Item | Value |
---|---|
geneid | 368 |
ensemblid | ENSG00000091262.17 |
hgncid | 57 |
symbol | ABCC6 |
name | ATP binding cassette subfamily C member 6 |
refseq_nuc | NM_001171.6 |
refseq_prot | NP_001162.5 |
ensembl_nuc | ENST00000205557.12 |
ensembl_prot | ENSP00000205557.7 |
mane_status | MANE Select |
chr | chr16 |
start | 16149565 |
end | 16223494 |
strand | - |
ver | v1.2 |
region | chr16:16149565-16223494 |
region5000 | chr16:16144565-16228494 |
regionname0 | ABCC6_chr16_16149565_16223494 |
regionname5000 | ABCC6_chr16_16144565_16228494 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1503 | 177 | 21 | 31 | 91 | 4 | 29 | 65 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0002 | 0/0 | 1503 | 45 | 17 | 12 | 12 | 2 | 2 | 8 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0003 | 0/0 | 1503 | 32 | 2 | 11 | 10 | 5 | 4 | 9 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0004 | 0/0 | 1503 | 12 | 4 | 0 | 4 | 4 | 0 | 3 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0005 | 0/0 | 1503 | 9 | 1 | 2 | 5 | 0 | 1 | 5 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0006 | 0/0 | 1503 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0007 | 0/0 | 1503 | 7 | 0 | 3 | 4 | 0 | 0 | 4 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0008 | 0/0 | 1503 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0009 | 0/0 | 1503 | 4 | 0 | 2 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0010 | 0/0 | 1503 | 4 | 1 | 3 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0011 | 0/0 | 1503 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0012 | 0/0 | 1503 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0013 | 0/0 | 1503 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0014 | 0/0 | 1503 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0015 | 0/0 | 1503 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0016 | 0/0 | 1503 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0017 | 0/0 | 1503 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0018 | 0/0 | 1503 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0019 | 0/0 | 1503 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0020 | 0/0 | 1503 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0021 | 0/0 | 1503 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0022 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0023 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0024 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0025 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0026 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0027 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0028 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0029 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0030 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0031 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0032 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0033 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0034 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0035 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0036 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0037 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0038 | 0/0 | 198 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(193): Show |
chr16 | 16144565 | 16228494 |
a0039 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0040 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0041 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0042 | 0/0 | 824 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(819): Show |
chr16 | 16144565 | 16228494 |
a0043 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0044 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
a0045 | 0/0 | 1503 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | MAAPA others(1498): Show |
chr16 | 16144565 | 16228494 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4509 | 92 | 9 | 20 | 43 | 1 | 19 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0001c0002 | 0/0 | 4509 | 32 | 5 | 0 | 23 | 0 | 4 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0001c0004 | 0/0 | 4509 | 19 | 2 | 9 | 5 | 2 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0001c0006 | 0/0 | 4509 | 17 | 0 | 1 | 15 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0001c0023 | 0/0 | 4509 | 2 | 0 | 0 | 0 | 0 | 2 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0001c0026 | 0/0 | 4509 | 2 | 1 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0001c0028 | 0/0 | 4509 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0001c0033 | 0/0 | 4509 | 2 | 0 | 0 | 0 | 1 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0001c0043 | 0/0 | 4509 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0001c0047 | 0/1 | 4509 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0001c0049 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0001c0052 | 0/0 | 4509 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0001c0055 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0001c0064 | 0/0 | 4509 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0001c0065 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0001c0067 | 0/0 | 4509 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0001c0072 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0002c0003 | 0/0 | 4509 | 27 | 14 | 4 | 7 | 1 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0002c0013 | 0/0 | 4509 | 5 | 0 | 4 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0002c0014 | 0/0 | 4509 | 5 | 0 | 0 | 5 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0002c0022 | 0/0 | 4509 | 2 | 0 | 1 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0002c0024 | 0/0 | 4509 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0002c0051 | 0/0 | 4509 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0002c0057 | 0/0 | 4509 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0002c0068 | 0/0 | 4509 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0002c0074 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0003c0005 | 0/0 | 4509 | 19 | 1 | 5 | 6 | 4 | 3 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0003c0007 | 0/0 | 4509 | 10 | 0 | 4 | 4 | 1 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0003c0021 | 0/0 | 4509 | 2 | 0 | 2 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0003c0071 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0004c0010 | 0/0 | 4509 | 7 | 2 | 0 | 1 | 4 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0004c0017 | 0/0 | 4509 | 4 | 1 | 0 | 3 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0004c0078 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0005c0012 | 0/0 | 4509 | 6 | 0 | 1 | 4 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0005c0031 | 0/0 | 4509 | 2 | 0 | 1 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0005c0048 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0006c0008 | 0/0 | 4509 | 7 | 6 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0007c0009 | 0/0 | 4509 | 7 | 0 | 3 | 4 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0008c0011 | 0/0 | 4509 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0009c0029 | 0/0 | 4509 | 2 | 0 | 2 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0009c0042 | 0/0 | 4509 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0009c0045 | 0/0 | 4509 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0010c0015 | 0/0 | 4509 | 4 | 1 | 3 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0011c0016 | 0/0 | 4509 | 4 | 3 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0012c0020 | 0/0 | 4509 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0012c0050 | 0/0 | 4509 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0013c0025 | 0/0 | 4509 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0013c0030 | 0/0 | 4509 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0014c0018 | 0/0 | 4509 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0015c0019 | 0/0 | 4509 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0016c0032 | 0/0 | 4509 | 2 | 0 | 1 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0017c0035 | 0/0 | 4509 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0018c0034 | 0/0 | 4509 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0019c0036 | 0/0 | 4509 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0020c0027 | 0/0 | 4509 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0021c0066 | 0/0 | 4509 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0022c0041 | 0/0 | 4509 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0023c0053 | 0/0 | 4509 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0024c0075 | 0/0 | 4509 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0025c0076 | 0/0 | 4509 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0026c0039 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0027c0073 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0028c0054 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0029c0069 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0030c0046 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0031c0058 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0032c0038 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0033c0077 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0034c0056 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0035c0060 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0036c0059 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0037c0062 | 0/0 | 4509 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0038c0079 | 0/0 | 4509 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0039c0037 | 0/0 | 4509 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0040c0040 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0041c0070 | 0/0 | 4509 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0042c0061 | 0/0 | 4522 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4517): Show |
chr16 | 16144565 | 16228494 | ||
a0043c0063 | 0/0 | 4509 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0044c0044 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 | ||
a0045c0080 | 0/0 | 4509 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | ATGGC others(4504): Show |
chr16 | 16144565 | 16228494 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5140 | 75 | 9 | 16 | 35 | 1 | 14 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0001c0001t0002 | 0/0 | 5140 | 12 | 0 | 1 | 6 | 0 | 5 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0001c0001t0004 | 0/0 | 5140 | 4 | 0 | 2 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0001c0001t0005 | 0/0 | 5141 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5136): Show |
chr16 | 16144565 | 16228494 |
a0001c0002t0001 | 0/0 | 5140 | 30 | 5 | 0 | 23 | 0 | 2 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0001c0002t0002 | 0/0 | 5140 | 2 | 0 | 0 | 0 | 0 | 2 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0001c0004t0001 | 0/0 | 5140 | 15 | 2 | 8 | 4 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0001c0004t0002 | 0/0 | 5140 | 4 | 0 | 1 | 1 | 1 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0001c0006t0001 | 0/0 | 5140 | 15 | 0 | 0 | 14 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0001c0006t0002 | 0/0 | 5140 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0001c0006t0009 | 0/0 | 5140 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0001c0023t0001 | 0/0 | 5140 | 2 | 0 | 0 | 0 | 0 | 2 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0001c0026t0001 | 0/0 | 5140 | 2 | 1 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0001c0028t0001 | 0/0 | 5140 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0001c0033t0001 | 0/0 | 5140 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0001c0033t0002 | 0/0 | 5140 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0001c0043t0001 | 0/0 | 5140 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0001c0047t0002 | 0/1 | 5140 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0001c0049t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0001c0052t0001 | 0/0 | 5140 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0001c0055t0012 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0001c0064t0005 | 0/0 | 5141 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5136): Show |
chr16 | 16144565 | 16228494 |
a0001c0065t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0001c0067t0001 | 0/0 | 5140 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0001c0072t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0002c0003t0001 | 0/0 | 5140 | 27 | 14 | 4 | 7 | 1 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0002c0013t0001 | 0/0 | 5140 | 5 | 0 | 4 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0002c0014t0001 | 0/0 | 5140 | 5 | 0 | 0 | 5 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0002c0022t0001 | 0/0 | 5140 | 2 | 0 | 1 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0002c0024t0001 | 0/0 | 5140 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0002c0051t0001 | 0/0 | 5140 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0002c0057t0001 | 0/0 | 5140 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0002c0068t0001 | 0/0 | 5140 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0002c0074t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0003c0005t0001 | 0/0 | 5140 | 17 | 1 | 5 | 5 | 4 | 2 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0003c0005t0005 | 0/0 | 5141 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5136): Show |
chr16 | 16144565 | 16228494 |
a0003c0005t0008 | 0/0 | 5140 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0003c0007t0001 | 0/0 | 5140 | 10 | 0 | 4 | 4 | 1 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0003c0021t0001 | 0/0 | 5140 | 2 | 0 | 2 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0003c0071t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0004c0010t0001 | 0/0 | 5140 | 7 | 2 | 0 | 1 | 4 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0004c0017t0001 | 0/0 | 5140 | 4 | 1 | 0 | 3 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0004c0078t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0005c0012t0001 | 0/0 | 5140 | 6 | 0 | 1 | 4 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0005c0031t0001 | 0/0 | 5140 | 2 | 0 | 1 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0005c0048t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0006c0008t0001 | 0/0 | 5140 | 7 | 6 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0007c0009t0001 | 0/0 | 5140 | 7 | 0 | 3 | 4 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0008c0011t0003 | 0/0 | 5140 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0009c0029t0001 | 0/0 | 5140 | 2 | 0 | 2 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0009c0042t0001 | 0/0 | 5140 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0009c0045t0001 | 0/0 | 5140 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0010c0015t0001 | 0/0 | 5140 | 4 | 1 | 3 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0011c0016t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0011c0016t0006 | 0/0 | 5140 | 2 | 1 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0011c0016t0011 | 0/0 | 5141 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5136): Show |
chr16 | 16144565 | 16228494 |
a0012c0020t0001 | 0/0 | 5140 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0012c0050t0001 | 0/0 | 5140 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0013c0025t0001 | 0/0 | 5140 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0013c0030t0001 | 0/0 | 5140 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0014c0018t0001 | 0/0 | 5140 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0015c0019t0001 | 0/0 | 5140 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0016c0032t0001 | 0/0 | 5140 | 2 | 0 | 1 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0017c0035t0001 | 0/0 | 5140 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0018c0034t0001 | 0/0 | 5140 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0019c0036t0001 | 0/0 | 5140 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0020c0027t0007 | 0/0 | 5140 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0021c0066t0001 | 0/0 | 5140 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0022c0041t0001 | 0/0 | 5140 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0023c0053t0001 | 0/0 | 5140 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0024c0075t0001 | 0/0 | 5140 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0025c0076t0001 | 0/0 | 5140 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0026c0039t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0027c0073t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0028c0054t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0029c0069t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0030c0046t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0031c0058t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0032c0038t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0033c0077t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0034c0056t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0035c0060t0010 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0036c0059t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0037c0062t0001 | 0/0 | 5140 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0038c0079t0001 | 0/0 | 5140 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0039c0037t0001 | 0/0 | 5140 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0040c0040t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0041c0070t0002 | 0/0 | 5140 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0042c0061t0001 | 0/0 | 5153 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5148): Show |
chr16 | 16144565 | 16228494 |
a0043c0063t0001 | 0/0 | 5140 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0044c0044t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
a0045c0080t0001 | 0/0 | 5140 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | AGTCT others(5135): Show |
chr16 | 16144565 | 16228494 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0001t0005g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0002g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0002t0002g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0004t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0004t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0004t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0004t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0004t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0004t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0004t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0004t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0004t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0004t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0004t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0004t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0004t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0004t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0004t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0004t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0004t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0006t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0006t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0006t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0006t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0006t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0006t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0006t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0006t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0006t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0006t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0006t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0006t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0006t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0006t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0006t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0006t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0006t0009g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0023t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0023t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0026t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0026t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0028t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0028t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0033t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0033t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0043t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0047t0002g0111 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0049t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0052t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0055t0012g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0064t0005g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0065t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0067t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0001c0072t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0003t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0013t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0013t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0013t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0013t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0013t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0014t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0014t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0014t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0014t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0014t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0022t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0022t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0024t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0024t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0051t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0057t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0068t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0002c0074t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0005t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0005t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0005t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0005t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0005t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0005t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0005t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0005t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0005t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0005t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0005t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0005t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0005t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0005t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0005t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0005t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0005t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0005t0005g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0005t0008g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0007t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0007t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0007t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0007t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0007t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0007t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0007t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0007t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0007t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0007t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0021t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0021t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0003c0071t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0004c0010t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0004c0010t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0004c0010t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0004c0010t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0004c0010t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0004c0010t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0004c0010t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0004c0017t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0004c0017t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0004c0017t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0004c0017t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0004c0078t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0005c0012t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0005c0012t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0005c0012t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0005c0012t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0005c0012t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0005c0012t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0005c0031t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0005c0031t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0005c0048t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0006c0008t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0006c0008t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0006c0008t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0006c0008t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0006c0008t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0006c0008t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0006c0008t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0007c0009t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0007c0009t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0007c0009t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0007c0009t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0007c0009t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0007c0009t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0007c0009t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0008c0011t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0008c0011t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0008c0011t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0008c0011t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0008c0011t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0008c0011t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0009c0029t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0009c0029t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0009c0042t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0009c0045t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0010c0015t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0010c0015t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0010c0015t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0010c0015t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0011c0016t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0011c0016t0006g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0011c0016t0006g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0011c0016t0011g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0012c0020t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0012c0020t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0012c0020t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0012c0050t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0013c0025t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0013c0025t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0013c0030t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0013c0030t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0014c0018t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0014c0018t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0014c0018t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0014c0018t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0015c0019t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0015c0019t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0015c0019t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0016c0032t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0016c0032t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0017c0035t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0017c0035t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0018c0034t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0019c0036t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0019c0036t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0020c0027t0007g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0020c0027t0007g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0021c0066t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0022c0041t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0023c0053t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0024c0075t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0025c0076t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0026c0039t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0027c0073t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0028c0054t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0029c0069t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0030c0046t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0031c0058t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0032c0038t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0033c0077t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0034c0056t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0035c0060t0010g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0036c0059t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0037c0062t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0038c0079t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0039c0037t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0040c0040t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0041c0070t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0042c0061t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0043c0063t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0044c0044t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
a0045c0080t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0007 | t0001 | g0245 | EUR | GBR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00099 | hp2 | a0021 | c0066 | t0001 | g0052 | EUR | GBR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00140 | hp1 | a0002 | c0003 | t0001 | g0151 | EUR | GBR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00140 | hp2 | a0003 | c0005 | t0001 | g0084 | EUR | GBR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00280 | hp1 | a0001 | c0004 | t0001 | g0103 | EUR | FIN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00280 | hp2 | a0009 | c0042 | t0001 | g0099 | EUR | FIN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00323 | hp1 | a0004 | c0010 | t0001 | g0046 | EUR | FIN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00323 | hp2 | a0009 | c0045 | t0001 | g0106 | EUR | FIN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00408 | hp1 | a0022 | c0041 | t0001 | g0216 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00438 | hp1 | a0023 | c0053 | t0001 | g0154 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00438 | hp2 | a0002 | c0003 | t0001 | g0320 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00544 | hp1 | a0001 | c0006 | t0001 | g0298 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00558 | hp1 | a0002 | c0003 | t0001 | g0152 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00558 | hp2 | a0001 | c0006 | t0001 | g0291 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00597 | hp1 | a0001 | c0006 | t0001 | g0329 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0354 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00639 | hp1 | a0005 | c0012 | t0001 | g0131 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00639 | hp2 | a0002 | c0068 | t0001 | g0097 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00642 | hp1 | a0024 | c0075 | t0001 | g0049 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00642 | hp2 | a0001 | c0004 | t0001 | g0209 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00733 | hp1 | a0007 | c0009 | t0001 | g0044 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00733 | hp2 | a0001 | c0004 | t0001 | g0220 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00735 | hp1 | a0001 | c0006 | t0002 | g0246 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00735 | hp2 | a0003 | c0007 | t0001 | g0210 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00741 | hp1 | a0002 | c0013 | t0001 | g0244 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG00741 | hp2 | a0001 | c0001 | t0005 | g0206 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01069 | hp1 | a0003 | c0007 | t0001 | g0109 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01069 | hp2 | a0009 | c0029 | t0001 | g0159 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01074 | hp2 | a0001 | c0004 | t0001 | g0163 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01081 | hp1 | a0025 | c0076 | t0001 | g0047 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01099 | hp2 | a0010 | c0015 | t0001 | g0019 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01106 | hp2 | a0002 | c0057 | t0001 | g0255 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01109 | hp1 | a0006 | c0008 | t0001 | g0256 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01109 | hp2 | a0002 | c0003 | t0001 | g0350 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01168 | hp1 | a0010 | c0015 | t0001 | g0018 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01169 | hp2 | a0001 | c0004 | t0001 | g0217 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01175 | hp1 | a0009 | c0029 | t0001 | g0230 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01175 | hp2 | a0001 | c0004 | t0001 | g0263 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01255 | hp2 | a0003 | c0007 | t0001 | g0036 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01256 | hp1 | a0002 | c0013 | t0001 | g0241 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01257 | hp1 | a0010 | c0015 | t0001 | g0022 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01257 | hp2 | a0003 | c0021 | t0001 | g0011 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01258 | hp2 | a0003 | c0021 | t0001 | g0012 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01261 | hp2 | a0005 | c0031 | t0001 | g0349 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01346 | hp1 | a0007 | c0009 | t0001 | g0050 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01346 | hp2 | a0001 | c0004 | t0001 | g0038 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01358 | hp1 | a0001 | c0004 | t0002 | g0218 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01361 | hp2 | a0002 | c0022 | t0001 | g0345 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01433 | hp2 | a0016 | c0032 | t0001 | g0051 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01496 | hp1 | a0002 | c0013 | t0001 | g0243 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01496 | hp2 | a0011 | c0016 | t0006 | g0271 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01515 | hp1 | a0003 | c0005 | t0001 | g0029 | EUR | IBS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01515 | hp2 | a0004 | c0010 | t0001 | g0045 | EUR | IBS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01516 | hp1 | a0004 | c0010 | t0001 | g0042 | EUR | IBS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01516 | hp2 | a0002 | c0022 | t0001 | g0095 | EUR | IBS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01517 | hp1 | a0003 | c0005 | t0001 | g0028 | EUR | IBS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01517 | hp2 | a0004 | c0010 | t0001 | g0043 | EUR | IBS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0175 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01884 | hp2 | a0002 | c0003 | t0001 | g0187 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01928 | hp1 | a0001 | c0001 | t0004 | g0223 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01928 | hp2 | a0012 | c0050 | t0001 | g0040 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01934 | hp1 | a0002 | c0003 | t0001 | g0142 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0348 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01975 | hp1 | a0002 | c0013 | t0001 | g0253 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0156 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01978 | hp1 | a0002 | c0003 | t0001 | g0224 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01978 | hp2 | a0003 | c0007 | t0001 | g0221 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01981 | hp1 | a0002 | c0003 | t0001 | g0225 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01981 | hp2 | a0003 | c0005 | t0001 | g0309 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01993 | hp1 | a0002 | c0051 | t0001 | g0353 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01993 | hp2 | a0001 | c0004 | t0001 | g0034 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02004 | hp2 | a0003 | c0005 | t0001 | g0135 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02040 | hp2 | a0003 | c0005 | t0001 | g0318 | EAS | KHV | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02055 | hp1 | a0005 | c0048 | t0001 | g0063 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02055 | hp2 | a0002 | c0003 | t0001 | g0333 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | KHV | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02056 | hp2 | a0001 | c0004 | t0001 | g0208 | EAS | KHV | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02071 | hp1 | a0004 | c0010 | t0001 | g0342 | EAS | KHV | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02074 | hp1 | a0001 | c0006 | t0001 | g0330 | EAS | KHV | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02132 | hp1 | a0001 | c0006 | t0001 | g0190 | EAS | KHV | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02132 | hp2 | a0001 | c0028 | t0001 | g0279 | EAS | KHV | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02135 | hp2 | a0001 | c0006 | t0001 | g0278 | EAS | KHV | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02145 | hp1 | a0006 | c0008 | t0001 | g0264 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02145 | hp2 | a0011 | c0016 | t0011 | g0301 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02155 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | CDX | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CDX | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02165 | hp1 | a0001 | c0006 | t0001 | g0297 | EAS | CDX | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02165 | hp2 | a0001 | c0006 | t0009 | g0285 | EAS | CDX | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02257 | hp1 | a0002 | c0003 | t0001 | g0176 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02258 | hp1 | a0014 | c0018 | t0001 | g0252 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02258 | hp2 | a0017 | c0035 | t0001 | g0078 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02273 | hp2 | a0003 | c0005 | t0001 | g0307 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02280 | hp1 | a0008 | c0011 | t0003 | g0091 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02280 | hp2 | a0026 | c0039 | t0001 | g0032 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02293 | hp1 | a0001 | c0004 | t0001 | g0037 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02293 | hp2 | a0003 | c0005 | t0001 | g0319 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02300 | hp1 | a0003 | c0005 | t0001 | g0178 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02300 | hp2 | a0007 | c0009 | t0001 | g0048 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02451 | hp1 | a0015 | c0019 | t0001 | g0125 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02451 | hp2 | a0027 | c0073 | t0001 | g0016 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02572 | hp1 | a0002 | c0003 | t0001 | g0267 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02572 | hp2 | a0001 | c0065 | t0001 | g0312 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02615 | hp1 | a0003 | c0005 | t0001 | g0260 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02615 | hp2 | a0006 | c0008 | t0001 | g0259 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02622 | hp1 | a0002 | c0003 | t0001 | g0169 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02622 | hp2 | a0008 | c0011 | t0003 | g0061 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02630 | hp1 | a0006 | c0008 | t0001 | g0053 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02630 | hp2 | a0001 | c0004 | t0001 | g0065 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02647 | hp2 | a0002 | c0024 | t0001 | g0155 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0068 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02698 | hp1 | a0003 | c0005 | t0001 | g0228 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02717 | hp1 | a0001 | c0004 | t0001 | g0006 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02717 | hp2 | a0029 | c0069 | t0001 | g0015 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0167 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02723 | hp2 | a0030 | c0046 | t0001 | g0304 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0332 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02809 | hp2 | a0008 | c0011 | t0003 | g0060 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02818 | hp1 | a0008 | c0011 | t0003 | g0062 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02886 | hp1 | a0031 | c0058 | t0001 | g0165 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02886 | hp2 | a0006 | c0008 | t0001 | g0262 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02895 | hp1 | a0013 | c0025 | t0001 | g0007 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02895 | hp2 | a0002 | c0003 | t0001 | g0168 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02897 | hp1 | a0012 | c0020 | t0001 | g0057 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02897 | hp2 | a0013 | c0025 | t0001 | g0008 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02922 | hp1 | a0008 | c0011 | t0003 | g0058 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02922 | hp2 | a0014 | c0018 | t0001 | g0251 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02965 | hp1 | a0014 | c0018 | t0001 | g0250 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02965 | hp2 | a0002 | c0003 | t0001 | g0074 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02970 | hp1 | a0004 | c0078 | t0001 | g0199 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02970 | hp2 | a0008 | c0011 | t0003 | g0059 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02976 | hp1 | a0002 | c0003 | t0001 | g0261 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02976 | hp2 | a0002 | c0074 | t0001 | g0186 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03098 | hp1 | a0010 | c0015 | t0001 | g0327 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03098 | hp2 | a0002 | c0003 | t0001 | g0123 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03130 | hp2 | a0015 | c0019 | t0001 | g0126 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03139 | hp1 | a0002 | c0003 | t0001 | g0306 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03139 | hp2 | a0011 | c0016 | t0001 | g0275 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03195 | hp1 | a0004 | c0010 | t0001 | g0073 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03195 | hp2 | a0001 | c0055 | t0012 | g0164 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03209 | hp1 | a0002 | c0003 | t0001 | g0013 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03209 | hp2 | a0032 | c0038 | t0001 | g0033 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03225 | hp2 | a0006 | c0008 | t0001 | g0265 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03239 | hp1 | a0003 | c0007 | t0001 | g0110 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03239 | hp2 | a0016 | c0032 | t0001 | g0150 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03453 | hp1 | a0002 | c0024 | t0001 | g0153 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03453 | hp2 | a0012 | c0020 | t0001 | g0055 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03486 | hp1 | a0034 | c0056 | t0001 | g0041 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03490 | hp1 | a0001 | c0023 | t0001 | g0066 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03490 | hp2 | a0001 | c0004 | t0002 | g0219 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0088 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03492 | hp1 | a0001 | c0023 | t0001 | g0100 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03516 | hp1 | a0015 | c0019 | t0001 | g0122 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03540 | hp1 | a0002 | c0003 | t0001 | g0257 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03540 | hp2 | a0035 | c0060 | t0010 | g0240 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03579 | hp1 | a0004 | c0010 | t0001 | g0075 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03579 | hp2 | a0001 | c0072 | t0001 | g0356 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03688 | hp1 | a0002 | c0013 | t0001 | g0266 | SAS | STU | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03688 | hp2 | a0005 | c0012 | t0001 | g0027 | SAS | STU | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03704 | hp2 | a0003 | c0005 | t0001 | g0197 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0340 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | BEB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03831 | hp2 | a0002 | c0003 | t0001 | g0082 | SAS | BEB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03834 | hp1 | a0001 | c0006 | t0001 | g0296 | SAS | BEB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03834 | hp2 | a0001 | c0043 | t0001 | g0236 | SAS | BEB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03927 | hp1 | a0003 | c0005 | t0005 | g0213 | SAS | BEB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0203 | SAS | BEB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | STU | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | STU | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0005 | SAS | STU | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG04204 | hp2 | a0001 | c0033 | t0001 | g0070 | SAS | STU | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0323 | SAS | STU | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | STU | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18522 | hp1 | a0006 | c0008 | t0001 | g0258 | AFR | YRI | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18522 | hp2 | a0002 | c0003 | t0001 | g0188 | AFR | YRI | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18747 | hp1 | a0002 | c0003 | t0001 | g0316 | EAS | CHB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | CHB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18906 | hp1 | a0013 | c0030 | t0001 | g0113 | AFR | YRI | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18906 | hp2 | a0036 | c0059 | t0001 | g0009 | AFR | YRI | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18939 | hp2 | a0005 | c0012 | t0001 | g0139 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18941 | hp2 | a0001 | c0006 | t0001 | g0300 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18942 | hp1 | a0004 | c0017 | t0001 | g0193 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18943 | hp2 | a0018 | c0034 | t0001 | g0001 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18944 | hp1 | a0019 | c0036 | t0001 | g0344 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18947 | hp1 | a0002 | c0003 | t0001 | g0080 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18949 | hp1 | a0003 | c0007 | t0001 | g0104 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18952 | hp1 | a0001 | c0006 | t0001 | g0286 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18952 | hp2 | a0001 | c0006 | t0001 | g0292 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18953 | hp1 | a0003 | c0005 | t0001 | g0314 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18953 | hp2 | a0001 | c0004 | t0002 | g0105 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18962 | hp1 | a0020 | c0027 | t0007 | g0294 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18964 | hp1 | a0001 | c0004 | t0001 | g0211 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18964 | hp2 | a0005 | c0012 | t0001 | g0140 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18968 | hp1 | a0001 | c0001 | t0004 | g0182 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18968 | hp2 | a0003 | c0007 | t0001 | g0102 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18969 | hp2 | a0001 | c0026 | t0001 | g0096 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18971 | hp1 | a0003 | c0007 | t0001 | g0098 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18977 | hp1 | a0037 | c0062 | t0001 | g0315 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18977 | hp2 | a0001 | c0064 | t0005 | g0324 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18978 | hp1 | a0007 | c0009 | t0001 | g0120 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18979 | hp1 | a0002 | c0014 | t0001 | g0288 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18981 | hp1 | a0001 | c0004 | t0001 | g0108 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18981 | hp2 | a0007 | c0009 | t0001 | g0119 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18983 | hp1 | a0004 | c0017 | t0001 | g0254 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18983 | hp2 | a0001 | c0004 | t0001 | g0212 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18985 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18985 | hp2 | a0002 | c0014 | t0001 | g0328 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18986 | hp2 | a0003 | c0005 | t0001 | g0282 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18987 | hp2 | a0001 | c0028 | t0001 | g0295 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18990 | hp2 | a0002 | c0014 | t0001 | g0289 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18993 | hp2 | a0003 | c0005 | t0001 | g0321 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18995 | hp2 | a0005 | c0012 | t0001 | g0179 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19000 | hp2 | a0038 | c0079 | t0001 | g0238 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19002 | hp2 | a0020 | c0027 | t0007 | g0293 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19003 | hp1 | a0001 | c0006 | t0001 | g0277 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19005 | hp1 | a0002 | c0014 | t0001 | g0284 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19007 | hp1 | a0007 | c0009 | t0001 | g0118 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19007 | hp2 | a0039 | c0037 | t0001 | g0355 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19010 | hp2 | a0002 | c0003 | t0001 | g0146 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19011 | hp1 | a0003 | c0005 | t0008 | g0317 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19011 | hp2 | a0002 | c0014 | t0001 | g0331 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19030 | hp2 | a0011 | c0016 | t0006 | g0280 | AFR | LWK | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19043 | hp1 | a0040 | c0040 | t0001 | g0031 | AFR | LWK | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19043 | hp2 | a0001 | c0049 | t0001 | g0352 | AFR | LWK | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19056 | hp1 | a0001 | c0006 | t0001 | g0276 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19060 | hp1 | a0003 | c0005 | t0001 | g0158 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19060 | hp2 | a0001 | c0006 | t0001 | g0290 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19065 | hp1 | a0019 | c0036 | t0001 | g0343 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19065 | hp2 | a0001 | c0006 | t0001 | g0299 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19066 | hp1 | a0003 | c0007 | t0001 | g0101 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19066 | hp2 | a0004 | c0017 | t0001 | g0214 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19070 | hp2 | a0005 | c0012 | t0001 | g0121 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19074 | hp1 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19074 | hp2 | a0041 | c0070 | t0002 | g0067 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19077 | hp1 | a0001 | c0052 | t0001 | g0283 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19077 | hp2 | a0042 | c0061 | t0001 | g0130 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19079 | hp2 | a0007 | c0009 | t0001 | g0116 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19081 | hp1 | a0002 | c0003 | t0001 | g0081 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0310 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19084 | hp1 | a0018 | c0034 | t0001 | g0001 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19084 | hp2 | a0043 | c0063 | t0001 | g0171 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19087 | hp2 | a0005 | c0031 | t0001 | g0133 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19240 | hp1 | a0004 | c0017 | t0001 | g0076 | AFR | YRI | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA19240 | hp2 | a0044 | c0044 | t0001 | g0302 | AFR | YRI | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA20129 | hp1 | a0012 | c0020 | t0001 | g0056 | AFR | ASW | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA20129 | hp2 | a0003 | c0071 | t0001 | g0035 | AFR | ASW | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA20752 | hp1 | a0003 | c0005 | t0001 | g0177 | EUR | TSI | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA20752 | hp2 | a0001 | c0033 | t0002 | g0196 | EUR | TSI | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA20805 | hp1 | a0001 | c0004 | t0002 | g0134 | EUR | TSI | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0227 | EUR | TSI | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | GIH | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA20905 | hp2 | a0045 | c0080 | t0001 | g0090 | SAS | GIH | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG01123 | hp2 | a0001 | c0067 | t0001 | g0351 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02109 | hp2 | a0013 | c0030 | t0001 | g0274 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02559 | hp1 | a0028 | c0054 | t0001 | g0072 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03471 | hp1 | a0002 | c0003 | t0001 | g0232 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG03471 | hp2 | a0033 | c0077 | t0001 | g0198 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG06807 | hp1 | a0014 | c0018 | t0001 | g0249 | AFR | USA | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
HG06807 | hp2 | a0001 | c0026 | t0001 | g0272 | AFR | USA | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA20300 | hp1 | a0017 | c0035 | t0001 | g0077 | AFR | USA | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | USA | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
homoSapiens | chm13v2 | a0001 | c0047 | t0002 | g0111 | REF | REF | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:16154767 | G | A | 1 | a0043 | 1 | NA19084.hp2 | missense_variant | MODERATE | c.4069C>T | p.Arg1357Trp | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/31 | 4129/5140 | 4069/4512 | 1357/1503 | chr16 | 16154767 | |||
chr16:16154934 | C | T | 1 | a0017 | 2 | HG02258.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.3980G>A | p.Gly1327Glu | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 28/31 | 4040/5140 | 3980/4512 | 1327/1503 | chr16 | 16154934 | |||
chr16:16155007 | C | T | 1 | a0037 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.3907G>A | p.Ala1303Thr | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 28/31 | 3967/5140 | 3907/4512 | 1303/1503 | chr16 | 16155007 | |||
chr16:16157674 | C | T | 6 | a0008 a0011 a0015 others(3): Show |
16 | HG01496.hp2 HG02145.hp2 HG02280.hp1 others(13): Show |
missense_variant | MODERATE | c.3871G>A | p.Ala1291Thr | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/31 | 3931/5140 | 3871/4512 | 1291/1503 | chr16 | 16157674 | |||
chr16:16157742 | C | T | 6 | a0003 a0005 a0009 others(3): Show |
49 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(46): Show |
missense_variant | MODERATE | c.3803G>A | p.Arg1268Gln | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/31 | 3863/5140 | 3803/4512 | 1268/1503 | chr16 | 16157742 | |||
chr16:16161509 | T | G | 1 | a0031 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.3562A>C | p.Thr1188Pro | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/31 | 3622/5140 | 3562/4512 | 1188/1503 | chr16 | 16161509 | |||
chr16:16165640 | G | T | 2 | a0024 a0044 |
2 | HG00642.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.3289C>A | p.Leu1097Ile | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/31 | 3349/5140 | 3289/4512 | 1097/1503 | chr16 | 16165640 | |||
chr16:16165739 | G | A | 2 | a0016 a0021 |
3 | HG00099.hp2 HG01433.hp2 HG03239.hp2 |
missense_variant | MODERATE | c.3190C>T | p.Arg1064Trp | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/31 | 3250/5140 | 3190/4512 | 1064/1503 | chr16 | 16165739 | |||
chr16:16165865 | G | C | 1 | a0034 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.3064C>G | p.Gln1022Glu | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/31 | 3124/5140 | 3064/4512 | 1022/1503 | chr16 | 16165865 | |||
chr16:16169805 | G | T | 1 | a0009 | 4 | HG00280.hp2 HG00323.hp2 HG01069.hp2 others(1): Show |
missense_variant | MODERATE | c.2836C>A | p.Leu946Ile | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/31 | 2896/5140 | 2836/4512 | 946/1503 | chr16 | 16169805 | |||
chr16:16173364 | C | G | 2 | a0013 a0030 |
5 | HG02109.hp2 HG02723.hp2 HG02895.hp1 others(2): Show |
missense_variant | MODERATE | c.2707G>C | p.Glu903Gln | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/31 | 2767/5140 | 2707/4512 | 903/1503 | chr16 | 16173364 | |||
chr16:16173375 | C | T | 1 | a0028 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.2696G>A | p.Arg899His | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/31 | 2756/5140 | 2696/4512 | 899/1503 | chr16 | 16173375 | |||
chr16:16173376 | G | A | 1 | a0015 | 3 | HG02451.hp1 HG03130.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.2695C>T | p.Arg899Cys | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/31 | 2755/5140 | 2695/4512 | 899/1503 | chr16 | 16173376 | |||
chr16:16177500 | T | C | 41 | a0001 a0002 a0003 others(38): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
missense_variant | MODERATE | c.2542A>G | p.Met848Val | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/31 | 2602/5140 | 2542/4512 | 848/1503 | chr16 | 16177500 | |||
chr16:16177618 | A | AATCCGTG others(6): Show |
1 | a0042 | 1 | NA19077.hp2 | frameshift_variant | HIGH | c.2416-5_2423dupCCCA others(9): Show |
p.Leu809fs | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/31 | 2483/5140 | 2423/4512 | 808/1503 | chr16 | 16177618 | |||
chr16:16182435 | T | C | 4 | a0024 a0035 a0036 others(1): Show |
4 | HG00642.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
missense_variant | MODERATE | c.2224A>G | p.Ile742Val | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/31 | 2284/5140 | 2224/4512 | 742/1503 | chr16 | 16182435 | |||
chr16:16182488 | C | T | 2 | a0035 a0036 |
2 | HG03540.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.2171G>A | p.Arg724Lys | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/31 | 2231/5140 | 2171/4512 | 724/1503 | chr16 | 16182488 | |||
chr16:16182519 | C | T | 1 | a0025 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.2140G>A | p.Gly714Arg | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/31 | 2200/5140 | 2140/4512 | 714/1503 | chr16 | 16182519 | |||
chr16:16182911 | G | T | 1 | a0030 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1963C>A | p.Gln655Lys | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 16/31 | 2023/5140 | 1963/4512 | 655/1503 | chr16 | 16182911 | |||
chr16:16185006 | G | T | 11 | a0002 a0003 a0007 others(8): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
missense_variant | MODERATE | c.1896C>A | p.His632Gln | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/31 | 1956/5140 | 1896/4512 | 632/1503 | chr16 | 16185006 | |||
chr16:16187150 | A | G | 14 | a0002 a0003 a0007 others(11): Show |
103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
missense_variant | MODERATE | c.1841T>C | p.Val614Ala | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/31 | 1901/5140 | 1841/4512 | 614/1503 | chr16 | 16187150 | |||
chr16:16190229 | C | A | 1 | a0029 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.1570G>T | p.Ala524Ser | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/31 | 1630/5140 | 1570/4512 | 524/1503 | chr16 | 16190229 | |||
chr16:16198076 | T | C | 1 | a0041 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.1283A>G | p.Asn428Ser | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/31 | 1343/5140 | 1283/4512 | 428/1503 | chr16 | 16198076 | |||
chr16:16198116 | C | T | 1 | a0023 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.1243G>A | p.Val415Met | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/31 | 1303/5140 | 1243/4512 | 415/1503 | chr16 | 16198116 | |||
chr16:16203453 | T | C | 1 | a0017 | 2 | HG02258.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.955A>G | p.Ile319Val | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/31 | 1015/5140 | 955/4512 | 319/1503 | chr16 | 16203453 | |||
chr16:16208729 | T | C | 7 | a0004 a0007 a0017 others(4): Show |
26 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(23): Show |
missense_variant&splice_region_variant | MODERATE | c.793A>G | p.Arg265Gly | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/31 | 853/5140 | 793/4512 | 265/1503 | chr16 | 16208729 | |||
chr16:16212240 | A | G | 1 | a0022 | 1 | HG00408.hp1 | missense_variant | MODERATE | c.607T>C | p.Cys203Arg | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/31 | 667/5140 | 607/4512 | 203/1503 | chr16 | 16212240 | |||
chr16:16214329 | G | A | 1 | a0038 | 1 | NA19000.hp2 | stop_gained | HIGH | c.595C>T | p.Gln199* | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/31 | 655/5140 | 595/4512 | 199/1503 | chr16 | 16214329 | |||
chr16:16214364 | G | A | 1 | a0045 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.560C>T | p.Ala187Val | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/31 | 620/5140 | 560/4512 | 187/1503 | chr16 | 16214364 | |||
chr16:16214437 | C | T | 3 | a0026 a0032 a0040 |
3 | HG02280.hp2 HG03209.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.487G>A | p.Asp163Asn | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/31 | 547/5140 | 487/4512 | 163/1503 | chr16 | 16214437 | |||
chr16:16219555 | G | A | 1 | a0014 | 4 | HG02258.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.473C>T | p.Ala158Val | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/31 | 533/5140 | 473/4512 | 158/1503 | chr16 | 16219555 | |||
chr16:16219655 | C | T | 1 | a0039 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.373G>A | p.Glu125Lys | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/31 | 433/5140 | 373/4512 | 125/1503 | chr16 | 16219655 | |||
chr16:16221759 | C | A | 1 | a0019 | 2 | NA18944.hp1 NA19065.hp1 |
missense_variant | MODERATE | c.109G>T | p.Val37Phe | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/31 | 169/5140 | 109/4512 | 37/1503 | chr16 | 16221759 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:16154660 | C | T | 1 | a0001c0049 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.4176G>A | p.Gln1392Gln | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/31 | 4236/5140 | 4176/4512 | 1392/1503 | chr16 | 16154660 | |||
chr16:16155011 | G | A | 1 | a0001c0064 | 1 | NA18977.hp2 | synonymous_variant | LOW | c.3903C>T | p.Thr1301Thr | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 28/31 | 3963/5140 | 3903/4512 | 1301/1503 | chr16 | 16155011 | |||
chr16:16157693 | G | A | 1 | a0001c0055 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.3852C>T | p.Gly1284Gly | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/31 | 3912/5140 | 3852/4512 | 1284/1503 | chr16 | 16157693 | |||
chr16:16163040 | G | A | 2 | a0001c0065 a0004c0078 |
2 | HG02572.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.3459C>T | p.Arg1153Arg | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/31 | 3519/5140 | 3459/4512 | 1153/1503 | chr16 | 16163040 | |||
chr16:16169806 | G | A | 15 | a0001c0002 a0001c0026 a0001c0028 others(12): Show |
59 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(56): Show |
synonymous_variant | LOW | c.2835C>T | p.Pro945Pro | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/31 | 2895/5140 | 2835/4512 | 945/1503 | chr16 | 16169806 | |||
chr16:16169806 | G | C | 1 | a0001c0067 | 1 | HG01123.hp2 | synonymous_variant | LOW | c.2835C>G | p.Pro945Pro | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/31 | 2895/5140 | 2835/4512 | 945/1503 | chr16 | 16169806 | |||
chr16:16173290 | G | A | 1 | a0015c0019 | 3 | HG02451.hp1 HG03130.hp2 HG03516.hp1 |
synonymous_variant | LOW | c.2781C>T | p.Tyr927Tyr | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/31 | 2841/5140 | 2781/4512 | 927/1503 | chr16 | 16173290 | |||
chr16:16177468 | T | A | 1 | a0001c0052 | 1 | NA19077.hp1 | synonymous_variant | LOW | c.2574A>T | p.Gly858Gly | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/31 | 2634/5140 | 2574/4512 | 858/1503 | chr16 | 16177468 | |||
chr16:16177552 | G | A | 12 | a0002c0003 a0002c0014 a0002c0022 others(9): Show |
53 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(50): Show |
synonymous_variant | LOW | c.2490C>T | p.Ala830Ala | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/31 | 2550/5140 | 2490/4512 | 830/1503 | chr16 | 16177552 | |||
chr16:16178813 | T | C | 76 | a0001c0001 a0001c0002 a0001c0004 others(73): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
synonymous_variant | LOW | c.2400A>G | p.Gly800Gly | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/31 | 2460/5140 | 2400/4512 | 800/1503 | chr16 | 16178813 | |||
chr16:16182484 | T | A | 4 | a0024c0075 a0035c0060 a0036c0059 others(1): Show |
4 | HG00642.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
synonymous_variant | LOW | c.2175A>T | p.Val725Val | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/31 | 2235/5140 | 2175/4512 | 725/1503 | chr16 | 16182484 | |||
chr16:16182574 | G | A | 1 | a0022c0041 | 1 | HG00408.hp1 | synonymous_variant | LOW | c.2085C>T | p.Tyr695Tyr | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/31 | 2145/5140 | 2085/4512 | 695/1503 | chr16 | 16182574 | |||
chr16:16185012 | G | C | 25 | a0002c0003 a0002c0013 a0002c0014 others(22): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
synonymous_variant | LOW | c.1890C>G | p.Thr630Thr | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/31 | 1950/5140 | 1890/4512 | 630/1503 | chr16 | 16185012 | |||
chr16:16187176 | G | A | 1 | a0002c0068 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.1815C>T | p.Leu605Leu | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/31 | 1875/5140 | 1815/4512 | 605/1503 | chr16 | 16187176 | |||
chr16:16192917 | C | T | 4 | a0001c0055 a0012c0020 a0028c0054 others(1): Show |
6 | HG02559.hp1 HG02897.hp1 HG03195.hp2 others(3): Show |
synonymous_variant | LOW | c.1344G>A | p.Leu448Leu | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/31 | 1404/5140 | 1344/4512 | 448/1503 | chr16 | 16192917 | |||
chr16:16198114 | C | T | 21 | a0001c0004 a0001c0023 a0001c0026 others(18): Show |
68 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(65): Show |
synonymous_variant | LOW | c.1245G>A | p.Val415Val | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/31 | 1305/5140 | 1245/4512 | 415/1503 | chr16 | 16198114 | |||
chr16:16198126 | A | G | 27 | a0001c0004 a0001c0006 a0001c0023 others(24): Show |
96 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(93): Show |
synonymous_variant | LOW | c.1233T>C | p.Asn411Asn | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/31 | 1293/5140 | 1233/4512 | 411/1503 | chr16 | 16198126 | |||
chr16:16198144 | C | T | 1 | a0001c0043 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.1215G>A | p.Ala405Ala | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/31 | 1275/5140 | 1215/4512 | 405/1503 | chr16 | 16198144 | |||
chr16:16202100 | T | C | 5 | a0001c0033 a0001c0072 a0002c0074 others(2): Show |
6 | HG02451.hp2 HG02976.hp2 HG03579.hp2 others(3): Show |
synonymous_variant | LOW | c.1077A>G | p.Ser359Ser | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/31 | 1137/5140 | 1077/4512 | 359/1503 | chr16 | 16202100 | |||
chr16:16203415 | C | A | 1 | a0012c0020 | 3 | HG02897.hp1 HG03453.hp2 NA20129.hp1 |
synonymous_variant | LOW | c.993G>T | p.Leu331Leu | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/31 | 1053/5140 | 993/4512 | 331/1503 | chr16 | 16203415 | |||
chr16:16212202 | C | T | 3 | a0001c0023 a0002c0022 a0009c0042 |
5 | HG00280.hp2 HG01361.hp2 HG01516.hp2 others(2): Show |
synonymous_variant | LOW | c.645G>A | p.Thr215Thr | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/31 | 705/5140 | 645/4512 | 215/1503 | chr16 | 16212202 | |||
chr16:16221678 | G | T | 1 | a0003c0021 | 2 | HG01257.hp2 HG01258.hp2 |
synonymous_variant | LOW | c.190C>A | p.Arg64Arg | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/31 | 250/5140 | 190/4512 | 64/1503 | chr16 | 16221678 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:16149668 | T | TG | 4 | a0001c0001t0005 a0001c0064t0005 a0003c0005t0005 others(1): Show |
4 | HG00741.hp2 HG02145.hp2 HG03927.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*464dupC | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 31/31 | 464 | chr16 | 16149668 | ||||||
chr16:16149675 | C | G | 2 | a0001c0055t0012 a0035c0060t0010 |
2 | HG03195.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*458G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 31/31 | 458 | chr16 | 16149675 | ||||||
chr16:16149685 | G | A | 2 | a0011c0016t0006 a0011c0016t0011 |
3 | HG01496.hp2 HG02145.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*448C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 31/31 | 448 | chr16 | 16149685 | ||||||
chr16:16149880 | C | T | 1 | a0008c0011t0003 | 6 | HG02280.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*253G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 31/31 | 253 | chr16 | 16149880 | ||||||
chr16:16149926 | C | T | 1 | a0001c0006t0009 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*207G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 31/31 | 207 | chr16 | 16149926 | ||||||
chr16:16149981 | T | C | 1 | a0001c0055t0012 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*152A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 31/31 | 152 | chr16 | 16149981 | ||||||
chr16:16150033 | C | T | 1 | a0003c0005t0008 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*100G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 31/31 | 100 | chr16 | 16150033 | ||||||
chr16:16150095 | C | T | 1 | a0001c0001t0004 | 4 | HG01928.hp1 HG01975.hp2 NA18968.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*38G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 31/31 | 38 | chr16 | 16150095 | ||||||
chr16:16150108 | C | A | 1 | a0020c0027t0007 | 2 | NA18962.hp1 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*25G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 31/31 | 25 | chr16 | 16150108 | ||||||
chr16:16150116 | C | T | 6 | a0001c0001t0002 a0001c0002t0002 a0001c0004t0002 others(3): Show |
21 | HG00735.hp1 HG01261.hp1 HG01358.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*17G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 31/31 | 17 | chr16 | 16150116 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:16150272 | T | C | 78 | a0001c0001t0001g0086 a0001c0001t0001g0201 a0001c0001t0001g0202 others(75): Show |
79 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.4404-31A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 30/30 | chr16 | 16150272 | |||||||
chr16:16150317 | T | C | 59 | a0001c0001t0001g0127 a0001c0001t0001g0239 a0001c0001t0001g0273 others(56): Show |
59 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.4404-76A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 30/30 | chr16 | 16150317 | |||||||
chr16:16150418 | C | G | 1 | a0001c0002t0001g0085 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.4403+160G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 30/30 | chr16 | 16150418 | |||||||
chr16:16150519 | G | A | 1 | a0035c0060t0010g0240 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4403+59C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 30/30 | chr16 | 16150519 | |||||||
chr16:16150780 | C | T | 1 | a0012c0050t0001g0040 | 1 | HG01928.hp2 | splice_region_variant&intron_variant | LOW | c.4209-8G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16150780 | |||||||
chr16:16150802 | C | T | 1 | a0002c0024t0001g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4209-30G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16150802 | |||||||
chr16:16150806 | C | T | 6 | a0008c0011t0003g0058 a0008c0011t0003g0059 a0008c0011t0003g0060 others(3): Show |
6 | HG02280.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.4209-34G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16150806 | |||||||
chr16:16150816 | C | T | 1 | a0002c0024t0001g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4209-44G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16150816 | |||||||
chr16:16151139 | G | A | 6 | a0008c0011t0003g0058 a0008c0011t0003g0059 a0008c0011t0003g0060 others(3): Show |
6 | HG02280.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.4209-367C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151139 | |||||||
chr16:16151222 | C | T | 1 | a0004c0017t0001g0193 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.4209-450G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151222 | |||||||
chr16:16151243 | G | A | 4 | a0001c0001t0001g0233 a0001c0001t0001g0305 a0001c0049t0001g0352 others(1): Show |
4 | HG00639.hp2 HG02109.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.4209-471C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151243 | |||||||
chr16:16151248 | G | C | 1 | a0001c0001t0001g0129 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.4209-476C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151248 | |||||||
chr16:16151267 | G | C | 55 | a0001c0001t0001g0184 a0001c0001t0001g0339 a0001c0002t0001g0014 others(52): Show |
55 | HG00438.hp2 HG00558.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.4209-495C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151267 | |||||||
chr16:16151268 | G | A | 8 | a0001c0001t0001g0239 a0002c0013t0001g0241 a0002c0013t0001g0243 others(5): Show |
8 | HG00741.hp1 HG01256.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.4209-496C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151268 | |||||||
chr16:16151396 | A | G | 1 | a0001c0055t0012g0164 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4209-624T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151396 | |||||||
chr16:16151412 | G | A | 1 | a0001c0055t0012g0164 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4209-640C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151412 | |||||||
chr16:16151491 | T | C | 1 | a0004c0017t0001g0254 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.4209-719A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151491 | |||||||
chr16:16151492 | G | C | 345 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(342): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.4209-720C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151492 | |||||||
chr16:16151519 | A | T | 1 | a0003c0007t0001g0101 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.4209-747T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151519 | |||||||
chr16:16151551 | G | A | 26 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0083 others(23): Show |
26 | HG00597.hp1 HG00639.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.4209-779C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151551 | |||||||
chr16:16151603 | T | C | 1 | a0001c0001t0001g0323 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4209-831A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151603 | |||||||
chr16:16151845 | G | T | 1 | a0011c0016t0001g0275 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4209-1073C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151845 | |||||||
chr16:16151866 | G | A | 4 | a0015c0019t0001g0122 a0015c0019t0001g0125 a0015c0019t0001g0126 others(1): Show |
4 | HG02451.hp1 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.4209-1094C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151866 | |||||||
chr16:16151872 | G | A | 48 | a0001c0004t0001g0263 a0003c0005t0001g0028 a0003c0005t0001g0029 others(45): Show |
49 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.4209-1100C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151872 | |||||||
chr16:16151914 | G | A | 6 | a0008c0011t0003g0058 a0008c0011t0003g0059 a0008c0011t0003g0060 others(3): Show |
6 | HG02280.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.4209-1142C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151914 | |||||||
chr16:16151921 | G | A | 1 | a0001c0002t0002g0004 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4209-1149C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151921 | |||||||
chr16:16151975 | G | A | 4 | a0015c0019t0001g0122 a0015c0019t0001g0125 a0015c0019t0001g0126 others(1): Show |
4 | HG02451.hp1 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.4209-1203C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151975 | |||||||
chr16:16152053 | G | A | 116 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(113): Show |
116 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.4209-1281C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152053 | |||||||
chr16:16152116 | C | T | 1 | a0041c0070t0002g0067 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.4209-1344G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152116 | |||||||
chr16:16152132 | CA | C | 149 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(146): Show |
149 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.4209-1361delT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152132 | |||||||
chr16:16152192 | C | CA | 91 | a0001c0001t0001g0127 a0001c0001t0001g0239 a0001c0001t0001g0339 others(88): Show |
91 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.4209-1421dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152192 | |||||||
chr16:16152192 | C | CAA | 64 | a0001c0001t0001g0184 a0001c0001t0002g0088 a0001c0002t0001g0014 others(61): Show |
65 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.4209-1422_4209-142 others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152192 | |||||||
chr16:16152192 | C | CAAA | 28 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0002g0030 others(25): Show |
28 | HG00323.hp1 HG00735.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.4209-1423_4209-142 others(7): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152192 | |||||||
chr16:16152192 | C | CAAAAA | 25 | a0001c0001t0001g0017 a0001c0001t0001g0128 a0001c0001t0001g0143 others(22): Show |
25 | HG00597.hp1 HG00639.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.4209-1425_4209-142 others(9): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152192 | |||||||
chr16:16152192 | C | CAAAAAA | 12 | a0001c0001t0001g0020 a0001c0001t0001g0089 a0001c0001t0001g0107 others(9): Show |
12 | HG01106.hp2 HG01358.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.4209-1426_4209-142 others(10): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152192 | |||||||
chr16:16152192 | C | CAAAAAAA | 78 | a0001c0001t0001g0039 a0001c0001t0001g0069 a0001c0001t0001g0079 others(75): Show |
78 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.4209-1427_4209-142 others(11): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152192 | |||||||
chr16:16152192 | C | CAAAAAAA others(1): Show |
28 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0137 others(25): Show |
28 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.4209-1428_4209-142 others(12): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152192 | |||||||
chr16:16152192 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0136 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.4209-1430_4209-142 others(14): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152192 | |||||||
chr16:16152192 | CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0001g0354 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.4209-1430_4209-142 others(14): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152192 | |||||||
chr16:16152222 | A | G | 151 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(148): Show |
151 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.4209-1450T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152222 | |||||||
chr16:16152307 | T | G | 50 | a0001c0002t0001g0014 a0001c0004t0001g0263 a0003c0005t0001g0028 others(47): Show |
51 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(48): Show |
intron_variant | MODIFIER | c.4209-1535A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152307 | |||||||
chr16:16152333 | A | G | 150 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(147): Show |
150 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.4209-1561T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152333 | |||||||
chr16:16152453 | A | G | 1 | a0027c0073t0001g0016 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4209-1681T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152453 | |||||||
chr16:16152722 | C | T | 4 | a0001c0001t0002g0203 a0011c0016t0006g0271 a0011c0016t0006g0280 others(1): Show |
4 | HG01496.hp2 HG02145.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.4208+1906G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152722 | |||||||
chr16:16152724 | G | A | 1 | a0004c0017t0001g0214 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.4208+1904C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152724 | |||||||
chr16:16152730 | G | A | 1 | a0001c0001t0004g0156 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.4208+1898C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152730 | |||||||
chr16:16152733 | G | C | 1 | a0005c0048t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4208+1895C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152733 | |||||||
chr16:16152906 | G | GT | 149 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(146): Show |
149 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.4208+1721dupA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152906 | |||||||
chr16:16152927 | T | C | 1 | a0001c0055t0012g0164 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4208+1701A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152927 | |||||||
chr16:16153036 | C | G | 1 | a0001c0055t0012g0164 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4208+1592G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153036 | |||||||
chr16:16153089 | G | A | 2 | a0001c0001t0001g0326 a0001c0001t0001g0338 |
2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4208+1539C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153089 | |||||||
chr16:16153175 | G | A | 5 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(2): Show |
5 | HG03491.hp1 HG03492.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.4208+1453C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153175 | |||||||
chr16:16153240 | T | G | 2 | a0013c0025t0001g0007 a0013c0025t0001g0008 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4208+1388A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153240 | |||||||
chr16:16153255 | A | T | 1 | a0011c0016t0001g0275 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4208+1373T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153255 | |||||||
chr16:16153439 | A | G | 1 | a0001c0055t0012g0164 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4208+1189T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153439 | |||||||
chr16:16153463 | C | T | 1 | a0001c0004t0001g0263 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4208+1165G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153463 | |||||||
chr16:16153493 | C | CA | 34 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0083 others(31): Show |
34 | HG00597.hp1 HG00639.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.4208+1134dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153493 | |||||||
chr16:16153520 | G | A | 2 | a0010c0015t0001g0327 a0034c0056t0001g0041 |
2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4208+1108C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153520 | |||||||
chr16:16153614 | A | T | 53 | a0001c0001t0001g0184 a0001c0001t0001g0339 a0001c0006t0009g0285 others(50): Show |
53 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.4208+1014T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153614 | |||||||
chr16:16153722 | G | A | 1 | a0035c0060t0010g0240 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4208+906C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153722 | |||||||
chr16:16153914 | GA | G | 94 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(91): Show |
94 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.4208+713delT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153914 | |||||||
chr16:16153969 | C | G | 1 | a0035c0060t0010g0240 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4208+659G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153969 | |||||||
chr16:16153996 | A | C | 1 | a0001c0055t0012g0164 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4208+632T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153996 | |||||||
chr16:16154088 | T | C | 2 | a0010c0015t0001g0327 a0034c0056t0001g0041 |
2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4208+540A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16154088 | |||||||
chr16:16154263 | CA | C | 7 | a0001c0001t0001g0233 a0001c0001t0001g0305 a0001c0049t0001g0352 others(4): Show |
7 | HG00639.hp2 HG01496.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.4208+364delT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16154263 | |||||||
chr16:16154369 | C | T | 2 | a0009c0042t0001g0099 a0009c0045t0001g0106 |
2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.4208+259G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16154369 | |||||||
chr16:16154371 | A | G | 1 | a0006c0008t0001g0258 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4208+257T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16154371 | |||||||
chr16:16154823 | C | T | 4 | a0001c0001t0001g0233 a0001c0001t0001g0305 a0001c0049t0001g0352 others(1): Show |
4 | HG00639.hp2 HG02109.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.4042-29G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 28/30 | chr16 | 16154823 | |||||||
chr16:16154824 | G | A | 52 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0069 others(49): Show |
52 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.4042-30C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 28/30 | chr16 | 16154824 | |||||||
chr16:16155038 | G | A | 1 | a0001c0002t0001g0287 | 1 | NA18939.hp1 | splice_region_variant&intron_variant | LOW | c.3883-7C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16155038 | |||||||
chr16:16155148 | T | G | 2 | a0013c0030t0001g0113 a0013c0030t0001g0274 |
2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3883-117A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16155148 | |||||||
chr16:16155333 | C | G | 89 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(86): Show |
89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.3883-302G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16155333 | |||||||
chr16:16155361 | CATCT | C | 92 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(89): Show |
92 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.3883-334_3883-331d others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16155361 | |||||||
chr16:16155373 | C | T | 1 | a0001c0001t0002g0088 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3883-342G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16155373 | |||||||
chr16:16155411 | GCCAT | G | 89 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(86): Show |
89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.3883-384_3883-381d others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16155411 | |||||||
chr16:16155687 | C | T | 1 | a0002c0013t0001g0266 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3883-656G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16155687 | |||||||
chr16:16155807 | A | C | 1 | a0001c0002t0001g0141 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.3883-776T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16155807 | |||||||
chr16:16155904 | C | CTTTA | 95 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(92): Show |
95 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.3883-877_3883-874d others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16155904 | |||||||
chr16:16155904 | CTTTA | C | 3 | a0004c0010t0001g0073 a0017c0035t0001g0077 a0017c0035t0001g0078 |
3 | HG02258.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3883-877_3883-874d others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16155904 | |||||||
chr16:16155980 | A | G | 1 | a0001c0055t0012g0164 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3883-949T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16155980 | |||||||
chr16:16156136 | A | T | 4 | a0009c0029t0001g0159 a0009c0029t0001g0230 a0009c0042t0001g0099 others(1): Show |
4 | HG00280.hp2 HG00323.hp2 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.3883-1105T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156136 | |||||||
chr16:16156402 | C | A | 1 | a0001c0001t0001g0337 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.3882+1261G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156402 | |||||||
chr16:16156437 | C | T | 3 | a0001c0002t0001g0054 a0001c0002t0001g0093 a0001c0002t0001g0310 |
3 | NA18990.hp1 NA18999.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.3882+1226G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156437 | |||||||
chr16:16156462 | G | A | 1 | a0029c0069t0001g0015 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3882+1201C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156462 | |||||||
chr16:16156499 | C | A | 19 | a0001c0001t0001g0039 a0001c0001t0001g0079 a0001c0001t0001g0144 others(16): Show |
19 | HG00642.hp2 HG00741.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.3882+1164G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156499 | |||||||
chr16:16156620 | G | C | 1 | a0003c0005t0001g0135 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3882+1043C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156620 | |||||||
chr16:16156639 | C | T | 1 | a0001c0055t0012g0164 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3882+1024G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156639 | |||||||
chr16:16156741 | C | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(204): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.3882+922G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156741 | |||||||
chr16:16156935 | T | A | 2 | a0001c0001t0002g0094 a0001c0001t0002g0311 |
2 | NA18959.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.3882+728A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156935 | |||||||
chr16:16156942 | C | CA | 123 | a0001c0001t0001g0086 a0001c0001t0001g0184 a0001c0001t0001g0201 others(120): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.3882+720dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156942 | |||||||
chr16:16156942 | C | CAA | 39 | a0001c0001t0001g0127 a0001c0002t0001g0024 a0001c0002t0001g0025 others(36): Show |
39 | HG00408.hp1 HG00544.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.3882+719_3882+720d others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156942 | |||||||
chr16:16156942 | C | CAAA | 14 | a0001c0002t0001g0010 a0001c0002t0001g0023 a0001c0002t0001g0085 others(11): Show |
14 | HG00597.hp2 HG00673.hp2 HG02738.hp2 others(11): Show |
intron_variant | MODIFIER | c.3882+718_3882+720d others(5): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156942 | |||||||
chr16:16156942 | CA | C | 37 | a0001c0001t0001g0069 a0001c0001t0001g0079 a0001c0001t0001g0083 others(34): Show |
37 | HG00438.hp1 HG00735.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.3882+720delT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156942 | |||||||
chr16:16156942 | CAA | C | 78 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(75): Show |
78 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.3882+719_3882+720d others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156942 | |||||||
chr16:16157003 | C | G | 3 | a0001c0001t0001g0270 a0001c0006t0001g0190 a0001c0006t0001g0298 |
3 | HG00544.hp1 HG02074.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.3882+660G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16157003 | |||||||
chr16:16157043 | C | T | 1 | a0003c0007t0001g0102 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3882+620G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16157043 | |||||||
chr16:16157402 | G | A | 23 | a0001c0001t0001g0083 a0001c0001t0002g0030 a0001c0001t0002g0087 others(20): Show |
23 | HG00735.hp1 HG01074.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.3882+261C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16157402 | |||||||
chr16:16157547 | A | G | 1 | a0003c0007t0001g0102 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3882+116T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16157547 | |||||||
chr16:16157578 | G | A | 343 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(340): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.3882+85C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16157578 | |||||||
chr16:16157600 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3882+63G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16157600 | |||||||
chr16:16157615 | C | T | 2 | a0001c0065t0001g0312 a0004c0078t0001g0199 |
2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3882+48G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16157615 | |||||||
chr16:16158042 | T | G | 36 | a0001c0001t0001g0003 a0001c0001t0001g0129 a0001c0001t0001g0136 others(33): Show |
36 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.3736-233A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158042 | |||||||
chr16:16158109 | T | C | 1 | a0004c0078t0001g0199 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3736-300A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158109 | |||||||
chr16:16158143 | T | G | 30 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0201 others(27): Show |
30 | HG00323.hp1 HG00735.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.3736-334A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158143 | |||||||
chr16:16158229 | T | A | 16 | a0008c0011t0003g0058 a0008c0011t0003g0059 a0008c0011t0003g0060 others(13): Show |
16 | HG01496.hp2 HG02145.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.3736-420A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158229 | |||||||
chr16:16158311 | G | A | 91 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(88): Show |
91 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.3736-502C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158311 | |||||||
chr16:16158330 | A | G | 1 | a0001c0001t0002g0088 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3736-521T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158330 | |||||||
chr16:16158367 | C | T | 80 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0107 others(77): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.3736-558G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158367 | |||||||
chr16:16158441 | G | C | 90 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(87): Show |
90 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.3736-632C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158441 | |||||||
chr16:16158455 | A | ATCCC | 74 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(71): Show |
74 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.3736-647_3736-646i others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158455 | |||||||
chr16:16158455 | A | C | 17 | a0001c0001t0001g0129 a0001c0001t0001g0136 a0001c0001t0001g0137 others(14): Show |
17 | HG00558.hp2 HG00673.hp1 HG03831.hp1 others(14): Show |
intron_variant | MODIFIER | c.3736-646T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158455 | |||||||
chr16:16158491 | T | C | 1 | a0004c0078t0001g0199 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3736-682A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158491 | |||||||
chr16:16158525 | C | A | 48 | a0003c0005t0001g0028 a0003c0005t0001g0029 a0003c0005t0001g0084 others(45): Show |
49 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.3736-716G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158525 | |||||||
chr16:16158630 | C | T | 2 | a0011c0016t0006g0280 a0011c0016t0011g0301 |
2 | HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3736-821G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158630 | |||||||
chr16:16158676 | T | C | 6 | a0010c0015t0001g0327 a0012c0020t0001g0055 a0012c0020t0001g0056 others(3): Show |
6 | HG02897.hp1 HG03098.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.3735+806A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158676 | |||||||
chr16:16158839 | T | C | 91 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(88): Show |
91 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.3735+643A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158839 | |||||||
chr16:16158900 | G | A | 6 | a0010c0015t0001g0327 a0012c0020t0001g0055 a0012c0020t0001g0056 others(3): Show |
6 | HG02897.hp1 HG03098.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.3735+582C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158900 | |||||||
chr16:16159181 | T | C | 7 | a0001c0004t0001g0065 a0001c0004t0001g0263 a0002c0057t0001g0255 others(4): Show |
7 | HG01106.hp2 HG01175.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.3735+301A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16159181 | |||||||
chr16:16159229 | C | T | 2 | a0001c0002t0001g0231 a0001c0004t0001g0212 |
2 | NA18962.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.3735+253G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16159229 | |||||||
chr16:16159364 | G | C | 1 | a0001c0004t0001g0034 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3735+118C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16159364 | |||||||
chr16:16159382 | G | A | 1 | a0001c0001t0001g0340 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3735+100C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16159382 | |||||||
chr16:16159382 | G | C | 1 | a0001c0001t0002g0087 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3735+100C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16159382 | |||||||
chr16:16159426 | GC | G | 341 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(338): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.3735+55delG | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16159426 | |||||||
chr16:16159435 | C | G | 8 | a0010c0015t0001g0327 a0012c0020t0001g0055 a0012c0020t0001g0056 others(5): Show |
8 | HG00642.hp1 HG02897.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.3735+47G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16159435 | |||||||
chr16:16159455 | A | AC | 6 | a0001c0001t0001g0189 a0001c0002t0001g0354 a0001c0004t0001g0034 others(3): Show |
6 | HG00597.hp2 HG01993.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.3735+26dupG | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16159455 | |||||||
chr16:16159587 | G | A | 1 | a0011c0016t0001g0275 | 1 | HG03139.hp2 | splice_region_variant&intron_variant | LOW | c.3634-4C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16159587 | |||||||
chr16:16159713 | C | T | 90 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(87): Show |
90 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.3634-130G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16159713 | |||||||
chr16:16159778 | C | T | 1 | a0002c0003t0001g0232 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3634-195G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16159778 | |||||||
chr16:16159835 | C | T | 1 | a0001c0055t0012g0164 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3634-252G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16159835 | |||||||
chr16:16159939 | G | A | 2 | a0001c0001t0001g0181 a0001c0004t0001g0103 |
2 | HG00280.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.3634-356C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16159939 | |||||||
chr16:16160059 | T | C | 1 | a0001c0001t0001g0269 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3634-476A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160059 | |||||||
chr16:16160300 | C | T | 6 | a0008c0011t0003g0058 a0008c0011t0003g0059 a0008c0011t0003g0060 others(3): Show |
6 | HG02280.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3634-717G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160300 | |||||||
chr16:16160316 | G | T | 1 | a0014c0018t0001g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3634-733C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160316 | |||||||
chr16:16160618 | C | T | 1 | a0005c0012t0001g0140 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.3633+820G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160618 | |||||||
chr16:16160628 | C | CA | 54 | a0001c0001t0001g0127 a0001c0001t0001g0239 a0001c0001t0001g0305 others(51): Show |
54 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.3633+809dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160628 | |||||||
chr16:16160628 | C | CAA | 71 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0189 others(68): Show |
72 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.3633+808_3633+809d others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160628 | |||||||
chr16:16160628 | C | CAAA | 38 | a0001c0001t0001g0017 a0001c0001t0001g0107 a0001c0001t0001g0170 others(35): Show |
38 | HG00639.hp1 HG00735.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.3633+807_3633+809d others(5): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160628 | |||||||
chr16:16160628 | C | CAAAA | 20 | a0001c0001t0001g0020 a0001c0001t0001g0128 a0001c0001t0001g0143 others(17): Show |
20 | HG00597.hp1 HG01981.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.3633+806_3633+809d others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160628 | |||||||
chr16:16160628 | C | CAAAAA | 7 | a0011c0016t0006g0271 a0011c0016t0006g0280 a0013c0030t0001g0113 others(4): Show |
7 | HG01496.hp2 HG02717.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3633+805_3633+809d others(7): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160628 | |||||||
chr16:16160628 | CA | C | 39 | a0001c0001t0001g0003 a0001c0001t0001g0129 a0001c0001t0001g0136 others(36): Show |
39 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.3633+809delT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160628 | |||||||
chr16:16160628 | CAA | C | 46 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0069 others(43): Show |
46 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.3633+808_3633+809d others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160628 | |||||||
chr16:16160628 | CAAAAA | C | 19 | a0001c0001t0001g0339 a0001c0026t0001g0272 a0002c0003t0001g0013 others(16): Show |
19 | HG01346.hp1 HG01516.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.3633+805_3633+809d others(7): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160628 | |||||||
chr16:16160628 | CAAAAAA | C | 28 | a0001c0001t0001g0184 a0001c0006t0009g0285 a0002c0003t0001g0002 others(25): Show |
28 | HG00438.hp2 HG00558.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.3633+804_3633+809d others(8): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160628 | |||||||
chr16:16160641 | A | C | 1 | a0006c0008t0001g0264 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3633+797T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160641 | |||||||
chr16:16160644 | A | G | 1 | a0001c0055t0012g0164 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3633+794T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160644 | |||||||
chr16:16160769 | C | T | 50 | a0001c0002t0001g0014 a0003c0005t0001g0028 a0003c0005t0001g0029 others(47): Show |
51 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(48): Show |
intron_variant | MODIFIER | c.3633+669G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160769 | |||||||
chr16:16160830 | C | T | 12 | a0008c0011t0003g0058 a0008c0011t0003g0059 a0008c0011t0003g0060 others(9): Show |
12 | HG01496.hp2 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.3633+608G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160830 | |||||||
chr16:16160909 | A | G | 57 | a0001c0001t0001g0086 a0001c0001t0001g0201 a0001c0001t0001g0202 others(54): Show |
58 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(55): Show |
intron_variant | MODIFIER | c.3633+529T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160909 | |||||||
chr16:16161054 | G | A | 1 | a0001c0006t0001g0286 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.3633+384C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16161054 | |||||||
chr16:16161058 | T | C | 2 | a0001c0001t0001g0313 a0001c0001t0001g0337 |
2 | NA18949.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.3633+380A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16161058 | |||||||
chr16:16161236 | ACAAGGAA others(11): Show |
A | 6 | a0001c0001t0001g0069 a0001c0001t0001g0180 a0001c0001t0001g0194 others(3): Show |
6 | HG00140.hp1 HG01123.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.3633+184_3633+201d others(20): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16161236 | |||||||
chr16:16161338 | T | G | 345 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(342): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.3633+100A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16161338 | |||||||
chr16:16161339 | T | G | 5 | a0001c0004t0001g0065 a0014c0018t0001g0249 a0014c0018t0001g0250 others(2): Show |
5 | HG02258.hp1 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3633+99A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16161339 | |||||||
chr16:16161348 | C | T | 90 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(87): Show |
90 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.3633+90G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16161348 | |||||||
chr16:16161383 | G | A | 90 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(87): Show |
90 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.3633+55C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16161383 | |||||||
chr16:16161567 | G | A | 4 | a0009c0029t0001g0159 a0009c0029t0001g0230 a0009c0042t0001g0099 others(1): Show |
4 | HG00280.hp2 HG00323.hp2 HG01069.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.3507-3C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16161567 | |||||||
chr16:16161580 | A | G | 32 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0107 others(29): Show |
32 | HG00597.hp1 HG00639.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.3507-16T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16161580 | |||||||
chr16:16161583 | G | A | 1 | a0002c0074t0001g0186 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3507-19C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16161583 | |||||||
chr16:16161594 | G | T | 1 | a0002c0013t0001g0266 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3507-30C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16161594 | |||||||
chr16:16161726 | C | T | 1 | a0001c0004t0001g0163 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3507-162G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16161726 | |||||||
chr16:16161771 | G | A | 1 | a0001c0002t0001g0026 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3507-207C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16161771 | |||||||
chr16:16161982 | T | C | 7 | a0002c0013t0001g0241 a0002c0013t0001g0243 a0002c0013t0001g0244 others(4): Show |
7 | HG00741.hp1 HG01256.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.3507-418A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16161982 | |||||||
chr16:16162293 | T | C | 2 | a0001c0065t0001g0312 a0004c0078t0001g0199 |
2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3506+700A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16162293 | |||||||
chr16:16162478 | G | A | 1 | a0005c0048t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3506+515C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16162478 | |||||||
chr16:16162562 | C | T | 1 | a0005c0048t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3506+431G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16162562 | |||||||
chr16:16162752 | G | C | 3 | a0005c0048t0001g0063 a0035c0060t0010g0240 a0036c0059t0001g0009 |
3 | HG02055.hp1 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3506+241C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16162752 | |||||||
chr16:16162821 | C | T | 29 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(26): Show |
29 | HG00597.hp1 HG00639.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.3506+172G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16162821 | |||||||
chr16:16162852 | T | C | 1 | a0005c0048t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3506+141A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16162852 | |||||||
chr16:16162879 | C | T | 1 | a0001c0002t0001g0332 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3506+114G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16162879 | |||||||
chr16:16162910 | T | A | 2 | a0016c0032t0001g0051 a0021c0066t0001g0052 |
2 | HG00099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.3506+83A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16162910 | |||||||
chr16:16162910 | T | G | 247 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(244): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.3506+83A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16162910 | |||||||
chr16:16163297 | G | C | 2 | a0001c0065t0001g0312 a0004c0078t0001g0199 |
2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3307-105C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16163297 | |||||||
chr16:16163412 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3307-220G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16163412 | |||||||
chr16:16163416 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3307-224A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16163416 | |||||||
chr16:16163443 | C | T | 4 | a0001c0001t0001g0128 a0001c0001t0001g0143 a0001c0001t0001g0200 others(1): Show |
4 | HG02135.hp1 HG02155.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.3307-251G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16163443 | |||||||
chr16:16163553 | C | A | 93 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(90): Show |
94 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.3307-361G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16163553 | |||||||
chr16:16163581 | T | C | 3 | a0001c0001t0001g0313 a0001c0001t0001g0335 a0001c0001t0001g0337 |
3 | NA18949.hp2 NA18971.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.3307-389A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16163581 | |||||||
chr16:16163615 | G | A | 2 | a0024c0075t0001g0049 a0044c0044t0001g0302 |
2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3307-423C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16163615 | |||||||
chr16:16163664 | G | T | 4 | a0001c0001t0001g0233 a0001c0001t0001g0305 a0001c0049t0001g0352 others(1): Show |
4 | HG00639.hp2 HG02109.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.3307-472C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16163664 | |||||||
chr16:16164089 | A | G | 62 | a0001c0001t0001g0127 a0001c0001t0001g0184 a0001c0002t0001g0010 others(59): Show |
62 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.3307-897T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16164089 | |||||||
chr16:16164092 | G | C | 1 | a0005c0048t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3307-900C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16164092 | |||||||
chr16:16164127 | G | A | 1 | a0001c0002t0001g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3307-935C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16164127 | |||||||
chr16:16164138 | A | G | 2 | a0001c0006t0001g0300 a0019c0036t0001g0343 |
2 | NA18941.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.3307-946T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16164138 | |||||||
chr16:16164182 | C | T | 2 | a0003c0005t0001g0228 a0003c0007t0001g0245 |
2 | HG00099.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.3307-990G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16164182 | |||||||
chr16:16164188 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.3307-996G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16164188 | |||||||
chr16:16164316 | G | A | 59 | a0001c0001t0001g0233 a0001c0001t0001g0239 a0001c0001t0001g0305 others(56): Show |
60 | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.3307-1124C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16164316 | |||||||
chr16:16164336 | C | T | 5 | a0013c0025t0001g0007 a0013c0025t0001g0008 a0013c0030t0001g0113 others(2): Show |
5 | HG02109.hp2 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.3307-1144G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16164336 | |||||||
chr16:16164391 | G | T | 2 | a0013c0030t0001g0113 a0013c0030t0001g0274 |
2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3307-1199C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16164391 | |||||||
chr16:16164973 | T | C | 254 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(251): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.3306+650A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16164973 | |||||||
chr16:16165034 | C | G | 2 | a0010c0015t0001g0327 a0034c0056t0001g0041 |
2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3306+589G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16165034 | |||||||
chr16:16165092 | G | A | 3 | a0004c0010t0001g0073 a0017c0035t0001g0077 a0017c0035t0001g0078 |
3 | HG02258.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3306+531C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16165092 | |||||||
chr16:16165092 | G | C | 1 | a0001c0001t0002g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3306+531C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16165092 | |||||||
chr16:16165124 | G | T | 1 | a0005c0048t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3306+499C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16165124 | |||||||
chr16:16165133 | G | A | 2 | a0035c0060t0010g0240 a0036c0059t0001g0009 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3306+490C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16165133 | |||||||
chr16:16165363 | A | G | 2 | a0024c0075t0001g0049 a0044c0044t0001g0302 |
2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3306+260T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16165363 | |||||||
chr16:16165432 | A | T | 2 | a0001c0001t0001g0340 a0003c0005t0005g0213 |
2 | HG03710.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.3306+191T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16165432 | |||||||
chr16:16165597 | C | T | 1 | a0005c0012t0001g0179 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.3306+26G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16165597 | |||||||
chr16:16166001 | G | A | 1 | a0002c0003t0001g0306 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2996-68C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166001 | |||||||
chr16:16166008 | T | TCTC | 3 | a0001c0006t0001g0276 a0001c0006t0001g0290 a0001c0006t0001g0292 |
3 | NA18952.hp2 NA19056.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.2996-78_2996-76dup others(3): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166008 | |||||||
chr16:16166162 | C | T | 247 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(244): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.2996-229G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166162 | |||||||
chr16:16166340 | C | T | 2 | a0001c0001t0001g0326 a0001c0001t0001g0338 |
2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2996-407G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166340 | |||||||
chr16:16166454 | C | CTAGAGGA others(3): Show |
2 | a0001c0065t0001g0312 a0004c0078t0001g0199 |
2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2996-522_2996-521i others(12): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166454 | |||||||
chr16:16166485 | C | T | 247 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(244): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.2996-552G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166485 | |||||||
chr16:16166570 | C | T | 244 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(241): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.2996-637G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166570 | |||||||
chr16:16166586 | A | G | 247 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(244): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.2996-653T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166586 | |||||||
chr16:16166593 | C | T | 4 | a0001c0001t0001g0233 a0001c0001t0001g0305 a0001c0049t0001g0352 others(1): Show |
4 | HG00639.hp2 HG02109.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2996-660G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166593 | |||||||
chr16:16166657 | A | G | 1 | a0001c0001t0001g0020 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2996-724T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166657 | |||||||
chr16:16166697 | C | T | 1 | a0040c0040t0001g0031 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2996-764G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166697 | |||||||
chr16:16166792 | G | C | 6 | a0001c0055t0012g0164 a0005c0048t0001g0063 a0024c0075t0001g0049 others(3): Show |
6 | HG00642.hp1 HG02055.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.2996-859C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166792 | |||||||
chr16:16166792 | G | T | 240 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(237): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.2996-859C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166792 | |||||||
chr16:16166796 | C | T | 61 | a0001c0001t0001g0239 a0001c0001t0001g0339 a0002c0003t0001g0002 others(58): Show |
62 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.2996-863G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166796 | |||||||
chr16:16166902 | A | AAAAC | 245 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(242): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.2996-973_2996-970d others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166902 | |||||||
chr16:16166902 | A | C | 1 | a0005c0048t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2996-969T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166902 | |||||||
chr16:16166961 | C | A | 4 | a0001c0001t0001g0233 a0001c0001t0001g0305 a0001c0049t0001g0352 others(1): Show |
4 | HG00639.hp2 HG02109.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2996-1028G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166961 | |||||||
chr16:16167146 | C | T | 241 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(238): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.2996-1213G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167146 | |||||||
chr16:16167276 | A | G | 1 | a0001c0004t0001g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2996-1343T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167276 | |||||||
chr16:16167286 | C | T | 347 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(344): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.2996-1353G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167286 | |||||||
chr16:16167313 | G | C | 244 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(241): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.2996-1380C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167313 | |||||||
chr16:16167366 | C | G | 1 | a0002c0051t0001g0353 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2996-1433G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167366 | |||||||
chr16:16167394 | C | T | 69 | a0001c0001t0001g0233 a0001c0001t0001g0239 a0001c0001t0001g0305 others(66): Show |
70 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.2996-1461G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167394 | |||||||
chr16:16167553 | C | T | 245 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(242): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.2996-1620G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167553 | |||||||
chr16:16167560 | C | G | 1 | a0001c0004t0001g0006 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2996-1627G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167560 | |||||||
chr16:16167573 | G | A | 1 | a0001c0026t0001g0272 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2996-1640C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167573 | |||||||
chr16:16167758 | C | T | 245 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(242): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.2996-1825G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167758 | |||||||
chr16:16167784 | T | G | 1 | a0001c0006t0001g0298 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2996-1851A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167784 | |||||||
chr16:16167816 | C | A | 1 | a0004c0017t0001g0076 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2995+1830G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167816 | |||||||
chr16:16167829 | C | T | 2 | a0004c0017t0001g0214 a0004c0017t0001g0254 |
2 | NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.2995+1817G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167829 | |||||||
chr16:16167830 | C | T | 2 | a0004c0017t0001g0214 a0004c0017t0001g0254 |
2 | NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.2995+1816G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167830 | |||||||
chr16:16168068 | T | G | 4 | a0001c0001t0001g0233 a0001c0001t0001g0305 a0001c0049t0001g0352 others(1): Show |
4 | HG00639.hp2 HG02109.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2995+1578A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168068 | |||||||
chr16:16168087 | C | T | 1 | a0002c0003t0001g0333 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2995+1559G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168087 | |||||||
chr16:16168088 | G | A | 2 | a0001c0001t0001g0234 a0001c0033t0001g0070 |
2 | HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2995+1558C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168088 | |||||||
chr16:16168111 | C | T | 6 | a0008c0011t0003g0058 a0008c0011t0003g0059 a0008c0011t0003g0060 others(3): Show |
6 | HG02280.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2995+1535G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168111 | |||||||
chr16:16168169 | C | A | 4 | a0015c0019t0001g0122 a0015c0019t0001g0125 a0015c0019t0001g0126 others(1): Show |
4 | HG02451.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2995+1477G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168169 | |||||||
chr16:16168206 | G | GCCAGGCC others(79): Show |
1 | a0001c0072t0001g0356 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2995+1439_2995+144 others(90): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168206 | |||||||
chr16:16168212 | C | A | 1 | a0001c0004t0001g0103 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2995+1434G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168212 | |||||||
chr16:16168218 | G | GTGGTGGC others(165): Show |
6 | a0001c0001t0001g0233 a0001c0001t0001g0305 a0001c0049t0001g0352 others(3): Show |
6 | HG00639.hp2 HG02109.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2995+1427_2995+142 others(176): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168218 | |||||||
chr16:16168218 | G | GTGGTGGC others(251): Show |
2 | a0010c0015t0001g0327 a0034c0056t0001g0041 |
2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2995+1427_2995+142 others(262): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168218 | |||||||
chr16:16168218 | G | GTGGTGGC others(251): Show |
57 | a0001c0001t0001g0239 a0001c0001t0001g0339 a0002c0003t0001g0002 others(54): Show |
58 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.2995+1427_2995+142 others(262): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168218 | |||||||
chr16:16168218 | G | GTGGTGGC others(79): Show |
44 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0201 others(41): Show |
44 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.2995+1427_2995+142 others(90): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168218 | |||||||
chr16:16168218 | G | GTGGTGGC others(251): Show |
1 | a0005c0048t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2995+1427_2995+142 others(262): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168218 | |||||||
chr16:16168218 | G | GTGGTGGC others(165): Show |
81 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(78): Show |
81 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.2995+1427_2995+142 others(176): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168218 | |||||||
chr16:16168218 | G | GTGGTGGC others(165): Show |
18 | a0001c0001t0001g0129 a0001c0001t0001g0136 a0001c0001t0001g0137 others(15): Show |
18 | HG00558.hp2 HG00673.hp1 HG03831.hp1 others(15): Show |
intron_variant | MODIFIER | c.2995+1427_2995+142 others(176): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168218 | |||||||
chr16:16168243 | A | ACACTTTG others(251): Show |
1 | a0003c0007t0001g0221 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2995+1402_2995+140 others(262): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168243 | |||||||
chr16:16168243 | A | ACACTTTG others(165): Show |
45 | a0002c0013t0001g0241 a0002c0013t0001g0243 a0002c0013t0001g0244 others(42): Show |
45 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.2995+1402_2995+140 others(176): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168243 | |||||||
chr16:16168317 | C | T | 204 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(201): Show |
205 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.2995+1329G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168317 | |||||||
chr16:16168353 | G | A | 4 | a0015c0019t0001g0122 a0015c0019t0001g0125 a0015c0019t0001g0126 others(1): Show |
4 | HG02451.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2995+1293C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168353 | |||||||
chr16:16168434 | C | T | 59 | a0001c0001t0001g0239 a0001c0001t0001g0339 a0002c0003t0001g0002 others(56): Show |
60 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2995+1212G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168434 | |||||||
chr16:16168485 | A | T | 1 | a0004c0010t0001g0342 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2995+1161T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168485 | |||||||
chr16:16168513 | G | A | 1 | a0007c0009t0001g0050 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2995+1133C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168513 | |||||||
chr16:16168663 | G | C | 103 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0201 others(100): Show |
104 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.2995+983C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168663 | |||||||
chr16:16168666 | G | T | 103 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0201 others(100): Show |
104 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.2995+980C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168666 | |||||||
chr16:16168674 | A | T | 1 | a0002c0014t0001g0288 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2995+972T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168674 | |||||||
chr16:16168715 | G | A | 80 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(77): Show |
80 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.2995+931C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168715 | |||||||
chr16:16168719 | A | T | 80 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(77): Show |
80 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.2995+927T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168719 | |||||||
chr16:16168810 | G | A | 80 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(77): Show |
80 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.2995+836C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168810 | |||||||
chr16:16168847 | G | C | 4 | a0001c0001t0001g0233 a0001c0001t0001g0305 a0001c0049t0001g0352 others(1): Show |
4 | HG00639.hp2 HG02109.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2995+799C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168847 | |||||||
chr16:16168878 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0201 |
2 | HG02683.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2995+768G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168878 | |||||||
chr16:16168952 | T | C | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02602.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2995+694A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168952 | |||||||
chr16:16169006 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2995+640G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16169006 | |||||||
chr16:16169023 | G | C | 28 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(25): Show |
28 | HG00597.hp1 HG01106.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.2995+623C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16169023 | |||||||
chr16:16169035 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2995+611C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16169035 | |||||||
chr16:16169046 | C | A | 261 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(258): Show |
262 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.2995+600G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16169046 | |||||||
chr16:16169127 | T | C | 34 | a0001c0001t0001g0233 a0001c0001t0001g0305 a0001c0049t0001g0352 others(31): Show |
35 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.2995+519A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16169127 | |||||||
chr16:16169221 | G | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0172 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2995+425C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16169221 | |||||||
chr16:16169293 | G | C | 347 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(344): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.2995+353C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16169293 | |||||||
chr16:16169403 | G | A | 1 | a0007c0009t0001g0050 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2995+243C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16169403 | |||||||
chr16:16169478 | G | C | 1 | a0002c0013t0001g0253 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2995+168C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16169478 | |||||||
chr16:16169495 | C | T | 5 | a0003c0005t0001g0135 a0003c0005t0001g0178 a0003c0005t0001g0307 others(2): Show |
5 | HG01981.hp2 HG02004.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.2995+151G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16169495 | |||||||
chr16:16169504 | G | A | 347 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(344): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.2995+142C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16169504 | |||||||
chr16:16169980 | T | C | 347 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(344): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.2788-127A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16169980 | |||||||
chr16:16170006 | G | A | 1 | a0007c0009t0001g0120 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2788-153C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170006 | |||||||
chr16:16170007 | A | G | 347 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(344): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.2788-154T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170007 | |||||||
chr16:16170094 | T | TTTTC | 4 | a0001c0001t0001g0180 a0015c0019t0001g0122 a0024c0075t0001g0049 others(1): Show |
4 | HG00642.hp1 HG01433.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2788-242_2788-241i others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170094 | |||||||
chr16:16170095 | T | TTTC | 339 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(336): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.2788-243_2788-242i others(5): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170095 | |||||||
chr16:16170096 | T | TTC | 4 | a0001c0001t0001g0207 a0001c0001t0001g0268 a0002c0003t0001g0074 others(1): Show |
4 | HG00438.hp1 HG01168.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2788-244_2788-243i others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170096 | |||||||
chr16:16170098 | G | T | 347 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(344): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.2788-245C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170098 | |||||||
chr16:16170160 | G | A | 32 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(29): Show |
32 | HG00597.hp1 HG01106.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.2788-307C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170160 | |||||||
chr16:16170241 | T | G | 347 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(344): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.2788-388A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170241 | |||||||
chr16:16170292 | A | G | 347 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(344): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.2788-439T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170292 | |||||||
chr16:16170337 | T | C | 347 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(344): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.2788-484A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170337 | |||||||
chr16:16170419 | C | T | 1 | a0001c0028t0001g0295 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2788-566G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170419 | |||||||
chr16:16170559 | A | G | 347 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(344): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.2788-706T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170559 | |||||||
chr16:16170758 | A | G | 1 | a0001c0001t0002g0087 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2788-905T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170758 | |||||||
chr16:16170875 | C | T | 1 | a0003c0005t0001g0282 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2788-1022G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170875 | |||||||
chr16:16170876 | A | G | 347 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(344): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.2788-1023T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170876 | |||||||
chr16:16170906 | T | A | 1 | a0001c0026t0001g0272 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2788-1053A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170906 | |||||||
chr16:16170906 | T | C | 352 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(349): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.2788-1053A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170906 | |||||||
chr16:16170936 | AAAAAAGA others(3): Show |
A | 1 | a0028c0054t0001g0072 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2788-1093_2788-108 others(14): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170936 | |||||||
chr16:16170938 | AAAAG | A | 66 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0064 others(63): Show |
66 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.2788-1089_2788-108 others(8): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170938 | |||||||
chr16:16170939 | AAAG | A | 62 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0079 others(59): Show |
62 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.2788-1089_2788-108 others(7): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170939 | |||||||
chr16:16170939 | AAAGAAAG | A | 14 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0054 others(11): Show |
14 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.2788-1093_2788-108 others(11): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170939 | |||||||
chr16:16170940 | AAG | A | 79 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0173 others(76): Show |
80 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.2788-1089_2788-108 others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170940 | |||||||
chr16:16170940 | AAGAAAG | A | 78 | a0001c0002t0001g0010 a0001c0002t0001g0014 a0001c0002t0001g0026 others(75): Show |
78 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.2788-1093_2788-108 others(10): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170940 | |||||||
chr16:16170941 | AG | A | 28 | a0001c0001t0001g0172 a0001c0001t0001g0184 a0001c0001t0001g0202 others(25): Show |
28 | HG00438.hp2 HG00558.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.2788-1089delC | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170941 | |||||||
chr16:16170941 | AGAAAG | A | 11 | a0001c0002t0001g0025 a0001c0002t0001g0085 a0001c0002t0001g0332 others(8): Show |
11 | HG00673.hp2 HG01496.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.2788-1093_2788-108 others(9): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170941 | |||||||
chr16:16170942 | G | A | 4 | a0001c0001t0001g0200 a0008c0011t0003g0059 a0035c0060t0010g0240 others(1): Show |
4 | HG02970.hp2 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2788-1089C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170942 | |||||||
chr16:16170946 | G | A | 186 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(183): Show |
186 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.2788-1093C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170946 | |||||||
chr16:16171121 | C | T | 242 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(239): Show |
242 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.2788-1268G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171121 | |||||||
chr16:16171124 | G | A | 347 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(344): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.2788-1271C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171124 | |||||||
chr16:16171196 | G | T | 347 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(344): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.2788-1343C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171196 | |||||||
chr16:16171223 | A | AT | 17 | a0001c0001t0001g0235 a0001c0001t0001g0247 a0001c0001t0001g0248 others(14): Show |
17 | HG00408.hp2 HG00544.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.2788-1371dupA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171223 | |||||||
chr16:16171375 | C | T | 1 | a0001c0055t0012g0164 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2788-1522G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171375 | |||||||
chr16:16171455 | G | A | 1 | a0003c0007t0001g0110 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2788-1602C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171455 | |||||||
chr16:16171557 | A | C | 32 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(29): Show |
32 | HG00597.hp1 HG01106.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.2788-1704T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171557 | |||||||
chr16:16171654 | G | A | 31 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(28): Show |
31 | HG00597.hp1 HG01106.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.2787+1630C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171654 | |||||||
chr16:16171704 | C | A | 150 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(147): Show |
150 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.2787+1580G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171704 | |||||||
chr16:16171705 | G | A | 1 | a0030c0046t0001g0304 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2787+1579C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171705 | |||||||
chr16:16171908 | T | C | 3 | a0001c0001t0001g0326 a0001c0001t0001g0338 a0001c0001t0001g0339 |
3 | HG02559.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2787+1376A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171908 | |||||||
chr16:16171923 | G | A | 1 | a0001c0002t0001g0157 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2787+1361C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171923 | |||||||
chr16:16171923 | G | GATGGATA others(15): Show |
3 | a0005c0048t0001g0063 a0024c0075t0001g0049 a0044c0044t0001g0302 |
3 | HG00642.hp1 HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2787+1360_2787+136 others(26): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171923 | |||||||
chr16:16171923 | G | GATGGATA others(94): Show |
2 | a0001c0006t0001g0329 a0038c0079t0001g0238 |
2 | HG00597.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2787+1360_2787+136 others(105): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171923 | |||||||
chr16:16171934 | G | A | 151 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(148): Show |
151 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.2787+1350C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171934 | |||||||
chr16:16171963 | G | GGTGGGTG others(14): Show |
5 | a0001c0002t0001g0014 a0001c0002t0001g0024 a0001c0055t0012g0164 others(2): Show |
5 | HG00544.hp2 HG03195.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2787+1320_2787+132 others(25): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171963 | |||||||
chr16:16171965 | T | C | 3 | a0001c0001t0001g0326 a0001c0001t0001g0338 a0001c0001t0001g0339 |
3 | HG02559.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2787+1319A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171965 | |||||||
chr16:16171983 | A | G | 52 | a0001c0002t0001g0010 a0001c0002t0001g0023 a0001c0002t0001g0025 others(49): Show |
52 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.2787+1301T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171983 | |||||||
chr16:16171989 | A | G | 52 | a0001c0002t0001g0010 a0001c0002t0001g0023 a0001c0002t0001g0025 others(49): Show |
52 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.2787+1295T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171989 | |||||||
chr16:16172004 | G | A | 52 | a0001c0002t0001g0010 a0001c0002t0001g0023 a0001c0002t0001g0025 others(49): Show |
52 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.2787+1280C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172004 | |||||||
chr16:16172005 | G | A | 52 | a0001c0002t0001g0010 a0001c0002t0001g0023 a0001c0002t0001g0025 others(49): Show |
52 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.2787+1279C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172005 | |||||||
chr16:16172007 | A | T | 52 | a0001c0002t0001g0010 a0001c0002t0001g0023 a0001c0002t0001g0025 others(49): Show |
52 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.2787+1277T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172007 | |||||||
chr16:16172010 | G | A | 52 | a0001c0002t0001g0010 a0001c0002t0001g0023 a0001c0002t0001g0025 others(49): Show |
52 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.2787+1274C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172010 | |||||||
chr16:16172026 | A | G | 52 | a0001c0002t0001g0010 a0001c0002t0001g0023 a0001c0002t0001g0025 others(49): Show |
52 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.2787+1258T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172026 | |||||||
chr16:16172028 | T | A | 52 | a0001c0002t0001g0010 a0001c0002t0001g0023 a0001c0002t0001g0025 others(49): Show |
52 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.2787+1256A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172028 | |||||||
chr16:16172029 | A | G | 53 | a0001c0002t0001g0010 a0001c0002t0001g0023 a0001c0002t0001g0025 others(50): Show |
53 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.2787+1255T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172029 | |||||||
chr16:16172039 | C | G | 53 | a0001c0002t0001g0010 a0001c0002t0001g0023 a0001c0002t0001g0025 others(50): Show |
53 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.2787+1245G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172039 | |||||||
chr16:16172047 | A | AGTAG | 52 | a0001c0002t0001g0010 a0001c0002t0001g0023 a0001c0002t0001g0025 others(49): Show |
52 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.2787+1236_2787+123 others(8): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172047 | |||||||
chr16:16172047 | A | AGTGGGAT others(35): Show |
1 | a0001c0002t0001g0024 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2787+1236_2787+123 others(46): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172047 | |||||||
chr16:16172047 | A | AGTGGGAT others(481): Show |
3 | a0004c0010t0001g0042 a0004c0010t0001g0043 a0004c0010t0001g0046 |
3 | HG00323.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2787+1236_2787+123 others(492): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172047 | |||||||
chr16:16172047 | A | AGTGGGAT others(502): Show |
3 | a0001c0001t0001g0086 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG01106.hp1 HG02683.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2787+1236_2787+123 others(513): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172047 | |||||||
chr16:16172047 | A | AGTGGGAT others(523): Show |
29 | a0001c0001t0002g0030 a0001c0001t0002g0087 a0001c0001t0002g0088 others(26): Show |
29 | HG00733.hp2 HG00735.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.2787+1236_2787+123 others(534): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172047 | |||||||
chr16:16172047 | A | AGTGGGAT others(330): Show |
3 | a0012c0020t0001g0055 a0012c0020t0001g0056 a0012c0020t0001g0057 |
3 | HG02897.hp1 HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2787+1236_2787+123 others(341): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172047 | |||||||
chr16:16172047 | A | AGTGGGAT others(523): Show |
2 | a0024c0075t0001g0049 a0044c0044t0001g0302 |
2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2787+1236_2787+123 others(534): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172047 | |||||||
chr16:16172047 | A | AGTGGGAT others(523): Show |
1 | a0004c0010t0001g0073 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2787+1236_2787+123 others(534): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172047 | |||||||
chr16:16172047 | AGTGGGAT others(14): Show |
A | 5 | a0001c0004t0001g0065 a0014c0018t0001g0249 a0014c0018t0001g0250 others(2): Show |
5 | HG02258.hp1 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2787+1216_2787+123 others(25): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172047 | |||||||
chr16:16172050 | G | GGGATGGA others(418): Show |
1 | a0001c0004t0001g0217 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2787+1233_2787+123 others(429): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172050 | |||||||
chr16:16172056 | G | C | 53 | a0001c0002t0001g0010 a0001c0002t0001g0023 a0001c0002t0001g0025 others(50): Show |
53 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.2787+1228C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172056 | |||||||
chr16:16172057 | A | ATAAATGA others(825): Show |
1 | a0001c0006t0001g0290 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2787+1226_2787+122 others(836): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172057 | |||||||
chr16:16172057 | A | ATAAATGA others(498): Show |
3 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0107 |
3 | NA18951.hp1 NA18980.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.2787+1226_2787+122 others(509): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172057 | |||||||
chr16:16172057 | A | ATAAATGA others(498): Show |
1 | a0001c0004t0001g0006 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2787+1226_2787+122 others(509): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172057 | |||||||
chr16:16172057 | A | ATAAATGA others(498): Show |
7 | a0001c0001t0001g0064 a0001c0001t0001g0189 a0001c0001t0001g0191 others(4): Show |
7 | HG01175.hp2 HG02040.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2787+1226_2787+122 others(509): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172057 | |||||||
chr16:16172057 | A | ATAAATGA others(140): Show |
1 | a0002c0003t0001g0151 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2787+1226_2787+122 others(151): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172057 | |||||||
chr16:16172057 | A | ATAAATGA others(56): Show |
1 | a0032c0038t0001g0033 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2787+1226_2787+122 others(67): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172057 | |||||||
chr16:16172057 | A | ATAAATGA others(35): Show |
1 | a0003c0007t0001g0110 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2787+1226_2787+122 others(46): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172057 | |||||||
chr16:16172057 | A | C | 1 | a0002c0014t0001g0288 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2787+1227T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172057 | |||||||
chr16:16172064 | A | AGTGGGTG others(695): Show |
2 | a0001c0001t0001g0192 a0001c0001t0001g0235 |
2 | HG00408.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2787+1219_2787+122 others(706): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172064 | |||||||
chr16:16172064 | AGTGG | A | 54 | a0001c0002t0001g0010 a0001c0002t0001g0023 a0001c0002t0001g0025 others(51): Show |
54 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.2787+1216_2787+121 others(8): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172064 | |||||||
chr16:16172065 | G | A | 1 | a0002c0024t0001g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2787+1219C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172065 | |||||||
chr16:16172068 | G | GGTGGGAT others(611): Show |
4 | a0001c0001t0001g0233 a0001c0001t0001g0305 a0001c0049t0001g0352 others(1): Show |
4 | HG00639.hp2 HG02109.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2787+1215_2787+121 others(622): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172068 | |||||||
chr16:16172068 | G | GGTGGGAT others(140): Show |
43 | a0002c0013t0001g0241 a0002c0013t0001g0243 a0002c0013t0001g0244 others(40): Show |
43 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.2787+1215_2787+121 others(151): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172068 | |||||||
chr16:16172068 | G | GGTGGGAT others(1065): Show |
1 | a0003c0007t0001g0104 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2787+1215_2787+121 others(1076): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172068 | |||||||
chr16:16172077 | G | C | 1 | a0002c0024t0001g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2787+1207C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172077 | |||||||
chr16:16172078 | A | C | 186 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(183): Show |
187 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.2787+1206T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172078 | |||||||
chr16:16172085 | A | G | 52 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(49): Show |
52 | HG00323.hp1 HG00642.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.2787+1199T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172085 | |||||||
chr16:16172089 | G | A | 1 | a0002c0024t0001g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2787+1195C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172089 | |||||||
chr16:16172099 | C | A | 186 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(183): Show |
187 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.2787+1185G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172099 | |||||||
chr16:16172106 | A | AATGGGTG others(35): Show |
175 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(172): Show |
176 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.2787+1177_2787+117 others(46): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172106 | |||||||
chr16:16172106 | A | G | 1 | a0002c0024t0001g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2787+1178T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172106 | |||||||
chr16:16172107 | G | A | 8 | a0001c0001t0001g0083 a0001c0002t0001g0014 a0004c0017t0001g0076 others(5): Show |
8 | HG01074.hp1 HG01109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.2787+1177C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172107 | |||||||
chr16:16172110 | G | GGTGGGAT others(10): Show |
1 | a0001c0001t0001g0083 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2787+1173_2787+117 others(21): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172110 | |||||||
chr16:16172119 | G | C | 7 | a0001c0002t0001g0014 a0004c0017t0001g0076 a0006c0008t0001g0256 others(4): Show |
7 | HG01109.hp1 HG02145.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2787+1165C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172119 | |||||||
chr16:16172126 | G | GAGGGGGT others(427): Show |
1 | a0003c0007t0001g0210 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2787+1157_2787+115 others(438): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172126 | |||||||
chr16:16172127 | A | G | 1 | a0001c0006t0001g0290 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2787+1157T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172127 | |||||||
chr16:16172128 | A | G | 241 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(238): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.2787+1156T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172128 | |||||||
chr16:16172131 | G | A | 7 | a0001c0002t0001g0014 a0004c0017t0001g0076 a0006c0008t0001g0256 others(4): Show |
7 | HG01109.hp1 HG02145.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2787+1153C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172131 | |||||||
chr16:16172132 | A | G | 352 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(349): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.2787+1152T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172132 | |||||||
chr16:16172140 | C | G | 65 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(62): Show |
65 | HG00323.hp1 HG00408.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.2787+1144G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172140 | |||||||
chr16:16172141 | A | C | 53 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(50): Show |
53 | HG00323.hp1 HG00642.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.2787+1143T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172141 | |||||||
chr16:16172148 | A | G | 3 | a0001c0002t0001g0014 a0001c0006t0001g0290 a0004c0017t0001g0076 |
3 | NA19060.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2787+1136T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172148 | |||||||
chr16:16172152 | A | AGTGGGAT others(56): Show |
5 | a0006c0008t0001g0256 a0006c0008t0001g0262 a0006c0008t0001g0264 others(2): Show |
5 | HG01109.hp1 HG02145.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2787+1131_2787+113 others(67): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172152 | |||||||
chr16:16172152 | A | G | 60 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(57): Show |
60 | HG00323.hp1 HG00408.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.2787+1132T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172152 | |||||||
chr16:16172169 | G | A | 3 | a0001c0002t0001g0014 a0001c0006t0001g0290 a0004c0017t0001g0076 |
3 | NA19060.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2787+1115C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172169 | |||||||
chr16:16172176 | G | GGGATGGA others(250): Show |
1 | a0008c0011t0003g0091 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2787+1107_2787+110 others(261): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172176 | |||||||
chr16:16172176 | G | GGGATGGA others(594): Show |
2 | a0001c0001t0001g0313 a0001c0001t0001g0337 |
2 | NA18949.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.2787+1107_2787+110 others(605): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172176 | |||||||
chr16:16172176 | G | GGGATGGA others(250): Show |
3 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0340 |
3 | HG01123.hp1 HG01358.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2787+1107_2787+110 others(261): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172176 | |||||||
chr16:16172176 | G | GGGATGGA others(443): Show |
1 | a0001c0001t0001g0200 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2787+1107_2787+110 others(454): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172176 | |||||||
chr16:16172182 | G | C | 2 | a0001c0002t0001g0014 a0004c0017t0001g0076 |
2 | NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2787+1102C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172182 | |||||||
chr16:16172183 | A | C | 6 | a0001c0001t0001g0192 a0001c0001t0001g0235 a0001c0004t0001g0217 others(3): Show |
6 | HG00408.hp2 HG01169.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2787+1101T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172183 | |||||||
chr16:16172190 | A | G | 54 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(51): Show |
54 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.2787+1094T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172190 | |||||||
chr16:16172199 | G | A | 8 | a0001c0001t0001g0064 a0001c0001t0001g0189 a0001c0001t0001g0191 others(5): Show |
8 | HG01175.hp2 HG02040.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2787+1085C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172199 | |||||||
chr16:16172199 | G | GATGGATA others(452): Show |
1 | a0001c0001t0001g0273 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2787+1084_2787+108 others(463): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172199 | |||||||
chr16:16172203 | C | G | 234 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(231): Show |
235 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.2787+1081G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172203 | |||||||
chr16:16172204 | A | ATAAATGA others(418): Show |
2 | a0008c0011t0003g0061 a0008c0011t0003g0062 |
2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(429): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(678): Show |
1 | a0001c0001t0001g0334 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(689): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(680): Show |
1 | a0001c0001t0001g0247 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(691): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(657): Show |
1 | a0001c0001t0001g0229 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(668): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(464): Show |
1 | a0001c0001t0001g0184 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(475): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(678): Show |
19 | a0001c0001t0001g0003 a0001c0001t0001g0268 a0001c0001t0001g0269 others(16): Show |
19 | HG00423.hp1 HG00544.hp1 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(689): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(678): Show |
1 | a0001c0006t0001g0292 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(689): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(699): Show |
7 | a0001c0001t0001g0129 a0001c0001t0001g0136 a0001c0001t0001g0137 others(4): Show |
7 | HG00558.hp2 HG00673.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(710): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(783): Show |
1 | a0001c0001t0001g0234 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(794): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(376): Show |
3 | a0001c0001t0001g0326 a0001c0001t0001g0338 a0001c0001t0001g0339 |
3 | HG02559.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(387): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(439): Show |
1 | a0029c0069t0001g0015 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(450): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(334): Show |
59 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0069 others(56): Show |
59 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(345): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(355): Show |
1 | a0001c0001t0001g0180 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(366): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(624): Show |
1 | a0002c0074t0001g0186 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(635): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(414): Show |
2 | a0035c0060t0010g0240 a0036c0059t0001g0009 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(425): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(582): Show |
5 | a0002c0003t0001g0013 a0002c0003t0001g0123 a0002c0003t0001g0176 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(593): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(519): Show |
2 | a0002c0003t0001g0168 a0031c0058t0001g0165 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(530): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(582): Show |
2 | a0002c0003t0001g0257 a0002c0024t0001g0155 |
2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(593): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(561): Show |
1 | a0002c0014t0001g0289 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(572): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(582): Show |
16 | a0002c0003t0001g0002 a0002c0003t0001g0074 a0002c0003t0001g0082 others(13): Show |
16 | HG00438.hp2 HG00558.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(593): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(561): Show |
1 | a0002c0022t0001g0095 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(572): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(561): Show |
1 | a0002c0024t0001g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(572): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(393): Show |
4 | a0013c0025t0001g0007 a0013c0025t0001g0008 a0013c0030t0001g0274 others(1): Show |
4 | HG02109.hp2 HG02723.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(404): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(582): Show |
3 | a0002c0003t0001g0080 a0002c0003t0001g0081 a0002c0014t0001g0288 |
3 | NA18947.hp1 NA18979.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(593): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(393): Show |
9 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(6): Show |
9 | HG00597.hp1 HG01106.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(404): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(351): Show |
1 | a0001c0001t0001g0174 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(362): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(411): Show |
1 | a0034c0056t0001g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(422): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | ATAAATGA others(712): Show |
1 | a0002c0003t0001g0267 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(723): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172204 | A | C | 2 | a0001c0004t0001g0217 a0001c0006t0001g0290 |
2 | HG01169.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2787+1080T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | |||||||
chr16:16172211 | A | AGTGGGTG others(418): Show |
2 | a0001c0065t0001g0312 a0004c0078t0001g0199 |
2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2787+1072_2787+107 others(429): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172211 | |||||||
chr16:16172211 | A | AGTGGGTG others(439): Show |
3 | a0015c0019t0001g0122 a0015c0019t0001g0125 a0015c0019t0001g0126 |
3 | HG02451.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2787+1072_2787+107 others(450): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172211 | |||||||
chr16:16172211 | A | AGTGGGTG others(418): Show |
1 | a0005c0048t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2787+1072_2787+107 others(429): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172211 | |||||||
chr16:16172211 | A | AGTGGGTG others(561): Show |
1 | a0002c0003t0001g0306 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2787+1072_2787+107 others(572): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172211 | |||||||
chr16:16172211 | A | AGTGGGTG others(393): Show |
1 | a0002c0003t0001g0146 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2787+1072_2787+107 others(404): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172211 | |||||||
chr16:16172211 | A | AGTGGGTG others(414): Show |
6 | a0002c0014t0001g0331 a0007c0009t0001g0116 a0007c0009t0001g0118 others(3): Show |
7 | NA18943.hp2 NA18978.hp1 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.2787+1072_2787+107 others(425): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172211 | |||||||
chr16:16172211 | A | AGTGGGTG others(582): Show |
1 | a0002c0003t0001g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2787+1072_2787+107 others(593): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172211 | |||||||
chr16:16172211 | A | AGTGGGTG others(582): Show |
2 | a0002c0003t0001g0225 a0002c0003t0001g0350 |
2 | HG01109.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.2787+1072_2787+107 others(593): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172211 | |||||||
chr16:16172211 | A | AGTGGGTG others(561): Show |
2 | a0002c0003t0001g0142 a0002c0003t0001g0224 |
2 | HG01934.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.2787+1072_2787+107 others(572): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172211 | |||||||
chr16:16172211 | A | AGTGGGTG others(603): Show |
1 | a0012c0050t0001g0040 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2787+1072_2787+107 others(614): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172211 | |||||||
chr16:16172211 | A | G | 2 | a0001c0002t0001g0014 a0004c0017t0001g0076 |
2 | NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2787+1073T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172211 | |||||||
chr16:16172212 | G | A | 1 | a0040c0040t0001g0031 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2787+1072C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172212 | |||||||
chr16:16172215 | A | AGTGGGAT others(497): Show |
4 | a0001c0001t0001g0233 a0001c0001t0001g0305 a0001c0049t0001g0352 others(1): Show |
4 | HG00639.hp2 HG02109.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2787+1068_2787+106 others(508): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172215 | |||||||
chr16:16172215 | A | G | 286 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(283): Show |
287 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.2787+1069T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172215 | |||||||
chr16:16172225 | A | C | 8 | a0001c0001t0001g0192 a0001c0001t0001g0235 a0001c0004t0001g0217 others(5): Show |
8 | HG00408.hp2 HG01169.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.2787+1059T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172225 | |||||||
chr16:16172232 | G | A | 55 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(52): Show |
55 | HG00323.hp1 HG00408.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.2787+1052C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172232 | |||||||
chr16:16172233 | G | A | 1 | a0040c0040t0001g0031 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2787+1051C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172233 | |||||||
chr16:16172246 | A | C | 5 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0313 others(2): Show |
5 | HG01123.hp1 HG01358.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.2787+1038T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172246 | |||||||
chr16:16172253 | G | A | 121 | a0001c0001t0001g0083 a0001c0001t0001g0194 a0001c0001t0001g0195 others(118): Show |
121 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.2787+1031C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172253 | |||||||
chr16:16172259 | T | A | 1 | a0008c0011t0003g0091 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2787+1025A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172259 | |||||||
chr16:16172260 | G | T | 1 | a0008c0011t0003g0091 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2787+1024C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172260 | |||||||
chr16:16172262 | G | A | 48 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(45): Show |
48 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2787+1022C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172262 | |||||||
chr16:16172267 | A | C | 50 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(47): Show |
50 | HG00323.hp1 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.2787+1017T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172267 | |||||||
chr16:16172274 | A | G | 6 | a0001c0001t0001g0192 a0001c0001t0001g0235 a0002c0024t0001g0153 others(3): Show |
6 | HG00408.hp2 HG02897.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2787+1010T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172274 | |||||||
chr16:16172283 | G | A | 1 | a0002c0024t0001g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2787+1001C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172283 | |||||||
chr16:16172283 | G | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0172 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2787+1001C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172283 | |||||||
chr16:16172287 | C | G | 236 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(233): Show |
237 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.2787+997G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172287 | |||||||
chr16:16172288 | A | C | 5 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0313 others(2): Show |
5 | HG01123.hp1 HG01358.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.2787+996T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172288 | |||||||
chr16:16172288 | ATAAATGA others(125): Show |
A | 5 | a0001c0004t0001g0065 a0014c0018t0001g0249 a0014c0018t0001g0250 others(2): Show |
5 | HG02258.hp1 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2787+864_2787+995d others(2): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172288 | |||||||
chr16:16172295 | A | G | 12 | a0001c0001t0001g0247 a0002c0003t0001g0146 a0002c0014t0001g0331 others(9): Show |
13 | HG02451.hp2 HG02809.hp2 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.2787+989T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172295 | |||||||
chr16:16172299 | A | G | 345 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(342): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.2787+985T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172299 | |||||||
chr16:16172308 | G | C | 108 | a0001c0001t0001g0083 a0001c0002t0001g0010 a0001c0002t0001g0023 others(105): Show |
108 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.2787+976C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172308 | |||||||
chr16:16172309 | A | C | 1 | a0001c0001t0001g0247 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2787+975T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172309 | |||||||
chr16:16172315 | G | GA | 108 | a0001c0001t0001g0083 a0001c0002t0001g0010 a0001c0002t0001g0023 others(105): Show |
108 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.2787+968_2787+969i others(3): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172315 | |||||||
chr16:16172316 | G | A | 15 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(12): Show |
15 | HG01175.hp2 HG02040.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2787+968C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172316 | |||||||
chr16:16172316 | GGTATGA | G | 83 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0069 others(80): Show |
83 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.2787+962_2787+967d others(8): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172316 | |||||||
chr16:16172318 | T | TGGGATGG others(558): Show |
1 | a0001c0001t0001g0083 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2787+965_2787+966i others(567): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGATGG others(527): Show |
1 | a0001c0002t0001g0157 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2787+965_2787+966i others(536): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGATGG others(730): Show |
2 | a0003c0005t0001g0028 a0003c0005t0001g0029 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2787+965_2787+966i others(739): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGATGG others(428): Show |
40 | a0002c0013t0001g0241 a0002c0013t0001g0243 a0002c0013t0001g0244 others(37): Show |
40 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.2787+965_2787+966i others(437): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGATGG others(449): Show |
1 | a0003c0005t0001g0197 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(458): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGATGG others(428): Show |
1 | a0003c0007t0001g0098 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2787+965_2787+966i others(437): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGATGG others(491): Show |
5 | a0006c0008t0001g0256 a0006c0008t0001g0262 a0006c0008t0001g0264 others(2): Show |
5 | HG01109.hp1 HG02145.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2787+965_2787+966i others(500): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGATGG others(512): Show |
1 | a0001c0055t0012g0164 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(521): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGATGG others(533): Show |
2 | a0001c0026t0001g0272 a0028c0054t0001g0072 |
2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2787+965_2787+966i others(542): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGATGG others(659): Show |
1 | a0002c0003t0001g0151 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2787+965_2787+966i others(668): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGATGG others(424): Show |
1 | a0003c0007t0001g0245 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2787+965_2787+966i others(433): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGATGG others(428): Show |
1 | a0003c0005t0001g0314 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2787+965_2787+966i others(437): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGATGG others(575): Show |
1 | a0032c0038t0001g0033 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(584): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGATGG others(491): Show |
1 | a0013c0030t0001g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2787+965_2787+966i others(500): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGATGG others(531): Show |
1 | a0001c0002t0001g0149 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(540): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGATGG others(906): Show |
1 | a0001c0002t0001g0024 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(915): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGATGG others(467): Show |
1 | a0001c0002t0001g0124 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(476): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGATGG others(488): Show |
43 | a0001c0002t0001g0010 a0001c0002t0001g0023 a0001c0002t0001g0025 others(40): Show |
43 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.2787+965_2787+966i others(497): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGATGG others(467): Show |
1 | a0005c0012t0001g0027 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(476): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGATGG others(509): Show |
2 | a0001c0002t0001g0068 a0001c0002t0001g0332 |
2 | HG02683.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2787+965_2787+966i others(518): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGTGGG others(8): Show |
12 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(9): Show |
12 | HG01175.hp2 HG02040.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2787+965_2787+966i others(17): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGTGGG others(29): Show |
1 | a0043c0063t0001g0171 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(38): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGTGGG others(555): Show |
1 | a0006c0008t0001g0259 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(564): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGTGGG others(576): Show |
2 | a0006c0008t0001g0053 a0006c0008t0001g0258 |
2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2787+965_2787+966i others(585): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGTGGG others(594): Show |
1 | a0040c0040t0001g0031 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2787+965_2787+966i others(603): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGTGGG others(492): Show |
2 | a0001c0002t0001g0014 a0004c0017t0001g0076 |
2 | NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2787+965_2787+966i others(501): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGTGGG others(29): Show |
2 | a0001c0001t0001g0313 a0001c0001t0001g0337 |
2 | NA18949.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.2787+965_2787+966i others(38): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGTGGG others(71): Show |
1 | a0002c0024t0001g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2787+965_2787+966i others(80): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGTGGG others(218): Show |
3 | a0012c0020t0001g0055 a0012c0020t0001g0056 a0012c0020t0001g0057 |
3 | HG02897.hp1 HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2787+965_2787+966i others(227): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGTGGG others(134): Show |
5 | a0002c0014t0001g0331 a0007c0009t0001g0118 a0007c0009t0001g0119 others(2): Show |
6 | NA18943.hp2 NA18978.hp1 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.2787+965_2787+966i others(143): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGTGGG others(155): Show |
1 | a0002c0003t0001g0146 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(164): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGTGGG others(176): Show |
1 | a0007c0009t0001g0116 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(185): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGTGGG others(8): Show |
41 | a0001c0001t0001g0003 a0001c0001t0001g0192 a0001c0001t0001g0229 others(38): Show |
41 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.2787+965_2787+966i others(17): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGTGGG others(50): Show |
1 | a0001c0001t0001g0335 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(59): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGTGGG others(29): Show |
70 | a0001c0001t0001g0129 a0001c0001t0001g0136 a0001c0001t0001g0137 others(67): Show |
70 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.2787+965_2787+966i others(38): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGTGGG others(218): Show |
1 | a0001c0004t0001g0217 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(227): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGTGGG others(50): Show |
8 | a0001c0001t0001g0233 a0001c0001t0001g0305 a0001c0049t0001g0352 others(5): Show |
8 | HG00639.hp2 HG01106.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2787+965_2787+966i others(59): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGTGGG others(134): Show |
1 | a0008c0011t0003g0091 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2787+965_2787+966i others(143): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGTGGG others(50): Show |
2 | a0008c0011t0003g0061 a0008c0011t0003g0062 |
2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2787+965_2787+966i others(59): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGTGGG others(29): Show |
1 | a0035c0060t0010g0240 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(38): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172318 | T | TGGGTGGG others(50): Show |
1 | a0036c0059t0001g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(59): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | |||||||
chr16:16172322 | A | AGTGGGTG others(35): Show |
43 | a0001c0002t0001g0010 a0001c0002t0001g0023 a0001c0002t0001g0025 others(40): Show |
43 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.2787+961_2787+962i others(44): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172322 | |||||||
chr16:16172322 | A | G | 32 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(29): Show |
32 | HG00639.hp2 HG01175.hp2 HG02040.hp1 others(29): Show |
intron_variant | MODIFIER | c.2787+962T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172322 | |||||||
chr16:16172336 | C | A | 186 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0129 others(183): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.2787+948G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172336 | |||||||
chr16:16172336 | C | CTAAATGA others(35): Show |
1 | a0001c0002t0001g0124 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2787+947_2787+948i others(44): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172336 | |||||||
chr16:16172343 | G | A | 208 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(205): Show |
208 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.2787+941C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172343 | |||||||
chr16:16172343 | G | AGTGGGTG others(35): Show |
1 | a0005c0012t0001g0027 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2787+941_2787+942i others(44): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172343 | |||||||
chr16:16172357 | C | A | 145 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(142): Show |
145 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.2787+927G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172357 | |||||||
chr16:16172364 | A | G | 55 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0170 others(52): Show |
55 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.2787+920T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172364 | |||||||
chr16:16172366 | T | C | 18 | a0001c0001t0001g0129 a0001c0001t0001g0136 a0001c0001t0001g0137 others(15): Show |
18 | HG00558.hp2 HG00673.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.2787+918A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172366 | |||||||
chr16:16172378 | C | A | 109 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0069 others(106): Show |
109 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.2787+906G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172378 | |||||||
chr16:16172378 | C | CTAAATGA others(14): Show |
1 | a0005c0048t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2787+905_2787+906i others(23): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172378 | |||||||
chr16:16172384 | G | GAGTGGGT others(123): Show |
1 | a0001c0004t0002g0105 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2787+899_2787+900i others(132): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172384 | |||||||
chr16:16172385 | A | GGTGGGTG others(35): Show |
64 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0069 others(61): Show |
64 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.2787+899_2787+900i others(44): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172385 | |||||||
chr16:16172385 | A | GGTGGGTG others(35): Show |
18 | a0001c0001t0001g0086 a0001c0001t0001g0201 a0001c0001t0001g0202 others(15): Show |
18 | HG01106.hp1 HG01261.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.2787+899_2787+900i others(44): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172385 | |||||||
chr16:16172387 | T | C | 19 | a0001c0001t0001g0003 a0001c0001t0001g0192 a0001c0001t0001g0229 others(16): Show |
19 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(16): Show |
intron_variant | MODIFIER | c.2787+897A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172387 | |||||||
chr16:16172399 | C | A | 118 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(115): Show |
118 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.2787+885G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172399 | |||||||
chr16:16172399 | C | CTAAATGA others(14): Show |
112 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(109): Show |
113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.2787+884_2787+885i others(23): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172399 | |||||||
chr16:16172406 | A | G | 3 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0340 |
3 | HG01123.hp1 HG01358.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2787+878T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172406 | |||||||
chr16:16172411 | G | GTGGGATG others(114): Show |
3 | a0015c0019t0001g0122 a0015c0019t0001g0125 a0015c0019t0001g0126 |
3 | HG02451.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2787+872_2787+873i others(123): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172411 | |||||||
chr16:16172420 | C | A | 112 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0069 others(109): Show |
112 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.2787+864G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172420 | |||||||
chr16:16172420 | C | CTAAATGA others(14): Show |
46 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0192 others(43): Show |
46 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.2787+843_2787+863d others(23): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172420 | |||||||
chr16:16172440 | G | C | 5 | a0001c0004t0001g0065 a0014c0018t0001g0249 a0014c0018t0001g0250 others(2): Show |
5 | HG02258.hp1 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2787+844C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172440 | |||||||
chr16:16172451 | G | T | 5 | a0001c0004t0001g0065 a0014c0018t0001g0249 a0014c0018t0001g0250 others(2): Show |
5 | HG02258.hp1 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2787+833C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172451 | |||||||
chr16:16172452 | GGTGGGAT | G | 5 | a0001c0004t0001g0065 a0014c0018t0001g0249 a0014c0018t0001g0250 others(2): Show |
5 | HG02258.hp1 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2787+825_2787+831d others(9): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172452 | |||||||
chr16:16172494 | G | A | 5 | a0001c0004t0001g0065 a0014c0018t0001g0249 a0014c0018t0001g0250 others(2): Show |
5 | HG02258.hp1 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2787+790C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172494 | |||||||
chr16:16172582 | G | T | 4 | a0002c0003t0001g0169 a0002c0003t0001g0187 a0002c0003t0001g0188 others(1): Show |
4 | HG01884.hp2 HG02622.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2787+702C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172582 | |||||||
chr16:16172719 | A | G | 1 | a0025c0076t0001g0047 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2787+565T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172719 | |||||||
chr16:16172741 | G | C | 158 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(155): Show |
158 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.2787+543C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172741 | |||||||
chr16:16172911 | A | C | 1 | a0036c0059t0001g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2787+373T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172911 | |||||||
chr16:16172915 | G | A | 59 | a0001c0002t0001g0010 a0001c0002t0001g0014 a0001c0002t0001g0023 others(56): Show |
59 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2787+369C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172915 | |||||||
chr16:16172961 | T | G | 347 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(344): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.2787+323A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172961 | |||||||
chr16:16172974 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2787+310G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172974 | |||||||
chr16:16172983 | A | C | 158 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(155): Show |
158 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.2787+301T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172983 | |||||||
chr16:16173065 | A | T | 1 | a0001c0028t0001g0295 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2787+219T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16173065 | |||||||
chr16:16173173 | G | A | 2 | a0024c0075t0001g0049 a0044c0044t0001g0302 |
2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2787+111C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16173173 | |||||||
chr16:16173180 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2787+104T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16173180 | |||||||
chr16:16173185 | A | G | 2 | a0001c0001t0002g0162 a0041c0070t0002g0067 |
2 | NA18943.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2787+99T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16173185 | |||||||
chr16:16173222 | A | G | 347 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(344): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.2787+62T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16173222 | |||||||
chr16:16173541 | A | G | 1 | a0001c0043t0001g0236 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2667-137T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16173541 | |||||||
chr16:16173583 | T | C | 1 | a0032c0038t0001g0033 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2667-179A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16173583 | |||||||
chr16:16173625 | C | T | 1 | a0001c0004t0002g0105 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2667-221G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16173625 | |||||||
chr16:16173692 | T | TTTTC | 136 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(133): Show |
136 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.2667-292_2667-289d others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16173692 | |||||||
chr16:16173696 | C | CT | 8 | a0001c0002t0001g0112 a0001c0002t0001g0149 a0001c0002t0001g0157 others(5): Show |
8 | HG01928.hp2 HG02300.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.2667-293dupA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16173696 | |||||||
chr16:16173696 | C | CTTTCT | 12 | a0001c0001t0001g0128 a0001c0001t0001g0166 a0001c0001t0001g0180 others(9): Show |
12 | HG01433.hp1 HG01433.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.2667-293_2667-292i others(7): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16173696 | |||||||
chr16:16173697 | T | TTTC | 8 | a0001c0001t0001g0079 a0001c0001t0001g0129 a0001c0001t0001g0229 others(5): Show |
8 | HG00099.hp2 HG01081.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.2667-294_2667-293i others(5): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16173697 | |||||||
chr16:16173807 | G | A | 1 | a0001c0006t0001g0286 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2667-403C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16173807 | |||||||
chr16:16173921 | A | T | 1 | a0042c0061t0001g0130 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2667-517T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16173921 | |||||||
chr16:16173928 | A | G | 1 | a0001c0001t0001g0268 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2667-524T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16173928 | |||||||
chr16:16173980 | G | A | 151 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(148): Show |
151 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.2667-576C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16173980 | |||||||
chr16:16174111 | A | G | 98 | a0002c0003t0001g0002 a0002c0003t0001g0013 a0002c0003t0001g0074 others(95): Show |
99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.2667-707T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174111 | |||||||
chr16:16174177 | G | A | 1 | a0002c0024t0001g0155 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2667-773C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174177 | |||||||
chr16:16174266 | CAACCGTT others(7): Show |
C | 1 | a0001c0001t0001g0334 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2667-876_2667-863d others(16): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174266 | |||||||
chr16:16174271 | G | A | 2 | a0035c0060t0010g0240 a0036c0059t0001g0009 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2667-867C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174271 | |||||||
chr16:16174373 | A | G | 98 | a0002c0003t0001g0002 a0002c0003t0001g0013 a0002c0003t0001g0074 others(95): Show |
99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.2667-969T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174373 | |||||||
chr16:16174438 | G | A | 3 | a0001c0001t0001g0336 a0001c0004t0001g0108 a0023c0053t0001g0154 |
3 | HG00438.hp1 HG02056.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.2667-1034C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174438 | |||||||
chr16:16174496 | C | T | 150 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0069 others(147): Show |
150 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.2667-1092G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174496 | |||||||
chr16:16174671 | C | T | 4 | a0015c0019t0001g0122 a0015c0019t0001g0125 a0015c0019t0001g0126 others(1): Show |
4 | HG02451.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2666+1240G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174671 | |||||||
chr16:16174742 | G | A | 1 | a0003c0005t0001g0307 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2666+1169C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174742 | |||||||
chr16:16174759 | A | ACCC | 3 | a0008c0011t0003g0058 a0008c0011t0003g0060 a0011c0016t0006g0271 |
3 | HG01496.hp2 HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2666+1151_2666+115 others(7): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | |||||||
chr16:16174759 | A | ACCCC | 9 | a0001c0001t0002g0092 a0001c0001t0002g0094 a0001c0004t0002g0105 others(6): Show |
9 | HG02280.hp1 HG02572.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.2666+1151_2666+115 others(8): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | |||||||
chr16:16174759 | A | ACCCCCCC | 9 | a0001c0001t0001g0161 a0001c0001t0001g0166 a0001c0001t0001g0227 others(6): Show |
9 | HG01256.hp2 HG02451.hp1 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.2666+1151_2666+115 others(11): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | |||||||
chr16:16174759 | A | ACCCCCCC others(1): Show |
18 | a0001c0001t0001g0039 a0001c0001t0001g0089 a0001c0001t0001g0127 others(15): Show |
18 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.2666+1151_2666+115 others(12): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | |||||||
chr16:16174759 | A | ACCCCCCC others(2): Show |
24 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0192 others(21): Show |
24 | HG00423.hp1 HG00423.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.2666+1151_2666+115 others(13): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | |||||||
chr16:16174759 | A | ACCCCCCC others(3): Show |
27 | a0001c0001t0001g0069 a0001c0001t0001g0079 a0001c0001t0001g0143 others(24): Show |
27 | HG00099.hp2 HG00408.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.2666+1151_2666+115 others(14): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | |||||||
chr16:16174759 | A | ACCCCCCC others(4): Show |
8 | a0001c0001t0001g0136 a0001c0001t0001g0145 a0001c0001t0001g0234 others(5): Show |
8 | HG00673.hp1 HG02273.hp1 HG04204.hp2 others(5): Show |
intron_variant | MODIFIER | c.2666+1151_2666+115 others(15): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | |||||||
chr16:16174759 | A | ACCCCCCC others(5): Show |
6 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0303 others(3): Show |
6 | HG02135.hp1 HG02135.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.2666+1151_2666+115 others(16): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | |||||||
chr16:16174759 | A | ACCCCCCC others(6): Show |
5 | a0001c0001t0001g0180 a0001c0001t0001g0338 a0001c0001t0001g0340 others(2): Show |
5 | HG00558.hp2 HG01433.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.2666+1151_2666+115 others(17): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | |||||||
chr16:16174759 | A | ACCCCCCC others(7): Show |
2 | a0001c0001t0001g0269 a0001c0001t0001g0308 |
2 | HG03831.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.2666+1151_2666+115 others(18): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | |||||||
chr16:16174759 | A | ACCCCCCC others(8): Show |
1 | a0001c0001t0001g0335 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2666+1151_2666+115 others(19): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | |||||||
chr16:16174759 | A | ACCCCCGC others(1): Show |
5 | a0001c0001t0001g0233 a0001c0001t0001g0305 a0002c0068t0001g0097 others(2): Show |
5 | HG00639.hp2 HG00642.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.2666+1151_2666+115 others(12): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | |||||||
chr16:16174759 | A | ACCCCCGC others(4): Show |
1 | a0005c0048t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2666+1151_2666+115 others(15): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | |||||||
chr16:16174759 | A | ACCCCGCC others(4): Show |
1 | a0001c0001t0001g0334 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2666+1151_2666+115 others(15): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | |||||||
chr16:16174759 | A | C | 1 | a0004c0010t0001g0342 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2666+1152T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | |||||||
chr16:16174760 | A | ACCCCCC | 25 | a0001c0002t0001g0014 a0001c0002t0001g0023 a0001c0002t0001g0024 others(22): Show |
25 | HG00408.hp1 HG00544.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.2666+1145_2666+115 others(10): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174760 | |||||||
chr16:16174760 | A | ACCCCCCC | 14 | a0001c0002t0001g0010 a0001c0002t0001g0085 a0001c0002t0001g0093 others(11): Show |
14 | HG00639.hp1 HG00673.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2666+1144_2666+115 others(11): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174760 | |||||||
chr16:16174760 | A | ACCCCCCC others(4): Show |
1 | a0001c0001t0001g0160 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2666+1150_2666+115 others(15): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174760 | |||||||
chr16:16174760 | A | C | 154 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(151): Show |
154 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.2666+1151T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174760 | |||||||
chr16:16174760 | A | G | 3 | a0001c0001t0002g0092 a0001c0001t0002g0094 a0001c0004t0002g0105 |
3 | HG02738.hp1 NA18953.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2666+1151T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174760 | |||||||
chr16:16174761 | C | CCCG | 28 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0201 others(25): Show |
28 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.2666+1149_2666+115 others(7): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174761 | |||||||
chr16:16174933 | T | A | 2 | a0024c0075t0001g0049 a0044c0044t0001g0302 |
2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2666+978A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174933 | |||||||
chr16:16174934 | T | A | 255 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(252): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.2666+977A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174934 | |||||||
chr16:16175011 | G | A | 45 | a0002c0013t0001g0241 a0002c0013t0001g0243 a0002c0013t0001g0244 others(42): Show |
45 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.2666+900C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16175011 | |||||||
chr16:16175069 | A | G | 212 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(209): Show |
212 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.2666+842T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16175069 | |||||||
chr16:16175261 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2666+650T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16175261 | |||||||
chr16:16175395 | C | A | 159 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(156): Show |
159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.2666+516G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16175395 | |||||||
chr16:16175412 | G | A | 51 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0201 others(48): Show |
51 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.2666+499C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16175412 | |||||||
chr16:16175566 | A | G | 158 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(155): Show |
158 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.2666+345T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16175566 | |||||||
chr16:16175575 | A | T | 1 | a0042c0061t0001g0130 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2666+336T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16175575 | |||||||
chr16:16175713 | A | G | 315 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(312): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.2666+198T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16175713 | |||||||
chr16:16175767 | A | C | 1 | a0042c0061t0001g0130 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2666+144T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16175767 | |||||||
chr16:16175771 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2666+140G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16175771 | |||||||
chr16:16175776 | TG | T | 309 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(306): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.2666+134delC | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16175776 | |||||||
chr16:16175896 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2666+15G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16175896 | |||||||
chr16:16176077 | C | A | 1 | a0001c0002t0001g0332 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2591-91G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176077 | |||||||
chr16:16176105 | G | A | 55 | a0001c0002t0001g0010 a0001c0002t0001g0014 a0001c0002t0001g0023 others(52): Show |
55 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.2591-119C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176105 | |||||||
chr16:16176189 | A | G | 60 | a0001c0002t0001g0010 a0001c0002t0001g0014 a0001c0002t0001g0023 others(57): Show |
60 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.2591-203T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176189 | |||||||
chr16:16176219 | T | G | 2 | a0001c0065t0001g0312 a0004c0078t0001g0199 |
2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2591-233A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176219 | |||||||
chr16:16176274 | C | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(103): Show |
106 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.2591-288G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176274 | |||||||
chr16:16176317 | T | C | 308 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(305): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2591-331A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176317 | |||||||
chr16:16176318 | T | C | 1 | a0001c0052t0001g0283 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2591-332A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176318 | |||||||
chr16:16176331 | TCTCACCT others(3): Show |
T | 1 | a0001c0001t0002g0088 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2591-355_2591-346d others(12): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176331 | |||||||
chr16:16176368 | A | C | 1 | a0001c0002t0001g0117 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2591-382T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176368 | |||||||
chr16:16176548 | C | T | 4 | a0009c0029t0001g0159 a0009c0029t0001g0230 a0009c0042t0001g0099 others(1): Show |
4 | HG00280.hp2 HG00323.hp2 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.2591-562G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176548 | |||||||
chr16:16176582 | C | T | 4 | a0015c0019t0001g0122 a0015c0019t0001g0125 a0015c0019t0001g0126 others(1): Show |
4 | HG02451.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2591-596G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176582 | |||||||
chr16:16176583 | A | C | 1 | a0042c0061t0001g0130 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2591-597T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176583 | |||||||
chr16:16176584 | C | A | 1 | a0042c0061t0001g0130 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2591-598G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176584 | |||||||
chr16:16176688 | A | T | 1 | a0042c0061t0001g0130 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2591-702T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176688 | |||||||
chr16:16176794 | T | G | 3 | a0015c0019t0001g0122 a0015c0019t0001g0125 a0015c0019t0001g0126 |
3 | HG02451.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2590+658A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176794 | |||||||
chr16:16176852 | A | G | 4 | a0015c0019t0001g0122 a0015c0019t0001g0125 a0015c0019t0001g0126 others(1): Show |
4 | HG02451.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2590+600T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176852 | |||||||
chr16:16176982 | A | C | 1 | a0002c0003t0001g0333 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2590+470T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176982 | |||||||
chr16:16176993 | C | T | 341 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(338): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.2590+459G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176993 | |||||||
chr16:16177020 | T | C | 202 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(199): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.2590+432A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16177020 | |||||||
chr16:16177047 | C | T | 54 | a0001c0002t0001g0010 a0001c0002t0001g0014 a0001c0002t0001g0023 others(51): Show |
54 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.2590+405G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16177047 | |||||||
chr16:16177165 | T | A | 1 | a0001c0001t0001g0336 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2590+287A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16177165 | |||||||
chr16:16177230 | A | AT | 4 | a0015c0019t0001g0122 a0015c0019t0001g0125 a0015c0019t0001g0126 others(1): Show |
4 | HG02451.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2590+221dupA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16177230 | |||||||
chr16:16177281 | G | A | 1 | a0029c0069t0001g0015 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2590+171C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16177281 | |||||||
chr16:16177407 | G | A | 2 | a0001c0004t0001g0108 a0023c0053t0001g0154 |
2 | HG00438.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.2590+45C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16177407 | |||||||
chr16:16177745 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2416-119G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16177745 | |||||||
chr16:16177760 | C | T | 6 | a0001c0001t0001g0127 a0001c0001t0001g0137 a0001c0001t0001g0166 others(3): Show |
6 | NA18941.hp2 NA18947.hp2 NA19064.hp1 others(3): Show |
intron_variant | MODIFIER | c.2416-134G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16177760 | |||||||
chr16:16177771 | C | T | 341 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(338): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.2416-145G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16177771 | |||||||
chr16:16177815 | C | A | 1 | a0001c0004t0002g0134 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2416-189G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16177815 | |||||||
chr16:16177848 | C | T | 1 | a0001c0001t0002g0088 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2416-222G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16177848 | |||||||
chr16:16177891 | C | T | 57 | a0001c0002t0001g0010 a0001c0002t0001g0014 a0001c0002t0001g0023 others(54): Show |
57 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.2416-265G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16177891 | |||||||
chr16:16177972 | A | G | 1 | a0001c0002t0001g0149 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2416-346T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16177972 | |||||||
chr16:16178129 | C | T | 1 | a0001c0004t0001g0217 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2416-503G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16178129 | |||||||
chr16:16178141 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2416-515G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16178141 | |||||||
chr16:16178219 | C | T | 1 | a0003c0007t0001g0104 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2415+579G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16178219 | |||||||
chr16:16178220 | G | A | 1 | a0011c0016t0001g0275 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2415+578C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16178220 | |||||||
chr16:16178258 | C | T | 1 | a0029c0069t0001g0015 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2415+540G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16178258 | |||||||
chr16:16178326 | C | CA | 55 | a0001c0002t0001g0010 a0001c0002t0001g0014 a0001c0002t0001g0023 others(52): Show |
55 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.2415+471dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16178326 | |||||||
chr16:16178406 | T | C | 2 | a0001c0065t0001g0312 a0004c0078t0001g0199 |
2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2415+392A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16178406 | |||||||
chr16:16178451 | C | T | 2 | a0024c0075t0001g0049 a0044c0044t0001g0302 |
2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2415+347G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16178451 | |||||||
chr16:16178621 | T | C | 2 | a0001c0065t0001g0312 a0004c0078t0001g0199 |
2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2415+177A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16178621 | |||||||
chr16:16178651 | G | A | 101 | a0001c0026t0001g0272 a0001c0055t0012g0164 a0002c0003t0001g0002 others(98): Show |
102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.2415+147C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16178651 | |||||||
chr16:16178707 | G | C | 2 | a0013c0030t0001g0113 a0013c0030t0001g0274 |
2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2415+91C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16178707 | |||||||
chr16:16179061 | G | C | 1 | a0022c0041t0001g0216 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2248-96C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16179061 | |||||||
chr16:16179180 | C | T | 5 | a0013c0025t0001g0007 a0013c0025t0001g0008 a0013c0030t0001g0113 others(2): Show |
5 | HG02109.hp2 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2248-215G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16179180 | |||||||
chr16:16179340 | G | T | 89 | a0001c0026t0001g0272 a0001c0055t0012g0164 a0002c0003t0001g0002 others(86): Show |
90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.2248-375C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16179340 | |||||||
chr16:16179517 | C | T | 268 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(265): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.2248-552G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16179517 | |||||||
chr16:16179563 | G | A | 1 | a0002c0024t0001g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2248-598C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16179563 | |||||||
chr16:16179595 | G | A | 1 | a0003c0005t0001g0319 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2248-630C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16179595 | |||||||
chr16:16179793 | G | A | 3 | a0015c0019t0001g0122 a0015c0019t0001g0125 a0015c0019t0001g0126 |
3 | HG02451.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2248-828C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16179793 | |||||||
chr16:16179834 | G | A | 156 | a0001c0002t0001g0010 a0001c0002t0001g0014 a0001c0002t0001g0023 others(153): Show |
157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.2248-869C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16179834 | |||||||
chr16:16179939 | A | G | 1 | a0001c0002t0001g0287 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2248-974T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16179939 | |||||||
chr16:16180349 | C | G | 160 | a0001c0002t0001g0010 a0001c0002t0001g0014 a0001c0002t0001g0023 others(157): Show |
161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.2248-1384G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16180349 | |||||||
chr16:16180475 | C | T | 1 | a0028c0054t0001g0072 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2248-1510G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16180475 | |||||||
chr16:16180829 | C | T | 4 | a0024c0075t0001g0049 a0035c0060t0010g0240 a0036c0059t0001g0009 others(1): Show |
4 | HG00642.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247+1583G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16180829 | |||||||
chr16:16180838 | G | A | 3 | a0001c0004t0002g0134 a0035c0060t0010g0240 a0036c0059t0001g0009 |
3 | HG03540.hp2 NA18906.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2247+1574C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16180838 | |||||||
chr16:16180905 | C | T | 2 | a0001c0002t0001g0068 a0001c0002t0001g0332 |
2 | HG02683.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2247+1507G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16180905 | |||||||
chr16:16180958 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2247+1454T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16180958 | |||||||
chr16:16181012 | A | C | 1 | a0005c0048t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2247+1400T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181012 | |||||||
chr16:16181286 | T | C | 4 | a0024c0075t0001g0049 a0035c0060t0010g0240 a0036c0059t0001g0009 others(1): Show |
4 | HG00642.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247+1126A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181286 | |||||||
chr16:16181344 | GA | G | 112 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(109): Show |
112 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.2247+1067delT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181344 | |||||||
chr16:16181344 | GAA | G | 13 | a0001c0001t0001g0136 a0001c0001t0001g0161 a0001c0001t0001g0189 others(10): Show |
13 | HG00642.hp2 HG00673.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.2247+1066_2247+106 others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181344 | |||||||
chr16:16181344 | GAAAAAAA | G | 36 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0202 others(33): Show |
36 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.2247+1061_2247+106 others(11): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181344 | |||||||
chr16:16181356 | A | G | 1 | a0001c0002t0002g0004 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2247+1056T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181356 | |||||||
chr16:16181357 | A | G | 154 | a0001c0002t0001g0010 a0001c0002t0001g0014 a0001c0002t0001g0023 others(151): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.2247+1055T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181357 | |||||||
chr16:16181358 | A | G | 1 | a0042c0061t0001g0130 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2247+1054T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181358 | |||||||
chr16:16181363 | AAAAAAG | A | 154 | a0001c0002t0001g0010 a0001c0002t0001g0014 a0001c0002t0001g0023 others(151): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.2247+1043_2247+104 others(10): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181363 | |||||||
chr16:16181367 | A | G | 2 | a0035c0060t0010g0240 a0036c0059t0001g0009 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2247+1045T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181367 | |||||||
chr16:16181403 | C | T | 4 | a0015c0019t0001g0122 a0015c0019t0001g0125 a0015c0019t0001g0126 others(1): Show |
4 | HG02451.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247+1009G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181403 | |||||||
chr16:16181413 | G | A | 2 | a0024c0075t0001g0049 a0044c0044t0001g0302 |
2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2247+999C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181413 | |||||||
chr16:16181488 | G | A | 102 | a0001c0026t0001g0272 a0001c0055t0012g0164 a0002c0003t0001g0002 others(99): Show |
103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.2247+924C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181488 | |||||||
chr16:16181609 | G | A | 4 | a0024c0075t0001g0049 a0035c0060t0010g0240 a0036c0059t0001g0009 others(1): Show |
4 | HG00642.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247+803C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181609 | |||||||
chr16:16181638 | C | A | 1 | a0001c0001t0004g0182 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2247+774G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181638 | |||||||
chr16:16181641 | G | A | 4 | a0024c0075t0001g0049 a0035c0060t0010g0240 a0036c0059t0001g0009 others(1): Show |
4 | HG00642.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247+771C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181641 | |||||||
chr16:16181662 | G | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG01123.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.2247+750C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181662 | |||||||
chr16:16181671 | T | G | 1 | a0003c0007t0001g0104 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2247+741A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181671 | |||||||
chr16:16181767 | TACTAAAA | T | 5 | a0013c0025t0001g0007 a0013c0025t0001g0008 a0013c0030t0001g0113 others(2): Show |
5 | HG02109.hp2 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2247+638_2247+644d others(9): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181767 | |||||||
chr16:16181855 | C | T | 1 | a0002c0068t0001g0097 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2247+557G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181855 | |||||||
chr16:16182023 | G | A | 4 | a0024c0075t0001g0049 a0035c0060t0010g0240 a0036c0059t0001g0009 others(1): Show |
4 | HG00642.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247+389C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16182023 | |||||||
chr16:16182123 | G | A | 1 | a0001c0004t0001g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2247+289C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16182123 | |||||||
chr16:16182172 | C | G | 2 | a0001c0001t0002g0203 a0001c0006t0002g0246 |
2 | HG00735.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.2247+240G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16182172 | |||||||
chr16:16182262 | C | T | 4 | a0024c0075t0001g0049 a0035c0060t0010g0240 a0036c0059t0001g0009 others(1): Show |
4 | HG00642.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247+150G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16182262 | |||||||
chr16:16182294 | C | T | 1 | a0036c0059t0001g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2247+118G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16182294 | |||||||
chr16:16182353 | A | G | 1 | a0001c0001t0004g0182 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2247+59T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16182353 | |||||||
chr16:16182354 | C | A | 1 | a0001c0001t0004g0182 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2247+58G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16182354 | |||||||
chr16:16182691 | G | A | 3 | a0001c0002t0001g0167 a0001c0002t0001g0175 a0040c0040t0001g0031 |
3 | HG01884.hp1 HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2071-103C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 16/30 | chr16 | 16182691 | |||||||
chr16:16183107 | C | T | 57 | a0001c0002t0001g0010 a0001c0002t0001g0014 a0001c0002t0001g0023 others(54): Show |
57 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.1944-177G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183107 | |||||||
chr16:16183133 | C | T | 1 | a0001c0055t0012g0164 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1944-203G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183133 | |||||||
chr16:16183307 | C | T | 1 | a0002c0068t0001g0097 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1944-377G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183307 | |||||||
chr16:16183343 | C | T | 5 | a0005c0048t0001g0063 a0024c0075t0001g0049 a0035c0060t0010g0240 others(2): Show |
5 | HG00642.hp1 HG02055.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1944-413G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183343 | |||||||
chr16:16183384 | C | T | 1 | a0002c0068t0001g0097 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1944-454G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183384 | |||||||
chr16:16183385 | G | C | 5 | a0005c0048t0001g0063 a0024c0075t0001g0049 a0035c0060t0010g0240 others(2): Show |
5 | HG00642.hp1 HG02055.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1944-455C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183385 | |||||||
chr16:16183415 | A | G | 5 | a0005c0048t0001g0063 a0024c0075t0001g0049 a0035c0060t0010g0240 others(2): Show |
5 | HG00642.hp1 HG02055.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1944-485T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183415 | |||||||
chr16:16183432 | C | A | 1 | a0001c0001t0004g0182 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1944-502G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183432 | |||||||
chr16:16183477 | G | A | 4 | a0024c0075t0001g0049 a0035c0060t0010g0240 a0036c0059t0001g0009 others(1): Show |
4 | HG00642.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1944-547C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183477 | |||||||
chr16:16183535 | G | C | 2 | a0035c0060t0010g0240 a0036c0059t0001g0009 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1944-605C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183535 | |||||||
chr16:16183563 | G | C | 1 | a0001c0001t0004g0182 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1944-633C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183563 | |||||||
chr16:16183593 | G | A | 5 | a0013c0025t0001g0007 a0013c0025t0001g0008 a0013c0030t0001g0113 others(2): Show |
5 | HG02109.hp2 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1944-663C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183593 | |||||||
chr16:16183755 | C | T | 5 | a0005c0048t0001g0063 a0024c0075t0001g0049 a0035c0060t0010g0240 others(2): Show |
5 | HG00642.hp1 HG02055.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1944-825G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183755 | |||||||
chr16:16183804 | G | A | 5 | a0005c0048t0001g0063 a0024c0075t0001g0049 a0035c0060t0010g0240 others(2): Show |
5 | HG00642.hp1 HG02055.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1944-874C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183804 | |||||||
chr16:16183826 | C | T | 26 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(23): Show |
26 | HG00597.hp1 HG01106.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.1944-896G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183826 | |||||||
chr16:16183828 | G | A | 38 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0201 others(35): Show |
38 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.1944-898C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183828 | |||||||
chr16:16183996 | T | G | 1 | a0001c0001t0004g0182 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1943+963A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183996 | |||||||
chr16:16183998 | G | T | 1 | a0001c0001t0004g0182 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1943+961C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183998 | |||||||
chr16:16184037 | A | G | 1 | a0028c0054t0001g0072 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1943+922T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184037 | |||||||
chr16:16184081 | C | G | 3 | a0005c0048t0001g0063 a0035c0060t0010g0240 a0036c0059t0001g0009 |
3 | HG02055.hp1 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1943+878G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184081 | |||||||
chr16:16184174 | G | A | 2 | a0035c0060t0010g0240 a0036c0059t0001g0009 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1943+785C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184174 | |||||||
chr16:16184179 | A | T | 2 | a0001c0023t0001g0066 a0001c0023t0001g0100 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1943+780T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184179 | |||||||
chr16:16184191 | T | C | 1 | a0001c0001t0004g0182 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1943+768A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184191 | |||||||
chr16:16184192 | C | T | 1 | a0001c0001t0004g0182 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1943+767G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184192 | |||||||
chr16:16184193 | C | T | 156 | a0001c0002t0001g0010 a0001c0002t0001g0014 a0001c0002t0001g0023 others(153): Show |
157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1943+766G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184193 | |||||||
chr16:16184198 | C | CA | 13 | a0001c0001t0001g0064 a0001c0001t0001g0172 a0001c0001t0001g0273 others(10): Show |
13 | HG01175.hp2 HG02055.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.1943+760dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184198 | |||||||
chr16:16184198 | CA | C | 128 | a0001c0001t0001g0069 a0001c0001t0001g0086 a0001c0001t0001g0173 others(125): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.1943+760delT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184198 | |||||||
chr16:16184198 | CAA | C | 147 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(144): Show |
147 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.1943+759_1943+760d others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184198 | |||||||
chr16:16184198 | CAAA | C | 9 | a0001c0001t0004g0156 a0001c0002t0001g0231 a0001c0026t0001g0272 others(6): Show |
9 | HG00642.hp1 HG01099.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1943+758_1943+760d others(5): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184198 | |||||||
chr16:16184198 | CAAAAAAA others(4): Show |
C | 1 | a0026c0039t0001g0032 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1943+750_1943+760d others(13): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184198 | |||||||
chr16:16184270 | T | C | 2 | a0024c0075t0001g0049 a0044c0044t0001g0302 |
2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1943+689A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184270 | |||||||
chr16:16184291 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1943+668C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184291 | |||||||
chr16:16184368 | C | A | 4 | a0024c0075t0001g0049 a0035c0060t0010g0240 a0036c0059t0001g0009 others(1): Show |
4 | HG00642.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1943+591G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184368 | |||||||
chr16:16184424 | C | T | 2 | a0035c0060t0010g0240 a0036c0059t0001g0009 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1943+535G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184424 | |||||||
chr16:16184446 | A | G | 1 | a0001c0001t0001g0325 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1943+513T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184446 | |||||||
chr16:16184459 | G | C | 1 | a0001c0004t0001g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1943+500C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184459 | |||||||
chr16:16184482 | C | G | 3 | a0001c0001t0001g0233 a0001c0001t0001g0305 a0001c0049t0001g0352 |
3 | HG02109.hp1 HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1943+477G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184482 | |||||||
chr16:16184494 | T | G | 2 | a0024c0075t0001g0049 a0044c0044t0001g0302 |
2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1943+465A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184494 | |||||||
chr16:16184589 | C | T | 100 | a0001c0001t0001g0089 a0002c0003t0001g0002 a0002c0003t0001g0013 others(97): Show |
101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.1943+370G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184589 | |||||||
chr16:16184754 | T | C | 1 | a0005c0012t0001g0140 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1943+205A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184754 | |||||||
chr16:16184808 | G | C | 1 | a0001c0004t0001g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1943+151C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184808 | |||||||
chr16:16184817 | C | T | 1 | a0001c0002t0001g0010 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1943+142G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184817 | |||||||
chr16:16184838 | A | T | 99 | a0002c0003t0001g0002 a0002c0003t0001g0013 a0002c0003t0001g0074 others(96): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.1943+121T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184838 | |||||||
chr16:16184868 | C | A | 1 | a0003c0005t0001g0319 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1943+91G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184868 | |||||||
chr16:16184949 | C | G | 1 | a0001c0055t0012g0164 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1943+10G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184949 | |||||||
chr16:16185091 | C | T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(98): Show |
101 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1868-57G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185091 | |||||||
chr16:16185118 | G | T | 1 | a0001c0001t0001g0308 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1868-84C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185118 | |||||||
chr16:16185118 | GC | G | 155 | a0001c0001t0001g0341 a0001c0002t0001g0010 a0001c0002t0001g0014 others(152): Show |
156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1868-85delG | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185118 | |||||||
chr16:16185124 | C | A | 33 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(30): Show |
33 | HG00597.hp1 HG00642.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1868-90G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185124 | |||||||
chr16:16185124 | C | G | 5 | a0002c0024t0001g0153 a0012c0020t0001g0055 a0012c0020t0001g0056 others(2): Show |
5 | HG02897.hp1 HG03209.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1868-90G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185124 | |||||||
chr16:16185125 | C | G | 1 | a0001c0049t0001g0352 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1868-91G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185125 | |||||||
chr16:16185191 | G | C | 153 | a0001c0002t0001g0010 a0001c0002t0001g0014 a0001c0002t0001g0023 others(150): Show |
154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1868-157C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185191 | |||||||
chr16:16185222 | C | T | 153 | a0001c0002t0001g0010 a0001c0002t0001g0014 a0001c0002t0001g0023 others(150): Show |
154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1868-188G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185222 | |||||||
chr16:16185225 | G | A | 1 | a0001c0026t0001g0272 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1868-191C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185225 | |||||||
chr16:16185426 | G | A | 151 | a0001c0002t0001g0010 a0001c0002t0001g0014 a0001c0002t0001g0023 others(148): Show |
152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.1868-392C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185426 | |||||||
chr16:16185470 | C | A | 1 | a0001c0006t0001g0277 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1868-436G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185470 | |||||||
chr16:16185626 | A | T | 1 | a0003c0005t0005g0213 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1868-592T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185626 | |||||||
chr16:16185728 | T | A | 34 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0089 others(31): Show |
34 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.1868-694A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185728 | |||||||
chr16:16185776 | CTG | C | 57 | a0002c0003t0001g0123 a0002c0003t0001g0151 a0002c0003t0001g0257 others(54): Show |
57 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(54): Show |
intron_variant | MODIFIER | c.1868-744_1868-743d others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185776 | |||||||
chr16:16185784 | C | T | 1 | a0002c0068t0001g0097 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1868-750G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185784 | |||||||
chr16:16185949 | G | A | 6 | a0008c0011t0003g0058 a0008c0011t0003g0059 a0008c0011t0003g0060 others(3): Show |
6 | HG02280.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1868-915C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185949 | |||||||
chr16:16186122 | T | C | 28 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(25): Show |
28 | HG00597.hp1 HG01496.hp2 HG02040.hp1 others(25): Show |
intron_variant | MODIFIER | c.1867+1002A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16186122 | |||||||
chr16:16186245 | C | T | 3 | a0013c0025t0001g0007 a0013c0025t0001g0008 a0030c0046t0001g0304 |
3 | HG02723.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1867+879G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16186245 | |||||||
chr16:16186346 | T | G | 1 | a0042c0061t0001g0130 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1867+778A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16186346 | |||||||
chr16:16186548 | C | T | 101 | a0002c0003t0001g0002 a0002c0003t0001g0013 a0002c0003t0001g0074 others(98): Show |
102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.1867+576G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16186548 | |||||||
chr16:16186790 | G | A | 1 | a0004c0010t0001g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1867+334C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16186790 | |||||||
chr16:16186919 | G | C | 33 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0089 others(30): Show |
33 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.1867+205C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16186919 | |||||||
chr16:16187032 | C | T | 101 | a0002c0003t0001g0002 a0002c0003t0001g0013 a0002c0003t0001g0074 others(98): Show |
102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.1867+92G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16187032 | |||||||
chr16:16187038 | A | G | 100 | a0002c0003t0001g0002 a0002c0003t0001g0013 a0002c0003t0001g0074 others(97): Show |
101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.1867+86T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16187038 | |||||||
chr16:16187064 | T | A | 3 | a0001c0004t0001g0034 a0001c0004t0001g0038 a0001c0067t0001g0351 |
3 | HG01123.hp2 HG01346.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1867+60A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16187064 | |||||||
chr16:16187064 | T | C | 335 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(332): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1867+60A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16187064 | |||||||
chr16:16187247 | A | T | 1 | a0003c0005t0001g0197 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1780-36T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187247 | |||||||
chr16:16187297 | C | A | 105 | a0001c0004t0002g0105 a0002c0003t0001g0002 a0002c0003t0001g0013 others(102): Show |
106 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.1780-86G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187297 | |||||||
chr16:16187330 | G | A | 6 | a0008c0011t0003g0058 a0008c0011t0003g0059 a0008c0011t0003g0060 others(3): Show |
6 | HG02280.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1780-119C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187330 | |||||||
chr16:16187434 | C | T | 1 | a0003c0005t0001g0197 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1780-223G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187434 | |||||||
chr16:16187704 | G | T | 3 | a0004c0010t0001g0073 a0017c0035t0001g0077 a0017c0035t0001g0078 |
3 | HG02258.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1780-493C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187704 | |||||||
chr16:16187781 | G | C | 2 | a0024c0075t0001g0049 a0044c0044t0001g0302 |
2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1780-570C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187781 | |||||||
chr16:16187819 | T | A | 2 | a0001c0006t0001g0277 a0001c0006t0001g0299 |
2 | NA19003.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1780-608A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187819 | |||||||
chr16:16187904 | AAAT | A | 49 | a0001c0001t0004g0071 a0001c0004t0001g0108 a0001c0004t0002g0105 others(46): Show |
49 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.1780-696_1780-694d others(5): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187904 | |||||||
chr16:16187904 | AAATT | A | 4 | a0024c0075t0001g0049 a0027c0073t0001g0016 a0036c0059t0001g0009 others(1): Show |
4 | HG00642.hp1 HG02451.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1780-697_1780-694d others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187904 | |||||||
chr16:16187907 | T | A | 3 | a0002c0013t0001g0241 a0003c0007t0001g0098 a0035c0060t0010g0240 |
3 | HG01256.hp1 HG03540.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1780-696A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187907 | |||||||
chr16:16187907 | T | TTAAA | 4 | a0001c0001t0001g0235 a0001c0001t0001g0326 a0001c0001t0001g0339 others(1): Show |
4 | HG00408.hp2 HG03130.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1780-700_1780-697d others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187907 | |||||||
chr16:16187907 | TTAAA | T | 176 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(173): Show |
177 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.1780-700_1780-697d others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187907 | |||||||
chr16:16187908 | T | A | 16 | a0001c0001t0001g0107 a0001c0001t0001g0170 a0001c0001t0001g0172 others(13): Show |
16 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1780-697A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187908 | |||||||
chr16:16187912 | T | A | 63 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(60): Show |
64 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1780-701A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187912 | |||||||
chr16:16187950 | G | A | 1 | a0001c0002t0001g0068 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1780-739C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187950 | |||||||
chr16:16187953 | C | T | 188 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(185): Show |
189 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1780-742G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187953 | |||||||
chr16:16187957 | C | T | 3 | a0027c0073t0001g0016 a0035c0060t0010g0240 a0036c0059t0001g0009 |
3 | HG02451.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1780-746G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187957 | |||||||
chr16:16187974 | G | A | 51 | a0001c0001t0004g0071 a0001c0004t0001g0108 a0001c0004t0002g0105 others(48): Show |
51 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.1780-763C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187974 | |||||||
chr16:16188082 | CAATA | C | 3 | a0011c0016t0006g0271 a0011c0016t0006g0280 a0011c0016t0011g0301 |
3 | HG01496.hp2 HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1779+745_1779+748d others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188082 | |||||||
chr16:16188173 | G | A | 3 | a0027c0073t0001g0016 a0035c0060t0010g0240 a0036c0059t0001g0009 |
3 | HG02451.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1779+658C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188173 | |||||||
chr16:16188225 | C | CA | 122 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(119): Show |
123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1779+605dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188225 | |||||||
chr16:16188225 | C | CAA | 10 | a0001c0001t0001g0189 a0001c0002t0001g0112 a0002c0014t0001g0288 others(7): Show |
10 | HG01257.hp1 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1779+604_1779+605d others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188225 | |||||||
chr16:16188225 | C | CAAA | 8 | a0001c0001t0001g0273 a0001c0001t0001g0341 a0001c0004t0001g0065 others(5): Show |
8 | HG01175.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1779+603_1779+605d others(5): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188225 | |||||||
chr16:16188279 | C | A | 1 | a0012c0050t0001g0040 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1779+552G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188279 | |||||||
chr16:16188449 | C | T | 1 | a0007c0009t0001g0050 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1779+382G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188449 | |||||||
chr16:16188450 | G | A | 50 | a0001c0004t0001g0108 a0001c0004t0001g0209 a0001c0004t0002g0105 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1779+381C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188450 | |||||||
chr16:16188667 | G | A | 9 | a0001c0001t0001g0273 a0001c0001t0001g0341 a0001c0004t0001g0065 others(6): Show |
9 | HG01175.hp2 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1779+164C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188667 | |||||||
chr16:16188686 | C | T | 1 | a0027c0073t0001g0016 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1779+145G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188686 | |||||||
chr16:16188721 | C | T | 2 | a0001c0001t0002g0242 a0001c0033t0002g0196 |
2 | HG01261.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1779+110G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188721 | |||||||
chr16:16188742 | C | T | 2 | a0003c0005t0001g0028 a0003c0005t0001g0029 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1779+89G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188742 | |||||||
chr16:16188793 | C | T | 1 | a0002c0024t0001g0155 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1779+38G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188793 | |||||||
chr16:16188984 | G | A | 2 | a0001c0055t0012g0164 a0029c0069t0001g0015 |
2 | HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1636-10C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16188984 | |||||||
chr16:16189086 | G | A | 12 | a0001c0001t0001g0233 a0001c0001t0001g0305 a0001c0055t0012g0164 others(9): Show |
12 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1636-112C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189086 | |||||||
chr16:16189101 | C | T | 1 | a0001c0072t0001g0356 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1636-127G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189101 | |||||||
chr16:16189185 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1636-211A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189185 | |||||||
chr16:16189214 | C | T | 54 | a0001c0001t0001g0145 a0001c0002t0001g0112 a0001c0002t0001g0167 others(51): Show |
55 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.1636-240G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189214 | |||||||
chr16:16189419 | C | CT | 8 | a0001c0001t0001g0185 a0001c0001t0001g0308 a0001c0001t0001g0335 others(5): Show |
8 | HG01928.hp2 HG02970.hp1 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.1636-446dupA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189419 | |||||||
chr16:16189419 | CTT | C | 73 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(70): Show |
73 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1636-447_1636-446d others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189419 | |||||||
chr16:16189456 | C | T | 3 | a0027c0073t0001g0016 a0035c0060t0010g0240 a0036c0059t0001g0009 |
3 | HG02451.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1636-482G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189456 | |||||||
chr16:16189552 | G | C | 1 | a0002c0003t0001g0261 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1636-578C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189552 | |||||||
chr16:16189720 | C | G | 2 | a0001c0004t0001g0006 a0011c0016t0001g0275 |
2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1635+444G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189720 | |||||||
chr16:16189754 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1635+410C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189754 | |||||||
chr16:16189822 | G | A | 2 | a0013c0025t0001g0007 a0013c0025t0001g0008 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1635+342C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189822 | |||||||
chr16:16189910 | C | A | 3 | a0001c0001t0001g0326 a0001c0001t0001g0338 a0001c0001t0001g0339 |
3 | HG02559.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1635+254G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189910 | |||||||
chr16:16189955 | C | A | 2 | a0001c0001t0001g0233 a0001c0001t0001g0305 |
2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1635+209G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189955 | |||||||
chr16:16190034 | C | A | 1 | a0001c0028t0001g0295 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1635+130G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16190034 | |||||||
chr16:16190035 | A | C | 1 | a0001c0028t0001g0295 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1635+129T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16190035 | |||||||
chr16:16190036 | G | A | 1 | a0001c0028t0001g0295 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1635+128C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16190036 | |||||||
chr16:16190085 | G | A | 1 | a0001c0001t0002g0030 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1635+79C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16190085 | |||||||
chr16:16190116 | G | A | 100 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(97): Show |
100 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1635+48C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16190116 | |||||||
chr16:16190408 | T | C | 101 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(98): Show |
101 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1432-41A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190408 | |||||||
chr16:16190415 | C | T | 335 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(332): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1432-48G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190415 | |||||||
chr16:16190503 | C | T | 2 | a0016c0032t0001g0051 a0021c0066t0001g0052 |
2 | HG00099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1432-136G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190503 | |||||||
chr16:16190552 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1432-185C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190552 | |||||||
chr16:16190573 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1432-206A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190573 | |||||||
chr16:16190668 | T | C | 5 | a0024c0075t0001g0049 a0027c0073t0001g0016 a0035c0060t0010g0240 others(2): Show |
5 | HG00642.hp1 HG02451.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1432-301A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190668 | |||||||
chr16:16190669 | G | A | 49 | a0001c0001t0001g0303 a0001c0004t0001g0108 a0001c0004t0001g0163 others(46): Show |
49 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.1432-302C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190669 | |||||||
chr16:16190685 | C | CT | 8 | a0001c0001t0002g0204 a0001c0001t0004g0182 a0001c0002t0001g0023 others(5): Show |
8 | HG01496.hp1 HG03688.hp1 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.1432-319dupA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190685 | |||||||
chr16:16190706 | A | C | 1 | a0003c0007t0001g0101 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1432-339T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190706 | |||||||
chr16:16190720 | G | A | 1 | a0001c0002t0001g0112 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1432-353C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190720 | |||||||
chr16:16190940 | G | A | 17 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(14): Show |
17 | HG00597.hp1 HG02040.hp1 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.1432-573C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190940 | |||||||
chr16:16190952 | C | G | 269 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(266): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1432-585G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190952 | |||||||
chr16:16190971 | G | A | 3 | a0001c0001t0001g0189 a0001c0049t0001g0352 a0011c0016t0001g0275 |
3 | HG03139.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1432-604C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190971 | |||||||
chr16:16191011 | G | C | 167 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0039 others(164): Show |
168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1432-644C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191011 | |||||||
chr16:16191067 | C | T | 339 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(336): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1432-700G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191067 | |||||||
chr16:16191083 | G | A | 1 | a0001c0001t0001g0189 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1432-716C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191083 | |||||||
chr16:16191085 | CG | C | 346 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(343): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1432-719delC | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191085 | |||||||
chr16:16191139 | C | T | 80 | a0001c0001t0001g0145 a0001c0001t0001g0303 a0001c0002t0001g0112 others(77): Show |
81 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1432-772G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191139 | |||||||
chr16:16191202 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1432-835C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191202 | |||||||
chr16:16191208 | T | C | 1 | a0041c0070t0002g0067 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1432-841A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191208 | |||||||
chr16:16191236 | T | C | 241 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(238): Show |
242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1432-869A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191236 | |||||||
chr16:16191241 | G | A | 1 | a0028c0054t0001g0072 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1432-874C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191241 | |||||||
chr16:16191265 | G | A | 3 | a0011c0016t0006g0271 a0011c0016t0006g0280 a0011c0016t0011g0301 |
3 | HG01496.hp2 HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1432-898C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191265 | |||||||
chr16:16191288 | G | A | 239 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0064 others(236): Show |
240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.1432-921C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191288 | |||||||
chr16:16191620 | T | C | 1 | a0036c0059t0001g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1431+1210A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191620 | |||||||
chr16:16191642 | CCTTTT | C | 260 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(257): Show |
261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1431+1183_1431+118 others(9): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191642 | |||||||
chr16:16191703 | G | T | 260 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(257): Show |
261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1431+1127C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191703 | |||||||
chr16:16191795 | C | T | 259 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(256): Show |
260 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.1431+1035G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191795 | |||||||
chr16:16191895 | G | C | 2 | a0001c0001t0002g0204 a0001c0002t0001g0093 |
2 | NA18987.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1431+935C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191895 | |||||||
chr16:16191911 | G | A | 12 | a0001c0001t0001g0273 a0001c0001t0001g0341 a0001c0004t0001g0065 others(9): Show |
12 | HG01175.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1431+919C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191911 | |||||||
chr16:16191966 | G | A | 1 | a0001c0002t0001g0141 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1431+864C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191966 | |||||||
chr16:16191990 | G | T | 127 | a0001c0001t0001g0064 a0001c0001t0001g0083 a0001c0001t0001g0086 others(124): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1431+840C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191990 | |||||||
chr16:16192105 | G | A | 2 | a0024c0075t0001g0049 a0044c0044t0001g0302 |
2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1431+725C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192105 | |||||||
chr16:16192111 | A | G | 1 | a0001c0004t0002g0219 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1431+719T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192111 | |||||||
chr16:16192231 | G | A | 1 | a0006c0008t0001g0264 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1431+599C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192231 | |||||||
chr16:16192258 | A | G | 1 | a0001c0002t0001g0222 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1431+572T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192258 | |||||||
chr16:16192373 | G | C | 1 | a0030c0046t0001g0304 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1431+457C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192373 | |||||||
chr16:16192444 | G | A | 1 | a0035c0060t0010g0240 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1431+386C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192444 | |||||||
chr16:16192505 | C | T | 352 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(349): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1431+325G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192505 | |||||||
chr16:16192515 | A | G | 3 | a0015c0019t0001g0122 a0015c0019t0001g0125 a0015c0019t0001g0126 |
3 | HG02451.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1431+315T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192515 | |||||||
chr16:16192577 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1431+253C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192577 | |||||||
chr16:16192662 | G | C | 130 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(127): Show |
130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1431+168C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192662 | |||||||
chr16:16192704 | C | T | 1 | a0001c0055t0012g0164 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1431+126G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192704 | |||||||
chr16:16192710 | A | G | 1 | a0001c0001t0002g0204 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1431+120T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192710 | |||||||
chr16:16192729 | C | T | 62 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0069 others(59): Show |
62 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1431+101G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192729 | |||||||
chr16:16192743 | C | T | 1 | a0014c0018t0001g0250 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1431+87G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192743 | |||||||
chr16:16192757 | G | C | 264 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(261): Show |
265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.1431+73C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192757 | |||||||
chr16:16192807 | C | T | 2 | a0024c0075t0001g0049 a0044c0044t0001g0302 |
2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1431+23G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192807 | |||||||
chr16:16193049 | T | A | 1 | a0011c0016t0001g0275 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1339-127A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193049 | |||||||
chr16:16193057 | C | T | 2 | a0035c0060t0010g0240 a0036c0059t0001g0009 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1339-135G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193057 | |||||||
chr16:16193096 | C | T | 1 | a0003c0005t0001g0321 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1339-174G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193096 | |||||||
chr16:16193154 | C | T | 1 | a0017c0035t0001g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1339-232G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193154 | |||||||
chr16:16193227 | C | T | 82 | a0001c0001t0001g0145 a0001c0001t0001g0303 a0001c0002t0001g0112 others(79): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1339-305G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193227 | |||||||
chr16:16193250 | A | G | 1 | a0001c0001t0001g0336 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1339-328T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193250 | |||||||
chr16:16193504 | A | G | 3 | a0015c0019t0001g0122 a0015c0019t0001g0125 a0015c0019t0001g0126 |
3 | HG02451.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1339-582T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193504 | |||||||
chr16:16193524 | G | C | 3 | a0011c0016t0006g0271 a0011c0016t0006g0280 a0011c0016t0011g0301 |
3 | HG01496.hp2 HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1339-602C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193524 | |||||||
chr16:16193527 | A | G | 3 | a0015c0019t0001g0122 a0015c0019t0001g0125 a0015c0019t0001g0126 |
3 | HG02451.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1339-605T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193527 | |||||||
chr16:16193552 | A | G | 1 | a0007c0009t0001g0048 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1339-630T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193552 | |||||||
chr16:16193568 | G | T | 34 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0089 others(31): Show |
34 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.1339-646C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193568 | |||||||
chr16:16193646 | G | A | 1 | a0001c0055t0012g0164 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1339-724C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193646 | |||||||
chr16:16193680 | C | T | 2 | a0024c0075t0001g0049 a0044c0044t0001g0302 |
2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1339-758G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193680 | |||||||
chr16:16193690 | G | C | 3 | a0008c0011t0003g0058 a0008c0011t0003g0059 a0008c0011t0003g0091 |
3 | HG02280.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1339-768C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193690 | |||||||
chr16:16193756 | G | T | 2 | a0005c0048t0001g0063 a0029c0069t0001g0015 |
2 | HG02055.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1339-834C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193756 | |||||||
chr16:16193762 | A | G | 130 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(127): Show |
130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1339-840T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193762 | |||||||
chr16:16193782 | C | T | 3 | a0001c0001t0001g0160 a0009c0029t0001g0159 a0009c0029t0001g0230 |
3 | HG01069.hp2 HG01175.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1339-860G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193782 | |||||||
chr16:16194015 | G | A | 1 | a0003c0005t0001g0260 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1339-1093C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194015 | |||||||
chr16:16194136 | T | A | 2 | a0001c0001t0002g0094 a0001c0001t0002g0311 |
2 | NA18959.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1339-1214A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194136 | |||||||
chr16:16194188 | C | A | 130 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(127): Show |
130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1339-1266G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194188 | |||||||
chr16:16194338 | A | C | 6 | a0001c0055t0012g0164 a0012c0020t0001g0055 a0012c0020t0001g0056 others(3): Show |
6 | HG02559.hp1 HG02897.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1339-1416T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194338 | |||||||
chr16:16194397 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1339-1475C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194397 | |||||||
chr16:16194397 | G | T | 81 | a0001c0001t0001g0145 a0001c0001t0001g0303 a0001c0002t0001g0112 others(78): Show |
82 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1339-1475C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194397 | |||||||
chr16:16194499 | G | A | 278 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(275): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.1339-1577C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194499 | |||||||
chr16:16194518 | G | A | 130 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(127): Show |
130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1339-1596C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194518 | |||||||
chr16:16194528 | G | A | 1 | a0001c0002t0001g0287 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1339-1606C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194528 | |||||||
chr16:16194535 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1339-1613C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194535 | |||||||
chr16:16194696 | G | A | 130 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(127): Show |
130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1339-1774C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194696 | |||||||
chr16:16194764 | C | T | 128 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(125): Show |
128 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.1339-1842G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194764 | |||||||
chr16:16194797 | G | T | 1 | a0040c0040t0001g0031 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1339-1875C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194797 | |||||||
chr16:16194809 | T | C | 1 | a0001c0001t0001g0247 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1339-1887A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194809 | |||||||
chr16:16194830 | A | G | 141 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(138): Show |
141 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.1339-1908T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194830 | |||||||
chr16:16194889 | A | G | 2 | a0001c0002t0001g0025 a0001c0002t0001g0026 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1339-1967T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194889 | |||||||
chr16:16194899 | C | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(127): Show |
130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1339-1977G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194899 | |||||||
chr16:16194953 | T | TACAGGTT others(6): Show |
1 | a0001c0004t0001g0108 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1339-2044_1339-203 others(17): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194953 | |||||||
chr16:16194993 | T | C | 6 | a0001c0055t0012g0164 a0012c0020t0001g0055 a0012c0020t0001g0056 others(3): Show |
6 | HG02559.hp1 HG02897.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1339-2071A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194993 | |||||||
chr16:16195035 | G | A | 1 | a0002c0003t0001g0188 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1339-2113C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195035 | |||||||
chr16:16195047 | C | G | 1 | a0005c0031t0001g0349 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1339-2125G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195047 | |||||||
chr16:16195147 | A | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(127): Show |
130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1339-2225T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195147 | |||||||
chr16:16195200 | A | G | 1 | a0035c0060t0010g0240 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1339-2278T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195200 | |||||||
chr16:16195234 | G | A | 2 | a0024c0075t0001g0049 a0044c0044t0001g0302 |
2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1339-2312C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195234 | |||||||
chr16:16195242 | A | T | 40 | a0001c0001t0001g0064 a0001c0001t0001g0083 a0001c0001t0001g0086 others(37): Show |
40 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1339-2320T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195242 | |||||||
chr16:16195269 | G | A | 2 | a0003c0021t0001g0011 a0003c0021t0001g0012 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1339-2347C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195269 | |||||||
chr16:16195269 | G | C | 130 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(127): Show |
130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1339-2347C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195269 | |||||||
chr16:16195282 | A | T | 1 | a0001c0001t0001g0338 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1339-2360T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195282 | |||||||
chr16:16195303 | A | AT | 41 | a0001c0001t0001g0069 a0001c0001t0001g0185 a0001c0001t0001g0201 others(38): Show |
41 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1339-2382dupA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195303 | |||||||
chr16:16195303 | AT | A | 49 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0064 others(46): Show |
49 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.1339-2382delA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195303 | |||||||
chr16:16195303 | ATT | A | 7 | a0001c0001t0001g0166 a0001c0001t0001g0183 a0001c0001t0002g0087 others(4): Show |
7 | HG02071.hp2 NA18906.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.1339-2383_1339-238 others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195303 | |||||||
chr16:16195303 | ATTTTT | A | 8 | a0001c0001t0001g0192 a0001c0001t0001g0335 a0001c0001t0004g0223 others(5): Show |
8 | HG01928.hp1 HG02572.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1339-2386_1339-238 others(9): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195303 | |||||||
chr16:16195303 | ATTTTTT | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0107 others(114): Show |
117 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1339-2387_1339-238 others(10): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195303 | |||||||
chr16:16195405 | C | T | 32 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0107 others(29): Show |
32 | HG00597.hp1 HG01884.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1339-2483G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195405 | |||||||
chr16:16195422 | C | T | 1 | a0001c0033t0001g0070 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1339-2500G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195422 | |||||||
chr16:16195496 | A | G | 5 | a0001c0004t0001g0065 a0014c0018t0001g0249 a0014c0018t0001g0250 others(2): Show |
5 | HG02258.hp1 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1338+2525T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195496 | |||||||
chr16:16195559 | G | T | 1 | a0028c0054t0001g0072 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1338+2462C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195559 | |||||||
chr16:16195675 | T | C | 124 | a0001c0001t0001g0064 a0001c0001t0001g0083 a0001c0001t0001g0086 others(121): Show |
125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.1338+2346A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195675 | |||||||
chr16:16195839 | T | C | 124 | a0001c0001t0001g0064 a0001c0001t0001g0083 a0001c0001t0001g0086 others(121): Show |
125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.1338+2182A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195839 | |||||||
chr16:16195887 | T | C | 1 | a0016c0032t0001g0150 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1338+2134A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195887 | |||||||
chr16:16195988 | T | C | 1 | a0028c0054t0001g0072 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1338+2033A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195988 | |||||||
chr16:16196073 | T | C | 135 | a0001c0001t0001g0064 a0001c0001t0001g0083 a0001c0001t0001g0086 others(132): Show |
136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1338+1948A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196073 | |||||||
chr16:16196083 | G | A | 62 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0069 others(59): Show |
62 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1338+1938C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196083 | |||||||
chr16:16196155 | A | G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0143 |
2 | HG02135.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1338+1866T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196155 | |||||||
chr16:16196158 | C | T | 1 | a0002c0013t0001g0266 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1338+1863G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196158 | |||||||
chr16:16196209 | C | CA | 84 | a0001c0001t0001g0205 a0001c0001t0001g0303 a0001c0002t0001g0112 others(81): Show |
85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1338+1811dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196209 | |||||||
chr16:16196209 | C | CAA | 87 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0069 others(84): Show |
87 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1338+1810_1338+181 others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196209 | |||||||
chr16:16196209 | C | CAAAA | 60 | a0001c0001t0001g0127 a0001c0001t0001g0145 a0001c0001t0001g0173 others(57): Show |
60 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1338+1808_1338+181 others(8): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196209 | |||||||
chr16:16196209 | C | CAAAAA | 35 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0107 others(32): Show |
35 | HG00597.hp1 HG00673.hp2 HG02040.hp1 others(32): Show |
intron_variant | MODIFIER | c.1338+1807_1338+181 others(9): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196209 | |||||||
chr16:16196209 | C | CAAAAAA | 41 | a0001c0001t0001g0003 a0001c0001t0001g0136 a0001c0001t0001g0137 others(38): Show |
41 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.1338+1806_1338+181 others(10): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196209 | |||||||
chr16:16196209 | CA | C | 9 | a0004c0010t0001g0073 a0004c0010t0001g0075 a0011c0016t0006g0271 others(6): Show |
9 | HG01496.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1338+1811delT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196209 | |||||||
chr16:16196234 | A | T | 2 | a0004c0010t0001g0042 a0004c0010t0001g0043 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1338+1787T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196234 | |||||||
chr16:16196245 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1338+1776G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196245 | |||||||
chr16:16196330 | A | G | 142 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(139): Show |
142 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.1338+1691T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196330 | |||||||
chr16:16196385 | A | G | 54 | a0001c0001t0001g0064 a0001c0001t0001g0083 a0001c0001t0001g0086 others(51): Show |
54 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1338+1636T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196385 | |||||||
chr16:16196473 | G | A | 42 | a0001c0001t0001g0064 a0001c0001t0001g0083 a0001c0001t0001g0086 others(39): Show |
42 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.1338+1548C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196473 | |||||||
chr16:16196484 | C | G | 1 | a0001c0001t0001g0303 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1338+1537G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196484 | |||||||
chr16:16196486 | C | T | 54 | a0001c0001t0001g0064 a0001c0001t0001g0083 a0001c0001t0001g0086 others(51): Show |
54 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1338+1535G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196486 | |||||||
chr16:16196489 | C | T | 3 | a0011c0016t0006g0271 a0011c0016t0006g0280 a0011c0016t0011g0301 |
3 | HG01496.hp2 HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1338+1532G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196489 | |||||||
chr16:16196520 | C | T | 242 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1338+1501G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196520 | |||||||
chr16:16196638 | A | G | 285 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1338+1383T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196638 | |||||||
chr16:16196678 | G | A | 13 | a0001c0001t0001g0235 a0001c0001t0001g0247 a0001c0001t0001g0313 others(10): Show |
13 | HG00408.hp2 HG00544.hp1 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1338+1343C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196678 | |||||||
chr16:16196679 | A | G | 1 | a0013c0030t0001g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1338+1342T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196679 | |||||||
chr16:16196801 | A | G | 1 | a0012c0020t0001g0055 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1338+1220T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196801 | |||||||
chr16:16196938 | C | T | 1 | a0007c0009t0001g0050 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1338+1083G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196938 | |||||||
chr16:16197011 | A | T | 251 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(248): Show |
251 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.1338+1010T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197011 | |||||||
chr16:16197012 | A | T | 1 | a0003c0005t0001g0314 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1338+1009T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197012 | |||||||
chr16:16197030 | C | T | 1 | a0002c0057t0001g0255 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1338+991G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197030 | |||||||
chr16:16197242 | A | G | 103 | a0001c0001t0001g0129 a0001c0001t0001g0136 a0001c0001t0001g0137 others(100): Show |
103 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1338+779T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197242 | |||||||
chr16:16197334 | G | C | 13 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(10): Show |
13 | HG02040.hp1 HG02056.hp2 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.1338+687C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197334 | |||||||
chr16:16197387 | A | G | 1 | a0001c0001t0001g0336 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1338+634T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197387 | |||||||
chr16:16197443 | G | A | 1 | a0001c0055t0012g0164 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1338+578C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197443 | |||||||
chr16:16197563 | G | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0069 others(138): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.1338+458C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197563 | |||||||
chr16:16197658 | C | T | 1 | a0002c0013t0001g0243 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1338+363G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197658 | |||||||
chr16:16197721 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1338+300C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197721 | |||||||
chr16:16197770 | G | A | 201 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(198): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1338+251C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197770 | |||||||
chr16:16197861 | C | T | 1 | a0036c0059t0001g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1338+160G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197861 | |||||||
chr16:16197942 | G | A | 1 | a0036c0059t0001g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1338+79C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197942 | |||||||
chr16:16197959 | G | C | 65 | a0001c0001t0001g0064 a0001c0001t0001g0079 a0001c0001t0001g0083 others(62): Show |
66 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.1338+62C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197959 | |||||||
chr16:16198001 | G | C | 256 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(253): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1338+20C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16198001 | |||||||
chr16:16198014 | G | C | 286 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(283): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
splice_region_variant&intron_variant | LOW | c.1338+7C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16198014 | |||||||
chr16:16198211 | A | C | 1 | a0001c0001t0001g0269 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1177-29T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198211 | |||||||
chr16:16198223 | C | T | 1 | a0001c0055t0012g0164 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1177-41G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198223 | |||||||
chr16:16198271 | C | T | 112 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(109): Show |
112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1177-89G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198271 | |||||||
chr16:16198276 | A | G | 112 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(109): Show |
112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1177-94T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198276 | |||||||
chr16:16198343 | G | C | 2 | a0001c0001t0002g0162 a0041c0070t0002g0067 |
2 | NA18943.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1177-161C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198343 | |||||||
chr16:16198466 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(136): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1177-284C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198466 | |||||||
chr16:16198486 | A | G | 1 | a0001c0002t0001g0138 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1177-304T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198486 | |||||||
chr16:16198633 | G | A | 111 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1177-451C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198633 | |||||||
chr16:16198659 | C | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1177-477G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198659 | |||||||
chr16:16198661 | C | T | 1 | a0013c0030t0001g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1177-479G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198661 | |||||||
chr16:16198721 | C | A | 111 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1177-539G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198721 | |||||||
chr16:16198721 | C | G | 1 | a0044c0044t0001g0302 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1177-539G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198721 | |||||||
chr16:16198721 | C | T | 1 | a0004c0017t0001g0193 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1177-539G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198721 | |||||||
chr16:16198733 | T | C | 118 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(115): Show |
119 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.1177-551A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198733 | |||||||
chr16:16198736 | A | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1177-554T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198736 | |||||||
chr16:16198739 | A | T | 1 | a0003c0007t0001g0104 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1177-557T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198739 | |||||||
chr16:16198747 | A | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG00673.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1177-565T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198747 | |||||||
chr16:16198851 | G | A | 51 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1177-669C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198851 | |||||||
chr16:16198909 | G | T | 1 | a0027c0073t0001g0016 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1177-727C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198909 | |||||||
chr16:16198962 | C | G | 1 | a0004c0017t0001g0076 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1177-780G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198962 | |||||||
chr16:16198999 | G | GAA | 57 | a0001c0001t0001g0189 a0001c0002t0001g0025 a0001c0002t0001g0026 others(54): Show |
57 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.1177-818_1177-817i others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198999 | |||||||
chr16:16198999 | G | GAC | 54 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(51): Show |
54 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.1177-818_1177-817i others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198999 | |||||||
chr16:16199000 | G | A | 112 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(109): Show |
112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1177-818C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199000 | |||||||
chr16:16199000 | G | GA | 171 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(168): Show |
171 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.1177-819dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199000 | |||||||
chr16:16199013 | A | T | 1 | a0001c0004t0001g0108 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1177-831T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199013 | |||||||
chr16:16199037 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1177-855C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199037 | |||||||
chr16:16199048 | T | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1177-866A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199048 | |||||||
chr16:16199055 | C | A | 1 | a0001c0001t0002g0088 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1177-873G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199055 | |||||||
chr16:16199125 | G | A | 1 | a0002c0003t0001g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1177-943C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199125 | |||||||
chr16:16199281 | G | GA | 5 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0239 others(2): Show |
5 | HG01123.hp1 HG01261.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1177-1100dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199281 | |||||||
chr16:16199298 | C | T | 1 | a0001c0002t0001g0010 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1177-1116G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199298 | |||||||
chr16:16199299 | G | T | 3 | a0015c0019t0001g0122 a0015c0019t0001g0125 a0015c0019t0001g0126 |
3 | HG02451.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1177-1117C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199299 | |||||||
chr16:16199333 | T | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1177-1151A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199333 | |||||||
chr16:16199350 | T | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1177-1168A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199350 | |||||||
chr16:16199401 | T | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1177-1219A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199401 | |||||||
chr16:16199431 | G | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1177-1249C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199431 | |||||||
chr16:16199459 | T | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1177-1277A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199459 | |||||||
chr16:16199560 | A | C | 114 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(111): Show |
114 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.1177-1378T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199560 | |||||||
chr16:16199567 | C | T | 1 | a0001c0002t0001g0157 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1177-1385G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199567 | |||||||
chr16:16199592 | T | A | 111 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1177-1410A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199592 | |||||||
chr16:16199623 | T | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1177-1441A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199623 | |||||||
chr16:16199659 | T | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1177-1477A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199659 | |||||||
chr16:16199735 | C | A | 111 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1177-1553G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199735 | |||||||
chr16:16199948 | A | T | 1 | a0001c0004t0001g0108 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1177-1766T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199948 | |||||||
chr16:16199958 | T | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1177-1776A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199958 | |||||||
chr16:16199982 | T | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1177-1800A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199982 | |||||||
chr16:16199983 | G | A | 111 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1177-1801C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199983 | |||||||
chr16:16200099 | A | T | 113 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(110): Show |
113 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.1176+1902T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200099 | |||||||
chr16:16200124 | G | C | 3 | a0001c0004t0001g0263 a0001c0072t0001g0356 a0002c0024t0001g0153 |
3 | HG01175.hp2 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1176+1877C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200124 | |||||||
chr16:16200159 | C | T | 4 | a0001c0001t0001g0326 a0001c0001t0001g0338 a0001c0001t0001g0339 others(1): Show |
4 | HG02559.hp2 HG03130.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1176+1842G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200159 | |||||||
chr16:16200169 | T | C | 2 | a0013c0025t0001g0007 a0013c0025t0001g0008 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1176+1832A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200169 | |||||||
chr16:16200216 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1176+1785C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200216 | |||||||
chr16:16200253 | A | G | 1 | a0001c0004t0001g0208 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1176+1748T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200253 | |||||||
chr16:16200286 | G | A | 113 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(110): Show |
113 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.1176+1715C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200286 | |||||||
chr16:16200297 | C | G | 1 | a0003c0005t0001g0135 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1176+1704G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200297 | |||||||
chr16:16200299 | C | T | 2 | a0001c0002t0001g0222 a0001c0002t0001g0354 |
2 | HG00597.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1176+1702G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200299 | |||||||
chr16:16200360 | C | T | 111 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1176+1641G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200360 | |||||||
chr16:16200387 | C | T | 111 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1176+1614G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200387 | |||||||
chr16:16200429 | G | GA | 23 | a0001c0001t0001g0089 a0001c0001t0001g0107 a0001c0001t0001g0185 others(20): Show |
23 | HG00323.hp2 HG00438.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1176+1571dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200429 | |||||||
chr16:16200429 | GA | G | 13 | a0001c0001t0001g0326 a0001c0001t0001g0338 a0001c0001t0001g0339 others(10): Show |
13 | HG01069.hp1 HG01515.hp2 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.1176+1571delT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200429 | |||||||
chr16:16200473 | T | C | 1 | a0001c0004t0001g0212 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1176+1528A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200473 | |||||||
chr16:16200511 | T | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1176+1490A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200511 | |||||||
chr16:16200537 | G | A | 111 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1176+1464C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200537 | |||||||
chr16:16200552 | G | A | 1 | a0013c0030t0001g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1176+1449C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200552 | |||||||
chr16:16200608 | T | C | 264 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0064 others(261): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1176+1393A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200608 | |||||||
chr16:16200644 | T | C | 115 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(112): Show |
115 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.1176+1357A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200644 | |||||||
chr16:16200662 | A | C | 115 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(112): Show |
115 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.1176+1339T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200662 | |||||||
chr16:16200684 | G | A | 1 | a0013c0030t0001g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1176+1317C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200684 | |||||||
chr16:16200704 | C | T | 111 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1176+1297G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200704 | |||||||
chr16:16200763 | A | G | 2 | a0013c0025t0001g0007 a0013c0025t0001g0008 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1176+1238T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200763 | |||||||
chr16:16200764 | C | T | 1 | a0013c0030t0001g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1176+1237G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200764 | |||||||
chr16:16200829 | C | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1176+1172G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200829 | |||||||
chr16:16200853 | A | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1176+1148T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200853 | |||||||
chr16:16200858 | C | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1176+1143G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200858 | |||||||
chr16:16200858 | C | T | 1 | a0018c0034t0001g0001 | 2 | NA18943.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1176+1143G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200858 | |||||||
chr16:16200885 | G | A | 7 | a0001c0001t0001g0273 a0001c0001t0001g0341 a0001c0002t0001g0014 others(4): Show |
7 | HG02109.hp2 HG02257.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1176+1116C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200885 | |||||||
chr16:16201027 | C | T | 1 | a0044c0044t0001g0302 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1176+974G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16201027 | |||||||
chr16:16201060 | G | A | 1 | a0001c0001t0002g0322 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1176+941C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16201060 | |||||||
chr16:16201210 | G | A | 1 | a0013c0030t0001g0274 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1176+791C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16201210 | |||||||
chr16:16201758 | G | A | 123 | a0001c0001t0001g0039 a0001c0001t0001g0064 a0001c0001t0001g0069 others(120): Show |
123 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.1176+243C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16201758 | |||||||
chr16:16202258 | ATGTGGAG others(26): Show |
A | 1 | a0001c0001t0002g0203 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.999-113_999-81delC others(32): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16202258 | |||||||
chr16:16202435 | T | C | 5 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(2): Show |
5 | HG03491.hp1 HG03492.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.999-257A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16202435 | |||||||
chr16:16202447 | G | C | 1 | a0001c0006t0001g0190 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.999-269C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16202447 | |||||||
chr16:16202509 | C | T | 2 | a0001c0006t0001g0329 a0004c0017t0001g0076 |
2 | HG00597.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.999-331G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16202509 | |||||||
chr16:16202568 | A | AC | 176 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(173): Show |
177 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.999-391_999-390ins others(1): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16202568 | |||||||
chr16:16202573 | G | T | 1 | a0003c0005t0001g0307 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.999-395C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16202573 | |||||||
chr16:16202603 | C | T | 1 | a0011c0016t0001g0275 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.999-425G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16202603 | |||||||
chr16:16202631 | G | A | 154 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(151): Show |
155 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.999-453C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16202631 | |||||||
chr16:16202930 | C | T | 1 | a0001c0043t0001g0236 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.998+480G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16202930 | |||||||
chr16:16203101 | C | T | 1 | a0001c0043t0001g0236 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.998+309G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16203101 | |||||||
chr16:16203114 | C | T | 1 | a0002c0003t0001g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.998+296G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16203114 | |||||||
chr16:16203212 | T | C | 1 | a0001c0049t0001g0352 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.998+198A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16203212 | |||||||
chr16:16203311 | C | T | 63 | a0001c0001t0001g0079 a0001c0001t0001g0083 a0001c0001t0001g0086 others(60): Show |
64 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.998+99G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16203311 | |||||||
chr16:16203938 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.795-325T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16203938 | |||||||
chr16:16204095 | C | T | 1 | a0023c0053t0001g0154 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.795-482G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204095 | |||||||
chr16:16204132 | C | T | 1 | a0002c0003t0001g0267 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.795-519G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204132 | |||||||
chr16:16204347 | C | T | 1 | a0010c0015t0001g0327 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.795-734G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204347 | |||||||
chr16:16204352 | G | A | 67 | a0001c0001t0001g0273 a0001c0001t0001g0281 a0001c0001t0001g0303 others(64): Show |
67 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.795-739C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204352 | |||||||
chr16:16204366 | T | C | 1 | a0002c0024t0001g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.795-753A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204366 | |||||||
chr16:16204391 | T | A | 1 | a0001c0004t0001g0108 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.795-778A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204391 | |||||||
chr16:16204398 | A | G | 4 | a0001c0001t0001g0326 a0001c0001t0001g0338 a0001c0001t0001g0339 others(1): Show |
4 | HG02559.hp2 HG03130.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.795-785T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204398 | |||||||
chr16:16204431 | G | T | 51 | a0001c0001t0001g0079 a0001c0001t0001g0083 a0001c0001t0001g0086 others(48): Show |
52 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.795-818C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204431 | |||||||
chr16:16204434 | A | T | 3 | a0008c0011t0003g0058 a0008c0011t0003g0059 a0008c0011t0003g0091 |
3 | HG02280.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.795-821T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204434 | |||||||
chr16:16204703 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.795-1090C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204703 | |||||||
chr16:16204723 | C | T | 1 | a0001c0002t0001g0354 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.795-1110G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204723 | |||||||
chr16:16204837 | C | CT | 61 | a0001c0001t0001g0079 a0001c0001t0001g0083 a0001c0001t0001g0086 others(58): Show |
62 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.795-1225dupA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204837 | |||||||
chr16:16204865 | C | T | 4 | a0014c0018t0001g0249 a0014c0018t0001g0250 a0014c0018t0001g0251 others(1): Show |
4 | HG02258.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.795-1252G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204865 | |||||||
chr16:16204896 | A | G | 2 | a0001c0001t0001g0273 a0013c0030t0001g0274 |
2 | HG02109.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.795-1283T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204896 | |||||||
chr16:16205009 | T | C | 1 | a0001c0067t0001g0351 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.795-1396A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205009 | |||||||
chr16:16205062 | C | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.795-1449G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205062 | |||||||
chr16:16205085 | C | T | 7 | a0001c0004t0001g0163 a0001c0004t0001g0217 a0001c0004t0001g0220 others(4): Show |
7 | HG00733.hp2 HG01074.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.795-1472G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205085 | |||||||
chr16:16205118 | G | A | 1 | a0001c0001t0001g0189 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.795-1505C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205118 | |||||||
chr16:16205131 | C | T | 1 | a0013c0030t0001g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.795-1518G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205131 | |||||||
chr16:16205174 | C | T | 4 | a0002c0024t0001g0155 a0015c0019t0001g0122 a0015c0019t0001g0125 others(1): Show |
4 | HG02451.hp1 HG02647.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.795-1561G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205174 | |||||||
chr16:16205291 | T | C | 6 | a0001c0001t0001g0200 a0001c0001t0001g0268 a0001c0001t0001g0269 others(3): Show |
6 | HG02074.hp2 NA18612.hp2 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.795-1678A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205291 | |||||||
chr16:16205376 | A | T | 1 | a0038c0079t0001g0238 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.795-1763T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205376 | |||||||
chr16:16205444 | G | GA | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.795-1832dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205444 | |||||||
chr16:16205474 | AC | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.795-1862delG | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205474 | |||||||
chr16:16205747 | A | G | 1 | a0001c0006t0001g0299 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.795-2134T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205747 | |||||||
chr16:16205751 | G | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.795-2138C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205751 | |||||||
chr16:16205898 | T | C | 27 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(24): Show |
27 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.795-2285A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205898 | |||||||
chr16:16205905 | A | G | 27 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(24): Show |
27 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.795-2292T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205905 | |||||||
chr16:16206092 | C | T | 1 | a0044c0044t0001g0302 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.795-2479G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16206092 | |||||||
chr16:16206347 | G | A | 1 | a0013c0030t0001g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.794+2381C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16206347 | |||||||
chr16:16206395 | C | T | 16 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(13): Show |
16 | HG00733.hp2 HG01074.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.794+2333G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16206395 | |||||||
chr16:16206466 | C | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.794+2262G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16206466 | |||||||
chr16:16206499 | T | C | 1 | a0001c0055t0012g0164 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.794+2229A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16206499 | |||||||
chr16:16206500 | G | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.794+2228C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16206500 | |||||||
chr16:16206503 | C | T | 1 | a0001c0001t0002g0242 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.794+2225G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16206503 | |||||||
chr16:16206609 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.794+2119C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16206609 | |||||||
chr16:16206625 | G | A | 1 | a0036c0059t0001g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.794+2103C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16206625 | |||||||
chr16:16206884 | C | G | 27 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(24): Show |
27 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.794+1844G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16206884 | |||||||
chr16:16207101 | C | T | 1 | a0001c0043t0001g0236 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.794+1627G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16207101 | |||||||
chr16:16207233 | T | G | 3 | a0001c0002t0001g0025 a0001c0002t0001g0026 a0010c0015t0001g0327 |
3 | HG02809.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.794+1495A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16207233 | |||||||
chr16:16207375 | T | C | 11 | a0001c0001t0001g0064 a0001c0004t0001g0065 a0005c0048t0001g0063 others(8): Show |
11 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.794+1353A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16207375 | |||||||
chr16:16207411 | G | A | 1 | a0023c0053t0001g0154 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.794+1317C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16207411 | |||||||
chr16:16207618 | C | T | 1 | a0004c0010t0001g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.794+1110G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16207618 | |||||||
chr16:16207673 | A | G | 27 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(24): Show |
27 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.794+1055T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16207673 | |||||||
chr16:16207901 | T | C | 7 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(4): Show |
7 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.794+827A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16207901 | |||||||
chr16:16208056 | T | C | 1 | a0002c0074t0001g0186 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.794+672A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208056 | |||||||
chr16:16208183 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.794+545G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208183 | |||||||
chr16:16208192 | C | T | 1 | a0001c0006t0001g0296 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.794+536G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208192 | |||||||
chr16:16208229 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.794+499T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208229 | |||||||
chr16:16208296 | C | A | 11 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(8): Show |
11 | HG01074.hp2 HG01099.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.794+432G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208296 | |||||||
chr16:16208297 | G | A | 3 | a0001c0001t0001g0326 a0001c0001t0001g0338 a0001c0001t0001g0339 |
3 | HG02559.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.794+431C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208297 | |||||||
chr16:16208342 | TTTTTTG | T | 10 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(7): Show |
10 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.794+380_794+385del others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208342 | |||||||
chr16:16208379 | G | GT | 8 | a0001c0001t0001g0166 a0001c0001t0001g0247 a0001c0001t0001g0346 others(5): Show |
8 | HG01256.hp1 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.794+348dupA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208379 | |||||||
chr16:16208379 | GT | G | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.794+348delA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208379 | |||||||
chr16:16208408 | T | C | 2 | a0001c0001t0001g0325 a0001c0064t0005g0324 |
2 | NA18977.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.794+320A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208408 | |||||||
chr16:16208447 | A | G | 1 | a0013c0030t0001g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.794+281T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208447 | |||||||
chr16:16208546 | C | G | 11 | a0001c0001t0001g0064 a0001c0004t0001g0065 a0005c0048t0001g0063 others(8): Show |
11 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.794+182G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208546 | |||||||
chr16:16208547 | T | C | 11 | a0001c0001t0001g0064 a0001c0004t0001g0065 a0005c0048t0001g0063 others(8): Show |
11 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.794+181A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208547 | |||||||
chr16:16208574 | A | G | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.794+154T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208574 | |||||||
chr16:16208615 | G | A | 1 | a0003c0005t0001g0197 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.794+113C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208615 | |||||||
chr16:16208618 | T | A | 1 | a0001c0043t0001g0236 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.794+110A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208618 | |||||||
chr16:16208652 | G | A | 4 | a0002c0024t0001g0155 a0015c0019t0001g0122 a0015c0019t0001g0125 others(1): Show |
4 | HG02451.hp1 HG02647.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.794+76C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208652 | |||||||
chr16:16208862 | G | A | 2 | a0002c0003t0001g0187 a0002c0003t0001g0188 |
2 | HG01884.hp2 NA18522.hp2 |
splice_region_variant&intron_variant | LOW | c.663-3C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16208862 | |||||||
chr16:16208960 | T | C | 1 | a0002c0003t0001g0123 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.663-101A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16208960 | |||||||
chr16:16208965 | G | C | 1 | a0002c0003t0001g0123 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.663-106C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16208965 | |||||||
chr16:16209097 | T | C | 1 | a0001c0001t0004g0156 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.663-238A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209097 | |||||||
chr16:16209544 | G | A | 10 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(7): Show |
10 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.663-685C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209544 | |||||||
chr16:16209557 | A | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.663-698T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209557 | |||||||
chr16:16209591 | CT | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.663-733delA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209591 | |||||||
chr16:16209602 | T | A | 1 | a0003c0007t0001g0109 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.663-743A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209602 | |||||||
chr16:16209621 | T | G | 15 | a0001c0001t0001g0064 a0001c0004t0001g0065 a0005c0048t0001g0063 others(12): Show |
15 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.663-762A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209621 | |||||||
chr16:16209644 | C | A | 7 | a0001c0006t0001g0278 a0001c0006t0001g0296 a0001c0006t0001g0297 others(4): Show |
7 | HG00544.hp1 HG02074.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.663-785G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209644 | |||||||
chr16:16209664 | T | C | 1 | a0001c0002t0002g0004 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.663-805A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209664 | |||||||
chr16:16209706 | C | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.663-847G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209706 | |||||||
chr16:16209706 | C | T | 1 | a0001c0002t0002g0004 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.663-847G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209706 | |||||||
chr16:16209713 | C | T | 1 | a0001c0002t0002g0004 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.663-854G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209713 | |||||||
chr16:16209799 | C | T | 3 | a0026c0039t0001g0032 a0032c0038t0001g0033 a0040c0040t0001g0031 |
3 | HG02280.hp2 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.663-940G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209799 | |||||||
chr16:16209804 | C | T | 1 | a0001c0006t0001g0286 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.663-945G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209804 | |||||||
chr16:16209820 | T | A | 1 | a0001c0002t0001g0157 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.663-961A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209820 | |||||||
chr16:16209927 | C | T | 1 | a0013c0030t0001g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.663-1068G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209927 | |||||||
chr16:16210119 | C | G | 1 | a0003c0007t0001g0098 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.663-1260G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210119 | |||||||
chr16:16210267 | A | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.663-1408T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210267 | |||||||
chr16:16210340 | TTGGTCAG others(2): Show |
T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.663-1490_663-1482d others(11): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210340 | |||||||
chr16:16210467 | C | T | 3 | a0026c0039t0001g0032 a0032c0038t0001g0033 a0040c0040t0001g0031 |
3 | HG02280.hp2 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.663-1608G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210467 | |||||||
chr16:16210528 | A | G | 1 | a0003c0005t0001g0307 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.662+1657T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210528 | |||||||
chr16:16210534 | G | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.662+1651C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210534 | |||||||
chr16:16210557 | A | G | 1 | a0030c0046t0001g0304 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.662+1628T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210557 | |||||||
chr16:16210736 | C | A | 12 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(9): Show |
12 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.662+1449G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210736 | |||||||
chr16:16210753 | T | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.662+1432A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210753 | |||||||
chr16:16210864 | G | T | 1 | a0002c0003t0001g0333 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.662+1321C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210864 | |||||||
chr16:16210904 | G | T | 1 | a0013c0030t0001g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.662+1281C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210904 | |||||||
chr16:16210909 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.662+1276G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210909 | |||||||
chr16:16210910 | G | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.662+1275C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210910 | |||||||
chr16:16210984 | G | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.662+1201C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210984 | |||||||
chr16:16211085 | A | T | 1 | a0013c0030t0001g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.662+1100T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211085 | |||||||
chr16:16211095 | C | CA | 73 | a0001c0001t0001g0069 a0001c0001t0001g0160 a0001c0001t0001g0161 others(70): Show |
73 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.662+1089dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211095 | |||||||
chr16:16211095 | CAA | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.662+1088_662+1089d others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211095 | |||||||
chr16:16211164 | A | G | 1 | a0001c0004t0001g0006 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.662+1021T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211164 | |||||||
chr16:16211200 | C | G | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.662+985G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211200 | |||||||
chr16:16211241 | A | C | 1 | a0001c0006t0009g0285 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.662+944T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211241 | |||||||
chr16:16211354 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.662+831A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211354 | |||||||
chr16:16211388 | C | T | 1 | a0005c0031t0001g0133 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.662+797G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211388 | |||||||
chr16:16211473 | C | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.662+712G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211473 | |||||||
chr16:16211498 | A | G | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.662+687T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211498 | |||||||
chr16:16211782 | A | G | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.662+403T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211782 | |||||||
chr16:16211880 | A | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.662+305T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211880 | |||||||
chr16:16211887 | G | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.662+298C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211887 | |||||||
chr16:16211939 | G | A | 1 | a0006c0008t0001g0053 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.662+246C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211939 | |||||||
chr16:16211975 | G | A | 4 | a0001c0001t0001g0326 a0001c0001t0001g0338 a0001c0001t0001g0339 others(1): Show |
4 | HG02559.hp2 HG03130.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.662+210C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211975 | |||||||
chr16:16212067 | G | A | 1 | a0001c0006t0001g0190 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.662+118C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16212067 | |||||||
chr16:16212071 | A | G | 156 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(153): Show |
157 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.662+114T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16212071 | |||||||
chr16:16212150 | G | T | 1 | a0002c0014t0001g0284 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.662+35C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16212150 | |||||||
chr16:16212173 | G | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(3): Show |
6 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.662+12C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16212173 | |||||||
chr16:16212288 | G | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-42C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16212288 | |||||||
chr16:16212328 | A | G | 3 | a0001c0002t0001g0025 a0001c0002t0001g0026 a0010c0015t0001g0327 |
3 | HG02809.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.601-82T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16212328 | |||||||
chr16:16212335 | G | T | 57 | a0001c0001t0001g0079 a0001c0001t0001g0083 a0001c0001t0001g0086 others(54): Show |
58 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.601-89C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16212335 | |||||||
chr16:16212340 | G | A | 1 | a0014c0018t0001g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.601-94C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16212340 | |||||||
chr16:16212366 | C | T | 1 | a0014c0018t0001g0249 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.601-120G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16212366 | |||||||
chr16:16212457 | C | T | 6 | a0001c0001t0001g0200 a0001c0001t0001g0268 a0001c0001t0001g0269 others(3): Show |
6 | HG02074.hp2 NA18612.hp2 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-211G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16212457 | |||||||
chr16:16212518 | C | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-272G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16212518 | |||||||
chr16:16212590 | A | G | 15 | a0001c0001t0001g0064 a0001c0004t0001g0065 a0005c0048t0001g0063 others(12): Show |
15 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.601-344T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16212590 | |||||||
chr16:16212615 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.601-369C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16212615 | |||||||
chr16:16212706 | G | A | 3 | a0003c0005t0001g0028 a0003c0005t0001g0029 a0005c0012t0001g0027 |
3 | HG01515.hp1 HG01517.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.601-460C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16212706 | |||||||
chr16:16212754 | A | C | 5 | a0001c0001t0001g0326 a0001c0001t0001g0338 a0001c0001t0001g0339 others(2): Show |
5 | HG02559.hp2 HG03098.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-508T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16212754 | |||||||
chr16:16212899 | G | A | 1 | a0001c0002t0001g0354 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.601-653C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16212899 | |||||||
chr16:16213082 | A | AT | 9 | a0001c0001t0001g0247 a0001c0002t0001g0132 a0002c0003t0001g0013 others(6): Show |
9 | HG00639.hp1 HG01109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-837dupA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213082 | |||||||
chr16:16213082 | A | ATT | 55 | a0001c0001t0001g0079 a0001c0001t0001g0083 a0001c0001t0001g0086 others(52): Show |
56 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.601-838_601-837dup others(2): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213082 | |||||||
chr16:16213082 | AT | A | 14 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(11): Show |
14 | HG01074.hp2 HG01257.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.601-837delA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213082 | |||||||
chr16:16213096 | T | C | 1 | a0002c0022t0001g0345 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.601-850A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213096 | |||||||
chr16:16213141 | A | G | 1 | a0006c0008t0001g0053 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.601-895T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213141 | |||||||
chr16:16213188 | A | C | 1 | a0001c0002t0001g0093 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.601-942T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213188 | |||||||
chr16:16213201 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.601-955A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213201 | |||||||
chr16:16213476 | C | G | 1 | a0001c0004t0001g0034 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.600+848G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213476 | |||||||
chr16:16213558 | CT | C | 327 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(324): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.600+765delA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213558 | |||||||
chr16:16213558 | CTT | C | 9 | a0001c0001t0001g0191 a0001c0006t0001g0300 a0003c0005t0001g0282 others(6): Show |
9 | HG02040.hp1 HG02559.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.600+764_600+765del others(2): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213558 | |||||||
chr16:16213589 | C | A | 1 | a0027c0073t0001g0016 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.600+735G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213589 | |||||||
chr16:16213603 | C | G | 1 | a0001c0001t0001g0079 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.600+721G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213603 | |||||||
chr16:16213607 | C | A | 2 | a0013c0025t0001g0007 a0013c0025t0001g0008 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.600+717G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213607 | |||||||
chr16:16213686 | G | A | 1 | a0044c0044t0001g0302 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.600+638C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213686 | |||||||
chr16:16213933 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.600+391G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213933 | |||||||
chr16:16214103 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.600+221C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16214103 | |||||||
chr16:16214143 | G | A | 1 | a0001c0001t0001g0348 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.600+181C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16214143 | |||||||
chr16:16214210 | G | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.600+114C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16214210 | |||||||
chr16:16214259 | G | C | 1 | a0027c0073t0001g0016 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.600+65C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16214259 | |||||||
chr16:16214488 | A | T | 1 | a0002c0068t0001g0097 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.475-39T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16214488 | |||||||
chr16:16214494 | G | A | 56 | a0001c0001t0001g0281 a0001c0001t0001g0303 a0001c0001t0001g0308 others(53): Show |
56 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.475-45C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16214494 | |||||||
chr16:16214778 | T | A | 11 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(8): Show |
11 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.475-329A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16214778 | |||||||
chr16:16214818 | C | T | 51 | a0001c0001t0001g0079 a0001c0001t0001g0083 a0001c0001t0001g0086 others(48): Show |
52 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.475-369G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16214818 | |||||||
chr16:16214950 | A | G | 2 | a0001c0002t0001g0117 a0007c0009t0001g0116 |
2 | NA18951.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.475-501T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16214950 | |||||||
chr16:16215098 | C | T | 1 | a0002c0003t0001g0333 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.475-649G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215098 | |||||||
chr16:16215438 | G | GGT | 36 | a0001c0001t0001g0003 a0001c0001t0002g0092 a0001c0001t0002g0094 others(33): Show |
37 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.475-991_475-990dup others(2): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215438 | |||||||
chr16:16215438 | G | GGTGT | 8 | a0001c0001t0002g0204 a0001c0002t0001g0014 a0003c0005t0005g0213 others(5): Show |
8 | HG00733.hp1 HG02559.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.475-993_475-990dup others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215438 | |||||||
chr16:16215438 | GGT | G | 152 | a0001c0001t0001g0017 a0001c0001t0001g0039 a0001c0001t0001g0064 others(149): Show |
152 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.475-991_475-990del others(2): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215438 | |||||||
chr16:16215438 | GGTGT | G | 32 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0192 others(29): Show |
32 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.475-993_475-990del others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215438 | |||||||
chr16:16215438 | GGTGTGT | G | 6 | a0001c0004t0001g0263 a0001c0049t0001g0352 a0001c0067t0001g0351 others(3): Show |
6 | HG01123.hp2 HG01175.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.475-995_475-990del others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215438 | |||||||
chr16:16215438 | GGTGTGTG others(3): Show |
G | 1 | a0002c0014t0001g0331 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.475-999_475-990del others(10): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215438 | |||||||
chr16:16215444 | T | G | 2 | a0001c0006t0001g0299 a0001c0006t0001g0300 |
2 | NA18941.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.475-995A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215444 | |||||||
chr16:16215478 | CT | C | 26 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(23): Show |
26 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.475-1030delA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215478 | |||||||
chr16:16215549 | C | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.475-1100G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215549 | |||||||
chr16:16215590 | T | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.475-1141A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215590 | |||||||
chr16:16215910 | T | C | 1 | a0002c0003t0001g0013 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.475-1461A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215910 | |||||||
chr16:16215950 | C | T | 4 | a0012c0020t0001g0055 a0012c0020t0001g0056 a0012c0020t0001g0057 others(1): Show |
4 | HG02559.hp1 HG02897.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-1501G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215950 | |||||||
chr16:16216069 | G | A | 1 | a0001c0004t0001g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.475-1620C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16216069 | |||||||
chr16:16216076 | C | T | 2 | a0001c0002t0001g0114 a0001c0002t0001g0115 |
2 | NA18963.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.475-1627G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16216076 | |||||||
chr16:16216260 | T | C | 1 | a0001c0001t0001g0341 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.475-1811A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16216260 | |||||||
chr16:16216270 | C | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.475-1821G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16216270 | |||||||
chr16:16216339 | C | T | 1 | a0002c0022t0001g0095 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.475-1890G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16216339 | |||||||
chr16:16216437 | G | T | 71 | a0001c0001t0001g0273 a0001c0001t0001g0281 a0001c0001t0001g0303 others(68): Show |
71 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.475-1988C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16216437 | |||||||
chr16:16216504 | A | G | 4 | a0012c0020t0001g0055 a0012c0020t0001g0056 a0012c0020t0001g0057 others(1): Show |
4 | HG02559.hp1 HG02897.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-2055T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16216504 | |||||||
chr16:16216638 | C | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.475-2189G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16216638 | |||||||
chr16:16216810 | A | C | 2 | a0002c0003t0001g0013 a0013c0030t0001g0113 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.475-2361T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16216810 | |||||||
chr16:16217045 | A | G | 3 | a0001c0002t0001g0112 a0004c0010t0001g0042 a0004c0010t0001g0043 |
3 | HG01516.hp1 HG01517.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.474+2509T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217045 | |||||||
chr16:16217144 | T | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+2410A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217144 | |||||||
chr16:16217188 | G | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+2366C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217188 | |||||||
chr16:16217409 | C | T | 2 | a0013c0025t0001g0007 a0013c0025t0001g0008 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.474+2145G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217409 | |||||||
chr16:16217438 | A | G | 1 | a0001c0052t0001g0283 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.474+2116T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217438 | |||||||
chr16:16217438 | A | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+2116T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217438 | |||||||
chr16:16217459 | C | T | 41 | a0001c0001t0001g0039 a0001c0001t0001g0107 a0001c0001t0002g0242 others(38): Show |
41 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.474+2095G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217459 | |||||||
chr16:16217489 | C | G | 3 | a0026c0039t0001g0032 a0032c0038t0001g0033 a0040c0040t0001g0031 |
3 | HG02280.hp2 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.474+2065G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217489 | |||||||
chr16:16217566 | G | A | 3 | a0001c0001t0001g0326 a0001c0001t0001g0338 a0001c0001t0001g0339 |
3 | HG02559.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.474+1988C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217566 | |||||||
chr16:16217609 | G | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+1945C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217609 | |||||||
chr16:16217721 | T | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+1833A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217721 | |||||||
chr16:16217807 | C | T | 1 | a0026c0039t0001g0032 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.474+1747G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217807 | |||||||
chr16:16217854 | C | T | 3 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0005g0206 |
3 | HG00741.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.474+1700G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217854 | |||||||
chr16:16217946 | T | C | 4 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0002g0092 others(1): Show |
4 | HG00741.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.474+1608A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217946 | |||||||
chr16:16218014 | C | CG | 3 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0005g0206 |
3 | HG00741.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.474+1539dupC | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218014 | |||||||
chr16:16218065 | G | T | 1 | a0001c0002t0001g0332 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.474+1489C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218065 | |||||||
chr16:16218274 | G | C | 10 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(7): Show |
10 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.474+1280C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218274 | |||||||
chr16:16218367 | G | A | 4 | a0001c0001t0002g0094 a0001c0001t0002g0204 a0001c0002t0001g0093 others(1): Show |
4 | NA18987.hp1 NA18990.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.474+1187C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218367 | |||||||
chr16:16218383 | A | C | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.474+1171T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218383 | |||||||
chr16:16218422 | C | T | 123 | a0001c0001t0001g0064 a0001c0001t0001g0079 a0001c0001t0001g0083 others(120): Show |
123 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.474+1132G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218422 | |||||||
chr16:16218491 | G | A | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.474+1063C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218491 | |||||||
chr16:16218613 | C | T | 1 | a0001c0001t0004g0071 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.474+941G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218613 | |||||||
chr16:16218650 | T | C | 6 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0239 others(3): Show |
6 | HG01123.hp1 HG01358.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.474+904A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218650 | |||||||
chr16:16218668 | T | C | 1 | a0001c0001t0001g0268 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.474+886A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218668 | |||||||
chr16:16218729 | C | G | 26 | a0001c0002t0001g0287 a0001c0006t0001g0276 a0001c0006t0001g0277 others(23): Show |
26 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.474+825G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218729 | |||||||
chr16:16218730 | G | A | 1 | a0003c0005t0001g0197 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.474+824C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218730 | |||||||
chr16:16218767 | G | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+787C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218767 | |||||||
chr16:16218824 | C | G | 1 | a0001c0033t0001g0070 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.474+730G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218824 | |||||||
chr16:16218838 | G | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+716C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218838 | |||||||
chr16:16218861 | TTTTAGTA others(28): Show |
T | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.474+658_474+692del others(35): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218861 | |||||||
chr16:16218872 | ATTTAGTA others(6): Show |
A | 1 | a0001c0002t0001g0124 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.474+669_474+681del others(13): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218872 | |||||||
chr16:16219059 | C | CA | 83 | a0001c0001t0001g0003 a0001c0001t0001g0200 a0001c0001t0001g0201 others(80): Show |
83 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.474+494dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219059 | |||||||
chr16:16219059 | CA | C | 30 | a0001c0001t0001g0064 a0001c0001t0001g0069 a0001c0001t0001g0268 others(27): Show |
30 | HG01256.hp2 HG01257.hp2 HG01975.hp1 others(27): Show |
intron_variant | MODIFIER | c.474+494delT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219059 | |||||||
chr16:16219059 | CAAAAAAA others(7): Show |
C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+481_474+494del others(14): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219059 | |||||||
chr16:16219059 | CAAAAAAA others(8): Show |
C | 1 | a0027c0073t0001g0016 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.474+480_474+494del others(15): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219059 | |||||||
chr16:16219066 | A | C | 1 | a0011c0016t0001g0275 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.474+488T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219066 | |||||||
chr16:16219107 | G | A | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.474+447C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219107 | |||||||
chr16:16219179 | C | A | 2 | a0011c0016t0006g0271 a0035c0060t0010g0240 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.474+375G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219179 | |||||||
chr16:16219253 | G | A | 6 | a0001c0001t0002g0242 a0001c0006t0002g0246 a0002c0013t0001g0241 others(3): Show |
6 | HG00099.hp1 HG00735.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.474+301C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219253 | |||||||
chr16:16219314 | T | A | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.474+240A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219314 | |||||||
chr16:16219339 | C | G | 2 | a0001c0002t0001g0054 a0039c0037t0001g0355 |
2 | NA18999.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.474+215G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219339 | |||||||
chr16:16219360 | T | G | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.474+194A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219360 | |||||||
chr16:16219454 | A | G | 1 | a0006c0008t0001g0053 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.474+100T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219454 | |||||||
chr16:16219495 | G | A | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | NA18947.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.474+59C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219495 | |||||||
chr16:16219511 | G | A | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.474+43C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219511 | |||||||
chr16:16219541 | C | T | 2 | a0016c0032t0001g0051 a0021c0066t0001g0052 |
2 | HG00099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.474+13G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219541 | |||||||
chr16:16219688 | C | T | 9 | a0004c0010t0001g0042 a0004c0010t0001g0043 a0004c0010t0001g0045 others(6): Show |
9 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.346-6G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 3/30 | chr16 | 16219688 | |||||||
chr16:16219796 | G | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.345+26C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 3/30 | chr16 | 16219796 | |||||||
chr16:16219810 | A | G | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.345+12T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 3/30 | chr16 | 16219810 | |||||||
chr16:16220010 | C | T | 4 | a0001c0001t0001g0273 a0013c0030t0001g0274 a0034c0056t0001g0041 others(1): Show |
4 | HG02109.hp2 HG02647.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-63G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220010 | |||||||
chr16:16220084 | C | A | 4 | a0002c0013t0001g0253 a0002c0057t0001g0255 a0004c0017t0001g0254 others(1): Show |
4 | HG01106.hp2 HG01975.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-137G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220084 | |||||||
chr16:16220087 | C | T | 9 | a0001c0001t0001g0039 a0001c0004t0001g0034 a0001c0004t0001g0037 others(6): Show |
9 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.220-140G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220087 | |||||||
chr16:16220183 | G | A | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.220-236C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220183 | |||||||
chr16:16220234 | G | C | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.220-287C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220234 | |||||||
chr16:16220234 | G | T | 343 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(340): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.220-287C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220234 | |||||||
chr16:16220238 | G | A | 1 | a0002c0013t0001g0266 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.220-291C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220238 | |||||||
chr16:16220314 | C | T | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.220-367G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220314 | |||||||
chr16:16220330 | G | A | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.220-383C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220330 | |||||||
chr16:16220433 | C | G | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.220-486G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220433 | |||||||
chr16:16220460 | G | A | 1 | a0002c0003t0001g0267 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.220-513C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220460 | |||||||
chr16:16220467 | G | T | 3 | a0026c0039t0001g0032 a0032c0038t0001g0033 a0040c0040t0001g0031 |
3 | HG02280.hp2 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.220-520C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220467 | |||||||
chr16:16220550 | A | G | 1 | a0002c0003t0001g0013 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.220-603T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220550 | |||||||
chr16:16220608 | G | A | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.220-661C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220608 | |||||||
chr16:16220608 | G | C | 3 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 |
3 | HG02074.hp2 NA18612.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.220-661C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220608 | |||||||
chr16:16220631 | T | C | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.220-684A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220631 | |||||||
chr16:16220660 | C | T | 2 | a0001c0002t0001g0014 a0029c0069t0001g0015 |
2 | HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.220-713G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220660 | |||||||
chr16:16220711 | C | T | 1 | a0001c0026t0001g0272 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.220-764G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220711 | |||||||
chr16:16220737 | A | G | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.220-790T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220737 | |||||||
chr16:16220897 | C | CA | 11 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(8): Show |
11 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.219+751dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220897 | |||||||
chr16:16220903 | A | C | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.219+746T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220903 | |||||||
chr16:16220908 | A | C | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.219+741T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220908 | |||||||
chr16:16220992 | C | T | 1 | a0001c0001t0002g0030 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.219+657G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220992 | |||||||
chr16:16221037 | C | T | 3 | a0003c0005t0001g0028 a0003c0005t0001g0029 a0005c0012t0001g0027 |
3 | HG01515.hp1 HG01517.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.219+612G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221037 | |||||||
chr16:16221038 | G | A | 1 | a0001c0026t0001g0272 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.219+611C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221038 | |||||||
chr16:16221087 | G | A | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.219+562C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221087 | |||||||
chr16:16221324 | T | C | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.219+325A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221324 | |||||||
chr16:16221327 | A | G | 2 | a0001c0002t0001g0025 a0001c0002t0001g0026 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.219+322T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221327 | |||||||
chr16:16221353 | T | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.219+296A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221353 | |||||||
chr16:16221475 | C | A | 70 | a0001c0001t0001g0273 a0001c0001t0001g0281 a0001c0001t0001g0303 others(67): Show |
70 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.219+174G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221475 | |||||||
chr16:16221489 | G | A | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.219+160C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221489 | |||||||
chr16:16221503 | C | G | 2 | a0001c0002t0001g0023 a0001c0002t0001g0024 |
2 | HG00544.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.219+146G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221503 | |||||||
chr16:16221550 | C | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.219+99G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221550 | |||||||
chr16:16221571 | A | G | 1 | a0002c0003t0001g0013 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.219+78T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221571 | |||||||
chr16:16221600 | G | C | 1 | a0004c0010t0001g0342 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.219+49C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221600 | |||||||
chr16:16221609 | G | C | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.219+40C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221609 | |||||||
chr16:16221611 | A | C | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.219+38T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221611 | |||||||
chr16:16221895 | A | G | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.37-64T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16221895 | |||||||
chr16:16221924 | A | G | 1 | a0001c0002t0001g0010 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.37-93T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16221924 | |||||||
chr16:16221942 | A | G | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.37-111T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16221942 | |||||||
chr16:16221948 | T | C | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.37-117A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16221948 | |||||||
chr16:16222072 | C | G | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.37-241G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222072 | |||||||
chr16:16222117 | A | T | 1 | a0036c0059t0001g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.37-286T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222117 | |||||||
chr16:16222236 | C | T | 2 | a0013c0025t0001g0007 a0013c0025t0001g0008 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.37-405G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222236 | |||||||
chr16:16222251 | G | A | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.37-420C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222251 | |||||||
chr16:16222254 | G | A | 1 | a0002c0022t0001g0345 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.37-423C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222254 | |||||||
chr16:16222260 | C | A | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.37-429G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222260 | |||||||
chr16:16222364 | G | A | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.37-533C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222364 | |||||||
chr16:16222370 | AT | A | 6 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0001g0348 others(3): Show |
6 | HG01109.hp2 HG01123.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.37-540delA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222370 | |||||||
chr16:16222450 | C | T | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.37-619G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222450 | |||||||
chr16:16222495 | G | A | 1 | a0001c0049t0001g0352 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.37-664C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222495 | |||||||
chr16:16222513 | G | A | 1 | a0002c0051t0001g0353 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.37-682C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222513 | |||||||
chr16:16222529 | A | C | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.37-698T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222529 | |||||||
chr16:16222610 | T | C | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.37-779A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222610 | |||||||
chr16:16222809 | C | T | 2 | a0001c0004t0001g0006 a0039c0037t0001g0355 |
2 | HG02717.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.36+590G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222809 | |||||||
chr16:16222855 | T | C | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.36+544A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222855 | |||||||
chr16:16222866 | A | T | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.36+533T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222866 | |||||||
chr16:16222904 | T | G | 2 | a0001c0002t0001g0354 a0039c0037t0001g0355 |
2 | HG00597.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.36+495A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222904 | |||||||
chr16:16223163 | A | G | 3 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0039c0037t0001g0355 |
3 | HG02602.hp1 HG04204.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.36+236T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16223163 | |||||||
chr16:16223173 | C | T | 1 | a0039c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.36+226G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16223173 | |||||||
chr16:16223224 | T | G | 2 | a0001c0072t0001g0356 a0039c0037t0001g0355 |
2 | HG03579.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.36+175A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16223224 | |||||||
chr16:16223283 | C | T | 2 | a0001c0001t0001g0003 a0002c0003t0001g0002 |
2 | HG00423.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.36+116G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16223283 |