 a0003c0003t0011g0078 a0003c0003t0011g0081 others(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 | a0001c0001t0003g0225 a0001c0001t0028g0064 a0001c0001t0033g0134 others(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 | a0001c0001t0003g0139 a0001c0001t0003g0153 a0001c0001t0003g0156 others(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 | a0001c0001t0076g0057 | 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 | 124 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(121): Show |
125 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(122): 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 | a0002c0002t0060g0015 | 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 | a0001c0001t0045g0009 a0002c0002t0059g0035 |
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 | 131 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(128): Show |
132 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(129): 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 | a0001c0001t0094g0173 | 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 | a0001c0001t0004g0182 | 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 | a0001c0001t0004g0178 | 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 | a0001c0001t0004g0125 a0001c0001t0004g0127 a0001c0001t0044g0004 |
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 | a0001c0001t0028g0103 a0001c0001t0066g0102 |
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 | a0001c0001t0073g0014 | 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 | a0002c0002t0046g0070 | 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 | a0001c0001t0023g0066 | 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 | a0001c0001t0004g0112 a0001c0001t0004g0169 a0001c0001t0004g0203 others(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 | a0001c0001t0016g0094 a0001c0001t0032g0108 a0002c0002t0013g0205 |
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 | a0001c0001t0004g0143 a0001c0001t0004g0144 a0001c0001t0029g0083 others(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 | a0001c0001t0013g0122 a0001c0001t0016g0077 a0001c0001t0071g0098 others(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 | a0001c0001t0039g0010 | 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 | a0001c0001t0003g0167 | 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 | a0001c0001t0023g0097 | 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 | a0001c0001t0004g0120 a0001c0001t0004g0171 a0001c0001t0026g0042 others(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 | a0001c0001t0004g0212 a0001c0001t0064g0087 |
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 | a0001c0001t0035g0245 a0001c0001t0067g0071 |
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 | a0001c0001t0003g0211 a0001c0001t0004g0207 a0001c0001t0008g0093 others(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 | a0001c0001t0013g0192 a0001c0001t0029g0082 a0001c0001t0074g0054 |
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 | a0001c0001t0021g0073 | 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 | a0001c0001t0003g0195 a0001c0001t0003g0198 a0001c0001t0047g0029 others(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 | a0002c0002t0012g0053 | 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 | a0001c0001t0004g0114 | 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 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0008g0036 others(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 | a0001c0001t0103g0157 a0002c0002t0001g0105 |
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 | a0001c0001t0035g0244 | 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 | a0002c0002t0024g0032 a0002c0002t0024g0050 |
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 | 174 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(171): Show |
175 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(172): 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 | a0003c0003t0011g0045 a0003c0003t0011g0074 a0003c0003t0011g0078 others(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 | a0001c0001t0004g0189 | 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 | a0002c0009t0108g0242 | 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 | a0001c0001t0028g0064 a0002c0009t0108g0242 a0006c0008t0109g0251 |
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 | a0001c0001t0021g0067 | 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 | a0001c0001t0004g0132 a0001c0001t0006g0113 a0001c0001t0006g0116 others(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 | a0001c0001t0073g0014 a0001c0001t0107g0240 a0002c0002t0007g0095 |
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 | 207 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(204): Show |
208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): 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 | a0001c0001t0073g0014 a0001c0001t0107g0240 a0002c0002t0007g0095 |
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 | a0001c0001t0003g0139 a0001c0001t0003g0153 a0001c0001t0003g0156 others(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 | a0001c0001t0003g0139 a0001c0001t0003g0153 a0001c0001t0003g0156 others(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 | a0001c0001t0033g0134 a0001c0001t0100g0168 |
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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 others(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 | a0001c0001t0033g0129 | 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 | a0001c0001t0110g0243 | 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 | a0001c0001t0038g0007 | 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 | a0001c0001t0003g0213 a0001c0001t0003g0214 |
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 | a0001c0001t0003g0139 a0001c0001t0003g0153 a0001c0001t0003g0156 others(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 | a0001c0001t0107g0240 a0002c0002t0024g0032 a0002c0002t0024g0050 |
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 | 200 | a0001c0001t0003g0124 a0001c0001t0003g0163 a0001c0001t0003g0166 others(197): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): 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 | a0001c0001t0003g0139 a0001c0001t0003g0153 a0001c0001t0003g0156 others(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 | a0001c0001t0021g0067 | 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 | a0001c0001t0073g0014 a0001c0001t0074g0054 a0001c0001t0103g0157 others(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 | a0001c0001t0072g0100 | 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 | a0001c0001t0022g0099 | 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 | a0001c0001t0003g0139 a0001c0001t0003g0153 a0001c0001t0003g0156 others(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 | a0001c0001t0073g0014 | 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 | a0002c0002t0009g0193 | 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 | a0001c0001t0107g0240 | 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 | a0006c0008t0109g0251 | 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 | a0001c0001t0004g0112 | 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 | a0002c0002t0024g0032 a0002c0002t0024g0050 |
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 | a0001c0001t0074g0054 | 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 | a0002c0002t0001g0204 a0002c0002t0002g0001 a0002c0002t0002g0126 others(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 | a0002c0002t0060g0015 | 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 | a0001c0001t0006g0113 a0001c0001t0006g0116 a0001c0001t0006g0158 others(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 | a0001c0001t0004g0127 | 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 | a0001c0001t0008g0085 a0001c0001t0008g0089 |
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 | a0001c0001t0022g0069 a0001c0001t0040g0008 a0001c0001t0078g0135 others(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 | a0002c0002t0005g0020 | 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 | a0003c0003t0051g0079 | 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 | a0001c0001t0015g0016 a0001c0001t0015g0034 a0001c0001t0020g0019 others(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 | a0001c0001t0023g0066 a0001c0001t0023g0097 a0001c0001t0034g0246 others(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 | a0001c0001t0004g0182 | 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 | a0002c0002t0001g0142 | 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 | a0001c0001t0048g0049 a0001c0001t0049g0046 |
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 | a0001c0001t0035g0244 a0001c0001t0035g0245 a0001c0001t0045g0009 others(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 | a0002c0002t0001g0118 | 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 |
79 | a0001c0001t0003g0124 a0001c0001t0003g0216 a0001c0001t0008g0086 others(76): Show |
79 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(76): 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 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(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 | a0002c0002t0009g0146 | 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 | a0001c0001t0014g0021 | 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 | a0002c0009t0108g0242 | 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 | a0001c0001t0004g0207 | 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 | a0001c0001t0063g0080 | 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 | a0002c0002t0046g0070 a0002c0002t0059g0035 |
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 | a0001c0001t0004g0132 a0001c0001t0006g0123 a0001c0001t0104g0121 |
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 | a0001c0001t0003g0213 a0001c0001t0003g0214 |
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 | a0001c0001t0014g0052 a0001c0001t0047g0029 |
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 | a0002c0002t0007g0088 a0002c0002t0089g0235 a0002c0002t0090g0200 |
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 | a0001c0001t0103g0157 a0002c0002t0001g0175 a0002c0002t0002g0174 |
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 | a0005c0005t0009g0104 | 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 | a0002c0002t0012g0053 | 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 | a0001c0001t0068g0030 a0002c0002t0005g0031 |
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 | a0002c0002t0030g0199 | 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 | a0001c0001t0022g0099 a0001c0001t0072g0100 |
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 | a0001c0001t0006g0141 | 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 | a0001c0001t0006g0141 | 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 | 213 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(210): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): 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 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(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 | a0006c0008t0109g0251 | 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 | a0006c0008t0109g0251 | 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 | a0002c0002t0001g0228 a0002c0002t0002g0229 |
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 | a0001c0001t0073g0014 | 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 | a0002c0002t0012g0051 | 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 | a0006c0008t0109g0251 | 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 | a0001c0001t0004g0132 a0001c0001t0006g0113 a0001c0001t0006g0116 others(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 | 77 | a0001c0001t0003g0124 a0001c0001t0003g0216 a0001c0001t0008g0086 others(74): Show |
78 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(75): 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 | a0006c0008t0109g0251 | 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 | 213 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(210): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.727+260C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69895441 | |||||||
chr18:69896073 | A | C | 236 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(233): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.383-28T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69896073 | |||||||
chr18:69896112 | T | C | 226 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): 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 | a0001c0001t0032g0107 a0001c0001t0032g0108 a0001c0001t0098g0106 others(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 | 113 | a0001c0001t0003g0124 a0001c0001t0003g0166 a0001c0001t0003g0167 others(110): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.383-137dupA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69896181 | |||||||
chr18:69896181 | C | CTT | 92 | a0001c0001t0003g0139 a0001c0001t0003g0153 a0001c0001t0003g0156 others(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 | a0001c0001t0004g0132 a0001c0001t0006g0113 a0001c0001t0006g0116 others(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 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(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 | a0006c0008t0109g0251 | 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 | a0001c0001t0100g0168 | 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 | a0003c0003t0011g0045 a0003c0003t0011g0078 a0003c0003t0011g0081 others(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 | a0001c0001t0102g0186 | 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 | a0001c0001t0003g0163 a0001c0001t0003g0225 a0001c0001t0006g0116 others(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 | a0001c0001t0003g0139 a0001c0001t0003g0153 a0001c0001t0003g0156 others(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 | a0002c0002t0009g0146 | 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 | a0002c0002t0009g0146 | 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 | a0002c0002t0009g0146 | 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 | a0001c0001t0028g0064 | 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 | a0001c0001t0006g0232 | 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 | a0002c0002t0046g0070 | 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 | a0001c0001t0003g0211 a0001c0001t0008g0093 |
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 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(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 | a0001c0001t0014g0018 a0001c0001t0028g0064 a0001c0001t0110g0243 |
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 | a0002c0002t0009g0146 | 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 | a0002c0002t0009g0146 | 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 | a0002c0002t0009g0146 | 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 | a0001c0001t0074g0054 | 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 | a0002c0002t0009g0146 | 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 | a0002c0002t0009g0146 | 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 | a0002c0002t0009g0146 | 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 | a0002c0002t0009g0146 | 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 | a0002c0002t0009g0146 | 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 | a0002c0002t0009g0146 | 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 | a0005c0005t0009g0104 | 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 | a0001c0001t0003g0139 a0001c0001t0003g0153 a0001c0001t0003g0156 others(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 | a0001c0001t0021g0067 | 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 | a0001c0001t0070g0013 a0001c0001t0076g0057 |
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 | a0001c0001t0105g0208 | 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 | 101 | a0001c0001t0003g0124 a0001c0001t0003g0167 a0001c0001t0003g0195 others(98): Show |
102 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.383-2298C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69898343 | |||||||
chr18:69898614 | T | C | 145 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0156 others(142): Show |
146 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.383-2569A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69898614 | |||||||
chr18:69898662 | T | C | 159 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0156 others(156): Show |
160 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(157): 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 | a0001c0001t0027g0025 a0001c0001t0027g0068 |
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 | 127 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0156 others(124): Show |
128 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(125): 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 | a0002c0002t0081g0111 | 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 | a0001c0001t0003g0153 a0001c0001t0045g0009 a0001c0001t0074g0054 others(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 | a0001c0001t0032g0107 a0001c0001t0032g0108 a0001c0001t0098g0106 others(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 | a0002c0002t0005g0020 a0002c0002t0005g0072 |
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 | a0001c0001t0021g0067 | 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 | a0001c0001t0003g0139 a0001c0001t0003g0156 a0001c0001t0003g0163 others(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 | a0002c0009t0108g0242 | 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 | a0001c0001t0063g0080 | 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 | a0001c0001t0006g0123 a0001c0001t0092g0194 a0001c0001t0104g0121 |
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 | a0002c0002t0025g0027 a0002c0002t0056g0028 |
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 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0211 others(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 | a0002c0002t0001g0175 a0002c0002t0002g0174 a0002c0002t0007g0088 others(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 | a0001c0001t0006g0123 a0001c0001t0092g0194 a0001c0001t0104g0121 |
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 | a0002c0002t0024g0032 a0002c0002t0024g0050 |
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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0003g0139 a0001c0001t0003g0156 a0001c0001t0003g0163 others(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 | a0001c0001t0003g0139 a0001c0001t0003g0156 a0001c0001t0003g0163 others(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 | a0001c0001t0021g0073 | 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 | a0001c0001t0003g0163 a0001c0001t0003g0166 |
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 | a0001c0001t0021g0067 | 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 | a0001c0001t0006g0123 a0001c0001t0092g0194 a0001c0001t0104g0121 |
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 | a0001c0001t0003g0139 a0001c0001t0003g0156 a0001c0001t0003g0163 others(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 | a0002c0002t0012g0056 | 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 | a0001c0001t0003g0139 a0001c0001t0003g0156 a0001c0001t0003g0163 others(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 | a0002c0009t0108g0242 | 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 | a0001c0001t0003g0153 a0001c0001t0100g0168 |
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 | a0001c0001t0003g0167 | 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 | a0001c0001t0045g0009 a0001c0001t0074g0054 a0001c0001t0103g0157 others(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 | a0001c0001t0028g0103 a0001c0001t0066g0102 |
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 | a0001c0001t0094g0173 | 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 | a0001c0001t0028g0103 a0001c0001t0066g0102 |
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 | a0001c0001t0003g0139 a0001c0001t0003g0167 a0001c0001t0003g0220 others(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 | a0001c0001t0053g0033 | 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 | 117 | a0001c0001t0003g0124 a0001c0001t0003g0153 a0001c0001t0003g0195 others(114): Show |
118 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.383-4616C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900661 | |||||||
chr18:69900664 | G | A | 116 | a0001c0001t0003g0124 a0001c0001t0003g0153 a0001c0001t0003g0195 others(113): Show |
117 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(114): 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 | a0001c0001t0003g0139 a0001c0001t0003g0156 a0001c0001t0003g0163 others(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 | a0002c0009t0108g0242 | 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 | a0001c0001t0006g0123 a0001c0001t0035g0244 a0001c0001t0035g0245 others(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 | a0001c0001t0050g0096 a0001c0001t0094g0173 a0002c0002t0001g0204 others(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 | a0001c0001t0003g0139 a0001c0001t0003g0163 a0001c0001t0003g0166 others(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 | a0001c0001t0003g0156 a0001c0001t0003g0187 a0001c0001t0003g0213 others(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 | a0001c0001t0047g0029 a0002c0002t0024g0032 a0002c0002t0024g0050 |
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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0002c0002t0007g0058 a0002c0002t0060g0015 |
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 | a0001c0001t0014g0018 a0001c0001t0014g0052 a0001c0001t0015g0016 others(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 | a0002c0002t0001g0145 | 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 | a0001c0001t0003g0139 a0001c0001t0003g0156 a0001c0001t0003g0163 others(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 | a0001c0001t0003g0139 a0001c0001t0003g0156 a0001c0001t0003g0163 others(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 | a0001c0001t0107g0240 a0002c0002t0005g0059 a0002c0002t0005g0060 others(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 | a0001c0001t0003g0139 a0001c0001t0003g0153 a0001c0001t0003g0163 others(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 | a0001c0001t0013g0122 a0001c0001t0013g0192 a0001c0001t0095g0209 others(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 | a0001c0001t0021g0067 a0001c0001t0022g0099 a0001c0001t0028g0103 others(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 | a0001c0001t0004g0120 | 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 | a0001c0001t0047g0029 | 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 | a0001c0001t0003g0139 a0001c0001t0003g0156 a0001c0001t0003g0163 others(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 | a0001c0001t0014g0052 a0001c0001t0111g0241 a0002c0002t0012g0051 |
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 | a0001c0001t0014g0052 a0002c0002t0012g0051 |
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 | a0001c0001t0003g0139 a0001c0001t0003g0156 a0001c0001t0003g0163 others(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 | a0001c0001t0003g0195 a0001c0001t0003g0198 a0001c0001t0004g0125 others(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 | a0001c0001t0003g0139 a0001c0001t0003g0156 a0001c0001t0003g0163 others(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 | a0001c0001t0004g0125 a0001c0001t0004g0127 a0001c0001t0027g0025 others(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 | a0001c0001t0028g0064 a0002c0002t0055g0063 |
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 | a0001c0001t0028g0064 a0001c0001t0078g0135 a0002c0002t0055g0063 |
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 | a0001c0001t0016g0084 a0001c0001t0092g0194 a0001c0001t0104g0121 |
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 | a0001c0001t0016g0084 a0001c0001t0092g0194 a0001c0001t0104g0121 |
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 | 138 | a0001c0001t0003g0124 a0001c0001t0003g0153 a0001c0001t0003g0166 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): 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 | a0001c0001t0006g0116 a0001c0001t0023g0066 a0002c0002t0001g0219 others(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 | 215 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(212): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): 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 | a0001c0001t0035g0244 a0001c0001t0107g0240 a0001c0001t0110g0243 others(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 | a0001c0001t0004g0120 a0001c0001t0004g0169 a0001c0001t0004g0171 others(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 | a0001c0001t0023g0097 | 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 | 163 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(160): Show |
164 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(161): 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 | a0002c0002t0005g0022 | 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 | a0001c0001t0014g0052 a0002c0002t0012g0051 |
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 | a0002c0002t0005g0065 | 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 | a0002c0002t0005g0022 | 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 | a0001c0001t0078g0135 | 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 | a0002c0002t0059g0035 | 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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 |
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 | a0001c0001t0014g0052 a0002c0002t0012g0051 |
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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0015g0016 others(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 | a0001c0001t0068g0030 a0002c0002t0005g0031 |
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 | a0002c0002t0001g0105 | 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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 |
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 | a0001c0001t0004g0143 a0001c0001t0004g0144 |
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 | a0001c0001t0028g0064 | 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 | a0002c0002t0002g0236 | 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 | a0001c0001t0047g0029 a0002c0002t0007g0095 |
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 | a0001c0001t0050g0096 a0001c0001t0063g0080 a0002c0002t0024g0032 others(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 | a0001c0001t0013g0160 a0001c0001t0014g0018 a0001c0001t0014g0021 others(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 | a0001c0001t0110g0243 a0001c0001t0111g0241 a0002c0009t0108g0242 |
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 | a0001c0001t0003g0124 | 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 | 220 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(217): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): 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 | a0001c0001t0006g0123 a0001c0001t0014g0018 a0001c0001t0014g0021 others(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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 others(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 | a0002c0002t0062g0090 | 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 | a0002c0002t0025g0026 | 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 | 171 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(168): Show |
172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): 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 | a0001c0001t0008g0036 | 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 | a0002c0002t0025g0026 a0002c0002t0025g0027 a0002c0002t0056g0028 |
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 | a0001c0001t0008g0012 a0001c0001t0048g0049 a0001c0001t0049g0046 others(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 | a0002c0002t0046g0070 | 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 | a0001c0001t0074g0054 | 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 | a0001c0001t0100g0168 | 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 | a0001c0001t0003g0163 a0002c0002t0001g0145 |
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 | a0001c0001t0106g0239 a0002c0002t0012g0075 |
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 | a0001c0001t0034g0246 a0001c0001t0034g0247 |
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 | a0001c0001t0069g0047 a0002c0002t0005g0048 |
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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 others(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 | a0001c0001t0008g0012 a0001c0001t0048g0049 a0001c0001t0049g0046 others(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 | a0001c0001t0022g0099 a0001c0001t0028g0103 a0001c0001t0066g0102 others(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 | a0001c0001t0022g0069 | 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 | 252 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(249): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.383-10528A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69906573 | |||||||
chr18:69906574 | G | A | 221 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(218): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): 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 | a0001c0001t0006g0158 a0001c0001t0106g0239 |
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 | a0002c0002t0012g0053 | 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 | a0001c0001t0023g0097 a0001c0001t0050g0096 |
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 | a0001c0001t0008g0036 a0002c0002t0059g0035 |
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 | a0001c0001t0003g0225 a0001c0001t0006g0123 a0001c0001t0092g0194 others(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 | a0003c0003t0011g0078 | 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 | a0001c0001t0004g0169 | 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 | a0001c0001t0022g0099 a0001c0001t0028g0103 a0001c0001t0066g0102 others(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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 others(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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | 206 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(203): Show |
207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.383-11346T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69907391 | |||||||
chr18:69907455 | A | G | 225 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(222): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): 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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 others(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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0003c0003t0011g0078 a0003c0003t0011g0081 a0003c0003t0051g0079 |
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 | a0002c0002t0001g0219 | 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 | a0001c0001t0016g0084 a0001c0001t0029g0082 a0001c0001t0029g0083 others(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 | a0001c0001t0013g0192 a0001c0001t0095g0209 a0002c0002t0001g0206 others(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 | a0001c0001t0111g0241 | 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 | a0001c0001t0022g0099 a0001c0001t0028g0103 a0001c0001t0066g0102 others(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 | a0001c0001t0004g0189 a0001c0001t0004g0203 a0001c0001t0004g0207 others(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 | a0001c0001t0003g0213 a0001c0001t0003g0214 a0001c0001t0003g0216 others(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 | a0001c0001t0004g0112 a0001c0001t0004g0114 a0001c0001t0006g0113 others(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 | a0001c0001t0022g0099 a0001c0001t0028g0103 a0001c0001t0066g0102 others(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 | a0001c0001t0053g0033 | 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 | a0001c0001t0107g0240 | 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 | a0002c0002t0012g0075 | 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 | a0001c0001t0068g0030 a0002c0002t0005g0031 |
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 | a0001c0001t0106g0239 | 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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0003g0213 a0001c0001t0003g0214 |
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 | a0001c0001t0068g0030 a0002c0002t0005g0031 |
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 | a0001c0001t0004g0125 | 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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0093g0176 | 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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0014g0052 | 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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 others(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 | a0002c0009t0108g0242 | 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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0063g0080 a0003c0003t0011g0078 a0003c0003t0011g0081 others(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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 others(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 | a0002c0002t0012g0053 | 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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | 205 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(202): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): 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 | a0002c0002t0079g0190 | 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 | 170 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(167): Show |
171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): 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 | a0001c0001t0008g0012 a0001c0001t0048g0049 a0001c0001t0049g0046 others(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 | a0002c0002t0057g0043 a0003c0003t0011g0045 |
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 | a0001c0001t0004g0203 | 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 | a0001c0001t0065g0038 | 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 | a0002c0002t0002g0130 | 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 | a0001c0001t0004g0143 a0001c0001t0004g0144 |
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 | a0001c0001t0008g0012 a0001c0001t0048g0049 a0001c0001t0049g0046 others(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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | 171 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(168): Show |
172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.383-17130G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69913175 | |||||||
chr18:69913184 | A | C | 202 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(199): Show |
203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): 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 | a0002c0002t0046g0070 | 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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0008g0036 a0002c0002t0059g0035 |
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 | a0001c0001t0008g0085 a0001c0001t0008g0089 a0001c0001t0064g0087 others(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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0106g0239 | 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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | 171 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(168): Show |
172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): 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 | a0001c0001t0004g0207 a0001c0001t0013g0192 a0001c0001t0095g0209 others(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 | a0001c0001t0102g0186 | 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 | a0001c0001t0003g0211 a0001c0001t0004g0132 a0001c0001t0008g0044 others(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 | a0001c0001t0008g0036 a0002c0002t0059g0035 |
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 | a0001c0001t0106g0239 | 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 | a0001c0001t0070g0013 | 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 | a0001c0001t0069g0047 a0002c0002t0005g0048 |
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 | a0002c0002t0079g0190 | 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 | a0001c0001t0008g0036 a0002c0002t0059g0035 |
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 | a0001c0001t0008g0036 a0002c0002t0059g0035 |
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 | a0001c0001t0069g0047 a0002c0002t0005g0048 |
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 | a0001c0001t0075g0055 | 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 | a0001c0001t0003g0195 a0001c0001t0003g0198 a0001c0001t0096g0197 others(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 | a0002c0002t0002g0159 | 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 | a0001c0001t0063g0080 a0003c0003t0011g0078 a0003c0003t0011g0081 others(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 | a0001c0001t0013g0160 | 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 | a0001c0001t0016g0084 a0001c0001t0029g0082 a0001c0001t0029g0083 |
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 | a0001c0001t0074g0054 | 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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 others(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 | a0002c0002t0001g0131 | 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 | a0001c0001t0070g0013 | 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 | a0002c0002t0002g0196 | 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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | 171 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(168): Show |
172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): 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 | a0002c0002t0041g0011 | 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 | a0002c0002t0001g0140 | 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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 |
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 | a0002c0002t0024g0032 a0002c0002t0024g0050 |
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 | a0002c0002t0001g0204 | 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 | a0001c0001t0003g0184 a0001c0001t0003g0187 a0001c0001t0004g0120 others(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 | a0001c0001t0023g0097 a0001c0001t0050g0096 |
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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0038g0007 | 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 | a0001c0001t0013g0160 a0001c0001t0026g0042 |
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 | 225 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(222): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): 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 | a0001c0001t0016g0084 a0001c0001t0029g0082 a0001c0001t0029g0083 |
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 | a0001c0001t0008g0086 | 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 | a0001c0001t0021g0073 a0001c0001t0028g0064 a0002c0002t0054g0061 others(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 | a0001c0001t0064g0087 | 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 | a0001c0001t0106g0239 a0002c0002t0012g0075 |
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 | a0001c0001t0003g0139 a0002c0004t0009g0136 |
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 | 199 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(196): Show |
200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): 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 | a0001c0001t0022g0099 a0001c0001t0028g0103 a0001c0001t0066g0102 others(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 | a0002c0002t0012g0053 | 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 | a0001c0001t0023g0097 | 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 | a0001c0001t0019g0249 | 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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0099g0109 | 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 | a0002c0002t0002g0161 | 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 | a0001c0001t0075g0055 | 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 | a0001c0001t0069g0047 a0002c0002t0005g0048 |
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 | a0001c0001t0016g0084 a0001c0001t0029g0082 a0001c0001t0029g0083 |
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 | a0001c0001t0076g0057 | 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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0022g0099 a0001c0001t0028g0103 a0001c0001t0066g0102 others(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 | a0001c0001t0106g0239 a0002c0002t0012g0075 |
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 | a0001c0001t0048g0049 | 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 | a0002c0002t0002g0236 | 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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0068g0030 a0002c0002t0005g0031 |
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 | a0001c0001t0101g0202 | 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 | a0001c0001t0016g0084 a0001c0001t0029g0082 a0001c0001t0029g0083 |
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 | 225 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(222): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): 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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0022g0099 a0001c0001t0028g0103 a0001c0001t0066g0102 others(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 | a0001c0001t0022g0099 a0001c0001t0028g0103 a0001c0001t0066g0102 others(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 | a0002c0002t0001g0140 | 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 | a0002c0002t0030g0227 | 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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0003g0213 a0001c0001t0003g0214 a0001c0001t0003g0216 others(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 | a0001c0001t0023g0097 a0001c0001t0050g0096 |
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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0033g0134 | 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 | a0001c0001t0053g0033 | 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 | a0002c0002t0012g0075 | 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 | a0001c0001t0008g0012 a0001c0001t0022g0099 a0001c0001t0028g0103 others(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 | a0001c0001t0048g0049 a0001c0001t0049g0046 a0002c0002t0024g0032 others(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 | a0002c0002t0005g0101 | 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 | 222 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): 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 | a0002c0002t0085g0162 | 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 | a0002c0002t0005g0072 | 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 | a0001c0001t0004g0132 | 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 | a0001c0001t0008g0036 a0002c0002t0059g0035 |
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 | a0001c0001t0016g0084 a0001c0001t0029g0082 a0001c0001t0029g0083 |
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 | a0002c0002t0001g0142 | 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 | a0001c0001t0008g0036 | 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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0008g0012 a0001c0001t0048g0049 a0001c0001t0049g0046 others(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 | a0001c0001t0023g0097 a0001c0001t0050g0096 |
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 | a0001c0001t0023g0097 a0001c0001t0050g0096 |
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 | a0001c0001t0107g0240 | 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 | a0001c0001t0023g0097 a0001c0001t0050g0096 |
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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 others(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 | a0001c0001t0003g0139 | 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 | 230 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(227): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): 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 | a0001c0001t0006g0141 | 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 | 226 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): 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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 others(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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 others(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 | a0001c0001t0106g0239 | 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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 others(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 | a0001c0001t0008g0012 a0001c0001t0068g0030 a0001c0001t0078g0135 others(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 | 150 | a0001c0001t0003g0124 a0001c0001t0003g0153 a0001c0001t0003g0156 others(147): Show |
151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): 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 | a0001c0001t0003g0139 a0001c0001t0003g0163 a0001c0001t0004g0114 others(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 | a0001c0001t0022g0099 a0001c0001t0028g0103 a0001c0001t0048g0049 others(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 | a0001c0001t0066g0102 a0002c0002t0005g0101 |
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 | a0001c0001t0016g0084 a0001c0001t0029g0082 a0001c0001t0029g0083 others(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 | a0001c0001t0004g0212 a0001c0001t0102g0186 |
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 | a0001c0001t0003g0166 a0001c0001t0003g0167 a0002c0002t0002g0234 |
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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0015g0016 others(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 | a0001c0001t0016g0084 a0001c0001t0029g0082 a0001c0001t0029g0083 |
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 | a0002c0002t0083g0119 | 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 | a0002c0002t0007g0040 | 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 | a0001c0001t0033g0134 | 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 | a0001c0001t0053g0033 a0001c0001t0110g0243 |
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 | a0001c0001t0016g0084 a0001c0001t0029g0082 a0001c0001t0029g0083 |
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 | a0002c0002t0009g0179 | 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 | a0002c0002t0088g0233 | 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 | a0001c0001t0074g0054 | 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 | a0001c0001t0100g0168 | 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 | a0001c0001t0074g0054 | 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 | a0001c0001t0027g0025 | 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 | a0007c0007t0011g0024 | 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 | a0001c0001t0107g0240 | 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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0064g0087 | 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 | a0002c0002t0030g0227 | 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 | a0001c0001t0063g0080 a0001c0001t0106g0239 a0003c0003t0011g0078 others(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 | a0002c0002t0002g0180 | 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 | 167 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(164): Show |
168 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(165): 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 | a0001c0001t0004g0207 a0001c0001t0008g0012 a0001c0001t0013g0192 others(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 | a0001c0001t0008g0036 a0001c0001t0019g0248 a0001c0001t0019g0249 others(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 | a0001c0001t0022g0099 a0001c0001t0028g0103 a0001c0001t0066g0102 others(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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0074g0054 | 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 | a0001c0001t0099g0109 | 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 | a0001c0001t0022g0099 a0001c0001t0028g0103 a0001c0001t0066g0102 others(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 | 222 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): 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 | a0001c0001t0106g0239 | 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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0016g0084 a0001c0001t0029g0082 a0001c0001t0029g0083 |
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 | 170 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(167): Show |
171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.382+18586G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69928148 | |||||||
chr18:69928213 | A | G | 170 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(167): Show |
171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.382+18521T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69928213 | |||||||
chr18:69928367 | G | A | 222 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.382+18367C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69928367 | |||||||
chr18:69928402 | G | A | 48 | a0001c0001t0003g0124 a0001c0001t0003g0153 a0001c0001t0003g0156 others(45): Show |
48 | HG00099.hp2 HG00280.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.382+18332C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69928402 | |||||||
chr18:69928692 | C | A | 170 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(167): Show |
171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.382+18042G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69928692 | |||||||
chr18:69928694 | A | G | 170 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(167): Show |
171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): 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 | a0001c0001t0074g0054 | 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 | a0001c0001t0069g0047 a0002c0002t0005g0048 |
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 | a0001c0001t0032g0107 a0001c0001t0032g0108 a0001c0001t0098g0106 others(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 | a0001c0001t0069g0047 a0002c0002t0005g0048 |
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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0003g0195 a0001c0001t0003g0198 a0001c0001t0096g0197 |
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 | a0001c0001t0028g0064 a0002c0002t0005g0059 a0002c0002t0005g0060 others(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 | 170 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(167): Show |
171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): 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 | a0001c0001t0049g0046 | 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 | a0001c0001t0048g0049 a0001c0001t0049g0046 a0002c0002t0024g0032 others(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 | 223 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(220): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): 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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0004g0182 a0001c0001t0100g0168 |
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 | a0002c0002t0091g0133 | 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 | 225 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(222): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.382+16205dupT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69930528 | |||||||
chr18:69930563 | C | T | 2 | a0001c0001t0048g0049 a0001c0001t0049g0046 |
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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | 170 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(167): Show |
171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.382+16121T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69930613 | |||||||
chr18:69930691 | T | C | 223 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(220): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.382+16043A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69930691 | |||||||
chr18:69930943 | C | T | 222 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): 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 | a0001c0001t0008g0012 a0001c0001t0048g0049 a0001c0001t0049g0046 others(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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | 170 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(167): Show |
171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): 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 | a0001c0001t0106g0239 | 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 | a0001c0001t0053g0033 | 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 | 171 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(168): Show |
172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): 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 | a0001c0001t0102g0186 | 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 | a0001c0001t0069g0047 a0002c0002t0005g0048 |
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 | 218 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(215): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): 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 | a0001c0001t0095g0209 | 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 | a0001c0001t0068g0030 a0002c0002t0005g0031 |
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 | a0002c0002t0001g0117 a0002c0002t0002g0110 |
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 | a0001c0001t0065g0038 | 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 | a0001c0001t0022g0099 a0001c0001t0028g0103 a0001c0001t0053g0033 others(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 | a0001c0001t0053g0033 | 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 | a0001c0001t0008g0012 a0001c0001t0048g0049 a0001c0001t0049g0046 others(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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0013g0122 a0004c0006t0001g0210 |
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 | 170 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(167): Show |
171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): 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 | a0001c0001t0053g0033 | 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 | a0001c0001t0008g0012 a0001c0001t0048g0049 a0001c0001t0049g0046 others(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 | 170 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(167): Show |
171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): 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 | a0001c0001t0099g0109 | 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 | 82 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(79): Show |
83 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(80): 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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 |
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 | a0001c0001t0022g0099 a0001c0001t0028g0103 a0001c0001t0066g0102 others(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 | a0001c0001t0044g0004 a0002c0002t0043g0005 |
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 | a0001c0001t0003g0184 a0001c0001t0003g0220 a0001c0001t0004g0127 others(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 | a0001c0001t0016g0077 a0001c0001t0048g0049 a0001c0001t0049g0046 others(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 | a0001c0001t0016g0084 a0001c0001t0021g0067 a0001c0001t0021g0073 others(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 | a0001c0001t0063g0080 a0001c0001t0070g0013 a0002c0002t0005g0065 others(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 | a0002c0002t0007g0058 a0002c0002t0012g0053 |
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 | a0001c0001t0014g0018 a0001c0001t0015g0016 a0001c0001t0015g0034 others(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 | a0001c0001t0014g0052 a0001c0001t0020g0019 a0002c0002t0012g0051 |
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 | a0001c0001t0014g0021 a0001c0001t0020g0023 a0001c0001t0073g0014 others(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 | a0001c0001t0027g0025 a0001c0001t0047g0029 a0002c0002t0025g0026 others(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 | a0001c0001t0008g0036 | 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 | 143 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(140): Show |
143 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(140): 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 | a0001c0001t0004g0132 a0001c0001t0008g0085 a0001c0001t0008g0086 others(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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 others(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 | 152 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(149): Show |
153 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(150): 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 | a0001c0001t0008g0012 a0001c0001t0070g0013 |
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 | a0001c0001t0003g0195 a0001c0001t0003g0198 a0001c0001t0096g0197 |
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 | a0001c0001t0016g0084 a0001c0001t0029g0082 a0001c0001t0029g0083 |
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 | a0001c0001t0053g0033 | 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 | a0001c0001t0063g0080 a0001c0001t0069g0047 a0002c0002t0005g0048 others(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 | a0001c0001t0008g0012 a0001c0001t0016g0084 a0001c0001t0019g0248 others(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 | 170 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(167): Show |
171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.382+11989A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69934745 | |||||||
chr18:69935024 | A | G | 222 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): 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 | a0001c0001t0008g0012 | 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 | a0001c0001t0053g0033 | 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 | a0002c0002t0002g0185 | 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 | a0001c0001t0053g0033 | 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 | a0001c0001t0021g0073 a0001c0001t0028g0064 a0002c0002t0005g0059 others(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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 others(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 | a0001c0001t0016g0084 a0001c0001t0029g0082 a0001c0001t0029g0083 |
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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 others(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 | a0001c0001t0008g0086 | 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 | a0001c0001t0106g0239 a0002c0002t0012g0075 |
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 | a0001c0001t0008g0036 | 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 | 199 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(196): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.382+10504delA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69936229 | |||||||
chr18:69936380 | T | A | 6 | a0001c0001t0022g0099 a0001c0001t0028g0103 a0001c0001t0066g0102 others(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 | a0001c0001t0039g0010 a0001c0001t0040g0008 a0001c0001t0045g0009 |
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 | 174 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(171): Show |
175 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(172): 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 | a0001c0001t0003g0211 a0001c0001t0008g0044 a0001c0001t0008g0093 |
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 | a0001c0001t0003g0213 a0001c0001t0003g0214 a0001c0001t0003g0216 others(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 | a0001c0001t0022g0099 a0001c0001t0028g0103 a0001c0001t0053g0033 others(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 | a0001c0001t0063g0080 a0003c0003t0011g0078 a0003c0003t0011g0081 others(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 | a0001c0001t0073g0014 | 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 | 171 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(168): Show |
172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): 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 | a0001c0001t0022g0099 a0001c0001t0028g0103 a0001c0001t0066g0102 others(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 | a0001c0001t0008g0012 a0001c0001t0048g0049 a0001c0001t0049g0046 others(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 | a0002c0002t0002g0196 | 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 | a0001c0001t0008g0012 a0001c0001t0016g0084 a0001c0001t0023g0097 others(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 | a0001c0001t0008g0036 | 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 | a0001c0001t0003g0187 a0001c0001t0097g0188 |
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 | a0001c0001t0069g0047 a0002c0002t0005g0048 |
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 | a0001c0001t0016g0084 a0001c0001t0029g0082 a0001c0001t0029g0083 |
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 | a0001c0001t0106g0239 a0002c0002t0012g0075 |
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 | a0001c0001t0053g0033 | 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 | a0001c0001t0004g0189 a0002c0002t0001g0222 |
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 | 209 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(206): Show |
210 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(207): 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 | a0001c0001t0003g0195 | 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 | a0001c0001t0110g0243 a0001c0001t0111g0241 a0002c0009t0108g0242 |
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 | a0001c0001t0022g0099 a0001c0001t0028g0103 a0001c0001t0053g0033 others(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 | a0001c0001t0008g0012 a0001c0001t0048g0049 a0001c0001t0049g0046 others(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 | a0001c0001t0022g0099 a0001c0001t0028g0103 a0001c0001t0066g0102 others(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 | a0001c0001t0008g0012 a0001c0001t0014g0018 a0001c0001t0014g0021 others(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 | a0001c0001t0003g0225 a0001c0001t0006g0123 a0001c0001t0092g0194 others(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 | a0001c0001t0092g0194 a0001c0001t0104g0121 |
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 | a0001c0001t0004g0114 | 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 | a0002c0002t0009g0193 | 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 | a0001c0001t0053g0033 | 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 | a0001c0001t0008g0036 a0002c0002t0059g0035 |
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 | a0001c0001t0023g0097 a0001c0001t0050g0096 |
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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0015g0016 others(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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 others(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 | a0001c0001t0032g0107 a0001c0001t0032g0108 a0001c0001t0098g0106 others(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 | a0001c0001t0008g0012 a0001c0001t0070g0013 |
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 | a0001c0001t0008g0012 a0001c0001t0016g0084 a0001c0001t0019g0248 others(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 | a0001c0001t0016g0084 a0001c0001t0029g0082 a0001c0001t0029g0083 |
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 | a0002c0002t0037g0002 | 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 | a0002c0002t0001g0131 | 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 | a0001c0001t0008g0012 a0001c0001t0016g0084 a0001c0001t0022g0099 others(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 | a0001c0001t0033g0129 a0002c0002t0002g0130 |
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 | a0002c0002t0079g0190 | 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 | a0001c0001t0008g0012 a0001c0001t0014g0018 a0001c0001t0014g0021 others(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 | a0001c0001t0008g0085 | 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 | a0001c0001t0008g0012 a0001c0001t0016g0084 a0001c0001t0019g0248 others(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 | 225 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(222): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): 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 | a0002c0002t0030g0227 | 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 | a0001c0001t0023g0097 a0001c0001t0050g0096 |
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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0013g0192 | 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 | a0001c0001t0068g0030 a0002c0002t0005g0031 |
2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.382+3698C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69943036 | |||||||
chr18:69943138 | T | C | 2 | a0001c0001t0106g0239 a0002c0002t0012g0075 |
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 | 229 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(226): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): 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 | a0001c0001t0023g0097 a0001c0001t0050g0096 |
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 | a0001c0001t0023g0097 a0001c0001t0050g0096 a0001c0001t0069g0047 others(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 | a0001c0001t0004g0125 a0001c0001t0004g0127 a0002c0002t0002g0001 others(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 | a0001c0001t0048g0049 a0001c0001t0049g0046 a0002c0002t0024g0032 others(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 | a0001c0001t0032g0107 a0001c0001t0032g0108 a0001c0001t0098g0106 others(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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0015g0016 others(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 | a0001c0001t0003g0195 a0001c0001t0003g0198 a0001c0001t0003g0211 others(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 | a0001c0001t0008g0012 a0001c0001t0023g0097 a0001c0001t0050g0096 others(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 | a0001c0001t0008g0012 a0001c0001t0023g0097 a0001c0001t0050g0096 others(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 | a0001c0001t0106g0239 a0002c0002t0012g0075 |
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 | a0002c0002t0012g0075 | 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 | a0001c0001t0048g0049 a0001c0001t0049g0046 a0002c0002t0024g0032 others(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 | a0001c0001t0003g0124 | 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 | 168 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(165): Show |
169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): 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 | a0001c0001t0008g0012 a0001c0001t0023g0097 a0001c0001t0050g0096 others(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 | a0002c0002t0030g0227 | 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 | a0002c0002t0001g0228 a0002c0002t0002g0229 |
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 | a0001c0001t0016g0084 a0001c0001t0029g0082 a0001c0001t0029g0083 |
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 | a0001c0001t0016g0084 a0001c0001t0029g0082 a0001c0001t0029g0083 |
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 | a0001c0001t0069g0047 a0002c0002t0005g0048 |
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 | a0001c0001t0008g0012 a0001c0001t0016g0084 a0001c0001t0023g0097 others(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 | a0001c0001t0048g0049 a0001c0001t0049g0046 a0001c0001t0053g0033 others(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 | a0001c0001t0022g0099 a0001c0001t0028g0103 a0001c0001t0066g0102 others(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 | a0001c0001t0014g0018 a0001c0001t0014g0021 a0001c0001t0014g0052 others(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 | a0001c0001t0053g0033 | 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 | a0001c0001t0008g0012 a0001c0001t0023g0097 a0001c0001t0050g0096 others(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 | a0001c0001t0006g0123 | 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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 others(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 | a0001c0001t0006g0230 a0001c0001t0006g0231 a0001c0001t0006g0232 |
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 | a0001c0001t0021g0067 a0001c0001t0021g0073 a0001c0001t0022g0069 others(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 | a0001c0001t0016g0084 a0001c0001t0019g0248 a0001c0001t0019g0249 others(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 | 152 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(149): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): 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 | a0001c0001t0004g0120 a0001c0001t0006g0123 a0001c0001t0008g0012 others(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 | a0001c0001t0006g0116 a0002c0002t0001g0115 |
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 | a0001c0001t0004g0112 a0001c0001t0004g0114 a0001c0001t0006g0113 others(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 | a0001c0001t0110g0243 a0001c0001t0111g0241 a0002c0009t0108g0242 |
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 | a0001c0001t0063g0080 a0003c0003t0011g0078 a0003c0003t0011g0081 others(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 | a0001c0001t0016g0084 a0001c0001t0029g0082 a0001c0001t0029g0083 |
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 | 224 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0153 others(221): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): 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 | a0001c0001t0016g0084 a0001c0001t0029g0082 a0001c0001t0029g0083 |
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 | a0001c0001t0008g0012 a0001c0001t0008g0085 a0001c0001t0008g0086 others(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 | a0001c0001t0019g0248 a0001c0001t0019g0249 a0001c0001t0019g0250 others(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 | a0002c0002t0002g0001 | 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 | a0001c0001t0023g0097 a0001c0001t0050g0096 |
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 | a0001c0001t0008g0012 a0001c0001t0070g0013 |
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 | a0001c0001t0022g0099 a0001c0001t0028g0103 a0001c0001t0066g0102 others(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 |