| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1545 | 246 | 41 | 43 | 128 | 5 | 28 | 100 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0002 | 0/0 | 1545 | 39 | 11 | 9 | 10 | 2 | 7 | 8 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0003 | 0/0 | 1545 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0004 | 0/0 | 1545 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0005 | 0/0 | 1545 | 4 | 1 | 2 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0006 | 0/0 | 1545 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0007 | 1/0 | 1545 | 3 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0008 | 0/0 | 1545 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0009 | 0/0 | 1545 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0010 | 0/0 | 1545 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0011 | 0/0 | 1545 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0012 | 0/0 | 99 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0013 | 0/0 | 1545 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0014 | 0/0 | 1545 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0015 | 0/0 | 1545 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0016 | 0/0 | 1545 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0017 | 0/0 | 1545 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0018 | 0/0 | 1545 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0019 | 0/0 | 1545 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0020 | 0/0 | 1545 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0021 | 0/0 | 1545 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0022 | 0/0 | 1545 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0023 | 0/0 | 1545 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0024 | 0/0 | 1545 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0025 | 0/0 | 1545 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0026 | 0/0 | 1545 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0027 | 0/0 | 1545 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0028 | 0/0 | 1545 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 4638 | 137 | 18 | 19 | 78 | 1 | 21 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0002 | 0/1 | 4638 | 88 | 13 | 22 | 43 | 3 | 6 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0003 | 0/0 | 4638 | 38 | 11 | 9 | 10 | 2 | 6 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0004 | 0/0 | 4638 | 9 | 8 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0005 | 0/0 | 4638 | 6 | 1 | 0 | 5 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0006 | 0/0 | 4638 | 6 | 5 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0007 | 0/0 | 4638 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0008 | 0/0 | 4638 | 4 | 1 | 2 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0009 | 0/0 | 4638 | 3 | 2 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0010 | 0/0 | 4638 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0011 | 0/0 | 4638 | 2 | 0 | 0 | 0 | 2 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0012 | 0/0 | 4638 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0013 | 0/0 | 4638 | 2 | 0 | 1 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0014 | 0/0 | 4638 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0015 | 0/0 | 4638 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0016 | 1/0 | 4638 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0017 | 0/0 | 4638 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0018 | 0/0 | 4638 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0019 | 0/0 | 4638 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0020 | 0/0 | 4638 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0021 | 0/0 | 4638 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0022 | 0/0 | 4638 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0023 | 0/0 | 4638 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0024 | 0/0 | 4638 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0025 | 0/0 | 4638 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0026 | 0/0 | 4638 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0027 | 0/0 | 4638 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0028 | 0/0 | 4638 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0029 | 0/0 | 4638 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0030 | 0/0 | 4638 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0031 | 0/0 | 4638 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0032 | 0/0 | 4638 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0033 | 0/0 | 4638 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0034 | 0/0 | 4638 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0035 | 0/0 | 4638 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0036 | 0/0 | 4638 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0037 | 0/0 | 4638 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0038 | 0/0 | 4638 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0039 | 0/0 | 4638 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0040 | 0/0 | 4638 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0041 | 0/0 | 4638 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| c0042 | 0/0 | 4638 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 1169 | 223 | 53 | 36 | 97 | 6 | 30 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| t0002 | 0/0 | 1169 | 56 | 3 | 10 | 37 | 3 | 3 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| t0003 | 0/1 | 1169 | 40 | 14 | 12 | 8 | 1 | 4 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| t0004 | 0/0 | 1169 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| t0005 | 0/0 | 1169 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| t0006 | 0/0 | 1169 | 3 | 0 | 3 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| t0007 | 0/0 | 1169 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| t0008 | 0/0 | 1169 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| t0009 | 0/0 | 1169 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| t0010 | 0/0 | 1169 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| t0011 | 0/0 | 1169 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0010 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0093 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 4638 | 137 | 18 | 19 | 78 | 1 | 21 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0002 | 0/1 | 4638 | 88 | 13 | 22 | 43 | 3 | 6 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0005 | 0/0 | 4638 | 6 | 1 | 0 | 5 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0007 | 0/0 | 4638 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0014 | 0/0 | 4638 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0017 | 0/0 | 4638 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0027 | 0/0 | 4638 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0030 | 0/0 | 4638 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0035 | 0/0 | 4638 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0036 | 0/0 | 4638 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0038 | 0/0 | 4638 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0042 | 0/0 | 4638 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0002c0003 | 0/0 | 4638 | 38 | 11 | 9 | 10 | 2 | 6 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0002c0021 | 0/0 | 4638 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0003c0004 | 0/0 | 4638 | 9 | 8 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0004c0006 | 0/0 | 4638 | 6 | 5 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0004c0029 | 0/0 | 4638 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0005c0008 | 0/0 | 4638 | 4 | 1 | 2 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0006c0009 | 0/0 | 4638 | 3 | 2 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0007c0010 | 0/0 | 4638 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0007c0016 | 1/0 | 4638 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0008c0011 | 0/0 | 4638 | 2 | 0 | 0 | 0 | 2 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0009c0012 | 0/0 | 4638 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0010c0013 | 0/0 | 4638 | 2 | 0 | 1 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0011c0015 | 0/0 | 4638 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0012c0041 | 0/0 | 4638 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0013c0018 | 0/0 | 4638 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0014c0039 | 0/0 | 4638 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0015c0020 | 0/0 | 4638 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0016c0019 | 0/0 | 4638 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0017c0037 | 0/0 | 4638 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0018c0022 | 0/0 | 4638 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0019c0023 | 0/0 | 4638 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0020c0024 | 0/0 | 4638 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0021c0026 | 0/0 | 4638 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0022c0028 | 0/0 | 4638 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0023c0034 | 0/0 | 4638 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0024c0033 | 0/0 | 4638 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0025c0031 | 0/0 | 4638 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0026c0032 | 0/0 | 4638 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0027c0025 | 0/0 | 4638 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0028c0040 | 0/0 | 4638 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | 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 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0001t0004 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0001t0005 | 0/0 | 5806 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0001t0008 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0001t0010 | 0/0 | 5806 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0002t0002 | 0/0 | 5806 | 51 | 3 | 8 | 35 | 2 | 3 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0002t0003 | 0/1 | 5806 | 32 | 8 | 12 | 8 | 1 | 2 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0002t0006 | 0/0 | 5806 | 2 | 0 | 2 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0002t0007 | 0/0 | 5806 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0002t0011 | 0/0 | 5806 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0005t0001 | 0/0 | 5806 | 6 | 1 | 0 | 5 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0007t0003 | 0/0 | 5806 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0014t0001 | 0/0 | 5806 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0017t0001 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0027t0001 | 0/0 | 5806 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0030t0001 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0035t0002 | 0/0 | 5806 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0036t0001 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0038t0001 | 0/0 | 5806 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0001c0042t0002 | 0/0 | 5806 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0002c0003t0001 | 0/0 | 5806 | 34 | 8 | 9 | 9 | 2 | 6 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0002c0003t0004 | 0/0 | 5806 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0002c0003t0009 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0002c0021t0003 | 0/0 | 5806 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0003c0004t0001 | 0/0 | 5806 | 9 | 8 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0004c0006t0001 | 0/0 | 5806 | 6 | 5 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0004c0029t0001 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0005c0008t0001 | 0/0 | 5806 | 4 | 1 | 2 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0006c0009t0001 | 0/0 | 5806 | 3 | 2 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0007c0010t0001 | 0/0 | 5806 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0007c0016t0001 | 1/0 | 5806 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0008c0011t0001 | 0/0 | 5806 | 2 | 0 | 0 | 0 | 2 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0009c0012t0001 | 0/0 | 5806 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0010c0013t0001 | 0/0 | 5806 | 2 | 0 | 1 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0011c0015t0001 | 0/0 | 5806 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0012c0041t0002 | 0/0 | 5806 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0013c0018t0001 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0014c0039t0001 | 0/0 | 5806 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0015c0020t0001 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0016c0019t0001 | 0/0 | 5806 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0017c0037t0001 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0018c0022t0001 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0019c0023t0001 | 0/0 | 5806 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0020c0024t0001 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0021c0026t0006 | 0/0 | 5806 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0022c0028t0001 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0023c0034t0002 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0024c0033t0003 | 0/0 | 5806 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0025c0031t0001 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0026c0032t0001 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0027c0025t0001 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| a0028c0040t0002 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | copy fasta | chr10 | 99777640 | 99857594 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0001g0157 | 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 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0207 | 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 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0222 | 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 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0268 | 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 |
| 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 |
| a0001c0001t0001g0274 | 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 |
| a0001c0001t0001g0277 | 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 | 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 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0283 | 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 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0293 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0313 | 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 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0005g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0008g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0001t0010g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0035 | 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 |
| a0001c0002t0002g0038 | 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 |
| a0001c0002t0002g0041 | 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 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0062 | 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 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0003g0093 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0113 | 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 |
| a0001c0002t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0006g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0006g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0007g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0007g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0002t0011g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0005t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0005t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0005t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0005t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0005t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0005t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0007t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0007t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0014t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0014t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0017t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0027t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0030t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0035t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0036t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0038t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0001c0042t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0002c0003t0001g0242 | 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 |
| a0002c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0001g0251 | 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 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0001g0257 | 0/0 | 1 | 1 | 0 | 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 |
| a0002c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0003t0004g0245 | 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 |
| a0002c0003t0009g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0002c0021t0003g0252 | 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 |
| a0003c0004t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0003c0004t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0003c0004t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0003c0004t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0003c0004t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0003c0004t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0004c0006t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0004c0006t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0004c0006t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0004c0006t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0004c0006t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0004c0006t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0004c0029t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0005c0008t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0005c0008t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0005c0008t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0005c0008t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0006c0009t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0006c0009t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0006c0009t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0007c0010t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0007c0010t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0007c0016t0001g0010 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0008c0011t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0008c0011t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0009c0012t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0009c0012t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0010c0013t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0010c0013t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0011c0015t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0011c0015t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0012c0041t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0013c0018t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0014c0039t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0015c0020t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0016c0019t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0017c0037t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0018c0022t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0019c0023t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0020c0024t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0021c0026t0006g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0022c0028t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0023c0034t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0024c0033t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0025c0031t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0026c0032t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0027c0025t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| a0028c0040t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | g0302 | EUR | GBR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00099 | hp2 | a0001 | c0035 | t0002 | g0044 | EUR | GBR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0115 | EUR | GBR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00140 | hp2 | a0005 | c0008 | t0001 | g0045 | EUR | GBR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00323 | hp1 | a0002 | c0003 | t0001 | g0326 | EUR | FIN | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00323 | hp2 | a0001 | c0002 | t0003 | g0068 | EUR | FIN | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00423 | hp1 | a0002 | c0003 | t0001 | g0261 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00423 | hp2 | a0018 | c0022 | t0001 | g0270 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0076 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0120 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00558 | hp1 | a0001 | c0030 | t0001 | g0299 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00597 | hp2 | a0023 | c0034 | t0002 | g0042 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00609 | hp2 | a0001 | c0002 | t0003 | g0057 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00621 | hp2 | a0002 | c0003 | t0001 | g0235 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00639 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00639 | hp2 | a0019 | c0023 | t0001 | g0219 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00642 | hp1 | a0001 | c0001 | t0010 | g0321 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00642 | hp2 | a0001 | c0002 | t0006 | g0016 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0055 | EAS | CHS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00733 | hp1 | a0016 | c0019 | t0001 | g0230 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0101 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00735 | hp1 | a0002 | c0003 | t0001 | g0309 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00735 | hp2 | a0001 | c0038 | t0001 | g0139 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0094 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0107 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01070 | hp1 | a0001 | c0002 | t0003 | g0018 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01070 | hp2 | a0010 | c0013 | t0001 | g0327 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01074 | hp1 | a0005 | c0008 | t0001 | g0028 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01074 | hp2 | a0002 | c0003 | t0001 | g0303 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0070 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0091 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01106 | hp2 | a0002 | c0003 | t0001 | g0258 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01109 | hp1 | a0006 | c0009 | t0001 | g0155 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01109 | hp2 | a0021 | c0026 | t0006 | g0019 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01167 | hp1 | a0001 | c0002 | t0003 | g0224 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0090 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01169 | hp2 | a0001 | c0002 | t0003 | g0276 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01175 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01175 | hp2 | a0001 | c0002 | t0003 | g0124 | AMR | PUR | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01255 | hp2 | a0001 | c0002 | t0003 | g0118 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0104 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01261 | hp2 | a0001 | c0002 | t0003 | g0061 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01346 | hp2 | a0002 | c0003 | t0001 | g0249 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0106 | 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 | g0119 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0116 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01496 | hp1 | a0001 | c0002 | t0006 | g0017 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01496 | hp2 | a0004 | c0006 | t0001 | g0138 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | IBS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01516 | hp2 | a0008 | c0011 | t0001 | g0320 | EUR | IBS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0046 | EUR | IBS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01517 | hp2 | a0008 | c0011 | t0001 | g0324 | EUR | IBS | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01884 | hp1 | a0002 | c0003 | t0001 | g0135 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0159 | 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 | a0006 | c0009 | t0001 | g0178 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01928 | hp2 | a0001 | c0002 | t0003 | g0113 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01952 | hp2 | a0001 | c0002 | t0003 | g0050 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01978 | hp1 | a0001 | c0042 | t0002 | g0064 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01978 | hp2 | a0001 | c0002 | t0003 | g0095 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02004 | hp1 | a0002 | c0003 | t0001 | g0250 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0105 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02015 | hp2 | a0025 | c0031 | t0001 | g0143 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0092 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0121 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02055 | hp1 | a0004 | c0029 | t0001 | g0331 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02055 | hp2 | a0001 | c0005 | t0001 | g0175 | 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 | g0062 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0214 | 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 | g0041 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02148 | hp2 | a0002 | c0003 | t0001 | g0253 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CDX | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02155 | hp2 | a0028 | c0040 | t0002 | g0089 | EAS | CDX | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0125 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02258 | hp2 | a0002 | c0003 | t0004 | g0245 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02273 | hp2 | a0012 | c0041 | t0002 | g0071 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02280 | hp1 | a0006 | c0009 | t0001 | g0161 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02280 | hp2 | a0001 | c0007 | t0003 | g0024 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0169 | 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 | g0184 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02300 | hp2 | a0005 | c0008 | t0001 | g0075 | AMR | PEL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02451 | hp1 | a0001 | c0002 | t0003 | g0054 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02451 | hp2 | a0020 | c0024 | t0001 | g0013 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0059 | EAS | KHV | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02602 | hp1 | a0002 | c0003 | t0001 | g0256 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02622 | hp1 | a0003 | c0004 | t0001 | g0144 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02622 | hp2 | a0004 | c0006 | t0001 | g0078 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02630 | hp1 | a0011 | c0015 | t0001 | g0014 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0069 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02698 | hp1 | a0002 | c0003 | t0001 | g0223 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02717 | hp1 | a0001 | c0002 | t0003 | g0097 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02717 | hp2 | a0011 | c0015 | t0001 | g0015 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02735 | hp1 | a0001 | c0027 | t0001 | g0145 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02735 | hp2 | a0002 | c0003 | t0001 | g0291 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02809 | hp1 | a0003 | c0004 | t0001 | g0171 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02809 | hp2 | a0007 | c0010 | t0001 | g0009 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02818 | hp1 | a0001 | c0002 | t0007 | g0129 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0077 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02886 | hp1 | a0001 | c0002 | t0003 | g0166 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02886 | hp2 | a0026 | c0032 | t0001 | g0127 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02895 | hp1 | a0003 | c0004 | t0001 | g0183 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02895 | hp2 | a0009 | c0012 | t0001 | g0218 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0284 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02896 | hp2 | a0004 | c0006 | t0001 | g0088 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0285 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02897 | hp2 | a0009 | c0012 | t0001 | g0217 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0301 | AFR | ESN | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02970 | hp2 | a0007 | c0010 | t0001 | g0008 | AFR | ESN | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03017 | hp1 | a0001 | c0002 | t0003 | g0048 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03017 | hp2 | a0010 | c0013 | t0001 | g0328 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03098 | hp1 | a0003 | c0004 | t0001 | g0182 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03098 | hp2 | a0001 | c0002 | t0003 | g0033 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03130 | hp1 | a0002 | c0003 | t0001 | g0136 | AFR | ESN | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03139 | hp1 | a0001 | c0002 | t0003 | g0131 | AFR | ESN | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03139 | hp2 | a0001 | c0017 | t0001 | g0165 | AFR | ESN | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03195 | hp1 | a0003 | c0004 | t0001 | g0164 | AFR | ESN | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03195 | hp2 | a0001 | c0002 | t0003 | g0130 | AFR | ESN | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03209 | hp1 | a0001 | c0007 | t0003 | g0027 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03225 | hp1 | a0003 | c0004 | t0001 | g0163 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03225 | hp2 | a0015 | c0020 | t0001 | g0314 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0316 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03453 | hp2 | a0013 | c0018 | t0001 | g0007 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03486 | hp1 | a0001 | c0014 | t0001 | g0128 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03486 | hp2 | a0002 | c0003 | t0001 | g0315 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03540 | hp1 | a0004 | c0006 | t0001 | g0020 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03540 | hp2 | a0001 | c0002 | t0003 | g0039 | AFR | GWD | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03579 | hp1 | a0001 | c0002 | t0007 | g0126 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03579 | hp2 | a0002 | c0003 | t0001 | g0152 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03669 | hp1 | a0024 | c0033 | t0003 | g0080 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | STU | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03688 | hp2 | a0002 | c0003 | t0001 | g0246 | SAS | STU | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03831 | hp2 | a0002 | c0003 | t0001 | g0254 | SAS | BEB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0102 | 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 | g0137 | SAS | BEB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG04199 | hp1 | a0001 | c0002 | t0011 | g0029 | SAS | STU | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG04199 | hp2 | a0002 | c0021 | t0003 | g0252 | SAS | STU | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0123 | SAS | STU | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG04204 | hp2 | a0002 | c0003 | t0001 | g0192 | SAS | STU | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | STU | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | YRI | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18522 | hp2 | a0002 | c0003 | t0004 | g0236 | AFR | YRI | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18906 | hp1 | a0004 | c0006 | t0001 | g0036 | AFR | YRI | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18906 | hp2 | a0001 | c0007 | t0003 | g0023 | AFR | YRI | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0141 | 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 | g0073 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18944 | hp2 | a0002 | c0003 | t0009 | g0244 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18954 | hp1 | a0002 | c0003 | t0001 | g0248 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18963 | hp1 | a0001 | c0036 | t0001 | g0234 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18964 | hp2 | a0001 | c0005 | t0001 | g0170 | 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 | g0158 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18970 | hp2 | a0017 | c0037 | t0001 | g0190 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18974 | hp1 | a0001 | c0005 | t0001 | g0153 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18974 | hp2 | a0001 | c0002 | t0003 | g0083 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18979 | hp2 | a0002 | c0003 | t0001 | g0231 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18982 | hp1 | a0002 | c0003 | t0001 | g0239 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18982 | hp2 | a0001 | c0002 | t0003 | g0081 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18983 | hp1 | a0002 | c0003 | t0001 | g0240 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18985 | hp1 | a0001 | c0002 | t0003 | g0031 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18987 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18992 | hp1 | a0001 | c0002 | t0003 | g0202 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18993 | hp2 | a0027 | c0025 | t0001 | g0156 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0096 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19003 | hp1 | a0001 | c0002 | t0003 | g0122 | 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 | g0087 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0109 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | LWK | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19030 | hp2 | a0001 | c0007 | t0003 | g0025 | AFR | LWK | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19043 | hp1 | a0002 | c0003 | t0001 | g0251 | AFR | LWK | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19043 | hp2 | a0002 | c0003 | t0001 | g0330 | AFR | LWK | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19055 | hp1 | a0002 | c0003 | t0001 | g0241 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19055 | hp2 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19056 | hp2 | a0001 | c0002 | t0003 | g0034 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19060 | hp2 | a0001 | c0001 | t0008 | g0292 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19065 | hp1 | a0001 | c0005 | t0001 | g0176 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19066 | hp2 | a0002 | c0003 | t0001 | g0242 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19079 | hp2 | a0001 | c0005 | t0001 | g0154 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19084 | hp1 | a0001 | c0002 | t0003 | g0030 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19084 | hp2 | a0002 | c0003 | t0001 | g0232 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0277 | 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 | g0100 | AFR | YRI | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA20129 | hp1 | a0001 | c0007 | t0003 | g0026 | AFR | ASW | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA20129 | hp2 | a0022 | c0028 | t0001 | g0280 | AFR | ASW | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA20905 | hp1 | a0014 | c0039 | t0001 | g0329 | SAS | GIH | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | GIH | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0082 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02109 | hp1 | a0004 | c0006 | t0001 | g0079 | 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 | g0149 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02559 | hp1 | a0001 | c0007 | t0003 | g0022 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG03471 | hp2 | a0001 | c0014 | t0001 | g0021 | AFR | MSL | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG06807 | hp1 | a0002 | c0003 | t0001 | g0257 | AFR | USA | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | USA | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA20300 | hp1 | a0001 | c0002 | t0003 | g0049 | AFR | USA | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0098 | AFR | USA | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA21309 | hp1 | a0005 | c0008 | t0001 | g0011 | AFR | LWK | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| NA21309 | hp2 | a0002 | c0003 | t0001 | g0247 | AFR | LWK | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0003 | g0093 | REF | REF | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| homoSapiens_grch38 | hp1 | a0007 | c0016 | t0001 | g0010 | REF | REF | ABCC2_chr10_99777640_99857594 | ABCC2 | chr10 | 99777640 | 99857594 |
| 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 | a0001a0002a0003others(24): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): 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 | a0012 | 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 | a0008 | 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 | a0028 | 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 | a0009a0013 | 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 | a0014 | 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 | a0002a0010a0014others(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 | a0017 | 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 | a0010 | 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 | a0018 | 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 | a0027 | 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 | a0019a0020 | 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 | a0019a0020 | 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 | a0019a0020 | 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 | a0016 | 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 | a0019a0020 | 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 | a0021 | 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 | a0005a0015a0019others(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 | a0023 | 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 | a0011 | 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 | a0006 | 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 | a0026 | 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 | a0025 | 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 | a0022 | 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 | a0004a0005a0013others(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 |
| 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 | a0019c0023a0020c0024 | 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 | a0001c0002a0001c0007a0001c0014others(9): Show | 106 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(103): 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 | a0004c0006a0013c0018 | 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 | a0005c0008a0015c0020a0019c0023others(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 | a0004c0006a0004c0029a0013c0018 | 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 | a0005c0008a0015c0020a0019c0023 | 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 |
| 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 | a0001c0002t0002a0001c0002t0011a0001c0035t0002others(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 | a0001c0001t0004a0002c0003t0004 | 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 | a0001c0002t0006a0021c0026t0006 | 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 | a0001c0002t0002a0001c0002t0003a0001c0002t0006others(11): Show | 102 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*932C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 32/32 | 932 | chr10 | 99852563 |
| 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 | a0001c0001t0001g0005a0001c0001t0001g0006 | 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 | 212 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(209): 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 | 110 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0056others(107): Show | 110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): 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 | a0001c0002t0002g0125 | 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 | a0001c0002t0003g0124 | 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 | a0001c0002t0003g0018a0001c0002t0006g0016a0001c0002t0006g0017others(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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0007g0126others(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 | 112 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0056others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): 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 | a0004c0029t0001g0331 | 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 | a0002c0003t0001g0330 | 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 | a0001c0014t0001g0021a0004c0006t0001g0020 | 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 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134 | 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 | a0002c0003t0001g0135a0002c0003t0001g0136 | 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 | a0002c0003t0001g0326a0010c0013t0001g0327a0010c0013t0001g0328others(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 | a0011c0015t0001g0014a0011c0015t0001g0015 | 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 | 83 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0137others(80): 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 | a0009c0012t0001g0217a0009c0012t0001g0218 | 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 | a0011c0015t0001g0014a0011c0015t0001g0015 | 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 | a0011c0015t0001g0014a0011c0015t0001g0015 | 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 | a0013c0018t0001g0007 | 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 | a0001c0007t0003g0022a0001c0007t0003g0023a0001c0007t0003g0024others(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 | a0005c0008t0001g0028 | 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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | a0001c0001t0001g0220 | 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 | a0001c0002t0002g0032a0001c0002t0003g0030a0001c0002t0003g0031others(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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0132others(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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | a0001c0001t0001g0137 | 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 | 204 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(201): 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 | a0001c0001t0001g0262a0001c0038t0001g0139a0002c0003t0001g0326others(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 | a0007c0010t0001g0008 | 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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | 110 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0056others(107): Show | 110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.207+2504C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99787285 | ||||||
| chr10:99787359
|
T | G | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | 216 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(213): 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 | 215 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(212): 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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | 83 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0137others(80): 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 | a0020c0024t0001g0013 | 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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | a0001c0001t0001g0012a0005c0008t0001g0011a0019c0023t0001g0219others(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 | a0001c0001t0001g0140 | 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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | 109 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0056others(106): Show | 109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): 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 | a0001c0002t0002g0123 | 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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | a0019c0023t0001g0219 | 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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0007g0126others(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 | a0001c0001t0001g0263a0001c0001t0001g0264 | 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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | a0013c0018t0001g0007 | 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 | a0005c0008t0001g0011 | 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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | 208 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(205): 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 | a0001c0001t0001g0264 | 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 | a0001c0001t0001g0141 | 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 | a0001c0001t0001g0215 | 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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | 112 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0056others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.208-3282C>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | chr10 | 99788952 | ||||||
| chr10:99789038
|
A | G | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0007g0126others(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 | a0001c0001t0001g0142 | 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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | a0025c0031t0001g0143 | 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 | a0001c0001t0001g0325 | 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 | a0003c0004t0001g0144 | 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 | a0001c0027t0001g0145 | 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 | 196 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(193): 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 | a0001c0001t0001g0002a0001c0001t0001g0221a0001c0001t0001g0265others(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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | a0001c0001t0001g0269 | 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 | a0001c0002t0003g0039 | 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 | a0001c0001t0001g0012a0005c0008t0001g0011a0019c0023t0001g0219others(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 | a0001c0002t0002g0040a0001c0002t0002g0041a0001c0002t0002g0043others(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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0215 | 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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0215 | 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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | a0001c0001t0001g0262a0001c0001t0001g0322a0001c0001t0001g0323 | 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 | 328 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(325): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): 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 | a0001c0001t0001g0262a0001c0001t0001g0322a0001c0001t0001g0323others(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 | a0001c0001t0001g0262a0001c0001t0001g0322a0001c0001t0001g0323 | 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 | a0008c0011t0001g0320a0008c0011t0001g0324 | 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 | a0018c0022t0001g0270 | 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 | a0013c0018t0001g0007 | 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 | a0001c0002t0011g0029 | 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 | 328 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(325): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): 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 | a0001c0035t0002g0044 | 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 | a0001c0001t0001g0222 | 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 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319 | 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 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(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 | 328 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(325): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): 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 | 110 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0056others(107): Show | 110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): 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 | a0001c0002t0003g0122 | 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 | a0013c0018t0001g0007 | 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 | 110 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0056others(107): Show | 110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): 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 | a0002c0003t0001g0223 | 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 | a0001c0001t0005g0316 | 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 | a0001c0001t0001g0213 | 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 | 328 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(325): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): 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 | a0011c0015t0001g0014a0011c0015t0001g0015 | 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 | a0013c0018t0001g0007 | 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 | a0001c0002t0002g0121 | 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 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0271others(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 | a0001c0005t0001g0153a0001c0005t0001g0154 | 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 | a0013c0018t0001g0007 | 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 | a0013c0018t0001g0007 | 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 | a0002c0003t0001g0261 | 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 | a0001c0002t0003g0224a0001c0002t0003g0276 | 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 | a0001c0001t0001g0012a0005c0008t0001g0011a0019c0023t0001g0219others(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 | a0001c0002t0002g0120 | 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 | 328 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(325): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): 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 | a0004c0006t0001g0020 | 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 | 92 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0137others(89): 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 | a0013c0018t0001g0007 | 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 | a0016c0019t0001g0230 | 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 | a0013c0018t0001g0007 | 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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0005a0001c0001t0001g0111a0001c0001t0001g0112others(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 | a0001c0001t0001g0137a0001c0001t0001g0140a0001c0001t0001g0146others(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 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0204others(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 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0027t0001g0145others(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 | a0001c0001t0001g0212 | 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 | a0001c0001t0001g0012a0005c0008t0001g0011a0019c0023t0001g0219others(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 | a0001c0007t0003g0022a0001c0007t0003g0023a0001c0007t0003g0024 | 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 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0162others(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 | 194 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(191): Show | 198 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(195): 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 | a0001c0001t0001g0279 | 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 | a0001c0001t0001g0221a0001c0002t0002g0040a0001c0002t0002g0046others(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 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0148others(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 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0149others(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 | 253 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(250): Show | 258 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(255): 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 | a0001c0002t0002g0115 | 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 | a0001c0001t0004g0098a0001c0002t0003g0039a0001c0002t0003g0054others(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 | a0001c0001t0001g0012 | 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 | 328 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(325): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): 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 | a0006c0009t0001g0178 | 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 | a0001c0001t0001g0151 | 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 | a0013c0018t0001g0007 | 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 | a0013c0018t0001g0007 | 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 | a0001c0001t0004g0098a0001c0002t0003g0039a0001c0002t0003g0054others(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 | a0001c0001t0001g0012a0005c0008t0001g0011a0019c0023t0001g0219 | 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 | a0001c0002t0003g0118a0001c0002t0003g0119 | 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 | a0011c0015t0001g0014a0011c0015t0001g0015 | 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 | a0001c0002t0002g0047 | 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 | a0013c0018t0001g0007 | 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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | a0001c0002t0002g0072 | 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 | a0002c0003t0001g0247 | 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 | a0011c0015t0001g0014a0011c0015t0001g0015 | 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 | a0001c0001t0001g0012a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0011c0015t0001g0014a0011c0015t0001g0015 | 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 | a0001c0002t0003g0030 | 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 | 98 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0056others(95): Show | 98 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.868-330A>T | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 7/31 | chr10 | 99798877 | ||||||
| chr10:99798989
|
G | T | 155 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0056others(152): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): 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 | a0004c0029t0001g0331 | 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 | a0001c0001t0001g0012a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0001c0001t0001g0052a0001c0001t0001g0053 | 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 | a0001c0001t0001g0179 | 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 | a0014c0039t0001g0329 | 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 | a0007c0010t0001g0009 | 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 | 325 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): 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 | a0021c0026t0006g0019 | 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 | a0001c0001t0001g0160a0001c0001t0001g0180a0027c0025t0001g0156 | 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 | a0001c0002t0003g0122 | 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 | a0001c0001t0001g0012a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0001c0001t0001g0237a0001c0001t0001g0283a0001c0001t0001g0286others(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 | a0005c0008t0001g0011 | 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 | a0001c0001t0001g0012a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0001c0002t0007g0129 | 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 | a0001c0027t0001g0145 | 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 | a0009c0012t0001g0217a0009c0012t0001g0218 | 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 | a0002c0003t0001g0152a0002c0003t0001g0330a0015c0020t0001g0314 | 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 | a0001c0001t0001g0132a0001c0001t0001g0133 | 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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0003g0224others(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 | a0001c0001t0001g0012a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0001c0001t0001g0056 | 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 | a0001c0001t0001g0002 | 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 | a0001c0001t0001g0002 | 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 | a0001c0001t0001g0181 | 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 | a0001c0002t0003g0057 | 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 | a0001c0038t0001g0139 | 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 | 321 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(318): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): 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 | 90 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0137others(87): 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 | a0005c0008t0001g0028a0005c0008t0001g0045a0005c0008t0001g0075 | 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 | a0001c0002t0002g0051a0001c0002t0002g0086a0001c0002t0002g0096 | 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 | a0020c0024t0001g0013 | 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 | a0004c0029t0001g0331 | 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 | a0001c0001t0001g0229 | 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 | 241 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(238): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): 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 | a0004c0029t0001g0331 | 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 | a0002c0003t0001g0253 | 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 | a0001c0001t0001g0012a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0001c0002t0002g0125 | 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 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0088 | 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 | a0001c0001t0001g0114 | 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 | a0005c0008t0001g0011 | 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 | a0004c0029t0001g0331 | 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 | a0001c0002t0003g0224a0001c0002t0003g0276 | 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 | a0001c0001t0001g0012a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0003g0224others(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 | a0013c0018t0001g0007 | 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 | a0005c0008t0001g0011 | 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 | a0001c0001t0001g0052 | 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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0003g0224others(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 | a0001c0001t0001g0012 | 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 | a0001c0014t0001g0128 | 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 | a0001c0002t0002g0051a0001c0002t0002g0086a0001c0002t0002g0096others(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 | a0001c0001t0001g0056a0001c0002t0002g0046a0001c0002t0002g0058others(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 |
71 | a0001c0001t0001g0060a0001c0001t0004g0098a0001c0002t0002g0032others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(68): 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 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0002t0002g0035others(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 | a0001c0001t0001g0114a0001c0002t0002g0076a0001c0002t0002g0125others(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 | a0001c0002t0002g0055a0004c0006t0001g0079 | 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 | a0019c0023t0001g0219 | 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 | a0001c0002t0002g0077a0001c0002t0002g0100 | 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 | a0001c0001t0001g0052a0001c0001t0001g0053 | 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 | a0001c0001t0001g0159a0001c0001t0001g0191a0001c0001t0001g0203others(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 | 149 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(146): 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 | a0001c0001t0001g0233a0002c0003t0001g0003a0002c0003t0001g0135others(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 | a0001c0002t0002g0101a0004c0029t0001g0331 | 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 | a0004c0029t0001g0331a0020c0024t0001g0013 | 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 | a0020c0024t0001g0013 | 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 | 325 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): 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 | a0001c0002t0002g0099 | 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 | a0001c0001t0001g0233a0002c0003t0001g0003a0002c0003t0001g0135others(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 | a0001c0001t0001g0114a0013c0018t0001g0007 | 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 | a0004c0029t0001g0331 | 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 | 325 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): 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 | a0001c0001t0001g0262a0001c0001t0001g0322a0001c0001t0001g0323others(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 | a0002c0003t0001g0256 | 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 | a0002c0003t0001g0003a0002c0003t0001g0135a0002c0003t0001g0136others(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 | a0024c0033t0003g0080 | 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 | a0001c0001t0001g0201 | 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 | 122 | a0001c0001t0001g0012a0001c0001t0001g0052a0001c0001t0001g0053others(119): Show | 122 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(119): 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0004 | 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 | a0001c0001t0001g0114a0013c0018t0001g0007 | 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 | a0001c0001t0001g0114a0013c0018t0001g0007 | 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 | a0001c0001t0001g0203 | 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 | a0001c0002t0002g0072 | 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 | a0001c0001t0001g0114a0013c0018t0001g0007 | 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 | a0001c0001t0001g0298 | 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 | a0001c0001t0001g0283 | 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 | a0001c0001t0001g0012a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0001c0001t0001g0167a0001c0001t0001g0181a0001c0001t0001g0184 | 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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0132others(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 | a0001c0001t0001g0012a0019c0023t0001g0219 | 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 | a0004c0029t0001g0331 | 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 | a0001c0001t0001g0114 | 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 | 325 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): 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 | a0001c0001t0001g0259 | 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 | 122 | a0001c0001t0001g0012a0001c0001t0001g0052a0001c0001t0001g0053others(119): Show | 122 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(119): 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 | a0001c0002t0002g0035 | 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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0003g0224others(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 | a0001c0001t0001g0238a0001c0001t0001g0297 | 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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0003g0224others(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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229 | 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 | a0021c0026t0006g0019 | 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 | a0001c0001t0001g0162a0006c0009t0001g0155a0006c0009t0001g0161others(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 | a0001c0001t0001g0012a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0001c0001t0001g0114a0013c0018t0001g0007 | 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 | a0004c0029t0001g0331 | 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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0215 | 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 | a0001c0001t0001g0114 | 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 | 222 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(219): 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 | a0001c0001t0004g0098 | 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 | a0001c0014t0001g0021a0004c0006t0001g0020 | 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 | 208 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(205): 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 | a0001c0001t0001g0114a0002c0003t0001g0136a0013c0018t0001g0007 | 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 | a0001c0001t0001g0262a0001c0001t0001g0322a0001c0001t0001g0323others(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 | a0003c0004t0001g0001a0003c0004t0001g0144a0003c0004t0001g0163others(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 | a0020c0024t0001g0013 | 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 | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0137others(85): 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 | a0001c0001t0001g0216 | 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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0003g0224others(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 | a0004c0029t0001g0331 | 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 | a0013c0018t0001g0007 | 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 | a0020c0024t0001g0013 | 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 | a0001c0001t0001g0264a0001c0002t0003g0130a0001c0002t0003g0131others(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 | a0001c0002t0002g0037a0001c0002t0002g0058 | 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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0003g0224others(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 | a0001c0001t0001g0114a0001c0002t0003g0130a0001c0002t0003g0131others(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 | a0001c0001t0001g0194 | 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 | a0005c0008t0001g0028a0005c0008t0001g0045a0005c0008t0001g0075others(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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0007g0126others(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 | a0028c0040t0002g0089 | 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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0132others(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 | 89 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0137others(86): 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 | a0001c0002t0002g0120 | 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 | 219 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(216): 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 | a0004c0029t0001g0331 | 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 | a0001c0002t0003g0068 | 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 | a0019c0023t0001g0219 | 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 | a0001c0001t0001g0185a0019c0023t0001g0219 | 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 | a0004c0029t0001g0331 | 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 | a0001c0001t0001g0114a0004c0029t0001g0331a0019c0023t0001g0219 | 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0146a0001c0001t0001g0157a0001c0001t0001g0159 | 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 | a0004c0006t0001g0036 | 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 | a0004c0029t0001g0331 | 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 | a0013c0018t0001g0007 | 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0185a0019c0023t0001g0219 | 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 | 11 | a0001c0001t0001g0006a0001c0001t0001g0191a0001c0001t0001g0203others(8): 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 | a0002c0003t0001g0152a0004c0029t0001g0331 | 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 | 186 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(183): 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 | a0001c0001t0001g0185 | 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 | a0019c0023t0001g0219 | 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 | a0001c0001t0001g0146a0001c0001t0001g0157a0001c0001t0001g0159 | 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 | a0001c0001t0001g0179a0002c0003t0001g0152 | 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0012a0002c0003t0001g0152a0005c0008t0001g0028others(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 | a0001c0001t0001g0146a0001c0001t0001g0157a0001c0001t0001g0159others(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 | 192 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(189): 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 | a0001c0002t0002g0066a0001c0002t0002g0067 | 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 | a0005c0008t0001g0028a0005c0008t0001g0045a0005c0008t0001g0075others(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 | a0001c0001t0001g0179a0002c0003t0001g0152 | 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 | a0001c0001t0001g0146a0001c0001t0001g0157a0001c0001t0001g0159 | 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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0132others(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 | 63 | a0001c0001t0001g0137a0001c0001t0001g0140a0001c0001t0001g0141others(60): 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 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0147others(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 | a0001c0001t0001g0179a0002c0003t0001g0152 | 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 | a0001c0002t0002g0123 | 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 | 71 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0140others(68): 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 | 183 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0132others(180): 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 | 70 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0140others(67): 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 | 64 | a0001c0001t0001g0137a0001c0001t0001g0140a0001c0001t0001g0141others(61): 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 | a0001c0001t0001g0146a0001c0001t0001g0157a0001c0001t0001g0159 | 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 | a0001c0001t0001g0005a0001c0001t0001g0147a0001c0001t0001g0215others(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 | 11 | a0001c0001t0001g0006a0001c0001t0001g0191a0001c0001t0001g0203others(8): 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 | 71 | a0001c0001t0001g0137a0001c0001t0001g0140a0001c0001t0001g0141others(68): 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 | a0001c0001t0001g0005a0001c0001t0001g0147a0001c0001t0001g0215others(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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0146a0001c0001t0001g0157a0001c0001t0001g0159others(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 | 71 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0137others(68): 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 | a0001c0002t0002g0090a0001c0002t0002g0091a0001c0002t0002g0102others(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 | a0001c0035t0002g0044 | 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 | 11 | a0001c0001t0001g0006a0001c0001t0001g0191a0001c0001t0001g0203others(8): 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 | a0001c0002t0002g0040a0001c0002t0002g0043a0001c0002t0002g0055others(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 | a0001c0001t0001g0005a0001c0001t0001g0147a0001c0001t0001g0215others(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 | a0002c0021t0003g0252 | 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 | a0001c0002t0002g0120 | 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 | a0001c0001t0001g0146a0001c0001t0001g0157a0001c0001t0001g0159others(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 | a0001c0001t0001g0146a0001c0001t0001g0157a0001c0001t0001g0159others(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 | a0001c0001t0001g0005a0001c0001t0001g0147a0001c0001t0001g0215others(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 | a0002c0003t0001g0003a0002c0003t0001g0291a0002c0003t0001g0302others(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 | a0002c0003t0001g0254 | 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 | a0001c0001t0001g0114a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0001c0001t0001g0146a0001c0001t0001g0157a0001c0001t0001g0159others(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 | a0001c0002t0002g0120 | 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 | a0005c0008t0001g0028a0005c0008t0001g0045a0005c0008t0001g0075others(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 | a0002c0003t0001g0258 | 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 | 68 | a0001c0001t0001g0012a0001c0001t0001g0137a0001c0001t0001g0140others(65): 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 | a0005c0008t0001g0028a0005c0008t0001g0045a0005c0008t0001g0075others(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 | 71 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0137others(68): 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 | a0001c0002t0002g0120a0004c0029t0001g0331a0013c0018t0001g0007 | 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 | a0001c0001t0001g0220a0001c0001t0005g0284a0001c0001t0005g0285others(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 | 68 | a0001c0001t0001g0012a0001c0001t0001g0137a0001c0001t0001g0140others(65): 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 | a0001c0001t0001g0005a0001c0001t0001g0147a0001c0001t0001g0215others(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 | a0001c0001t0001g0142a0001c0001t0001g0199a0001c0001t0001g0200others(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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0132others(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 | a0001c0014t0001g0021a0004c0006t0001g0020a0004c0006t0001g0078others(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 | 11 | a0001c0001t0001g0006a0001c0001t0001g0191a0001c0001t0001g0203others(8): 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 | a0001c0001t0001g0146a0001c0001t0001g0157a0001c0001t0001g0159 | 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 | 78 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0140others(75): 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 | a0001c0001t0001g0114a0004c0029t0001g0331 | 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 | a0005c0008t0001g0028a0005c0008t0001g0045a0007c0010t0001g0008others(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 | a0001c0001t0001g0012a0001c0001t0001g0298 | 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 | a0001c0001t0001g0012a0001c0001t0001g0114 | 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 | a0001c0001t0001g0298 | 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 | a0001c0001t0001g0146a0001c0001t0001g0157a0001c0001t0001g0159 | 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 | 80 | a0001c0001t0001g0012a0001c0001t0001g0137a0001c0001t0001g0140others(77): 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 | a0020c0024t0001g0013 | 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 | a0019c0023t0001g0219 | 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 | a0001c0001t0001g0114 | 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 | a0001c0002t0003g0018a0001c0002t0006g0016a0001c0002t0006g0017others(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 | a0001c0001t0001g0146a0001c0001t0001g0157a0001c0001t0001g0159others(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 | a0004c0029t0001g0331 | 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 | a0001c0001t0001g0146a0001c0001t0001g0157a0001c0001t0001g0159 | 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 | 16 | a0001c0001t0001g0005a0001c0001t0001g0147a0001c0001t0001g0191others(13): 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 | a0004c0029t0001g0331 | 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 | a0001c0001t0001g0006a0001c0002t0003g0130a0001c0002t0003g0131others(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 | a0001c0001t0001g0006a0001c0002t0003g0130a0001c0002t0003g0131others(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 | 17 | a0001c0001t0001g0005a0001c0001t0001g0147a0001c0001t0001g0191others(14): 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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0003g0224others(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 | a0001c0001t0001g0012a0001c0001t0001g0177a0001c0001t0001g0208others(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 | 98 | a0001c0001t0001g0137a0001c0001t0001g0140a0001c0001t0001g0141others(95): 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 | a0001c0001t0001g0005a0001c0001t0001g0052a0001c0001t0001g0053 | 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 | a0001c0002t0003g0039 | 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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0003g0224others(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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0003g0224others(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 | a0001c0001t0001g0146a0001c0001t0001g0157a0001c0001t0001g0159others(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 | a0019c0023t0001g0219 | 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 | a0005c0008t0001g0028a0005c0008t0001g0045a0005c0008t0001g0075others(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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0003g0224others(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 | a0001c0001t0001g0157a0001c0001t0001g0159a0001c0001t0001g0172others(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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0147a0001c0001t0001g0215a0001c0001t0001g0225others(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 | a0005c0008t0001g0045a0005c0008t0001g0075a0007c0010t0001g0008others(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 | 62 | a0001c0001t0001g0137a0001c0001t0001g0140a0001c0001t0001g0141others(59): 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 | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0191others(9): 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 | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0191others(9): 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 | a0004c0029t0001g0331a0005c0008t0001g0028a0013c0018t0001g0007others(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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0003g0224others(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 | a0001c0001t0001g0142a0001c0001t0001g0146a0001c0001t0001g0147others(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 | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0005t0001g0153others(5): 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 | a0001c0002t0003g0030 | 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 | a0001c0001t0001g0191a0001c0001t0001g0203a0001c0001t0001g0209others(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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0003g0224others(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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0012a0001c0002t0003g0130a0001c0002t0003g0131others(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 | a0001c0001t0001g0172a0001c0001t0001g0213a0006c0009t0001g0155 | 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 | a0004c0029t0001g0331 | 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 | a0001c0001t0001g0012a0013c0018t0001g0007 | 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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0002c0003t0001g0249 | 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 | a0002c0003t0001g0003a0002c0003t0001g0135a0002c0003t0001g0136others(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 | a0001c0001t0001g0191a0001c0001t0001g0203a0001c0001t0001g0209others(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 | 212 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(209): 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 | a0001c0002t0002g0035 | 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 | a0001c0002t0002g0065a0001c0002t0003g0033 | 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 | a0001c0001t0001g0191a0001c0001t0001g0203a0001c0001t0001g0209others(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 | a0002c0003t0001g0232a0002c0003t0001g0243a0002c0003t0001g0250others(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 | a0001c0002t0003g0116 | 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 | a0001c0001t0001g0210 | 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 | a0005c0008t0001g0028a0005c0008t0001g0045a0005c0008t0001g0075 | 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 | a0001c0001t0001g0325 | 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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0001c0002t0003g0018a0001c0002t0006g0016a0001c0002t0006g0017others(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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0001c0002t0003g0224a0001c0002t0003g0276 | 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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0005c0008t0001g0028a0005c0008t0001g0045a0005c0008t0001g0075others(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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0003g0224others(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 | a0002c0003t0001g0152 | 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 | 207 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(204): 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 | a0001c0001t0001g0012a0001c0001t0001g0114 | 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 | a0001c0001t0001g0052a0001c0001t0001g0053 | 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 | a0001c0001t0001g0012 | 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 | a0013c0018t0001g0007 | 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 | a0001c0002t0002g0067 | 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 | a0001c0002t0002g0115a0001c0002t0003g0113a0001c0002t0003g0117others(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 | a0004c0006t0001g0020 | 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 | a0001c0001t0001g0147a0001c0002t0007g0126a0001c0002t0007g0129others(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 | a0001c0002t0002g0125 | 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 | a0001c0002t0002g0123 | 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 | a0004c0006t0001g0036 | 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 | 217 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(214): 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 | a0001c0001t0001g0237a0001c0001t0001g0283a0001c0001t0001g0286others(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 | 216 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(213): 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 | a0002c0003t0001g0249 | 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 | a0001c0001t0001g0237a0001c0001t0001g0283a0001c0001t0001g0286others(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 | a0004c0006t0001g0036 | 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 | a0001c0001t0001g0237a0001c0001t0001g0283a0001c0001t0001g0286others(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 | a0001c0001t0001g0237a0001c0001t0001g0283a0001c0001t0001g0286others(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 | a0001c0001t0001g0141a0001c0001t0001g0179a0001c0001t0001g0194others(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 | a0001c0001t0001g0237a0001c0001t0001g0283a0001c0001t0001g0286others(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 | a0001c0001t0001g0237a0001c0001t0001g0283a0001c0001t0001g0286others(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 | a0001c0001t0001g0237a0001c0001t0001g0283a0001c0001t0001g0286others(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 | a0001c0001t0001g0237a0001c0001t0001g0283a0001c0001t0001g0286others(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 | a0001c0001t0008g0292 | 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 | a0001c0001t0001g0237a0001c0001t0001g0283a0001c0001t0001g0286others(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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0132others(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 | a0004c0006t0001g0036 | 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 | a0004c0006t0001g0036 | 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 | a0001c0001t0001g0114a0001c0001t0001g0238a0001c0001t0001g0278others(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 | a0004c0006t0001g0036 | 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 | a0001c0001t0001g0238a0001c0001t0001g0278a0001c0001t0001g0287others(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 | a0004c0006t0001g0036 | 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 | a0004c0006t0001g0036 | 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 | a0001c0001t0001g0233a0001c0001t0001g0237a0001c0001t0001g0269others(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 | a0009c0012t0001g0217a0009c0012t0001g0218 | 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 | 64 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0140others(61): 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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0238a0001c0001t0001g0278a0001c0001t0001g0287others(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 | a0019c0023t0001g0219 | 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 | a0020c0024t0001g0013 | 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 | a0013c0018t0001g0007 | 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 | a0001c0001t0001g0132a0001c0001t0001g0134a0001c0001t0001g0233others(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 | a0001c0001t0001g0263 | 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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0133a0001c0001t0001g0262a0001c0001t0001g0322others(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 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0279others(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 | a0001c0001t0001g0260 | 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 | a0001c0001t0001g0002a0001c0001t0001g0221a0001c0001t0001g0265others(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 | a0001c0001t0001g0275a0001c0001t0001g0300a0001c0001t0001g0308others(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 | a0001c0001t0001g0220a0001c0001t0001g0313a0001c0001t0005g0284others(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 | a0001c0001t0001g0004 | 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 | a0001c0001t0001g0272a0001c0001t0001g0274 | 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 | a0001c0001t0001g0282 | 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 | a0001c0001t0001g0211a0002c0003t0001g0231a0002c0003t0001g0232others(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 | a0015c0020t0001g0314 | 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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0162a0001c0002t0003g0166a0002c0003t0001g0192others(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 | a0001c0001t0001g0137a0001c0001t0001g0146a0001c0001t0001g0147others(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 | a0001c0005t0001g0153a0001c0005t0001g0154a0003c0004t0001g0001others(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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0150a0001c0001t0001g0151a0002c0003t0001g0003others(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 | a0002c0003t0001g0235a0002c0003t0001g0243a0002c0003t0001g0247others(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 | a0011c0015t0001g0014a0011c0015t0001g0015 | 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 | a0002c0003t0001g0261 | 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 | a0002c0003t0001g0223 | 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 | a0001c0002t0002g0100 | 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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0002t0002g0051others(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 | a0001c0001t0001g0114a0001c0002t0003g0130a0001c0002t0003g0131others(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 | a0001c0001t0001g0259a0001c0001t0001g0290a0001c0001t0001g0307others(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 | a0001c0001t0001g0237a0001c0001t0001g0283a0001c0001t0001g0286others(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 | a0002c0003t0001g0135a0002c0003t0001g0136a0002c0003t0001g0152others(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 | a0001c0001t0001g0157a0001c0001t0001g0159 | 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 | a0001c0002t0002g0125 | 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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0001c0001t0008g0292 | 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 | a0001c0001t0001g0238a0001c0001t0001g0278a0001c0001t0001g0287others(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 | a0001c0001t0001g0157a0001c0001t0001g0159a0001c0001t0001g0237others(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 | a0001c0001t0001g0297 | 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 | a0001c0001t0001g0238 | 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 | a0001c0001t0001g0287a0001c0001t0001g0294 | 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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0157a0001c0001t0001g0159a0001c0001t0001g0237others(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 | a0001c0001t0001g0298a0001c0001t0001g0325 | 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 | a0001c0001t0001g0137a0001c0001t0001g0146a0001c0001t0001g0147others(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 | a0009c0012t0001g0217a0009c0012t0001g0218 | 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 | a0001c0001t0001g0237a0001c0001t0001g0259a0001c0001t0001g0283others(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 | a0001c0001t0001g0238a0001c0001t0001g0278a0001c0001t0001g0287others(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 | a0001c0001t0001g0298a0001c0001t0001g0325 | 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 | a0001c0001t0001g0220a0001c0001t0001g0260a0001c0001t0001g0262others(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 | a0004c0029t0001g0331a0013c0018t0001g0007 | 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 | a0001c0001t0001g0238a0001c0001t0001g0278a0001c0001t0001g0287others(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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0001c0001t0001g0162a0002c0003t0001g0249a0006c0009t0001g0161 | 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 | a0001c0001t0001g0211a0001c0001t0001g0259a0001c0001t0001g0290others(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 |
46 | a0001c0001t0001g0005a0001c0001t0001g0141a0001c0001t0001g0142others(43): 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 | a0001c0001t0001g0200a0001c0017t0001g0165 | 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 | a0001c0001t0001g0169 | 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 | a0001c0001t0001g0140a0001c0001t0001g0204a0002c0003t0001g0242others(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 | a0001c0001t0001g0006 | 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 | a0001c0001t0001g0264a0001c0001t0001g0300a0001c0001t0001g0308others(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 | a0001c0001t0001g0004a0013c0018t0001g0007 | 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 | a0001c0042t0002g0064a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134 | 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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0002c0003t0001g0309 | 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 | a0001c0001t0001g0162a0006c0009t0001g0161a0019c0023t0001g0219 | 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 | a0006c0009t0001g0178 | 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 | a0006c0009t0001g0155 | 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 | a0001c0001t0001g0012a0001c0001t0001g0172a0001c0001t0001g0188others(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 | a0001c0002t0002g0072a0001c0002t0002g0073a0001c0002t0002g0074 | 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 | a0001c0001t0001g0225a0001c0007t0003g0022a0001c0007t0003g0023others(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 | a0005c0008t0001g0028 | 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 | a0005c0008t0001g0045a0005c0008t0001g0075 | 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 | a0001c0001t0001g0114a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0221others(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 | a0001c0001t0001g0304a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0007c0010t0001g0008a0007c0010t0001g0009 | 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 | a0001c0002t0003g0049a0001c0002t0003g0050a0001c0042t0002g0064 | 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 | 153 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0137others(150): 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 | a0001c0002t0003g0039a0001c0002t0003g0166a0001c0014t0001g0021others(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 | a0004c0006t0001g0078 | 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 | a0001c0002t0002g0035a0001c0002t0002g0043a0001c0002t0002g0047others(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 | a0001c0001t0001g0172a0001c0001t0001g0213a0001c0002t0002g0040 | 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 | a0001c0001t0001g0216 | 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 | a0001c0001t0001g0002a0001c0001t0001g0221a0001c0001t0001g0265others(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 | a0001c0002t0002g0123a0012c0041t0002g0071 | 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0004a0001c0001t0001g0132a0001c0001t0001g0133others(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 | a0001c0001t0001g0002a0001c0001t0001g0221a0001c0001t0001g0265others(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 | a0001c0001t0001g0233a0001c0001t0001g0237a0001c0001t0001g0283others(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 | a0002c0003t0001g0231a0002c0003t0001g0239a0002c0003t0001g0248others(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 | a0013c0018t0001g0007 | 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 | a0013c0018t0001g0007 | 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 | a0013c0018t0001g0007 | 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 | a0001c0002t0002g0077a0001c0002t0002g0100a0013c0018t0001g0007 | 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 | a0001c0001t0001g0012 | 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 | a0004c0029t0001g0331a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0001c0002t0002g0062a0001c0002t0002g0066a0001c0002t0002g0067others(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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0220others(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 | a0001c0017t0001g0165 | 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 | a0001c0001t0001g0188a0001c0001t0001g0198a0025c0031t0001g0143 | 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 | a0001c0001t0001g0267a0001c0001t0001g0308 | 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 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134 | 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 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0308 | 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 | a0001c0002t0007g0129 | 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 | a0001c0002t0007g0126 | 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 | a0001c0002t0003g0130a0001c0002t0003g0131 | 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 | a0001c0014t0001g0128 | 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 | a0001c0001t0001g0233a0001c0001t0001g0237a0001c0001t0001g0283others(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 | a0001c0001t0001g0293 | 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 | a0001c0001t0001g0311a0001c0001t0001g0312 | 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 | a0001c0001t0001g0264 | 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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(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 | a0001c0001t0001g0189a0001c0002t0003g0118a0001c0002t0003g0119others(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 | a0002c0003t0001g0231a0002c0003t0001g0239a0002c0003t0001g0248 | 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 | a0002c0003t0001g0240 | 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 | a0001c0001t0001g0162a0002c0003t0001g0247a0006c0009t0001g0155others(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 | a0006c0009t0001g0161 | 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 | a0001c0001t0001g0307a0001c0001t0001g0310a0001c0001t0001g0317 | 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 | a0001c0001t0001g0259 | 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 | a0001c0002t0003g0224a0001c0002t0003g0276 | 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 | a0026c0032t0001g0127 | 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 | a0001c0001t0001g0012a0001c0002t0003g0130a0001c0002t0003g0131others(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 | a0001c0001t0001g0004a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0001c0001t0001g0300a0018c0022t0001g0270 | 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 | a0002c0003t0001g0003a0002c0003t0001g0291a0002c0003t0001g0302others(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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0004 | 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 | a0004c0006t0001g0020 | 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 | a0001c0001t0001g0114a0001c0002t0003g0048a0013c0018t0001g0007 | 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 | a0001c0001t0001g0114a0013c0018t0001g0007 | 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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0003g0224others(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 | a0001c0001t0001g0114a0001c0002t0003g0130a0001c0002t0003g0131others(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 | a0002c0003t0001g0003a0002c0003t0001g0291a0002c0003t0001g0302others(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 | a0001c0001t0001g0012a0001c0002t0003g0130a0001c0002t0003g0131others(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 | a0001c0001t0001g0114a0013c0018t0001g0007 | 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 | 129 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0137others(126): 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 | a0001c0005t0001g0153a0001c0005t0001g0154a0002c0003t0001g0250 | 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 | 209 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(206): 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 | a0001c0038t0001g0139 | 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 | a0021c0026t0006g0019 | 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 | a0001c0001t0001g0200 | 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 | a0001c0002t0003g0118 | 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 | a0001c0001t0001g0114a0013c0018t0001g0007 | 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 | 222 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(219): 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 | a0001c0001t0001g0114a0013c0018t0001g0007 | 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 | a0001c0001t0001g0114a0013c0018t0001g0007 | 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 | a0001c0002t0003g0130a0001c0002t0003g0131 | 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 | a0005c0008t0001g0028a0005c0008t0001g0045a0005c0008t0001g0075others(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 | 217 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(214): 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 | a0005c0008t0001g0028a0005c0008t0001g0045a0005c0008t0001g0075others(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 | a0001c0002t0003g0061 | 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 | a0004c0029t0001g0331 | 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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0003g0224others(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 | a0001c0001t0001g0207 | 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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0020c0024t0001g0013 | 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 | a0013c0018t0001g0007 | 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 | a0001c0007t0003g0027 | 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 | a0001c0001t0001g0006a0001c0001t0001g0148a0001c0001t0001g0160others(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 | a0001c0001t0001g0198a0001c0002t0002g0090a0005c0008t0001g0028others(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 | a0004c0029t0001g0331 | 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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0215 | 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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0114a0001c0002t0003g0130a0001c0002t0003g0131others(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 | a0001c0002t0003g0095 | 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 | a0002c0003t0001g0291 | 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 | a0001c0001t0001g0114a0013c0018t0001g0007 | 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 | a0002c0003t0001g0003a0002c0003t0001g0192a0002c0003t0001g0231others(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 | a0002c0003t0001g0003a0002c0003t0001g0135a0002c0003t0001g0136others(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 | a0001c0002t0002g0059 | 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 | a0001c0001t0001g0298 | 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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0001c0001t0001g0114a0013c0018t0001g0007 | 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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0002c0003t0001g0254 | 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 | 222 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(219): 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 | a0001c0001t0001g0114a0013c0018t0001g0007 | 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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0003g0224others(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 | a0002c0003t0001g0223 | 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 | a0004c0029t0001g0331 | 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 | a0001c0001t0001g0012 | 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 | a0004c0029t0001g0331 | 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 | a0001c0002t0002g0059a0001c0002t0002g0108 | 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 | 130 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0137others(127): 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 | a0001c0001t0001g0278a0001c0001t0001g0281a0001c0001t0001g0298 | 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 | a0001c0002t0003g0033 | 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 | a0001c0002t0002g0082a0001c0002t0002g0106a0001c0002t0002g0107others(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 | a0001c0002t0002g0046a0001c0002t0002g0094 | 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 | a0001c0001t0001g0185 | 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 | a0001c0002t0002g0069 | 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 | a0001c0001t0001g0012a0001c0002t0003g0130a0001c0002t0003g0131others(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 | 95 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0137others(92): 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 | a0001c0001t0001g0157a0001c0001t0001g0159a0001c0002t0003g0166others(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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0012a0004c0029t0001g0331 | 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 | a0004c0029t0001g0331 | 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 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0088 | 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 | a0001c0001t0001g0012a0001c0002t0003g0130a0001c0002t0003g0131others(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 | a0001c0001t0001g0114 | 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 | 247 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(244): 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 | a0001c0002t0003g0166a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0004c0006t0001g0036 | 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 | a0013c0018t0001g0007 | 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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0132others(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 | a0001c0001t0001g0012a0001c0002t0003g0130a0001c0002t0003g0131others(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 | a0001c0002t0003g0116 | 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 | a0001c0001t0001g0142a0001c0001t0001g0167a0001c0001t0001g0174others(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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | a0020c0024t0001g0013 | 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 | a0001c0001t0001g0313 | 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0012a0001c0002t0003g0130a0001c0002t0003g0131others(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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0012a0001c0002t0003g0130a0001c0002t0003g0131others(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 | a0005c0008t0001g0028a0005c0008t0001g0045a0005c0008t0001g0075others(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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0114 | 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 | a0011c0015t0001g0014 | 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 | a0001c0001t0001g0262 | 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 | a0002c0003t0001g0249 | 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 | a0001c0002t0002g0125 | 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 | a0020c0024t0001g0013 | 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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0012a0001c0002t0003g0130a0001c0002t0003g0131others(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 | a0001c0002t0003g0118a0001c0002t0003g0119 | 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 | a0004c0029t0001g0331 | 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 | a0009c0012t0001g0217a0009c0012t0001g0218a0011c0015t0001g0014others(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 | a0004c0029t0001g0331a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0001c0001t0001g0012a0001c0002t0003g0130a0001c0002t0003g0131others(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 | a0001c0001t0001g0012a0001c0002t0003g0130a0001c0002t0003g0131others(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 | a0001c0001t0001g0260 | 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 | a0001c0001t0001g0012 | 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 | a0004c0029t0001g0331 | 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 | a0001c0001t0001g0012a0001c0014t0001g0021a0005c0008t0001g0011 | 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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): 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 | a0004c0029t0001g0331a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0001c0001t0001g0151 | 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0260 | 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 | a0001c0001t0001g0114 | 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 | 95 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0137others(92): 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 | a0001c0001t0001g0012a0001c0002t0003g0130a0001c0002t0003g0131others(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 | a0001c0001t0001g0215 | 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 | a0001c0001t0001g0012a0001c0002t0003g0130a0001c0002t0003g0131others(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 | 248 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(245): 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 | a0001c0001t0001g0114 | 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 | a0001c0002t0002g0046a0001c0002t0002g0094 | 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 | a0001c0001t0001g0167a0001c0001t0001g0181a0001c0001t0001g0184others(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 | a0005c0008t0001g0028a0005c0008t0001g0045a0005c0008t0001g0075others(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 | a0004c0029t0001g0331a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0001c0001t0001g0012a0001c0002t0003g0130a0001c0002t0003g0131others(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 | a0004c0029t0001g0331a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | 225 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(222): 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 | a0025c0031t0001g0143 | 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 | a0001c0001t0005g0301a0002c0003t0001g0003a0002c0003t0001g0135others(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 | a0001c0001t0001g0012a0001c0001t0001g0114a0001c0002t0003g0130others(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 | a0001c0001t0001g0214 | 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 | 221 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(218): 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 | 224 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(221): 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 | a0001c0001t0001g0193 | 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 | 221 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(218): 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 | a0001c0001t0001g0012 | 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 | 224 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(221): 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 | 224 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(221): 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 | a0003c0004t0001g0182 | 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 | a0001c0001t0001g0212 | 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 | a0001c0001t0001g0149 | 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 | 212 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(209): 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 | a0001c0001t0001g0167 | 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 | 212 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(209): 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 | a0001c0002t0002g0101 | 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 | 220 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(217): 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 | a0001c0001t0001g0056 | 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 | 221 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(218): 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 | a0001c0001t0001g0298 | 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 | 223 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(220): 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 | a0019c0023t0001g0219a0020c0024t0001g0013a0022c0028t0001g0280 | 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 | 223 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(220): 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 | 221 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(218): 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 | 221 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(218): 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 | a0004c0029t0001g0331 | 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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0004c0029t0001g0331 | 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 | a0019c0023t0001g0219 | 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 | 4 | a0001c0002t0003g0093a0001c0002t0003g0113a0001c0002t0003g0117others(1): Show | 4 | HG01928.hp2 HG03669.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2621-4679C>G | ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 19/31 | chr10 | 99825628 | ||||||
| chr10:99825640
|
G | A | 1 | a0020c0024t0001g0013 | 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 | a0005c0008t0001g0028 | 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 | 223 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(220): 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 | a0001c0001t0001g0213 | 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 | a0004c0029t0001g0331 | 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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | 221 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(218): 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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0003g0224others(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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0193 | 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 | a0001c0002t0002g0086 | 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 | a0001c0002t0002g0106 | 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 | a0011c0015t0001g0014a0011c0015t0001g0015 | 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 | a0002c0003t0001g0152a0020c0024t0001g0013 | 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 | a0004c0006t0001g0020 | 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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0003g0224others(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 | a0001c0001t0001g0168 | 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 | a0002c0003t0001g0247 | 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 | a0001c0002t0003g0116 | 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 | a0013c0018t0001g0007 | 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 | 223 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(220): 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 | a0001c0001t0001g0012a0001c0002t0003g0130a0001c0002t0003g0131others(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 | 212 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(209): 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 | a0001c0002t0002g0041 | 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 | 225 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(222): 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 | a0001c0001t0001g0193 | 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 | a0013c0018t0001g0007 | 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 | a0001c0001t0001g0177 | 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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0003g0224others(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 | a0001c0001t0001g0053 | 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 | 221 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(218): 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 | a0005c0008t0001g0028a0005c0008t0001g0045a0005c0008t0001g0075others(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 | a0005c0008t0001g0028a0005c0008t0001g0045a0005c0008t0001g0075others(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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0019c0023t0001g0219 | 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 | 220 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(217): 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 | a0001c0001t0001g0114 | 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 | 225 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(222): 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0287a0001c0001t0001g0294 | 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 | a0001c0001t0001g0279 | 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 | a0002c0003t0001g0003a0002c0003t0001g0135a0002c0003t0001g0136others(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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0001c0002t0002g0121 | 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 | a0001c0002t0007g0126a0001c0002t0007g0129a0001c0014t0001g0128others(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 | a0004c0029t0001g0331a0013c0018t0001g0007 | 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 | a0001c0005t0001g0170 | 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 |
219 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(216): Show | 224 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(221): 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 |
107 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0056others(104): Show | 107 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(104): 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 | a0001c0001t0001g0278 | 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 | 91 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0137others(88): 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 | a0019c0023t0001g0219 | 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 | a0004c0029t0001g0331 | 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 | a0001c0001t0001g0220 | 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 | a0001c0002t0011g0029 | 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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0003g0224others(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 | a0005c0008t0001g0011 | 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 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0088 | 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 | a0001c0002t0002g0123 | 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 | a0005c0008t0001g0028a0005c0008t0001g0045a0005c0008t0001g0075 | 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 | 226 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(223): 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 | a0005c0008t0001g0028a0005c0008t0001g0045a0005c0008t0001g0075others(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 | a0002c0003t0001g0256 | 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 | 223 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(220): 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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0001c0002t0003g0166 | 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 | a0001c0002t0002g0110 | 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 | 91 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0137others(88): 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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0003c0004t0001g0001a0003c0004t0001g0144a0003c0004t0001g0163others(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 | a0001c0002t0002g0076a0001c0002t0002g0087a0001c0002t0002g0099 | 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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0002c0003t0001g0003a0002c0003t0001g0135a0002c0003t0001g0136others(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 | a0001c0002t0002g0069a0001c0002t0002g0082a0001c0002t0002g0106others(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 | a0001c0001t0001g0114 | 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 | a0001c0002t0002g0087 | 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 | a0005c0008t0001g0028a0005c0008t0001g0045a0005c0008t0001g0075others(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 | 2 | a0001c0001t0001g0197a0001c0001t0001g0206 | 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 | a0019c0023t0001g0219a0020c0024t0001g0013 | 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 | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0003g0224others(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 | 220 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(217): 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 | a0020c0024t0001g0013 | 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 | 200 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(197): 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 | 200 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(197): 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 | 200 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(197): 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 | 197 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(194): 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 | a0020c0024t0001g0013 | 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 | a0001c0001t0001g0191a0001c0001t0001g0203a0001c0001t0001g0209 | 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 | a0020c0024t0001g0013 | 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 | a0001c0001t0001g0177 | 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 | 226 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(223): 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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0001t0001g0149 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0002t0002g0069 | 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 | a0001c0002t0003g0095 | 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 | a0001c0001t0001g0060 | 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 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229 | 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 | a0002c0003t0001g0231a0002c0003t0001g0248 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0036 | 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0213 | 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 | a0001c0001t0001g0238a0001c0001t0001g0269a0001c0001t0001g0287others(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 | a0002c0003t0001g0254 | 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 | a0001c0001t0001g0147a0001c0001t0004g0098a0002c0003t0001g0135others(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 | a0003c0004t0001g0183 | 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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0020c0024t0001g0013 | 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 | a0007c0010t0001g0008a0007c0010t0001g0009 | 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 | a0001c0001t0001g0201 | 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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0311a0001c0001t0001g0312 | 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 | a0020c0024t0001g0013 | 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 | a0001c0001t0001g0052a0001c0001t0001g0053 | 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 | a0001c0002t0002g0063a0001c0002t0002g0084a0001c0002t0002g0085others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0020c0024t0001g0013 | 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 | a0004c0029t0001g0331 | 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 | a0002c0003t0001g0257 | 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 | a0005c0008t0001g0028 | 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 | a0020c0024t0001g0013 | 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 | a0004c0029t0001g0331 | 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 | a0001c0002t0002g0058 | 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 | a0019c0023t0001g0219 | 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 | a0001c0002t0002g0058 | 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 | a0001c0001t0001g0220a0011c0015t0001g0014a0011c0015t0001g0015 | 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 | a0004c0006t0001g0088 | 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 | 164 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(161): Show | 166 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(163): 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 | a0001c0001t0001g0114a0001c0001t0001g0147a0001c0001t0001g0271others(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 | a0004c0006t0001g0036a0004c0006t0001g0078a0004c0006t0001g0079others(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 | a0004c0029t0001g0331 | 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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0138 | 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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0001c0001t0001g0147a0001c0001t0001g0319a0001c0002t0002g0032others(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 | a0026c0032t0001g0127 | 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 | a0001c0001t0001g0111a0001c0001t0001g0142a0001c0001t0001g0148others(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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0053a0001c0001t0001g0265a0001c0001t0001g0286others(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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0020c0024t0001g0013 | 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 | a0001c0002t0002g0065a0004c0006t0001g0020a0004c0006t0001g0036others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0002t0002g0090 | 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 | a0001c0007t0003g0022 | 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 | a0001c0001t0001g0195a0001c0001t0001g0208 | 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 | a0001c0001t0001g0147a0001c0001t0004g0098a0002c0003t0001g0135others(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 | a0020c0024t0001g0013 | 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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0001t0001g0304 | 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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0005c0008t0001g0045a0005c0008t0001g0075 | 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 | a0001c0014t0001g0021a0001c0014t0001g0128 | 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 | a0005c0008t0001g0045a0005c0008t0001g0075 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0036 | 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 | a0001c0014t0001g0021a0001c0014t0001g0128 | 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 | a0020c0024t0001g0013 | 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 | a0001c0001t0001g0274 | 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 | a0001c0014t0001g0021a0001c0014t0001g0128a0005c0008t0001g0011 | 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 | a0001c0001t0001g0298 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0138others(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 | a0005c0008t0001g0011 | 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 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0088 | 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 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0088 | 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 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0088 | 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 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0088 | 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 | a0004c0029t0001g0331 | 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 | a0001c0014t0001g0021a0001c0014t0001g0128 | 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 | a0001c0002t0006g0016a0001c0002t0006g0017a0005c0008t0001g0028others(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 | a0005c0008t0001g0011 | 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 | a0007c0010t0001g0008a0007c0010t0001g0009 | 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 | a0005c0008t0001g0011 | 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 | a0019c0023t0001g0219 | 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 | a0001c0001t0001g0274a0001c0014t0001g0021a0001c0014t0001g0128others(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 | a0009c0012t0001g0217a0009c0012t0001g0218 | 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 | a0001c0002t0006g0016a0001c0002t0006g0017a0021c0026t0006g0019 | 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 | a0001c0002t0006g0016a0001c0002t0006g0017a0021c0026t0006g0019 | 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 | a0001c0002t0006g0016a0001c0002t0006g0017a0021c0026t0006g0019 | 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 | a0001c0001t0001g0271a0001c0001t0008g0292 | 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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0001c0001t0001g0319 | 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 | a0001c0001t0001g0053a0002c0021t0003g0252 | 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 | a0001c0014t0001g0021a0001c0014t0001g0128a0004c0006t0001g0020others(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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0007c0010t0001g0008a0007c0010t0001g0009a0026c0032t0001g0127 | 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 | a0001c0002t0002g0109 | 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 | a0001c0014t0001g0021a0001c0014t0001g0128 | 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 | a0001c0001t0001g0004 | 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 | a0001c0001t0001g0271a0001c0001t0008g0292a0001c0002t0006g0016others(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 | a0001c0001t0001g0114a0009c0012t0001g0217a0009c0012t0001g0218 | 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 | a0005c0008t0001g0028a0015c0020t0001g0314 | 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 | a0001c0001t0001g0238 | 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 | a0001c0001t0001g0271a0001c0001t0008g0292a0001c0002t0006g0016others(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 | a0001c0002t0002g0058 | 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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0185a0001c0001t0001g0271a0001c0001t0008g0292others(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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0002c0003t0001g0254 | 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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0132others(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 | a0002c0021t0003g0252 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0308 | 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 | a0002c0003t0001g0135a0002c0003t0001g0136a0002c0003t0001g0152others(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 | a0005c0008t0001g0028a0015c0020t0001g0314 | 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 | a0005c0008t0001g0028a0015c0020t0001g0314 | 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 | a0001c0002t0002g0058 | 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 | a0001c0002t0002g0058 | 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 | a0001c0002t0002g0058 | 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 | a0001c0001t0001g0274 | 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 | a0001c0001t0001g0275 | 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 | a0020c0024t0001g0013 | 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 | a0020c0024t0001g0013 | 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 | a0001c0001t0001g0274 | 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 | a0001c0001t0001g0271a0001c0001t0001g0274a0001c0001t0008g0292others(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 | a0001c0001t0001g0274 | 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 | a0019c0023t0001g0219 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0001t0001g0274 | 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 | a0019c0023t0001g0219 | 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 | a0005c0008t0001g0011a0005c0008t0001g0045a0005c0008t0001g0075others(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 | a0001c0001t0001g0274 | 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 | a0007c0010t0001g0008a0007c0010t0001g0009 | 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 | a0013c0018t0001g0007 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0001t0001g0271 | 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 | a0001c0001t0008g0292a0001c0014t0001g0021a0001c0014t0001g0128others(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 | a0001c0002t0006g0016a0001c0002t0006g0017 | 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 | a0001c0001t0001g0274 | 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 | a0001c0001t0001g0271a0001c0001t0001g0274a0001c0001t0008g0292others(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 | a0001c0001t0001g0271a0001c0001t0001g0274a0001c0001t0008g0292others(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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0132others(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 | a0001c0001t0001g0271a0001c0001t0001g0274a0001c0001t0008g0292others(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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0019c0023t0001g0219 | 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 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0056others(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 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0272others(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 | a0001c0001t0001g0308a0002c0021t0003g0252 | 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 | a0001c0001t0001g0134a0001c0001t0001g0319 | 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 | a0001c0001t0001g0275 | 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 | a0001c0001t0001g0274 | 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 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0056others(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 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0056others(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 | a0005c0008t0001g0028a0015c0020t0001g0314 | 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 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0056others(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 | a0001c0001t0001g0160a0001c0001t0001g0180a0027c0025t0001g0156 | 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 | a0001c0002t0002g0123a0001c0002t0003g0113 | 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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0132others(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 | a0001c0001t0001g0271a0001c0001t0008g0292a0001c0002t0002g0072others(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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0056others(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 | a0001c0001t0001g0271a0001c0001t0008g0292a0001c0002t0006g0016others(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 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0056others(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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0132others(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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0221others(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 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0237others(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 | a0001c0001t0001g0271a0001c0001t0008g0292 | 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 | a0004c0029t0001g0331 | 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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0001c0001t0001g0212a0001c0002t0006g0016a0001c0002t0006g0017others(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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0001c0001t0001g0212 | 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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0001c0001t0001g0308 | 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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0001c0002t0006g0016a0001c0002t0006g0017a0001c0014t0001g0021others(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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0001c0002t0006g0016a0001c0002t0006g0017a0001c0014t0001g0021others(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 | a0001c0001t0001g0212a0001c0001t0001g0271a0001c0001t0008g0292others(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 | a0001c0002t0006g0016a0001c0002t0006g0017a0001c0014t0001g0021others(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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0001t0001g0271a0001c0001t0008g0292a0001c0002t0006g0016others(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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0001c0001t0001g0142 | 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 | a0001c0001t0001g0212 | 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 | a0001c0001t0001g0271a0001c0001t0008g0292 | 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 | a0001c0002t0006g0016a0001c0002t0006g0017a0001c0014t0001g0021others(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 | a0001c0002t0006g0016a0001c0002t0006g0017a0021c0026t0006g0019 | 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 | a0001c0014t0001g0021a0001c0014t0001g0128 | 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 | a0005c0008t0001g0028a0015c0020t0001g0314a0019c0023t0001g0219 | 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 | a0005c0008t0001g0011a0005c0008t0001g0045a0005c0008t0001g0075others(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 | a0005c0008t0001g0011a0019c0023t0001g0219a0022c0028t0001g0280 | 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 | a0001c0001t0001g0271a0001c0001t0008g0292a0005c0008t0001g0028others(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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0001c0001t0001g0238 | 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 | a0001c0002t0006g0016a0001c0002t0006g0017a0001c0014t0001g0021others(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 | a0001c0001t0001g0271a0001c0001t0008g0292a0005c0008t0001g0011others(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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0001c0002t0002g0069 | 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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0001c0014t0001g0021a0001c0014t0001g0128 | 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 | a0004c0029t0001g0331 | 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 | a0001c0001t0001g0317 | 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 | a0001c0002t0002g0058 | 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 | a0004c0029t0001g0331 | 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 | a0001c0014t0001g0021a0001c0014t0001g0128 | 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 | a0001c0002t0006g0017a0021c0026t0006g0019 | 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 | a0001c0002t0006g0016 | 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 | a0001c0002t0003g0034a0001c0002t0003g0130a0001c0002t0003g0131others(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 | a0001c0002t0002g0037a0001c0002t0002g0125a0026c0032t0001g0127 | 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(578): Show |
1 | a0001c0002t0003g0093 | 1 | homoSapiens_chm13v2.hp1 | 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 |
3 | a0001c0002t0003g0070a0001c0002t0003g0097a0001c0002t0003g0166 | 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 | a0001c0007t0003g0025 | 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 | a0001c0002t0002g0038a0001c0002t0002g0040a0001c0002t0002g0043others(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 | a0001c0002t0002g0076a0001c0002t0002g0084a0001c0002t0002g0120others(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 | a0001c0002t0002g0092 | 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 | a0001c0002t0011g0029 | 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 | a0001c0002t0003g0124 | 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 | a0001c0002t0002g0032 | 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 | a0001c0002t0003g0117a0024c0033t0003g0080 | 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 | a0001c0002t0002g0035 | 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 | a0001c0002t0002g0041a0001c0002t0002g0055a0001c0002t0002g0063others(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 | a0001c0002t0002g0087a0001c0002t0003g0049a0001c0002t0003g0061others(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 | a0001c0002t0002g0099 | 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 | a0001c0002t0002g0047a0001c0007t0003g0024 | 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 | a0001c0002t0003g0057 | 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 | a0001c0002t0002g0074 | 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 | a0002c0003t0001g0223 | 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 | a0001c0002t0003g0054 | 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 | a0001c0002t0002g0058 | 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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0002c0003t0001g0330 | 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 | a0001c0001t0001g0227 | 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 | a0009c0012t0001g0217 | 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 | a0009c0012t0001g0218 | 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 | a0007c0010t0001g0008a0007c0010t0001g0009 | 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 | a0001c0001t0001g0220 | 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 | a0006c0009t0001g0155a0006c0009t0001g0178 | 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 | a0001c0001t0001g0222a0011c0015t0001g0014a0011c0015t0001g0015 | 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 | a0001c0005t0001g0153 | 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 | a0001c0001t0001g0199 | 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 |
4 | a0001c0001t0001g0197a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 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 |
47 | a0001c0001t0001g0141a0001c0001t0001g0147a0001c0001t0001g0148others(44): 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0006 | 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 | a0001c0001t0001g0160a0001c0001t0001g0180a0027c0025t0001g0156 | 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 | a0001c0001t0001g0322a0002c0003t0001g0256a0003c0004t0001g0182 | 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 | a0001c0001t0001g0151 | 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 | a0002c0003t0001g0326 | 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 | a0001c0001t0001g0209 | 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 | a0001c0001t0001g0185 | 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 | a0002c0003t0001g0253 | 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 | a0006c0009t0001g0161 | 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 | a0001c0005t0001g0154 | 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0140a0001c0001t0001g0195 | 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 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0168others(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 | a0001c0001t0001g0137 | 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 | a0002c0003t0001g0232 | 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 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0210others(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 | a0002c0003t0001g0257 | 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 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0196 | 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 | a0002c0003t0001g0136 | 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 | a0001c0001t0004g0098a0002c0003t0001g0235a0002c0003t0001g0249others(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 | a0002c0003t0004g0245 | 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 | a0002c0003t0001g0315 | 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 | a0001c0001t0001g0146 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0002t0003g0048 | 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 | a0001c0002t0003g0039 | 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 | a0001c0002t0003g0122 | 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 | a0002c0003t0001g0192 | 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 | a0001c0002t0002g0096 | 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 | a0001c0002t0002g0102 | 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 | a0001c0002t0002g0062 | 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 | a0002c0003t0009g0244 | 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 | a0002c0003t0001g0135 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | 122 | a0001c0002t0002g0032a0001c0002t0002g0035a0001c0002t0002g0037others(119): Show | 122 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(119): 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0002t0002g0107 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0002t0002g0107 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0138others(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 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0088 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0002t0002g0037a0001c0002t0002g0125a0002c0003t0001g0223others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0001c0002t0002g0037a0001c0002t0002g0125a0002c0003t0001g0223others(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 | a0001c0002t0002g0037a0001c0002t0002g0125a0002c0003t0001g0223others(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 | a0004c0029t0001g0331 | 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 | a0001c0002t0002g0037a0001c0002t0002g0125a0002c0003t0001g0223others(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 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0259others(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 | a0001c0001t0001g0137a0001c0001t0001g0141a0001c0001t0001g0169others(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 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0259others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0002t0002g0037a0001c0002t0002g0125a0002c0003t0001g0223others(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 | a0001c0001t0001g0157a0001c0001t0001g0159 | 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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0001c0002t0002g0069 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0002t0002g0037a0001c0002t0002g0125a0002c0003t0001g0223others(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 | a0001c0002t0002g0037a0001c0002t0002g0125a0002c0003t0001g0223others(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 | a0004c0029t0001g0331 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0001t0001g0220 | 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 | a0001c0002t0002g0037a0001c0002t0002g0125a0002c0003t0001g0223others(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 | a0001c0001t0001g0220 | 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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0004c0029t0001g0331 | 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 | a0001c0002t0002g0037a0001c0002t0002g0125 | 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 | a0002c0003t0001g0223a0004c0006t0001g0020a0004c0006t0001g0036others(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 | a0002c0003t0001g0223a0002c0003t0001g0326a0004c0006t0001g0020others(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 | a0004c0029t0001g0331 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0002c0003t0001g0223a0026c0032t0001g0127 | 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 | a0026c0032t0001g0127 | 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 | a0002c0003t0001g0223 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0029t0001g0331 | 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 | a0001c0001t0001g0168 | 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 | 117 | a0001c0001t0001g0220a0001c0001t0001g0271a0001c0001t0008g0292others(114): Show | 117 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(114): 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 | a0001c0002t0002g0058 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0001t0001g0134a0001c0001t0001g0146a0001c0001t0001g0185others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0001t0001g0220a0001c0001t0008g0292 | 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 | a0002c0003t0001g0223a0026c0032t0001g0127 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0001t0001g0271a0004c0006t0001g0020a0004c0006t0001g0036others(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 | a0001c0001t0001g0271a0004c0006t0001g0020a0004c0006t0001g0036others(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 | a0001c0002t0003g0224a0001c0002t0003g0276 | 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 | a0004c0029t0001g0331 | 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 | a0005c0008t0001g0011 | 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 | a0001c0001t0001g0271 | 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 | a0004c0029t0001g0331 | 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 | a0001c0001t0001g0271a0001c0001t0008g0292a0001c0002t0002g0037others(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 | a0001c0001t0001g0271a0001c0001t0008g0292a0001c0002t0002g0037others(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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0001c0001t0008g0292a0004c0006t0001g0020a0004c0006t0001g0036others(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 | a0001c0002t0002g0037a0001c0002t0002g0125a0002c0003t0001g0223others(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 | a0001c0001t0001g0271 | 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 | a0004c0029t0001g0331 | 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 | a0001c0001t0001g0271a0001c0002t0002g0037a0001c0002t0002g0125others(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 | a0001c0001t0008g0292 | 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 | a0001c0001t0001g0168a0001c0001t0001g0194a0001c0001t0001g0212others(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 | 99 | a0001c0002t0002g0032a0001c0002t0002g0035a0001c0002t0002g0038others(96): Show | 99 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(96): 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 | a0001c0001t0008g0292a0004c0006t0001g0020a0004c0006t0001g0036others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0001t0001g0272 | 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 | a0001c0001t0001g0228 | 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 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0001g0293others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0002c0003t0001g0223 | 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 | a0001c0001t0001g0271a0001c0001t0008g0292a0001c0002t0002g0037others(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 | a0001c0001t0008g0292a0001c0002t0002g0125 | 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 | a0001c0002t0002g0037 | 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 | a0004c0029t0001g0331 | 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 | a0004c0029t0001g0331 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0001t0008g0292 | 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 | a0001c0001t0001g0271a0001c0001t0008g0292a0001c0002t0002g0125others(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 | a0001c0002t0002g0058 | 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 | a0001c0002t0002g0058 | 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 | a0001c0002t0002g0058 | 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 | a0004c0029t0001g0331 | 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 | a0001c0001t0001g0271 | 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 | a0026c0032t0001g0127 | 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 | a0001c0002t0002g0125 | 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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0001c0001t0001g0308 | 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 | a0004c0029t0001g0331 | 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 | a0001c0001t0008g0292 | 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 | a0001c0001t0008g0292 | 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 | a0001c0001t0008g0292 | 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 | a0004c0029t0001g0331 | 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 | a0001c0001t0008g0292 | 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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0001c0001t0001g0298a0004c0006t0001g0020a0004c0006t0001g0036others(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 | a0001c0001t0001g0271a0001c0001t0001g0283a0001c0001t0001g0286others(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 | a0004c0029t0001g0331 | 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 | a0004c0029t0001g0331 | 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 | a0001c0001t0001g0271a0001c0001t0001g0283a0001c0001t0001g0286others(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 | a0001c0001t0008g0292 | 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 | a0001c0001t0001g0271a0001c0001t0001g0283a0001c0001t0001g0286others(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 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0259others(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 | a0001c0001t0001g0146a0001c0001t0001g0169a0001c0001t0001g0177others(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 | a0001c0002t0007g0126a0001c0002t0007g0129 | 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 | a0020c0024t0001g0013 | 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 | a0002c0003t0001g0315 | 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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0004c0029t0001g0331 | 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 | a0004c0029t0001g0331 | 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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0001t0001g0222a0013c0018t0001g0007 | 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 | a0001c0001t0001g0005a0004c0006t0001g0020a0004c0006t0001g0036others(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 | a0022c0028t0001g0280 | 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 | a0022c0028t0001g0280 | 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 | a0002c0003t0001g0315 | 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 | 256 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(253): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): 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 | a0001c0002t0002g0058 | 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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0002c0003t0001g0246 | 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 | a0005c0008t0001g0028a0005c0008t0001g0045a0005c0008t0001g0075others(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 | a0001c0001t0001g0271 | 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 | a0001c0002t0003g0224a0001c0002t0003g0276 | 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 | a0001c0002t0002g0090a0001c0002t0002g0091a0001c0002t0002g0102others(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 | a0001c0001t0005g0284a0001c0001t0005g0285a0001c0001t0005g0301others(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 | a0005c0008t0001g0028 | 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 | a0001c0001t0001g0160a0001c0001t0001g0180a0027c0025t0001g0156 | 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 | a0001c0001t0001g0160a0001c0001t0001g0180a0027c0025t0001g0156 | 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 | a0026c0032t0001g0127 | 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 | a0022c0028t0001g0280 | 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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0007c0010t0001g0008a0007c0010t0001g0009 | 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 | a0002c0003t0001g0223 | 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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0271 | 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 | a0011c0015t0001g0014a0011c0015t0001g0015 | 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 | a0001c0002t0003g0057 | 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 | a0004c0029t0001g0331 | 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 | a0001c0001t0001g0207 | 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 | a0001c0001t0001g0114 | 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 | a0001c0002t0003g0039 | 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 | a0001c0002t0002g0082a0001c0002t0002g0106a0001c0002t0002g0107 | 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 | a0009c0012t0001g0217a0009c0012t0001g0218 | 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 | a0004c0029t0001g0331 | 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 | a0004c0029t0001g0331 | 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 | 105 | a0001c0002t0002g0032a0001c0002t0002g0035a0001c0002t0002g0037others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(102): 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0002t0003g0081 | 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 | a0020c0024t0001g0013 | 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 | a0019c0023t0001g0219 | 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 | a0001c0001t0001g0313 | 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 | a0001c0002t0003g0081 | 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 | a0001c0002t0003g0081 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0002t0003g0081 | 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 | a0001c0002t0003g0081 | 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 | a0001c0002t0003g0081 | 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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | 101 | a0001c0002t0002g0032a0001c0002t0002g0035a0001c0002t0002g0037others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(98): 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 | a0001c0001t0001g0191 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0001t0001g0278a0001c0001t0001g0281 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0002t0003g0031 | 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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0001c0002t0002g0120 | 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 | a0004c0029t0001g0331 | 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 | a0001c0002t0003g0048 | 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 | a0004c0029t0001g0331 | 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 | 218 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(215): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0007t0003g0022a0001c0007t0003g0023a0001c0007t0003g0024others(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 | a0026c0032t0001g0127 | 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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0001c0001t0001g0220a0011c0015t0001g0014a0011c0015t0001g0015 | 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 | a0002c0003t0001g0241 | 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 | a0001c0001t0001g0325 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0002t0002g0032 | 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 | a0001c0002t0002g0032 | 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 | 103 | a0001c0002t0002g0032a0001c0002t0002g0035a0001c0002t0002g0037others(100): Show | 103 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(100): 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 | a0001c0001t0001g0114 | 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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0001c0002t0003g0124 | 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 | a0005c0008t0001g0028 | 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 | a0001c0002t0003g0033 | 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 | a0020c0024t0001g0013 | 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 | a0001c0002t0002g0094 | 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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0026c0032t0001g0127 | 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 | a0001c0002t0002g0032 | 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 | a0001c0002t0002g0032 | 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 | a0001c0001t0001g0147a0001c0001t0004g0098a0002c0003t0001g0135others(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 | a0019c0023t0001g0219 | 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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0001c0002t0002g0087 | 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 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0052others(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 | a0001c0002t0002g0066a0001c0002t0002g0067 | 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 | a0001c0001t0001g0004 | 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 | 2 | a0001c0002t0003g0093a0024c0033t0003g0080 | 2 | HG03669.hp1 homoSapiens_chm13v2.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 | a0001c0001t0001g0147a0001c0001t0004g0098a0002c0003t0001g0135others(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 | a0015c0020t0001g0314 | 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 | a0002c0003t0001g0315 | 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 | a0001c0002t0003g0118a0001c0002t0003g0119a0001c0007t0003g0022others(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 | a0026c0032t0001g0127 | 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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0003c0004t0001g0001a0003c0004t0001g0144a0003c0004t0001g0163others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0001t0001g0147a0001c0001t0001g0160a0001c0001t0004g0098others(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 | a0020c0024t0001g0013 | 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 | a0002c0003t0001g0247 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0026c0032t0001g0127 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0001c0001t0001g0147a0001c0001t0001g0160a0001c0001t0004g0098others(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 | a0006c0009t0001g0155a0006c0009t0001g0161a0006c0009t0001g0178 | 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 | a0001c0014t0001g0128 | 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0214 | 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 | 2 | a0001c0001t0001g0197a0001c0001t0001g0206 | 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 | a0001c0002t0002g0102 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0002c0003t0001g0257 | 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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0001c0001t0004g0098 | 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 | a0001c0002t0007g0126 | 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 | a0001c0002t0003g0048 | 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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | 103 | a0001c0002t0002g0032a0001c0002t0002g0035a0001c0002t0002g0037others(100): Show | 103 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(100): 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 | a0020c0024t0001g0013 | 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 | a0004c0029t0001g0331 | 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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0001c0001t0001g0304 | 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 | a0001c0002t0003g0166 | 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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0020c0024t0001g0013 | 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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0001c0001t0001g0137a0001c0027t0001g0145 | 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 | a0001c0001t0001g0308 | 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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0002c0003t0001g0231 | 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 | a0001c0001t0001g0160a0001c0001t0004g0098a0002c0003t0001g0223others(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 | a0002c0003t0001g0254 | 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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0001c0002t0002g0047 | 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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0001g0269others(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 | a0005c0008t0001g0011a0005c0008t0001g0028a0005c0008t0001g0045others(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 | a0001c0001t0001g0287a0001c0001t0001g0294 | 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 | a0005c0008t0001g0028 | 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 | 122 | a0001c0002t0002g0032a0001c0002t0002g0035a0001c0002t0002g0037others(119): Show | 122 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(119): 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 | a0023c0034t0002g0042 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 | a0001c0002t0003g0130a0001c0002t0003g0131 | 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 | a0002c0003t0001g0135a0002c0003t0001g0136 | 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 | a0020c0024t0001g0013 | 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 | a0004c0006t0001g0020a0004c0006t0001g0036a0004c0006t0001g0078others(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 |