Item | Value |
---|---|
geneid | 1244 |
ensemblid | ENSG00000023839.12 |
hgncid | 53 |
symbol | ABCC2 |
name | ATP binding cassette subfamily C member 2 |
refseq_nuc | NM_000392.5 |
refseq_prot | NP_000383.2 |
ensembl_nuc | ENST00000647814.1 |
ensembl_prot | ENSP00000497274.1 |
mane_status | MANE Select |
chr | chr10 |
start | 99782640 |
end | 99852594 |
strand | + |
ver | v1.2 |
region | chr10:99782640-99852594 |
region5000 | chr10:99777640-99857594 |
regionname0 | ABCC2_chr10_99782640_99852594 |
regionname5000 | ABCC2_chr10_99777640_99857594 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1545 | 246 | 41 | 43 | 128 | 5 | 28 | 100 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0002 | 0/0 | 1545 | 39 | 11 | 9 | 10 | 2 | 7 | 8 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0003 | 0/0 | 1545 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0004 | 0/0 | 1545 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0005 | 0/0 | 1545 | 4 | 1 | 2 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0006 | 1/0 | 1545 | 3 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0007 | 0/0 | 1545 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0008 | 0/0 | 1545 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0009 | 0/0 | 1545 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0010 | 0/0 | 1545 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0011 | 0/0 | 1545 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0012 | 0/0 | 1545 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0013 | 0/0 | 1545 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0014 | 0/0 | 1545 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0015 | 0/0 | 1545 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0016 | 0/0 | 1545 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0017 | 0/0 | 1545 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0018 | 0/0 | 1545 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0019 | 0/0 | 99 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(94): Show |
chr10 | 99777640 | 99857594 |
a0020 | 0/0 | 1545 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0021 | 0/0 | 1545 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0022 | 0/0 | 1545 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0023 | 0/0 | 1545 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0024 | 0/0 | 1545 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0025 | 0/0 | 1545 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0026 | 0/0 | 1545 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0027 | 0/0 | 1545 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
a0028 | 0/0 | 1545 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | MLEKF others(1540): Show |
chr10 | 99777640 | 99857594 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4635 | 137 | 18 | 19 | 78 | 1 | 21 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0001c0002 | 0/1 | 4635 | 88 | 13 | 22 | 43 | 3 | 6 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0001c0005 | 0/0 | 4635 | 6 | 1 | 0 | 5 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0001c0007 | 0/0 | 4635 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0001c0014 | 0/0 | 4635 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0001c0017 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0001c0027 | 0/0 | 4635 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0001c0030 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0001c0035 | 0/0 | 4635 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0001c0036 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0001c0038 | 0/0 | 4635 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0001c0042 | 0/0 | 4635 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0002c0003 | 0/0 | 4635 | 38 | 11 | 9 | 10 | 2 | 6 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0002c0021 | 0/0 | 4635 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0003c0004 | 0/0 | 4635 | 9 | 8 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0004c0006 | 0/0 | 4635 | 6 | 5 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0004c0029 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0005c0008 | 0/0 | 4635 | 4 | 1 | 2 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0006c0010 | 0/0 | 4635 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0006c0016 | 1/0 | 4635 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0007c0009 | 0/0 | 4635 | 3 | 2 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0008c0013 | 0/0 | 4635 | 2 | 0 | 1 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0009c0011 | 0/0 | 4635 | 2 | 0 | 0 | 0 | 2 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0010c0015 | 0/0 | 4635 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0011c0012 | 0/0 | 4635 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0012c0022 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0013c0034 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0014c0023 | 0/0 | 4635 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0015c0019 | 0/0 | 4635 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0016c0026 | 0/0 | 4635 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0017c0031 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0018c0040 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0019c0041 | 0/0 | 4635 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0020c0024 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0021c0032 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0022c0020 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0023c0018 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0024c0033 | 0/0 | 4635 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0025c0037 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0026c0025 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0027c0028 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 | ||
a0028c0039 | 0/0 | 4635 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | ATGCT others(4630): Show |
chr10 | 99777640 | 99857594 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5806 | 130 | 13 | 18 | 77 | 1 | 21 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0001c0001t0004 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0001c0001t0005 | 0/0 | 5806 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0001c0001t0008 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0001c0001t0010 | 0/0 | 5806 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0001c0002t0002 | 0/0 | 5806 | 51 | 3 | 8 | 35 | 2 | 3 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0001c0002t0003 | 0/1 | 5806 | 32 | 8 | 12 | 8 | 1 | 2 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0001c0002t0006 | 0/0 | 5806 | 2 | 0 | 2 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0001c0002t0007 | 0/0 | 5806 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0001c0002t0011 | 0/0 | 5806 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0001c0005t0001 | 0/0 | 5806 | 6 | 1 | 0 | 5 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0001c0007t0003 | 0/0 | 5806 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0001c0014t0001 | 0/0 | 5806 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0001c0017t0001 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0001c0027t0001 | 0/0 | 5806 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0001c0030t0001 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0001c0035t0002 | 0/0 | 5806 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0001c0036t0001 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0001c0038t0001 | 0/0 | 5806 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0001c0042t0002 | 0/0 | 5806 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0002c0003t0001 | 0/0 | 5806 | 34 | 8 | 9 | 9 | 2 | 6 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0002c0003t0004 | 0/0 | 5806 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0002c0003t0009 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0002c0021t0003 | 0/0 | 5806 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0003c0004t0001 | 0/0 | 5806 | 9 | 8 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0004c0006t0001 | 0/0 | 5806 | 6 | 5 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0004c0029t0001 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0005c0008t0001 | 0/0 | 5806 | 4 | 1 | 2 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0006c0010t0001 | 0/0 | 5806 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0006c0016t0001 | 1/0 | 5806 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0007c0009t0001 | 0/0 | 5806 | 3 | 2 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0008c0013t0001 | 0/0 | 5806 | 2 | 0 | 1 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0009c0011t0001 | 0/0 | 5806 | 2 | 0 | 0 | 0 | 2 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0010c0015t0001 | 0/0 | 5806 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0011c0012t0001 | 0/0 | 5806 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0012c0022t0001 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0013c0034t0002 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0014c0023t0001 | 0/0 | 5806 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0015c0019t0001 | 0/0 | 5806 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0016c0026t0006 | 0/0 | 5806 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0017c0031t0001 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0018c0040t0002 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0019c0041t0002 | 0/0 | 5806 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0020c0024t0001 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0021c0032t0001 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0022c0020t0001 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0023c0018t0001 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0024c0033t0003 | 0/0 | 5806 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0025c0037t0001 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0026c0025t0001 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0027c0028t0001 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
a0028c0039t0001 | 0/0 | 5806 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | AGTCA others(5801): Show |
chr10 | 99777640 | 99857594 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0005g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0008g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0001t0010g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0095 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0006g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0006g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0007g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0002t0011g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0005t0001g0003 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0005t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0005t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0005t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0005t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0007t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0007t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0007t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0007t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0007t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0007t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0014t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0014t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0017t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0027t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0030t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0035t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0036t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0038t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0001c0042t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0003t0009g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0002c0021t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0003c0004t0001g0001 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0003c0004t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0003c0004t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0003c0004t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0003c0004t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0003c0004t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0003c0004t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0004c0006t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0004c0006t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0004c0006t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0004c0006t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0004c0006t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0004c0006t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0004c0029t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0005c0008t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0005c0008t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0005c0008t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0005c0008t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0006c0010t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0006c0010t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0006c0016t0001g0012 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0007c0009t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0007c0009t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0007c0009t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0008c0013t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0008c0013t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0009c0011t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0009c0011t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0010c0015t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0010c0015t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0011c0012t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0011c0012t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0012c0022t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0013c0034t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0014c0023t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0015c0019t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0016c0026t0006g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0017c0031t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0018c0040t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0019c0041t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0020c0024t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0021c0032t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0022c0020t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0023c0018t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0024c0033t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0025c0037t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0026c0025t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0027c0028t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
a0028c0039t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0003 | t0001 | g0311 | EUR | GBR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00099 | hp2 | a0001 | c0035 | t0002 | g0046 | EUR | GBR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00140 | hp1 | a0001 | c0002 | t0002 | g0089 | EUR | GBR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00140 | hp2 | a0005 | c0008 | t0001 | g0047 | EUR | GBR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00323 | hp1 | a0002 | c0003 | t0001 | g0324 | EUR | FIN | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00323 | hp2 | a0001 | c0002 | t0003 | g0070 | EUR | FIN | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00423 | hp1 | a0002 | c0003 | t0001 | g0259 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00423 | hp2 | a0012 | c0022 | t0001 | g0268 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0078 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0122 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00558 | hp1 | a0001 | c0030 | t0001 | g0293 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00597 | hp2 | a0013 | c0034 | t0002 | g0044 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00609 | hp2 | a0001 | c0002 | t0003 | g0059 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0092 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00621 | hp2 | a0002 | c0003 | t0001 | g0233 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00639 | hp1 | a0002 | c0003 | t0001 | g0006 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00639 | hp2 | a0014 | c0023 | t0001 | g0217 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00642 | hp1 | a0001 | c0001 | t0010 | g0319 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00642 | hp2 | a0001 | c0002 | t0006 | g0018 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00673 | hp2 | a0001 | c0002 | t0002 | g0057 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00733 | hp1 | a0015 | c0019 | t0001 | g0228 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00733 | hp2 | a0001 | c0002 | t0002 | g0097 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00735 | hp1 | a0002 | c0003 | t0001 | g0312 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00735 | hp2 | a0001 | c0038 | t0001 | g0141 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0108 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00741 | hp1 | a0001 | c0002 | t0002 | g0106 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01070 | hp1 | a0001 | c0002 | t0003 | g0020 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01070 | hp2 | a0008 | c0013 | t0001 | g0326 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01074 | hp1 | a0005 | c0008 | t0001 | g0030 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01074 | hp2 | a0002 | c0003 | t0001 | g0313 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01081 | hp1 | a0001 | c0002 | t0003 | g0072 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01106 | hp1 | a0001 | c0002 | t0002 | g0103 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01106 | hp2 | a0002 | c0003 | t0001 | g0256 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01109 | hp1 | a0007 | c0009 | t0001 | g0157 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01109 | hp2 | a0016 | c0026 | t0006 | g0021 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01167 | hp1 | a0001 | c0002 | t0003 | g0222 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0100 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01169 | hp2 | a0001 | c0002 | t0003 | g0274 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01175 | hp1 | a0002 | c0003 | t0001 | g0006 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01175 | hp2 | a0001 | c0002 | t0003 | g0126 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01255 | hp2 | a0001 | c0002 | t0003 | g0090 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0102 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01261 | hp2 | a0001 | c0002 | t0003 | g0064 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01346 | hp2 | a0002 | c0003 | t0001 | g0251 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0105 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01358 | hp2 | a0003 | c0004 | t0001 | g0001 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01433 | hp1 | a0001 | c0002 | t0003 | g0091 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01433 | hp2 | a0001 | c0002 | t0003 | g0111 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01496 | hp1 | a0001 | c0002 | t0006 | g0019 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01496 | hp2 | a0004 | c0006 | t0001 | g0140 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | IBS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01516 | hp2 | a0009 | c0011 | t0001 | g0318 | EUR | IBS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01517 | hp1 | a0001 | c0002 | t0002 | g0048 | EUR | IBS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01517 | hp2 | a0009 | c0011 | t0001 | g0322 | EUR | IBS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01884 | hp1 | a0002 | c0003 | t0001 | g0137 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01891 | hp1 | a0002 | c0003 | t0004 | g0255 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01891 | hp2 | a0007 | c0009 | t0001 | g0210 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01928 | hp2 | a0001 | c0002 | t0003 | g0116 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01952 | hp2 | a0001 | c0002 | t0003 | g0052 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01978 | hp1 | a0001 | c0042 | t0002 | g0067 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01978 | hp2 | a0001 | c0002 | t0003 | g0110 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02004 | hp1 | a0002 | c0003 | t0001 | g0253 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02015 | hp2 | a0017 | c0031 | t0001 | g0145 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0107 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0123 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02055 | hp1 | a0004 | c0029 | t0001 | g0329 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02055 | hp2 | a0001 | c0005 | t0001 | g0003 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02148 | hp2 | a0002 | c0003 | t0001 | g0258 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | CDX | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02155 | hp2 | a0018 | c0040 | t0002 | g0099 | EAS | CDX | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02258 | hp1 | a0001 | c0002 | t0002 | g0127 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02258 | hp2 | a0002 | c0003 | t0004 | g0244 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02273 | hp2 | a0019 | c0041 | t0002 | g0073 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02280 | hp1 | a0007 | c0009 | t0001 | g0163 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02280 | hp2 | a0001 | c0007 | t0003 | g0026 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02293 | hp2 | a0002 | c0003 | t0001 | g0243 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02300 | hp2 | a0005 | c0008 | t0001 | g0077 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02451 | hp1 | a0001 | c0002 | t0003 | g0056 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02451 | hp2 | a0020 | c0024 | t0001 | g0015 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02523 | hp2 | a0001 | c0002 | t0002 | g0061 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02602 | hp1 | a0002 | c0003 | t0001 | g0248 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02622 | hp1 | a0003 | c0004 | t0001 | g0146 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02622 | hp2 | a0004 | c0006 | t0001 | g0080 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02630 | hp1 | a0010 | c0015 | t0001 | g0017 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0071 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02698 | hp1 | a0002 | c0003 | t0001 | g0221 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02717 | hp1 | a0001 | c0002 | t0003 | g0120 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02717 | hp2 | a0010 | c0015 | t0001 | g0016 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02735 | hp1 | a0001 | c0027 | t0001 | g0147 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02735 | hp2 | a0002 | c0003 | t0001 | g0289 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02809 | hp1 | a0003 | c0004 | t0001 | g0178 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02809 | hp2 | a0006 | c0010 | t0001 | g0011 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02818 | hp1 | a0001 | c0002 | t0007 | g0131 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02818 | hp2 | a0001 | c0002 | t0002 | g0079 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02886 | hp1 | a0001 | c0002 | t0003 | g0168 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02886 | hp2 | a0021 | c0032 | t0001 | g0129 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02895 | hp1 | a0003 | c0004 | t0001 | g0177 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02895 | hp2 | a0011 | c0012 | t0001 | g0216 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02896 | hp1 | a0001 | c0001 | t0005 | g0283 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02896 | hp2 | a0004 | c0006 | t0001 | g0096 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02897 | hp1 | a0001 | c0001 | t0005 | g0282 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02897 | hp2 | a0011 | c0012 | t0001 | g0215 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0292 | AFR | ESN | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02970 | hp2 | a0006 | c0010 | t0001 | g0010 | AFR | ESN | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03017 | hp1 | a0001 | c0002 | t0003 | g0050 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03017 | hp2 | a0008 | c0013 | t0001 | g0325 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03098 | hp1 | a0003 | c0004 | t0001 | g0176 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03098 | hp2 | a0001 | c0002 | t0003 | g0036 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03130 | hp1 | a0002 | c0003 | t0001 | g0138 | AFR | ESN | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03139 | hp1 | a0001 | c0002 | t0003 | g0133 | AFR | ESN | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03139 | hp2 | a0001 | c0017 | t0001 | g0167 | AFR | ESN | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03195 | hp1 | a0003 | c0004 | t0001 | g0166 | AFR | ESN | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03195 | hp2 | a0001 | c0002 | t0003 | g0132 | AFR | ESN | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03209 | hp1 | a0001 | c0007 | t0003 | g0029 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03225 | hp1 | a0003 | c0004 | t0001 | g0165 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03225 | hp2 | a0022 | c0020 | t0001 | g0309 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0314 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03453 | hp2 | a0023 | c0018 | t0001 | g0009 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03486 | hp1 | a0001 | c0014 | t0001 | g0130 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03486 | hp2 | a0002 | c0003 | t0001 | g0310 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03540 | hp1 | a0004 | c0006 | t0001 | g0022 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03540 | hp2 | a0001 | c0002 | t0003 | g0041 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03579 | hp1 | a0001 | c0002 | t0007 | g0128 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03579 | hp2 | a0002 | c0003 | t0001 | g0154 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03669 | hp1 | a0024 | c0033 | t0003 | g0082 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | STU | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03688 | hp2 | a0002 | c0003 | t0001 | g0239 | SAS | STU | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03831 | hp2 | a0002 | c0003 | t0001 | g0250 | SAS | BEB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0098 | SAS | BEB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG04184 | hp1 | a0001 | c0002 | t0003 | g0117 | SAS | BEB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG04199 | hp1 | a0001 | c0002 | t0011 | g0031 | SAS | STU | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG04199 | hp2 | a0002 | c0021 | t0003 | g0257 | SAS | STU | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0125 | SAS | STU | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG04204 | hp2 | a0002 | c0003 | t0001 | g0209 | SAS | STU | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | STU | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | STU | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | YRI | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18522 | hp2 | a0002 | c0003 | t0004 | g0234 | AFR | YRI | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18906 | hp1 | a0004 | c0006 | t0001 | g0038 | AFR | YRI | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18906 | hp2 | a0001 | c0007 | t0003 | g0025 | AFR | YRI | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18940 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18944 | hp2 | a0002 | c0003 | t0009 | g0242 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18954 | hp1 | a0002 | c0003 | t0001 | g0249 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18962 | hp1 | a0001 | c0002 | t0002 | g0109 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18963 | hp1 | a0001 | c0036 | t0001 | g0232 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18964 | hp2 | a0001 | c0005 | t0001 | g0172 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18967 | hp2 | a0001 | c0005 | t0001 | g0160 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18968 | hp1 | a0001 | c0002 | t0002 | g0101 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18970 | hp2 | a0025 | c0037 | t0001 | g0201 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18971 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18974 | hp1 | a0001 | c0005 | t0001 | g0155 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18974 | hp2 | a0001 | c0002 | t0003 | g0085 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18978 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18979 | hp2 | a0002 | c0003 | t0001 | g0229 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18982 | hp1 | a0002 | c0003 | t0001 | g0237 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18982 | hp2 | a0001 | c0002 | t0003 | g0083 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18983 | hp1 | a0002 | c0003 | t0001 | g0238 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18985 | hp1 | a0001 | c0002 | t0003 | g0033 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18987 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0113 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18992 | hp1 | a0001 | c0002 | t0003 | g0207 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18992 | hp2 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18993 | hp2 | a0026 | c0025 | t0001 | g0158 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18995 | hp1 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18998 | hp1 | a0001 | c0002 | t0002 | g0119 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19003 | hp1 | a0001 | c0002 | t0003 | g0124 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19004 | hp1 | a0001 | c0002 | t0002 | g0093 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19005 | hp2 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19009 | hp1 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19012 | hp1 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | LWK | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19030 | hp2 | a0001 | c0007 | t0003 | g0027 | AFR | LWK | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19043 | hp1 | a0002 | c0003 | t0001 | g0254 | AFR | LWK | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19043 | hp2 | a0002 | c0003 | t0001 | g0328 | AFR | LWK | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19055 | hp1 | a0002 | c0003 | t0001 | g0240 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19055 | hp2 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19056 | hp2 | a0001 | c0002 | t0003 | g0035 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19060 | hp2 | a0001 | c0001 | t0008 | g0291 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19065 | hp1 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19066 | hp2 | a0002 | c0003 | t0001 | g0241 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19079 | hp2 | a0001 | c0005 | t0001 | g0156 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19083 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19084 | hp1 | a0001 | c0002 | t0003 | g0032 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19084 | hp2 | a0002 | c0003 | t0001 | g0230 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19240 | hp1 | a0003 | c0004 | t0001 | g0001 | AFR | YRI | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA19240 | hp2 | a0001 | c0002 | t0002 | g0094 | AFR | YRI | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA20129 | hp1 | a0001 | c0007 | t0003 | g0028 | AFR | ASW | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA20129 | hp2 | a0027 | c0028 | t0001 | g0277 | AFR | ASW | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA20905 | hp1 | a0028 | c0039 | t0001 | g0327 | SAS | GIH | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | GIH | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0084 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02109 | hp1 | a0004 | c0006 | t0001 | g0081 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02109 | hp2 | a0003 | c0004 | t0001 | g0001 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02559 | hp1 | a0001 | c0007 | t0003 | g0024 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG03471 | hp2 | a0001 | c0014 | t0001 | g0023 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG06807 | hp1 | a0002 | c0003 | t0001 | g0252 | AFR | USA | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | USA | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA18955 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA20300 | hp1 | a0001 | c0002 | t0003 | g0051 | AFR | USA | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0121 | AFR | USA | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA21309 | hp1 | a0005 | c0008 | t0001 | g0013 | AFR | LWK | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
NA21309 | hp2 | a0002 | c0003 | t0001 | g0245 | AFR | LWK | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
homoSapiens | chm13v2 | a0001 | c0002 | t0003 | g0095 | REF | REF | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
homoSapiens | grch38p0 | a0006 | c0016 | t0001 | g0012 | REF | REF | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:99784690 | A | T | 27 | a0001 a0002 a0003 others(24): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
missense_variant | MODERATE | c.116A>T | p.Tyr39Phe | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/32 | 321/5806 | 116/4638 | 39/1545 | chr10 | 99784690 | |||
chr10:99792324 | C | T | 1 | a0019 | 1 | HG02273.hp2 | stop_gained | HIGH | c.298C>T | p.Arg100* | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 3/32 | 503/5806 | 298/4638 | 100/1545 | chr10 | 99792324 | |||
chr10:99797306 | G | A | 1 | a0009 | 2 | HG01516.hp2 HG01517.hp2 |
missense_variant | MODERATE | c.842G>A | p.Ser281Asn | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 7/32 | 1047/5806 | 842/4638 | 281/1545 | chr10 | 99797306 | |||
chr10:99799297 | A | G | 1 | a0018 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.958A>G | p.Met320Val | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 8/32 | 1163/5806 | 958/4638 | 320/1545 | chr10 | 99799297 | |||
chr10:99800412 | G | A | 2 | a0011 a0023 |
3 | HG02895.hp2 HG02897.hp2 HG03453.hp2 |
missense_variant | MODERATE | c.1058G>A | p.Arg353His | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/32 | 1263/5806 | 1058/4638 | 353/1545 | chr10 | 99800412 | |||
chr10:99800525 | A | G | 1 | a0028 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.1171A>G | p.Lys391Glu | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/32 | 1376/5806 | 1171/4638 | 391/1545 | chr10 | 99800525 | |||
chr10:99804058 | G | A | 5 | a0002 a0008 a0015 others(2): Show |
44 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(41): Show |
missense_variant | MODERATE | c.1249G>A | p.Val417Ile | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 10/32 | 1454/5806 | 1249/4638 | 417/1545 | chr10 | 99804058 | |||
chr10:99804266 | C | T | 1 | a0025 | 1 | NA18970.hp2 | missense_variant | MODERATE | c.1457C>T | p.Thr486Ile | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 10/32 | 1662/5806 | 1457/4638 | 486/1545 | chr10 | 99804266 | |||
chr10:99805400 | A | G | 1 | a0008 | 2 | HG01070.hp2 HG03017.hp2 |
missense_variant | MODERATE | c.1483A>G | p.Lys495Glu | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/32 | 1688/5806 | 1483/4638 | 495/1545 | chr10 | 99805400 | |||
chr10:99811599 | G | A | 1 | a0012 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.1964G>A | p.Arg655Gln | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 15/32 | 2169/5806 | 1964/4638 | 655/1545 | chr10 | 99811599 | |||
chr10:99830363 | G | C | 1 | a0026 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.2677G>C | p.Glu893Gln | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 20/32 | 2882/5806 | 2677/4638 | 893/1545 | chr10 | 99830363 | |||
chr10:99830429 | C | T | 2 | a0014 a0020 |
2 | HG00639.hp2 HG02451.hp2 |
missense_variant | MODERATE | c.2743C>T | p.Arg915Cys | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 20/32 | 2948/5806 | 2743/4638 | 915/1545 | chr10 | 99830429 | |||
chr10:99830781 | G | A | 2 | a0014 a0020 |
2 | HG00639.hp2 HG02451.hp2 |
missense_variant | MODERATE | c.2813G>A | p.Ser938Asn | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 21/32 | 3018/5806 | 2813/4638 | 938/1545 | chr10 | 99830781 | |||
chr10:99831671 | A | G | 2 | a0014 a0020 |
2 | HG00639.hp2 HG02451.hp2 |
missense_variant | MODERATE | c.2944A>G | p.Ile982Val | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 22/32 | 3149/5806 | 2944/4638 | 982/1545 | chr10 | 99831671 | |||
chr10:99831980 | T | C | 1 | a0015 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.3107T>C | p.Ile1036Thr | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 23/32 | 3312/5806 | 3107/4638 | 1036/1545 | chr10 | 99831980 | |||
chr10:99832061 | A | G | 2 | a0014 a0020 |
2 | HG00639.hp2 HG02451.hp2 |
missense_variant | MODERATE | c.3188A>G | p.Asn1063Ser | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 23/32 | 3393/5806 | 3188/4638 | 1063/1545 | chr10 | 99832061 | |||
chr10:99832109 | G | A | 1 | a0016 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.3236G>A | p.Arg1079Gln | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 23/32 | 3441/5806 | 3236/4638 | 1079/1545 | chr10 | 99832109 | |||
chr10:99836218 | G | T | 1 | a0003 | 9 | HG01358.hp2 HG02109.hp2 HG02622.hp1 others(6): Show |
missense_variant | MODERATE | c.3542G>T | p.Arg1181Leu | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/32 | 3747/5806 | 3542/4638 | 1181/1545 | chr10 | 99836218 | |||
chr10:99836239 | T | A | 4 | a0005 a0014 a0022 others(1): Show |
7 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(4): Show |
missense_variant | MODERATE | c.3563T>A | p.Val1188Glu | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/32 | 3768/5806 | 3563/4638 | 1188/1545 | chr10 | 99836239 | |||
chr10:99843856 | G | T | 1 | a0013 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.3799G>T | p.Val1267Leu | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 27/32 | 4004/5806 | 3799/4638 | 1267/1545 | chr10 | 99843856 | |||
chr10:99843874 | A | G | 1 | a0010 | 2 | HG02630.hp1 HG02717.hp2 |
missense_variant | MODERATE | c.3817A>G | p.Thr1273Ala | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 27/32 | 4022/5806 | 3817/4638 | 1273/1545 | chr10 | 99843874 | |||
chr10:99844350 | C | T | 1 | a0007 | 3 | HG01109.hp1 HG01891.hp2 HG02280.hp1 |
missense_variant | MODERATE | c.3872C>T | p.Pro1291Leu | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 28/32 | 4077/5806 | 3872/4638 | 1291/1545 | chr10 | 99844350 | |||
chr10:99845711 | A | C | 1 | a0021 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.4075A>C | p.Ile1359Leu | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 29/32 | 4280/5806 | 4075/4638 | 1359/1545 | chr10 | 99845711 | |||
chr10:99847054 | C | T | 1 | a0017 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.4240C>T | p.His1414Tyr | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/32 | 4445/5806 | 4240/4638 | 1414/1545 | chr10 | 99847054 | |||
chr10:99850783 | A | G | 1 | a0027 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.4495A>G | p.Met1499Val | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 31/32 | 4700/5806 | 4495/4638 | 1499/1545 | chr10 | 99850783 | |||
chr10:99851537 | G | A | 7 | a0004 a0005 a0014 others(4): Show |
16 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(13): Show |
missense_variant | MODERATE | c.4544G>A | p.Cys1515Tyr | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 32/32 | 4749/5806 | 4544/4638 | 1515/1545 | chr10 | 99851537 | |||
chr10:99851561 | A | C | 1 | a0024 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.4568A>C | p.Gln1523Pro | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 32/32 | 4773/5806 | 4568/4638 | 1523/1545 | chr10 | 99851561 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:99784724 | C | T | 1 | a0001c0042 | 1 | HG01978.hp1 | synonymous_variant | LOW | c.150C>T | p.His50His | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/32 | 355/5806 | 150/4638 | 50/1545 | chr10 | 99784724 | |||
chr10:99793556 | G | A | 1 | a0001c0017 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.339G>A | p.Leu113Leu | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 4/32 | 544/5806 | 339/4638 | 113/1545 | chr10 | 99793556 | |||
chr10:99804028 | C | T | 1 | a0001c0007 | 6 | HG02280.hp2 HG02559.hp1 HG03209.hp1 others(3): Show |
synonymous_variant | LOW | c.1219C>T | p.Leu407Leu | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 10/32 | 1424/5806 | 1219/4638 | 407/1545 | chr10 | 99804028 | |||
chr10:99804255 | C | G | 1 | a0001c0038 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.1446C>G | p.Thr482Thr | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 10/32 | 1651/5806 | 1446/4638 | 482/1545 | chr10 | 99804255 | |||
chr10:99813123 | C | A | 2 | a0014c0023 a0020c0024 |
2 | HG00639.hp2 HG02451.hp2 |
synonymous_variant | LOW | c.2073C>A | p.Val691Val | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/32 | 2278/5806 | 2073/4638 | 691/1545 | chr10 | 99813123 | |||
chr10:99831661 | G | A | 1 | a0001c0005 | 6 | HG02055.hp2 NA18964.hp2 NA18967.hp2 others(3): Show |
synonymous_variant | LOW | c.2934G>A | p.Ser978Ser | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 22/32 | 3139/5806 | 2934/4638 | 978/1545 | chr10 | 99831661 | |||
chr10:99831766 | C | T | 1 | a0001c0036 | 1 | NA18963.hp1 | synonymous_variant | LOW | c.3039C>T | p.Thr1013Thr | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 22/32 | 3244/5806 | 3039/4638 | 1013/1545 | chr10 | 99831766 | |||
chr10:99834517 | T | C | 1 | a0001c0027 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.3396T>C | p.Ile1132Ile | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 24/32 | 3601/5806 | 3396/4638 | 1132/1545 | chr10 | 99834517 | |||
chr10:99836168 | C | T | 1 | a0001c0035 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.3492C>T | p.Ser1164Ser | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/32 | 3697/5806 | 3492/4638 | 1164/1545 | chr10 | 99836168 | |||
chr10:99844450 | C | T | 12 | a0001c0002 a0001c0007 a0001c0014 others(9): Show |
105 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(102): Show |
synonymous_variant | LOW | c.3972C>T | p.Ile1324Ile | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 28/32 | 4177/5806 | 3972/4638 | 1324/1545 | chr10 | 99844450 | |||
chr10:99845698 | C | T | 1 | a0001c0014 | 2 | HG03471.hp2 HG03486.hp1 |
synonymous_variant | LOW | c.4062C>T | p.Ala1354Ala | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 29/32 | 4267/5806 | 4062/4638 | 1354/1545 | chr10 | 99845698 | |||
chr10:99845746 | C | T | 2 | a0004c0006 a0023c0018 |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
synonymous_variant | LOW | c.4110C>T | p.Leu1370Leu | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 29/32 | 4315/5806 | 4110/4638 | 1370/1545 | chr10 | 99845746 | |||
chr10:99847104 | G | T | 5 | a0005c0008 a0014c0023 a0020c0024 others(2): Show |
8 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(5): Show |
synonymous_variant | LOW | c.4290G>T | p.Val1430Val | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/32 | 4495/5806 | 4290/4638 | 1430/1545 | chr10 | 99847104 | |||
chr10:99850695 | A | G | 1 | a0001c0030 | 1 | HG00558.hp1 | synonymous_variant | LOW | c.4407A>G | p.Leu1469Leu | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 31/32 | 4612/5806 | 4407/4638 | 1469/1545 | chr10 | 99850695 | |||
chr10:99850698 | G | A | 3 | a0004c0006 a0004c0029 a0023c0018 |
8 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
synonymous_variant | LOW | c.4410G>A | p.Glu1470Glu | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 31/32 | 4615/5806 | 4410/4638 | 1470/1545 | chr10 | 99850698 | |||
chr10:99850776 | C | T | 3 | a0005c0008 a0014c0023 a0022c0020 |
6 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(3): Show |
synonymous_variant | LOW | c.4488C>T | p.His1496His | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 31/32 | 4693/5806 | 4488/4638 | 1496/1545 | chr10 | 99850776 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:99782821 | C | T | 7 | a0001c0002t0002 a0001c0002t0011 a0001c0035t0002 others(4): Show |
57 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(54): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-24C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 1/32 | chr10 | 99782821 | |||||||
chr10:99782822 | G | C | 1 | a0001c0001t0008 | 1 | NA19060.hp2 | 5_prime_UTR_variant | MODIFIER | c.-23G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 1/32 | 23 | chr10 | 99782822 | ||||||
chr10:99851735 | G | A | 1 | a0002c0003t0009 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*104G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 32/32 | 104 | chr10 | 99851735 | ||||||
chr10:99851832 | C | T | 1 | a0001c0002t0007 | 2 | HG02818.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*201C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 32/32 | 201 | chr10 | 99851832 | ||||||
chr10:99851890 | G | T | 1 | a0001c0001t0010 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*259G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 32/32 | 259 | chr10 | 99851890 | ||||||
chr10:99851927 | C | A | 1 | a0001c0002t0011 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*296C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 32/32 | 296 | chr10 | 99851927 | ||||||
chr10:99852041 | T | G | 2 | a0001c0001t0004 a0002c0003t0004 |
4 | HG01891.hp1 HG02258.hp2 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*410T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 32/32 | 410 | chr10 | 99852041 | ||||||
chr10:99852407 | T | A | 2 | a0001c0002t0006 a0016c0026t0006 |
3 | HG00642.hp2 HG01109.hp2 HG01496.hp1 |
3_prime_UTR_variant | MODIFIER | c.*776T>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 32/32 | 776 | chr10 | 99852407 | ||||||
chr10:99852510 | T | C | 1 | a0001c0001t0005 | 4 | HG02896.hp1 HG02897.hp1 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*879T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 32/32 | 879 | chr10 | 99852510 | ||||||
chr10:99852563 | C | T | 14 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0006 others(11): Show |
101 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*932C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 32/32 | 932 | chr10 | 99852563 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:99783103 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG03654.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.33+226T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 1/31 | chr10 | 99783103 | |||||||
chr10:99783206 | A | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(207): Show |
217 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.33+329A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 1/31 | chr10 | 99783206 | |||||||
chr10:99783290 | A | C | 109 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0058 others(106): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.33+413A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 1/31 | chr10 | 99783290 | |||||||
chr10:99783365 | A | G | 1 | a0001c0002t0002g0127 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.33+488A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 1/31 | chr10 | 99783365 | |||||||
chr10:99783831 | A | G | 1 | a0001c0002t0003g0126 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.34-777A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 1/31 | chr10 | 99783831 | |||||||
chr10:99783984 | GCCCACCC | G | 4 | a0001c0002t0003g0020 a0001c0002t0006g0018 a0001c0002t0006g0019 others(1): Show |
4 | HG00642.hp2 HG01070.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.34-612_34-606delCC others(5): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr10 | 99783984 | ||||||
chr10:99783994 | C | A | 6 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0007g0128 others(3): Show |
6 | HG02818.hp1 HG02886.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.34-614C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 1/31 | chr10 | 99783994 | |||||||
chr10:99784269 | C | T | 111 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0058 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.34-339C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 1/31 | chr10 | 99784269 | |||||||
chr10:99784440 | A | T | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.34-168A>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 1/31 | chr10 | 99784440 | |||||||
chr10:99784508 | A | G | 1 | a0002c0003t0001g0328 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.34-100A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 1/31 | chr10 | 99784508 | |||||||
chr10:99784600 | G | A | 2 | a0001c0014t0001g0023 a0004c0006t0001g0022 |
2 | HG03471.hp2 HG03540.hp1 |
splice_region_variant&intron_variant | LOW | c.34-8G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 1/31 | chr10 | 99784600 | |||||||
chr10:99784973 | T | G | 3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 |
3 | HG02027.hp2 HG02056.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.207+192T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99784973 | |||||||
chr10:99785348 | G | A | 2 | a0002c0003t0001g0137 a0002c0003t0001g0138 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.207+567G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99785348 | |||||||
chr10:99785581 | A | G | 4 | a0002c0003t0001g0324 a0008c0013t0001g0325 a0008c0013t0001g0326 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+800A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99785581 | |||||||
chr10:99785777 | C | T | 2 | a0010c0015t0001g0016 a0010c0015t0001g0017 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.207+996C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99785777 | |||||||
chr10:99785801 | G | C | 81 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): Show |
85 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(82): Show |
intron_variant | MODIFIER | c.207+1020G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99785801 | |||||||
chr10:99785829 | T | G | 2 | a0011c0012t0001g0215 a0011c0012t0001g0216 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.207+1048T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99785829 | |||||||
chr10:99785902 | G | A | 2 | a0010c0015t0001g0016 a0010c0015t0001g0017 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.207+1121G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99785902 | |||||||
chr10:99786318 | C | A | 2 | a0010c0015t0001g0016 a0010c0015t0001g0017 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.207+1537C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99786318 | |||||||
chr10:99786597 | T | A | 1 | a0023c0018t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.207+1816T>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99786597 | |||||||
chr10:99786787 | G | A | 6 | a0001c0007t0003g0024 a0001c0007t0003g0025 a0001c0007t0003g0026 others(3): Show |
6 | HG02280.hp2 HG02559.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+2006G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99786787 | |||||||
chr10:99786801 | G | A | 1 | a0005c0008t0001g0030 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.207+2020G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99786801 | |||||||
chr10:99786875 | C | T | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.207+2094C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99786875 | |||||||
chr10:99786997 | G | A | 1 | a0001c0001t0001g0218 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.207+2216G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99786997 | |||||||
chr10:99787001 | C | CA | 6 | a0001c0002t0002g0034 a0001c0002t0003g0032 a0001c0002t0003g0033 others(3): Show |
6 | HG03098.hp2 HG04199.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.207+2237dupA | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr10 | 99787001 | ||||||
chr10:99787001 | CA | C | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0134 others(70): Show |
76 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.207+2237delA | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr10 | 99787001 | ||||||
chr10:99787050 | C | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.207+2269C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99787050 | |||||||
chr10:99787095 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.207+2314G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99787095 | |||||||
chr10:99787155 | C | CA | 202 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(199): Show |
209 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.207+2388dupA | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr10 | 99787155 | ||||||
chr10:99787155 | C | CAA | 8 | a0001c0001t0001g0260 a0001c0038t0001g0141 a0002c0003t0001g0324 others(5): Show |
8 | HG00323.hp1 HG00735.hp2 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+2387_207+2388d others(4): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr10 | 99787155 | ||||||
chr10:99787206 | T | C | 1 | a0006c0010t0001g0010 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.207+2425T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99787206 | |||||||
chr10:99787264 | C | A | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.207+2483C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99787264 | |||||||
chr10:99787285 | C | T | 109 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0058 others(106): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.207+2504C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99787285 | |||||||
chr10:99787359 | T | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.207+2578T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99787359 | |||||||
chr10:99787459 | G | T | 214 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(211): Show |
221 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.207+2678G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99787459 | |||||||
chr10:99787460 | G | T | 213 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(210): Show |
220 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.207+2679G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99787460 | |||||||
chr10:99787461 | G | T | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.207+2680G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99787461 | |||||||
chr10:99787483 | G | A | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.207+2702G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99787483 | |||||||
chr10:99787519 | G | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): Show |
85 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(82): Show |
intron_variant | MODIFIER | c.207+2738G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99787519 | |||||||
chr10:99787526 | A | G | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.207+2745A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99787526 | |||||||
chr10:99787568 | C | T | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.207+2787C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99787568 | |||||||
chr10:99787571 | C | T | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.207+2790C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99787571 | |||||||
chr10:99787590 | C | T | 4 | a0001c0001t0001g0014 a0005c0008t0001g0013 a0014c0023t0001g0217 others(1): Show |
4 | HG00639.hp2 HG02451.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+2809C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99787590 | |||||||
chr10:99787663 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.207+2882T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99787663 | |||||||
chr10:99787694 | A | AT | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.207+2919dupT | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr10 | 99787694 | ||||||
chr10:99787855 | C | T | 108 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0058 others(105): Show |
108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.207+3074C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99787855 | |||||||
chr10:99787860 | C | T | 1 | a0001c0002t0002g0125 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.207+3079C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99787860 | |||||||
chr10:99787890 | G | A | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.207+3109G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99787890 | |||||||
chr10:99787904 | A | G | 1 | a0014c0023t0001g0217 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.207+3123A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99787904 | |||||||
chr10:99787906 | T | A | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.207+3125T>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99787906 | |||||||
chr10:99787915 | T | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.207+3134T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99787915 | |||||||
chr10:99787997 | G | A | 6 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0007g0128 others(3): Show |
6 | HG02818.hp1 HG02886.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+3216G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99787997 | |||||||
chr10:99788011 | G | A | 2 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
2 | NA18948.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.207+3230G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99788011 | |||||||
chr10:99788026 | C | T | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.207+3245C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99788026 | |||||||
chr10:99788066 | CAA | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.207+3295_207+3296d others(4): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr10 | 99788066 | ||||||
chr10:99788127 | C | G | 1 | a0023c0018t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.207+3346C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99788127 | |||||||
chr10:99788144 | G | C | 1 | a0005c0008t0001g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.207+3363G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99788144 | |||||||
chr10:99788420 | A | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.207+3639A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99788420 | |||||||
chr10:99788711 | G | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(203): Show |
213 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.208-3523G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99788711 | |||||||
chr10:99788770 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.208-3464C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99788770 | |||||||
chr10:99788829 | C | A | 1 | a0001c0001t0001g0143 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.208-3405C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99788829 | |||||||
chr10:99788834 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.208-3400C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99788834 | |||||||
chr10:99788859 | C | T | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.208-3375C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99788859 | |||||||
chr10:99788952 | C | T | 111 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0058 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.208-3282C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99788952 | |||||||
chr10:99789038 | A | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.208-3196A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99789038 | |||||||
chr10:99789105 | A | G | 6 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0007g0128 others(3): Show |
6 | HG02818.hp1 HG02886.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-3129A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99789105 | |||||||
chr10:99789139 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.208-3095G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99789139 | |||||||
chr10:99789217 | G | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.208-3017G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99789217 | |||||||
chr10:99789506 | G | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.208-2728G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99789506 | |||||||
chr10:99789628 | T | A | 1 | a0017c0031t0001g0145 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.208-2606T>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99789628 | |||||||
chr10:99789646 | C | T | 1 | a0001c0001t0001g0323 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.208-2588C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99789646 | |||||||
chr10:99789697 | G | A | 1 | a0003c0004t0001g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.208-2537G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99789697 | |||||||
chr10:99789709 | C | A | 1 | a0001c0027t0001g0147 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.208-2525C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99789709 | |||||||
chr10:99789709 | C | CA | 194 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(191): Show |
200 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.208-2508dupA | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr10 | 99789709 | ||||||
chr10:99789709 | C | CAA | 10 | a0001c0001t0001g0004 a0001c0001t0001g0219 a0001c0001t0001g0263 others(7): Show |
11 | HG02818.hp1 HG02886.hp2 HG03486.hp1 others(8): Show |
intron_variant | MODIFIER | c.208-2509_208-2508d others(4): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr10 | 99789709 | ||||||
chr10:99789775 | A | AG | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.208-2458dupG | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr10 | 99789775 | ||||||
chr10:99789829 | T | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.208-2405T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99789829 | |||||||
chr10:99790008 | G | A | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.208-2226G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99790008 | |||||||
chr10:99790154 | G | A | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.208-2080G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99790154 | |||||||
chr10:99790319 | T | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.208-1915T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99790319 | |||||||
chr10:99790372 | T | C | 1 | a0001c0001t0001g0267 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.208-1862T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99790372 | |||||||
chr10:99790661 | G | A | 1 | a0001c0002t0003g0041 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.208-1573G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99790661 | |||||||
chr10:99790764 | C | A | 4 | a0001c0001t0001g0014 a0005c0008t0001g0013 a0014c0023t0001g0217 others(1): Show |
4 | HG00639.hp2 HG02451.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-1470C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99790764 | |||||||
chr10:99790910 | G | A | 4 | a0001c0002t0002g0042 a0001c0002t0002g0043 a0001c0002t0002g0045 others(1): Show |
4 | HG00597.hp2 HG02083.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-1324G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99790910 | |||||||
chr10:99790933 | AG | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0213 |
3 | HG01255.hp1 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.208-1300delG | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99790933 | |||||||
chr10:99790944 | A | G | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0213 |
3 | HG01255.hp1 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.208-1290A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99790944 | |||||||
chr10:99791224 | A | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.208-1010A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99791224 | |||||||
chr10:99791234 | C | T | 3 | a0001c0001t0001g0260 a0001c0001t0001g0320 a0001c0001t0001g0321 |
3 | HG00741.hp2 HG01081.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.208-1000C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99791234 | |||||||
chr10:99791349 | C | A | 325 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(322): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.208-885C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99791349 | |||||||
chr10:99791856 | C | G | 6 | a0001c0001t0001g0260 a0001c0001t0001g0320 a0001c0001t0001g0321 others(3): Show |
6 | HG00642.hp1 HG00741.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.208-378C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99791856 | |||||||
chr10:99791886 | C | T | 3 | a0001c0001t0001g0260 a0001c0001t0001g0320 a0001c0001t0001g0321 |
3 | HG00741.hp2 HG01081.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.208-348C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99791886 | |||||||
chr10:99791887 | G | A | 2 | a0009c0011t0001g0318 a0009c0011t0001g0322 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.208-347G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99791887 | |||||||
chr10:99791904 | T | G | 1 | a0012c0022t0001g0268 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.208-330T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99791904 | |||||||
chr10:99792120 | G | A | 1 | a0023c0018t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.208-114G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99792120 | |||||||
chr10:99792144 | G | A | 1 | a0001c0002t0011g0031 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.208-90G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99792144 | |||||||
chr10:99792145 | C | T | 325 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(322): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.208-89C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99792145 | |||||||
chr10:99792557 | G | C | 1 | a0001c0035t0002g0046 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.333+198G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 3/31 | chr10 | 99792557 | |||||||
chr10:99792678 | T | A | 1 | a0001c0001t0001g0220 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.333+319T>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 3/31 | chr10 | 99792678 | |||||||
chr10:99792924 | C | T | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | NA18952.hp2 NA18969.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.333+565C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 3/31 | chr10 | 99792924 | |||||||
chr10:99792950 | T | G | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+591T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 3/31 | chr10 | 99792950 | |||||||
chr10:99793061 | G | GCA | 325 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(322): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.334-489_334-488ins others(2): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr10 | 99793061 | ||||||
chr10:99793129 | A | T | 109 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0058 others(106): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.334-422A>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 3/31 | chr10 | 99793129 | |||||||
chr10:99793256 | A | G | 1 | a0001c0002t0003g0124 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.334-295A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 3/31 | chr10 | 99793256 | |||||||
chr10:99793385 | G | A | 1 | a0023c0018t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.334-166G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 3/31 | chr10 | 99793385 | |||||||
chr10:99793502 | C | T | 109 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0058 others(106): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.334-49C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 3/31 | chr10 | 99793502 | |||||||
chr10:99793505 | G | A | 1 | a0002c0003t0001g0221 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.334-46G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 3/31 | chr10 | 99793505 | |||||||
chr10:99793538 | A | C | 1 | a0001c0001t0005g0314 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.334-13A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 3/31 | chr10 | 99793538 | |||||||
chr10:99794102 | A | C | 1 | a0001c0001t0001g0211 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.576+103A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 5/31 | chr10 | 99794102 | |||||||
chr10:99794152 | G | GAGT | 325 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(322): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.576+155_576+157dup others(3): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr10 | 99794152 | ||||||
chr10:99794273 | C | T | 2 | a0010c0015t0001g0016 a0010c0015t0001g0017 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.577-140C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 5/31 | chr10 | 99794273 | |||||||
chr10:99794393 | G | A | 1 | a0023c0018t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.577-20G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 5/31 | chr10 | 99794393 | |||||||
chr10:99794551 | A | T | 1 | a0001c0002t0002g0123 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.632+83A>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99794551 | |||||||
chr10:99794554 | T | A | 11 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0269 others(8): Show |
11 | HG00609.hp1 HG02155.hp1 NA18948.hp1 others(8): Show |
intron_variant | MODIFIER | c.632+86T>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99794554 | |||||||
chr10:99794734 | G | A | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | NA18974.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.632+266G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99794734 | |||||||
chr10:99794780 | T | A | 1 | a0023c0018t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.632+312T>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99794780 | |||||||
chr10:99794810 | G | A | 1 | a0023c0018t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.632+342G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99794810 | |||||||
chr10:99794972 | A | G | 1 | a0002c0003t0001g0259 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.632+504A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99794972 | |||||||
chr10:99795002 | G | A | 2 | a0001c0002t0003g0222 a0001c0002t0003g0274 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.632+534G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99795002 | |||||||
chr10:99795096 | G | A | 4 | a0001c0001t0001g0014 a0005c0008t0001g0013 a0014c0023t0001g0217 others(1): Show |
4 | HG00639.hp2 HG02451.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.632+628G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99795096 | |||||||
chr10:99795203 | A | G | 1 | a0001c0002t0002g0122 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.632+735A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99795203 | |||||||
chr10:99795426 | T | C | 325 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(322): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.632+958T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99795426 | |||||||
chr10:99795516 | T | C | 1 | a0004c0006t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.632+1048T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99795516 | |||||||
chr10:99795662 | G | A | 90 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(87): Show |
94 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(91): Show |
intron_variant | MODIFIER | c.632+1194G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99795662 | |||||||
chr10:99795723 | G | GAAAGAAA others(60): Show |
1 | a0023c0018t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.632+1265_632+1266i others(69): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr10 | 99795723 | ||||||
chr10:99795726 | AGAAAGAA others(5): Show |
A | 1 | a0015c0019t0001g0228 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.632+1270_632+1281d others(14): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr10 | 99795726 | ||||||
chr10:99795738 | G | A | 1 | a0023c0018t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.632+1270G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99795738 | |||||||
chr10:99795738 | G | GAAGAAAG others(3): Show |
1 | a0001c0001t0001g0281 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.632+1270_632+1271i others(12): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99795738 | |||||||
chr10:99795738 | GGAAA | G | 64 | a0001c0001t0001g0007 a0001c0001t0001g0114 a0001c0001t0001g0115 others(61): Show |
67 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.633-1296_633-1293d others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr10 | 99795738 | ||||||
chr10:99795738 | GGAAAGAA others(1): Show |
G | 38 | a0001c0001t0001g0002 a0001c0001t0001g0139 a0001c0001t0001g0142 others(35): Show |
38 | HG00140.hp1 HG00438.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.633-1300_633-1293d others(10): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr10 | 99795738 | ||||||
chr10:99795738 | GGAAAGAA others(5): Show |
G | 21 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(18): Show |
22 | HG00438.hp1 HG00609.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.633-1304_633-1293d others(14): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr10 | 99795738 | ||||||
chr10:99795738 | GGAAAGAA others(9): Show |
G | 5 | a0001c0001t0001g0184 a0001c0001t0001g0196 a0001c0027t0001g0147 others(2): Show |
5 | HG00558.hp2 HG02735.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.633-1308_633-1293d others(18): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr10 | 99795738 | ||||||
chr10:99795738 | GGAAAGAA others(25): Show |
G | 1 | a0001c0001t0001g0185 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.632+1305_633-1293d others(34): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr10 | 99795738 | ||||||
chr10:99795738 | GGAAAGAA others(29): Show |
G | 4 | a0001c0001t0001g0014 a0005c0008t0001g0013 a0014c0023t0001g0217 others(1): Show |
4 | HG00639.hp2 HG02451.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.632+1301_633-1293d others(38): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr10 | 99795738 | ||||||
chr10:99795775 | G | GAAAGAA | 3 | a0001c0007t0003g0024 a0001c0007t0003g0025 a0001c0007t0003g0026 |
3 | HG02280.hp2 HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.632+1309_632+1314d others(8): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr10 | 99795775 | ||||||
chr10:99795797 | A | AAGAT | 55 | a0001c0001t0001g0004 a0001c0001t0001g0162 a0001c0001t0001g0164 others(52): Show |
56 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.633-1297_633-1296i others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr10 | 99795797 | ||||||
chr10:99795797 | A | T | 191 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(188): Show |
197 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.633-1300A>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99795797 | |||||||
chr10:99795801 | A | AAGAAAGA others(25): Show |
1 | a0001c0001t0001g0276 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.633-1293_633-1292i others(34): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr10 | 99795801 | ||||||
chr10:99795801 | A | AAGAAAGA others(9): Show |
7 | a0001c0001t0001g0219 a0001c0002t0002g0042 a0001c0002t0002g0048 others(4): Show |
7 | HG00140.hp2 HG01109.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.633-1293_633-1292i others(18): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr10 | 99795801 | ||||||
chr10:99795801 | A | AAGAAAGA others(5): Show |
19 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0150 others(16): Show |
19 | HG00642.hp2 HG00738.hp1 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.633-1293_633-1292i others(14): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr10 | 99795801 | ||||||
chr10:99795801 | A | AAGATAGA others(1): Show |
45 | a0001c0001t0001g0058 a0001c0001t0001g0062 a0001c0001t0001g0151 others(42): Show |
45 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.633-1292_633-1291i others(10): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr10 | 99795801 | ||||||
chr10:99795801 | A | G | 250 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(247): Show |
257 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(254): Show |
intron_variant | MODIFIER | c.633-1296A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99795801 | |||||||
chr10:99795801 | A | T | 1 | a0001c0002t0002g0089 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.633-1296A>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99795801 | |||||||
chr10:99795808 | C | G | 5 | a0001c0001t0004g0121 a0001c0002t0003g0041 a0001c0002t0003g0056 others(2): Show |
5 | HG01081.hp1 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.633-1289C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99795808 | |||||||
chr10:99795934 | G | C | 1 | a0001c0001t0001g0014 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.633-1163G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99795934 | |||||||
chr10:99795960 | C | G | 325 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(322): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.633-1137C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99795960 | |||||||
chr10:99796112 | C | G | 1 | a0007c0009t0001g0210 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.633-985C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99796112 | |||||||
chr10:99796684 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.633-413C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99796684 | |||||||
chr10:99796695 | C | G | 1 | a0023c0018t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.633-402C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99796695 | |||||||
chr10:99796711 | A | G | 1 | a0023c0018t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.633-386A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99796711 | |||||||
chr10:99796899 | A | C | 5 | a0001c0001t0004g0121 a0001c0002t0003g0041 a0001c0002t0003g0056 others(2): Show |
5 | HG01081.hp1 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.633-198A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99796899 | |||||||
chr10:99797067 | G | T | 3 | a0001c0001t0001g0014 a0005c0008t0001g0013 a0014c0023t0001g0217 |
3 | HG00639.hp2 HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.633-30G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 6/31 | chr10 | 99797067 | |||||||
chr10:99797363 | G | A | 2 | a0001c0002t0003g0090 a0001c0002t0003g0091 |
2 | HG01255.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.867+32G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 7/31 | chr10 | 99797363 | |||||||
chr10:99797441 | G | A | 2 | a0010c0015t0001g0016 a0010c0015t0001g0017 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.867+110G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 7/31 | chr10 | 99797441 | |||||||
chr10:99797479 | A | G | 1 | a0001c0002t0002g0049 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.867+148A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 7/31 | chr10 | 99797479 | |||||||
chr10:99797480 | C | T | 1 | a0023c0018t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.867+149C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 7/31 | chr10 | 99797480 | |||||||
chr10:99797572 | A | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.867+241A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 7/31 | chr10 | 99797572 | |||||||
chr10:99797797 | C | T | 1 | a0001c0002t0002g0074 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.867+466C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 7/31 | chr10 | 99797797 | |||||||
chr10:99798137 | G | A | 1 | a0002c0003t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.867+806G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 7/31 | chr10 | 99798137 | |||||||
chr10:99798521 | G | T | 2 | a0010c0015t0001g0016 a0010c0015t0001g0017 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.868-686G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 7/31 | chr10 | 99798521 | |||||||
chr10:99798526 | G | A | 3 | a0001c0001t0001g0014 a0014c0023t0001g0217 a0020c0024t0001g0015 |
3 | HG00639.hp2 HG02451.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.868-681G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 7/31 | chr10 | 99798526 | |||||||
chr10:99798658 | C | T | 2 | a0010c0015t0001g0016 a0010c0015t0001g0017 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.868-549C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 7/31 | chr10 | 99798658 | |||||||
chr10:99798819 | G | T | 1 | a0001c0002t0003g0032 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.868-388G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 7/31 | chr10 | 99798819 | |||||||
chr10:99798877 | A | T | 97 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0058 others(94): Show |
97 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.868-330A>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 7/31 | chr10 | 99798877 | |||||||
chr10:99798989 | G | T | 154 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0058 others(151): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.868-218G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 7/31 | chr10 | 99798989 | |||||||
chr10:99799094 | G | T | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.868-113G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 7/31 | chr10 | 99799094 | |||||||
chr10:99799401 | A | C | 3 | a0001c0001t0001g0014 a0014c0023t0001g0217 a0020c0024t0001g0015 |
3 | HG00639.hp2 HG02451.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1031+31A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 8/31 | chr10 | 99799401 | |||||||
chr10:99799429 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG00738.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1031+59C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 8/31 | chr10 | 99799429 | |||||||
chr10:99799538 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1031+168G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 8/31 | chr10 | 99799538 | |||||||
chr10:99799554 | A | G | 1 | a0028c0039t0001g0327 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1031+184A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 8/31 | chr10 | 99799554 | |||||||
chr10:99799602 | G | C | 1 | a0006c0010t0001g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1031+232G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 8/31 | chr10 | 99799602 | |||||||
chr10:99799658 | A | G | 322 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1031+288A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 8/31 | chr10 | 99799658 | |||||||
chr10:99799673 | A | G | 1 | a0016c0026t0006g0021 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1031+303A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 8/31 | chr10 | 99799673 | |||||||
chr10:99799908 | G | A | 3 | a0001c0001t0001g0162 a0001c0001t0001g0174 a0026c0025t0001g0158 |
3 | HG00673.hp1 NA18984.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1032-478G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 8/31 | chr10 | 99799908 | |||||||
chr10:99800177 | C | A | 1 | a0001c0002t0003g0124 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1032-209C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 8/31 | chr10 | 99800177 | |||||||
chr10:99800349 | C | A | 3 | a0001c0001t0001g0014 a0014c0023t0001g0217 a0020c0024t0001g0015 |
3 | HG00639.hp2 HG02451.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1032-37C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 8/31 | chr10 | 99800349 | |||||||
chr10:99800778 | T | C | 5 | a0001c0001t0001g0235 a0001c0001t0001g0280 a0001c0001t0001g0284 others(2): Show |
5 | NA18950.hp2 NA18968.hp2 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.1209+215T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | chr10 | 99800778 | |||||||
chr10:99800863 | T | C | 1 | a0005c0008t0001g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1209+300T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | chr10 | 99800863 | |||||||
chr10:99800939 | T | C | 3 | a0001c0001t0001g0014 a0014c0023t0001g0217 a0020c0024t0001g0015 |
3 | HG00639.hp2 HG02451.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1209+376T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | chr10 | 99800939 | |||||||
chr10:99801058 | A | C | 1 | a0001c0002t0007g0131 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1209+495A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | chr10 | 99801058 | |||||||
chr10:99801121 | G | A | 1 | a0001c0027t0001g0147 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1209+558G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | chr10 | 99801121 | |||||||
chr10:99801218 | G | A | 2 | a0011c0012t0001g0215 a0011c0012t0001g0216 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1209+655G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | chr10 | 99801218 | |||||||
chr10:99801231 | T | C | 3 | a0002c0003t0001g0154 a0002c0003t0001g0328 a0022c0020t0001g0309 |
3 | HG03225.hp2 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1209+668T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | chr10 | 99801231 | |||||||
chr10:99801265 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02027.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1209+702C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | chr10 | 99801265 | |||||||
chr10:99801340 | G | C | 8 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0003g0222 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209+777G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | chr10 | 99801340 | |||||||
chr10:99801416 | T | G | 3 | a0001c0001t0001g0014 a0014c0023t0001g0217 a0020c0024t0001g0015 |
3 | HG00639.hp2 HG02451.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1209+853T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | chr10 | 99801416 | |||||||
chr10:99801469 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1209+906G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | chr10 | 99801469 | |||||||
chr10:99801715 | G | A | 1 | a0001c0001t0001g0004 | 2 | NA18970.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1209+1152G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | chr10 | 99801715 | |||||||
chr10:99801716 | T | C | 1 | a0001c0001t0001g0004 | 2 | NA18970.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1209+1153T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | chr10 | 99801716 | |||||||
chr10:99801868 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1209+1305G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | chr10 | 99801868 | |||||||
chr10:99801979 | T | C | 1 | a0001c0002t0003g0059 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1209+1416T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | chr10 | 99801979 | |||||||
chr10:99802216 | C | T | 1 | a0001c0038t0001g0141 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1209+1653C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | chr10 | 99802216 | |||||||
chr10:99802499 | GT | G | 318 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(315): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.1210-1507delT | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr10 | 99802499 | ||||||
chr10:99802512 | T | C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
92 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(89): Show |
intron_variant | MODIFIER | c.1210-1507T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | chr10 | 99802512 | |||||||
chr10:99802867 | A | T | 3 | a0005c0008t0001g0030 a0005c0008t0001g0047 a0005c0008t0001g0077 |
3 | HG00140.hp2 HG01074.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1210-1152A>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | chr10 | 99802867 | |||||||
chr10:99802921 | A | G | 3 | a0001c0002t0002g0053 a0001c0002t0002g0088 a0001c0002t0002g0119 |
3 | NA18945.hp2 NA18995.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1210-1098A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | chr10 | 99802921 | |||||||
chr10:99802942 | T | A | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1210-1077T>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | chr10 | 99802942 | |||||||
chr10:99802989 | G | C | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1210-1030G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | chr10 | 99802989 | |||||||
chr10:99803083 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1210-936C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | chr10 | 99803083 | |||||||
chr10:99803096 | G | C | 240 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(237): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1210-923G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | chr10 | 99803096 | |||||||
chr10:99803710 | G | T | 1 | a0001c0002t0003g0117 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1210-309G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | chr10 | 99803710 | |||||||
chr10:99803912 | A | G | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1210-107A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 9/31 | chr10 | 99803912 | |||||||
chr10:99804516 | C | T | 1 | a0002c0003t0001g0258 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1464+243C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 10/31 | chr10 | 99804516 | |||||||
chr10:99804604 | C | T | 3 | a0001c0001t0001g0014 a0014c0023t0001g0217 a0020c0024t0001g0015 |
3 | HG00639.hp2 HG02451.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1464+331C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 10/31 | chr10 | 99804604 | |||||||
chr10:99804700 | G | A | 1 | a0001c0002t0002g0127 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1464+427G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 10/31 | chr10 | 99804700 | |||||||
chr10:99804769 | T | C | 3 | a0004c0006t0001g0080 a0004c0006t0001g0081 a0004c0006t0001g0096 |
3 | HG02109.hp1 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1464+496T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 10/31 | chr10 | 99804769 | |||||||
chr10:99805141 | T | A | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1465-241T>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 10/31 | chr10 | 99805141 | |||||||
chr10:99805205 | C | T | 1 | a0005c0008t0001g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1465-177C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 10/31 | chr10 | 99805205 | |||||||
chr10:99805553 | G | A | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1530+106G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | chr10 | 99805553 | |||||||
chr10:99805594 | C | A | 2 | a0001c0002t0003g0222 a0001c0002t0003g0274 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1530+147C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | chr10 | 99805594 | |||||||
chr10:99805606 | G | A | 3 | a0001c0001t0001g0014 a0014c0023t0001g0217 a0020c0024t0001g0015 |
3 | HG00639.hp2 HG02451.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1530+159G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | chr10 | 99805606 | |||||||
chr10:99805737 | G | GA | 8 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0003g0222 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1530+292dupA | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr10 | 99805737 | ||||||
chr10:99805900 | G | T | 1 | a0023c0018t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1530+453G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | chr10 | 99805900 | |||||||
chr10:99806071 | C | T | 1 | a0005c0008t0001g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1530+624C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | chr10 | 99806071 | |||||||
chr10:99806073 | C | CTCTCTCT others(3): Show |
1 | a0001c0001t0001g0054 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1530+627_1530+628i others(12): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr10 | 99806073 | ||||||
chr10:99806075 | G | GTCTCTCT others(5): Show |
7 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0003g0222 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1530+631_1530+632i others(14): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr10 | 99806075 | ||||||
chr10:99806077 | C | CTCTCTCT others(9): Show |
1 | a0001c0001t0001g0014 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1530+631_1530+632i others(18): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr10 | 99806077 | ||||||
chr10:99806077 | C | CTCTCTGT others(7): Show |
1 | a0001c0014t0001g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1530+631_1530+632i others(16): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr10 | 99806077 | ||||||
chr10:99806077 | C | CTCTG | 6 | a0001c0002t0002g0053 a0001c0002t0002g0088 a0001c0002t0002g0098 others(3): Show |
6 | HG02451.hp1 HG03942.hp2 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.1530+631_1530+632i others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr10 | 99806077 | ||||||
chr10:99806077 | C | CTCTGTG | 6 | a0001c0001t0001g0058 a0001c0002t0002g0048 a0001c0002t0002g0060 others(3): Show |
6 | HG01517.hp1 HG03471.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1530+631_1530+632i others(8): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr10 | 99806077 | ||||||
chr10:99806077 | C | CTCTGTGT others(1): Show |
70 | a0001c0001t0001g0062 a0001c0001t0004g0121 a0001c0002t0002g0034 others(67): Show |
70 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1530+631_1530+632i others(10): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr10 | 99806077 | ||||||
chr10:99806077 | C | CTCTGTGT others(3): Show |
12 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0002t0002g0037 others(9): Show |
12 | HG00621.hp1 HG01169.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1530+631_1530+632i others(12): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr10 | 99806077 | ||||||
chr10:99806077 | C | CTCTGTGT others(5): Show |
7 | a0001c0001t0001g0118 a0001c0002t0002g0078 a0001c0002t0002g0127 others(4): Show |
7 | HG00544.hp1 HG01928.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1530+631_1530+632i others(14): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr10 | 99806077 | ||||||
chr10:99806077 | C | CTCTGTGT others(7): Show |
2 | a0001c0002t0002g0057 a0004c0006t0001g0081 |
2 | HG00673.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1530+631_1530+632i others(16): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr10 | 99806077 | ||||||
chr10:99806077 | C | CTCTGTGT others(9): Show |
1 | a0014c0023t0001g0217 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1530+631_1530+632i others(18): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr10 | 99806077 | ||||||
chr10:99806077 | C | CTCTGTGT others(11): Show |
2 | a0001c0002t0002g0079 a0001c0002t0002g0094 |
2 | HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1530+631_1530+632i others(20): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr10 | 99806077 | ||||||
chr10:99806077 | C | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG00738.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1530+630C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | chr10 | 99806077 | |||||||
chr10:99806077 | CTG | C | 11 | a0001c0001t0001g0161 a0001c0001t0001g0205 a0001c0001t0001g0206 others(8): Show |
11 | HG01884.hp2 HG02683.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.1530+664_1530+665d others(4): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr10 | 99806077 | ||||||
chr10:99806077 | CTGTG | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(144): Show |
153 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.1530+662_1530+665d others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr10 | 99806077 | ||||||
chr10:99806077 | CTGTGTG | C | 48 | a0001c0001t0001g0231 a0002c0003t0001g0006 a0002c0003t0001g0137 others(45): Show |
49 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.1530+660_1530+665d others(8): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr10 | 99806077 | ||||||
chr10:99806083 | G | C | 2 | a0001c0002t0002g0097 a0004c0029t0001g0329 |
2 | HG00733.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1530+636G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | chr10 | 99806083 | |||||||
chr10:99806085 | G | C | 2 | a0004c0029t0001g0329 a0020c0024t0001g0015 |
2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1530+638G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | chr10 | 99806085 | |||||||
chr10:99806087 | G | C | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1530+640G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | chr10 | 99806087 | |||||||
chr10:99806217 | C | T | 322 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1530+770C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | chr10 | 99806217 | |||||||
chr10:99806245 | G | A | 1 | a0001c0002t0002g0092 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1530+798G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | chr10 | 99806245 | |||||||
chr10:99806253 | C | T | 44 | a0001c0001t0001g0231 a0002c0003t0001g0006 a0002c0003t0001g0137 others(41): Show |
45 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.1530+806C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | chr10 | 99806253 | |||||||
chr10:99806275 | A | G | 2 | a0001c0001t0001g0118 a0023c0018t0001g0009 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1530+828A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | chr10 | 99806275 | |||||||
chr10:99806284 | G | A | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1530+837G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | chr10 | 99806284 | |||||||
chr10:99806422 | A | G | 322 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1531-962A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | chr10 | 99806422 | |||||||
chr10:99806511 | A | C | 6 | a0001c0001t0001g0260 a0001c0001t0001g0320 a0001c0001t0001g0321 others(3): Show |
6 | HG00642.hp1 HG00741.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.1531-873A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | chr10 | 99806511 | |||||||
chr10:99806530 | T | C | 1 | a0002c0003t0001g0248 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1531-854T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | chr10 | 99806530 | |||||||
chr10:99807109 | T | A | 24 | a0002c0003t0001g0006 a0002c0003t0001g0137 a0002c0003t0001g0138 others(21): Show |
25 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.1531-275T>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | chr10 | 99807109 | |||||||
chr10:99807560 | G | C | 1 | a0024c0033t0003g0082 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1668+39G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 12/31 | chr10 | 99807560 | |||||||
chr10:99807657 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1668+136C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 12/31 | chr10 | 99807657 | |||||||
chr10:99807669 | A | G | 121 | a0001c0001t0001g0014 a0001c0001t0001g0054 a0001c0001t0001g0055 others(118): Show |
121 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.1668+148A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 12/31 | chr10 | 99807669 | |||||||
chr10:99807744 | C | A | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1668+223C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 12/31 | chr10 | 99807744 | |||||||
chr10:99807765 | A | G | 1 | a0001c0001t0001g0005 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1668+244A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 12/31 | chr10 | 99807765 | |||||||
chr10:99807863 | A | C | 2 | a0001c0001t0001g0118 a0023c0018t0001g0009 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1669-220A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 12/31 | chr10 | 99807863 | |||||||
chr10:99807915 | G | A | 2 | a0001c0001t0001g0118 a0023c0018t0001g0009 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1669-168G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 12/31 | chr10 | 99807915 | |||||||
chr10:99807961 | C | T | 1 | a0001c0001t0001g0208 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1669-122C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 12/31 | chr10 | 99807961 | |||||||
chr10:99807965 | G | C | 1 | a0001c0002t0002g0074 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1669-118G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 12/31 | chr10 | 99807965 | |||||||
chr10:99808256 | C | G | 2 | a0001c0001t0001g0118 a0023c0018t0001g0009 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1815+27C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 13/31 | chr10 | 99808256 | |||||||
chr10:99808405 | C | T | 1 | a0001c0001t0001g0308 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1815+176C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 13/31 | chr10 | 99808405 | |||||||
chr10:99808543 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1815+314C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 13/31 | chr10 | 99808543 | |||||||
chr10:99808677 | A | G | 3 | a0001c0001t0001g0014 a0014c0023t0001g0217 a0020c0024t0001g0015 |
3 | HG00639.hp2 HG02451.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1815+448A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 13/31 | chr10 | 99808677 | |||||||
chr10:99809075 | T | TG | 3 | a0001c0001t0001g0169 a0001c0001t0001g0175 a0001c0001t0001g0179 |
3 | HG01928.hp1 HG01943.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1815+848dupG | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr10 | 99809075 | ||||||
chr10:99809156 | C | A | 68 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0134 others(65): Show |
70 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1815+927C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 13/31 | chr10 | 99809156 | |||||||
chr10:99809446 | C | A | 2 | a0001c0001t0001g0014 a0014c0023t0001g0217 |
2 | HG00639.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1816-688C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 13/31 | chr10 | 99809446 | |||||||
chr10:99809559 | T | G | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1816-575T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 13/31 | chr10 | 99809559 | |||||||
chr10:99809578 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1816-556T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 13/31 | chr10 | 99809578 | |||||||
chr10:99809614 | T | C | 322 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1816-520T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 13/31 | chr10 | 99809614 | |||||||
chr10:99809692 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1816-442G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 13/31 | chr10 | 99809692 | |||||||
chr10:99809726 | T | C | 121 | a0001c0001t0001g0014 a0001c0001t0001g0054 a0001c0001t0001g0055 others(118): Show |
121 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.1816-408T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 13/31 | chr10 | 99809726 | |||||||
chr10:99809761 | G | C | 1 | a0001c0002t0002g0037 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1816-373G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 13/31 | chr10 | 99809761 | |||||||
chr10:99809802 | G | A | 8 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0003g0222 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1816-332G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 13/31 | chr10 | 99809802 | |||||||
chr10:99809826 | C | T | 2 | a0001c0001t0001g0236 a0001c0001t0001g0307 |
2 | NA18953.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1816-308C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 13/31 | chr10 | 99809826 | |||||||
chr10:99809915 | A | G | 8 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0003g0222 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1816-219A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 13/31 | chr10 | 99809915 | |||||||
chr10:99810240 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1900+22T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 14/31 | chr10 | 99810240 | |||||||
chr10:99810468 | A | G | 3 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 |
3 | NA18948.hp2 NA18978.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1900+250A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 14/31 | chr10 | 99810468 | |||||||
chr10:99810499 | G | A | 1 | a0016c0026t0006g0021 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1900+281G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 14/31 | chr10 | 99810499 | |||||||
chr10:99810548 | G | C | 4 | a0001c0001t0001g0164 a0007c0009t0001g0157 a0007c0009t0001g0163 others(1): Show |
4 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1900+330G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 14/31 | chr10 | 99810548 | |||||||
chr10:99810671 | T | A | 3 | a0001c0001t0001g0014 a0014c0023t0001g0217 a0020c0024t0001g0015 |
3 | HG00639.hp2 HG02451.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1900+453T>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 14/31 | chr10 | 99810671 | |||||||
chr10:99810752 | C | T | 2 | a0001c0001t0001g0118 a0023c0018t0001g0009 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1900+534C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 14/31 | chr10 | 99810752 | |||||||
chr10:99810790 | C | T | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1900+572C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 14/31 | chr10 | 99810790 | |||||||
chr10:99811109 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1901-427T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 14/31 | chr10 | 99811109 | |||||||
chr10:99811187 | G | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0213 |
3 | HG01255.hp1 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1901-349G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 14/31 | chr10 | 99811187 | |||||||
chr10:99811208 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1901-328G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 14/31 | chr10 | 99811208 | |||||||
chr10:99811236 | C | A | 220 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(217): Show |
227 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.1901-300C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 14/31 | chr10 | 99811236 | |||||||
chr10:99811258 | A | G | 1 | a0001c0001t0004g0121 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1901-278A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 14/31 | chr10 | 99811258 | |||||||
chr10:99811685 | G | A | 2 | a0001c0014t0001g0023 a0004c0006t0001g0022 |
2 | HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1967+83G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 15/31 | chr10 | 99811685 | |||||||
chr10:99811771 | C | T | 206 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(203): Show |
213 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.1967+169C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 15/31 | chr10 | 99811771 | |||||||
chr10:99811907 | C | T | 3 | a0001c0001t0001g0118 a0002c0003t0001g0138 a0023c0018t0001g0009 |
3 | HG03130.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1967+305C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 15/31 | chr10 | 99811907 | |||||||
chr10:99812098 | A | C | 4 | a0001c0001t0001g0260 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG00642.hp1 HG00741.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.1967+496A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 15/31 | chr10 | 99812098 | |||||||
chr10:99812259 | C | A | 8 | a0003c0004t0001g0001 a0003c0004t0001g0146 a0003c0004t0001g0165 others(5): Show |
10 | HG01358.hp2 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1967+657C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 15/31 | chr10 | 99812259 | |||||||
chr10:99812444 | G | A | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1968-574G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 15/31 | chr10 | 99812444 | |||||||
chr10:99812586 | A | C | 86 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(83): Show |
90 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.1968-432A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 15/31 | chr10 | 99812586 | |||||||
chr10:99812655 | C | G | 1 | a0001c0001t0001g0214 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1968-363C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 15/31 | chr10 | 99812655 | |||||||
chr10:99812699 | G | A | 8 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0003g0222 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1968-319G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 15/31 | chr10 | 99812699 | |||||||
chr10:99813269 | G | A | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2094+125G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99813269 | |||||||
chr10:99813394 | G | A | 1 | a0023c0018t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2094+250G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99813394 | |||||||
chr10:99813426 | G | A | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2094+282G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99813426 | |||||||
chr10:99813709 | C | CA | 8 | a0001c0001t0001g0262 a0001c0002t0003g0132 a0001c0002t0003g0133 others(5): Show |
8 | HG02818.hp1 HG02886.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.2094+577dupA | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99813709 | ||||||
chr10:99813802 | G | C | 2 | a0001c0002t0002g0039 a0001c0002t0002g0060 |
2 | NA18987.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2094+658G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99813802 | |||||||
chr10:99813894 | A | ATAT | 8 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0003g0222 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2094+751_2094+753d others(5): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99813894 | ||||||
chr10:99813973 | T | C | 13 | a0001c0001t0001g0118 a0001c0002t0003g0132 a0001c0002t0003g0133 others(10): Show |
13 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.2094+829T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99813973 | |||||||
chr10:99813986 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2094+842T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99813986 | |||||||
chr10:99814073 | A | G | 5 | a0005c0008t0001g0030 a0005c0008t0001g0047 a0005c0008t0001g0077 others(2): Show |
5 | HG00140.hp2 HG01074.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.2094+929A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814073 | |||||||
chr10:99814077 | G | GTATGTGT others(23): Show |
6 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0007g0128 others(3): Show |
6 | HG02818.hp1 HG02886.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2094+961_2094+962i others(32): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814077 | ||||||
chr10:99814083 | GTATATAC others(5): Show |
G | 1 | a0018c0040t0002g0099 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2094+950_2094+961d others(14): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814083 | ||||||
chr10:99814088 | T | TAC | 119 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0134 others(116): Show |
122 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.2094+948_2094+949d others(4): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814088 | ||||||
chr10:99814094 | T | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(84): Show |
91 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.2094+950T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814094 | |||||||
chr10:99814095 | ATATATAC others(11): Show |
A | 1 | a0001c0002t0002g0122 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2094+971_2094+988d others(20): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814095 | ||||||
chr10:99814106 | C | T | 217 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(214): Show |
224 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.2094+962C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814106 | |||||||
chr10:99814109 | A | G | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2094+965A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814109 | |||||||
chr10:99814115 | A | G | 1 | a0001c0002t0003g0070 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2094+971A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814115 | |||||||
chr10:99814120 | C | CACATATA others(3): Show |
1 | a0014c0023t0001g0217 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2094+979_2094+980i others(12): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814120 | ||||||
chr10:99814126 | T | C | 2 | a0001c0001t0001g0183 a0014c0023t0001g0217 |
2 | HG00639.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.2094+982T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814126 | |||||||
chr10:99814127 | A | G | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2094+983A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814127 | |||||||
chr10:99814129 | G | A | 3 | a0001c0001t0001g0118 a0004c0029t0001g0329 a0014c0023t0001g0217 |
3 | HG00639.hp2 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2094+985G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814129 | |||||||
chr10:99814131 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2094+987G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814131 | |||||||
chr10:99814132 | T | TGTATATA others(5): Show |
3 | a0001c0001t0001g0149 a0001c0001t0001g0159 a0001c0001t0001g0161 |
3 | HG01884.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2094+989_2094+1000 others(15): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814132 | ||||||
chr10:99814132 | TGTATATA others(23): Show |
T | 1 | a0004c0006t0001g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2094+1019_2094+104 others(34): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814132 | ||||||
chr10:99814133 | G | A | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2094+989G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814133 | |||||||
chr10:99814135 | A | G | 1 | a0023c0018t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2094+991A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814135 | |||||||
chr10:99814138 | T | C | 1 | a0001c0001t0001g0183 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2094+994T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814138 | |||||||
chr10:99814140 | T | C | 2 | a0001c0001t0001g0183 a0014c0023t0001g0217 |
2 | HG00639.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.2094+996T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814140 | |||||||
chr10:99814140 | TACACACA others(11): Show |
T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0205 a0001c0001t0001g0206 others(7): Show |
11 | HG02055.hp2 HG03942.hp1 NA18940.hp1 others(8): Show |
intron_variant | MODIFIER | c.2094+1001_2094+101 others(22): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814140 | ||||||
chr10:99814142 | C | T | 2 | a0002c0003t0001g0154 a0004c0029t0001g0329 |
2 | HG02055.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2094+998C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814142 | |||||||
chr10:99814144 | CACAT | C | 185 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(182): Show |
191 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.2094+1001_2094+100 others(8): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814144 | |||||||
chr10:99814144 | CACATGTA others(63): Show |
C | 1 | a0001c0001t0001g0183 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2094+1001_2094+107 others(74): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814144 | |||||||
chr10:99814146 | C | T | 1 | a0014c0023t0001g0217 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2094+1002C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814146 | |||||||
chr10:99814147 | A | ATATG | 3 | a0001c0001t0001g0149 a0001c0001t0001g0159 a0001c0001t0001g0161 |
3 | HG01884.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2094+1004_2094+100 others(8): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814147 | ||||||
chr10:99814147 | A | G | 2 | a0001c0001t0001g0173 a0002c0003t0001g0154 |
2 | HG03579.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.2094+1003A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814147 | |||||||
chr10:99814148 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2094+1004T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814148 | |||||||
chr10:99814149 | G | A | 7 | a0001c0001t0001g0014 a0002c0003t0001g0154 a0005c0008t0001g0030 others(4): Show |
7 | HG00140.hp2 HG01074.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.2094+1005G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814149 | |||||||
chr10:99814151 | A | G | 9 | a0001c0001t0001g0149 a0001c0001t0001g0159 a0001c0001t0001g0161 others(6): Show |
9 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.2094+1007A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814151 | |||||||
chr10:99814153 | G | A | 191 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(188): Show |
197 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.2094+1009G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814153 | |||||||
chr10:99814153 | G | GTATACAC others(7): Show |
2 | a0001c0002t0002g0065 a0001c0002t0002g0069 |
2 | NA18992.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.2094+1019_2094+103 others(18): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814153 | ||||||
chr10:99814154 | TATACACA others(1): Show |
T | 5 | a0005c0008t0001g0030 a0005c0008t0001g0047 a0005c0008t0001g0077 others(2): Show |
5 | HG00140.hp2 HG01074.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.2094+1011_2094+101 others(12): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814154 | |||||||
chr10:99814156 | T | C | 2 | a0001c0001t0001g0173 a0002c0003t0001g0154 |
2 | HG03579.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.2094+1012T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814156 | |||||||
chr10:99814158 | C | T | 3 | a0001c0001t0001g0149 a0001c0001t0001g0159 a0001c0001t0001g0161 |
3 | HG01884.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2094+1014C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814158 | |||||||
chr10:99814162 | C | CAT | 117 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0134 others(114): Show |
120 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.2094+1018_2094+101 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814162 | |||||||
chr10:99814162 | C | CATAT | 62 | a0001c0001t0001g0002 a0001c0001t0001g0139 a0001c0001t0001g0142 others(59): Show |
65 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.2094+1018_2094+101 others(8): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814162 | |||||||
chr10:99814162 | C | CATATGT | 7 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0148 others(4): Show |
7 | HG01255.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2094+1018_2094+101 others(10): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814162 | |||||||
chr10:99814162 | C | T | 2 | a0001c0001t0001g0173 a0002c0003t0001g0154 |
2 | HG03579.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.2094+1018C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814162 | |||||||
chr10:99814162 | CGTATATA others(27): Show |
C | 1 | a0001c0002t0002g0125 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2094+1037_2094+107 others(38): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814162 | ||||||
chr10:99814165 | A | G | 70 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0139 others(67): Show |
73 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.2094+1021A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814165 | |||||||
chr10:99814167 | A | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(179): Show |
188 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.2094+1023A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814167 | |||||||
chr10:99814172 | C | T | 69 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0139 others(66): Show |
72 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.2094+1028C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814172 | |||||||
chr10:99814174 | C | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0139 a0001c0001t0001g0142 others(60): Show |
66 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.2094+1030C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814174 | |||||||
chr10:99814176 | C | CAT | 3 | a0001c0001t0001g0149 a0001c0001t0001g0159 a0001c0001t0001g0161 |
3 | HG01884.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2094+1033_2094+103 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814176 | ||||||
chr10:99814177 | A | G | 6 | a0001c0001t0001g0007 a0001c0001t0001g0148 a0001c0001t0001g0213 others(3): Show |
6 | HG01255.hp1 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+1033A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814177 | |||||||
chr10:99814177 | ATG | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0205 a0001c0001t0001g0206 others(7): Show |
11 | HG02055.hp2 HG03942.hp1 NA18940.hp1 others(8): Show |
intron_variant | MODIFIER | c.2094+1035_2094+103 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814177 | ||||||
chr10:99814178 | T | C | 70 | a0001c0001t0001g0002 a0001c0001t0001g0139 a0001c0001t0001g0142 others(67): Show |
73 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.2094+1034T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814178 | |||||||
chr10:99814179 | G | A | 11 | a0001c0001t0001g0007 a0001c0001t0001g0148 a0001c0001t0001g0213 others(8): Show |
11 | HG00140.hp2 HG01074.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.2094+1035G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814179 | |||||||
chr10:99814180 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2094+1036T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814180 | |||||||
chr10:99814181 | A | G | 8 | a0001c0001t0001g0149 a0001c0001t0001g0159 a0001c0001t0001g0161 others(5): Show |
8 | HG00140.hp2 HG01074.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.2094+1037A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814181 | |||||||
chr10:99814183 | G | A | 70 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(67): Show |
73 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.2094+1039G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814183 | |||||||
chr10:99814183 | G | GTATACAC others(11): Show |
6 | a0001c0002t0002g0098 a0001c0002t0002g0100 a0001c0002t0002g0101 others(3): Show |
6 | HG01106.hp1 HG01167.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2094+1079_2094+109 others(22): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814183 | ||||||
chr10:99814183 | G | GTATACAC others(29): Show |
1 | a0001c0035t0002g0046 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2094+1061_2094+109 others(40): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814183 | ||||||
chr10:99814183 | GTATACAC others(3): Show |
G | 10 | a0001c0001t0001g0008 a0001c0001t0001g0205 a0001c0001t0001g0206 others(7): Show |
11 | HG02055.hp2 HG03942.hp1 NA18940.hp1 others(8): Show |
intron_variant | MODIFIER | c.2094+1041_2094+105 others(14): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814183 | ||||||
chr10:99814183 | GTATACAC others(11): Show |
G | 8 | a0001c0002t0002g0042 a0001c0002t0002g0045 a0001c0002t0002g0057 others(5): Show |
8 | HG00673.hp2 HG01255.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2094+1079_2094+109 others(22): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814183 | ||||||
chr10:99814186 | T | C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0148 a0001c0001t0001g0213 others(3): Show |
6 | HG01255.hp1 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+1042T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814186 | |||||||
chr10:99814187 | A | G | 1 | a0002c0021t0003g0257 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2094+1043A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814187 | |||||||
chr10:99814188 | C | CACACGTA others(5): Show |
1 | a0001c0002t0002g0122 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2094+1048_2094+104 others(16): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814188 | ||||||
chr10:99814188 | C | T | 8 | a0001c0001t0001g0149 a0001c0001t0001g0159 a0001c0001t0001g0161 others(5): Show |
8 | HG00140.hp2 HG01074.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.2094+1044C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814188 | |||||||
chr10:99814190 | C | T | 9 | a0001c0001t0001g0149 a0001c0001t0001g0159 a0001c0001t0001g0161 others(6): Show |
9 | HG00140.hp2 HG01070.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.2094+1046C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814190 | |||||||
chr10:99814192 | C | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0148 a0001c0001t0001g0213 others(3): Show |
6 | HG01255.hp1 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+1048C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814192 | |||||||
chr10:99814192 | CAT | C | 5 | a0002c0003t0001g0006 a0002c0003t0001g0289 a0002c0003t0001g0311 others(2): Show |
6 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.2094+1049_2094+105 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814192 | |||||||
chr10:99814193 | A | G | 1 | a0002c0003t0001g0250 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2094+1049A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814193 | |||||||
chr10:99814193 | ATG | A | 6 | a0001c0001t0001g0118 a0005c0008t0001g0030 a0005c0008t0001g0047 others(3): Show |
6 | HG00140.hp2 HG01074.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+1053_2094+105 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814193 | ||||||
chr10:99814194 | T | C | 4 | a0001c0001t0001g0149 a0001c0001t0001g0159 a0001c0001t0001g0161 others(1): Show |
4 | HG00544.hp2 HG01884.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2094+1050T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814194 | |||||||
chr10:99814195 | G | A | 1 | a0001c0002t0002g0122 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2094+1051G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814195 | |||||||
chr10:99814196 | T | C | 5 | a0005c0008t0001g0030 a0005c0008t0001g0047 a0005c0008t0001g0077 others(2): Show |
5 | HG00140.hp2 HG01074.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.2094+1052T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814196 | |||||||
chr10:99814196 | TGTATATA others(45): Show |
T | 1 | a0002c0003t0001g0256 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2094+1057_2094+110 others(56): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814196 | ||||||
chr10:99814197 | G | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0139 others(64): Show |
70 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.2094+1053G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814197 | |||||||
chr10:99814197 | G | T | 5 | a0005c0008t0001g0030 a0005c0008t0001g0047 a0005c0008t0001g0077 others(2): Show |
5 | HG00140.hp2 HG01074.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.2094+1053G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814197 | |||||||
chr10:99814199 | A | G | 70 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(67): Show |
73 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.2094+1055A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814199 | |||||||
chr10:99814201 | A | G | 3 | a0001c0002t0002g0122 a0004c0029t0001g0329 a0023c0018t0001g0009 |
3 | HG00544.hp2 HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2094+1057A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814201 | |||||||
chr10:99814201 | ATATACAC others(73): Show |
A | 6 | a0001c0001t0001g0218 a0001c0001t0005g0282 a0001c0001t0005g0283 others(3): Show |
6 | HG02896.hp1 HG02897.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2094+1068_2094+114 others(84): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814201 | ||||||
chr10:99814204 | T | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0139 others(64): Show |
70 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.2094+1060T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814204 | |||||||
chr10:99814206 | C | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0148 a0001c0001t0001g0213 others(3): Show |
6 | HG01255.hp1 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+1062C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814206 | |||||||
chr10:99814206 | CACACATG others(43): Show |
C | 45 | a0001c0001t0001g0144 a0001c0001t0001g0202 a0001c0001t0001g0203 others(42): Show |
46 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.2094+1068_2094+111 others(54): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814206 | ||||||
chr10:99814206 | CACACATG others(57): Show |
C | 65 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0134 others(62): Show |
67 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.2094+1068_2094+113 others(68): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814206 | ||||||
chr10:99814208 | C | T | 5 | a0001c0014t0001g0023 a0004c0006t0001g0022 a0004c0006t0001g0080 others(2): Show |
5 | HG02109.hp1 HG02622.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2094+1064C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814208 | |||||||
chr10:99814208 | CACATGT | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0205 a0001c0001t0001g0206 others(7): Show |
11 | HG02055.hp2 HG03942.hp1 NA18940.hp1 others(8): Show |
intron_variant | MODIFIER | c.2094+1065_2094+107 others(10): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814208 | |||||||
chr10:99814210 | C | T | 3 | a0001c0001t0001g0149 a0001c0001t0001g0159 a0001c0001t0001g0161 |
3 | HG01884.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2094+1066C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814210 | |||||||
chr10:99814210 | CATGT | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0139 others(74): Show |
80 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.2094+1067_2094+107 others(8): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814210 | |||||||
chr10:99814211 | A | G | 2 | a0001c0001t0001g0118 a0004c0029t0001g0329 |
2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2094+1067A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814211 | |||||||
chr10:99814211 | ATG | A | 4 | a0005c0008t0001g0030 a0005c0008t0001g0047 a0006c0010t0001g0010 others(1): Show |
4 | HG00140.hp2 HG01074.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2094+1071_2094+107 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814211 | ||||||
chr10:99814212 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0308 |
2 | HG02486.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.2094+1068T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814212 | |||||||
chr10:99814213 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0118 |
2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2094+1069G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814213 | |||||||
chr10:99814214 | TGTATATA others(85): Show |
T | 1 | a0001c0001t0001g0308 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2094+1071_2094+116 others(96): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814214 | |||||||
chr10:99814217 | A | G | 3 | a0001c0001t0001g0149 a0001c0001t0001g0159 a0001c0001t0001g0161 |
3 | HG01884.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2094+1073A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814217 | |||||||
chr10:99814219 | A | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0139 others(76): Show |
82 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.2094+1075A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814219 | |||||||
chr10:99814219 | ATATACAC others(41): Show |
A | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2094+1085_2094+113 others(52): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814219 | ||||||
chr10:99814221 | A | G | 1 | a0014c0023t0001g0217 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2094+1077A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814221 | |||||||
chr10:99814222 | TACACACA others(57): Show |
T | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2094+1085_2094+114 others(68): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814222 | ||||||
chr10:99814223 | A | G | 5 | a0001c0002t0003g0020 a0001c0002t0006g0018 a0001c0002t0006g0019 others(2): Show |
5 | HG00642.hp2 HG01070.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2094+1079A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814223 | |||||||
chr10:99814224 | C | T | 4 | a0001c0001t0001g0149 a0001c0001t0001g0159 a0001c0001t0001g0161 others(1): Show |
4 | HG00639.hp2 HG01884.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2094+1080C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814224 | |||||||
chr10:99814225 | A | G | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2094+1081A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814225 | |||||||
chr10:99814228 | CATGT | C | 3 | a0001c0001t0001g0149 a0001c0001t0001g0159 a0001c0001t0001g0161 |
3 | HG01884.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2094+1085_2094+108 others(8): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814228 | |||||||
chr10:99814229 | ATG | A | 15 | a0001c0001t0001g0007 a0001c0001t0001g0148 a0001c0001t0001g0205 others(12): Show |
16 | HG01255.hp1 HG02055.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.2094+1089_2094+109 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814229 | ||||||
chr10:99814230 | T | C | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2094+1086T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814230 | |||||||
chr10:99814233 | G | A | 9 | a0001c0001t0001g0008 a0001c0002t0003g0132 a0001c0002t0003g0133 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.2094+1089G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814233 | |||||||
chr10:99814235 | A | G | 9 | a0001c0001t0001g0008 a0001c0002t0003g0132 a0001c0002t0003g0133 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.2094+1091A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814235 | |||||||
chr10:99814237 | A | G | 16 | a0001c0001t0001g0007 a0001c0001t0001g0148 a0001c0001t0001g0205 others(13): Show |
17 | HG01255.hp1 HG02055.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.2094+1093A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814237 | |||||||
chr10:99814240 | T | C | 8 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0003g0222 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2094+1096T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814240 | |||||||
chr10:99814240 | TGC | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0186 a0001c0001t0001g0188 others(1): Show |
4 | HG01074.hp1 HG02486.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.2094+1097_2094+109 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814240 | |||||||
chr10:99814241 | G | A | 96 | a0001c0001t0001g0002 a0001c0001t0001g0139 a0001c0001t0001g0142 others(93): Show |
100 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.2094+1097G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814241 | |||||||
chr10:99814241 | GCA | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0055 |
3 | HG00738.hp1 HG01516.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.2094+1103_2094+110 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814241 | ||||||
chr10:99814242 | CACACACG others(7): Show |
C | 1 | a0001c0002t0003g0041 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2094+1133_2094+114 others(18): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814242 | ||||||
chr10:99814246 | C | T | 8 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0003g0222 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2094+1102C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814246 | |||||||
chr10:99814247 | A | G | 8 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0003g0222 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2094+1103A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814247 | |||||||
chr10:99814248 | C | T | 17 | a0001c0001t0001g0149 a0001c0001t0001g0159 a0001c0001t0001g0161 others(14): Show |
17 | HG00140.hp2 HG00639.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.2094+1104C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814248 | |||||||
chr10:99814250 | TATGTATA others(5): Show |
T | 1 | a0014c0023t0001g0217 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2094+1107_2094+111 others(16): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814250 | |||||||
chr10:99814251 | A | G | 5 | a0005c0008t0001g0030 a0005c0008t0001g0047 a0005c0008t0001g0077 others(2): Show |
5 | HG00140.hp2 HG01074.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.2094+1107A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814251 | |||||||
chr10:99814253 | G | A | 13 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0003g0222 others(10): Show |
13 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.2094+1109G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814253 | |||||||
chr10:99814256 | T | TAC | 5 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0197 others(2): Show |
5 | HG01109.hp1 HG01884.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.2094+1117_2094+111 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814256 | ||||||
chr10:99814256 | T | TACACACA others(29): Show |
1 | a0001c0001t0001g0149 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2094+1118_2094+111 others(40): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814256 | ||||||
chr10:99814256 | T | TACACACA others(13): Show |
5 | a0001c0001t0001g0148 a0001c0001t0001g0213 a0001c0001t0001g0223 others(2): Show |
5 | HG01255.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2094+1118_2094+111 others(24): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814256 | ||||||
chr10:99814257 | ACACACGT others(3): Show |
A | 4 | a0005c0008t0001g0047 a0005c0008t0001g0077 a0006c0010t0001g0010 others(1): Show |
4 | HG00140.hp2 HG02300.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2094+1114_2094+112 others(14): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814257 | |||||||
chr10:99814258 | CACACGTA others(5): Show |
C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0139 a0001c0001t0001g0142 others(58): Show |
64 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.2094+1119_2094+113 others(16): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814258 | ||||||
chr10:99814263 | G | A | 11 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0205 others(8): Show |
12 | HG02055.hp2 HG03654.hp2 HG03942.hp1 others(9): Show |
intron_variant | MODIFIER | c.2094+1119G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814263 | |||||||
chr10:99814265 | A | G | 11 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0205 others(8): Show |
12 | HG02055.hp2 HG03654.hp2 HG03942.hp1 others(9): Show |
intron_variant | MODIFIER | c.2094+1121A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814265 | |||||||
chr10:99814267 | G | A | 4 | a0004c0029t0001g0329 a0005c0008t0001g0030 a0014c0023t0001g0217 others(1): Show |
4 | HG00639.hp2 HG01074.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.2094+1123G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814267 | |||||||
chr10:99814270 | T | C | 14 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0003g0222 others(11): Show |
14 | HG00140.hp2 HG01074.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.2094+1126T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814270 | |||||||
chr10:99814270 | T | TAC | 57 | a0001c0001t0001g0144 a0001c0001t0001g0148 a0001c0001t0001g0149 others(54): Show |
58 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.2094+1131_2094+113 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814270 | ||||||
chr10:99814270 | T | TATATAC | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0005t0001g0003 others(4): Show |
8 | HG02055.hp2 HG03654.hp2 HG03942.hp1 others(5): Show |
intron_variant | MODIFIER | c.2094+1127_2094+112 others(10): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814270 | ||||||
chr10:99814270 | TACACACG others(9): Show |
T | 1 | a0001c0002t0003g0032 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2094+1148_2094+116 others(20): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814270 | ||||||
chr10:99814271 | ACACACGT others(3): Show |
A | 4 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0208 others(1): Show |
4 | NA18940.hp1 NA18971.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.2094+1128_2094+113 others(14): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814271 | |||||||
chr10:99814276 | C | CAT | 8 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0003g0222 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2094+1132_2094+113 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814276 | |||||||
chr10:99814277 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2094+1133G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814277 | |||||||
chr10:99814279 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2094+1135A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814279 | |||||||
chr10:99814281 | G | A | 9 | a0001c0001t0001g0014 a0001c0002t0003g0132 a0001c0002t0003g0133 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2094+1137G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814281 | |||||||
chr10:99814286 | C | CACACATG others(7): Show |
3 | a0001c0001t0001g0197 a0001c0001t0001g0211 a0007c0009t0001g0157 |
3 | HG01109.hp1 HG03490.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2094+1147_2094+114 others(18): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814286 | ||||||
chr10:99814286 | C | CACACATG others(97): Show |
1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2094+1147_2094+114 others(108): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814286 | ||||||
chr10:99814286 | C | T | 2 | a0001c0001t0001g0014 a0023c0018t0001g0009 |
2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2094+1142C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814286 | |||||||
chr10:99814292 | C | T | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2094+1148C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814292 | |||||||
chr10:99814297 | G | A | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2094+1153G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814297 | |||||||
chr10:99814302 | CACACATG others(5): Show |
C | 1 | a0002c0003t0001g0251 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2094+1164_2094+117 others(16): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814302 | ||||||
chr10:99814304 | C | T | 41 | a0002c0003t0001g0006 a0002c0003t0001g0137 a0002c0003t0001g0138 others(38): Show |
42 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.2094+1160C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814304 | |||||||
chr10:99814306 | C | CACGT | 4 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0208 others(1): Show |
4 | NA18940.hp1 NA18971.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.2094+1163_2094+116 others(8): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814306 | ||||||
chr10:99814309 | G | GTA | 210 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(207): Show |
217 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.2094+1170_2094+117 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814309 | ||||||
chr10:99814309 | G | GTATATAC others(23): Show |
1 | a0001c0002t0002g0037 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2094+1206_2094+123 others(34): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814309 | ||||||
chr10:99814309 | GTATATAC others(23): Show |
G | 2 | a0001c0002t0002g0063 a0001c0002t0003g0036 |
2 | HG03098.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.2094+1206_2094+123 others(34): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814309 | ||||||
chr10:99814314 | T | C | 4 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0208 others(1): Show |
4 | NA18940.hp1 NA18971.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.2094+1170T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814314 | |||||||
chr10:99814314 | T | TATAC | 4 | a0002c0003t0001g0230 a0002c0003t0001g0243 a0002c0003t0001g0253 others(1): Show |
4 | HG02004.hp1 HG02148.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.2094+1171_2094+117 others(8): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814314 | ||||||
chr10:99814315 | A | G | 1 | a0001c0002t0003g0111 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2094+1171A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814315 | |||||||
chr10:99814325 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2094+1181G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814325 | |||||||
chr10:99814326 | T | C | 3 | a0005c0008t0001g0030 a0005c0008t0001g0047 a0005c0008t0001g0077 |
3 | HG00140.hp2 HG01074.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.2094+1182T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814326 | |||||||
chr10:99814330 | C | T | 1 | a0001c0001t0001g0323 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2094+1186C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814330 | |||||||
chr10:99814341 | A | G | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2094+1197A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814341 | |||||||
chr10:99814344 | TAC | T | 4 | a0001c0002t0003g0020 a0001c0002t0006g0018 a0001c0002t0006g0019 others(1): Show |
4 | HG00642.hp2 HG01070.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.2094+1205_2094+120 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814344 | ||||||
chr10:99814348 | C | T | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2094+1204C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814348 | |||||||
chr10:99814351 | G | A | 2 | a0001c0002t0003g0222 a0001c0002t0003g0274 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2094+1207G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814351 | |||||||
chr10:99814353 | A | G | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2094+1209A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814353 | |||||||
chr10:99814356 | T | C | 5 | a0005c0008t0001g0030 a0005c0008t0001g0047 a0005c0008t0001g0077 others(2): Show |
5 | HG00140.hp2 HG01074.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.2094+1212T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814356 | |||||||
chr10:99814357 | A | G | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2094+1213A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814357 | |||||||
chr10:99814360 | C | T | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2094+1216C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814360 | |||||||
chr10:99814362 | C | T | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2094+1218C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814362 | |||||||
chr10:99814365 | A | G | 8 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0003g0222 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2094+1221A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814365 | |||||||
chr10:99814369 | A | G | 1 | a0002c0003t0001g0154 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2094+1225A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814369 | |||||||
chr10:99814370 | TATATACA others(1): Show |
T | 205 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(202): Show |
212 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.2094+1232_2094+123 others(12): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814370 | ||||||
chr10:99814377 | A | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0118 |
2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2094+1233A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814377 | |||||||
chr10:99814408 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG00738.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.2094+1264C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814408 | |||||||
chr10:99814425 | A | C | 1 | a0001c0001t0001g0014 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2094+1281A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814425 | |||||||
chr10:99814429 | A | C | 1 | a0023c0018t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2094+1285A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814429 | |||||||
chr10:99814434 | T | TATACACA others(17): Show |
1 | a0001c0002t0002g0069 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2094+1324_2094+134 others(28): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814434 | ||||||
chr10:99814434 | TATACACA others(17): Show |
T | 5 | a0001c0002t0002g0089 a0001c0002t0003g0116 a0001c0002t0003g0117 others(2): Show |
5 | HG00140.hp1 HG01928.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.2094+1324_2094+134 others(28): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814434 | ||||||
chr10:99814440 | CACATATG others(37): Show |
C | 1 | a0004c0006t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2094+1300_2094+134 others(48): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814440 | ||||||
chr10:99814444 | TA | T | 5 | a0001c0001t0001g0148 a0001c0002t0007g0128 a0001c0002t0007g0131 others(2): Show |
5 | HG01255.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2094+1301delA | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814444 | |||||||
chr10:99814456 | T | C | 1 | a0001c0002t0002g0127 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2094+1312T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814456 | |||||||
chr10:99814460 | T | C | 1 | a0001c0002t0002g0125 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2094+1316T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814460 | |||||||
chr10:99814460 | T | TACACACA others(49): Show |
1 | a0004c0006t0001g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2094+1323_2094+132 others(60): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814460 | ||||||
chr10:99814462 | C | T | 215 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(212): Show |
222 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.2094+1318C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814462 | |||||||
chr10:99814466 | C | CAAACATA others(11): Show |
5 | a0001c0001t0001g0235 a0001c0001t0001g0280 a0001c0001t0001g0284 others(2): Show |
5 | NA18950.hp2 NA18968.hp2 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.2094+1323_2094+132 others(22): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814466 | ||||||
chr10:99814467 | AT | A | 214 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(211): Show |
221 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.2094+1324delT | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814467 | |||||||
chr10:99814468 | T | TATGTGTG others(16): Show |
1 | a0002c0003t0001g0251 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2094+1341_2094+134 others(27): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814468 | ||||||
chr10:99814475 | G | A | 6 | a0001c0001t0001g0235 a0001c0001t0001g0280 a0001c0001t0001g0284 others(3): Show |
6 | NA18906.hp1 NA18950.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+1331G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814475 | |||||||
chr10:99814480 | T | C | 1 | a0004c0006t0001g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2094+1336T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814480 | |||||||
chr10:99814486 | C | T | 7 | a0001c0001t0001g0235 a0001c0001t0001g0280 a0001c0001t0001g0284 others(4): Show |
7 | HG03453.hp2 NA18906.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.2094+1342C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814486 | |||||||
chr10:99814492 | A | C | 6 | a0001c0001t0001g0235 a0001c0001t0001g0280 a0001c0001t0001g0284 others(3): Show |
6 | NA18906.hp1 NA18950.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+1348A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814492 | |||||||
chr10:99814494 | CAT | C | 13 | a0001c0001t0001g0143 a0001c0001t0001g0173 a0001c0001t0001g0181 others(10): Show |
13 | HG01074.hp2 HG01978.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.2094+1355_2094+135 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814494 | ||||||
chr10:99814499 | A | G | 6 | a0001c0001t0001g0235 a0001c0001t0001g0280 a0001c0001t0001g0284 others(3): Show |
6 | NA18906.hp1 NA18950.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+1355A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814499 | |||||||
chr10:99814503 | G | A | 6 | a0001c0001t0001g0235 a0001c0001t0001g0280 a0001c0001t0001g0284 others(3): Show |
6 | NA18906.hp1 NA18950.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+1359G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814503 | |||||||
chr10:99814505 | G | A | 6 | a0001c0001t0001g0235 a0001c0001t0001g0280 a0001c0001t0001g0284 others(3): Show |
6 | NA18906.hp1 NA18950.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+1361G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814505 | |||||||
chr10:99814506 | T | TACACATA others(7): Show |
4 | a0001c0001t0001g0235 a0001c0001t0001g0280 a0001c0001t0001g0284 others(1): Show |
4 | NA18950.hp2 NA18968.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.2094+1362_2094+136 others(18): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814506 | |||||||
chr10:99814506 | T | TACACATA others(85): Show |
1 | a0001c0001t0008g0291 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2094+1362_2094+136 others(96): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814506 | |||||||
chr10:99814507 | G | A | 6 | a0001c0001t0001g0235 a0001c0001t0001g0280 a0001c0001t0001g0284 others(3): Show |
6 | NA18906.hp1 NA18950.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+1363G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814507 | |||||||
chr10:99814507 | G | GTA | 58 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0134 others(55): Show |
60 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2094+1365_2094+136 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814507 | ||||||
chr10:99814508 | T | C | 1 | a0004c0006t0001g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2094+1364T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814508 | |||||||
chr10:99814510 | T | C | 1 | a0004c0006t0001g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2094+1366T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814510 | |||||||
chr10:99814511 | G | A | 10 | a0001c0001t0001g0118 a0001c0001t0001g0236 a0001c0001t0001g0281 others(7): Show |
10 | HG02895.hp2 HG02897.hp2 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.2094+1367G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814511 | |||||||
chr10:99814513 | G | A | 1 | a0004c0006t0001g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2094+1369G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814513 | |||||||
chr10:99814515 | A | G | 7 | a0001c0001t0001g0236 a0001c0001t0001g0281 a0001c0001t0001g0287 others(4): Show |
7 | HG02895.hp2 HG02897.hp2 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.2094+1371A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814515 | |||||||
chr10:99814516 | T | C | 1 | a0004c0006t0001g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2094+1372T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814516 | |||||||
chr10:99814518 | T | C | 1 | a0004c0006t0001g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2094+1374T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814518 | |||||||
chr10:99814520 | T | C | 12 | a0001c0001t0001g0231 a0001c0001t0001g0235 a0001c0001t0001g0267 others(9): Show |
12 | HG00423.hp2 HG00558.hp1 NA18906.hp1 others(9): Show |
intron_variant | MODIFIER | c.2094+1376T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814520 | |||||||
chr10:99814522 | C | T | 2 | a0011c0012t0001g0215 a0011c0012t0001g0216 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2094+1378C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814522 | |||||||
chr10:99814522 | CAT | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(59): Show |
64 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.2094+1386_2094+138 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814522 | ||||||
chr10:99814523 | A | ACATACAC others(141): Show |
1 | a0001c0001t0001g0306 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2094+1379_2094+138 others(152): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814523 | |||||||
chr10:99814524 | T | C | 9 | a0001c0001t0001g0236 a0001c0001t0001g0281 a0001c0001t0001g0287 others(6): Show |
9 | HG02895.hp2 HG02897.hp2 NA18953.hp2 others(6): Show |
intron_variant | MODIFIER | c.2094+1380T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814524 | |||||||
chr10:99814525 | A | ACATATAC others(121): Show |
1 | a0014c0023t0001g0217 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2094+1381_2094+138 others(132): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814525 | |||||||
chr10:99814525 | A | ACATATAC others(121): Show |
1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2094+1381_2094+138 others(132): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814525 | |||||||
chr10:99814525 | A | ACATATAC others(252): Show |
1 | a0023c0018t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2094+1381_2094+138 others(263): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814525 | |||||||
chr10:99814525 | A | ATACACAC others(87): Show |
7 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0231 others(4): Show |
7 | HG00558.hp1 HG02056.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.2094+1383_2094+138 others(98): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814525 | A | ATACACAC others(115): Show |
1 | a0001c0001t0001g0261 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2094+1383_2094+138 others(126): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814525 | A | ATACACAC others(139): Show |
1 | a0001c0001t0001g0267 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2094+1383_2094+138 others(150): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814525 | A | ATACACAC others(113): Show |
5 | a0001c0001t0001g0136 a0001c0001t0001g0260 a0001c0001t0001g0320 others(2): Show |
5 | HG00642.hp1 HG00741.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.2094+1383_2094+138 others(124): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814525 | A | ATACACAC others(141): Show |
9 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0276 others(6): Show |
9 | HG01516.hp2 HG01517.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.2094+1383_2094+138 others(152): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814525 | A | ATACACAC others(169): Show |
1 | a0001c0001t0001g0247 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2094+1383_2094+138 others(180): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814525 | A | ATACACAC others(165): Show |
9 | a0001c0001t0001g0004 a0001c0001t0001g0219 a0001c0001t0001g0263 others(6): Show |
10 | HG03669.hp2 HG03688.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.2094+1383_2094+138 others(176): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814525 | A | ATACACAC others(139): Show |
4 | a0001c0001t0001g0271 a0001c0001t0001g0304 a0001c0001t0001g0305 others(1): Show |
4 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(1): Show |
intron_variant | MODIFIER | c.2094+1383_2094+138 others(150): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814525 | A | ATACACAC others(167): Show |
7 | a0001c0001t0001g0218 a0001c0001t0001g0303 a0001c0001t0005g0282 others(4): Show |
7 | HG02896.hp1 HG02897.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2094+1383_2094+138 others(178): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814525 | A | ATACACAC others(163): Show |
1 | a0001c0001t0001g0005 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2094+1383_2094+138 others(174): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814525 | A | ATACACAC others(137): Show |
2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02155.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2094+1383_2094+138 others(148): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814525 | A | ATACACAC others(165): Show |
1 | a0001c0001t0001g0279 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2094+1383_2094+138 others(176): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814525 | A | ATATACAC others(19): Show |
7 | a0001c0001t0001g0196 a0002c0003t0001g0229 a0002c0003t0001g0230 others(4): Show |
7 | HG06807.hp1 NA18953.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.2094+1385_2094+138 others(30): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814525 | A | ATATACAC others(45): Show |
1 | a0022c0020t0001g0309 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2094+1385_2094+138 others(56): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814525 | A | ATATACAC others(71): Show |
1 | a0001c0001t0001g0150 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2094+1385_2094+138 others(82): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814525 | A | ATATACAC others(47): Show |
7 | a0001c0001t0001g0164 a0001c0002t0003g0168 a0002c0003t0001g0209 others(4): Show |
7 | HG00323.hp1 HG01070.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2094+1385_2094+138 others(58): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814525 | A | ATATACAC others(73): Show |
8 | a0001c0001t0001g0139 a0001c0001t0001g0148 a0001c0001t0001g0149 others(5): Show |
8 | HG01255.hp1 HG02486.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2094+1385_2094+138 others(84): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814525 | A | ATATACAC others(99): Show |
9 | a0001c0005t0001g0155 a0001c0005t0001g0156 a0003c0004t0001g0001 others(6): Show |
11 | HG01358.hp2 HG01496.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2094+1385_2094+138 others(110): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814525 | A | ATATACAC others(125): Show |
1 | a0001c0001t0001g0200 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2094+1385_2094+138 others(136): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814525 | A | ATATACAC others(45): Show |
14 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0002c0003t0001g0006 others(11): Show |
15 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.2094+1385_2094+138 others(56): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814525 | A | ATATACAC others(71): Show |
12 | a0002c0003t0001g0233 a0002c0003t0001g0243 a0002c0003t0001g0245 others(9): Show |
12 | HG00621.hp2 HG00733.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.2094+1385_2094+138 others(82): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814525 | A | ATATACAC others(29): Show |
2 | a0010c0015t0001g0016 a0010c0015t0001g0017 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2094+1385_2094+138 others(40): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814525 | A | ATATACAC others(43): Show |
1 | a0002c0003t0001g0259 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2094+1385_2094+138 others(54): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814525 | A | ATATACAC others(71): Show |
1 | a0002c0003t0001g0221 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2094+1385_2094+138 others(82): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814525 | A | ATATATAC others(21): Show |
1 | a0001c0002t0002g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2094+1458_2094+148 others(32): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814525 | A | G | 1 | a0001c0001t0001g0306 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2094+1381A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814525 | |||||||
chr10:99814525 | ATATATAC others(21): Show |
A | 12 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0002t0002g0053 others(9): Show |
12 | HG01169.hp1 HG01175.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.2094+1458_2094+148 others(32): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814525 | ||||||
chr10:99814526 | T | C | 10 | a0001c0001t0001g0118 a0001c0002t0003g0132 a0001c0002t0003g0133 others(7): Show |
10 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.2094+1382T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814526 | |||||||
chr10:99814527 | A | ACACACAC others(7): Show |
7 | a0001c0001t0001g0246 a0001c0001t0001g0288 a0001c0001t0001g0295 others(4): Show |
7 | HG00438.hp1 HG03239.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.2094+1383_2094+138 others(18): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814527 | |||||||
chr10:99814527 | A | ACACACAT others(5): Show |
4 | a0001c0001t0001g0235 a0001c0001t0001g0280 a0001c0001t0001g0284 others(1): Show |
4 | NA18950.hp2 NA18968.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.2094+1383_2094+138 others(16): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814527 | |||||||
chr10:99814527 | A | ATACACAT others(17): Show |
5 | a0002c0003t0001g0137 a0002c0003t0001g0138 a0002c0003t0001g0154 others(2): Show |
5 | HG01884.hp1 HG03130.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2094+1385_2094+138 others(28): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814527 | ||||||
chr10:99814527 | A | ATACACAT others(71): Show |
2 | a0001c0001t0001g0159 a0001c0001t0001g0161 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2094+1385_2094+138 others(82): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814527 | ||||||
chr10:99814527 | A | ATATACAC others(21): Show |
1 | a0001c0002t0002g0127 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2094+1410_2094+141 others(32): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814527 | ||||||
chr10:99814527 | A | G | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2094+1383A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814527 | |||||||
chr10:99814528 | T | C | 1 | a0001c0001t0008g0291 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2094+1384T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814528 | |||||||
chr10:99814530 | T | C | 8 | a0001c0001t0001g0236 a0001c0001t0001g0281 a0001c0001t0001g0287 others(5): Show |
8 | NA18953.hp2 NA18967.hp1 NA18987.hp2 others(5): Show |
intron_variant | MODIFIER | c.2094+1386T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814530 | |||||||
chr10:99814532 | C | T | 18 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0235 others(15): Show |
18 | HG00438.hp1 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.2094+1388C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814532 | |||||||
chr10:99814534 | C | CACATATG others(135): Show |
1 | a0001c0001t0001g0307 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2094+1391_2094+139 others(146): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814534 | ||||||
chr10:99814534 | C | CACATATG others(135): Show |
1 | a0001c0001t0001g0236 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2094+1391_2094+139 others(146): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814534 | ||||||
chr10:99814534 | C | CACATATG others(159): Show |
2 | a0001c0001t0001g0287 a0001c0001t0001g0294 |
2 | NA18967.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.2094+1391_2094+139 others(170): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814534 | ||||||
chr10:99814534 | C | CACATATG others(135): Show |
1 | a0001c0001t0001g0281 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2094+1391_2094+139 others(146): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814534 | ||||||
chr10:99814536 | T | C | 17 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0235 others(14): Show |
17 | HG00438.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2094+1392T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814536 | |||||||
chr10:99814538 | T | TGTGTATA others(137): Show |
2 | a0001c0001t0001g0308 a0001c0001t0001g0323 |
2 | NA18987.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.2094+1394_2094+139 others(148): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814538 | |||||||
chr10:99814538 | TAC | T | 28 | a0001c0001t0001g0139 a0001c0001t0001g0148 a0001c0001t0001g0149 others(25): Show |
28 | HG00558.hp1 HG01255.hp1 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.2094+1402_2094+140 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814538 | ||||||
chr10:99814540 | C | CACACACA others(73): Show |
2 | a0011c0012t0001g0215 a0011c0012t0001g0216 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2094+1421_2094+142 others(84): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814540 | ||||||
chr10:99814540 | C | T | 12 | a0001c0001t0001g0235 a0001c0001t0001g0246 a0001c0001t0001g0280 others(9): Show |
12 | HG00438.hp1 NA18950.hp2 NA18952.hp1 others(9): Show |
intron_variant | MODIFIER | c.2094+1396C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814540 | |||||||
chr10:99814542 | C | CATAT | 6 | a0001c0001t0001g0236 a0001c0001t0001g0281 a0001c0001t0001g0287 others(3): Show |
6 | NA18953.hp2 NA18967.hp1 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+1399_2094+140 others(8): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814542 | ||||||
chr10:99814542 | C | T | 2 | a0001c0001t0001g0308 a0001c0001t0001g0323 |
2 | NA18987.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.2094+1398C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814542 | |||||||
chr10:99814544 | CACAT | C | 26 | a0001c0001t0001g0218 a0001c0001t0001g0247 a0001c0001t0001g0260 others(23): Show |
26 | HG00642.hp1 HG00741.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.2094+1402_2094+140 others(8): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814544 | ||||||
chr10:99814546 | C | T | 2 | a0004c0029t0001g0329 a0023c0018t0001g0009 |
2 | HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2094+1402C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814546 | |||||||
chr10:99814548 | T | C | 8 | a0001c0001t0001g0236 a0001c0001t0001g0281 a0001c0001t0001g0287 others(5): Show |
8 | NA18953.hp2 NA18967.hp1 NA18987.hp2 others(5): Show |
intron_variant | MODIFIER | c.2094+1404T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814548 | |||||||
chr10:99814555 | A | G | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2094+1411A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814555 | |||||||
chr10:99814566 | T | C | 3 | a0001c0001t0001g0164 a0002c0003t0001g0251 a0007c0009t0001g0163 |
3 | HG01346.hp2 HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2094+1422T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814566 | |||||||
chr10:99814566 | TAC | T | 11 | a0001c0001t0001g0196 a0001c0001t0001g0246 a0001c0001t0001g0288 others(8): Show |
11 | HG00438.hp1 HG00735.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.2094+1430_2094+143 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814566 | ||||||
chr10:99814568 | C | CACACACA others(45): Show |
44 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0143 others(41): Show |
46 | HG00558.hp2 HG00673.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.2094+1457_2094+145 others(56): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814568 | ||||||
chr10:99814568 | C | CACACACA others(71): Show |
2 | a0001c0001t0001g0202 a0001c0017t0001g0167 |
2 | HG02004.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2094+1457_2094+145 others(82): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814568 | ||||||
chr10:99814568 | C | CACACACA others(97): Show |
1 | a0001c0001t0001g0171 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2094+1457_2094+145 others(108): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814568 | ||||||
chr10:99814568 | C | CACACATA others(17): Show |
5 | a0001c0001t0001g0142 a0001c0001t0001g0182 a0002c0003t0001g0241 others(2): Show |
5 | HG00438.hp2 HG02602.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2094+1429_2094+143 others(28): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814568 | ||||||
chr10:99814568 | C | CACACATA others(43): Show |
1 | a0001c0001t0001g0008 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2094+1429_2094+143 others(54): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814568 | ||||||
chr10:99814572 | CACAT | C | 4 | a0001c0001t0001g0262 a0001c0001t0001g0304 a0001c0001t0001g0305 others(1): Show |
4 | HG00423.hp2 HG00597.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.2094+1430_2094+143 others(8): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814572 | ||||||
chr10:99814574 | C | T | 2 | a0001c0001t0001g0005 a0023c0018t0001g0009 |
3 | HG03453.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2094+1430C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814574 | |||||||
chr10:99814574 | CAT | C | 6 | a0001c0042t0002g0067 a0005c0008t0001g0030 a0005c0008t0001g0047 others(3): Show |
6 | HG00140.hp2 HG01074.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.2094+1433_2094+143 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814574 | ||||||
chr10:99814574 | CATAT | C | 3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 |
3 | HG02027.hp2 HG02056.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.2094+1431_2094+143 others(8): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814574 | |||||||
chr10:99814583 | A | G | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2094+1439A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814583 | |||||||
chr10:99814590 | C | T | 1 | a0002c0003t0001g0312 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2094+1446C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814590 | |||||||
chr10:99814594 | T | C | 3 | a0001c0001t0001g0164 a0007c0009t0001g0163 a0014c0023t0001g0217 |
3 | HG00639.hp2 HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2094+1450T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814594 | |||||||
chr10:99814594 | T | TACACACA others(47): Show |
1 | a0007c0009t0001g0210 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2094+1460_2094+146 others(58): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814594 | ||||||
chr10:99814594 | T | TACACACA others(47): Show |
1 | a0007c0009t0001g0157 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2094+1457_2094+145 others(58): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814594 | ||||||
chr10:99814594 | TAC | T | 19 | a0001c0001t0001g0014 a0001c0001t0001g0197 a0001c0001t0001g0198 others(16): Show |
19 | HG00323.hp2 HG00438.hp1 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.2094+1458_2094+145 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814594 | ||||||
chr10:99814596 | C | CACACACA others(19): Show |
3 | a0001c0002t0002g0074 a0001c0002t0002g0075 a0001c0002t0002g0076 |
3 | NA18944.hp1 NA18964.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.2094+1486_2094+151 others(30): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814596 | ||||||
chr10:99814596 | CACACACA others(19): Show |
C | 7 | a0001c0001t0001g0223 a0001c0007t0003g0024 a0001c0007t0003g0025 others(4): Show |
7 | HG02280.hp2 HG02559.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2094+1486_2094+151 others(30): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814596 | ||||||
chr10:99814598 | C | CACATGTG others(37): Show |
1 | a0005c0008t0001g0030 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2094+1457_2094+145 others(48): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814598 | ||||||
chr10:99814598 | C | CACATGTG others(61): Show |
2 | a0005c0008t0001g0047 a0005c0008t0001g0077 |
2 | HG00140.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.2094+1457_2094+145 others(72): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814598 | ||||||
chr10:99814602 | C | CAT | 3 | a0001c0001t0001g0118 a0014c0023t0001g0217 a0020c0024t0001g0015 |
3 | HG00639.hp2 HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2094+1461_2094+146 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814602 | ||||||
chr10:99814602 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0219 others(8): Show |
13 | HG03453.hp2 HG03490.hp1 HG03492.hp2 others(10): Show |
intron_variant | MODIFIER | c.2094+1458C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814602 | |||||||
chr10:99814604 | T | C | 4 | a0001c0001t0001g0299 a0005c0008t0001g0030 a0005c0008t0001g0047 others(1): Show |
4 | HG00140.hp2 HG01074.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.2094+1460T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814604 | |||||||
chr10:99814604 | T | TGTGTATA others(65): Show |
2 | a0006c0010t0001g0010 a0006c0010t0001g0011 |
2 | HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2094+1460_2094+146 others(76): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814604 | |||||||
chr10:99814622 | T | C | 3 | a0001c0002t0003g0051 a0001c0002t0003g0052 a0001c0042t0002g0067 |
3 | HG01952.hp2 HG01978.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2094+1478T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814622 | |||||||
chr10:99814622 | T | TAC | 151 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(148): Show |
156 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.2094+1484_2094+148 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814622 | ||||||
chr10:99814622 | T | TACACACA others(23): Show |
6 | a0001c0002t0003g0041 a0001c0002t0003g0168 a0001c0014t0001g0023 others(3): Show |
6 | HG02109.hp1 HG02886.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+1485_2094+148 others(34): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814622 | ||||||
chr10:99814622 | T | TACACACA others(51): Show |
1 | a0004c0006t0001g0080 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2094+1485_2094+148 others(62): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814622 | ||||||
chr10:99814622 | T | TACACACA others(21): Show |
9 | a0001c0002t0002g0037 a0001c0002t0002g0045 a0001c0002t0002g0049 others(6): Show |
9 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.2094+1513_2094+154 others(32): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814622 | ||||||
chr10:99814622 | T | TACACACA others(49): Show |
3 | a0001c0001t0001g0197 a0001c0001t0001g0211 a0001c0002t0002g0042 |
3 | HG03490.hp2 HG03834.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.2094+1485_2094+154 others(60): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814622 | ||||||
chr10:99814622 | T | TACACACA others(77): Show |
1 | a0001c0001t0001g0214 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2094+1540_2094+154 others(88): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814622 | ||||||
chr10:99814622 | TAC | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0219 a0001c0001t0001g0263 others(5): Show |
9 | HG03669.hp2 HG03688.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.2094+1484_2094+148 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814622 | ||||||
chr10:99814622 | TACACACA others(21): Show |
T | 2 | a0001c0002t0002g0125 a0019c0041t0002g0073 |
2 | HG02273.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2094+1513_2094+154 others(32): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814622 | ||||||
chr10:99814628 | C | CACATATA others(137): Show |
1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2094+1485_2094+148 others(148): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814628 | ||||||
chr10:99814628 | C | CAT | 42 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(39): Show |
43 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.2094+1487_2094+148 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814628 | ||||||
chr10:99814628 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0219 a0001c0001t0001g0263 others(5): Show |
9 | HG03669.hp2 HG03688.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.2094+1484C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814628 | |||||||
chr10:99814628 | CAT | C | 10 | a0001c0001t0001g0231 a0001c0001t0001g0235 a0001c0001t0001g0280 others(7): Show |
10 | HG00558.hp1 HG02809.hp2 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.2094+1487_2094+148 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814628 | ||||||
chr10:99814630 | T | C | 7 | a0002c0003t0001g0229 a0002c0003t0001g0237 a0002c0003t0001g0249 others(4): Show |
7 | HG00140.hp2 HG01074.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.2094+1486T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814630 | |||||||
chr10:99814633 | G | A | 1 | a0023c0018t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2094+1489G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814633 | |||||||
chr10:99814637 | A | G | 1 | a0023c0018t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2094+1493A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814637 | |||||||
chr10:99814642 | C | T | 1 | a0023c0018t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2094+1498C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814642 | |||||||
chr10:99814646 | T | C | 3 | a0001c0002t0002g0079 a0001c0002t0002g0094 a0023c0018t0001g0009 |
3 | HG02818.hp2 HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2094+1502T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814646 | |||||||
chr10:99814646 | T | TACACACA others(45): Show |
1 | a0001c0001t0001g0014 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2094+1503_2094+150 others(56): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814646 | ||||||
chr10:99814648 | T | C | 3 | a0004c0029t0001g0329 a0014c0023t0001g0217 a0020c0024t0001g0015 |
3 | HG00639.hp2 HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2094+1504T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814648 | |||||||
chr10:99814648 | TAC | T | 8 | a0001c0002t0002g0065 a0001c0002t0002g0066 a0001c0002t0002g0069 others(5): Show |
8 | HG01891.hp1 HG02040.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.2094+1512_2094+151 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814648 | ||||||
chr10:99814648 | TACAC | T | 42 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0218 others(39): Show |
44 | HG00609.hp1 HG00642.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.2094+1510_2094+151 others(8): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814648 | ||||||
chr10:99814650 | C | CACACACA others(19): Show |
1 | a0001c0017t0001g0167 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2094+1514_2094+153 others(30): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814650 | ||||||
chr10:99814650 | C | CACACACA others(47): Show |
3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0017c0031t0001g0145 |
3 | HG02015.hp2 HG02083.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.2094+1540_2094+154 others(58): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814650 | ||||||
chr10:99814650 | C | CATATATG others(13): Show |
2 | a0001c0001t0001g0263 a0001c0001t0001g0305 |
2 | HG00597.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.2094+1507_2094+150 others(24): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814650 | ||||||
chr10:99814652 | C | CACATATA others(17): Show |
3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 |
3 | HG02027.hp2 HG02056.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.2094+1511_2094+151 others(28): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814652 | ||||||
chr10:99814652 | C | T | 3 | a0001c0001t0001g0247 a0001c0001t0001g0263 a0001c0001t0001g0305 |
3 | HG00597.hp1 NA18955.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.2094+1508C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814652 | |||||||
chr10:99814656 | C | CATATATG others(81): Show |
1 | a0001c0002t0007g0131 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2094+1516_2094+151 others(92): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814656 | ||||||
chr10:99814656 | C | CATATATG others(81): Show |
1 | a0001c0002t0007g0128 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2094+1516_2094+151 others(92): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814656 | ||||||
chr10:99814656 | C | CATATATG others(51): Show |
2 | a0001c0002t0003g0132 a0001c0002t0003g0133 |
2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2094+1516_2094+151 others(62): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814656 | ||||||
chr10:99814656 | C | CATATGTG others(109): Show |
1 | a0001c0014t0001g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2094+1540_2094+154 others(120): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814656 | ||||||
chr10:99814656 | C | CATATGTG others(73): Show |
8 | a0001c0001t0001g0231 a0001c0001t0001g0235 a0001c0001t0001g0280 others(5): Show |
8 | HG00558.hp1 HG03239.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.2094+1540_2094+154 others(84): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814656 | ||||||
chr10:99814656 | C | CATATGTG others(69): Show |
1 | a0001c0001t0001g0290 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2094+1539_2094+154 others(80): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814656 | ||||||
chr10:99814656 | C | CATATGTG others(121): Show |
2 | a0001c0001t0001g0297 a0001c0001t0001g0298 |
2 | NA18954.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2094+1539_2094+154 others(132): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814656 | ||||||
chr10:99814656 | C | CATATGTG others(17): Show |
1 | a0001c0001t0001g0262 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2094+1535_2094+153 others(28): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814656 | ||||||
chr10:99814656 | C | T | 77 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(74): Show |
81 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.2094+1512C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814656 | |||||||
chr10:99814656 | CATAT | C | 4 | a0001c0001t0001g0200 a0001c0002t0003g0090 a0001c0002t0003g0091 others(1): Show |
4 | HG00423.hp1 HG01255.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.2094+1513_2094+151 others(8): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814656 | |||||||
chr10:99814658 | T | C | 3 | a0002c0003t0001g0229 a0002c0003t0001g0237 a0002c0003t0001g0249 |
3 | NA18954.hp1 NA18979.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.2094+1514T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814658 | |||||||
chr10:99814658 | T | TATGTGTA others(19): Show |
1 | a0002c0003t0001g0238 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2094+1515_2094+154 others(30): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814658 | ||||||
chr10:99814660 | T | TGTGTATA others(17): Show |
4 | a0001c0001t0001g0164 a0002c0003t0001g0245 a0007c0009t0001g0157 others(1): Show |
4 | HG01109.hp1 HG01891.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2094+1534_2094+155 others(28): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814660 | ||||||
chr10:99814660 | T | TGTGTATA others(41): Show |
1 | a0007c0009t0001g0163 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2094+1557_2094+155 others(52): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814660 | ||||||
chr10:99814660 | T | TGTGTATA others(145): Show |
3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0315 |
3 | HG00438.hp1 NA18952.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.2094+1539_2094+154 others(156): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814660 | ||||||
chr10:99814660 | T | TGTGTATA others(169): Show |
1 | a0001c0001t0001g0246 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2094+1539_2094+154 others(180): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814660 | ||||||
chr10:99814672 | C | CATATACA others(109): Show |
2 | a0001c0002t0003g0222 a0001c0002t0003g0274 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2094+1540_2094+154 others(120): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814672 | ||||||
chr10:99814672 | C | CATATACA others(79): Show |
1 | a0021c0032t0001g0129 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2094+1540_2094+154 others(90): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814672 | ||||||
chr10:99814672 | C | T | 9 | a0001c0001t0001g0014 a0001c0002t0003g0132 a0001c0002t0003g0133 others(6): Show |
9 | HG00639.hp2 HG02055.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2094+1528C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814672 | |||||||
chr10:99814676 | TAC | T | 6 | a0001c0001t0001g0005 a0005c0008t0001g0030 a0005c0008t0001g0047 others(3): Show |
7 | HG00140.hp2 HG01074.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.2094+1539_2094+154 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814676 | ||||||
chr10:99814678 | C | CATATATG others(15): Show |
2 | a0001c0001t0001g0304 a0012c0022t0001g0268 |
2 | HG00423.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2094+1535_2094+153 others(26): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814678 | ||||||
chr10:99814684 | C | CATAT | 6 | a0002c0003t0001g0006 a0002c0003t0001g0289 a0002c0003t0001g0311 others(3): Show |
7 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.2094+1540_2094+154 others(8): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814684 | |||||||
chr10:99814701 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2094+1557A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814701 | |||||||
chr10:99814743 | A | ATGTATGT others(23): Show |
1 | a0001c0001t0001g0005 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2094+1620_2094+164 others(34): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814743 | ||||||
chr10:99814743 | A | G | 1 | a0004c0006t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2094+1599A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814743 | |||||||
chr10:99814754 | TAC | T | 3 | a0001c0001t0001g0118 a0001c0002t0003g0050 a0023c0018t0001g0009 |
3 | HG03017.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2094+1618_2094+161 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814754 | ||||||
chr10:99814762 | C | T | 2 | a0001c0001t0001g0118 a0023c0018t0001g0009 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2094+1618C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814762 | |||||||
chr10:99814764 | T | C | 11 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0003g0222 others(8): Show |
11 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.2094+1620T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814764 | |||||||
chr10:99814767 | A | G | 11 | a0001c0001t0001g0118 a0001c0002t0003g0132 a0001c0002t0003g0133 others(8): Show |
11 | HG01167.hp1 HG01169.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.2094+1623A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814767 | |||||||
chr10:99814769 | G | A | 5 | a0002c0003t0001g0006 a0002c0003t0001g0289 a0002c0003t0001g0311 others(2): Show |
6 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.2094+1625G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814769 | |||||||
chr10:99814769 | GTGTGTGT others(21): Show |
G | 12 | a0001c0001t0001g0014 a0001c0002t0003g0132 a0001c0002t0003g0133 others(9): Show |
12 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.2094+1633_2094+166 others(32): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814769 | ||||||
chr10:99814794 | C | T | 2 | a0001c0001t0001g0118 a0023c0018t0001g0009 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2094+1650C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814794 | |||||||
chr10:99814795 | A | ATG | 127 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(124): Show |
132 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.2094+1652_2094+165 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99814795 | ||||||
chr10:99814795 | A | G | 3 | a0001c0005t0001g0155 a0001c0005t0001g0156 a0002c0003t0001g0253 |
3 | HG02004.hp1 NA18974.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2094+1651A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814795 | |||||||
chr10:99814797 | A | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(204): Show |
214 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.2094+1653A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814797 | |||||||
chr10:99814809 | A | G | 1 | a0001c0038t0001g0141 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2094+1665A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814809 | |||||||
chr10:99814817 | A | T | 1 | a0016c0026t0006g0021 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2094+1673A>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99814817 | |||||||
chr10:99815042 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2094+1898T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99815042 | |||||||
chr10:99815045 | G | C | 1 | a0001c0002t0003g0090 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2094+1901G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99815045 | |||||||
chr10:99815049 | T | C | 2 | a0001c0001t0001g0118 a0023c0018t0001g0009 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2094+1905T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99815049 | |||||||
chr10:99815174 | G | C | 220 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(217): Show |
227 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.2094+2030G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99815174 | |||||||
chr10:99815382 | G | A | 2 | a0001c0001t0001g0118 a0023c0018t0001g0009 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2095-1926G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99815382 | |||||||
chr10:99815396 | A | G | 2 | a0001c0001t0001g0118 a0023c0018t0001g0009 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2095-1912A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99815396 | |||||||
chr10:99815479 | A | G | 2 | a0001c0002t0003g0132 a0001c0002t0003g0133 |
2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2095-1829A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99815479 | |||||||
chr10:99815502 | G | GAT | 5 | a0005c0008t0001g0030 a0005c0008t0001g0047 a0005c0008t0001g0077 others(2): Show |
5 | HG00140.hp2 HG01074.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.2095-1806_2095-180 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99815502 | |||||||
chr10:99815503 | C | A | 215 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(212): Show |
222 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.2095-1805C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99815503 | |||||||
chr10:99815503 | C | T | 5 | a0005c0008t0001g0030 a0005c0008t0001g0047 a0005c0008t0001g0077 others(2): Show |
5 | HG00140.hp2 HG01074.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.2095-1805C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99815503 | |||||||
chr10:99815575 | A | G | 1 | a0001c0002t0003g0064 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2095-1733A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99815575 | |||||||
chr10:99815616 | C | T | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2095-1692C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99815616 | |||||||
chr10:99815746 | C | CA | 8 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0003g0222 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2095-1555dupA | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99815746 | ||||||
chr10:99815773 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2095-1535A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99815773 | |||||||
chr10:99815797 | A | G | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2095-1511A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99815797 | |||||||
chr10:99815842 | G | A | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2095-1466G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99815842 | |||||||
chr10:99815851 | G | C | 1 | a0023c0018t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2095-1457G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99815851 | |||||||
chr10:99815923 | GTTCTTCC others(7): Show |
G | 1 | a0001c0007t0003g0029 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2095-1384_2095-137 others(18): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99815923 | |||||||
chr10:99815969 | G | GT | 25 | a0001c0001t0001g0008 a0001c0001t0001g0150 a0001c0001t0001g0162 others(22): Show |
25 | HG00597.hp2 HG01884.hp1 HG02071.hp1 others(22): Show |
intron_variant | MODIFIER | c.2095-1322dupT | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99815969 | ||||||
chr10:99815969 | GT | G | 7 | a0001c0001t0001g0198 a0001c0002t0002g0100 a0005c0008t0001g0030 others(4): Show |
7 | HG00140.hp2 HG01074.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.2095-1322delT | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99815969 | ||||||
chr10:99816024 | A | C | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2095-1284A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99816024 | |||||||
chr10:99816037 | C | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0213 |
3 | HG01255.hp1 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2095-1271C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99816037 | |||||||
chr10:99816053 | C | T | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2095-1255C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99816053 | |||||||
chr10:99816073 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2095-1235A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99816073 | |||||||
chr10:99816278 | TTTTG | T | 13 | a0001c0001t0001g0118 a0001c0002t0003g0132 a0001c0002t0003g0133 others(10): Show |
13 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.2095-1009_2095-100 others(8): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | 99816278 | ||||||
chr10:99816387 | G | A | 1 | a0001c0002t0003g0110 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2095-921G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99816387 | |||||||
chr10:99816398 | C | T | 1 | a0002c0003t0001g0289 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2095-910C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99816398 | |||||||
chr10:99816531 | C | T | 2 | a0001c0001t0001g0118 a0023c0018t0001g0009 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2095-777C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99816531 | |||||||
chr10:99816562 | G | A | 18 | a0002c0003t0001g0006 a0002c0003t0001g0209 a0002c0003t0001g0229 others(15): Show |
19 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.2095-746G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99816562 | |||||||
chr10:99816570 | G | A | 43 | a0002c0003t0001g0006 a0002c0003t0001g0137 a0002c0003t0001g0138 others(40): Show |
44 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.2095-738G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99816570 | |||||||
chr10:99816710 | G | A | 1 | a0001c0002t0002g0061 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2095-598G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99816710 | |||||||
chr10:99816717 | G | A | 1 | a0001c0001t0001g0308 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2095-591G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99816717 | |||||||
chr10:99816725 | T | C | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2095-583T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99816725 | |||||||
chr10:99816782 | T | C | 2 | a0001c0001t0001g0118 a0023c0018t0001g0009 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2095-526T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99816782 | |||||||
chr10:99816900 | A | C | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2095-408A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99816900 | |||||||
chr10:99817005 | T | A | 1 | a0002c0003t0001g0250 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2095-303T>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99817005 | |||||||
chr10:99817203 | T | C | 220 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(217): Show |
227 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.2095-105T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99817203 | |||||||
chr10:99817261 | G | A | 2 | a0001c0001t0001g0118 a0023c0018t0001g0009 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2095-47G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99817261 | |||||||
chr10:99817278 | T | A | 8 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0003g0222 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2095-30T>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99817278 | |||||||
chr10:99817302 | A | G | 1 | a0002c0003t0001g0221 | 1 | HG02698.hp1 | splice_region_variant&intron_variant | LOW | c.2095-6A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | 99817302 | |||||||
chr10:99817520 | G | T | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2271+36G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 17/31 | chr10 | 99817520 | |||||||
chr10:99817811 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2271+327G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 17/31 | chr10 | 99817811 | |||||||
chr10:99818038 | C | A | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2271+554C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 17/31 | chr10 | 99818038 | |||||||
chr10:99818195 | C | T | 2 | a0001c0002t0002g0061 a0001c0002t0002g0109 |
2 | HG02523.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.2272-595C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 17/31 | chr10 | 99818195 | |||||||
chr10:99818222 | C | CA | 128 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(125): Show |
133 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.2272-557dupA | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr10 | 99818222 | ||||||
chr10:99818375 | A | G | 3 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0001g0308 |
3 | NA18979.hp1 NA18987.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.2272-415A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 17/31 | chr10 | 99818375 | |||||||
chr10:99818521 | C | A | 1 | a0001c0002t0003g0036 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2272-269C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 17/31 | chr10 | 99818521 | |||||||
chr10:99818525 | T | C | 4 | a0001c0002t0002g0084 a0001c0002t0002g0089 a0001c0002t0002g0105 others(1): Show |
4 | HG00140.hp1 HG00741.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.2272-265T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 17/31 | chr10 | 99818525 | |||||||
chr10:99818560 | C | T | 2 | a0001c0002t0002g0048 a0001c0002t0002g0108 |
2 | HG00738.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2272-230C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 17/31 | chr10 | 99818560 | |||||||
chr10:99818959 | T | C | 1 | a0001c0001t0001g0183 | 1 | NA19012.hp2 | splice_donor_variant&intron_variant | HIGH | c.2439+2T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 18/31 | chr10 | 99818959 | |||||||
chr10:99819056 | G | T | 1 | a0001c0002t0002g0071 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2440-33G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 18/31 | chr10 | 99819056 | |||||||
chr10:99819325 | T | C | 12 | a0001c0001t0001g0014 a0001c0002t0003g0132 a0001c0002t0003g0133 others(9): Show |
12 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.2620+56T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99819325 | |||||||
chr10:99819413 | CTG | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): Show |
97 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(94): Show |
intron_variant | MODIFIER | c.2620+148_2620+149d others(4): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | INFO_REALIGN_3_PRIME | chr10 | 99819413 | ||||||
chr10:99819609 | T | C | 4 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0002t0003g0168 others(1): Show |
4 | HG01884.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2620+340T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99819609 | |||||||
chr10:99819698 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2620+429T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99819698 | |||||||
chr10:99820129 | C | T | 2 | a0001c0001t0001g0014 a0004c0029t0001g0329 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2620+860C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99820129 | |||||||
chr10:99820162 | C | T | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2620+893C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99820162 | |||||||
chr10:99820163 | G | T | 3 | a0004c0006t0001g0080 a0004c0006t0001g0081 a0004c0006t0001g0096 |
3 | HG02109.hp1 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2620+894G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99820163 | |||||||
chr10:99820280 | G | A | 12 | a0001c0001t0001g0014 a0001c0002t0003g0132 a0001c0002t0003g0133 others(9): Show |
12 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.2620+1011G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99820280 | |||||||
chr10:99820346 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2620+1077G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99820346 | |||||||
chr10:99820390 | TCA | T | 245 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(242): Show |
252 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.2620+1140_2620+114 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | INFO_REALIGN_3_PRIME | chr10 | 99820390 | ||||||
chr10:99820409 | C | A | 6 | a0001c0002t0003g0168 a0005c0008t0001g0030 a0005c0008t0001g0047 others(3): Show |
6 | HG00140.hp2 HG01074.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.2620+1140C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99820409 | |||||||
chr10:99820578 | T | A | 1 | a0004c0006t0001g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2620+1309T>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99820578 | |||||||
chr10:99820653 | C | T | 1 | a0023c0018t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2620+1384C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99820653 | |||||||
chr10:99820908 | A | G | 68 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0134 others(65): Show |
70 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.2620+1639A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99820908 | |||||||
chr10:99820944 | A | G | 9 | a0001c0001t0001g0014 a0001c0002t0003g0132 a0001c0002t0003g0133 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2620+1675A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99820944 | |||||||
chr10:99820958 | G | A | 1 | a0001c0002t0003g0111 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2620+1689G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99820958 | |||||||
chr10:99821086 | GA | G | 13 | a0001c0001t0001g0144 a0001c0001t0001g0169 a0001c0001t0001g0175 others(10): Show |
13 | HG00735.hp2 HG01928.hp1 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.2620+1818delA | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821086 | |||||||
chr10:99821094 | C | T | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.2620+1825C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821094 | |||||||
chr10:99821095 | G | A | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2620+1826G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821095 | |||||||
chr10:99821130 | G | T | 1 | a0001c0001t0001g0303 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2620+1861G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821130 | |||||||
chr10:99821180 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2620+1911T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821180 | |||||||
chr10:99821229 | G | A | 9 | a0001c0001t0001g0014 a0001c0002t0003g0132 a0001c0002t0003g0133 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2620+1960G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821229 | |||||||
chr10:99821311 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2620+2042A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821311 | |||||||
chr10:99821356 | C | T | 12 | a0001c0001t0001g0014 a0001c0002t0003g0132 a0001c0002t0003g0133 others(9): Show |
12 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.2620+2087C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821356 | |||||||
chr10:99821378 | G | C | 5 | a0005c0008t0001g0030 a0005c0008t0001g0047 a0005c0008t0001g0077 others(2): Show |
5 | HG00140.hp2 HG01074.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.2620+2109G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821378 | |||||||
chr10:99821381 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2620+2112C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821381 | |||||||
chr10:99821406 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2620+2137C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821406 | |||||||
chr10:99821428 | C | T | 1 | a0010c0015t0001g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2620+2159C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821428 | |||||||
chr10:99821429 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2620+2160G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821429 | |||||||
chr10:99821447 | A | G | 1 | a0002c0003t0001g0251 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2620+2178A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821447 | |||||||
chr10:99821503 | G | A | 1 | a0001c0002t0002g0127 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2620+2234G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821503 | |||||||
chr10:99821564 | C | T | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2620+2295C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821564 | |||||||
chr10:99821565 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2620+2296G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821565 | |||||||
chr10:99821612 | A | G | 9 | a0001c0001t0001g0014 a0001c0002t0003g0132 a0001c0002t0003g0133 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2620+2343A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821612 | |||||||
chr10:99821649 | A | T | 2 | a0001c0002t0003g0090 a0001c0002t0003g0091 |
2 | HG01255.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.2620+2380A>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821649 | |||||||
chr10:99821655 | C | T | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2620+2386C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821655 | |||||||
chr10:99821664 | C | T | 4 | a0010c0015t0001g0016 a0010c0015t0001g0017 a0011c0012t0001g0215 others(1): Show |
4 | HG02630.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2620+2395C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821664 | |||||||
chr10:99821672 | G | A | 3 | a0004c0029t0001g0329 a0014c0023t0001g0217 a0020c0024t0001g0015 |
3 | HG00639.hp2 HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2620+2403G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821672 | |||||||
chr10:99821689 | T | C | 9 | a0001c0001t0001g0014 a0001c0002t0003g0132 a0001c0002t0003g0133 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2620+2420T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821689 | |||||||
chr10:99821695 | G | A | 12 | a0001c0001t0001g0014 a0001c0002t0003g0132 a0001c0002t0003g0133 others(9): Show |
12 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.2620+2426G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821695 | |||||||
chr10:99821718 | A | G | 1 | a0001c0001t0001g0247 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2620+2449A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821718 | |||||||
chr10:99821824 | C | A | 1 | a0001c0001t0001g0014 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2620+2555C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821824 | |||||||
chr10:99821825 | G | A | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2620+2556G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821825 | |||||||
chr10:99821831 | G | A | 3 | a0001c0001t0001g0014 a0001c0014t0001g0023 a0005c0008t0001g0013 |
3 | HG02486.hp2 HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2620+2562G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821831 | |||||||
chr10:99821955 | T | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.2620+2686T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821955 | |||||||
chr10:99821987 | G | A | 3 | a0004c0029t0001g0329 a0014c0023t0001g0217 a0020c0024t0001g0015 |
3 | HG00639.hp2 HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2620+2718G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99821987 | |||||||
chr10:99822000 | A | C | 1 | a0001c0001t0001g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2620+2731A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99822000 | |||||||
chr10:99822016 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2620+2747G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99822016 | |||||||
chr10:99822083 | C | A | 1 | a0001c0001t0001g0247 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2620+2814C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99822083 | |||||||
chr10:99822166 | G | C | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2620+2897G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99822166 | |||||||
chr10:99822230 | C | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): Show |
97 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(94): Show |
intron_variant | MODIFIER | c.2620+2961C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99822230 | |||||||
chr10:99822310 | G | A | 12 | a0001c0001t0001g0014 a0001c0002t0003g0132 a0001c0002t0003g0133 others(9): Show |
12 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.2620+3041G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99822310 | |||||||
chr10:99822414 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2620+3145C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99822414 | |||||||
chr10:99822424 | C | T | 12 | a0001c0001t0001g0014 a0001c0002t0003g0132 a0001c0002t0003g0133 others(9): Show |
12 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.2620+3155C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99822424 | |||||||
chr10:99822427 | T | C | 246 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(243): Show |
253 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.2620+3158T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99822427 | |||||||
chr10:99822437 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2620+3168G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99822437 | |||||||
chr10:99822469 | G | A | 2 | a0001c0002t0002g0048 a0001c0002t0002g0108 |
2 | HG00738.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2620+3200G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99822469 | |||||||
chr10:99822503 | C | T | 4 | a0001c0001t0001g0169 a0001c0001t0001g0175 a0001c0001t0001g0179 others(1): Show |
4 | HG01928.hp1 HG01943.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.2620+3234C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99822503 | |||||||
chr10:99822822 | T | C | 5 | a0005c0008t0001g0030 a0005c0008t0001g0047 a0005c0008t0001g0077 others(2): Show |
5 | HG00140.hp2 HG01074.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.2620+3553T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99822822 | |||||||
chr10:99822940 | C | T | 3 | a0004c0029t0001g0329 a0014c0023t0001g0217 a0020c0024t0001g0015 |
3 | HG00639.hp2 HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2620+3671C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99822940 | |||||||
chr10:99822975 | GT | G | 12 | a0001c0001t0001g0014 a0001c0002t0003g0132 a0001c0002t0003g0133 others(9): Show |
12 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.2620+3713delT | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | INFO_REALIGN_3_PRIME | chr10 | 99822975 | ||||||
chr10:99823018 | C | T | 3 | a0004c0029t0001g0329 a0014c0023t0001g0217 a0020c0024t0001g0015 |
3 | HG00639.hp2 HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2620+3749C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99823018 | |||||||
chr10:99823047 | A | G | 223 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(220): Show |
230 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.2620+3778A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99823047 | |||||||
chr10:99823144 | C | T | 1 | a0017c0031t0001g0145 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2620+3875C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99823144 | |||||||
chr10:99823280 | T | C | 44 | a0001c0001t0005g0292 a0002c0003t0001g0006 a0002c0003t0001g0137 others(41): Show |
45 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.2620+4011T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99823280 | |||||||
chr10:99823350 | C | G | 13 | a0001c0001t0001g0014 a0001c0001t0001g0118 a0001c0002t0003g0132 others(10): Show |
13 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.2620+4081C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99823350 | |||||||
chr10:99823508 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2620+4239T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99823508 | |||||||
chr10:99823573 | G | A | 219 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(216): Show |
226 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.2620+4304G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99823573 | |||||||
chr10:99823585 | G | A | 222 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(219): Show |
229 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.2620+4316G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99823585 | |||||||
chr10:99823600 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2620+4331C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99823600 | |||||||
chr10:99823887 | C | T | 219 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(216): Show |
226 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.2620+4618C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99823887 | |||||||
chr10:99824062 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2620+4793T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99824062 | |||||||
chr10:99824287 | T | C | 222 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(219): Show |
229 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.2620+5018T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99824287 | |||||||
chr10:99824387 | A | G | 222 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(219): Show |
229 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.2620+5118A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99824387 | |||||||
chr10:99824479 | T | C | 1 | a0003c0004t0001g0176 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2620+5210T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99824479 | |||||||
chr10:99824579 | C | A | 1 | a0001c0001t0001g0185 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2620+5310C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99824579 | |||||||
chr10:99824642 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2620+5373G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99824642 | |||||||
chr10:99824741 | G | A | 210 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(207): Show |
217 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.2620+5472G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99824741 | |||||||
chr10:99824746 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2620+5477G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99824746 | |||||||
chr10:99824852 | C | T | 210 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(207): Show |
217 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.2621-5455C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99824852 | |||||||
chr10:99824853 | G | A | 1 | a0001c0002t0002g0097 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2621-5454G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99824853 | |||||||
chr10:99824858 | C | T | 218 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(215): Show |
225 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.2621-5449C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99824858 | |||||||
chr10:99824868 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2621-5439A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99824868 | |||||||
chr10:99824870 | G | A | 219 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(216): Show |
226 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.2621-5437G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99824870 | |||||||
chr10:99824951 | C | T | 1 | a0001c0001t0001g0308 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2621-5356C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99824951 | |||||||
chr10:99825008 | T | C | 221 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(218): Show |
228 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.2621-5299T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99825008 | |||||||
chr10:99825014 | T | C | 3 | a0014c0023t0001g0217 a0020c0024t0001g0015 a0027c0028t0001g0277 |
3 | HG00639.hp2 HG02451.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2621-5293T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99825014 | |||||||
chr10:99825017 | C | A | 221 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(218): Show |
228 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.2621-5290C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99825017 | |||||||
chr10:99825175 | C | T | 219 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(216): Show |
226 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.2621-5132C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99825175 | |||||||
chr10:99825328 | T | A | 219 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(216): Show |
226 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.2621-4979T>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99825328 | |||||||
chr10:99825350 | G | A | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2621-4957G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99825350 | |||||||
chr10:99825433 | A | C | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2621-4874A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99825433 | |||||||
chr10:99825500 | G | A | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2621-4807G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99825500 | |||||||
chr10:99825627 | C | T | 1 | a0014c0023t0001g0217 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2621-4680C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99825627 | |||||||
chr10:99825628 | C | G | 3 | a0001c0002t0003g0116 a0001c0002t0003g0117 a0024c0033t0003g0082 |
3 | HG01928.hp2 HG03669.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2621-4679C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99825628 | |||||||
chr10:99825640 | G | A | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2621-4667G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99825640 | |||||||
chr10:99825684 | C | A | 1 | a0005c0008t0001g0030 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2621-4623C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99825684 | |||||||
chr10:99825752 | T | C | 221 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(218): Show |
228 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.2621-4555T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99825752 | |||||||
chr10:99825754 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2621-4553T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99825754 | |||||||
chr10:99825774 | G | T | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2621-4533G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99825774 | |||||||
chr10:99825779 | C | T | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2621-4528C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99825779 | |||||||
chr10:99825835 | C | T | 219 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(216): Show |
226 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.2621-4472C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99825835 | |||||||
chr10:99825841 | G | A | 8 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0003g0222 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2621-4466G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99825841 | |||||||
chr10:99825890 | G | T | 1 | a0001c0001t0001g0180 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2621-4417G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99825890 | |||||||
chr10:99825900 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2621-4407G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99825900 | |||||||
chr10:99825981 | C | A | 1 | a0001c0002t0002g0088 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2621-4326C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99825981 | |||||||
chr10:99825989 | G | A | 1 | a0001c0002t0002g0105 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2621-4318G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99825989 | |||||||
chr10:99825995 | C | A | 2 | a0010c0015t0001g0016 a0010c0015t0001g0017 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2621-4312C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99825995 | |||||||
chr10:99825996 | G | A | 2 | a0002c0003t0001g0154 a0020c0024t0001g0015 |
2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2621-4311G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99825996 | |||||||
chr10:99826047 | T | C | 1 | a0004c0006t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2621-4260T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99826047 | |||||||
chr10:99826128 | T | C | 8 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0003g0222 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2621-4179T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99826128 | |||||||
chr10:99826207 | C | A | 1 | a0001c0001t0001g0170 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2621-4100C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99826207 | |||||||
chr10:99826219 | C | A | 1 | a0002c0003t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2621-4088C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99826219 | |||||||
chr10:99826374 | T | C | 1 | a0001c0002t0003g0111 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2621-3933T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99826374 | |||||||
chr10:99826401 | C | T | 1 | a0023c0018t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2621-3906C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99826401 | |||||||
chr10:99826414 | T | C | 221 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(218): Show |
228 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.2621-3893T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99826414 | |||||||
chr10:99826621 | T | C | 13 | a0001c0001t0001g0014 a0001c0002t0003g0132 a0001c0002t0003g0133 others(10): Show |
13 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.2621-3686T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99826621 | |||||||
chr10:99826621 | T | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(207): Show |
217 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.2621-3686T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99826621 | |||||||
chr10:99826823 | A | G | 1 | a0001c0002t0002g0043 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2621-3484A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99826823 | |||||||
chr10:99826832 | T | G | 223 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(220): Show |
230 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.2621-3475T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99826832 | |||||||
chr10:99826907 | A | C | 1 | a0001c0001t0001g0180 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2621-3400A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99826907 | |||||||
chr10:99826912 | T | G | 1 | a0023c0018t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2621-3395T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99826912 | |||||||
chr10:99826980 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2621-3327G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99826980 | |||||||
chr10:99827028 | T | C | 8 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0003g0222 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2621-3279T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99827028 | |||||||
chr10:99827029 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2621-3278C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99827029 | |||||||
chr10:99827055 | G | A | 219 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(216): Show |
226 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.2621-3252G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99827055 | |||||||
chr10:99827125 | GATATCC | G | 5 | a0005c0008t0001g0030 a0005c0008t0001g0047 a0005c0008t0001g0077 others(2): Show |
5 | HG00140.hp2 HG01074.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.2621-3178_2621-317 others(10): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | INFO_REALIGN_3_PRIME | chr10 | 99827125 | ||||||
chr10:99827133 | T | A | 5 | a0005c0008t0001g0030 a0005c0008t0001g0047 a0005c0008t0001g0077 others(2): Show |
5 | HG00140.hp2 HG01074.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.2621-3174T>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99827133 | |||||||
chr10:99827175 | G | A | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2621-3132G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99827175 | |||||||
chr10:99827198 | C | T | 1 | a0014c0023t0001g0217 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2621-3109C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99827198 | |||||||
chr10:99827245 | C | T | 218 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(215): Show |
225 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.2621-3062C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99827245 | |||||||
chr10:99827281 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2621-3026G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99827281 | |||||||
chr10:99827285 | C | T | 223 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(220): Show |
230 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.2621-3022C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99827285 | |||||||
chr10:99827498 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2621-2809G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99827498 | |||||||
chr10:99827672 | C | T | 2 | a0001c0001t0001g0287 a0001c0001t0001g0294 |
2 | NA18967.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.2621-2635C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99827672 | |||||||
chr10:99827679 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2621-2628C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99827679 | |||||||
chr10:99827812 | C | T | 43 | a0002c0003t0001g0006 a0002c0003t0001g0137 a0002c0003t0001g0138 others(40): Show |
44 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.2621-2495C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99827812 | |||||||
chr10:99827877 | G | T | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2621-2430G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99827877 | |||||||
chr10:99827886 | C | T | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2621-2421C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99827886 | |||||||
chr10:99827913 | C | T | 1 | a0001c0002t0002g0123 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2621-2394C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99827913 | |||||||
chr10:99827917 | C | T | 4 | a0001c0002t0007g0128 a0001c0002t0007g0131 a0001c0014t0001g0130 others(1): Show |
4 | HG02818.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2621-2390C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99827917 | |||||||
chr10:99827980 | C | CCACACCT others(211): Show |
2 | a0004c0029t0001g0329 a0023c0018t0001g0009 |
2 | HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2621-2319_2621-231 others(222): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | INFO_REALIGN_3_PRIME | chr10 | 99827980 | ||||||
chr10:99827980 | C | CCACACCT others(211): Show |
1 | a0001c0005t0001g0172 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2621-2319_2621-231 others(222): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | INFO_REALIGN_3_PRIME | chr10 | 99827980 | ||||||
chr10:99827980 | C | CCACACCT others(211): Show |
106 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0058 others(103): Show |
106 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.2621-2319_2621-231 others(222): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | INFO_REALIGN_3_PRIME | chr10 | 99827980 | ||||||
chr10:99827980 | C | CCACACCT others(211): Show |
1 | a0001c0001t0001g0281 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2621-2319_2621-231 others(222): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | INFO_REALIGN_3_PRIME | chr10 | 99827980 | ||||||
chr10:99828174 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
93 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.2621-2133C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99828174 | |||||||
chr10:99828232 | G | A | 1 | a0014c0023t0001g0217 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2621-2075G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99828232 | |||||||
chr10:99828337 | G | T | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2621-1970G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99828337 | |||||||
chr10:99828441 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2621-1866C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99828441 | |||||||
chr10:99828546 | G | A | 1 | a0001c0002t0011g0031 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2621-1761G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99828546 | |||||||
chr10:99828582 | G | C | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2621-1725G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99828582 | |||||||
chr10:99828664 | C | T | 8 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0003g0222 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2621-1643C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99828664 | |||||||
chr10:99828764 | C | G | 1 | a0005c0008t0001g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2621-1543C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99828764 | |||||||
chr10:99828983 | G | A | 3 | a0004c0006t0001g0080 a0004c0006t0001g0081 a0004c0006t0001g0096 |
3 | HG02109.hp1 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2621-1324G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99828983 | |||||||
chr10:99829269 | T | C | 1 | a0001c0002t0002g0125 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2621-1038T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99829269 | |||||||
chr10:99829275 | G | A | 3 | a0005c0008t0001g0030 a0005c0008t0001g0047 a0005c0008t0001g0077 |
3 | HG00140.hp2 HG01074.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.2621-1032G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99829275 | |||||||
chr10:99829453 | A | AT | 224 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(221): Show |
231 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.2621-849dupT | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | INFO_REALIGN_3_PRIME | chr10 | 99829453 | ||||||
chr10:99829467 | T | C | 5 | a0005c0008t0001g0030 a0005c0008t0001g0047 a0005c0008t0001g0077 others(2): Show |
5 | HG00140.hp2 HG01074.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.2621-840T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99829467 | |||||||
chr10:99829489 | G | A | 1 | a0002c0003t0001g0248 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2621-818G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99829489 | |||||||
chr10:99829545 | ATATTT | A | 221 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(218): Show |
228 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.2621-745_2621-741d others(7): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | INFO_REALIGN_3_PRIME | chr10 | 99829545 | ||||||
chr10:99829568 | C | A | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2621-739C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99829568 | |||||||
chr10:99829568 | C | T | 1 | a0001c0002t0003g0168 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2621-739C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99829568 | |||||||
chr10:99829569 | G | A | 1 | a0001c0002t0002g0113 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2621-738G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99829569 | |||||||
chr10:99829571 | G | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
93 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.2621-736G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99829571 | |||||||
chr10:99829609 | T | G | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2621-698T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99829609 | |||||||
chr10:99829647 | G | T | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2621-660G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99829647 | |||||||
chr10:99829672 | C | T | 8 | a0003c0004t0001g0001 a0003c0004t0001g0146 a0003c0004t0001g0165 others(5): Show |
10 | HG01358.hp2 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2621-635C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99829672 | |||||||
chr10:99829762 | G | A | 3 | a0001c0002t0002g0078 a0001c0002t0002g0092 a0001c0002t0002g0093 |
3 | HG00544.hp1 HG00621.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.2621-545G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99829762 | |||||||
chr10:99829931 | G | A | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2621-376G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99829931 | |||||||
chr10:99830168 | G | A | 43 | a0002c0003t0001g0006 a0002c0003t0001g0137 a0002c0003t0001g0138 others(40): Show |
44 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.2621-139G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99830168 | |||||||
chr10:99830263 | G | A | 5 | a0001c0002t0002g0071 a0001c0002t0002g0084 a0001c0002t0002g0089 others(2): Show |
5 | HG00140.hp1 HG00741.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.2621-44G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99830263 | |||||||
chr10:99830536 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2747+103C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 20/31 | chr10 | 99830536 | |||||||
chr10:99830550 | C | T | 1 | a0001c0002t0002g0093 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2747+117C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 20/31 | chr10 | 99830550 | |||||||
chr10:99830862 | C | T | 5 | a0005c0008t0001g0030 a0005c0008t0001g0047 a0005c0008t0001g0077 others(2): Show |
5 | HG00140.hp2 HG01074.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.2883+11C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 21/31 | chr10 | 99830862 | |||||||
chr10:99831298 | C | T | 1 | a0001c0001t0001g0002 | 2 | HG02523.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2884-313C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 21/31 | chr10 | 99831298 | |||||||
chr10:99831543 | C | A | 2 | a0014c0023t0001g0217 a0020c0024t0001g0015 |
2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2884-68C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 21/31 | chr10 | 99831543 | |||||||
chr10:99831577 | G | T | 8 | a0001c0002t0003g0132 a0001c0002t0003g0133 a0001c0002t0003g0222 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2884-34G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 21/31 | chr10 | 99831577 | |||||||
chr10:99832187 | T | C | 218 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(215): Show |
225 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.3258+56T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 23/31 | chr10 | 99832187 | |||||||
chr10:99832286 | C | G | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3258+155C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 23/31 | chr10 | 99832286 | |||||||
chr10:99832400 | A | ATGTGT | 198 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(195): Show |
203 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.3258+269_3258+270i others(7): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 23/31 | chr10 | 99832400 | |||||||
chr10:99832401 | A | G | 198 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(195): Show |
203 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.3258+270A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 23/31 | chr10 | 99832401 | |||||||
chr10:99832402 | C | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(195): Show |
203 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.3258+271C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 23/31 | chr10 | 99832402 | |||||||
chr10:99832563 | A | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(192): Show |
202 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.3258+432A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 23/31 | chr10 | 99832563 | |||||||
chr10:99832615 | G | A | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3258+484G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 23/31 | chr10 | 99832615 | |||||||
chr10:99832632 | G | C | 3 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0208 |
3 | NA18940.hp1 NA18971.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.3258+501G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 23/31 | chr10 | 99832632 | |||||||
chr10:99832634 | T | C | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3258+503T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 23/31 | chr10 | 99832634 | |||||||
chr10:99832826 | C | A | 1 | a0001c0001t0001g0186 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.3258+695C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 23/31 | chr10 | 99832826 | |||||||
chr10:99832865 | A | G | 224 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(221): Show |
231 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.3258+734A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 23/31 | chr10 | 99832865 | |||||||
chr10:99832932 | T | G | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(64): Show |
69 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.3258+801T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 23/31 | chr10 | 99832932 | |||||||
chr10:99833086 | A | G | 9 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(6): Show |
9 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.3258+955A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 23/31 | chr10 | 99833086 | |||||||
chr10:99833147 | A | G | 9 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(6): Show |
9 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.3258+1016A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 23/31 | chr10 | 99833147 | |||||||
chr10:99833422 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3259-958G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 23/31 | chr10 | 99833422 | |||||||
chr10:99833628 | G | A | 8 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(5): Show |
8 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3259-752G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 23/31 | chr10 | 99833628 | |||||||
chr10:99833776 | A | T | 8 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(5): Show |
8 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3259-604A>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 23/31 | chr10 | 99833776 | |||||||
chr10:99833993 | A | G | 17 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(14): Show |
17 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.3259-387A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 23/31 | chr10 | 99833993 | |||||||
chr10:99834036 | G | A | 1 | a0001c0002t0002g0071 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3259-344G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 23/31 | chr10 | 99834036 | |||||||
chr10:99834160 | G | A | 1 | a0001c0002t0003g0110 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3259-220G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 23/31 | chr10 | 99834160 | |||||||
chr10:99834285 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3259-95A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 23/31 | chr10 | 99834285 | |||||||
chr10:99834560 | T | C | 3 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 |
3 | NA18948.hp2 NA18978.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.3414+25T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 24/31 | chr10 | 99834560 | |||||||
chr10:99834643 | C | T | 2 | a0002c0003t0001g0229 a0002c0003t0001g0249 |
2 | NA18954.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.3414+108C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 24/31 | chr10 | 99834643 | |||||||
chr10:99834652 | G | T | 9 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(6): Show |
9 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.3414+117G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 24/31 | chr10 | 99834652 | |||||||
chr10:99834679 | T | C | 1 | a0004c0006t0001g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3414+144T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 24/31 | chr10 | 99834679 | |||||||
chr10:99834737 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3414+202C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 24/31 | chr10 | 99834737 | |||||||
chr10:99834796 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3414+261C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 24/31 | chr10 | 99834796 | |||||||
chr10:99834887 | C | T | 5 | a0001c0001t0001g0236 a0001c0001t0001g0267 a0001c0001t0001g0287 others(2): Show |
5 | NA18953.hp2 NA18967.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.3414+352C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 24/31 | chr10 | 99834887 | |||||||
chr10:99834888 | G | A | 1 | a0002c0003t0001g0250 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3414+353G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 24/31 | chr10 | 99834888 | |||||||
chr10:99834972 | G | A | 25 | a0001c0001t0001g0148 a0001c0001t0004g0121 a0002c0003t0001g0137 others(22): Show |
25 | HG00423.hp1 HG00621.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.3414+437G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 24/31 | chr10 | 99834972 | |||||||
chr10:99835036 | C | T | 1 | a0003c0004t0001g0177 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3414+501C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 24/31 | chr10 | 99835036 | |||||||
chr10:99835096 | C | T | 7 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(4): Show |
7 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.3414+561C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 24/31 | chr10 | 99835096 | |||||||
chr10:99835097 | G | A | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3414+562G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 24/31 | chr10 | 99835097 | |||||||
chr10:99835262 | C | T | 2 | a0006c0010t0001g0010 a0006c0010t0001g0011 |
2 | HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3414+727C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 24/31 | chr10 | 99835262 | |||||||
chr10:99835263 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3414+728G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 24/31 | chr10 | 99835263 | |||||||
chr10:99835308 | C | T | 6 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(3): Show |
6 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.3414+773C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 24/31 | chr10 | 99835308 | |||||||
chr10:99835410 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.3415-681C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 24/31 | chr10 | 99835410 | |||||||
chr10:99835463 | G | A | 2 | a0001c0001t0001g0297 a0001c0001t0001g0298 |
2 | NA18954.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.3415-628G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 24/31 | chr10 | 99835463 | |||||||
chr10:99835549 | C | T | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3415-542C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 24/31 | chr10 | 99835549 | |||||||
chr10:99835592 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG00738.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.3415-499C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 24/31 | chr10 | 99835592 | |||||||
chr10:99835597 | C | T | 4 | a0001c0002t0002g0068 a0001c0002t0002g0086 a0001c0002t0002g0087 others(1): Show |
4 | NA18990.hp2 NA19005.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.3415-494C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 24/31 | chr10 | 99835597 | |||||||
chr10:99835616 | T | C | 9 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(6): Show |
9 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.3415-475T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 24/31 | chr10 | 99835616 | |||||||
chr10:99835726 | T | C | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3415-365T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 24/31 | chr10 | 99835726 | |||||||
chr10:99835736 | C | T | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3415-355C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 24/31 | chr10 | 99835736 | |||||||
chr10:99835799 | T | C | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3415-292T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 24/31 | chr10 | 99835799 | |||||||
chr10:99836355 | G | A | 1 | a0002c0003t0001g0252 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3614+65G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99836355 | |||||||
chr10:99836374 | C | G | 1 | a0005c0008t0001g0030 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3614+84C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99836374 | |||||||
chr10:99836419 | G | A | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3614+129G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99836419 | |||||||
chr10:99836483 | G | A | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3614+193G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99836483 | |||||||
chr10:99836636 | C | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3614+346C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99836636 | |||||||
chr10:99836639 | A | G | 1 | a0014c0023t0001g0217 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3614+349A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99836639 | |||||||
chr10:99836639 | A | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3614+349A>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99836639 | |||||||
chr10:99836794 | G | C | 3 | a0001c0001t0001g0218 a0010c0015t0001g0016 a0010c0015t0001g0017 |
3 | HG02630.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3614+504G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99836794 | |||||||
chr10:99836840 | C | T | 1 | a0004c0006t0001g0096 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3614+550C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99836840 | |||||||
chr10:99837137 | C | CT | 163 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(160): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.3614+864dupT | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99837137 | ||||||
chr10:99837137 | C | CTT | 33 | a0001c0001t0001g0118 a0001c0001t0001g0148 a0001c0001t0001g0269 others(30): Show |
33 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.3614+863_3614+864d others(4): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99837137 | ||||||
chr10:99837137 | C | CTTTT | 9 | a0004c0006t0001g0038 a0004c0006t0001g0080 a0004c0006t0001g0081 others(6): Show |
9 | HG00140.hp2 HG00639.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.3614+861_3614+864d others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99837137 | ||||||
chr10:99837325 | C | T | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3614+1035C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99837325 | |||||||
chr10:99837326 | G | A | 6 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(3): Show |
6 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.3614+1036G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99837326 | |||||||
chr10:99837384 | A | G | 16 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(13): Show |
16 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.3614+1094A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99837384 | |||||||
chr10:99837448 | ATTCTTTT others(2): Show |
A | 6 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(3): Show |
6 | HG02109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3614+1170_3614+117 others(13): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99837448 | ||||||
chr10:99837451 | CTTTTTTT others(3): Show |
C | 1 | a0004c0006t0001g0140 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3614+1170_3614+117 others(14): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99837451 | ||||||
chr10:99837456 | TTTTC | T | 7 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(4): Show |
7 | HG00140.hp2 HG01074.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614+1170_3614+117 others(8): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99837456 | ||||||
chr10:99837460 | C | CT | 26 | a0001c0001t0001g0148 a0001c0001t0001g0317 a0001c0002t0002g0034 others(23): Show |
26 | HG00423.hp1 HG00621.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.3614+1187dupT | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99837460 | ||||||
chr10:99837460 | C | T | 1 | a0021c0032t0001g0129 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3614+1170C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99837460 | |||||||
chr10:99837460 | CT | C | 21 | a0001c0001t0001g0114 a0001c0001t0001g0144 a0001c0001t0001g0150 others(18): Show |
21 | HG00323.hp1 HG01169.hp1 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.3614+1187delT | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99837460 | ||||||
chr10:99837468 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3614+1178T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99837468 | |||||||
chr10:99837477 | TA | T | 6 | a0001c0001t0001g0055 a0001c0001t0001g0265 a0001c0001t0001g0284 others(3): Show |
6 | HG01167.hp1 HG01516.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.3614+1190delA | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99837477 | ||||||
chr10:99837478 | A | T | 74 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(71): Show |
76 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.3614+1188A>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99837478 | |||||||
chr10:99837596 | T | C | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3614+1306T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99837596 | |||||||
chr10:99837615 | C | T | 17 | a0001c0002t0002g0063 a0004c0006t0001g0022 a0004c0006t0001g0038 others(14): Show |
17 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.3614+1325C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99837615 | |||||||
chr10:99837726 | T | C | 16 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(13): Show |
16 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.3614+1436T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99837726 | |||||||
chr10:99837813 | C | G | 1 | a0001c0002t0002g0100 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3614+1523C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99837813 | |||||||
chr10:99837846 | A | G | 1 | a0001c0007t0003g0024 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3614+1556A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99837846 | |||||||
chr10:99837928 | G | C | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | NA18989.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.3614+1638G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99837928 | |||||||
chr10:99837945 | T | A | 43 | a0001c0001t0001g0148 a0001c0001t0004g0121 a0002c0003t0001g0137 others(40): Show |
43 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.3614+1655T>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99837945 | |||||||
chr10:99838001 | C | T | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3614+1711C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838001 | |||||||
chr10:99838002 | G | C | 7 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(4): Show |
7 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.3614+1712G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838002 | |||||||
chr10:99838016 | G | A | 8 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(5): Show |
8 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3614+1726G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838016 | |||||||
chr10:99838023 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3614+1733G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838023 | |||||||
chr10:99838036 | C | T | 65 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(62): Show |
67 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.3614+1746C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838036 | |||||||
chr10:99838104 | T | C | 2 | a0005c0008t0001g0047 a0005c0008t0001g0077 |
2 | HG00140.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.3614+1814T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838104 | |||||||
chr10:99838107 | C | CCCCCCAA others(220): Show |
2 | a0001c0014t0001g0023 a0001c0014t0001g0130 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3614+1822_3614+182 others(231): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838107 | ||||||
chr10:99838108 | CCCCCCCA others(218): Show |
C | 2 | a0005c0008t0001g0047 a0005c0008t0001g0077 |
2 | HG00140.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.3614+1825_3614+204 others(4): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838108 | ||||||
chr10:99838134 | C | T | 8 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(5): Show |
8 | HG01496.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.3614+1844C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838134 | |||||||
chr10:99838143 | G | A | 1 | a0004c0006t0001g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3614+1853G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838143 | |||||||
chr10:99838154 | T | C | 2 | a0001c0014t0001g0023 a0001c0014t0001g0130 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3614+1864T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838154 | |||||||
chr10:99838158 | C | A | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3614+1868C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838158 | |||||||
chr10:99838163 | A | AACCTCCC others(347): Show |
1 | a0001c0001t0001g0272 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3614+1905_3614+190 others(358): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838163 | ||||||
chr10:99838163 | A | C | 3 | a0001c0014t0001g0023 a0001c0014t0001g0130 a0005c0008t0001g0013 |
3 | HG03471.hp2 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3614+1873A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838163 | |||||||
chr10:99838168 | C | A | 1 | a0001c0001t0001g0308 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.3614+1878C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838168 | |||||||
chr10:99838183 | CGGCTGGC others(9): Show |
C | 5 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0140 others(2): Show |
5 | HG01496.hp2 HG02055.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.3614+1899_3614+191 others(20): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838183 | ||||||
chr10:99838184 | G | A | 1 | a0005c0008t0001g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3614+1894G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838184 | |||||||
chr10:99838188 | G | GACCCCCC others(9): Show |
3 | a0004c0006t0001g0080 a0004c0006t0001g0081 a0004c0006t0001g0096 |
3 | HG02109.hp1 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.3614+1898_3614+189 others(20): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838188 | |||||||
chr10:99838189 | G | C | 3 | a0004c0006t0001g0080 a0004c0006t0001g0081 a0004c0006t0001g0096 |
3 | HG02109.hp1 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.3614+1899G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838189 | |||||||
chr10:99838194 | G | A | 3 | a0004c0006t0001g0080 a0004c0006t0001g0081 a0004c0006t0001g0096 |
3 | HG02109.hp1 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.3614+1904G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838194 | |||||||
chr10:99838199 | G | GC | 3 | a0004c0006t0001g0080 a0004c0006t0001g0081 a0004c0006t0001g0096 |
3 | HG02109.hp1 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.3614+1909_3614+191 others(5): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838199 | |||||||
chr10:99838202 | C | A | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3614+1912C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838202 | |||||||
chr10:99838203 | T | C | 2 | a0001c0014t0001g0023 a0001c0014t0001g0130 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3614+1913T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838203 | |||||||
chr10:99838217 | CCCTCCCG others(71): Show |
C | 5 | a0001c0002t0006g0018 a0001c0002t0006g0019 a0005c0008t0001g0030 others(2): Show |
5 | HG00642.hp2 HG01074.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.3614+1957_3614+203 others(82): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838217 | ||||||
chr10:99838222 | C | G | 1 | a0005c0008t0001g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3614+1932C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838222 | |||||||
chr10:99838225 | G | A | 2 | a0006c0010t0001g0010 a0006c0010t0001g0011 |
2 | HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3614+1935G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838225 | |||||||
chr10:99838233 | G | A | 1 | a0005c0008t0001g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3614+1943G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838233 | |||||||
chr10:99838245 | AGAGGGGC others(121): Show |
A | 1 | a0014c0023t0001g0217 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3614+1957_3614+208 others(4): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838245 | ||||||
chr10:99838278 | A | G | 14 | a0001c0001t0001g0272 a0001c0014t0001g0023 a0001c0014t0001g0130 others(11): Show |
14 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.3614+1988A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838278 | |||||||
chr10:99838288 | G | A | 2 | a0011c0012t0001g0215 a0011c0012t0001g0216 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3614+1998G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838288 | |||||||
chr10:99838305 | C | T | 3 | a0001c0002t0006g0018 a0001c0002t0006g0019 a0016c0026t0006g0021 |
3 | HG00642.hp2 HG01109.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.3614+2015C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838305 | |||||||
chr10:99838308 | G | C | 3 | a0001c0002t0006g0018 a0001c0002t0006g0019 a0016c0026t0006g0021 |
3 | HG00642.hp2 HG01109.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.3614+2018G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838308 | |||||||
chr10:99838309 | G | A | 3 | a0001c0002t0006g0018 a0001c0002t0006g0019 a0016c0026t0006g0021 |
3 | HG00642.hp2 HG01109.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.3614+2019G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838309 | |||||||
chr10:99838309 | G | GCGGCTGG others(169): Show |
2 | a0001c0001t0001g0269 a0001c0001t0008g0291 |
2 | NA19060.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.3614+2032_3614+203 others(180): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838309 | ||||||
chr10:99838318 | C | CGGGCGGA others(218): Show |
60 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(57): Show |
62 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.3614+2032_3614+203 others(229): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838318 | ||||||
chr10:99838318 | C | CGGGCGGA others(219): Show |
1 | a0001c0001t0001g0317 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3614+2032_3614+203 others(230): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838318 | ||||||
chr10:99838318 | C | CGGGCGGA others(219): Show |
2 | a0001c0001t0001g0055 a0002c0021t0003g0257 |
2 | HG01516.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.3614+2032_3614+203 others(230): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838318 | ||||||
chr10:99838322 | CA | C | 9 | a0001c0014t0001g0023 a0001c0014t0001g0130 a0004c0006t0001g0022 others(6): Show |
9 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.3614+2033delA | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838322 | |||||||
chr10:99838323 | A | G | 68 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(65): Show |
70 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.3614+2033A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838323 | |||||||
chr10:99838331 | C | T | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(69): Show |
74 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.3614+2041C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838331 | |||||||
chr10:99838334 | C | CCCCCCCC others(43): Show |
3 | a0006c0010t0001g0010 a0006c0010t0001g0011 a0021c0032t0001g0129 |
3 | HG02809.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3614+2051_3614+205 others(54): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838334 | ||||||
chr10:99838334 | CCCCCCCC others(42): Show |
C | 1 | a0001c0002t0002g0112 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.3614+2133_3614+218 others(53): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838334 | ||||||
chr10:99838335 | C | CCCCCCAC others(41): Show |
2 | a0001c0014t0001g0023 a0001c0014t0001g0130 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3614+2050_3614+205 others(52): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838335 | ||||||
chr10:99838339 | C | A | 1 | a0001c0001t0001g0005 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3614+2049C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838339 | |||||||
chr10:99838357 | G | A | 7 | a0001c0001t0001g0269 a0001c0001t0008g0291 a0001c0002t0006g0018 others(4): Show |
7 | HG00642.hp2 HG01109.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.3614+2067G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838357 | |||||||
chr10:99838359 | G | A | 3 | a0001c0001t0001g0118 a0011c0012t0001g0215 a0011c0012t0001g0216 |
3 | HG02895.hp2 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3614+2069G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838359 | |||||||
chr10:99838362 | G | A | 2 | a0005c0008t0001g0030 a0022c0020t0001g0309 |
2 | HG01074.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3614+2072G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838362 | |||||||
chr10:99838369 | C | A | 1 | a0001c0001t0001g0236 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3614+2079C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838369 | |||||||
chr10:99838369 | C | T | 7 | a0001c0001t0001g0269 a0001c0001t0008g0291 a0001c0002t0006g0018 others(4): Show |
7 | HG00642.hp2 HG01109.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.3614+2079C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838369 | |||||||
chr10:99838372 | G | C | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3614+2082G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838372 | |||||||
chr10:99838373 | C | CAGAGGGG others(72): Show |
1 | a0001c0001t0001g0288 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3614+2083_3614+208 others(83): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838373 | |||||||
chr10:99838373 | C | CG | 9 | a0001c0001t0001g0183 a0001c0001t0001g0269 a0001c0001t0008g0291 others(6): Show |
9 | HG00642.hp2 HG01109.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.3614+2089dupG | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838373 | ||||||
chr10:99838381 | C | T | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(69): Show |
74 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.3614+2091C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838381 | |||||||
chr10:99838383 | A | ACCCCCCC others(530): Show |
1 | a0002c0003t0001g0250 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3614+2132_3614+213 others(541): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838383 | ||||||
chr10:99838383 | A | ACCCCCCC others(123): Show |
50 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(47): Show |
52 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.3614+2132_3614+213 others(134): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838383 | ||||||
chr10:99838383 | A | ACCCCCCC others(124): Show |
8 | a0001c0001t0001g0055 a0001c0001t0001g0058 a0001c0001t0001g0135 others(5): Show |
8 | HG01516.hp1 HG02132.hp1 HG04228.hp1 others(5): Show |
intron_variant | MODIFIER | c.3614+2132_3614+213 others(135): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838383 | ||||||
chr10:99838383 | A | ACCCCCCC others(126): Show |
1 | a0002c0021t0003g0257 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3614+2132_3614+213 others(137): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838383 | ||||||
chr10:99838383 | A | ACCCCCCC others(125): Show |
1 | a0001c0001t0001g0302 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3614+2132_3614+213 others(136): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838383 | ||||||
chr10:99838383 | A | ACCCCCCC others(124): Show |
1 | a0001c0001t0001g0305 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3614+2100_3614+210 others(135): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838383 | ||||||
chr10:99838385 | C | A | 5 | a0002c0003t0001g0137 a0002c0003t0001g0138 a0002c0003t0001g0154 others(2): Show |
5 | HG01884.hp1 HG03130.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.3614+2095C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838385 | |||||||
chr10:99838400 | C | G | 2 | a0005c0008t0001g0030 a0022c0020t0001g0309 |
2 | HG01074.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3614+2110C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838400 | |||||||
chr10:99838410 | CGGCTGGC others(169): Show |
C | 2 | a0005c0008t0001g0030 a0022c0020t0001g0309 |
2 | HG01074.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3614+2133_3614+230 others(4): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838410 | ||||||
chr10:99838414 | T | C | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3614+2124T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838414 | |||||||
chr10:99838415 | G | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3614+2125G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838415 | |||||||
chr10:99838417 | C | G | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3614+2127C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838417 | |||||||
chr10:99838422 | C | CAGAGGGG others(170): Show |
1 | a0001c0001t0001g0272 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3614+2132_3614+213 others(181): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838422 | |||||||
chr10:99838422 | C | CAGAGGGG others(124): Show |
1 | a0001c0001t0001g0271 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3614+2132_3614+213 others(135): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838422 | |||||||
chr10:99838422 | C | T | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3614+2132C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838422 | |||||||
chr10:99838423 | GGGGGGCC others(395): Show |
G | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3614+2139_3614+254 others(4): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838423 | ||||||
chr10:99838428 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3614+2138G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838428 | |||||||
chr10:99838430 | C | T | 9 | a0001c0001t0001g0269 a0001c0001t0001g0272 a0001c0001t0008g0291 others(6): Show |
9 | HG00639.hp2 HG00642.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.3614+2140C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838430 | |||||||
chr10:99838441 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3614+2151C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838441 | |||||||
chr10:99838449 | C | G | 1 | a0014c0023t0001g0217 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3614+2159C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838449 | |||||||
chr10:99838450 | C | G | 8 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(5): Show |
8 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3614+2160C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838450 | |||||||
chr10:99838459 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3614+2169C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838459 | |||||||
chr10:99838460 | G | A | 1 | a0014c0023t0001g0217 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3614+2170G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838460 | |||||||
chr10:99838468 | GGGCAGAG others(346): Show |
G | 4 | a0005c0008t0001g0013 a0005c0008t0001g0047 a0005c0008t0001g0077 others(1): Show |
4 | HG00140.hp2 HG02300.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.3614+2181_3614+253 others(4): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838468 | ||||||
chr10:99838472 | A | T | 1 | a0001c0001t0001g0272 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3614+2182A>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838472 | |||||||
chr10:99838476 | G | C | 2 | a0006c0010t0001g0010 a0006c0010t0001g0011 |
2 | HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3614+2186G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838476 | |||||||
chr10:99838522 | A | ACCTCCCG others(46): Show |
1 | a0023c0018t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3614+2238_3614+223 others(57): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838522 | ||||||
chr10:99838522 | A | ACCTCCCG others(47): Show |
7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.3614+2238_3614+223 others(58): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838522 | ||||||
chr10:99838522 | A | ACCTCCCG others(45): Show |
1 | a0001c0001t0001g0269 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3614+2238_3614+223 others(56): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838522 | ||||||
chr10:99838522 | A | ACCTCCCG others(46): Show |
4 | a0001c0001t0008g0291 a0001c0014t0001g0023 a0001c0014t0001g0130 others(1): Show |
4 | HG01109.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3614+2238_3614+223 others(57): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838522 | ||||||
chr10:99838522 | A | ACCTCCCG others(47): Show |
2 | a0001c0002t0006g0018 a0001c0002t0006g0019 |
2 | HG00642.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.3614+2238_3614+223 others(58): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838522 | ||||||
chr10:99838525 | T | G | 1 | a0001c0001t0001g0272 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3614+2235T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838525 | |||||||
chr10:99838529 | A | G | 18 | a0001c0001t0001g0269 a0001c0001t0001g0272 a0001c0001t0008g0291 others(15): Show |
18 | HG00639.hp2 HG00642.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.3614+2239A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838529 | |||||||
chr10:99838552 | A | G | 17 | a0001c0001t0001g0269 a0001c0001t0001g0272 a0001c0001t0008g0291 others(14): Show |
17 | HG00639.hp2 HG00642.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.3614+2262A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838552 | |||||||
chr10:99838555 | G | GCTGACCC others(92): Show |
48 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0135 others(45): Show |
50 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.3614+2269_3614+227 others(103): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838555 | ||||||
chr10:99838557 | T | C | 9 | a0001c0001t0001g0269 a0001c0001t0001g0272 a0001c0001t0008g0291 others(6): Show |
9 | HG00639.hp2 HG00642.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.3614+2267T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838557 | |||||||
chr10:99838560 | G | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(78): Show |
83 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.3614+2270G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838560 | |||||||
chr10:99838564 | CCCATCTC others(165): Show |
C | 1 | a0014c0023t0001g0217 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3614+2277_3614+244 others(4): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838564 | ||||||
chr10:99838565 | C | CCACCTCC others(219): Show |
4 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0058 others(1): Show |
4 | HG00738.hp1 HG01516.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.3614+2277_3614+227 others(230): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838565 | ||||||
chr10:99838565 | C | CCACCTCC others(219): Show |
6 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0270 others(3): Show |
6 | NA18948.hp1 NA18952.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.3614+2277_3614+227 others(230): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838565 | ||||||
chr10:99838565 | C | CCACCTCC others(220): Show |
1 | a0001c0001t0001g0287 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.3614+2277_3614+227 others(231): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838565 | ||||||
chr10:99838565 | C | CCACCTCC others(221): Show |
2 | a0001c0001t0001g0305 a0002c0021t0003g0257 |
2 | HG00597.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.3614+2277_3614+227 others(232): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838565 | ||||||
chr10:99838565 | C | CCCACCTC others(220): Show |
2 | a0001c0001t0001g0134 a0001c0001t0001g0317 |
2 | HG02056.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.3614+2276_3614+227 others(231): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838565 | ||||||
chr10:99838565 | C | CCCACCTC others(221): Show |
1 | a0001c0001t0001g0271 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3614+2276_3614+227 others(232): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838565 | ||||||
chr10:99838565 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3614+2275C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838565 | |||||||
chr10:99838568 | T | C | 32 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0058 others(29): Show |
32 | HG00597.hp1 HG00609.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.3614+2278T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838568 | |||||||
chr10:99838586 | T | C | 32 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0058 others(29): Show |
32 | HG00597.hp1 HG00609.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.3614+2296T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838586 | |||||||
chr10:99838587 | G | A | 2 | a0005c0008t0001g0030 a0022c0020t0001g0309 |
2 | HG01074.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3614+2297G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838587 | |||||||
chr10:99838599 | T | A | 34 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0058 others(31): Show |
34 | HG00597.hp1 HG00609.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.3614+2309T>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838599 | |||||||
chr10:99838628 | G | A | 3 | a0001c0001t0001g0162 a0001c0001t0001g0174 a0026c0025t0001g0158 |
3 | HG00673.hp1 NA18984.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.3614+2338G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838628 | |||||||
chr10:99838649 | A | ACCTCCCA others(42): Show |
2 | a0001c0002t0002g0125 a0001c0002t0003g0116 |
2 | HG01928.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.3614+2365_3614+236 others(53): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838649 | ||||||
chr10:99838652 | T | G | 48 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0135 others(45): Show |
50 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.3614+2362T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838652 | |||||||
chr10:99838656 | G | A | 8 | a0001c0001t0001g0269 a0001c0001t0008g0291 a0001c0002t0002g0074 others(5): Show |
8 | HG00642.hp2 HG01109.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.3614+2366G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838656 | |||||||
chr10:99838660 | G | C | 1 | a0001c0001t0001g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3614+2370G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838660 | |||||||
chr10:99838676 | C | CA | 26 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0058 others(23): Show |
26 | HG00597.hp1 HG00609.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.3614+2386_3614+238 others(5): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838676 | |||||||
chr10:99838677 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3614+2387G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838677 | |||||||
chr10:99838679 | G | A | 7 | a0001c0001t0001g0269 a0001c0001t0008g0291 a0001c0002t0006g0018 others(4): Show |
7 | HG00642.hp2 HG01109.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.3614+2389G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838679 | |||||||
chr10:99838684 | T | A | 17 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0058 others(14): Show |
17 | HG00597.hp1 HG00609.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.3614+2394T>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838684 | |||||||
chr10:99838684 | T | C | 58 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0135 others(55): Show |
60 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.3614+2394T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838684 | |||||||
chr10:99838686 | A | ACCCCCTC others(125): Show |
29 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0219 others(26): Show |
31 | HG00558.hp1 HG02071.hp1 HG02897.hp1 others(28): Show |
intron_variant | MODIFIER | c.3614+2401_3614+240 others(136): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838686 | ||||||
chr10:99838686 | A | ACCCCCTC others(126): Show |
19 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0235 others(16): Show |
19 | HG00423.hp2 HG00438.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.3614+2401_3614+240 others(137): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838686 | ||||||
chr10:99838687 | CCCCCCCA others(42): Show |
C | 2 | a0001c0001t0001g0269 a0001c0001t0008g0291 |
2 | NA19060.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.3614+2418_3614+246 others(53): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838687 | ||||||
chr10:99838689 | CCCCCACC others(40): Show |
C | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3614+2404_3614+245 others(51): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838689 | ||||||
chr10:99838708 | T | C | 80 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(77): Show |
82 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.3614+2418T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838708 | |||||||
chr10:99838709 | G | A | 6 | a0001c0001t0001g0185 a0001c0002t0006g0018 a0001c0002t0006g0019 others(3): Show |
6 | HG00642.hp2 HG01109.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.3614+2419G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838709 | |||||||
chr10:99838711 | C | G | 80 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(77): Show |
82 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.3614+2421C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838711 | |||||||
chr10:99838712 | A | G | 80 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(77): Show |
82 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.3614+2422A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838712 | |||||||
chr10:99838721 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3614+2431C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838721 | |||||||
chr10:99838732 | G | C | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(70): Show |
75 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.3614+2442G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838732 | |||||||
chr10:99838734 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3614+2444T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838734 | |||||||
chr10:99838734 | T | G | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(70): Show |
75 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.3614+2444T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838734 | |||||||
chr10:99838735 | G | A | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(70): Show |
75 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.3614+2445G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838735 | |||||||
chr10:99838736 | A | C | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(70): Show |
75 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.3614+2446A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838736 | |||||||
chr10:99838742 | C | CT | 5 | a0001c0002t0006g0018 a0001c0002t0006g0019 a0001c0014t0001g0023 others(2): Show |
5 | HG00642.hp2 HG01109.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.3614+2452_3614+245 others(5): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838742 | |||||||
chr10:99838758 | A | G | 82 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(79): Show |
84 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.3614+2468A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838758 | |||||||
chr10:99838770 | T | C | 86 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(83): Show |
88 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.3614+2480T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838770 | |||||||
chr10:99838774 | C | T | 5 | a0001c0002t0006g0018 a0001c0002t0006g0019 a0001c0014t0001g0023 others(2): Show |
5 | HG00642.hp2 HG01109.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.3614+2484C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838774 | |||||||
chr10:99838774 | CG | C | 14 | a0001c0001t0001g0185 a0001c0001t0001g0269 a0001c0001t0008g0291 others(11): Show |
14 | HG00639.hp2 HG01074.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.3614+2491delG | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838774 | ||||||
chr10:99838781 | G | A | 5 | a0001c0002t0006g0018 a0001c0002t0006g0019 a0001c0014t0001g0023 others(2): Show |
5 | HG00642.hp2 HG01109.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.3614+2491G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838781 | |||||||
chr10:99838781 | G | C | 65 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(62): Show |
67 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.3614+2491G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838781 | |||||||
chr10:99838782 | CTG | C | 65 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(62): Show |
67 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.3614+2493_3614+249 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838782 | |||||||
chr10:99838783 | T | C | 11 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(8): Show |
11 | HG00639.hp2 HG01074.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.3614+2493T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838783 | |||||||
chr10:99838785 | AC | A | 18 | a0001c0001t0001g0269 a0001c0001t0008g0291 a0001c0002t0006g0018 others(15): Show |
18 | HG00639.hp2 HG00642.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.3614+2503delC | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838785 | ||||||
chr10:99838786 | C | A | 65 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(62): Show |
67 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.3614+2496C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838786 | |||||||
chr10:99838786 | C | CCCCCCCA others(754): Show |
1 | a0001c0001t0001g0144 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.3614+2502_3614+250 others(765): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838786 | ||||||
chr10:99838786 | C | CCCCCCCA others(760): Show |
1 | a0001c0001t0001g0185 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3614+2502_3614+250 others(771): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838786 | ||||||
chr10:99838793 | C | T | 2 | a0001c0001t0001g0269 a0001c0001t0008g0291 |
2 | NA19060.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.3614+2503C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838793 | |||||||
chr10:99838795 | C | T | 5 | a0001c0002t0006g0018 a0001c0002t0006g0019 a0001c0014t0001g0023 others(2): Show |
5 | HG00642.hp2 HG01109.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.3614+2505C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838795 | |||||||
chr10:99838801 | T | TCCCGGAC others(71): Show |
3 | a0001c0002t0006g0018 a0001c0002t0006g0019 a0016c0026t0006g0021 |
3 | HG00642.hp2 HG01109.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.3614+2522_3614+252 others(82): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838801 | ||||||
chr10:99838801 | T | TCCCGGAC others(71): Show |
2 | a0001c0014t0001g0023 a0001c0014t0001g0130 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3614+2522_3614+252 others(82): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838801 | ||||||
chr10:99838824 | G | GT | 3 | a0005c0008t0001g0030 a0014c0023t0001g0217 a0022c0020t0001g0309 |
3 | HG00639.hp2 HG01074.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3614+2534_3614+253 others(5): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838824 | |||||||
chr10:99838824 | G | T | 4 | a0005c0008t0001g0013 a0005c0008t0001g0047 a0005c0008t0001g0077 others(1): Show |
4 | HG00140.hp2 HG02300.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.3614+2534G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838824 | |||||||
chr10:99838825 | C | G | 3 | a0005c0008t0001g0013 a0014c0023t0001g0217 a0027c0028t0001g0277 |
3 | HG00639.hp2 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3614+2535C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838825 | |||||||
chr10:99838825 | C | T | 6 | a0001c0001t0001g0269 a0001c0001t0008g0291 a0005c0008t0001g0030 others(3): Show |
6 | HG00140.hp2 HG01074.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.3614+2535C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838825 | |||||||
chr10:99838833 | T | C | 80 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(77): Show |
82 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.3614+2543T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838833 | |||||||
chr10:99838835 | AC | A | 8 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(5): Show |
8 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.3614+2552delC | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838835 | ||||||
chr10:99838836 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3614+2546C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838836 | |||||||
chr10:99838841 | C | T | 5 | a0001c0002t0006g0018 a0001c0002t0006g0019 a0001c0014t0001g0023 others(2): Show |
5 | HG00642.hp2 HG01109.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.3614+2551C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838841 | |||||||
chr10:99838844 | C | T | 10 | a0001c0001t0001g0269 a0001c0001t0008g0291 a0005c0008t0001g0013 others(7): Show |
10 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.3614+2554C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838844 | |||||||
chr10:99838862 | C | CGGCTGGC others(498): Show |
1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3614+2584_3614+258 others(509): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838862 | ||||||
chr10:99838862 | C | T | 77 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(74): Show |
79 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.3614+2572C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838862 | |||||||
chr10:99838875 | A | AGGGGGGC others(322): Show |
1 | a0001c0002t0002g0071 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3614+2586_3614+258 others(333): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838875 | ||||||
chr10:99838875 | A | T | 78 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(75): Show |
80 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.3614+2585A>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838875 | |||||||
chr10:99838878 | G | A | 2 | a0001c0014t0001g0023 a0001c0014t0001g0130 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3614+2588G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838878 | |||||||
chr10:99838880 | G | T | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3614+2590G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838880 | |||||||
chr10:99838903 | C | T | 1 | a0001c0001t0001g0315 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.3614+2613C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838903 | |||||||
chr10:99838924 | C | CTCACCTC others(587): Show |
1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3614+2634_3614+263 others(598): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838924 | |||||||
chr10:99838925 | A | ACCTCCCG others(48): Show |
1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3614+2645_3614+264 others(59): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838925 | ||||||
chr10:99838925 | A | ACCTCCCG others(45): Show |
2 | a0001c0014t0001g0023 a0001c0014t0001g0130 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3614+2662_3614+266 others(56): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838925 | ||||||
chr10:99838925 | A | ACCTCCCG others(46): Show |
2 | a0001c0002t0006g0019 a0016c0026t0006g0021 |
2 | HG01109.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.3614+2662_3614+266 others(57): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838925 | ||||||
chr10:99838925 | A | ACCTCCCG others(47): Show |
1 | a0001c0002t0006g0018 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(58): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838925 | ||||||
chr10:99838925 | A | ACCTCCCG others(578): Show |
5 | a0001c0002t0003g0035 a0001c0002t0003g0132 a0001c0002t0003g0133 others(2): Show |
5 | HG02818.hp1 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.3614+2662_3614+266 others(589): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838925 | ||||||
chr10:99838925 | A | ACCTCCCG others(46): Show |
3 | a0001c0002t0002g0039 a0001c0002t0002g0127 a0021c0032t0001g0129 |
3 | HG02258.hp1 HG02886.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.3614+2662_3614+266 others(57): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838925 | ||||||
chr10:99838925 | A | ACCTCCCG others(579): Show |
3 | a0001c0002t0003g0072 a0001c0002t0003g0120 a0001c0002t0003g0168 |
3 | HG01081.hp1 HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.3614+2662_3614+266 others(590): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838925 | ||||||
chr10:99838925 | A | ACCTCCCG others(578): Show |
1 | a0001c0007t0003g0027 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(589): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838925 | ||||||
chr10:99838925 | A | ACCTCCCG others(579): Show |
42 | a0001c0002t0002g0040 a0001c0002t0002g0042 a0001c0002t0002g0045 others(39): Show |
42 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.3614+2662_3614+266 others(590): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838925 | ||||||
chr10:99838925 | A | ACCTCCCG others(580): Show |
4 | a0001c0002t0002g0078 a0001c0002t0002g0086 a0001c0002t0002g0122 others(1): Show |
4 | HG00544.hp1 HG00544.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.3614+2662_3614+266 others(591): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838925 | ||||||
chr10:99838925 | A | ACCTCCCG others(579): Show |
1 | a0001c0002t0002g0107 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(590): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838925 | ||||||
chr10:99838925 | A | ACCTCCCG others(581): Show |
1 | a0001c0002t0011g0031 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(592): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838925 | ||||||
chr10:99838925 | A | ACCTCCCG others(581): Show |
1 | a0001c0002t0003g0126 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(592): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838925 | ||||||
chr10:99838925 | A | ACCTCCCG others(580): Show |
1 | a0001c0002t0002g0034 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(591): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838925 | ||||||
chr10:99838925 | A | ACCTCCCG others(579): Show |
2 | a0001c0002t0003g0117 a0024c0033t0003g0082 |
2 | HG03669.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.3614+2662_3614+266 others(590): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838925 | ||||||
chr10:99838925 | A | ACCTCCCG others(579): Show |
1 | a0001c0002t0002g0037 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(590): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838925 | ||||||
chr10:99838925 | A | ACCTCCCG others(580): Show |
14 | a0001c0002t0002g0043 a0001c0002t0002g0057 a0001c0002t0002g0068 others(11): Show |
14 | HG00673.hp2 HG00733.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.3614+2662_3614+266 others(591): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838925 | ||||||
chr10:99838925 | A | ACCTCCCG others(581): Show |
4 | a0001c0002t0002g0093 a0001c0002t0003g0051 a0001c0002t0003g0064 others(1): Show |
4 | HG00597.hp2 HG01261.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.3614+2662_3614+266 others(592): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838925 | ||||||
chr10:99838925 | A | ACCTCCCG others(582): Show |
1 | a0001c0002t0002g0092 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(593): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838925 | ||||||
chr10:99838925 | A | ACCTCCCG others(582): Show |
2 | a0001c0002t0002g0049 a0001c0007t0003g0026 |
2 | HG02280.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.3614+2662_3614+266 others(593): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838925 | ||||||
chr10:99838925 | A | ACCTCCCG others(582): Show |
1 | a0001c0002t0003g0059 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(593): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838925 | ||||||
chr10:99838925 | A | ACCTCCCG others(583): Show |
1 | a0001c0002t0002g0076 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(594): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838925 | ||||||
chr10:99838925 | A | ACCTCCCG others(48): Show |
1 | a0002c0003t0001g0221 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(59): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838925 | ||||||
chr10:99838925 | A | ACCTCCCG others(526): Show |
1 | a0001c0002t0003g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3614+2677_3614+267 others(537): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838925 | ||||||
chr10:99838925 | A | C | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3614+2635A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838925 | |||||||
chr10:99838928 | T | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(68): Show |
73 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.3614+2638T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838928 | |||||||
chr10:99838928 | T | TCCCAGAC others(805): Show |
1 | a0002c0003t0001g0328 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3614+2641_3614+264 others(816): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(805): Show |
1 | a0001c0001t0001g0225 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(816): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(804): Show |
1 | a0011c0012t0001g0215 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(815): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(805): Show |
1 | a0011c0012t0001g0216 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(816): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(399): Show |
2 | a0006c0010t0001g0010 a0006c0010t0001g0011 |
2 | HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3614+2662_3614+266 others(410): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(399): Show |
1 | a0001c0001t0001g0218 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(410): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(803): Show |
2 | a0007c0009t0001g0157 a0007c0009t0001g0210 |
2 | HG01109.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.3614+2662_3614+266 others(814): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(803): Show |
3 | a0001c0001t0001g0220 a0010c0015t0001g0016 a0010c0015t0001g0017 |
3 | HG02630.hp1 HG02717.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.3614+2662_3614+266 others(814): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(805): Show |
1 | a0001c0005t0001g0155 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(816): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(755): Show |
1 | a0001c0001t0001g0203 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(766): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(804): Show |
3 | a0001c0001t0001g0002 a0001c0001t0001g0188 a0001c0001t0001g0195 |
4 | HG02040.hp2 HG02523.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.3614+2662_3614+266 others(815): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(804): Show |
46 | a0001c0001t0001g0143 a0001c0001t0001g0148 a0001c0001t0001g0150 others(43): Show |
49 | HG00099.hp1 HG00735.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.3614+2662_3614+266 others(815): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(2700): Show |
1 | a0001c0001t0001g0212 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(2711): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(1209): Show |
1 | a0001c0001t0001g0008 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(1220): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(804): Show |
3 | a0001c0001t0001g0162 a0001c0001t0001g0174 a0026c0025t0001g0158 |
3 | HG00673.hp1 NA18984.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.3614+2662_3614+266 others(815): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(805): Show |
3 | a0001c0001t0001g0320 a0002c0003t0001g0248 a0003c0004t0001g0176 |
3 | HG00741.hp2 HG02602.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3614+2662_3614+266 others(816): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(807): Show |
1 | a0001c0001t0001g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(818): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(804): Show |
1 | a0002c0003t0001g0324 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(815): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(805): Show |
1 | a0001c0001t0001g0206 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(816): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(806): Show |
1 | a0001c0001t0001g0183 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(817): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(400): Show |
1 | a0002c0003t0001g0258 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(411): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(804): Show |
1 | a0007c0009t0001g0163 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(815): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(806): Show |
1 | a0001c0005t0001g0156 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(817): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(805): Show |
1 | a0001c0001t0001g0199 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(816): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(805): Show |
2 | a0001c0001t0001g0142 a0001c0001t0001g0189 |
2 | HG00438.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.3614+2662_3614+266 others(816): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(805): Show |
28 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0170 others(25): Show |
29 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.3614+2662_3614+266 others(816): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(806): Show |
1 | a0001c0001t0001g0139 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(817): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(806): Show |
1 | a0002c0003t0001g0230 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(817): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(806): Show |
6 | a0001c0001t0001g0182 a0001c0001t0001g0184 a0001c0001t0001g0193 others(3): Show |
6 | HG00558.hp2 HG00642.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.3614+2662_3614+266 others(817): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(806): Show |
1 | a0002c0003t0001g0252 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(817): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(807): Show |
1 | a0001c0001t0001g0190 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(818): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(807): Show |
1 | a0001c0001t0001g0192 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(818): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(805): Show |
1 | a0002c0003t0001g0138 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(816): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(806): Show |
7 | a0001c0001t0004g0121 a0002c0003t0001g0233 a0002c0003t0001g0251 others(4): Show |
7 | HG00423.hp1 HG00621.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614+2662_3614+266 others(817): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(807): Show |
1 | a0002c0003t0001g0243 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(818): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(807): Show |
1 | a0002c0003t0004g0244 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(818): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(808): Show |
1 | a0002c0003t0001g0310 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(819): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838928 | T | TCCCGGAC others(805): Show |
1 | a0001c0001t0001g0149 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(816): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838928 | ||||||
chr10:99838932 | G | A | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614+2642G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838932 | |||||||
chr10:99838936 | G | GGGGCGGC others(579): Show |
1 | a0001c0002t0003g0050 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(590): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838936 | ||||||
chr10:99838949 | G | GGGCAGGG others(95): Show |
1 | a0001c0002t0003g0041 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(106): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838949 | ||||||
chr10:99838952 | C | CAGGGGGG others(580): Show |
1 | a0001c0002t0003g0124 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(591): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838952 | |||||||
chr10:99838952 | C | CAGGGGGG others(807): Show |
1 | a0002c0003t0001g0209 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(818): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838952 | |||||||
chr10:99838952 | C | CAGGGGGG others(582): Show |
1 | a0001c0002t0002g0119 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(593): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838952 | |||||||
chr10:99838952 | C | CAGGGGGG others(582): Show |
1 | a0001c0002t0002g0098 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(593): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838952 | |||||||
chr10:99838952 | C | CAGGGGGG others(586): Show |
1 | a0001c0002t0002g0066 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(597): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838952 | |||||||
chr10:99838952 | C | CAGGGGGG others(807): Show |
1 | a0002c0003t0009g0242 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(818): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838952 | |||||||
chr10:99838952 | C | CAGGGGGG others(810): Show |
1 | a0002c0003t0001g0137 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3614+2662_3614+266 others(821): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838952 | |||||||
chr10:99838955 | G | A | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614+2665G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838955 | |||||||
chr10:99838960 | C | T | 8 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(5): Show |
8 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3614+2670C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838960 | |||||||
chr10:99838968 | T | C | 121 | a0001c0002t0002g0034 a0001c0002t0002g0037 a0001c0002t0002g0039 others(118): Show |
121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.3614+2678T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838968 | |||||||
chr10:99838985 | G | A | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614+2695G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99838985 | |||||||
chr10:99838996 | C | CCGGGCGG others(268): Show |
1 | a0001c0002t0002g0106 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3614+2711_3614+271 others(279): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99838996 | ||||||
chr10:99839001 | CA | C | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614+2712delA | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839001 | |||||||
chr10:99839002 | A | T | 1 | a0001c0002t0002g0106 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3614+2712A>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839002 | |||||||
chr10:99839004 | A | G | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614+2714A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839004 | |||||||
chr10:99839010 | T | TGACCCCC others(3): Show |
7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614+2720_3614+272 others(14): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839010 | |||||||
chr10:99839014 | CA | C | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614+2725delA | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839014 | |||||||
chr10:99839017 | T | C | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614+2727T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839017 | |||||||
chr10:99839022 | A | G | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614+2732A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839022 | |||||||
chr10:99839024 | T | A | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614+2734T>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839024 | |||||||
chr10:99839025 | A | C | 4 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0140 others(1): Show |
4 | HG01496.hp2 HG03453.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.3614+2735A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839025 | |||||||
chr10:99839025 | A | T | 3 | a0004c0006t0001g0080 a0004c0006t0001g0081 a0004c0006t0001g0096 |
3 | HG02109.hp1 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.3614+2735A>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839025 | |||||||
chr10:99839030 | C | CGGCT | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614+2743_3614+274 others(8): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839030 | ||||||
chr10:99839044 | C | G | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614+2754C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839044 | |||||||
chr10:99839047 | C | T | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614+2757C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839047 | |||||||
chr10:99839054 | C | T | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614+2764C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839054 | |||||||
chr10:99839059 | G | A | 19 | a0001c0002t0002g0039 a0001c0002t0002g0127 a0002c0003t0001g0221 others(16): Show |
19 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.3614+2769G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839059 | |||||||
chr10:99839061 | A | T | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614+2771A>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839061 | |||||||
chr10:99839062 | C | A | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614+2772C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839062 | |||||||
chr10:99839071 | TGGCCGGG others(5): Show |
T | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614+2784_3614+279 others(16): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839071 | ||||||
chr10:99839075 | C | CGGGCAGG others(1): Show |
54 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(51): Show |
56 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.3614+2792_3614+279 others(12): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839075 | ||||||
chr10:99839079 | CA | C | 12 | a0001c0002t0002g0039 a0001c0002t0002g0127 a0002c0003t0001g0221 others(9): Show |
12 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.3614+2790delA | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839079 | |||||||
chr10:99839083 | G | A | 12 | a0001c0002t0002g0039 a0001c0002t0002g0127 a0002c0003t0001g0221 others(9): Show |
12 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.3614+2793G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839083 | |||||||
chr10:99839088 | A | C | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3614+2798A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839088 | |||||||
chr10:99839088 | A | T | 12 | a0001c0002t0002g0039 a0001c0002t0002g0127 a0002c0003t0001g0221 others(9): Show |
12 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.3614+2798A>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839088 | |||||||
chr10:99839089 | G | GGGGGGCA others(2): Show |
9 | a0001c0001t0001g0055 a0001c0001t0001g0058 a0001c0001t0001g0246 others(6): Show |
9 | HG00597.hp1 HG01516.hp1 HG03239.hp1 others(6): Show |
intron_variant | MODIFIER | c.3614+2799_3614+280 others(13): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839089 | |||||||
chr10:99839090 | A | AC | 43 | a0001c0001t0001g0139 a0001c0001t0001g0143 a0001c0001t0001g0171 others(40): Show |
44 | HG00544.hp1 HG00558.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.3614+2810dupC | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839090 | ||||||
chr10:99839090 | A | C | 9 | a0001c0001t0001g0055 a0001c0001t0001g0058 a0001c0001t0001g0246 others(6): Show |
9 | HG00597.hp1 HG01516.hp1 HG03239.hp1 others(6): Show |
intron_variant | MODIFIER | c.3614+2800A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839090 | |||||||
chr10:99839091 | C | G | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614+2801C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839091 | |||||||
chr10:99839092 | C | G | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614+2802C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839092 | |||||||
chr10:99839094 | C | G | 15 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(12): Show |
15 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.3614+2804C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839094 | |||||||
chr10:99839099 | C | T | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614+2809C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839099 | |||||||
chr10:99839101 | ACCTC | A | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614+2818_3614+282 others(8): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839101 | ||||||
chr10:99839112 | G | A | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614+2822G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839112 | |||||||
chr10:99839116 | G | A | 4 | a0001c0002t0002g0039 a0001c0002t0002g0127 a0002c0003t0001g0221 others(1): Show |
4 | HG02258.hp1 HG02698.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3614+2826G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839116 | |||||||
chr10:99839120 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0161 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3614+2830C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839120 | |||||||
chr10:99839129 | G | A | 8 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(5): Show |
8 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.3615-2838G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839129 | |||||||
chr10:99839132 | C | CGGGGGGC others(174): Show |
1 | a0001c0002t0002g0071 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3615-2786_3615-278 others(185): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839132 | ||||||
chr10:99839135 | G | A | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3615-2832G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839135 | |||||||
chr10:99839140 | C | T | 19 | a0001c0002t0002g0039 a0001c0002t0002g0127 a0002c0003t0001g0221 others(16): Show |
19 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.3615-2827C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839140 | |||||||
chr10:99839149 | C | T | 12 | a0001c0002t0002g0039 a0001c0002t0002g0127 a0002c0003t0001g0221 others(9): Show |
12 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.3615-2818C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839149 | |||||||
chr10:99839161 | G | GGACGGGG others(71): Show |
1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3615-2786_3615-278 others(82): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839161 | ||||||
chr10:99839178 | G | A | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3615-2789G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839178 | |||||||
chr10:99839179 | G | T | 1 | a0001c0001t0001g0218 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3615-2788G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839179 | |||||||
chr10:99839181 | C | T | 12 | a0001c0002t0002g0039 a0001c0002t0002g0127 a0002c0003t0001g0221 others(9): Show |
12 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.3615-2786C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839181 | |||||||
chr10:99839182 | G | C | 1 | a0001c0001t0001g0218 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3615-2785G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839182 | |||||||
chr10:99839182 | GGGGGGCC others(41): Show |
G | 8 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(5): Show |
8 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.3615-2779_3615-273 others(52): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839182 | ||||||
chr10:99839184 | G | A | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3615-2783G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839184 | |||||||
chr10:99839187 | G | GACTGACC others(254): Show |
2 | a0001c0002t0002g0039 a0001c0002t0002g0127 |
2 | HG02258.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.3615-2780_3615-277 others(265): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839187 | |||||||
chr10:99839189 | C | T | 10 | a0002c0003t0001g0221 a0004c0006t0001g0022 a0004c0006t0001g0038 others(7): Show |
10 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.3615-2778C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839189 | |||||||
chr10:99839190 | A | G | 11 | a0002c0003t0001g0221 a0002c0003t0001g0324 a0004c0006t0001g0022 others(8): Show |
11 | HG00323.hp1 HG01496.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.3615-2777A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839190 | |||||||
chr10:99839196 | C | T | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3615-2771C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839196 | |||||||
chr10:99839198 | C | T | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3615-2769C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839198 | |||||||
chr10:99839200 | C | T | 2 | a0002c0003t0001g0221 a0021c0032t0001g0129 |
2 | HG02698.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3615-2767C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839200 | |||||||
chr10:99839206 | T | TCCCGGAC others(71): Show |
1 | a0021c0032t0001g0129 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3615-2751_3615-275 others(82): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839206 | ||||||
chr10:99839206 | T | TCCCGGAC others(71): Show |
1 | a0002c0003t0001g0221 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3615-2751_3615-275 others(82): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839206 | ||||||
chr10:99839207 | C | A | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3615-2760C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839207 | |||||||
chr10:99839214 | G | A | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3615-2753G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839214 | |||||||
chr10:99839217 | C | CCGGCTGG others(42): Show |
1 | a0001c0001t0001g0170 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.3615-2736_3615-268 others(53): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839217 | ||||||
chr10:99839217 | C | G | 116 | a0001c0001t0001g0218 a0001c0001t0001g0269 a0001c0001t0008g0291 others(113): Show |
116 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.3615-2750C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839217 | |||||||
chr10:99839218 | C | G | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3615-2749C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839218 | |||||||
chr10:99839229 | G | GT | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3615-2738_3615-273 others(5): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839229 | |||||||
chr10:99839230 | C | CG | 13 | a0001c0001t0001g0134 a0001c0001t0001g0149 a0001c0001t0001g0183 others(10): Show |
13 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.3615-2731dupG | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839230 | ||||||
chr10:99839230 | C | G | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3615-2737C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839230 | |||||||
chr10:99839238 | C | T | 16 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(13): Show |
16 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.3615-2729C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839238 | |||||||
chr10:99839246 | C | CCACCTCC others(120): Show |
2 | a0001c0001t0001g0218 a0001c0001t0008g0291 |
2 | NA19030.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.3615-2701_3615-270 others(131): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839246 | ||||||
chr10:99839246 | C | T | 2 | a0002c0003t0001g0221 a0021c0032t0001g0129 |
2 | HG02698.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3615-2721C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839246 | |||||||
chr10:99839249 | C | T | 15 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(12): Show |
15 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.3615-2718C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839249 | |||||||
chr10:99839267 | C | T | 16 | a0001c0001t0001g0269 a0004c0006t0001g0022 a0004c0006t0001g0038 others(13): Show |
16 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.3615-2700C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839267 | |||||||
chr10:99839280 | A | T | 16 | a0001c0001t0001g0269 a0004c0006t0001g0022 a0004c0006t0001g0038 others(13): Show |
16 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.3615-2687A>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839280 | |||||||
chr10:99839299 | C | G | 2 | a0001c0002t0003g0222 a0001c0002t0003g0274 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3615-2668C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839299 | |||||||
chr10:99839312 | C | T | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3615-2655C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839312 | |||||||
chr10:99839318 | G | A | 1 | a0005c0008t0001g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3615-2649G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839318 | |||||||
chr10:99839333 | T | G | 1 | a0001c0001t0001g0269 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3615-2634T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839333 | |||||||
chr10:99839337 | G | A | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3615-2630G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839337 | |||||||
chr10:99839341 | A | G | 22 | a0001c0001t0001g0269 a0001c0001t0008g0291 a0001c0002t0002g0039 others(19): Show |
22 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.3615-2626A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839341 | |||||||
chr10:99839353 | T | C | 14 | a0001c0001t0001g0269 a0001c0001t0008g0291 a0001c0002t0002g0039 others(11): Show |
14 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.3615-2614T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839353 | |||||||
chr10:99839353 | T | G | 8 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(5): Show |
8 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.3615-2614T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839353 | |||||||
chr10:99839357 | CG | C | 17 | a0001c0001t0008g0291 a0004c0006t0001g0022 a0004c0006t0001g0038 others(14): Show |
17 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.3615-2603delG | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839357 | ||||||
chr10:99839358 | G | A | 4 | a0001c0002t0002g0039 a0001c0002t0002g0127 a0002c0003t0001g0221 others(1): Show |
4 | HG02258.hp1 HG02698.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3615-2609G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839358 | |||||||
chr10:99839358 | G | GGGGGGCC others(128): Show |
1 | a0001c0001t0001g0269 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3615-2604_3615-260 others(139): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839358 | ||||||
chr10:99839361 | G | A | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3615-2606G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839361 | |||||||
chr10:99839366 | T | A | 5 | a0001c0001t0001g0269 a0001c0002t0002g0039 a0001c0002t0002g0127 others(2): Show |
5 | HG02258.hp1 HG02698.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3615-2601T>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839366 | |||||||
chr10:99839366 | T | C | 1 | a0001c0001t0008g0291 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3615-2601T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839366 | |||||||
chr10:99839368 | A | AC | 15 | a0001c0001t0001g0170 a0001c0001t0001g0181 a0001c0001t0001g0185 others(12): Show |
15 | HG00597.hp1 HG01081.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.3615-2590dupC | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839368 | ||||||
chr10:99839368 | AC | A | 98 | a0001c0002t0002g0034 a0001c0002t0002g0037 a0001c0002t0002g0040 others(95): Show |
98 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.3615-2590delC | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839368 | ||||||
chr10:99839368 | ACC | A | 17 | a0001c0001t0008g0291 a0004c0006t0001g0022 a0004c0006t0001g0038 others(14): Show |
17 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.3615-2591_3615-259 others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839368 | ||||||
chr10:99839392 | C | T | 15 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(12): Show |
15 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.3615-2575C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839392 | |||||||
chr10:99839395 | G | C | 15 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(12): Show |
15 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.3615-2572G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839395 | |||||||
chr10:99839396 | G | A | 15 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(12): Show |
15 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.3615-2571G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839396 | |||||||
chr10:99839397 | C | T | 1 | a0001c0001t0001g0273 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3615-2570C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839397 | |||||||
chr10:99839398 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.3615-2569G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839398 | |||||||
chr10:99839403 | GCCGGGCG others(74): Show |
G | 5 | a0001c0001t0001g0280 a0001c0001t0001g0284 a0001c0001t0001g0290 others(2): Show |
5 | NA18950.hp2 NA18954.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.3615-2559_3615-247 others(85): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839403 | ||||||
chr10:99839406 | G | A | 16 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(13): Show |
16 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.3615-2561G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839406 | |||||||
chr10:99839409 | CGGGGGGC others(43): Show |
C | 1 | a0002c0003t0001g0221 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3615-2541_3615-249 others(54): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839409 | ||||||
chr10:99839417 | T | C | 5 | a0001c0001t0001g0269 a0001c0001t0008g0291 a0001c0002t0002g0039 others(2): Show |
5 | HG02258.hp1 HG02886.hp2 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.3615-2550T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839417 | |||||||
chr10:99839418 | G | A | 2 | a0001c0001t0008g0291 a0001c0002t0002g0127 |
2 | HG02258.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.3615-2549G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839418 | |||||||
chr10:99839419 | A | ACCCCCCC others(220): Show |
1 | a0001c0002t0002g0039 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3615-2522_3615-252 others(231): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839419 | ||||||
chr10:99839426 | C | T | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3615-2541C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839426 | |||||||
chr10:99839435 | C | A | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3615-2532C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839435 | |||||||
chr10:99839441 | C | T | 15 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(12): Show |
15 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.3615-2526C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839441 | |||||||
chr10:99839444 | G | C | 15 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(12): Show |
15 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.3615-2523G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839444 | |||||||
chr10:99839445 | G | A | 15 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(12): Show |
15 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.3615-2522G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839445 | |||||||
chr10:99839445 | G | C | 1 | a0001c0001t0008g0291 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3615-2522G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839445 | |||||||
chr10:99839446 | T | C | 20 | a0001c0001t0001g0269 a0001c0001t0008g0291 a0001c0002t0002g0127 others(17): Show |
20 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.3615-2521T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839446 | |||||||
chr10:99839454 | C | G | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3615-2513C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839454 | |||||||
chr10:99839457 | G | C | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3615-2510G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839457 | |||||||
chr10:99839458 | C | G | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3615-2509C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839458 | |||||||
chr10:99839458 | C | T | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3615-2509C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839458 | |||||||
chr10:99839459 | G | GGGGGGCC others(168): Show |
1 | a0001c0001t0001g0269 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3615-2503_3615-250 others(179): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839459 | ||||||
chr10:99839459 | G | GGGGGGCC others(173): Show |
1 | a0021c0032t0001g0129 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3615-2503_3615-250 others(184): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839459 | ||||||
chr10:99839459 | G | GGGGGGCC others(170): Show |
1 | a0001c0002t0002g0127 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3615-2503_3615-250 others(181): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839459 | ||||||
chr10:99839459 | GGGGGGGC others(41): Show |
G | 51 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(48): Show |
53 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.3615-2443_3615-239 others(52): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839459 | ||||||
chr10:99839460 | GGGGGGCT others(40): Show |
G | 1 | a0001c0001t0001g0305 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3615-2501_3615-245 others(51): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839460 | ||||||
chr10:99839465 | G | A | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3615-2502G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839465 | |||||||
chr10:99839465 | G | C | 1 | a0001c0001t0008g0291 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3615-2502G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839465 | |||||||
chr10:99839467 | T | G | 1 | a0001c0001t0008g0291 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3615-2500T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839467 | |||||||
chr10:99839468 | G | A | 1 | a0001c0001t0008g0291 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3615-2499G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839468 | |||||||
chr10:99839469 | A | ACCCCCCC others(170): Show |
1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3615-2492_3615-249 others(181): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839469 | ||||||
chr10:99839469 | A | C | 1 | a0001c0001t0008g0291 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3615-2498A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839469 | |||||||
chr10:99839469 | ACCCCCCA others(92): Show |
A | 8 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(5): Show |
8 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.3615-2477_3615-237 others(103): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839469 | ||||||
chr10:99839470 | CCCCCCAC others(40): Show |
C | 8 | a0001c0001t0001g0308 a0004c0006t0001g0022 a0004c0006t0001g0038 others(5): Show |
8 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.3615-2491_3615-244 others(51): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839470 | ||||||
chr10:99839490 | T | C | 9 | a0001c0001t0001g0269 a0001c0001t0001g0280 a0001c0001t0001g0284 others(6): Show |
9 | HG02258.hp1 HG02886.hp2 NA18950.hp2 others(6): Show |
intron_variant | MODIFIER | c.3615-2477T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839490 | |||||||
chr10:99839493 | G | C | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3615-2474G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839493 | |||||||
chr10:99839494 | G | A | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3615-2473G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839494 | |||||||
chr10:99839495 | C | T | 8 | a0001c0001t0001g0269 a0001c0001t0001g0280 a0001c0001t0001g0284 others(5): Show |
8 | HG02258.hp1 HG02886.hp2 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.3615-2472C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839495 | |||||||
chr10:99839507 | C | CAGAGGGG others(142): Show |
1 | a0001c0001t0008g0291 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3615-2460_3615-245 others(153): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839507 | |||||||
chr10:99839507 | C | CG | 11 | a0001c0001t0001g0269 a0001c0001t0001g0280 a0001c0001t0001g0284 others(8): Show |
11 | HG02055.hp1 HG02056.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.3615-2454dupG | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839507 | ||||||
chr10:99839518 | CCCCCCAC others(40): Show |
C | 6 | a0001c0001t0001g0055 a0001c0001t0001g0058 a0001c0001t0001g0246 others(3): Show |
6 | HG00609.hp1 HG01516.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.3615-2443_3615-239 others(51): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839518 | ||||||
chr10:99839565 | A | AC | 22 | a0001c0001t0001g0149 a0001c0001t0001g0171 a0001c0001t0001g0183 others(19): Show |
22 | HG00597.hp2 HG01978.hp2 HG02056.hp2 others(19): Show |
intron_variant | MODIFIER | c.3615-2393dupC | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | 99839565 | ||||||
chr10:99839570 | C | G | 2 | a0001c0002t0007g0128 a0001c0002t0007g0131 |
2 | HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3615-2397C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839570 | |||||||
chr10:99839572 | C | A | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3615-2395C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839572 | |||||||
chr10:99839573 | C | T | 1 | a0002c0003t0001g0310 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3615-2394C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839573 | |||||||
chr10:99839574 | C | A | 6 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(3): Show |
6 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.3615-2393C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839574 | |||||||
chr10:99839601 | C | G | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3615-2366C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839601 | |||||||
chr10:99839630 | G | A | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3615-2337G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839630 | |||||||
chr10:99839632 | G | A | 68 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(65): Show |
70 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.3615-2335G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839632 | |||||||
chr10:99839658 | T | C | 16 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(13): Show |
16 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.3615-2309T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839658 | |||||||
chr10:99839669 | C | T | 2 | a0001c0001t0001g0220 a0023c0018t0001g0009 |
2 | HG03453.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.3615-2298C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839669 | |||||||
chr10:99839759 | G | A | 9 | a0001c0001t0001g0007 a0004c0006t0001g0022 a0004c0006t0001g0038 others(6): Show |
9 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.3615-2208G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839759 | |||||||
chr10:99839793 | T | G | 1 | a0027c0028t0001g0277 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3615-2174T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839793 | |||||||
chr10:99839794 | C | T | 1 | a0027c0028t0001g0277 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3615-2173C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839794 | |||||||
chr10:99839826 | T | C | 1 | a0002c0003t0001g0310 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3615-2141T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839826 | |||||||
chr10:99839834 | A | C | 255 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(252): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.3615-2133A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839834 | |||||||
chr10:99839834 | A | G | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3615-2133A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839834 | |||||||
chr10:99839866 | T | C | 6 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(3): Show |
6 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.3615-2101T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839866 | |||||||
chr10:99839871 | G | C | 1 | a0002c0003t0001g0239 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3615-2096G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839871 | |||||||
chr10:99839871 | G | T | 4 | a0005c0008t0001g0030 a0005c0008t0001g0047 a0005c0008t0001g0077 others(1): Show |
4 | HG00140.hp2 HG01074.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.3615-2096G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839871 | |||||||
chr10:99839888 | C | T | 1 | a0001c0001t0001g0269 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3615-2079C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839888 | |||||||
chr10:99839924 | C | T | 2 | a0001c0002t0003g0222 a0001c0002t0003g0274 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3615-2043C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839924 | |||||||
chr10:99839949 | G | T | 4 | a0001c0002t0002g0098 a0001c0002t0002g0100 a0001c0002t0002g0102 others(1): Show |
4 | HG01106.hp1 HG01167.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.3615-2018G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839949 | |||||||
chr10:99839956 | G | T | 4 | a0001c0001t0005g0282 a0001c0001t0005g0283 a0001c0001t0005g0292 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.3615-2011G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839956 | |||||||
chr10:99839964 | C | T | 1 | a0005c0008t0001g0030 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3615-2003C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839964 | |||||||
chr10:99839976 | T | A | 3 | a0001c0001t0001g0162 a0001c0001t0001g0174 a0026c0025t0001g0158 |
3 | HG00673.hp1 NA18984.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.3615-1991T>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839976 | |||||||
chr10:99839977 | C | A | 3 | a0001c0001t0001g0162 a0001c0001t0001g0174 a0026c0025t0001g0158 |
3 | HG00673.hp1 NA18984.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.3615-1990C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839977 | |||||||
chr10:99839983 | T | G | 1 | a0021c0032t0001g0129 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3615-1984T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99839983 | |||||||
chr10:99840019 | C | T | 1 | a0027c0028t0001g0277 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3615-1948C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840019 | |||||||
chr10:99840020 | G | A | 8 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(5): Show |
8 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.3615-1947G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840020 | |||||||
chr10:99840033 | G | A | 2 | a0006c0010t0001g0010 a0006c0010t0001g0011 |
2 | HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3615-1934G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840033 | |||||||
chr10:99840058 | C | T | 1 | a0002c0003t0001g0221 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3615-1909C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840058 | |||||||
chr10:99840066 | C | T | 1 | a0001c0001t0001g0269 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3615-1901C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840066 | |||||||
chr10:99840067 | A | G | 1 | a0001c0001t0001g0269 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3615-1900A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840067 | |||||||
chr10:99840071 | G | A | 2 | a0010c0015t0001g0016 a0010c0015t0001g0017 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.3615-1896G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840071 | |||||||
chr10:99840090 | G | A | 1 | a0001c0002t0003g0059 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3615-1877G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840090 | |||||||
chr10:99840100 | G | A | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3615-1867G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840100 | |||||||
chr10:99840115 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3615-1852G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840115 | |||||||
chr10:99840168 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3615-1799C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840168 | |||||||
chr10:99840171 | C | T | 1 | a0001c0002t0003g0041 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3615-1796C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840171 | |||||||
chr10:99840274 | C | G | 3 | a0001c0002t0002g0084 a0001c0002t0002g0105 a0001c0002t0002g0106 |
3 | HG00741.hp1 HG01123.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.3615-1693C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840274 | |||||||
chr10:99840342 | C | T | 2 | a0011c0012t0001g0215 a0011c0012t0001g0216 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3615-1625C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840342 | |||||||
chr10:99840353 | G | A | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3615-1614G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840353 | |||||||
chr10:99840354 | G | A | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3615-1613G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840354 | |||||||
chr10:99840399 | C | G | 104 | a0001c0002t0002g0034 a0001c0002t0002g0037 a0001c0002t0002g0039 others(101): Show |
104 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.3615-1568C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840399 | |||||||
chr10:99840400 | G | A | 8 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(5): Show |
8 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3615-1567G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840400 | |||||||
chr10:99840401 | G | T | 1 | a0001c0002t0003g0083 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.3615-1566G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840401 | |||||||
chr10:99840405 | G | T | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3615-1562G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840405 | |||||||
chr10:99840431 | C | T | 1 | a0014c0023t0001g0217 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3615-1536C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840431 | |||||||
chr10:99840467 | G | A | 1 | a0001c0001t0001g0303 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3615-1500G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840467 | |||||||
chr10:99840473 | T | C | 1 | a0001c0002t0003g0083 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.3615-1494T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840473 | |||||||
chr10:99840474 | C | A | 1 | a0001c0002t0003g0083 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.3615-1493C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840474 | |||||||
chr10:99840558 | T | A | 8 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(5): Show |
8 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3615-1409T>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840558 | |||||||
chr10:99840598 | C | A | 1 | a0001c0002t0003g0083 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.3615-1369C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840598 | |||||||
chr10:99840599 | A | G | 1 | a0001c0002t0003g0083 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.3615-1368A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840599 | |||||||
chr10:99840601 | G | T | 1 | a0001c0002t0003g0083 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.3615-1366G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840601 | |||||||
chr10:99840980 | C | A | 8 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(5): Show |
8 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.3615-987C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99840980 | |||||||
chr10:99841479 | C | T | 100 | a0001c0002t0002g0034 a0001c0002t0002g0037 a0001c0002t0002g0039 others(97): Show |
100 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.3615-488C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99841479 | |||||||
chr10:99841531 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3615-436G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99841531 | |||||||
chr10:99841657 | T | C | 8 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(5): Show |
8 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3615-310T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99841657 | |||||||
chr10:99841705 | C | T | 2 | a0001c0001t0001g0278 a0001c0001t0001g0281 |
2 | NA18979.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.3615-262C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99841705 | |||||||
chr10:99841907 | T | C | 8 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(5): Show |
8 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3615-60T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | chr10 | 99841907 | |||||||
chr10:99842123 | G | A | 1 | a0001c0002t0003g0033 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3741+30G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 26/31 | chr10 | 99842123 | |||||||
chr10:99842247 | T | C | 65 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(62): Show |
67 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.3741+154T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 26/31 | chr10 | 99842247 | |||||||
chr10:99842496 | G | A | 1 | a0001c0002t0002g0122 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3741+403G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 26/31 | chr10 | 99842496 | |||||||
chr10:99842594 | C | A | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3741+501C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 26/31 | chr10 | 99842594 | |||||||
chr10:99842680 | GAACTAAT others(5): Show |
G | 1 | a0001c0002t0003g0050 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3741+588_3741+599d others(14): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 26/31 | chr10 | 99842680 | |||||||
chr10:99842688 | T | C | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3741+595T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 26/31 | chr10 | 99842688 | |||||||
chr10:99842816 | A | G | 217 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(214): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.3741+723A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 26/31 | chr10 | 99842816 | |||||||
chr10:99842824 | T | C | 8 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(5): Show |
8 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3741+731T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 26/31 | chr10 | 99842824 | |||||||
chr10:99843034 | C | G | 6 | a0001c0007t0003g0024 a0001c0007t0003g0025 a0001c0007t0003g0026 others(3): Show |
6 | HG02280.hp2 HG02559.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.3742-765C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 26/31 | chr10 | 99843034 | |||||||
chr10:99843036 | G | C | 1 | a0021c0032t0001g0129 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3742-763G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 26/31 | chr10 | 99843036 | |||||||
chr10:99843052 | C | CA | 66 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(63): Show |
68 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.3742-732dupA | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 26/31 | INFO_REALIGN_3_PRIME | chr10 | 99843052 | ||||||
chr10:99843138 | A | G | 3 | a0001c0001t0001g0218 a0010c0015t0001g0016 a0010c0015t0001g0017 |
3 | HG02630.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3742-661A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 26/31 | chr10 | 99843138 | |||||||
chr10:99843329 | G | T | 1 | a0002c0003t0001g0240 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3742-470G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 26/31 | chr10 | 99843329 | |||||||
chr10:99843333 | C | T | 1 | a0001c0001t0001g0323 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3742-466C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 26/31 | chr10 | 99843333 | |||||||
chr10:99843765 | T | C | 16 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(13): Show |
16 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.3742-34T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 26/31 | chr10 | 99843765 | |||||||
chr10:99843962 | T | G | 1 | a0001c0002t0002g0034 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3843+62T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 27/31 | chr10 | 99843962 | |||||||
chr10:99844003 | T | G | 1 | a0001c0002t0002g0034 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3843+103T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 27/31 | chr10 | 99844003 | |||||||
chr10:99844024 | C | G | 102 | a0001c0002t0002g0034 a0001c0002t0002g0037 a0001c0002t0002g0039 others(99): Show |
102 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.3843+124C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 27/31 | chr10 | 99844024 | |||||||
chr10:99844079 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3843+179G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 27/31 | chr10 | 99844079 | |||||||
chr10:99844249 | A | G | 8 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(5): Show |
8 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.3844-73A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 27/31 | chr10 | 99844249 | |||||||
chr10:99844259 | G | C | 1 | a0001c0002t0003g0126 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3844-63G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 27/31 | chr10 | 99844259 | |||||||
chr10:99844486 | C | T | 1 | a0005c0008t0001g0030 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3987+21C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 28/31 | chr10 | 99844486 | |||||||
chr10:99844555 | A | C | 1 | a0001c0002t0003g0036 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3987+90A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 28/31 | chr10 | 99844555 | |||||||
chr10:99844575 | G | C | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3987+110G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 28/31 | chr10 | 99844575 | |||||||
chr10:99844663 | C | T | 1 | a0001c0002t0002g0108 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3987+198C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 28/31 | chr10 | 99844663 | |||||||
chr10:99844724 | T | C | 7 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(4): Show |
7 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.3987+259T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 28/31 | chr10 | 99844724 | |||||||
chr10:99844953 | C | T | 1 | a0021c0032t0001g0129 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3987+488C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 28/31 | chr10 | 99844953 | |||||||
chr10:99845014 | T | G | 1 | a0001c0002t0002g0034 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3987+549T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 28/31 | chr10 | 99845014 | |||||||
chr10:99845023 | T | G | 1 | a0001c0002t0002g0034 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3987+558T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 28/31 | chr10 | 99845023 | |||||||
chr10:99845179 | G | A | 24 | a0001c0001t0001g0148 a0001c0001t0004g0121 a0002c0003t0001g0137 others(21): Show |
24 | HG00423.hp1 HG00621.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.3988-445G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 28/31 | chr10 | 99845179 | |||||||
chr10:99845559 | A | C | 1 | a0014c0023t0001g0217 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3988-65A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 28/31 | chr10 | 99845559 | |||||||
chr10:99845793 | G | C | 8 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(5): Show |
8 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.4146+11G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 29/31 | chr10 | 99845793 | |||||||
chr10:99845918 | C | T | 1 | a0001c0002t0002g0093 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.4146+136C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 29/31 | chr10 | 99845918 | |||||||
chr10:99845936 | A | G | 82 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0054 others(79): Show |
84 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.4146+154A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 29/31 | chr10 | 99845936 | |||||||
chr10:99846130 | T | A | 2 | a0001c0002t0002g0065 a0001c0002t0002g0069 |
2 | NA18992.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.4146+348T>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 29/31 | chr10 | 99846130 | |||||||
chr10:99846156 | A | G | 1 | a0001c0001t0001g0005 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.4146+374A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 29/31 | chr10 | 99846156 | |||||||
chr10:99846380 | C | T | 1 | a0024c0033t0003g0082 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4147-581C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 29/31 | chr10 | 99846380 | |||||||
chr10:99846447 | CCT | C | 24 | a0001c0001t0001g0148 a0001c0001t0004g0121 a0002c0003t0001g0137 others(21): Show |
24 | HG00423.hp1 HG00621.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.4147-511_4147-510d others(4): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr10 | 99846447 | ||||||
chr10:99846589 | A | G | 1 | a0022c0020t0001g0309 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4147-372A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 29/31 | chr10 | 99846589 | |||||||
chr10:99846631 | C | G | 1 | a0002c0003t0001g0310 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4147-330C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 29/31 | chr10 | 99846631 | |||||||
chr10:99846675 | G | C | 8 | a0001c0002t0003g0090 a0001c0002t0003g0091 a0001c0007t0003g0024 others(5): Show |
8 | HG01255.hp2 HG01433.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.4147-286G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 29/31 | chr10 | 99846675 | |||||||
chr10:99846686 | C | G | 1 | a0021c0032t0001g0129 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4147-275C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 29/31 | chr10 | 99846686 | |||||||
chr10:99846693 | T | C | 8 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(5): Show |
8 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.4147-268T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 29/31 | chr10 | 99846693 | |||||||
chr10:99846728 | A | AACTC | 8 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(5): Show |
8 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.4147-232_4147-231i others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr10 | 99846728 | ||||||
chr10:99846779 | C | G | 7 | a0003c0004t0001g0001 a0003c0004t0001g0146 a0003c0004t0001g0165 others(4): Show |
9 | HG01358.hp2 HG02109.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.4147-182C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 29/31 | chr10 | 99846779 | |||||||
chr10:99846786 | G | C | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.4147-175G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 29/31 | chr10 | 99846786 | |||||||
chr10:99846926 | G | A | 26 | a0001c0001t0001g0148 a0001c0001t0001g0162 a0001c0001t0004g0121 others(23): Show |
26 | HG00423.hp1 HG00621.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.4147-35G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 29/31 | chr10 | 99846926 | |||||||
chr10:99847138 | A | C | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4313+11A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99847138 | |||||||
chr10:99847219 | A | G | 1 | a0002c0003t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4313+92A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99847219 | |||||||
chr10:99847274 | C | G | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.4313+147C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99847274 | |||||||
chr10:99847340 | G | A | 8 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(5): Show |
8 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.4313+213G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99847340 | |||||||
chr10:99847400 | G | A | 1 | a0021c0032t0001g0129 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4313+273G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99847400 | |||||||
chr10:99847459 | T | G | 16 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(13): Show |
16 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.4313+332T>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99847459 | |||||||
chr10:99847560 | A | G | 8 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(5): Show |
8 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.4313+433A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99847560 | |||||||
chr10:99847601 | T | TA | 26 | a0001c0001t0001g0148 a0001c0001t0001g0162 a0001c0001t0004g0121 others(23): Show |
26 | HG00423.hp1 HG00621.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.4313+486dupA | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr10 | 99847601 | ||||||
chr10:99847631 | T | C | 3 | a0007c0009t0001g0157 a0007c0009t0001g0163 a0007c0009t0001g0210 |
3 | HG01109.hp1 HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.4313+504T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99847631 | |||||||
chr10:99847690 | G | C | 1 | a0001c0014t0001g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4313+563G>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99847690 | |||||||
chr10:99847721 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.4313+594C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99847721 | |||||||
chr10:99847747 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.4313+620C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99847747 | |||||||
chr10:99847843 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG02523.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.4313+716G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99847843 | |||||||
chr10:99847911 | C | G | 1 | a0001c0002t0002g0098 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4313+784C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99847911 | |||||||
chr10:99847918 | A | AAAAC | 17 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(14): Show |
17 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.4313+811_4313+814d others(6): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr10 | 99847918 | ||||||
chr10:99847958 | G | A | 8 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(5): Show |
8 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.4313+831G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99847958 | |||||||
chr10:99847971 | A | C | 1 | a0002c0003t0001g0252 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4313+844A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99847971 | |||||||
chr10:99848144 | G | A | 7 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(4): Show |
7 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.4313+1017G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99848144 | |||||||
chr10:99848148 | C | T | 1 | a0001c0001t0004g0121 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4313+1021C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99848148 | |||||||
chr10:99848352 | G | A | 1 | a0001c0002t0007g0128 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4313+1225G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99848352 | |||||||
chr10:99848399 | A | G | 1 | a0001c0002t0003g0050 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4313+1272A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99848399 | |||||||
chr10:99848492 | G | A | 8 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(5): Show |
8 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.4313+1365G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99848492 | |||||||
chr10:99848765 | C | G | 102 | a0001c0002t0002g0034 a0001c0002t0002g0037 a0001c0002t0002g0039 others(99): Show |
102 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.4313+1638C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99848765 | |||||||
chr10:99848803 | A | G | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4313+1676A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99848803 | |||||||
chr10:99848855 | G | T | 1 | a0004c0029t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4313+1728G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99848855 | |||||||
chr10:99848973 | C | T | 8 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(5): Show |
8 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.4314-1629C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99848973 | |||||||
chr10:99848991 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4314-1611G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99848991 | |||||||
chr10:99849154 | C | T | 1 | a0001c0002t0003g0168 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4314-1448C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99849154 | |||||||
chr10:99849162 | G | A | 6 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(3): Show |
6 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.4314-1440G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99849162 | |||||||
chr10:99849241 | G | A | 17 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(14): Show |
17 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.4314-1361G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99849241 | |||||||
chr10:99849253 | T | C | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4314-1349T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99849253 | |||||||
chr10:99849294 | C | T | 7 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(4): Show |
7 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.4314-1308C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99849294 | |||||||
chr10:99849646 | C | T | 2 | a0001c0001t0001g0139 a0001c0027t0001g0147 |
2 | HG02735.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.4314-956C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99849646 | |||||||
chr10:99849708 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.4314-894T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99849708 | |||||||
chr10:99849816 | T | C | 8 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(5): Show |
8 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.4314-786T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99849816 | |||||||
chr10:99849905 | G | A | 8 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(5): Show |
8 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.4314-697G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99849905 | |||||||
chr10:99850012 | G | A | 1 | a0002c0003t0001g0229 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.4314-590G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99850012 | |||||||
chr10:99850049 | G | A | 19 | a0001c0001t0001g0162 a0001c0001t0004g0121 a0002c0003t0001g0221 others(16): Show |
19 | HG00423.hp1 HG00621.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.4314-553G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99850049 | |||||||
chr10:99850265 | G | T | 1 | a0002c0003t0001g0250 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4314-337G>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99850265 | |||||||
chr10:99850346 | G | A | 8 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(5): Show |
8 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.4314-256G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99850346 | |||||||
chr10:99850369 | C | G | 1 | a0001c0002t0002g0049 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.4314-233C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99850369 | |||||||
chr10:99850510 | A | G | 1 | a0001c0001t0001g0275 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.4314-92A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99850510 | |||||||
chr10:99850549 | C | T | 10 | a0001c0001t0001g0231 a0001c0001t0001g0236 a0001c0001t0001g0267 others(7): Show |
10 | HG00558.hp1 HG02071.hp1 NA18953.hp2 others(7): Show |
intron_variant | MODIFIER | c.4314-53C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 30/31 | chr10 | 99850549 | |||||||
chr10:99850808 | G | A | 8 | a0005c0008t0001g0013 a0005c0008t0001g0030 a0005c0008t0001g0047 others(5): Show |
8 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.4508+12G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 31/31 | chr10 | 99850808 | |||||||
chr10:99850827 | A | C | 2 | a0001c0001t0001g0287 a0001c0001t0001g0294 |
2 | NA18967.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.4508+31A>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 31/31 | chr10 | 99850827 | |||||||
chr10:99850870 | C | T | 1 | a0005c0008t0001g0030 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.4508+74C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 31/31 | chr10 | 99850870 | |||||||
chr10:99850966 | A | G | 121 | a0001c0002t0002g0034 a0001c0002t0002g0037 a0001c0002t0002g0039 others(118): Show |
121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.4508+170A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 31/31 | chr10 | 99850966 | |||||||
chr10:99851068 | A | G | 1 | a0013c0034t0002g0044 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.4508+272A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 31/31 | chr10 | 99851068 | |||||||
chr10:99851236 | C | A | 8 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(5): Show |
8 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.4509-266C>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 31/31 | chr10 | 99851236 | |||||||
chr10:99851288 | C | T | 2 | a0001c0002t0003g0132 a0001c0002t0003g0133 |
2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.4509-214C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 31/31 | chr10 | 99851288 | |||||||
chr10:99851364 | T | C | 2 | a0002c0003t0001g0137 a0002c0003t0001g0138 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4509-138T>C | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 31/31 | chr10 | 99851364 | |||||||
chr10:99851404 | G | A | 1 | a0020c0024t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4509-98G>A | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 31/31 | chr10 | 99851404 | |||||||
chr10:99851412 | A | G | 7 | a0004c0006t0001g0022 a0004c0006t0001g0038 a0004c0006t0001g0080 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.4509-90A>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 31/31 | chr10 | 99851412 |