Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 8714 |
|---|---|
| ensemblid | ENSG00000108846.16 |
| hgncid | 54 |
| symbol | ABCC3 |
| name | ATP binding cassette subfamily C member 3 |
| refseq_nuc | NM_003786.4 |
| refseq_prot | NP_003777.2 |
| ensembl_nuc | ENST00000285238.13 |
| ensembl_prot | ENSP00000285238.8 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 50634881 |
| end | 50692253 |
| strand | + |
| ver | v1.2 |
| region | chr17:50634881-50692253 |
| region5000 | chr17:50629881-50697253 |
| regionname0 | ABCC3_chr17_50634881_50692253 |
| regionname5000 | ABCC3_chr17_50629881_50697253 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1527 | 286 | 47 | 56 | 139 | 9 | 33 | 105 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0002 | 0/0 | 1527 | 12 | 11 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0003 | 0/0 | 1527 | 8 | 1 | 5 | 0 | 2 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0004 | 0/0 | 1527 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0005 | 0/0 | 1527 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0006 | 0/0 | 1527 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0007 | 0/0 | 1527 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0008 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0009 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0010 | 0/0 | 1527 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0011 | 0/0 | 1527 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0012 | 0/0 | 726 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0013 | 0/0 | 1527 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0014 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0015 | 0/0 | 1244 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0016 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0017 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0018 | 0/0 | 1527 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0019 | 0/0 | 1527 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0020 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0021 | 0/0 | 1527 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0022 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0023 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0024 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0025 | 0/0 | 1527 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 4584 | 204 | 31 | 42 | 104 | 5 | 21 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0002 | 0/0 | 4584 | 25 | 5 | 8 | 7 | 2 | 3 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0003 | 0/0 | 4584 | 22 | 0 | 3 | 16 | 1 | 2 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0004 | 0/1 | 4584 | 15 | 4 | 2 | 5 | 0 | 3 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0005 | 0/0 | 4584 | 8 | 1 | 5 | 0 | 2 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0006 | 0/0 | 4584 | 7 | 7 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0007 | 0/0 | 4584 | 6 | 5 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0008 | 0/0 | 4584 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0009 | 0/0 | 4584 | 5 | 4 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0010 | 0/0 | 4584 | 4 | 3 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0011 | 0/0 | 4584 | 3 | 0 | 0 | 3 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0012 | 0/0 | 4584 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0013 | 0/0 | 4584 | 2 | 1 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0014 | 0/0 | 4584 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0015 | 0/0 | 4584 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0016 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0017 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0018 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0019 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0020 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0021 | 0/0 | 4584 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0022 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0023 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0024 | 0/0 | 4584 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0025 | 0/0 | 4570 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0026 | 0/0 | 4584 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0027 | 0/0 | 4584 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0028 | 0/0 | 4584 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0029 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0030 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0031 | 0/0 | 4584 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0032 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0033 | 0/0 | 4584 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0034 | 0/0 | 4584 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0035 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0036 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0037 | 0/0 | 4584 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0038 | 0/0 | 4584 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0039 | 0/0 | 4584 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0040 | 0/0 | 4584 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0041 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0042 | 0/0 | 4584 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0043 | 0/0 | 4584 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0044 | 0/0 | 4584 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| c0045 | 0/0 | 4584 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| 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 | 1110 | 313 | 72 | 55 | 144 | 8 | 33 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| t0002 | 0/1 | 1110 | 20 | 4 | 8 | 3 | 4 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| t0003 | 0/0 | 1110 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| t0004 | 0/0 | 1110 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| t0005 | 0/0 | 1110 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| t0006 | 0/0 | 1110 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| 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 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0278 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0293 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 4584 | 204 | 31 | 42 | 104 | 5 | 21 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0002 | 0/0 | 4584 | 25 | 5 | 8 | 7 | 2 | 3 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0003 | 0/0 | 4584 | 22 | 0 | 3 | 16 | 1 | 2 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0004 | 0/1 | 4584 | 15 | 4 | 2 | 5 | 0 | 3 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0009 | 0/0 | 4584 | 5 | 4 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0013 | 0/0 | 4584 | 2 | 1 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0014 | 0/0 | 4584 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0017 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0022 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0024 | 0/0 | 4584 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0026 | 0/0 | 4584 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0027 | 0/0 | 4584 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0037 | 0/0 | 4584 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0038 | 0/0 | 4584 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0039 | 0/0 | 4584 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0042 | 0/0 | 4584 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0043 | 0/0 | 4584 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0045 | 0/0 | 4584 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0002c0006 | 0/0 | 4584 | 7 | 7 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0002c0010 | 0/0 | 4584 | 4 | 3 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0002c0036 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0003c0005 | 0/0 | 4584 | 8 | 1 | 5 | 0 | 2 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0004c0007 | 0/0 | 4584 | 6 | 5 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0004c0023 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0005c0008 | 0/0 | 4584 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0006c0011 | 0/0 | 4584 | 3 | 0 | 0 | 3 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0007c0012 | 0/0 | 4584 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0008c0016 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0009c0019 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0010c0021 | 0/0 | 4584 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0011c0040 | 0/0 | 4584 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0012c0025 | 0/0 | 4570 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0013c0034 | 0/0 | 4584 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0014c0018 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0015c0033 | 0/0 | 4584 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0016c0032 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0017c0029 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0018c0031 | 0/0 | 4584 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0019c0028 | 0/0 | 4584 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0020c0030 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0021c0044 | 0/0 | 4584 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0022c0035 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0023c0020 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0024c0041 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0025c0015 | 0/0 | 4584 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5693 | 191 | 26 | 39 | 101 | 3 | 21 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0001t0002 | 0/0 | 5693 | 10 | 3 | 3 | 2 | 2 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0001t0003 | 0/0 | 5693 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0001t0004 | 0/0 | 5693 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0002t0001 | 0/0 | 5693 | 24 | 5 | 7 | 7 | 2 | 3 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0002t0006 | 0/0 | 5693 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0003t0001 | 0/0 | 5693 | 22 | 0 | 3 | 16 | 1 | 2 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0004t0001 | 0/0 | 5693 | 13 | 3 | 2 | 5 | 0 | 3 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0004t0002 | 0/1 | 5693 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0004t0003 | 0/0 | 5693 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0009t0001 | 0/0 | 5693 | 4 | 3 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0009t0003 | 0/0 | 5693 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0013t0001 | 0/0 | 5693 | 2 | 1 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0014t0001 | 0/0 | 5693 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0017t0001 | 0/0 | 5693 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0022t0001 | 0/0 | 5693 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0024t0001 | 0/0 | 5693 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0026t0001 | 0/0 | 5693 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0027t0001 | 0/0 | 5693 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0037t0001 | 0/0 | 5693 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0038t0001 | 0/0 | 5693 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0039t0001 | 0/0 | 5693 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0042t0001 | 0/0 | 5693 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0043t0001 | 0/0 | 5693 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0001c0045t0001 | 0/0 | 5693 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0002c0006t0001 | 0/0 | 5693 | 7 | 7 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0002c0010t0001 | 0/0 | 5693 | 4 | 3 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0002c0036t0001 | 0/0 | 5693 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0003c0005t0002 | 0/0 | 5693 | 8 | 1 | 5 | 0 | 2 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0004c0007t0001 | 0/0 | 5693 | 6 | 5 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0004c0023t0001 | 0/0 | 5693 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0005c0008t0001 | 0/0 | 5693 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0006c0011t0001 | 0/0 | 5693 | 3 | 0 | 0 | 3 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0007c0012t0003 | 0/0 | 5693 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0008c0016t0001 | 0/0 | 5693 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0009c0019t0001 | 0/0 | 5693 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0010c0021t0001 | 0/0 | 5693 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0011c0040t0002 | 0/0 | 5693 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0012c0025t0001 | 0/0 | 5679 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0013c0034t0001 | 0/0 | 5693 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0014c0018t0001 | 0/0 | 5693 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0015c0033t0001 | 0/0 | 5693 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0016c0032t0001 | 0/0 | 5693 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0017c0029t0001 | 0/0 | 5693 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0018c0031t0005 | 0/0 | 5693 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0019c0028t0001 | 0/0 | 5693 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0020c0030t0001 | 0/0 | 5693 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0021c0044t0001 | 0/0 | 5693 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0022c0035t0001 | 0/0 | 5693 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0023c0020t0001 | 0/0 | 5693 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0024c0041t0001 | 0/0 | 5693 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| a0025c0015t0001 | 0/0 | 5693 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | copy fasta | chr17 | 50629881 | 50697253 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0293 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0002t0006g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0003t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0003t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0003t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0003t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0003t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0004t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0004t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0004t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0004t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0004t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0004t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0004t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0004t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0004t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0004t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0004t0002g0278 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0004t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0009t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0009t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0009t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0009t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0009t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0013t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0013t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0014t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0014t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0017t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0022t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0024t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0026t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0027t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0037t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0038t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0039t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0042t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0043t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0001c0045t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0002c0006t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0002c0006t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0002c0006t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0002c0006t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0002c0006t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0002c0006t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0002c0006t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0002c0010t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0002c0010t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0002c0010t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0002c0010t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0002c0036t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0003c0005t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0003c0005t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0003c0005t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0003c0005t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0003c0005t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0003c0005t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0003c0005t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0003c0005t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0004c0007t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0004c0007t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0004c0007t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0004c0007t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0004c0007t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0004c0007t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0004c0023t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0005c0008t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0005c0008t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0005c0008t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0005c0008t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0005c0008t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0005c0008t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0006c0011t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0006c0011t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0006c0011t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0007c0012t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0007c0012t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0008c0016t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0009c0019t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0010c0021t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0011c0040t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0012c0025t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0013c0034t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0014c0018t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0015c0033t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0016c0032t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0017c0029t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0018c0031t0005g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0019c0028t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0020c0030t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0021c0044t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0022c0035t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0023c0020t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0024c0041t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| a0025c0015t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0005 | t0002 | g0303 | EUR | GBR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0099 | EUR | GBR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0093 | EUR | FIN | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0204 | EUR | FIN | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0280 | EUR | FIN | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0322 | EUR | FIN | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | CHS | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00423 | hp1 | a0001 | c0003 | t0001 | g0214 | EAS | CHS | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00544 | hp1 | a0021 | c0044 | t0001 | g0245 | EAS | CHS | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00544 | hp2 | a0001 | c0004 | t0001 | g0061 | EAS | CHS | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00558 | hp2 | a0001 | c0003 | t0001 | g0153 | EAS | CHS | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00621 | hp2 | a0011 | c0040 | t0002 | g0056 | EAS | CHS | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00639 | hp2 | a0001 | c0037 | t0001 | g0288 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00642 | hp1 | a0015 | c0033 | t0001 | g0020 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0228 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01069 | hp2 | a0004 | c0007 | t0001 | g0060 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0094 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01081 | hp1 | a0003 | c0005 | t0002 | g0302 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01081 | hp2 | a0002 | c0010 | t0001 | g0065 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0070 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01099 | hp2 | a0001 | c0003 | t0001 | g0158 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0090 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01106 | hp2 | a0003 | c0005 | t0002 | g0277 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0301 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01168 | hp2 | a0003 | c0005 | t0002 | g0078 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0296 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01243 | hp1 | a0001 | c0002 | t0006 | g0266 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0226 | AMR | CLM | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01258 | hp1 | a0001 | c0003 | t0001 | g0284 | AMR | CLM | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | CLM | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01346 | hp2 | a0003 | c0005 | t0002 | g0085 | AMR | CLM | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | CLM | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0294 | AMR | CLM | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0225 | EUR | IBS | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01516 | hp2 | a0025 | c0015 | t0001 | g0328 | EUR | IBS | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01517 | hp1 | a0001 | c0026 | t0001 | g0148 | EUR | IBS | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0227 | EUR | IBS | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01884 | hp1 | a0001 | c0009 | t0003 | g0006 | AFR | ACB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01884 | hp2 | a0001 | c0004 | t0003 | g0267 | AFR | ACB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01891 | hp1 | a0004 | c0023 | t0001 | g0004 | AFR | ACB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01891 | hp2 | a0002 | c0006 | t0001 | g0232 | AFR | ACB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01928 | hp1 | a0001 | c0004 | t0001 | g0059 | AMR | PEL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01934 | hp1 | a0001 | c0004 | t0001 | g0243 | AMR | PEL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | KHV | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02027 | hp1 | a0001 | c0003 | t0001 | g0213 | EAS | KHV | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02040 | hp1 | a0001 | c0004 | t0001 | g0237 | EAS | KHV | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02055 | hp1 | a0003 | c0005 | t0002 | g0300 | AFR | ACB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02056 | hp2 | a0001 | c0027 | t0001 | g0015 | EAS | KHV | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02071 | hp1 | a0001 | c0003 | t0001 | g0215 | EAS | KHV | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02074 | hp1 | a0001 | c0004 | t0001 | g0145 | EAS | KHV | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02080 | hp2 | a0001 | c0014 | t0001 | g0121 | EAS | KHV | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02135 | hp1 | a0001 | c0003 | t0001 | g0176 | EAS | KHV | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0274 | AFR | ACB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02148 | hp1 | a0003 | c0005 | t0002 | g0297 | AMR | PEL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | CDX | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CDX | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0027 | EAS | CDX | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CDX | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02280 | hp1 | a0001 | c0022 | t0001 | g0122 | AFR | ACB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02280 | hp2 | a0004 | c0007 | t0001 | g0005 | AFR | ACB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0276 | AFR | ACB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02451 | hp2 | a0001 | c0004 | t0001 | g0318 | AFR | ACB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02572 | hp2 | a0004 | c0007 | t0001 | g0119 | AFR | GWD | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02615 | hp2 | a0007 | c0012 | t0003 | g0304 | AFR | GWD | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02622 | hp1 | a0001 | c0017 | t0001 | g0233 | AFR | GWD | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0291 | AFR | GWD | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02630 | hp1 | a0004 | c0007 | t0001 | g0203 | AFR | GWD | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0073 | AFR | GWD | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02647 | hp2 | a0001 | c0004 | t0001 | g0117 | AFR | GWD | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02717 | hp2 | a0014 | c0018 | t0001 | g0074 | AFR | GWD | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02738 | hp1 | a0001 | c0004 | t0001 | g0197 | SAS | PJL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02738 | hp2 | a0001 | c0003 | t0001 | g0295 | SAS | PJL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02809 | hp1 | a0001 | c0009 | t0001 | g0102 | AFR | GWD | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02809 | hp2 | a0009 | c0019 | t0001 | g0071 | AFR | GWD | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | GWD | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02886 | hp2 | a0022 | c0035 | t0001 | g0040 | AFR | GWD | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02922 | hp1 | a0002 | c0010 | t0001 | g0026 | AFR | ESN | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02965 | hp1 | a0016 | c0032 | t0001 | g0033 | AFR | ESN | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | ESN | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0292 | AFR | ESN | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | ESN | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02976 | hp1 | a0002 | c0006 | t0001 | g0003 | AFR | ESN | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0321 | SAS | PJL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | MSL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03098 | hp2 | a0005 | c0008 | t0001 | g0028 | AFR | MSL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0092 | AFR | ESN | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03139 | hp2 | a0001 | c0009 | t0001 | g0007 | AFR | ESN | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03209 | hp1 | a0005 | c0008 | t0001 | g0103 | AFR | MSL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03209 | hp2 | a0002 | c0006 | t0001 | g0001 | AFR | MSL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03225 | hp1 | a0002 | c0010 | t0001 | g0116 | AFR | MSL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03225 | hp2 | a0001 | c0013 | t0001 | g0098 | AFR | MSL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03453 | hp1 | a0002 | c0006 | t0001 | g0023 | AFR | MSL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03453 | hp2 | a0002 | c0006 | t0001 | g0097 | AFR | MSL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | MSL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03492 | hp2 | a0001 | c0004 | t0001 | g0198 | SAS | PJL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03516 | hp2 | a0005 | c0008 | t0001 | g0002 | AFR | ESN | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03540 | hp1 | a0017 | c0029 | t0001 | g0229 | AFR | GWD | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03540 | hp2 | a0005 | c0008 | t0001 | g0313 | AFR | GWD | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03579 | hp1 | a0001 | c0004 | t0001 | g0100 | AFR | MSL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03579 | hp2 | a0004 | c0007 | t0001 | g0058 | AFR | MSL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0082 | SAS | PJL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03654 | hp2 | a0001 | c0039 | t0001 | g0126 | SAS | PJL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0155 | SAS | STU | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03688 | hp2 | a0001 | c0004 | t0001 | g0205 | SAS | STU | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0333 | SAS | BEB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03942 | hp1 | a0001 | c0024 | t0001 | g0287 | SAS | BEB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | STU | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG04115 | hp2 | a0001 | c0009 | t0001 | g0339 | SAS | STU | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | STU | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0326 | SAS | STU | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | STU | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | YRI | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0316 | AFR | YRI | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | YRI | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18940 | hp2 | a0001 | c0003 | t0001 | g0219 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18952 | hp2 | a0001 | c0003 | t0001 | g0234 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18960 | hp1 | a0001 | c0013 | t0001 | g0236 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18961 | hp1 | a0001 | c0003 | t0001 | g0336 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18962 | hp1 | a0001 | c0038 | t0001 | g0191 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18962 | hp2 | a0001 | c0004 | t0001 | g0319 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18967 | hp2 | a0001 | c0003 | t0001 | g0209 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18968 | hp1 | a0006 | c0011 | t0001 | g0270 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18970 | hp2 | a0001 | c0003 | t0001 | g0217 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0342 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18974 | hp1 | a0001 | c0003 | t0001 | g0218 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18975 | hp1 | a0001 | c0045 | t0001 | g0062 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18981 | hp2 | a0001 | c0003 | t0001 | g0242 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19003 | hp1 | a0012 | c0025 | t0001 | g0151 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19003 | hp2 | a0006 | c0011 | t0001 | g0269 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19007 | hp2 | a0019 | c0028 | t0001 | g0138 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19043 | hp1 | a0002 | c0006 | t0001 | g0104 | AFR | LWK | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19043 | hp2 | a0002 | c0006 | t0001 | g0334 | AFR | LWK | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19057 | hp1 | a0001 | c0003 | t0001 | g0241 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19060 | hp1 | a0013 | c0034 | t0001 | g0144 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19060 | hp2 | a0010 | c0021 | t0001 | g0067 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19079 | hp2 | a0006 | c0011 | t0001 | g0268 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19080 | hp1 | a0001 | c0003 | t0001 | g0239 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19081 | hp1 | a0001 | c0003 | t0001 | g0244 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19081 | hp2 | a0001 | c0004 | t0001 | g0202 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19085 | hp1 | a0001 | c0014 | t0001 | g0171 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19085 | hp2 | a0001 | c0003 | t0001 | g0238 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19091 | hp2 | a0001 | c0042 | t0001 | g0050 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19240 | hp1 | a0008 | c0016 | t0001 | g0037 | AFR | YRI | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | YRI | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ASW | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA20129 | hp2 | a0005 | c0008 | t0001 | g0030 | AFR | ASW | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA20805 | hp1 | a0003 | c0005 | t0002 | g0298 | EUR | TSI | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0315 | EUR | TSI | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA20905 | hp1 | a0001 | c0043 | t0001 | g0335 | SAS | GIH | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA20905 | hp2 | a0018 | c0031 | t0005 | g0283 | SAS | GIH | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0083 | AMR | CLM | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02109 | hp1 | a0007 | c0012 | t0003 | g0069 | AFR | ACB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0314 | AFR | ACB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02559 | hp1 | a0001 | c0009 | t0001 | g0101 | AFR | ACB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG02559 | hp2 | a0002 | c0036 | t0001 | g0230 | AFR | ACB | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | MSL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG03471 | hp2 | a0023 | c0020 | t0001 | g0063 | AFR | MSL | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG06807 | hp1 | a0004 | c0007 | t0001 | g0118 | AFR | USA | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| HG06807 | hp2 | a0020 | c0030 | t0001 | g0337 | AFR | USA | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA20300 | hp1 | a0002 | c0010 | t0001 | g0247 | AFR | USA | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | USA | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA21309 | hp1 | a0005 | c0008 | t0001 | g0029 | AFR | LWK | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| NA21309 | hp2 | a0024 | c0041 | t0001 | g0095 | AFR | LWK | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0004 | t0002 | g0278 | REF | REF | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0293 | REF | REF | ABCC3_chr17_50629881_50697253 | ABCC3 | chr17 | 50629881 | 50697253 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:50634968
|
G | A | 1 | a0006 | 3 | NA18968.hp1 NA19003.hp2 NA19079.hp2 |
missense_variant | MODERATE | c.32G>A | p.Gly11Asp | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/31 | 88/5693 | 32/4584 | 11/1527 | chr17 | 50634968 | ||
| chr17:50634975
|
G | C | 1 | a0025 | 1 | HG01516.hp2 | missense_variant | MODERATE | c.39G>C | p.Lys13Asn | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/31 | 95/5693 | 39/4584 | 13/1527 | chr17 | 50634975 | ||
| chr17:50656775
|
G | A | 1 | a0008 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.296G>A | p.Arg99Gln | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 3/31 | 352/5693 | 296/4584 | 99/1527 | chr17 | 50656775 | ||
| chr17:50660987
|
C | T | 1 | a0024 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.871C>T | p.Arg291Trp | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/31 | 927/5693 | 871/4584 | 291/1527 | chr17 | 50660987 | ||
| chr17:50661096
|
T | C | 1 | a0024 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.980T>C | p.Ile327Thr | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/31 | 1036/5693 | 980/4584 | 327/1527 | chr17 | 50661096 | ||
| chr17:50663760
|
T | C | 1 | a0009 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1078T>C | p.Ser360Pro | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 9/31 | 1134/5693 | 1078/4584 | 360/1527 | chr17 | 50663760 | ||
| chr17:50663839
|
T | G | 1 | a0023 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.1157T>G | p.Met386Arg | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 9/31 | 1213/5693 | 1157/4584 | 386/1527 | chr17 | 50663839 | ||
| chr17:50665235
|
G | A | 1 | a0010 | 1 | NA19060.hp2 | missense_variant | MODERATE | c.1421G>A | p.Arg474His | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 11/31 | 1477/5693 | 1421/4584 | 474/1527 | chr17 | 50665235 | ||
| chr17:50667698
|
C | T | 1 | a0011 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.1576C>T | p.Arg526Cys | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 12/31 | 1632/5693 | 1576/4584 | 526/1527 | chr17 | 50667698 | ||
| chr17:50668467
|
G | A | 1 | a0004 | 7 | HG01069.hp2 HG01891.hp1 HG02280.hp2 others(4): Show |
missense_variant | MODERATE | c.1820G>A | p.Ser607Asn | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 14/31 | 1876/5693 | 1820/4584 | 607/1527 | chr17 | 50668467 | ||
| chr17:50669464
|
CCTGTGCC others(7): Show |
C | 1 | a0012 | 1 | NA19003.hp1 | frameshift_variant | HIGH | c.2181_2194delTGCCTT others(8): Show |
p.Cys727fs | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/31 | 2237/5693 | 2181/4584 | 727/1527 | INFO_REALIGN_3_PRIME | chr17 | 50669464 | |
| chr17:50673022
|
G | C | 1 | a0004 | 7 | HG01069.hp2 HG01891.hp1 HG02280.hp2 others(4): Show |
missense_variant | MODERATE | c.2293G>C | p.Val765Leu | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 18/31 | 2349/5693 | 2293/4584 | 765/1527 | chr17 | 50673022 | ||
| chr17:50673462
|
T | TCCCCAGA others(15): Show |
1 | a0001 | 1 | NA19067.hp1 | frameshift_variant | HIGH | c.2410-5_2426dupCCCA others(18): Show |
p.His810fs | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/31 | 2483/5693 | 2427/4584 | 809/1527 | INFO_REALIGN_3_PRIME | chr17 | 50673462 | |
| chr17:50675674
|
C | T | 1 | a0002 | 12 | HG01081.hp2 HG01891.hp2 HG02559.hp2 others(9): Show |
missense_variant | MODERATE | c.2758C>T | p.Pro920Ser | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 21/31 | 2814/5693 | 2758/4584 | 920/1527 | chr17 | 50675674 | ||
| chr17:50676314
|
C | T | 1 | a0022 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.3104C>T | p.Ala1035Val | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 23/31 | 3160/5693 | 3104/4584 | 1035/1527 | chr17 | 50676314 | ||
| chr17:50676485
|
A | G | 1 | a0021 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.3275A>G | p.Asn1092Ser | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 23/31 | 3331/5693 | 3275/4584 | 1092/1527 | chr17 | 50676485 | ||
| chr17:50677825
|
A | C | 1 | a0013 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.3460A>C | p.Thr1154Pro | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 24/31 | 3516/5693 | 3460/4584 | 1154/1527 | chr17 | 50677825 | ||
| chr17:50677861
|
C | T | 1 | a0014 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.3496C>T | p.Arg1166Cys | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 24/31 | 3552/5693 | 3496/4584 | 1166/1527 | chr17 | 50677861 | ||
| chr17:50679825
|
C | T | 1 | a0015 | 1 | HG00642.hp1 | stop_gained | HIGH | c.3733C>T | p.Arg1245* | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/31 | 3789/5693 | 3733/4584 | 1245/1527 | chr17 | 50679825 | ||
| chr17:50679829
|
T | G | 1 | a0013 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.3737T>G | p.Met1246Arg | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/31 | 3793/5693 | 3737/4584 | 1246/1527 | chr17 | 50679829 | ||
| chr17:50683658
|
C | G | 1 | a0016 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.3856C>G | p.Arg1286Gly | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 27/31 | 3912/5693 | 3856/4584 | 1286/1527 | chr17 | 50683658 | ||
| chr17:50683692
|
G | A | 1 | a0003 | 8 | HG00099.hp1 HG01081.hp1 HG01106.hp2 others(5): Show |
missense_variant | MODERATE | c.3890G>A | p.Arg1297His | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 27/31 | 3946/5693 | 3890/4584 | 1297/1527 | chr17 | 50683692 | ||
| chr17:50683751
|
G | A | 1 | a0011 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.3949G>A | p.Glu1317Lys | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 27/31 | 4005/5693 | 3949/4584 | 1317/1527 | chr17 | 50683751 | ||
| chr17:50683965
|
G | A | 1 | a0017 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.3971G>A | p.Arg1324His | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 28/31 | 4027/5693 | 3971/4584 | 1324/1527 | chr17 | 50683965 | ||
| chr17:50684024
|
A | G | 1 | a0018 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.4030A>G | p.Lys1344Glu | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 28/31 | 4086/5693 | 4030/4584 | 1344/1527 | chr17 | 50684024 | ||
| chr17:50684036
|
C | T | 2 | a0005a0009 | 7 | HG02809.hp2 HG03098.hp2 HG03209.hp1 others(4): Show |
missense_variant | MODERATE | c.4042C>T | p.Arg1348Cys | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 28/31 | 4098/5693 | 4042/4584 | 1348/1527 | chr17 | 50684036 | ||
| chr17:50684048
|
C | T | 1 | a0007 | 2 | HG02109.hp1 HG02615.hp2 |
missense_variant | MODERATE | c.4054C>T | p.Leu1352Phe | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 28/31 | 4110/5693 | 4054/4584 | 1352/1527 | chr17 | 50684048 | ||
| chr17:50684088
|
A | G | 1 | a0020 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.4094A>G | p.Gln1365Arg | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 28/31 | 4150/5693 | 4094/4584 | 1365/1527 | chr17 | 50684088 | ||
| chr17:50684812
|
C | T | 1 | a0019 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.4217C>T | p.Thr1406Met | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/31 | 4273/5693 | 4217/4584 | 1406/1527 | chr17 | 50684812 | ||
| chr17:50684829
|
C | A | 1 | a0016 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.4234C>A | p.Pro1412Thr | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/31 | 4290/5693 | 4234/4584 | 1412/1527 | chr17 | 50684829 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:50655921
|
G | T | 1 | a0001c0014 | 2 | HG02080.hp2 NA19085.hp1 |
synonymous_variant | LOW | c.135G>T | p.Leu45Leu | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 2/31 | 191/5693 | 135/4584 | 45/1527 | chr17 | 50655921 | ||
| chr17:50657087
|
C | T | 2 | a0001c0045a0021c0044 | 2 | HG00544.hp1 NA18975.hp1 |
synonymous_variant | LOW | c.390C>T | p.Gly130Gly | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 4/31 | 446/5693 | 390/4584 | 130/1527 | chr17 | 50657087 | ||
| chr17:50658189
|
C | T | 1 | a0001c0043 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.594C>T | p.Ser198Ser | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 5/31 | 650/5693 | 594/4584 | 198/1527 | chr17 | 50658189 | ||
| chr17:50658455
|
C | T | 1 | a0001c0042 | 1 | NA19091.hp2 | synonymous_variant | LOW | c.633C>T | p.Ser211Ser | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 6/31 | 689/5693 | 633/4584 | 211/1527 | chr17 | 50658455 | ||
| chr17:50658476
|
G | A | 2 | a0001c0017a0014c0018 | 2 | HG02622.hp1 HG02717.hp2 |
synonymous_variant | LOW | c.654G>A | p.Leu218Leu | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 6/31 | 710/5693 | 654/4584 | 218/1527 | chr17 | 50658476 | ||
| chr17:50663982
|
G | A | 1 | a0024c0041 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.1209G>A | p.Ala403Ala | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 10/31 | 1265/5693 | 1209/4584 | 403/1527 | chr17 | 50663982 | ||
| chr17:50667592
|
G | C | 1 | a0001c0022 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.1470G>C | p.Leu490Leu | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 12/31 | 1526/5693 | 1470/4584 | 490/1527 | chr17 | 50667592 | ||
| chr17:50668908
|
C | A | 1 | a0001c0024 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.1926C>A | p.Pro642Pro | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 15/31 | 1982/5693 | 1926/4584 | 642/1527 | chr17 | 50668908 | ||
| chr17:50669242
|
G | A | 1 | a0007c0012 | 2 | HG02109.hp1 HG02615.hp2 |
synonymous_variant | LOW | c.2040G>A | p.Lys680Lys | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 16/31 | 2096/5693 | 2040/4584 | 680/1527 | chr17 | 50669242 | ||
| chr17:50672980
|
C | T | 1 | a0001c0039 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.2251C>T | p.Leu751Leu | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 18/31 | 2307/5693 | 2251/4584 | 751/1527 | chr17 | 50672980 | ||
| chr17:50673117
|
A | G | 1 | a0001c0038 | 1 | NA18962.hp1 | synonymous_variant | LOW | c.2388A>G | p.Pro796Pro | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 18/31 | 2444/5693 | 2388/4584 | 796/1527 | chr17 | 50673117 | ||
| chr17:50675658
|
G | T | 1 | a0001c0037 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.2742G>T | p.Gly914Gly | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 21/31 | 2798/5693 | 2742/4584 | 914/1527 | chr17 | 50675658 | ||
| chr17:50676062
|
C | T | 9 | a0001c0003a0001c0009a0001c0013others(6): Show | 40 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(37): Show |
synonymous_variant | LOW | c.3039C>T | p.Gly1013Gly | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 22/31 | 3095/5693 | 3039/4584 | 1013/1527 | chr17 | 50676062 | ||
| chr17:50678186
|
G | A | 1 | a0002c0036 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.3672G>A | p.Gly1224Gly | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 25/31 | 3728/5693 | 3672/4584 | 1224/1527 | chr17 | 50678186 | ||
| chr17:50683744
|
C | T | 22 | a0001c0002a0001c0003a0001c0004others(19): Show | 96 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(93): Show |
synonymous_variant | LOW | c.3942C>T | p.His1314His | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 27/31 | 3998/5693 | 3942/4584 | 1314/1527 | chr17 | 50683744 | ||
| chr17:50684002
|
G | A | 1 | a0001c0026 | 1 | HG01517.hp1 | synonymous_variant | LOW | c.4008G>A | p.Leu1336Leu | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 28/31 | 4064/5693 | 4008/4584 | 1336/1527 | chr17 | 50684002 | ||
| chr17:50687623
|
C | T | 1 | a0001c0027 | 1 | HG02056.hp2 | synonymous_variant | LOW | c.4368C>T | p.Ile1456Ile | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 30/31 | 4424/5693 | 4368/4584 | 1456/1527 | chr17 | 50687623 | ||
| chr17:50691125
|
A | G | 5 | a0001c0002a0001c0013a0001c0042others(2): Show | 30 | HG00642.hp1 HG00733.hp2 HG01070.hp1 others(27): Show |
synonymous_variant | LOW | c.4509A>G | p.Glu1503Glu | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 31/31 | 4565/5693 | 4509/4584 | 1503/1527 | chr17 | 50691125 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:50691458
|
G | C | 4 | a0001c0001t0003a0001c0004t0003a0001c0009t0003others(1): Show | 6 | HG01884.hp1 HG01884.hp2 HG02109.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*258G>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 31/31 | 258 | chr17 | 50691458 | |||||
| chr17:50691559
|
T | C | 1 | a0001c0001t0004 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*359T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 31/31 | 359 | chr17 | 50691559 | |||||
| chr17:50691661
|
A | T | 1 | a0001c0002t0006 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*461A>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 31/31 | 461 | chr17 | 50691661 | |||||
| chr17:50691851
|
A | C | 1 | a0018c0031t0005 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*651A>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 31/31 | 651 | chr17 | 50691851 | |||||
| chr17:50691968
|
C | T | 4 | a0001c0001t0002a0001c0004t0002a0003c0005t0002others(1): Show | 20 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*768C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 31/31 | 768 | chr17 | 50691968 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:50635017
|
C | T | 1 | a0001c0001t0002g0342 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.45+36C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50635017 | ||||||
| chr17:50635160
|
G | A | 28 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(25): Show | 28 | HG00438.hp1 HG00642.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.45+179G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50635160 | ||||||
| chr17:50635344
|
G | A | 276 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(273): Show | 276 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.45+363G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50635344 | ||||||
| chr17:50635350
|
C | G | 314 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(311): Show | 314 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.45+369C>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50635350 | ||||||
| chr17:50635663
|
C | CAG | 5 | a0001c0001t0001g0031a0001c0002t0001g0032a0005c0008t0001g0028others(2): Show | 5 | HG02886.hp1 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+689_45+690dupAG | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50635663 | |||||
| chr17:50635735
|
C | T | 288 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0035others(285): Show | 288 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.45+754C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50635735 | ||||||
| chr17:50635819
|
A | G | 251 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0035others(248): Show | 251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.45+838A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50635819 | ||||||
| chr17:50635862
|
G | A | 251 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0035others(248): Show | 251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.45+881G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50635862 | ||||||
| chr17:50635876
|
C | T | 1 | a0001c0001t0001g0275 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.45+895C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50635876 | ||||||
| chr17:50635909
|
A | G | 1 | a0001c0002t0001g0274 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.45+928A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50635909 | ||||||
| chr17:50636207
|
T | G | 97 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(94): Show | 97 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.45+1226T>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50636207 | ||||||
| chr17:50636329
|
A | C | 1 | a0020c0030t0001g0337 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.45+1348A>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50636329 | ||||||
| chr17:50636689
|
C | T | 7 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(4): Show | 7 | NA18968.hp1 NA18969.hp1 NA19003.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+1708C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50636689 | ||||||
| chr17:50636822
|
T | C | 3 | a0001c0001t0001g0066a0001c0001t0001g0068a0010c0021t0001g0067 | 3 | NA19060.hp2 NA19066.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.45+1841T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50636822 | ||||||
| chr17:50636908
|
G | T | 1 | a0001c0003t0001g0336 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.45+1927G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50636908 | ||||||
| chr17:50637051
|
C | T | 34 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0064others(31): Show | 34 | HG00099.hp1 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.45+2070C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50637051 | ||||||
| chr17:50637358
|
G | A | 4 | a0001c0001t0001g0034a0007c0012t0003g0069a0007c0012t0003g0304others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+2377G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50637358 | ||||||
| chr17:50637441
|
C | T | 1 | a0002c0010t0001g0247 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.45+2460C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50637441 | ||||||
| chr17:50637666
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | NA18955.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.45+2685G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50637666 | ||||||
| chr17:50637751
|
T | C | 20 | a0001c0001t0001g0072a0001c0001t0001g0305a0001c0001t0001g0306others(17): Show | 20 | HG01099.hp1 HG02486.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.45+2770T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50637751 | ||||||
| chr17:50637793
|
G | A | 21 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(18): Show | 21 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.45+2812G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50637793 | ||||||
| chr17:50637858
|
T | C | 33 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0038others(30): Show | 33 | HG00099.hp1 HG00558.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.45+2877T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50637858 | ||||||
| chr17:50637910
|
A | G | 298 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(295): Show | 298 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.45+2929A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50637910 | ||||||
| chr17:50638219
|
C | T | 1 | a0023c0020t0001g0063 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.45+3238C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50638219 | ||||||
| chr17:50638344
|
G | A | 1 | a0001c0002t0001g0294 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.45+3363G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50638344 | ||||||
| chr17:50638389
|
A | G | 1 | a0001c0001t0001g0246 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.45+3408A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50638389 | ||||||
| chr17:50638434
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.45+3453G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50638434 | ||||||
| chr17:50638567
|
C | T | 3 | a0001c0001t0003g0314a0005c0008t0001g0313a0008c0016t0001g0037 | 3 | HG02486.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.45+3586C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50638567 | ||||||
| chr17:50638743
|
C | T | 1 | a0023c0020t0001g0063 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.45+3762C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50638743 | ||||||
| chr17:50638864
|
G | A | 1 | a0002c0006t0001g0001 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.45+3883G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50638864 | ||||||
| chr17:50638883
|
G | GC | 19 | a0001c0001t0001g0008a0001c0001t0003g0314a0001c0002t0006g0266others(16): Show | 19 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.45+3904dupC | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50638883 | |||||
| chr17:50638946
|
C | T | 1 | a0001c0001t0001g0265 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.45+3965C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50638946 | ||||||
| chr17:50638955
|
A | C | 19 | a0001c0001t0001g0008a0001c0001t0003g0314a0001c0002t0006g0266others(16): Show | 19 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.45+3974A>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50638955 | ||||||
| chr17:50638976
|
G | A | 2 | a0007c0012t0003g0069a0007c0012t0003g0304 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.45+3995G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50638976 | ||||||
| chr17:50639087
|
G | A | 4 | a0001c0001t0001g0034a0007c0012t0003g0069a0007c0012t0003g0304others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+4106G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50639087 | ||||||
| chr17:50639207
|
C | A | 1 | a0001c0002t0001g0009 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.45+4226C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50639207 | ||||||
| chr17:50639359
|
A | G | 146 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(143): Show | 146 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.45+4378A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50639359 | ||||||
| chr17:50639391
|
G | A | 1 | a0001c0002t0001g0276 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.45+4410G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50639391 | ||||||
| chr17:50639440
|
C | G | 1 | a0001c0001t0001g0312 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.45+4459C>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50639440 | ||||||
| chr17:50639458
|
G | A | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0216others(22): Show | 25 | HG00408.hp1 HG00423.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.45+4477G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50639458 | ||||||
| chr17:50639767
|
C | CT | 10 | a0001c0001t0001g0008a0001c0001t0001g0212a0001c0004t0001g0061others(7): Show | 10 | HG00544.hp2 HG01884.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.45+4800dupT | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50639767 | |||||
| chr17:50639767
|
CT | C | 68 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(65): Show | 68 | HG00323.hp1 HG00544.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.45+4800delT | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50639767 | |||||
| chr17:50639767
|
CTT | C | 27 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(24): Show | 27 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.45+4799_45+4800del others(2): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50639767 | |||||
| chr17:50639780
|
T | G | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG01255.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.45+4799T>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50639780 | ||||||
| chr17:50639871
|
C | T | 1 | a0001c0002t0001g0231 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.45+4890C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50639871 | ||||||
| chr17:50639899
|
G | T | 1 | a0002c0010t0001g0026 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.45+4918G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50639899 | ||||||
| chr17:50639984
|
A | C | 4 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+5003A>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50639984 | ||||||
| chr17:50640035
|
A | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0027t0001g0015 | 3 | HG00438.hp1 HG02056.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.45+5054A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50640035 | ||||||
| chr17:50640046
|
G | A | 1 | a0001c0014t0001g0121 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.45+5065G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50640046 | ||||||
| chr17:50640111
|
A | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0210a0001c0001t0001g0211others(1): Show | 4 | HG01109.hp1 HG01261.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+5130A>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50640111 | ||||||
| chr17:50640177
|
A | C | 1 | a0021c0044t0001g0245 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.45+5196A>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50640177 | ||||||
| chr17:50640226
|
G | A | 8 | a0001c0001t0001g0008a0001c0009t0001g0007a0001c0009t0003g0006others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+5245G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50640226 | ||||||
| chr17:50640377
|
G | A | 20 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0003g0314others(17): Show | 20 | HG01099.hp1 HG01243.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.45+5396G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50640377 | ||||||
| chr17:50640455
|
C | A | 1 | a0001c0004t0001g0061 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.45+5474C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50640455 | ||||||
| chr17:50640530
|
T | C | 1 | a0001c0002t0001g0021 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.45+5549T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50640530 | ||||||
| chr17:50640668
|
G | A | 13 | a0001c0001t0001g0072a0001c0001t0001g0305a0001c0001t0001g0306others(10): Show | 13 | HG02486.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.45+5687G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50640668 | ||||||
| chr17:50640780
|
C | A | 1 | a0001c0001t0001g0039 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.45+5799C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50640780 | ||||||
| chr17:50640983
|
G | C | 37 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0038others(34): Show | 37 | HG00099.hp1 HG00558.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.45+6002G>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50640983 | ||||||
| chr17:50641093
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0249a0001c0001t0001g0250 | 3 | HG01255.hp1 HG01256.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.45+6112C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50641093 | ||||||
| chr17:50641109
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.45+6128C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50641109 | ||||||
| chr17:50641119
|
G | A | 1 | a0002c0010t0001g0026 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.45+6138G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50641119 | ||||||
| chr17:50641170
|
T | C | 37 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0024others(34): Show | 37 | HG00408.hp1 HG00423.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.45+6189T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50641170 | ||||||
| chr17:50641170
|
T | G | 1 | a0002c0010t0001g0026 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.45+6189T>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50641170 | ||||||
| chr17:50641379
|
G | A | 1 | a0002c0010t0001g0026 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.45+6398G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50641379 | ||||||
| chr17:50641525
|
A | C | 3 | a0001c0001t0001g0072a0001c0001t0003g0073a0014c0018t0001g0074 | 3 | HG02486.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.45+6544A>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50641525 | ||||||
| chr17:50641611
|
T | C | 5 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG01256.hp2 HG01258.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+6630T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50641611 | ||||||
| chr17:50641642
|
C | T | 16 | a0001c0001t0001g0072a0001c0001t0001g0305a0001c0001t0001g0306others(13): Show | 16 | HG02486.hp1 HG02486.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.45+6661C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50641642 | ||||||
| chr17:50641733
|
T | C | 1 | a0001c0001t0001g0251 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.45+6752T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50641733 | ||||||
| chr17:50641780
|
T | C | 10 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(7): Show | 10 | HG02615.hp1 HG02717.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.45+6799T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50641780 | ||||||
| chr17:50641802
|
T | C | 26 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0120others(23): Show | 26 | HG00408.hp1 HG00423.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.45+6821T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50641802 | ||||||
| chr17:50641841
|
T | C | 10 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(7): Show | 10 | HG02615.hp1 HG02717.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.45+6860T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50641841 | ||||||
| chr17:50641993
|
G | GA | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0120others(22): Show | 25 | HG00408.hp1 HG00423.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.45+7012_45+7013ins others(1): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50641993 | ||||||
| chr17:50641994
|
G | A | 64 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0024others(61): Show | 64 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.45+7013G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50641994 | ||||||
| chr17:50642213
|
G | C | 1 | a0001c0001t0001g0128 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.45+7232G>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50642213 | ||||||
| chr17:50642216
|
C | G | 1 | a0002c0010t0001g0247 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.45+7235C>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50642216 | ||||||
| chr17:50642229
|
G | C | 66 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(63): Show | 66 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.45+7248G>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50642229 | ||||||
| chr17:50642243
|
G | A | 2 | a0001c0004t0001g0117a0005c0008t0001g0002 | 2 | HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.45+7262G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50642243 | ||||||
| chr17:50642254
|
T | A | 132 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(129): Show | 132 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.45+7273T>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50642254 | ||||||
| chr17:50642320
|
G | A | 5 | a0001c0002t0001g0274a0001c0002t0001g0276a0007c0012t0003g0069others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+7339G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50642320 | ||||||
| chr17:50642447
|
T | C | 49 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041others(46): Show | 49 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.45+7466T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50642447 | ||||||
| chr17:50642474
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.45+7493C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50642474 | ||||||
| chr17:50642487
|
C | T | 21 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(18): Show | 21 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.45+7506C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50642487 | ||||||
| chr17:50642528
|
T | G | 61 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0024others(58): Show | 61 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.45+7547T>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50642528 | ||||||
| chr17:50642713
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.45+7732C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50642713 | ||||||
| chr17:50642752
|
C | T | 3 | a0001c0002t0001g0276a0007c0012t0003g0069a0007c0012t0003g0304 | 3 | HG02109.hp1 HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.45+7771C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50642752 | ||||||
| chr17:50643333
|
T | A | 2 | a0001c0001t0003g0314a0005c0008t0001g0313 | 2 | HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.45+8352T>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50643333 | ||||||
| chr17:50643447
|
G | T | 28 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(25): Show | 28 | HG00438.hp1 HG00544.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.45+8466G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50643447 | ||||||
| chr17:50643497
|
C | T | 1 | a0002c0036t0001g0230 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.45+8516C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50643497 | ||||||
| chr17:50643531
|
G | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0120a0017c0029t0001g0229 | 3 | HG02818.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.45+8550G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50643531 | ||||||
| chr17:50643535
|
C | T | 1 | a0019c0028t0001g0138 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.45+8554C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50643535 | ||||||
| chr17:50643610
|
C | T | 1 | a0001c0004t0001g0205 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.45+8629C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50643610 | ||||||
| chr17:50643651
|
A | C | 2 | a0002c0006t0001g0334a0002c0010t0001g0026 | 2 | HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.45+8670A>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50643651 | ||||||
| chr17:50643666
|
G | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0120a0017c0029t0001g0229 | 3 | HG02818.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.45+8685G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50643666 | ||||||
| chr17:50643846
|
T | TG | 66 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.45+8873dupG | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50643846 | |||||
| chr17:50644096
|
A | G | 1 | a0001c0001t0001g0248 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.45+9115A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50644096 | ||||||
| chr17:50644164
|
A | G | 2 | a0001c0001t0003g0314a0005c0008t0001g0313 | 2 | HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.45+9183A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50644164 | ||||||
| chr17:50644178
|
G | A | 97 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(94): Show | 97 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.45+9197G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50644178 | ||||||
| chr17:50644181
|
G | C | 97 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(94): Show | 97 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.45+9200G>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50644181 | ||||||
| chr17:50644182
|
G | A | 97 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(94): Show | 97 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.45+9201G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50644182 | ||||||
| chr17:50644185
|
T | C | 97 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(94): Show | 97 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.45+9204T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50644185 | ||||||
| chr17:50644251
|
C | T | 1 | a0002c0036t0001g0230 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.45+9270C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50644251 | ||||||
| chr17:50644260
|
A | G | 226 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(223): Show | 226 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.45+9279A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50644260 | ||||||
| chr17:50644263
|
G | A | 226 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(223): Show | 226 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.45+9282G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50644263 | ||||||
| chr17:50644298
|
C | G | 129 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(126): Show | 129 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.45+9317C>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50644298 | ||||||
| chr17:50644310
|
C | CA | 7 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0055others(4): Show | 7 | HG01106.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.45+9351dupA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50644310 | |||||
| chr17:50644310
|
C | CAA | 84 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0024others(81): Show | 84 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.45+9350_45+9351dup others(2): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50644310 | |||||
| chr17:50644310
|
C | CAAA | 16 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0044others(13): Show | 16 | HG00621.hp1 HG00733.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.45+9349_45+9351dup others(3): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50644310 | |||||
| chr17:50644310
|
C | CAAAA | 32 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(29): Show | 32 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.45+9348_45+9351dup others(4): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50644310 | |||||
| chr17:50644310
|
C | CAAAAA | 71 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(68): Show | 71 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.45+9347_45+9351dup others(5): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50644310 | |||||
| chr17:50644310
|
C | CAAAAAA | 14 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0038others(11): Show | 14 | HG00735.hp1 HG01175.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.45+9346_45+9351dup others(6): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50644310 | |||||
| chr17:50644333
|
G | A | 1 | a0001c0001t0001g0223 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.45+9352G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50644333 | ||||||
| chr17:50644335
|
A | G | 1 | a0001c0001t0001g0223 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.45+9354A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50644335 | ||||||
| chr17:50644875
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.45+9894G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50644875 | ||||||
| chr17:50644879
|
A | G | 212 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0016others(209): Show | 212 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.45+9898A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50644879 | ||||||
| chr17:50645200
|
T | TA | 18 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0305others(15): Show | 18 | HG02109.hp1 HG02148.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.45+10235dupA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50645200 | |||||
| chr17:50645200
|
TA | T | 12 | a0001c0001t0001g0019a0001c0001t0001g0087a0001c0001t0001g0088others(9): Show | 12 | HG01069.hp1 HG02015.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.45+10235delA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50645200 | |||||
| chr17:50645221
|
G | T | 25 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(22): Show | 25 | HG00639.hp2 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.45+10240G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50645221 | ||||||
| chr17:50645226
|
T | A | 28 | a0001c0001t0001g0034a0001c0001t0001g0075a0001c0001t0001g0076others(25): Show | 28 | HG00639.hp2 HG00733.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.45+10245T>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50645226 | ||||||
| chr17:50645233
|
C | A | 2 | a0001c0002t0001g0082a0001c0002t0001g0083 | 2 | HG01123.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.45+10252C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50645233 | ||||||
| chr17:50645253
|
A | T | 2 | a0002c0006t0001g0232a0004c0007t0001g0060 | 2 | HG01069.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.45+10272A>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50645253 | ||||||
| chr17:50645371
|
C | CA | 31 | a0001c0001t0001g0010a0001c0001t0001g0106a0001c0001t0001g0130others(28): Show | 31 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.45+10418dupA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50645371 | |||||
| chr17:50645371
|
C | CAA | 10 | a0001c0001t0001g0043a0001c0002t0001g0032a0001c0002t0001g0294others(7): Show | 10 | HG01361.hp2 HG02040.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.45+10417_45+10418d others(4): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50645371 | |||||
| chr17:50645371
|
CA | C | 42 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0072others(39): Show | 42 | HG00099.hp2 HG00621.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.45+10418delA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50645371 | |||||
| chr17:50645371
|
CAA | C | 76 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(73): Show | 76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.45+10417_45+10418d others(4): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50645371 | |||||
| chr17:50645371
|
CAAA | C | 10 | a0001c0001t0001g0235a0001c0001t0001g0251a0001c0001t0001g0305others(7): Show | 10 | HG00639.hp2 HG01517.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.45+10416_45+10418d others(5): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50645371 | |||||
| chr17:50645371
|
CAAAAA | C | 7 | a0001c0001t0001g0031a0001c0001t0001g0307a0001c0001t0001g0308others(4): Show | 7 | HG02615.hp1 HG02970.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+10414_45+10418d others(7): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50645371 | |||||
| chr17:50645371
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0004t0001g0205 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.45+10405_45+10418d others(16): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50645371 | |||||
| chr17:50645564
|
C | G | 25 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(22): Show | 25 | HG00639.hp2 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.46-10268C>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50645564 | ||||||
| chr17:50645762
|
G | A | 81 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(78): Show | 81 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.46-10070G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50645762 | ||||||
| chr17:50645764
|
T | G | 1 | a0001c0001t0001g0045 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.46-10068T>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50645764 | ||||||
| chr17:50645800
|
A | G | 2 | a0001c0004t0001g0197a0001c0004t0001g0198 | 2 | HG02738.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.46-10032A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50645800 | ||||||
| chr17:50645929
|
A | G | 1 | a0001c0043t0001g0335 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.46-9903A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50645929 | ||||||
| chr17:50646137
|
CA | C | 3 | a0001c0001t0001g0223a0001c0001t0001g0253a0001c0002t0001g0231 | 3 | NA18964.hp1 NA18982.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.46-9694delA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50646137 | ||||||
| chr17:50646181
|
T | A | 25 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(22): Show | 25 | HG00639.hp2 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.46-9651T>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50646181 | ||||||
| chr17:50646224
|
G | A | 81 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(78): Show | 81 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.46-9608G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50646224 | ||||||
| chr17:50646533
|
C | G | 7 | a0001c0001t0001g0031a0001c0001t0001g0307a0001c0001t0001g0308others(4): Show | 7 | HG02615.hp1 HG02970.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-9299C>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50646533 | ||||||
| chr17:50646569
|
G | C | 3 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0312 | 3 | HG02717.hp1 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.46-9263G>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50646569 | ||||||
| chr17:50646676
|
A | C | 219 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0016others(216): Show | 219 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.46-9156A>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50646676 | ||||||
| chr17:50646838
|
A | C | 121 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(118): Show | 121 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.46-8994A>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50646838 | ||||||
| chr17:50646840
|
C | G | 2 | a0001c0001t0003g0314a0005c0008t0001g0313 | 2 | HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.46-8992C>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50646840 | ||||||
| chr17:50646960
|
C | T | 7 | a0001c0001t0001g0031a0001c0001t0001g0307a0001c0001t0001g0308others(4): Show | 7 | HG02615.hp1 HG02970.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-8872C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50646960 | ||||||
| chr17:50646987
|
A | T | 121 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(118): Show | 121 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.46-8845A>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50646987 | ||||||
| chr17:50647168
|
T | C | 220 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0016others(217): Show | 220 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.46-8664T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50647168 | ||||||
| chr17:50647172
|
C | T | 1 | a0001c0014t0001g0121 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.46-8660C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50647172 | ||||||
| chr17:50647203
|
A | T | 1 | a0001c0002t0001g0032 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.46-8629A>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50647203 | ||||||
| chr17:50647469
|
C | T | 29 | a0001c0001t0001g0034a0001c0001t0001g0075a0001c0001t0001g0076others(26): Show | 29 | HG00639.hp2 HG00733.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.46-8363C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50647469 | ||||||
| chr17:50647590
|
A | G | 2 | a0002c0006t0001g0097a0002c0006t0001g0104 | 2 | HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.46-8242A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50647590 | ||||||
| chr17:50647863
|
A | AC | 6 | a0001c0001t0001g0223a0001c0001t0001g0305a0001c0001t0001g0306others(3): Show | 6 | HG02145.hp1 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-7965dupC | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50647863 | |||||
| chr17:50647931
|
C | T | 1 | a0001c0002t0001g0221 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.46-7901C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50647931 | ||||||
| chr17:50647946
|
G | T | 3 | a0001c0004t0003g0267a0001c0017t0001g0233a0002c0006t0001g0001 | 3 | HG01884.hp2 HG02622.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.46-7886G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50647946 | ||||||
| chr17:50647985
|
G | A | 1 | a0001c0002t0001g0296 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.46-7847G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50647985 | ||||||
| chr17:50648042
|
GA | G | 9 | a0001c0001t0001g0081a0001c0001t0001g0086a0001c0001t0001g0087others(6): Show | 9 | HG00408.hp1 HG00735.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-7779delA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50648042 | |||||
| chr17:50648082
|
A | G | 3 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0003t0001g0209 | 3 | HG01109.hp1 HG02300.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.46-7750A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50648082 | ||||||
| chr17:50648150
|
T | TA | 52 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(49): Show | 52 | HG00438.hp1 HG00544.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.46-7679dupA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50648150 | |||||
| chr17:50648154
|
G | A | 220 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0016others(217): Show | 220 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.46-7678G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50648154 | ||||||
| chr17:50648221
|
A | G | 1 | a0001c0001t0001g0223 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.46-7611A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50648221 | ||||||
| chr17:50648243
|
G | T | 25 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(22): Show | 25 | HG00639.hp2 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.46-7589G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50648243 | ||||||
| chr17:50648505
|
C | T | 2 | a0001c0002t0001g0032a0001c0002t0001g0276 | 2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.46-7327C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50648505 | ||||||
| chr17:50648748
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.46-7084C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50648748 | ||||||
| chr17:50648771
|
A | T | 25 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(22): Show | 25 | HG00639.hp2 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.46-7061A>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50648771 | ||||||
| chr17:50648901
|
A | G | 120 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(117): Show | 120 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.46-6931A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50648901 | ||||||
| chr17:50648942
|
C | CCAT | 220 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0016others(217): Show | 220 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.46-6889_46-6888ins others(3): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50648942 | |||||
| chr17:50649046
|
A | G | 1 | a0014c0018t0001g0074 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.46-6786A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50649046 | ||||||
| chr17:50649111
|
C | CA | 16 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0046others(13): Show | 16 | HG00544.hp1 HG02040.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.46-6704dupA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50649111 | |||||
| chr17:50649111
|
CA | C | 57 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0038others(54): Show | 57 | HG00099.hp1 HG00558.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.46-6704delA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50649111 | |||||
| chr17:50649585
|
AAAG | A | 125 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0016others(122): Show | 125 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.46-6243_46-6241del others(3): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50649585 | |||||
| chr17:50649587
|
A | G | 2 | a0002c0006t0001g0232a0004c0007t0001g0060 | 2 | HG01069.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.46-6245A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50649587 | ||||||
| chr17:50649589
|
A | G | 1 | a0001c0017t0001g0233 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.46-6243A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50649589 | ||||||
| chr17:50649727
|
A | G | 58 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042others(55): Show | 58 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.46-6105A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50649727 | ||||||
| chr17:50649737
|
A | G | 1 | a0001c0002t0001g0294 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.46-6095A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50649737 | ||||||
| chr17:50649781
|
A | G | 1 | a0005c0008t0001g0029 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.46-6051A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50649781 | ||||||
| chr17:50649806
|
C | A | 2 | a0001c0001t0003g0314a0005c0008t0001g0313 | 2 | HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.46-6026C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50649806 | ||||||
| chr17:50649892
|
G | C | 218 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0016others(215): Show | 218 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.46-5940G>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50649892 | ||||||
| chr17:50650003
|
C | T | 153 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0016others(150): Show | 153 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.46-5829C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50650003 | ||||||
| chr17:50650129
|
A | C | 1 | a0001c0001t0001g0189 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.46-5703A>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50650129 | ||||||
| chr17:50650201
|
G | T | 2 | a0001c0001t0003g0314a0005c0008t0001g0313 | 2 | HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.46-5631G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50650201 | ||||||
| chr17:50650219
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.46-5613C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50650219 | ||||||
| chr17:50650473
|
T | C | 1 | a0002c0010t0001g0116 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.46-5359T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50650473 | ||||||
| chr17:50650560
|
A | G | 1 | a0001c0002t0001g0276 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46-5272A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50650560 | ||||||
| chr17:50650795
|
G | A | 2 | a0002c0006t0001g0232a0004c0007t0001g0060 | 2 | HG01069.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.46-5037G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50650795 | ||||||
| chr17:50650926
|
G | A | 4 | a0001c0001t0001g0146a0001c0002t0001g0156a0001c0002t0001g0157others(1): Show | 4 | HG01517.hp1 HG02155.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-4906G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50650926 | ||||||
| chr17:50651066
|
G | GAAAA | 31 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0024others(28): Show | 31 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.46-4750_46-4747dup others(4): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50651066 | |||||
| chr17:50651066
|
G | GAAAAAA | 23 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(20): Show | 23 | HG00639.hp2 HG00733.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.46-4752_46-4747dup others(6): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50651066 | |||||
| chr17:50651066
|
G | GAAAAAAA | 11 | a0001c0001t0001g0031a0001c0001t0001g0251a0001c0001t0001g0308others(8): Show | 11 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.46-4753_46-4747dup others(7): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50651066 | |||||
| chr17:50651066
|
G | GAAAAAAA others(1): Show |
65 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0018others(62): Show | 65 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.46-4754_46-4747dup others(8): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50651066 | |||||
| chr17:50651066
|
G | GAAAAAAA others(2): Show |
15 | a0001c0001t0001g0008a0001c0001t0001g0087a0001c0001t0001g0306others(12): Show | 15 | HG01175.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.46-4755_46-4747dup others(9): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50651066 | |||||
| chr17:50651066
|
G | GAAAAAAA others(3): Show |
3 | a0001c0001t0003g0073a0001c0003t0001g0242a0001c0009t0003g0006 | 3 | HG01884.hp1 HG02630.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.46-4756_46-4747dup others(10): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50651066 | |||||
| chr17:50651066
|
G | GAAAAAAA others(5): Show |
6 | a0002c0006t0001g0003a0004c0007t0001g0005a0004c0007t0001g0118others(3): Show | 6 | HG01891.hp1 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-4758_46-4747dup others(12): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50651066 | |||||
| chr17:50651067
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.46-4765A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50651067 | ||||||
| chr17:50651107
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.46-4725C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50651107 | ||||||
| chr17:50651222
|
A | G | 7 | a0001c0001t0001g0286a0001c0001t0001g0317a0001c0001t0002g0096others(4): Show | 7 | HG00639.hp2 HG01123.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-4610A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50651222 | ||||||
| chr17:50651651
|
G | C | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.46-4181G>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50651651 | ||||||
| chr17:50651817
|
A | T | 1 | a0002c0010t0001g0247 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.46-4015A>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50651817 | ||||||
| chr17:50652137
|
C | G | 84 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0017others(81): Show | 84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.46-3695C>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50652137 | ||||||
| chr17:50652402
|
A | AT | 228 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0016others(225): Show | 228 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.46-3423dupT | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50652402 | |||||
| chr17:50652403
|
T | C | 1 | a0001c0001t0001g0330 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.46-3429T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50652403 | ||||||
| chr17:50652420
|
T | A | 26 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(23): Show | 26 | HG00639.hp2 HG00733.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.46-3412T>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50652420 | ||||||
| chr17:50652456
|
C | A | 224 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0016others(221): Show | 224 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.46-3376C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50652456 | ||||||
| chr17:50652481
|
G | A | 7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0235others(4): Show | 7 | HG00544.hp1 NA18952.hp2 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-3351G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50652481 | ||||||
| chr17:50652628
|
C | A | 1 | a0001c0002t0001g0009 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.46-3204C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50652628 | ||||||
| chr17:50652700
|
C | T | 1 | a0001c0001t0001g0341 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.46-3132C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50652700 | ||||||
| chr17:50652848
|
A | C | 1 | a0023c0020t0001g0063 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.46-2984A>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50652848 | ||||||
| chr17:50653067
|
C | T | 1 | a0001c0004t0001g0319 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.46-2765C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50653067 | ||||||
| chr17:50653068
|
G | A | 1 | a0001c0002t0001g0294 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.46-2764G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50653068 | ||||||
| chr17:50653244
|
G | T | 2 | a0001c0002t0001g0274a0022c0035t0001g0040 | 2 | HG02145.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.46-2588G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50653244 | ||||||
| chr17:50653283
|
T | C | 156 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0016others(153): Show | 156 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.46-2549T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50653283 | ||||||
| chr17:50653306
|
A | G | 81 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(78): Show | 81 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.46-2526A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50653306 | ||||||
| chr17:50653333
|
C | T | 2 | a0001c0002t0001g0032a0001c0002t0001g0276 | 2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.46-2499C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50653333 | ||||||
| chr17:50653344
|
C | CA | 35 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0129others(32): Show | 35 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.46-2469dupA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50653344 | |||||
| chr17:50653344
|
CA | C | 14 | a0001c0001t0001g0019a0001c0001t0001g0089a0001c0001t0001g0146others(11): Show | 14 | HG01069.hp1 HG01099.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.46-2469delA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50653344 | |||||
| chr17:50653344
|
CAA | C | 6 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0312others(3): Show | 6 | HG02145.hp1 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-2470_46-2469del others(2): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50653344 | |||||
| chr17:50653357
|
AAAAAAAG | A | 6 | a0001c0001t0001g0016a0001c0001t0001g0139a0001c0001t0001g0140others(3): Show | 6 | HG00423.hp2 HG00438.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-2469_46-2463del others(7): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50653357 | |||||
| chr17:50653358
|
A | G | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | NA18963.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.46-2474A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50653358 | ||||||
| chr17:50653383
|
G | A | 1 | a0008c0016t0001g0037 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.46-2449G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50653383 | ||||||
| chr17:50653428
|
C | T | 1 | a0004c0007t0001g0060 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.46-2404C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50653428 | ||||||
| chr17:50653477
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.46-2355G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50653477 | ||||||
| chr17:50653581
|
T | TTTC | 35 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0024others(32): Show | 35 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.46-2249_46-2247dup others(3): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50653581 | |||||
| chr17:50653758
|
G | GA | 155 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0016others(152): Show | 155 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.46-2060dupA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50653758 | |||||
| chr17:50653758
|
G | GAA | 6 | a0001c0001t0001g0084a0001c0001t0001g0305a0001c0001t0001g0306others(3): Show | 6 | HG01192.hp1 HG02148.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-2061_46-2060dup others(2): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50653758 | |||||
| chr17:50653849
|
A | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG00639.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.46-1983A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50653849 | ||||||
| chr17:50654031
|
G | A | 156 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0016others(153): Show | 156 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.46-1801G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50654031 | ||||||
| chr17:50654311
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.46-1521C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50654311 | ||||||
| chr17:50654578
|
T | G | 1 | a0014c0018t0001g0074 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.46-1254T>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50654578 | ||||||
| chr17:50654588
|
G | T | 1 | a0001c0002t0001g0032 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.46-1244G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50654588 | ||||||
| chr17:50654605
|
C | A | 1 | a0001c0003t0001g0158 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.46-1227C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50654605 | ||||||
| chr17:50654720
|
C | T | 1 | a0008c0016t0001g0037 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.46-1112C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50654720 | ||||||
| chr17:50654823
|
T | C | 1 | a0002c0036t0001g0230 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.46-1009T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50654823 | ||||||
| chr17:50654937
|
C | CA | 155 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0014others(152): Show | 155 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.46-882dupA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50654937 | |||||
| chr17:50655056
|
C | T | 1 | a0001c0009t0001g0339 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.46-776C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50655056 | ||||||
| chr17:50655099
|
C | CA | 9 | a0001c0001t0001g0031a0001c0001t0001g0208a0001c0001t0001g0307others(6): Show | 9 | HG02615.hp1 HG02970.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.46-713dupA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50655099 | |||||
| chr17:50655099
|
CA | C | 272 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(269): Show | 272 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.46-713delA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50655099 | |||||
| chr17:50655140
|
C | G | 341 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(338): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.46-692C>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50655140 | ||||||
| chr17:50655141
|
G | C | 1 | a0001c0002t0001g0231 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.46-691G>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50655141 | ||||||
| chr17:50655141
|
G | GC | 340 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(337): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.46-691_46-690insC | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50655141 | ||||||
| chr17:50655203
|
C | G | 7 | a0001c0001t0001g0031a0001c0001t0001g0307a0001c0001t0001g0308others(4): Show | 7 | HG02615.hp1 HG02970.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-629C>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50655203 | ||||||
| chr17:50655320
|
C | T | 3 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0312 | 3 | HG02717.hp1 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.46-512C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50655320 | ||||||
| chr17:50655331
|
G | A | 7 | a0001c0001t0001g0031a0001c0001t0001g0307a0001c0001t0001g0308others(4): Show | 7 | HG02615.hp1 HG02970.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-501G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50655331 | ||||||
| chr17:50655404
|
C | CA | 19 | a0001c0001t0001g0041a0001c0001t0001g0066a0001c0001t0001g0091others(16): Show | 19 | HG00438.hp2 HG01952.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.46-411dupA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50655404 | |||||
| chr17:50655404
|
C | CAA | 15 | a0001c0001t0001g0072a0001c0001t0001g0077a0001c0001t0001g0108others(12): Show | 15 | HG00639.hp2 HG00733.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.46-412_46-411dupAA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50655404 | |||||
| chr17:50655404
|
C | CAAA | 10 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0079others(7): Show | 10 | HG00735.hp2 HG01175.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.46-413_46-411dupAA others(1): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50655404 | |||||
| chr17:50655404
|
C | CAAAA | 66 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(63): Show | 66 | HG00099.hp1 HG00544.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.46-414_46-411dupAA others(2): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50655404 | |||||
| chr17:50655404
|
C | CAAAAA | 45 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(42): Show | 45 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.46-415_46-411dupAA others(3): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50655404 | |||||
| chr17:50655404
|
C | CAAAAAA | 7 | a0001c0001t0001g0220a0001c0001t0001g0257a0001c0001t0001g0306others(4): Show | 7 | HG00408.hp1 HG01069.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-416_46-411dupAA others(4): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50655404 | |||||
| chr17:50655404
|
CA | C | 6 | a0001c0001t0001g0031a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02615.hp1 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-411delA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | 50655404 | |||||
| chr17:50655415
|
A | C | 1 | a0002c0036t0001g0230 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.46-417A>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50655415 | ||||||
| chr17:50655422
|
C | A | 154 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0016others(151): Show | 154 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.46-410C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50655422 | ||||||
| chr17:50655428
|
C | A | 5 | a0001c0001t0001g0286a0001c0002t0001g0225a0001c0004t0001g0059others(2): Show | 5 | HG00639.hp2 HG01123.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-404C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50655428 | ||||||
| chr17:50655645
|
C | A | 5 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0312others(2): Show | 5 | HG02145.hp1 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-187C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | chr17 | 50655645 | ||||||
| chr17:50656046
|
C | T | 1 | a0001c0004t0002g0278 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.222+38C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 2/30 | chr17 | 50656046 | ||||||
| chr17:50656076
|
T | A | 2 | a0001c0001t0001g0081a0001c0003t0001g0209 | 2 | HG00735.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.222+68T>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 2/30 | chr17 | 50656076 | ||||||
| chr17:50656160
|
A | G | 7 | a0001c0001t0001g0031a0001c0001t0001g0307a0001c0001t0001g0308others(4): Show | 7 | HG02615.hp1 HG02970.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+152A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 2/30 | chr17 | 50656160 | ||||||
| chr17:50656276
|
G | A | 35 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0024others(32): Show | 35 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.222+268G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 2/30 | chr17 | 50656276 | ||||||
| chr17:50656384
|
G | C | 60 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.223-318G>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 2/30 | chr17 | 50656384 | ||||||
| chr17:50656454
|
T | C | 240 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.223-248T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 2/30 | chr17 | 50656454 | ||||||
| chr17:50656956
|
C | T | 1 | a0001c0004t0002g0278 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.349-90C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 3/30 | chr17 | 50656956 | ||||||
| chr17:50656993
|
G | A | 37 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0024others(34): Show | 37 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.349-53G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 3/30 | chr17 | 50656993 | ||||||
| chr17:50657022
|
G | T | 1 | a0001c0001t0001g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.349-24G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 3/30 | chr17 | 50657022 | ||||||
| chr17:50657440
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.486+257C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 4/30 | chr17 | 50657440 | ||||||
| chr17:50657570
|
T | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.486+387T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 4/30 | chr17 | 50657570 | ||||||
| chr17:50657669
|
T | C | 2 | a0001c0017t0001g0233a0014c0018t0001g0074 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.487-413T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 4/30 | chr17 | 50657669 | ||||||
| chr17:50657732
|
C | T | 1 | a0001c0004t0003g0267 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.487-350C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 4/30 | chr17 | 50657732 | ||||||
| chr17:50657841
|
G | A | 1 | a0001c0003t0001g0244 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.487-241G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 4/30 | chr17 | 50657841 | ||||||
| chr17:50658225
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.612+18G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 5/30 | chr17 | 50658225 | ||||||
| chr17:50658280
|
C | A | 6 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(3): Show | 6 | HG00639.hp2 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.612+73C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 5/30 | chr17 | 50658280 | ||||||
| chr17:50658413
|
G | A | 98 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(95): Show | 98 | HG00438.hp2 HG00738.hp1 HG01069.hp1 others(95): Show |
intron_variant | MODIFIER | c.613-22G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 5/30 | chr17 | 50658413 | ||||||
| chr17:50658652
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.674+156T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 6/30 | chr17 | 50658652 | ||||||
| chr17:50658709
|
C | T | 1 | a0014c0018t0001g0074 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.674+213C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 6/30 | chr17 | 50658709 | ||||||
| chr17:50658815
|
A | G | 1 | a0024c0041t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.674+319A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 6/30 | chr17 | 50658815 | ||||||
| chr17:50658928
|
G | C | 93 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(90): Show | 93 | HG00438.hp2 HG00639.hp2 HG00738.hp1 others(90): Show |
intron_variant | MODIFIER | c.675-309G>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 6/30 | chr17 | 50658928 | ||||||
| chr17:50658964
|
G | A | 14 | a0001c0002t0001g0221a0001c0003t0001g0213a0001c0003t0001g0214others(11): Show | 14 | HG00423.hp1 HG02027.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.675-273G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 6/30 | chr17 | 50658964 | ||||||
| chr17:50659042
|
G | A | 92 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(89): Show | 92 | HG00438.hp2 HG00639.hp2 HG00738.hp1 others(89): Show |
intron_variant | MODIFIER | c.675-195G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 6/30 | chr17 | 50659042 | ||||||
| chr17:50659121
|
C | T | 1 | a0001c0017t0001g0233 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.675-116C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 6/30 | chr17 | 50659121 | ||||||
| chr17:50659200
|
T | G | 1 | a0001c0003t0001g0070 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.675-37T>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 6/30 | chr17 | 50659200 | ||||||
| chr17:50659432
|
C | T | 1 | a0001c0001t0002g0292 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.806+64C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 7/30 | chr17 | 50659432 | ||||||
| chr17:50659442
|
C | A | 1 | a0001c0038t0001g0191 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.806+74C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 7/30 | chr17 | 50659442 | ||||||
| chr17:50659506
|
G | A | 1 | a0004c0007t0001g0060 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.806+138G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 7/30 | chr17 | 50659506 | ||||||
| chr17:50659540
|
C | G | 123 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0018others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.806+172C>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 7/30 | chr17 | 50659540 | ||||||
| chr17:50659555
|
C | T | 1 | a0024c0041t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.806+187C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 7/30 | chr17 | 50659555 | ||||||
| chr17:50659641
|
A | T | 1 | a0001c0001t0001g0275 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.806+273A>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 7/30 | chr17 | 50659641 | ||||||
| chr17:50659650
|
A | G | 46 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0038others(43): Show | 46 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.806+282A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 7/30 | chr17 | 50659650 | ||||||
| chr17:50659700
|
T | TG | 124 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0018others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.806+336dupG | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr17 | 50659700 | |||||
| chr17:50659709
|
G | A | 1 | a0001c0001t0002g0093 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.806+341G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 7/30 | chr17 | 50659709 | ||||||
| chr17:50659746
|
A | G | 111 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(108): Show | 111 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.806+378A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 7/30 | chr17 | 50659746 | ||||||
| chr17:50659776
|
A | G | 124 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0018others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.806+408A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 7/30 | chr17 | 50659776 | ||||||
| chr17:50659779
|
G | C | 46 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0038others(43): Show | 46 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.806+411G>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 7/30 | chr17 | 50659779 | ||||||
| chr17:50659915
|
G | A | 8 | a0002c0006t0001g0003a0004c0007t0001g0005a0004c0007t0001g0058others(5): Show | 8 | HG01069.hp2 HG01891.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.806+547G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 7/30 | chr17 | 50659915 | ||||||
| chr17:50660087
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.806+719G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 7/30 | chr17 | 50660087 | ||||||
| chr17:50660221
|
A | G | 1 | a0001c0002t0001g0094 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.807-702A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 7/30 | chr17 | 50660221 | ||||||
| chr17:50660500
|
C | G | 130 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(127): Show | 130 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.807-423C>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 7/30 | chr17 | 50660500 | ||||||
| chr17:50660666
|
G | A | 1 | a0002c0010t0001g0116 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.807-257G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 7/30 | chr17 | 50660666 | ||||||
| chr17:50660681
|
G | T | 3 | a0001c0001t0001g0031a0001c0001t0001g0113a0001c0001t0001g0307 | 3 | HG02970.hp2 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.807-242G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 7/30 | chr17 | 50660681 | ||||||
| chr17:50660896
|
C | T | 1 | a0002c0010t0001g0247 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.807-27C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 7/30 | chr17 | 50660896 | ||||||
| chr17:50660905
|
C | T | 41 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0038others(38): Show | 41 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.807-18C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 7/30 | chr17 | 50660905 | ||||||
| chr17:50661130
|
G | A | 2 | a0001c0001t0001g0299a0001c0001t0001g0332 | 2 | HG00642.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.998+16G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50661130 | ||||||
| chr17:50661315
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.998+201T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50661315 | ||||||
| chr17:50661316
|
A | G | 1 | a0018c0031t0005g0283 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.998+202A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50661316 | ||||||
| chr17:50661388
|
G | T | 2 | a0001c0001t0001g0034a0008c0016t0001g0037 | 2 | HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.998+274G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50661388 | ||||||
| chr17:50661485
|
C | T | 1 | a0001c0013t0001g0098 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.998+371C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50661485 | ||||||
| chr17:50661573
|
C | T | 21 | a0001c0001t0001g0031a0001c0001t0001g0112a0001c0001t0001g0113others(18): Show | 21 | HG01069.hp2 HG01891.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.998+459C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50661573 | ||||||
| chr17:50661647
|
T | C | 10 | a0001c0017t0001g0233a0002c0006t0001g0003a0004c0007t0001g0005others(7): Show | 10 | HG01069.hp2 HG01891.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.998+533T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50661647 | ||||||
| chr17:50661663
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.998+549G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50661663 | ||||||
| chr17:50662182
|
T | C | 119 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0034others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.998+1068T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50662182 | ||||||
| chr17:50662193
|
A | C | 1 | a0001c0001t0001g0320 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.998+1079A>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50662193 | ||||||
| chr17:50662209
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.998+1095G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50662209 | ||||||
| chr17:50662481
|
T | C | 134 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(131): Show | 134 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.999-1200T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50662481 | ||||||
| chr17:50662592
|
G | A | 2 | a0001c0003t0001g0295a0001c0003t0001g0321 | 2 | HG02738.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.999-1089G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50662592 | ||||||
| chr17:50662629
|
C | T | 7 | a0001c0001t0001g0091a0001c0001t0001g0188a0001c0001t0003g0314others(4): Show | 7 | HG02145.hp1 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.999-1052C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50662629 | ||||||
| chr17:50662637
|
C | CA | 29 | a0001c0001t0001g0034a0001c0001t0001g0051a0001c0001t0001g0128others(26): Show | 29 | HG00639.hp2 HG01069.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.999-1023dupA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | INFO_REALIGN_3_PRIME | chr17 | 50662637 | |||||
| chr17:50662637
|
C | CAA | 69 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0041others(66): Show | 69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.999-1024_999-1023d others(4): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | INFO_REALIGN_3_PRIME | chr17 | 50662637 | |||||
| chr17:50662637
|
C | CAAA | 6 | a0001c0001t0001g0044a0001c0001t0001g0305a0001c0001t0001g0306others(3): Show | 6 | HG00621.hp1 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.999-1025_999-1023d others(5): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | INFO_REALIGN_3_PRIME | chr17 | 50662637 | |||||
| chr17:50662637
|
CA | C | 13 | a0001c0001t0001g0054a0001c0001t0001g0072a0001c0001t0001g0089others(10): Show | 13 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(10): Show |
intron_variant | MODIFIER | c.999-1023delA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | INFO_REALIGN_3_PRIME | chr17 | 50662637 | |||||
| chr17:50662655
|
A | AG | 16 | a0001c0001t0001g0136a0001c0001t0001g0261a0001c0001t0002g0096others(13): Show | 16 | HG00099.hp2 HG00621.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.999-1026_999-1025i others(3): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50662655 | ||||||
| chr17:50662655
|
A | G | 1 | a0003c0005t0002g0303 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.999-1026A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50662655 | ||||||
| chr17:50662657
|
A | G | 22 | a0001c0001t0001g0057a0001c0001t0001g0080a0001c0001t0001g0136others(19): Show | 22 | HG00099.hp1 HG00099.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.999-1024A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50662657 | ||||||
| chr17:50662695
|
T | G | 6 | a0001c0003t0001g0214a0001c0003t0001g0217a0001c0003t0001g0218others(3): Show | 6 | HG00423.hp1 NA18940.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.999-986T>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50662695 | ||||||
| chr17:50662755
|
T | G | 112 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0041others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.999-926T>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50662755 | ||||||
| chr17:50662883
|
C | T | 1 | a0001c0002t0001g0221 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.999-798C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50662883 | ||||||
| chr17:50662894
|
A | G | 1 | a0024c0041t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.999-787A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50662894 | ||||||
| chr17:50662938
|
G | A | 2 | a0001c0003t0001g0217a0001c0003t0001g0218 | 2 | NA18970.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.999-743G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50662938 | ||||||
| chr17:50662992
|
G | T | 1 | a0001c0004t0002g0278 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.999-689G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50662992 | ||||||
| chr17:50663001
|
C | T | 1 | a0024c0041t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.999-680C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50663001 | ||||||
| chr17:50663003
|
G | A | 1 | a0001c0001t0001g0330 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.999-678G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50663003 | ||||||
| chr17:50663284
|
G | A | 1 | a0002c0036t0001g0230 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.999-397G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50663284 | ||||||
| chr17:50663437
|
C | G | 117 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0034others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.999-244C>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50663437 | ||||||
| chr17:50663441
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.999-240G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50663441 | ||||||
| chr17:50663449
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.999-232G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50663449 | ||||||
| chr17:50663488
|
G | A | 1 | a0002c0010t0001g0247 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.999-193G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50663488 | ||||||
| chr17:50663543
|
G | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0080 | 2 | HG02071.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.999-138G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50663543 | ||||||
| chr17:50663588
|
C | T | 1 | a0017c0029t0001g0229 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.999-93C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | chr17 | 50663588 | ||||||
| chr17:50663915
|
C | T | 1 | a0001c0022t0001g0122 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1177-35C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 9/30 | chr17 | 50663915 | ||||||
| chr17:50664298
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1338+187G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 10/30 | chr17 | 50664298 | ||||||
| chr17:50664331
|
A | T | 1 | a0001c0002t0006g0266 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1338+220A>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 10/30 | chr17 | 50664331 | ||||||
| chr17:50664450
|
A | G | 9 | a0002c0006t0001g0003a0004c0007t0001g0005a0004c0007t0001g0058others(6): Show | 9 | HG01069.hp2 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1338+339A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 10/30 | chr17 | 50664450 | ||||||
| chr17:50664511
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1338+400C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 10/30 | chr17 | 50664511 | ||||||
| chr17:50664702
|
C | CA | 57 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0035others(54): Show | 57 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.1339-426dupA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 10/30 | INFO_REALIGN_3_PRIME | chr17 | 50664702 | |||||
| chr17:50664702
|
CA | C | 43 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0049others(40): Show | 43 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1339-426delA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 10/30 | INFO_REALIGN_3_PRIME | chr17 | 50664702 | |||||
| chr17:50664702
|
CAA | C | 11 | a0001c0002t0001g0231a0001c0022t0001g0122a0002c0006t0001g0003others(8): Show | 11 | HG01069.hp2 HG01891.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1339-427_1339-426d others(4): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 10/30 | INFO_REALIGN_3_PRIME | chr17 | 50664702 | |||||
| chr17:50664803
|
G | A | 1 | a0001c0022t0001g0122 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1339-350G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 10/30 | chr17 | 50664803 | ||||||
| chr17:50664820
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1339-333T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 10/30 | chr17 | 50664820 | ||||||
| chr17:50665082
|
C | T | 1 | a0001c0003t0001g0070 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1339-71C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 10/30 | chr17 | 50665082 | ||||||
| chr17:50665551
|
A | T | 1 | a0001c0001t0001g0115 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1431+306A>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 11/30 | chr17 | 50665551 | ||||||
| chr17:50665608
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1431+363C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 11/30 | chr17 | 50665608 | ||||||
| chr17:50665608
|
CT | C | 86 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0041others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1431+378delT | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr17 | 50665608 | |||||
| chr17:50665609
|
T | C | 1 | a0001c0001t0001g0046 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1431+364T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 11/30 | chr17 | 50665609 | ||||||
| chr17:50665616
|
T | A | 84 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0041others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1431+371T>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 11/30 | chr17 | 50665616 | ||||||
| chr17:50665657
|
A | G | 71 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0017others(68): Show | 71 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1431+412A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 11/30 | chr17 | 50665657 | ||||||
| chr17:50665709
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1431+464G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 11/30 | chr17 | 50665709 | ||||||
| chr17:50665745
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1431+500A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 11/30 | chr17 | 50665745 | ||||||
| chr17:50665780
|
A | AT | 26 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0049others(23): Show | 26 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.1431+546dupT | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr17 | 50665780 | |||||
| chr17:50665914
|
T | C | 30 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0049others(27): Show | 30 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.1431+669T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 11/30 | chr17 | 50665914 | ||||||
| chr17:50666123
|
G | A | 1 | a0015c0033t0001g0020 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1431+878G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 11/30 | chr17 | 50666123 | ||||||
| chr17:50666170
|
G | A | 26 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0049others(23): Show | 26 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.1431+925G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 11/30 | chr17 | 50666170 | ||||||
| chr17:50666190
|
G | A | 2 | a0001c0001t0001g0034a0008c0016t0001g0037 | 2 | HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1431+945G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 11/30 | chr17 | 50666190 | ||||||
| chr17:50666223
|
G | C | 1 | a0024c0041t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1431+978G>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 11/30 | chr17 | 50666223 | ||||||
| chr17:50666238
|
G | A | 70 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0017others(67): Show | 70 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1431+993G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 11/30 | chr17 | 50666238 | ||||||
| chr17:50666442
|
A | G | 61 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0024others(58): Show | 61 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.1432-1112A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 11/30 | chr17 | 50666442 | ||||||
| chr17:50666471
|
CA | C | 8 | a0001c0001t0001g0174a0004c0007t0001g0005a0004c0007t0001g0058others(5): Show | 8 | HG01069.hp2 HG01891.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1432-1073delA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr17 | 50666471 | |||||
| chr17:50666563
|
C | T | 31 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0041others(28): Show | 31 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.1432-991C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 11/30 | chr17 | 50666563 | ||||||
| chr17:50666662
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1432-892G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 11/30 | chr17 | 50666662 | ||||||
| chr17:50666673
|
C | A | 1 | a0001c0001t0001g0216 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1432-881C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 11/30 | chr17 | 50666673 | ||||||
| chr17:50666716
|
C | T | 31 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0041others(28): Show | 31 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.1432-838C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 11/30 | chr17 | 50666716 | ||||||
| chr17:50667171
|
T | C | 1 | a0001c0001t0001g0163 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1432-383T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 11/30 | chr17 | 50667171 | ||||||
| chr17:50667251
|
G | T | 196 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.1432-303G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 11/30 | chr17 | 50667251 | ||||||
| chr17:50667444
|
G | T | 1 | a0001c0001t0001g0105 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1432-110G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 11/30 | chr17 | 50667444 | ||||||
| chr17:50667841
|
AC | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0150a0001c0001t0001g0192 | 3 | NA18983.hp1 NA18988.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1636-21delC | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 12/30 | chr17 | 50667841 | ||||||
| chr17:50668056
|
G | T | 1 | a0001c0043t0001g0335 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1782+47G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 13/30 | chr17 | 50668056 | ||||||
| chr17:50668426
|
G | A | 8 | a0001c0022t0001g0122a0004c0007t0001g0005a0004c0007t0001g0058others(5): Show | 8 | HG01069.hp2 HG01891.hp1 HG02280.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.1783-4G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 13/30 | chr17 | 50668426 | ||||||
| chr17:50668627
|
C | G | 7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0043others(4): Show | 7 | HG02040.hp2 NA18971.hp2 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.1870+110C>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 14/30 | chr17 | 50668627 | ||||||
| chr17:50668774
|
C | T | 270 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.1871-79C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 14/30 | chr17 | 50668774 | ||||||
| chr17:50669327
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2065-25C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 16/30 | chr17 | 50669327 | ||||||
| chr17:50669336
|
T | TTTCTCCT others(3): Show |
1 | a0001c0001t0001g0135 | 1 | NA18974.hp2 | splice_region_variant&intron_variant | LOW | c.2065-15_2065-6dupT others(9): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 16/30 | INFO_REALIGN_3_PRIME | chr17 | 50669336 | |||||
| chr17:50669562
|
G | C | 278 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(275): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.2241+34G>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50669562 | ||||||
| chr17:50669792
|
CT | C | 278 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(275): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.2241+275delT | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr17 | 50669792 | |||||
| chr17:50669803
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2241+275T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50669803 | ||||||
| chr17:50669813
|
T | C | 1 | a0002c0006t0001g0104 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2241+285T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50669813 | ||||||
| chr17:50669925
|
A | G | 1 | a0024c0041t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2241+397A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50669925 | ||||||
| chr17:50670061
|
A | G | 1 | a0001c0004t0001g0205 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2241+533A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50670061 | ||||||
| chr17:50670230
|
G | A | 1 | a0001c0037t0001g0288 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2241+702G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50670230 | ||||||
| chr17:50670438
|
A | T | 1 | a0001c0001t0001g0317 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2241+910A>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50670438 | ||||||
| chr17:50670688
|
G | A | 1 | a0001c0003t0001g0321 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2241+1160G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50670688 | ||||||
| chr17:50670706
|
A | T | 7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0043others(4): Show | 7 | HG02040.hp2 NA18971.hp2 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.2241+1178A>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50670706 | ||||||
| chr17:50670707
|
T | A | 7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0043others(4): Show | 7 | HG02040.hp2 NA18971.hp2 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.2241+1179T>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50670707 | ||||||
| chr17:50670799
|
C | A | 2 | a0007c0012t0003g0069a0007c0012t0003g0304 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2241+1271C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50670799 | ||||||
| chr17:50670815
|
A | G | 341 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(338): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.2241+1287A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50670815 | ||||||
| chr17:50670824
|
A | G | 247 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(244): Show | 247 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.2241+1296A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50670824 | ||||||
| chr17:50670997
|
G | C | 28 | a0001c0001t0001g0057a0001c0001t0001g0080a0001c0001t0001g0091others(25): Show | 28 | HG01081.hp2 HG01243.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.2241+1469G>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50670997 | ||||||
| chr17:50671125
|
G | A | 3 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0312 | 3 | HG02717.hp1 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2241+1597G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50671125 | ||||||
| chr17:50671194
|
T | G | 2 | a0001c0001t0001g0034a0008c0016t0001g0037 | 2 | HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2241+1666T>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50671194 | ||||||
| chr17:50671225
|
A | T | 1 | a0016c0032t0001g0033 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2241+1697A>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50671225 | ||||||
| chr17:50671247
|
A | AAGACTCT others(5): Show |
1 | a0001c0001t0001g0034 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2241+1721_2242-171 others(16): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr17 | 50671247 | |||||
| chr17:50671259
|
T | TA | 6 | a0001c0001t0001g0127a0001c0001t0001g0252a0001c0001t0001g0279others(3): Show | 6 | HG00642.hp1 HG01952.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.2242-1698dupA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr17 | 50671259 | |||||
| chr17:50671274
|
G | A | 28 | a0001c0001t0001g0057a0001c0001t0001g0080a0001c0001t0001g0091others(25): Show | 28 | HG01081.hp2 HG01243.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.2242-1697G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50671274 | ||||||
| chr17:50671275
|
A | G | 28 | a0001c0001t0001g0057a0001c0001t0001g0080a0001c0001t0001g0091others(25): Show | 28 | HG01081.hp2 HG01243.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.2242-1696A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50671275 | ||||||
| chr17:50671344
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2242-1627C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50671344 | ||||||
| chr17:50671357
|
C | A | 1 | a0001c0004t0001g0318 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2242-1614C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50671357 | ||||||
| chr17:50671372
|
A | C | 16 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0049others(13): Show | 16 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.2242-1599A>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50671372 | ||||||
| chr17:50671603
|
C | G | 11 | a0001c0001t0001g0091a0001c0001t0003g0073a0001c0001t0003g0314others(8): Show | 11 | HG02486.hp1 HG02572.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.2242-1368C>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50671603 | ||||||
| chr17:50671702
|
C | CT | 50 | a0001c0001t0001g0008a0001c0001t0001g0044a0001c0001t0001g0046others(47): Show | 50 | HG00423.hp2 HG00544.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.2242-1239dupT | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr17 | 50671702 | |||||
| chr17:50671702
|
C | CTT | 59 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0019others(56): Show | 59 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.2242-1240_2242-123 others(6): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr17 | 50671702 | |||||
| chr17:50671702
|
C | CTTT | 55 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0022others(52): Show | 55 | HG00438.hp2 HG00733.hp2 HG01123.hp1 others(52): Show |
intron_variant | MODIFIER | c.2242-1241_2242-123 others(7): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr17 | 50671702 | |||||
| chr17:50671702
|
C | CTTTTTT | 16 | a0001c0001t0002g0099a0001c0001t0002g0175a0001c0001t0002g0281others(13): Show | 16 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.2242-1244_2242-123 others(10): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr17 | 50671702 | |||||
| chr17:50671702
|
C | CTTTTTTT | 9 | a0001c0001t0001g0189a0001c0001t0002g0096a0001c0001t0002g0292others(6): Show | 9 | HG00621.hp2 HG01081.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2242-1245_2242-123 others(11): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr17 | 50671702 | |||||
| chr17:50671702
|
CT | C | 16 | a0001c0001t0001g0135a0001c0001t0001g0320a0001c0002t0001g0090others(13): Show | 16 | HG00423.hp1 HG01099.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.2242-1239delT | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr17 | 50671702 | |||||
| chr17:50671702
|
CTT | C | 16 | a0001c0002t0001g0092a0001c0002t0001g0276a0001c0003t0001g0070others(13): Show | 16 | HG00280.hp2 HG00639.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.2242-1240_2242-123 others(6): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr17 | 50671702 | |||||
| chr17:50671702
|
CTTTTTTT others(3): Show |
C | 13 | a0001c0001t0001g0057a0001c0001t0001g0072a0001c0001t0001g0080others(10): Show | 13 | HG01891.hp1 HG02015.hp2 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.2242-1248_2242-123 others(14): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr17 | 50671702 | |||||
| chr17:50671702
|
CTTTTTTT others(4): Show |
C | 15 | a0001c0001t0001g0178a0001c0001t0001g0188a0001c0001t0001g0305others(12): Show | 15 | HG01069.hp2 HG01081.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.2242-1249_2242-123 others(15): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr17 | 50671702 | |||||
| chr17:50671702
|
CTTTTTTT others(5): Show |
C | 1 | a0002c0006t0001g0334 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2242-1250_2242-123 others(16): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr17 | 50671702 | |||||
| chr17:50671705
|
T | C | 1 | a0022c0035t0001g0040 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2242-1266T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50671705 | ||||||
| chr17:50671706
|
T | C | 1 | a0022c0035t0001g0040 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2242-1265T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50671706 | ||||||
| chr17:50671839
|
A | G | 1 | a0001c0001t0001g0038 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2242-1132A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50671839 | ||||||
| chr17:50671870
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2242-1101C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50671870 | ||||||
| chr17:50671914
|
G | A | 5 | a0001c0001t0001g0057a0001c0001t0001g0080a0001c0001t0001g0257others(2): Show | 5 | HG02015.hp2 HG02071.hp2 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.2242-1057G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50671914 | ||||||
| chr17:50671970
|
C | A | 1 | a0001c0001t0001g0038 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2242-1001C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50671970 | ||||||
| chr17:50671974
|
G | A | 1 | a0008c0016t0001g0037 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2242-997G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50671974 | ||||||
| chr17:50672015
|
C | T | 30 | a0001c0001t0001g0091a0001c0001t0001g0136a0001c0001t0001g0189others(27): Show | 30 | HG00099.hp1 HG00099.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.2242-956C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50672015 | ||||||
| chr17:50672161
|
A | T | 211 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2242-810A>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50672161 | ||||||
| chr17:50672162
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2242-809C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50672162 | ||||||
| chr17:50672190
|
A | G | 1 | a0001c0001t0004g0027 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2242-781A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50672190 | ||||||
| chr17:50672241
|
G | T | 1 | a0002c0006t0001g0334 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2242-730G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50672241 | ||||||
| chr17:50672297
|
A | T | 1 | a0001c0001t0001g0038 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2242-674A>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50672297 | ||||||
| chr17:50672382
|
T | C | 30 | a0001c0001t0001g0091a0001c0001t0001g0136a0001c0001t0001g0189others(27): Show | 30 | HG00099.hp1 HG00099.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.2242-589T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50672382 | ||||||
| chr17:50672399
|
G | T | 1 | a0001c0038t0001g0191 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2242-572G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50672399 | ||||||
| chr17:50672415
|
G | A | 2 | a0007c0012t0003g0069a0007c0012t0003g0304 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2242-556G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50672415 | ||||||
| chr17:50672473
|
G | A | 2 | a0007c0012t0003g0069a0007c0012t0003g0304 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2242-498G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50672473 | ||||||
| chr17:50672479
|
C | A | 1 | a0001c0001t0001g0091 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2242-492C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50672479 | ||||||
| chr17:50672522
|
A | G | 30 | a0001c0001t0001g0091a0001c0001t0001g0136a0001c0001t0001g0189others(27): Show | 30 | HG00099.hp1 HG00099.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.2242-449A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50672522 | ||||||
| chr17:50672559
|
T | C | 36 | a0001c0001t0001g0261a0001c0002t0001g0090a0001c0002t0001g0092others(33): Show | 36 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.2242-412T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50672559 | ||||||
| chr17:50672627
|
G | A | 1 | a0024c0041t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2242-344G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50672627 | ||||||
| chr17:50672634
|
G | A | 1 | a0001c0001t0001g0331 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2242-337G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50672634 | ||||||
| chr17:50672718
|
T | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0120a0001c0017t0001g0233 | 3 | HG02622.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2242-253T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50672718 | ||||||
| chr17:50672742
|
C | A | 2 | a0001c0001t0001g0014a0001c0027t0001g0015 | 2 | HG02056.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.2242-229C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50672742 | ||||||
| chr17:50672794
|
C | G | 1 | a0001c0001t0001g0038 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2242-177C>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50672794 | ||||||
| chr17:50672835
|
G | A | 10 | a0001c0004t0001g0059a0001c0004t0001g0100a0001c0004t0001g0145others(7): Show | 10 | HG00544.hp1 HG01928.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.2242-136G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | chr17 | 50672835 | ||||||
| chr17:50672870
|
G | GA | 17 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0066others(14): Show | 17 | HG00639.hp2 HG01175.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.2242-86dupA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr17 | 50672870 | |||||
| chr17:50673185
|
C | T | 2 | a0001c0002t0001g0090a0001c0002t0001g0092 | 2 | HG01106.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2409+47C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 18/30 | chr17 | 50673185 | ||||||
| chr17:50673235
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0323 | 2 | NA18971.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.2409+97G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 18/30 | chr17 | 50673235 | ||||||
| chr17:50673418
|
A | G | 1 | a0024c0041t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2410-51A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 18/30 | chr17 | 50673418 | ||||||
| chr17:50673441
|
G | A | 9 | a0001c0001t0001g0201a0001c0001t0001g0224a0001c0001t0001g0240others(6): Show | 9 | HG02135.hp2 HG02273.hp1 NA18961.hp2 others(6): Show |
intron_variant | MODIFIER | c.2410-28G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 18/30 | chr17 | 50673441 | ||||||
| chr17:50673443
|
G | T | 2 | a0007c0012t0003g0069a0007c0012t0003g0304 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2410-26G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 18/30 | chr17 | 50673443 | ||||||
| chr17:50673753
|
C | T | 96 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0017others(93): Show | 96 | HG00323.hp2 HG00438.hp2 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.2599+95C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673753 | ||||||
| chr17:50673803
|
T | G | 203 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.2599+145T>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673803 | ||||||
| chr17:50673824
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0039a0001c0001t0001g0054others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2599+166G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673824 | ||||||
| chr17:50673886
|
G | C | 1 | a0001c0001t0001g0091 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2599+228G>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673886 | ||||||
| chr17:50673900
|
T | TTTTC | 3 | a0001c0001t0001g0107a0001c0001t0001g0154a0001c0002t0001g0274 | 3 | HG01175.hp1 HG02145.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2599+320_2599+323d others(6): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673900 | |||||
| chr17:50673900
|
T | TTTTCTTT others(13): Show |
1 | a0001c0001t0004g0027 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2599+304_2599+323d others(22): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673900 | |||||
| chr17:50673914
|
T | C | 8 | a0001c0004t0001g0059a0001c0004t0001g0100a0001c0004t0001g0145others(5): Show | 8 | HG01928.hp1 HG01934.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.2599+256T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673914 | ||||||
| chr17:50673918
|
T | C | 1 | a0001c0004t0001g0243 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2599+260T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673918 | ||||||
| chr17:50673919
|
T | C | 3 | a0001c0001t0001g0051a0001c0001t0001g0252a0002c0010t0001g0026 | 3 | HG02922.hp1 NA18612.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.2599+261T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673919 | ||||||
| chr17:50673933
|
T | TTTCTTTC others(7): Show |
1 | a0001c0001t0001g0183 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2599+284_2599+285i others(16): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673933 | |||||
| chr17:50673936
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2599+278C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673936 | ||||||
| chr17:50673937
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2599+279T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673937 | ||||||
| chr17:50673941
|
TTTCTTTC others(4): Show |
T | 1 | a0013c0034t0001g0144 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2599+286_2599+296d others(13): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673941 | |||||
| chr17:50673958
|
T | TTCTTTCT others(7): Show |
1 | a0001c0001t0001g0066 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2599+302_2599+315d others(16): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673958 | |||||
| chr17:50673958
|
T | TTCTTTCT others(23): Show |
2 | a0001c0001t0001g0010a0001c0001t0001g0024 | 2 | NA18983.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.2599+323_2599+324i others(32): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673958 | |||||
| chr17:50673958
|
T | TTCTTTCT others(27): Show |
1 | a0017c0029t0001g0229 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2599+323_2599+324i others(36): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673958 | |||||
| chr17:50673961
|
T | C | 2 | a0001c0003t0001g0238a0001c0003t0001g0241 | 2 | NA19057.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2599+303T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673961 | ||||||
| chr17:50673961
|
T | TTTCTTTC others(12): Show |
1 | a0001c0001t0001g0057 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2599+305_2599+323d others(21): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673961 | |||||
| chr17:50673962
|
T | TTCTTTCT others(7): Show |
4 | a0001c0001t0001g0068a0001c0001t0001g0195a0001c0001t0001g0289others(1): Show | 4 | HG00738.hp1 HG02015.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.2599+306_2599+319d others(16): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673962 | |||||
| chr17:50673962
|
T | TTCTTTCT others(15): Show |
1 | a0001c0001t0001g0286 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2599+319_2599+320i others(24): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673962 | |||||
| chr17:50673962
|
T | TTCTTTCT others(15): Show |
2 | a0001c0001t0001g0035a0010c0021t0001g0067 | 2 | NA18955.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.2599+323_2599+324i others(24): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673962 | |||||
| chr17:50673962
|
T | TTCTTTCT others(19): Show |
3 | a0001c0001t0001g0170a0001c0001t0001g0190a0001c0001t0001g0192 | 3 | HG01952.hp1 NA18941.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.2599+323_2599+324i others(28): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673962 | |||||
| chr17:50673962
|
T | TTCTTTCT others(27): Show |
1 | a0001c0001t0001g0250 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2599+323_2599+324i others(36): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673962 | |||||
| chr17:50673963
|
T | C | 1 | a0007c0012t0003g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2599+305T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673963 | ||||||
| chr17:50673964
|
CTTTCTTT others(7): Show |
C | 1 | a0024c0041t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2599+308_2599+321d others(16): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673964 | |||||
| chr17:50673965
|
T | C | 2 | a0001c0003t0001g0238a0001c0003t0001g0241 | 2 | NA19057.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2599+307T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673965 | ||||||
| chr17:50673965
|
T | TTTCTTTC others(16): Show |
1 | a0001c0001t0001g0257 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2599+323_2599+324i others(25): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673965 | |||||
| chr17:50673966
|
T | TTCTTTCT others(3): Show |
2 | a0001c0001t0001g0149a0001c0001t0001g0187 | 2 | HG00438.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.2599+310_2599+319d others(12): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673966 | |||||
| chr17:50673966
|
T | TTCTTTCT others(15): Show |
1 | a0001c0001t0001g0043 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2599+323_2599+324i others(24): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673966 | |||||
| chr17:50673967
|
T | C | 1 | a0007c0012t0003g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2599+309T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673967 | ||||||
| chr17:50673969
|
T | C | 9 | a0001c0001t0002g0096a0001c0001t0002g0099a0001c0003t0001g0158others(6): Show | 9 | HG00099.hp1 HG00099.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.2599+311T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673969 | ||||||
| chr17:50673970
|
T | C | 2 | a0002c0036t0001g0230a0004c0023t0001g0004 | 2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2599+312T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673970 | ||||||
| chr17:50673970
|
T | TTCTTTCT others(19): Show |
1 | a0001c0001t0001g0164 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2599+323_2599+324i others(28): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673970 | |||||
| chr17:50673970
|
TTCTTTCT others(5): Show |
T | 1 | a0001c0001t0001g0091 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2599+316_2599+327d others(14): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673970 | |||||
| chr17:50673970
|
TTCTTTCT others(7): Show |
T | 1 | a0002c0006t0001g0023 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2599+316_2599+329d others(16): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673970 | |||||
| chr17:50673971
|
T | C | 1 | a0007c0012t0003g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2599+313T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673971 | ||||||
| chr17:50673973
|
T | C | 20 | a0001c0001t0001g0136a0001c0001t0001g0189a0001c0001t0002g0096others(17): Show | 20 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.2599+315T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673973 | ||||||
| chr17:50673974
|
T | C | 5 | a0001c0001t0001g0139a0001c0001t0001g0188a0001c0004t0001g0319others(2): Show | 5 | HG01891.hp1 HG02145.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.2599+316T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673974 | ||||||
| chr17:50673974
|
TTCTTTCT others(11): Show |
T | 1 | a0001c0001t0001g0141 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2599+320_2599+337d others(20): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673974 | |||||
| chr17:50673974
|
TTCTTTCT others(13): Show |
T | 2 | a0001c0001t0001g0049a0001c0001t0001g0206 | 2 | HG00423.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.2599+320_2599+339d others(22): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673974 | |||||
| chr17:50673975
|
T | C | 2 | a0007c0012t0003g0069a0007c0012t0003g0304 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2599+317T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673975 | ||||||
| chr17:50673976
|
C | G | 1 | a0001c0001t0001g0169 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2599+318C>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673976 | ||||||
| chr17:50673977
|
T | C | 33 | a0001c0001t0001g0120a0001c0001t0001g0136a0001c0001t0001g0189others(30): Show | 33 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.2599+319T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673977 | ||||||
| chr17:50673977
|
T | TCTTTCTT others(10): Show |
1 | a0001c0001t0001g0162 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2599+319_2599+320i others(19): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673977 | ||||||
| chr17:50673977
|
T | TTTCTTTC others(28): Show |
1 | a0001c0001t0001g0223 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2599+323_2599+324i others(37): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673977 | |||||
| chr17:50673977
|
TTTCTCTC others(4): Show |
T | 1 | a0001c0001t0001g0045 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2599+321_2599+331d others(13): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673977 | |||||
| chr17:50673978
|
T | C | 16 | a0001c0001t0001g0046a0001c0001t0001g0051a0001c0001t0001g0081others(13): Show | 16 | HG00735.hp1 HG00738.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2599+320T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673978 | ||||||
| chr17:50673978
|
T | TTCTCTCT others(64): Show |
1 | a0001c0001t0001g0124 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2599+358_2599+359i others(73): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTCTTT others(19): Show |
1 | a0001c0001t0001g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2599+325_2599+326i others(28): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTTTCT others(13): Show |
1 | a0001c0001t0001g0240 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2599+323_2599+324i others(22): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTTTCT others(61): Show |
1 | a0001c0039t0001g0126 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2599+323_2599+324i others(70): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTTTCT others(69): Show |
1 | a0001c0001t0001g0110 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2599+323_2599+324i others(78): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTTTCT others(5): Show |
1 | a0001c0001t0001g0089 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2599+323_2599+324i others(14): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTTTCT others(19): Show |
1 | a0001c0001t0001g0246 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2599+323_2599+324i others(28): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTTTCT others(45): Show |
1 | a0001c0001t0001g0039 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2599+323_2599+324i others(54): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTTTCT others(61): Show |
1 | a0001c0001t0001g0111 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2599+323_2599+324i others(70): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTTTCT others(71): Show |
1 | a0001c0001t0001g0271 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2599+323_2599+324i others(80): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTTTCT others(87): Show |
1 | a0001c0001t0001g0055 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2599+323_2599+324i others(96): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTTTCT others(21): Show |
1 | a0001c0001t0001g0075 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2599+323_2599+324i others(30): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTTTCT others(25): Show |
2 | a0001c0001t0001g0012a0001c0001t0001g0166 | 2 | HG01261.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.2599+323_2599+324i others(34): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTTTCT others(31): Show |
1 | a0001c0001t0001g0299 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2599+323_2599+324i others(40): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTTTCT others(86): Show |
1 | a0001c0001t0001g0087 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2599+323_2599+324i others(95): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTTTCT others(11): Show |
1 | a0001c0001t0001g0048 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2599+323_2599+324i others(20): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTTTCT others(53): Show |
1 | a0001c0001t0001g0329 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2599+323_2599+324i others(62): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTTTCT others(79): Show |
1 | a0001c0001t0001g0134 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2599+323_2599+324i others(88): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTTTCT others(29): Show |
1 | a0001c0001t0001g0173 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2599+323_2599+324i others(38): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTTTCT others(70): Show |
1 | a0001c0001t0001g0086 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2599+323_2599+324i others(79): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTTTCT others(111): Show |
1 | a0001c0001t0001g0201 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2599+323_2599+324i others(120): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTTTCT others(56): Show |
1 | a0001c0001t0001g0224 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2599+323_2599+324i others(65): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTTTCT others(37): Show |
1 | a0001c0001t0001g0019 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2599+323_2599+324i others(46): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTTTCT others(67): Show |
1 | a0001c0001t0001g0211 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2599+323_2599+324i others(76): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTTTCT others(77): Show |
1 | a0001c0001t0001g0273 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2599+323_2599+324i others(86): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTTTCT others(117): Show |
1 | a0001c0001t0001g0331 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2599+323_2599+324i others(126): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
T | TTCTTTCT others(25): Show |
1 | a0001c0001t0001g0264 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2599+323_2599+324i others(34): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
TTCTCTC | T | 3 | a0001c0002t0001g0009a0001c0002t0001g0021a0001c0002t0001g0231 | 3 | NA18947.hp1 NA19010.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.2599+374_2599+379d others(8): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
TTCTCTCT others(3): Show |
T | 5 | a0001c0002t0001g0082a0001c0002t0001g0294a0001c0002t0001g0326others(2): Show | 5 | HG00642.hp1 HG01361.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.2599+370_2599+379d others(12): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
TTCTCTCT others(5): Show |
T | 1 | a0006c0011t0001g0270 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2599+368_2599+379d others(14): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
TTCTCTCT others(7): Show |
T | 3 | a0001c0001t0001g0165a0001c0002t0001g0225a0001c0002t0001g0227 | 3 | HG01516.hp1 HG01517.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.2599+366_2599+379d others(16): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
TTCTCTCT others(9): Show |
T | 1 | a0001c0004t0001g0145 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2599+364_2599+379d others(18): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
TTCTCTCT others(11): Show |
T | 3 | a0001c0002t0001g0156a0001c0002t0001g0160a0001c0002t0001g0276 | 3 | HG02155.hp1 HG02451.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.2599+362_2599+379d others(20): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
TTCTCTCT others(13): Show |
T | 1 | a0001c0004t0001g0243 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2599+360_2599+379d others(22): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
TTCTCTCT others(15): Show |
T | 1 | a0001c0002t0001g0094 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2599+358_2599+379d others(24): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673978
|
TTCTCTCT others(19): Show |
T | 1 | a0001c0002t0001g0226 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2599+354_2599+379d others(28): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673978 | |||||
| chr17:50673979
|
T | C | 2 | a0007c0012t0003g0069a0007c0012t0003g0304 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2599+321T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673979 | ||||||
| chr17:50673980
|
C | CCTTCCTT others(7): Show |
1 | a0001c0001t0001g0136 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2599+322_2599+323i others(16): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673980 | ||||||
| chr17:50673980
|
C | CCTTCCTT others(15): Show |
2 | a0001c0001t0001g0189a0001c0017t0001g0233 | 2 | HG02622.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2599+322_2599+323i others(24): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673980 | ||||||
| chr17:50673980
|
C | CCTTCCTT others(19): Show |
1 | a0001c0001t0001g0120 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2599+322_2599+323i others(28): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673980 | ||||||
| chr17:50673980
|
C | CCTTCCTT others(31): Show |
2 | a0001c0001t0001g0034a0008c0016t0001g0037 | 2 | HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2599+322_2599+323i others(40): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673980 | ||||||
| chr17:50673980
|
C | CTCTTTCT others(5): Show |
1 | a0001c0001t0001g0052 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2599+325_2599+326i others(14): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673980 | |||||
| chr17:50673980
|
C | CTT | 8 | a0001c0001t0001g0014a0001c0001t0001g0068a0001c0001t0001g0149others(5): Show | 8 | HG00438.hp2 HG00738.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.2599+323_2599+324i others(4): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673980 | |||||
| chr17:50673980
|
C | CTTTCTCT others(5): Show |
1 | a0001c0001t0001g0260 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2599+323_2599+324i others(14): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673980 | |||||
| chr17:50673980
|
C | CTTTCTCT others(9): Show |
1 | a0001c0001t0001g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2599+323_2599+324i others(18): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673980 | |||||
| chr17:50673980
|
C | CTTTCTCT others(13): Show |
1 | a0001c0001t0001g0022 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2599+323_2599+324i others(22): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673980 | |||||
| chr17:50673980
|
C | CTTTCTCT others(17): Show |
1 | a0001c0001t0001g0263 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2599+323_2599+324i others(26): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673980 | |||||
| chr17:50673980
|
C | CTTTCTT | 3 | a0001c0001t0001g0199a0001c0001t0001g0220a0001c0043t0001g0335 | 3 | HG00408.hp1 NA19064.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2599+323_2599+324i others(8): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673980 | |||||
| chr17:50673980
|
C | CTTTCTTT others(5): Show |
1 | a0001c0001t0001g0168 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2599+323_2599+324i others(14): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673980 | |||||
| chr17:50673980
|
C | CTTTCTTT others(9): Show |
3 | a0001c0001t0001g0254a0001c0014t0001g0121a0004c0007t0001g0118 | 3 | HG02080.hp2 HG06807.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.2599+323_2599+324i others(18): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673980 | |||||
| chr17:50673980
|
C | CTTTCTTT others(13): Show |
4 | a0001c0001t0001g0018a0001c0001t0001g0038a0001c0001t0001g0169others(1): Show | 4 | HG03942.hp2 NA18906.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.2599+323_2599+324i others(22): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673980 | |||||
| chr17:50673980
|
C | CTTTCTTT others(17): Show |
2 | a0001c0001t0001g0017a0001c0001t0001g0249 | 2 | HG01255.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.2599+323_2599+324i others(26): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673980 | |||||
| chr17:50673980
|
C | CTTTCTTT others(20): Show |
1 | a0012c0025t0001g0151 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2599+323_2599+324i others(29): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673980 | |||||
| chr17:50673980
|
C | CTTTCTTT others(21): Show |
1 | a0001c0001t0001g0150 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2599+323_2599+324i others(30): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673980 | |||||
| chr17:50673980
|
C | CTTTCTTT others(3): Show |
2 | a0001c0001t0001g0041a0001c0004t0002g0278 | 2 | NA18992.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2599+323_2599+324i others(12): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673980 | |||||
| chr17:50673980
|
C | CTTTCTTT others(9): Show |
2 | a0001c0001t0001g0262a0004c0007t0001g0060 | 2 | HG01069.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.2599+323_2599+324i others(18): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673980 | |||||
| chr17:50673980
|
C | CTTTCTTT others(13): Show |
1 | a0001c0001t0001g0251 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2599+323_2599+324i others(22): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673980 | |||||
| chr17:50673980
|
C | CTTTCTTT others(7): Show |
2 | a0001c0001t0001g0207a0001c0002t0001g0032 | 2 | HG02886.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.2599+323_2599+324i others(16): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673980 | |||||
| chr17:50673980
|
C | CTTTCTTT others(13): Show |
1 | a0001c0004t0001g0100 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2599+323_2599+324i others(22): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673980 | |||||
| chr17:50673980
|
C | CTTTCTTT others(11): Show |
1 | a0001c0004t0001g0237 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2599+323_2599+324i others(20): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673980 | |||||
| chr17:50673980
|
C | T | 4 | a0001c0001t0001g0051a0001c0001t0001g0185a0001c0001t0001g0248others(1): Show | 4 | HG02886.hp2 NA18612.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.2599+322C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673980 | ||||||
| chr17:50673980
|
CTCT | C | 4 | a0001c0003t0001g0242a0001c0013t0001g0236a0003c0005t0002g0085others(1): Show | 4 | HG01346.hp2 NA18960.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.2599+323_2599+325d others(5): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673980 | ||||||
| chr17:50673980
|
CTCTCTCT | C | 3 | a0001c0001t0002g0281a0001c0003t0001g0234a0003c0005t0002g0302 | 3 | HG00735.hp2 HG01081.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.2599+323_2599+329d others(9): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673980 | ||||||
| chr17:50673980
|
CTCTCTCT others(4): Show |
C | 5 | a0001c0001t0002g0093a0001c0001t0002g0282a0001c0003t0001g0215others(2): Show | 5 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(2): Show |
intron_variant | MODIFIER | c.2599+323_2599+333d others(13): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673980 | ||||||
| chr17:50673980
|
CTCTCTCT others(8): Show |
C | 4 | a0001c0003t0001g0204a0001c0003t0001g0321a0001c0022t0001g0122others(1): Show | 4 | HG00280.hp2 HG02280.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.2599+323_2599+337d others(17): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673980 | ||||||
| chr17:50673980
|
CTCTCTCT others(12): Show |
C | 9 | a0001c0001t0002g0342a0001c0003t0001g0239a0001c0003t0001g0284others(6): Show | 9 | HG01258.hp1 HG02055.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.2599+323_2599+341d others(21): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673980 | ||||||
| chr17:50673980
|
CTCTCTCT others(16): Show |
C | 9 | a0001c0001t0003g0314a0001c0003t0001g0153a0001c0003t0001g0158others(6): Show | 9 | HG00558.hp2 HG01099.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.2599+323_2599+345d others(25): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673980 | ||||||
| chr17:50673980
|
CTCTCTCT others(20): Show |
C | 1 | a0001c0003t0001g0070 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2599+323_2599+349d others(29): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673980 | ||||||
| chr17:50673980
|
CTCTCTCT others(24): Show |
C | 3 | a0001c0009t0001g0007a0005c0008t0001g0313a0023c0020t0001g0063 | 3 | HG03139.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2599+323_2599+353d others(33): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673980 | ||||||
| chr17:50673980
|
CTCTCTCT others(32): Show |
C | 2 | a0001c0003t0001g0238a0001c0003t0001g0241 | 2 | NA19057.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2599+323_2599+361d others(41): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673980 | ||||||
| chr17:50673981
|
T | C | 2 | a0001c0003t0001g0295a0003c0005t0002g0277 | 2 | HG01106.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.2599+323T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673981 | ||||||
| chr17:50673981
|
TC | T | 3 | a0001c0001t0001g0317a0001c0004t0003g0267a0001c0027t0001g0015 | 3 | HG01884.hp2 HG02056.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2599+324delC | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673981 | ||||||
| chr17:50673982
|
C | CCT | 9 | a0001c0001t0001g0034a0001c0001t0001g0120a0001c0001t0001g0136others(6): Show | 9 | HG00099.hp2 HG02622.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.2599+324_2599+325i others(4): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673982 | ||||||
| chr17:50673982
|
C | CTTTCTTT others(10): Show |
1 | a0001c0001t0001g0290 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2599+325_2599+326i others(19): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673982 | |||||
| chr17:50673982
|
C | T | 134 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(131): Show | 134 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.2599+324C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673982 | ||||||
| chr17:50673984
|
C | T | 50 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0038others(47): Show | 50 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2599+326C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673984 | ||||||
| chr17:50673984
|
CTCTCTCT others(4): Show |
C | 1 | a0001c0001t0002g0301 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2599+327_2599+337d others(13): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673984 | ||||||
| chr17:50673984
|
CTCTCTCT others(16): Show |
C | 1 | a0001c0013t0001g0098 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2599+327_2599+349d others(25): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673984 | ||||||
| chr17:50673985
|
T | C | 15 | a0001c0001t0001g0034a0001c0001t0001g0120a0001c0001t0001g0136others(12): Show | 15 | HG00099.hp2 HG01106.hp2 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.2599+327T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673985 | ||||||
| chr17:50673985
|
TC | T | 6 | a0001c0001t0001g0053a0001c0001t0001g0114a0001c0003t0001g0242others(3): Show | 6 | HG00733.hp1 HG01346.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2599+328delC | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673985 | ||||||
| chr17:50673985
|
TCTCTCTC others(4): Show |
T | 1 | a0001c0001t0001g0265 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2599+328_2599+338d others(13): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673985 | ||||||
| chr17:50673986
|
C | CTTCTTTC others(14): Show |
1 | a0001c0002t0001g0090 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2599+329_2599+330i others(23): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673986 | |||||
| chr17:50673986
|
C | CTTTCTTT others(3): Show |
1 | a0001c0001t0001g0025 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2599+329_2599+330i others(12): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673986 | |||||
| chr17:50673986
|
C | CTTTCTTT others(7): Show |
1 | a0001c0001t0001g0235 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2599+329_2599+330i others(16): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673986 | |||||
| chr17:50673986
|
C | CTTTCTTT others(11): Show |
1 | a0001c0001t0001g0036 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2599+329_2599+330i others(20): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673986 | |||||
| chr17:50673986
|
C | T | 102 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0031others(99): Show | 102 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.2599+328C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673986 | ||||||
| chr17:50673988
|
C | CCTTCCTT others(35): Show |
1 | a0001c0001t0001g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2599+330_2599+331i others(44): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673988 | ||||||
| chr17:50673988
|
C | CTCTCTCT others(65): Show |
1 | a0001c0001t0001g0008 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2599+363_2599+364i others(74): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673988 | |||||
| chr17:50673988
|
C | T | 51 | a0001c0001t0001g0018a0001c0001t0001g0051a0001c0001t0001g0052others(48): Show | 51 | HG00323.hp2 HG01069.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.2599+330C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673988 | ||||||
| chr17:50673988
|
CTCT | C | 3 | a0001c0003t0001g0209a0001c0003t0001g0218a0001c0045t0001g0062 | 3 | NA18967.hp2 NA18974.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.2599+331_2599+333d others(5): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673988 | ||||||
| chr17:50673988
|
CTCTCTCT others(8): Show |
C | 1 | a0001c0009t0003g0006 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2599+331_2599+345d others(17): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673988 | ||||||
| chr17:50673988
|
CTCTCTCT others(12): Show |
C | 1 | a0001c0001t0003g0073 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2599+331_2599+349d others(21): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673988 | ||||||
| chr17:50673989
|
T | C | 20 | a0001c0001t0001g0120a0001c0001t0001g0136a0001c0001t0001g0189others(17): Show | 20 | HG00099.hp2 HG00423.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.2599+331T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673989 | ||||||
| chr17:50673989
|
T | TCTCTCTC others(71): Show |
1 | a0001c0001t0001g0320 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2599+350_2599+351i others(80): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673989 | |||||
| chr17:50673989
|
T | TTTCTTTC others(24): Show |
1 | a0001c0001t0001g0146 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2599+331_2599+332i others(33): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673989 | ||||||
| chr17:50673989
|
TC | T | 4 | a0001c0001t0002g0281a0001c0003t0001g0234a0003c0005t0002g0078others(1): Show | 4 | HG00735.hp2 HG01081.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.2599+332delC | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673989 | ||||||
| chr17:50673990
|
C | CTTTCTTT others(3): Show |
1 | a0001c0004t0001g0197 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2599+333_2599+334i others(12): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673990 | |||||
| chr17:50673990
|
C | CTTTCTTT others(7): Show |
5 | a0001c0001t0001g0143a0001c0001t0001g0167a0001c0001t0001g0182others(2): Show | 5 | HG01346.hp1 HG02155.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2599+333_2599+334i others(16): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673990 | |||||
| chr17:50673990
|
C | CTTTCTTT others(11): Show |
2 | a0001c0001t0001g0261a0001c0001t0001g0340 | 2 | HG02015.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2599+333_2599+334i others(20): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673990 | |||||
| chr17:50673990
|
C | CTTTCTTT others(19): Show |
2 | a0001c0002t0001g0316a0001c0002t0006g0266 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2599+333_2599+334i others(28): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673990 | |||||
| chr17:50673990
|
C | T | 70 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0031others(67): Show | 70 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2599+332C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673990 | ||||||
| chr17:50673991
|
T | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0224 | 2 | HG02135.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2599+333T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673991 | ||||||
| chr17:50673992
|
C | CTTTCTTT others(8): Show |
1 | a0001c0001t0001g0011 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2599+335_2599+336i others(17): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673992 | |||||
| chr17:50673992
|
C | T | 54 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0076others(51): Show | 54 | HG00323.hp2 HG00642.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.2599+334C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673992 | ||||||
| chr17:50673992
|
CTCTCTCT others(4): Show |
C | 1 | a0005c0008t0001g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2599+335_2599+345d others(13): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673992 | ||||||
| chr17:50673993
|
T | C | 25 | a0001c0001t0001g0120a0001c0001t0001g0136a0001c0001t0001g0189others(22): Show | 25 | HG00099.hp2 HG00423.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.2599+335T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673993 | ||||||
| chr17:50673993
|
T | TTTCTTTC others(8): Show |
1 | a0004c0007t0001g0119 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2599+335_2599+336i others(17): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673993 | ||||||
| chr17:50673993
|
TC | T | 9 | a0001c0001t0002g0093a0001c0001t0002g0282a0001c0003t0001g0209others(6): Show | 9 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.2599+336delC | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673993 | ||||||
| chr17:50673993
|
TCTCTCTC others(4): Show |
T | 1 | a0002c0010t0001g0116 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2599+336_2599+346d others(13): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673993 | ||||||
| chr17:50673994
|
C | CTTTCTTT others(7): Show |
1 | a0001c0001t0001g0253 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2599+337_2599+338i others(16): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673994 | |||||
| chr17:50673994
|
C | T | 67 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0047others(64): Show | 67 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.2599+336C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673994 | ||||||
| chr17:50673995
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2599+337T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673995 | ||||||
| chr17:50673996
|
C | T | 51 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0076others(48): Show | 51 | HG00323.hp2 HG00642.hp1 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.2599+338C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673996 | ||||||
| chr17:50673997
|
T | C | 33 | a0001c0001t0001g0136a0001c0001t0001g0189a0001c0001t0002g0093others(30): Show | 33 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.2599+339T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673997 | ||||||
| chr17:50673997
|
TC | T | 5 | a0001c0001t0002g0301a0001c0003t0001g0204a0001c0003t0001g0321others(2): Show | 5 | HG00280.hp2 HG01109.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.2599+340delC | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673997 | ||||||
| chr17:50673997
|
TCTCTCTC others(6): Show |
T | 1 | a0001c0002t0001g0228 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2599+340_2599+352d others(15): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673997 | ||||||
| chr17:50673998
|
C | CTTTCTTT others(15): Show |
1 | a0001c0004t0001g0318 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2599+341_2599+342i others(24): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50673998 | |||||
| chr17:50673998
|
C | T | 70 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0057others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.2599+340C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673998 | ||||||
| chr17:50673999
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2599+341T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50673999 | ||||||
| chr17:50674000
|
C | CCTTCCTT others(3): Show |
1 | a0011c0040t0002g0056 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2599+342_2599+343i others(12): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674000 | ||||||
| chr17:50674000
|
C | T | 42 | a0001c0001t0001g0013a0001c0001t0001g0107a0001c0001t0001g0108others(39): Show | 42 | HG00323.hp2 HG00544.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.2599+342C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674000 | ||||||
| chr17:50674001
|
T | C | 37 | a0001c0001t0001g0136a0001c0001t0001g0189a0001c0001t0002g0093others(34): Show | 37 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.2599+343T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674001 | ||||||
| chr17:50674001
|
TC | T | 10 | a0001c0001t0002g0342a0001c0002t0001g0221a0001c0003t0001g0239others(7): Show | 10 | HG01258.hp1 HG02055.hp1 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.2599+344delC | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674001 | ||||||
| chr17:50674002
|
C | CCTTCCTT others(23): Show |
1 | a0007c0012t0003g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2599+344_2599+345i others(32): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674002 | ||||||
| chr17:50674002
|
C | T | 74 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0034others(71): Show | 74 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.2599+344C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674002 | ||||||
| chr17:50674002
|
CTCTCTCT others(40): Show |
C | 1 | a0002c0036t0001g0230 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2599+346_2599+392d others(49): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674002 | |||||
| chr17:50674004
|
C | T | 28 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0159others(25): Show | 28 | HG00544.hp1 HG00642.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.2599+346C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674004 | ||||||
| chr17:50674005
|
T | C | 48 | a0001c0001t0001g0136a0001c0001t0001g0189a0001c0001t0002g0093others(45): Show | 48 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(45): Show |
intron_variant | MODIFIER | c.2599+347T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674005 | ||||||
| chr17:50674005
|
TC | T | 11 | a0001c0001t0003g0314a0001c0003t0001g0153a0001c0003t0001g0158others(8): Show | 11 | HG00558.hp2 HG01099.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.2599+348delC | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674005 | ||||||
| chr17:50674006
|
C | T | 90 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0019others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2599+348C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674006 | ||||||
| chr17:50674007
|
T | C | 1 | a0001c0001t0001g0240 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2599+349T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674007 | ||||||
| chr17:50674008
|
C | T | 20 | a0001c0001t0001g0159a0001c0001t0001g0165a0001c0001t0001g0172others(17): Show | 20 | HG00544.hp1 HG00642.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.2599+350C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674008 | ||||||
| chr17:50674009
|
T | C | 60 | a0001c0001t0001g0034a0001c0001t0001g0136a0001c0001t0001g0189others(57): Show | 60 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.2599+351T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674009 | ||||||
| chr17:50674009
|
TC | T | 3 | a0001c0001t0003g0073a0001c0003t0001g0070a0001c0013t0001g0098 | 3 | HG01099.hp1 HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2599+352delC | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674009 | ||||||
| chr17:50674010
|
C | CTTCTTTC others(14): Show |
1 | a0001c0001t0001g0080 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2599+353_2599+354i others(23): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674010 | |||||
| chr17:50674010
|
C | T | 109 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.2599+352C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674010 | ||||||
| chr17:50674012
|
C | T | 12 | a0001c0002t0001g0225a0001c0002t0001g0227a0001c0004t0001g0059others(9): Show | 12 | HG00544.hp1 HG00642.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.2599+354C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674012 | ||||||
| chr17:50674013
|
T | C | 62 | a0001c0001t0001g0136a0001c0001t0001g0189a0001c0001t0002g0093others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.2599+355T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674013 | ||||||
| chr17:50674013
|
TC | T | 3 | a0001c0009t0001g0007a0005c0008t0001g0313a0023c0020t0001g0063 | 3 | HG03139.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2599+356delC | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674013 | ||||||
| chr17:50674014
|
C | T | 123 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.2599+356C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674014 | ||||||
| chr17:50674014
|
CTCTCTCT others(37): Show |
C | 2 | a0001c0004t0003g0267a0004c0023t0001g0004 | 2 | HG01884.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.2599+360_2599+403d others(46): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674014 | |||||
| chr17:50674015
|
T | TCTCTCTC others(78): Show |
1 | a0001c0001t0001g0272 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2599+379_2599+380i others(87): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674015 | |||||
| chr17:50674016
|
C | T | 9 | a0001c0004t0001g0059a0001c0004t0001g0145a0001c0004t0001g0243others(6): Show | 9 | HG00544.hp1 HG00642.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.2599+358C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674016 | ||||||
| chr17:50674016
|
CTCTCTCT others(22): Show |
C | 1 | a0016c0032t0001g0033 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2599+360_2599+388d others(31): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674016 | |||||
| chr17:50674017
|
T | C | 66 | a0001c0001t0001g0120a0001c0001t0001g0136a0001c0001t0001g0189others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.2599+359T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674017 | ||||||
| chr17:50674018
|
C | CCTTCCTT others(43): Show |
1 | a0007c0012t0003g0304 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2599+360_2599+361i others(52): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674018 | ||||||
| chr17:50674018
|
C | T | 141 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.2599+360C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674018 | ||||||
| chr17:50674018
|
CTCTCTCT others(21): Show |
C | 1 | a0002c0006t0001g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2599+364_2599+391d others(30): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674018 | |||||
| chr17:50674020
|
C | T | 6 | a0001c0004t0001g0059a0001c0004t0001g0145a0001c0004t0001g0243others(3): Show | 6 | HG01928.hp1 HG01934.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.2599+362C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674020 | ||||||
| chr17:50674020
|
CTCTCTCT others(31): Show |
C | 1 | a0001c0001t0001g0310 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2599+366_2599+403d others(40): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674020 | |||||
| chr17:50674021
|
T | C | 67 | a0001c0001t0001g0013a0001c0001t0001g0136a0001c0001t0001g0189others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.2599+363T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674021 | ||||||
| chr17:50674022
|
C | T | 161 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.2599+364C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674022 | ||||||
| chr17:50674022
|
CTCTCTCT others(9): Show |
C | 1 | a0001c0001t0001g0152 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2599+368_2599+383d others(18): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674022 | |||||
| chr17:50674022
|
CTCTCTCT others(17): Show |
C | 1 | a0001c0001t0001g0044 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2599+368_2599+391d others(26): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674022 | |||||
| chr17:50674024
|
C | T | 3 | a0001c0004t0001g0145a0001c0004t0001g0243a0013c0034t0001g0144 | 3 | HG01934.hp1 HG02074.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2599+366C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674024 | ||||||
| chr17:50674024
|
CTCTCTCT others(18): Show |
C | 1 | a0002c0006t0001g0334 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2599+368_2599+392d others(27): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674024 | |||||
| chr17:50674024
|
CTCTCTCT others(27): Show |
C | 1 | a0001c0001t0001g0188 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2599+370_2599+403d others(36): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674024 | |||||
| chr17:50674024
|
CTCTCTCT others(31): Show |
C | 1 | a0001c0001t0001g0125 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2599+370_2599+407d others(40): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674024 | |||||
| chr17:50674025
|
T | C | 67 | a0001c0001t0001g0136a0001c0001t0001g0189a0001c0001t0002g0093others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.2599+367T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674025 | ||||||
| chr17:50674026
|
C | T | 178 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.2599+368C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674026 | ||||||
| chr17:50674026
|
CTCTCTCT others(5): Show |
C | 1 | a0001c0001t0001g0142 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2599+372_2599+383d others(14): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674026 | |||||
| chr17:50674026
|
CTCTCTCT others(9): Show |
C | 1 | a0001c0001t0001g0046 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2599+372_2599+387d others(18): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674026 | |||||
| chr17:50674028
|
C | T | 2 | a0001c0004t0001g0145a0013c0034t0001g0144 | 2 | HG02074.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2599+370C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674028 | ||||||
| chr17:50674028
|
CTCTCTCT others(11): Show |
C | 1 | a0002c0006t0001g0097 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2599+374_2599+391d others(20): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674028 | |||||
| chr17:50674028
|
CTCTCTCT others(27): Show |
C | 1 | a0001c0001t0001g0127 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2599+374_2599+407d others(36): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674028 | |||||
| chr17:50674029
|
T | C | 67 | a0001c0001t0001g0136a0001c0001t0001g0189a0001c0001t0002g0093others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.2599+371T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674029 | ||||||
| chr17:50674030
|
C | CTCTTCTT others(12): Show |
1 | a0001c0001t0001g0210 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2599+375_2599+376i others(21): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674030 | |||||
| chr17:50674030
|
C | CTCTTCTT others(16): Show |
1 | a0001c0038t0001g0191 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2599+375_2599+376i others(25): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674030 | |||||
| chr17:50674030
|
C | CTCTTTCT others(25): Show |
1 | a0001c0001t0001g0212 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2599+375_2599+376i others(34): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674030 | |||||
| chr17:50674030
|
C | CTTCTTTC others(26): Show |
1 | a0001c0001t0001g0185 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2599+373_2599+374i others(35): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674030 | |||||
| chr17:50674030
|
C | T | 189 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.2599+372C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674030 | ||||||
| chr17:50674030
|
CTCTCTCT others(9): Show |
C | 3 | a0001c0004t0001g0061a0002c0006t0001g0001a0002c0006t0001g0104 | 3 | HG00544.hp2 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2599+376_2599+391d others(18): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674030 | |||||
| chr17:50674030
|
CTCTCTCT others(21): Show |
C | 1 | a0020c0030t0001g0337 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2599+376_2599+403d others(30): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674030 | |||||
| chr17:50674033
|
T | C | 66 | a0001c0001t0001g0136a0001c0001t0001g0189a0001c0001t0002g0093others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.2599+375T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674033 | ||||||
| chr17:50674033
|
T | TCTCTCTC others(86): Show |
1 | a0001c0001t0001g0054 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2599+379_2599+380i others(95): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674033 | |||||
| chr17:50674034
|
C | CTCTCTCT others(23): Show |
1 | a0001c0001t0001g0184 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2599+379_2599+380i others(32): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674034 | |||||
| chr17:50674034
|
C | CTCTCTCT others(35): Show |
1 | a0001c0001t0001g0079 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2599+379_2599+380i others(44): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674034 | |||||
| chr17:50674034
|
C | CTCTCTCT others(33): Show |
1 | a0001c0001t0001g0174 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2599+379_2599+380i others(42): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674034 | |||||
| chr17:50674034
|
C | CTCTCTCT others(23): Show |
3 | a0001c0001t0001g0077a0001c0001t0001g0179a0001c0026t0001g0148 | 3 | HG01517.hp1 HG01993.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.2599+379_2599+380i others(32): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674034 | |||||
| chr17:50674034
|
C | CTCTCTCT others(27): Show |
2 | a0001c0001t0001g0109a0001c0001t0001g0333 | 2 | HG01169.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2599+379_2599+380i others(36): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674034 | |||||
| chr17:50674034
|
C | CTCTCTCT others(33): Show |
1 | a0001c0001t0001g0222 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2599+379_2599+380i others(42): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674034 | |||||
| chr17:50674034
|
C | CTCTCTTT others(23): Show |
1 | a0001c0001t0001g0143 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2599+379_2599+380i others(32): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674034 | |||||
| chr17:50674034
|
C | CTCTCTTT others(27): Show |
2 | a0001c0001t0001g0108a0001c0001t0001g0172 | 2 | HG01070.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.2599+379_2599+380i others(36): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674034 | |||||
| chr17:50674034
|
C | CTCTTCTT others(16): Show |
1 | a0001c0001t0001g0322 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2599+380_2599+381i others(25): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674034 | |||||
| chr17:50674034
|
C | CTCTTTCT others(21): Show |
1 | a0001c0001t0001g0076 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2599+390_2599+417d others(30): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674034 | |||||
| chr17:50674034
|
C | CTCTTTCT others(25): Show |
2 | a0001c0001t0001g0275a0001c0001t0001g0330 | 2 | HG01167.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.2599+386_2599+417d others(34): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674034 | |||||
| chr17:50674034
|
C | CTCTTTCT others(29): Show |
1 | a0001c0001t0001g0159 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2599+382_2599+417d others(38): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674034 | |||||
| chr17:50674034
|
C | CTTCTTTC others(22): Show |
1 | a0001c0001t0001g0167 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2599+377_2599+378i others(31): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674034 | |||||
| chr17:50674034
|
C | CTTCTTTC others(26): Show |
1 | a0001c0024t0001g0287 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2599+377_2599+378i others(35): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674034 | |||||
| chr17:50674034
|
C | CTTTCTTT others(19): Show |
1 | a0001c0001t0001g0182 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2599+377_2599+378i others(28): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674034 | |||||
| chr17:50674034
|
C | CTTTCTTT others(27): Show |
2 | a0001c0001t0001g0193a0001c0001t0001g0253 | 2 | NA18964.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2599+377_2599+378i others(36): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674034 | |||||
| chr17:50674034
|
C | CTTTCTTT others(35): Show |
1 | a0001c0001t0001g0186 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2599+377_2599+378i others(44): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674034 | |||||
| chr17:50674034
|
C | T | 200 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.2599+376C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674034 | ||||||
| chr17:50674034
|
CTCTT | C | 3 | a0001c0001t0001g0128a0001c0001t0001g0194a0019c0028t0001g0138 | 3 | HG02165.hp2 NA19007.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.2599+414_2599+417d others(6): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674034 | |||||
| chr17:50674034
|
CTCTTTCT others(1): Show |
C | 3 | a0001c0001t0001g0115a0001c0001t0001g0327a0002c0006t0001g0232 | 3 | HG01891.hp2 HG03130.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.2599+410_2599+417d others(10): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674034 | |||||
| chr17:50674034
|
CTCTTTCT others(5): Show |
C | 3 | a0001c0001t0001g0113a0001c0001t0001g0133a0001c0001t0001g0208 | 3 | HG03927.hp1 NA18522.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2599+406_2599+417d others(14): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674034 | |||||
| chr17:50674034
|
CTCTTTCT others(9): Show |
C | 2 | a0001c0001t0001g0309a0001c0014t0001g0171 | 2 | NA19085.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2599+402_2599+417d others(18): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674034 | |||||
| chr17:50674034
|
CTCTTTCT others(13): Show |
C | 2 | a0001c0001t0001g0196a0001c0001t0001g0323 | 2 | NA18940.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.2599+398_2599+417d others(22): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674034 | |||||
| chr17:50674034
|
CTCTTTCT others(17): Show |
C | 4 | a0001c0001t0001g0106a0001c0001t0001g0112a0001c0001t0001g0307others(1): Show | 4 | HG02055.hp2 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2599+394_2599+417d others(26): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674034 | |||||
| chr17:50674036
|
CTT | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0130a0001c0001t0001g0135others(2): Show | 5 | HG00438.hp1 HG02886.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.2599+380_2599+381d others(4): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674036 | |||||
| chr17:50674036
|
CTTTCTTT others(3): Show |
C | 3 | a0002c0006t0001g0023a0002c0010t0001g0116a0024c0041t0001g0095 | 3 | HG03225.hp1 HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2599+380_2599+389d others(12): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674036 | |||||
| chr17:50674036
|
CTTTCTTT others(7): Show |
C | 9 | a0001c0001t0001g0064a0001c0001t0001g0081a0001c0001t0001g0084others(6): Show | 9 | HG00735.hp1 HG01081.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.2599+380_2599+393d others(16): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674036 | |||||
| chr17:50674036
|
CTTTCTTT others(11): Show |
C | 4 | a0001c0001t0001g0031a0001c0001t0001g0131a0001c0001t0001g0132others(1): Show | 4 | HG01952.hp2 HG02976.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.2599+380_2599+397d others(20): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674036 | |||||
| chr17:50674036
|
CTTTCTTT others(15): Show |
C | 3 | a0001c0001t0001g0053a0001c0001t0001g0114a0001c0004t0001g0319 | 3 | HG00733.hp1 HG02109.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.2599+380_2599+401d others(24): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674036 | |||||
| chr17:50674037
|
T | C | 65 | a0001c0001t0001g0136a0001c0001t0001g0189a0001c0001t0002g0093others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.2599+379T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674037 | ||||||
| chr17:50674038
|
T | C | 53 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0039others(50): Show | 53 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.2599+380T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674038 | ||||||
| chr17:50674038
|
T | TCTCTCTC others(65): Show |
1 | a0001c0001t0001g0123 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2599+380_2599+381i others(74): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674038 | ||||||
| chr17:50674041
|
T | C | 65 | a0001c0001t0001g0136a0001c0001t0001g0189a0001c0001t0002g0093others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.2599+383T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674041 | ||||||
| chr17:50674042
|
T | C | 46 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0039others(43): Show | 46 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.2599+384T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674042 | ||||||
| chr17:50674044
|
CTTTCTTT others(14): Show |
C | 1 | a0001c0001t0001g0325 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2599+389_2599+409d others(23): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674044 | |||||
| chr17:50674045
|
T | C | 65 | a0001c0001t0001g0136a0001c0001t0001g0189a0001c0001t0002g0093others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.2599+387T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674045 | ||||||
| chr17:50674046
|
T | C | 45 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0039others(42): Show | 45 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.2599+388T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674046 | ||||||
| chr17:50674049
|
T | C | 32 | a0001c0001t0001g0136a0001c0001t0001g0189a0001c0001t0002g0093others(29): Show | 32 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.2599+391T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674049 | ||||||
| chr17:50674050
|
T | C | 46 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0039others(43): Show | 46 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.2599+392T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674050 | ||||||
| chr17:50674053
|
T | C | 1 | a0002c0010t0001g0026 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2599+395T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674053 | ||||||
| chr17:50674053
|
TTTCTTTC others(4): Show |
T | 1 | a0001c0001t0001g0047 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2599+398_2599+408d others(13): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674053 | |||||
| chr17:50674054
|
T | C | 53 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0039others(50): Show | 53 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.2599+396T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674054 | ||||||
| chr17:50674055
|
T | C | 1 | a0001c0001t0001g0320 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2599+397T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674055 | ||||||
| chr17:50674058
|
T | C | 59 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0031others(56): Show | 59 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.2599+400T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674058 | ||||||
| chr17:50674062
|
T | C | 54 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0039others(51): Show | 54 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.2599+404T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674062 | ||||||
| chr17:50674065
|
T | C | 1 | a0001c0001t0001g0047 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2599+407T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674065 | ||||||
| chr17:50674065
|
T | TCTCTCTC others(6): Show |
1 | a0001c0001t0001g0088 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2599+407_2599+408i others(15): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674065 | ||||||
| chr17:50674066
|
T | C | 2 | a0001c0001t0001g0201a0001c0001t0001g0207 | 2 | HG02273.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.2599+408T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674066 | ||||||
| chr17:50674072
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2599+414C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674072 | ||||||
| chr17:50674075
|
T | C | 1 | a0001c0002t0001g0155 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2599+417T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674075 | ||||||
| chr17:50674075
|
T | TCTTTCTT others(22): Show |
1 | a0001c0001t0001g0107 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2599+417_2599+418i others(31): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674075 | ||||||
| chr17:50674077
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2599+419T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674077 | ||||||
| chr17:50674081
|
C | A | 1 | a0001c0003t0001g0176 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2599+423C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674081 | ||||||
| chr17:50674136
|
A | G | 2 | a0007c0012t0003g0069a0007c0012t0003g0304 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2599+478A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674136 | ||||||
| chr17:50674215
|
C | T | 1 | a0001c0001t0003g0073 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2599+557C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674215 | ||||||
| chr17:50674216
|
G | A | 2 | a0007c0012t0003g0069a0007c0012t0003g0304 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2599+558G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674216 | ||||||
| chr17:50674224
|
G | A | 26 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0001g0042others(23): Show | 26 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.2599+566G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674224 | ||||||
| chr17:50674260
|
TTTCACCA others(6): Show |
T | 1 | a0001c0001t0001g0320 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2599+603_2599+615d others(15): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674260 | ||||||
| chr17:50674360
|
C | T | 31 | a0001c0001t0001g0136a0001c0001t0001g0189a0001c0001t0002g0093others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.2599+702C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674360 | ||||||
| chr17:50674375
|
T | G | 1 | a0001c0001t0001g0054 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2599+717T>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674375 | ||||||
| chr17:50674391
|
A | G | 1 | a0001c0001t0001g0199 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2599+733A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674391 | ||||||
| chr17:50674394
|
A | G | 1 | a0022c0035t0001g0040 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2599+736A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674394 | ||||||
| chr17:50674400
|
G | A | 96 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0017others(93): Show | 96 | HG00323.hp2 HG00438.hp2 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.2599+742G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674400 | ||||||
| chr17:50674798
|
A | AT | 84 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0034others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.2600-546dupT | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674798 | |||||
| chr17:50674798
|
A | ATT | 18 | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0048others(15): Show | 18 | HG00408.hp2 HG00738.hp2 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.2600-547_2600-546d others(4): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674798 | |||||
| chr17:50674816
|
TG | T | 13 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0124others(10): Show | 13 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.2600-542delG | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | 50674816 | |||||
| chr17:50674817
|
G | T | 327 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(324): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.2600-545G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674817 | ||||||
| chr17:50674818
|
G | T | 1 | a0001c0001t0001g0054 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2600-544G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674818 | ||||||
| chr17:50674902
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2600-460C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674902 | ||||||
| chr17:50674924
|
C | T | 5 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0120others(2): Show | 5 | HG02622.hp1 HG02818.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2600-438C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674924 | ||||||
| chr17:50674961
|
G | A | 2 | a0001c0002t0001g0032a0001c0004t0001g0318 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2600-401G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674961 | ||||||
| chr17:50674989
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2600-373G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50674989 | ||||||
| chr17:50675018
|
T | C | 30 | a0001c0001t0001g0136a0001c0001t0002g0093a0001c0001t0002g0096others(27): Show | 30 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(27): Show |
intron_variant | MODIFIER | c.2600-344T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50675018 | ||||||
| chr17:50675038
|
G | A | 2 | a0001c0003t0001g0204a0001c0003t0001g0284 | 2 | HG00280.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2600-324G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50675038 | ||||||
| chr17:50675044
|
T | C | 67 | a0001c0001t0001g0136a0001c0001t0002g0093a0001c0001t0002g0096others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.2600-318T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50675044 | ||||||
| chr17:50675077
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2600-285C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50675077 | ||||||
| chr17:50675103
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0120a0001c0017t0001g0233 | 3 | HG02622.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2600-259C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50675103 | ||||||
| chr17:50675216
|
T | C | 4 | a0001c0001t0001g0308a0001c0001t0001g0309a0001c0001t0001g0310others(1): Show | 4 | HG02615.hp1 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2600-146T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50675216 | ||||||
| chr17:50675238
|
C | A | 12 | a0002c0006t0001g0001a0002c0006t0001g0003a0002c0006t0001g0023others(9): Show | 12 | HG01081.hp2 HG01891.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.2600-124C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50675238 | ||||||
| chr17:50675239
|
C | T | 108 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0017others(105): Show | 108 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.2600-123C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | 50675239 | ||||||
| chr17:50675505
|
C | T | 108 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0017others(105): Show | 108 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.2714+29C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 20/30 | chr17 | 50675505 | ||||||
| chr17:50675529
|
G | A | 216 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(213): Show | 216 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.2714+53G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 20/30 | chr17 | 50675529 | ||||||
| chr17:50675602
|
T | C | 1 | a0013c0034t0001g0144 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2715-29T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 20/30 | chr17 | 50675602 | ||||||
| chr17:50675603
|
C | T | 1 | a0013c0034t0001g0144 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2715-28C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 20/30 | chr17 | 50675603 | ||||||
| chr17:50676161
|
C | T | 22 | a0001c0001t0001g0136a0001c0001t0002g0093a0001c0001t0002g0099others(19): Show | 22 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(19): Show |
intron_variant | MODIFIER | c.3067+71C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 22/30 | chr17 | 50676161 | ||||||
| chr17:50676205
|
G | A | 1 | a0001c0004t0001g0145 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3068-73G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 22/30 | chr17 | 50676205 | ||||||
| chr17:50676615
|
G | A | 6 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0120others(3): Show | 6 | HG02622.hp1 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.3378+27G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 23/30 | chr17 | 50676615 | ||||||
| chr17:50676635
|
G | A | 2 | a0001c0001t0001g0286a0001c0001t0001g0338 | 2 | HG00738.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.3378+47G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 23/30 | chr17 | 50676635 | ||||||
| chr17:50676651
|
G | T | 1 | a0001c0001t0001g0084 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3378+63G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 23/30 | chr17 | 50676651 | ||||||
| chr17:50676707
|
G | C | 1 | a0001c0001t0001g0054 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3378+119G>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 23/30 | chr17 | 50676707 | ||||||
| chr17:50676708
|
C | A | 1 | a0001c0001t0001g0054 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3378+120C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 23/30 | chr17 | 50676708 | ||||||
| chr17:50676709
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3378+121A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 23/30 | chr17 | 50676709 | ||||||
| chr17:50676847
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3378+259G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 23/30 | chr17 | 50676847 | ||||||
| chr17:50676879
|
T | G | 101 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0017others(98): Show | 101 | HG00323.hp2 HG00438.hp2 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.3378+291T>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 23/30 | chr17 | 50676879 | ||||||
| chr17:50676885
|
TTGGG | T | 102 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0017others(99): Show | 102 | HG00323.hp2 HG00438.hp2 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.3378+298_3378+301d others(6): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 23/30 | chr17 | 50676885 | ||||||
| chr17:50676886
|
TG | T | 31 | a0001c0001t0001g0091a0001c0003t0001g0070a0001c0003t0001g0153others(28): Show | 31 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.3378+310delG | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 23/30 | INFO_REALIGN_3_PRIME | chr17 | 50676886 | |||||
| chr17:50676886
|
TGG | T | 22 | a0001c0001t0001g0013a0001c0001t0001g0120a0001c0001t0001g0135others(19): Show | 22 | HG00738.hp2 HG01069.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.3378+309_3378+310d others(4): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 23/30 | INFO_REALIGN_3_PRIME | chr17 | 50676886 | |||||
| chr17:50676886
|
TGGG | T | 140 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0016others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.3378+308_3378+310d others(5): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 23/30 | INFO_REALIGN_3_PRIME | chr17 | 50676886 | |||||
| chr17:50676887
|
G | T | 1 | a0001c0003t0001g0219 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3378+299G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 23/30 | chr17 | 50676887 | ||||||
| chr17:50676889
|
G | T | 3 | a0001c0001t0001g0135a0001c0001t0001g0180a0003c0005t0002g0085 | 3 | HG00738.hp2 HG01346.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.3378+301G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 23/30 | chr17 | 50676889 | ||||||
| chr17:50676892
|
G | T | 214 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(211): Show | 214 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.3378+304G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 23/30 | chr17 | 50676892 | ||||||
| chr17:50676895
|
G | C | 1 | a0001c0004t0003g0267 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3378+307G>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 23/30 | chr17 | 50676895 | ||||||
| chr17:50677004
|
C | T | 11 | a0002c0006t0001g0001a0002c0006t0001g0003a0002c0006t0001g0023others(8): Show | 11 | HG01081.hp2 HG01891.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.3378+416C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 23/30 | chr17 | 50677004 | ||||||
| chr17:50677199
|
T | A | 1 | a0001c0001t0001g0169 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3379-545T>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 23/30 | chr17 | 50677199 | ||||||
| chr17:50677374
|
TC | T | 3 | a0001c0002t0001g0156a0001c0002t0001g0157a0001c0002t0001g0160 | 3 | HG02155.hp1 NA18955.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.3379-367delC | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 23/30 | INFO_REALIGN_3_PRIME | chr17 | 50677374 | |||||
| chr17:50677593
|
G | A | 1 | a0017c0029t0001g0229 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3379-151G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 23/30 | chr17 | 50677593 | ||||||
| chr17:50677641
|
G | A | 78 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0031others(75): Show | 78 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.3379-103G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 23/30 | chr17 | 50677641 | ||||||
| chr17:50678027
|
C | T | 37 | a0001c0003t0001g0070a0001c0003t0001g0153a0001c0003t0001g0158others(34): Show | 37 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.3579-66C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 24/30 | chr17 | 50678027 | ||||||
| chr17:50678045
|
G | GCCCTGCC others(4): Show |
2 | a0001c0004t0001g0117a0023c0020t0001g0063 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3579-39_3579-29dup others(11): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 24/30 | INFO_REALIGN_3_PRIME | chr17 | 50678045 | |||||
| chr17:50678089
|
A | G | 4 | a0001c0002t0001g0156a0001c0002t0001g0157a0001c0002t0001g0160others(1): Show | 4 | HG02155.hp1 NA18955.hp2 NA18963.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.3579-4A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 24/30 | chr17 | 50678089 | ||||||
| chr17:50678280
|
C | T | 9 | a0002c0006t0001g0001a0002c0006t0001g0003a0002c0006t0001g0023others(6): Show | 9 | HG01081.hp2 HG01891.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3705+61C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 25/30 | chr17 | 50678280 | ||||||
| chr17:50678377
|
A | T | 11 | a0002c0006t0001g0001a0002c0006t0001g0003a0002c0006t0001g0023others(8): Show | 11 | HG01081.hp2 HG01891.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.3705+158A>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 25/30 | chr17 | 50678377 | ||||||
| chr17:50678519
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3705+300G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 25/30 | chr17 | 50678519 | ||||||
| chr17:50678652
|
G | C | 1 | a0001c0001t0001g0161 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.3705+433G>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 25/30 | chr17 | 50678652 | ||||||
| chr17:50678876
|
C | T | 1 | a0002c0010t0001g0247 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3705+657C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 25/30 | chr17 | 50678876 | ||||||
| chr17:50678926
|
GA | G | 63 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0001g0042others(60): Show | 63 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.3705+718delA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 25/30 | INFO_REALIGN_3_PRIME | chr17 | 50678926 | |||||
| chr17:50679201
|
C | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0159others(1): Show | 4 | HG01069.hp1 HG01070.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.3706-597C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 25/30 | chr17 | 50679201 | ||||||
| chr17:50679351
|
A | G | 7 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0159others(4): Show | 7 | HG01069.hp1 HG01070.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.3706-447A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 25/30 | chr17 | 50679351 | ||||||
| chr17:50679576
|
C | T | 94 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0017others(91): Show | 94 | HG00323.hp2 HG00438.hp2 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.3706-222C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 25/30 | chr17 | 50679576 | ||||||
| chr17:50679920
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3807+21G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50679920 | ||||||
| chr17:50680246
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3807+347G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50680246 | ||||||
| chr17:50680417
|
C | T | 1 | a0024c0041t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3807+518C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50680417 | ||||||
| chr17:50680486
|
C | T | 10 | a0002c0006t0001g0001a0002c0006t0001g0003a0002c0006t0001g0097others(7): Show | 10 | HG01081.hp2 HG01891.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.3807+587C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50680486 | ||||||
| chr17:50680550
|
G | A | 28 | a0001c0001t0001g0136a0001c0001t0002g0093a0001c0001t0002g0099others(25): Show | 28 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.3807+651G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50680550 | ||||||
| chr17:50680587
|
C | G | 9 | a0002c0006t0001g0001a0002c0006t0001g0003a0002c0006t0001g0097others(6): Show | 9 | HG01081.hp2 HG01891.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3807+688C>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50680587 | ||||||
| chr17:50680927
|
A | G | 3 | a0001c0002t0001g0090a0001c0002t0001g0092a0001c0002t0001g0276 | 3 | HG01106.hp1 HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3807+1028A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50680927 | ||||||
| chr17:50680927
|
A | T | 338 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(335): Show | 338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.3807+1028A>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50680927 | ||||||
| chr17:50680940
|
G | A | 91 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0034others(88): Show | 91 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.3807+1041G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50680940 | ||||||
| chr17:50680950
|
C | G | 3 | a0001c0002t0001g0090a0001c0002t0001g0092a0001c0002t0001g0276 | 3 | HG01106.hp1 HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3807+1051C>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50680950 | ||||||
| chr17:50681074
|
TA | T | 10 | a0001c0004t0001g0059a0001c0004t0001g0100a0001c0004t0001g0145others(7): Show | 10 | HG00544.hp1 HG01928.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.3807+1188delA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr17 | 50681074 | |||||
| chr17:50681269
|
C | G | 1 | a0001c0027t0001g0015 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3807+1370C>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50681269 | ||||||
| chr17:50681455
|
C | T | 1 | a0016c0032t0001g0033 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3807+1556C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50681455 | ||||||
| chr17:50681810
|
C | G | 1 | a0001c0004t0003g0267 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3808-1800C>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50681810 | ||||||
| chr17:50681825
|
G | T | 1 | a0001c0004t0003g0267 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3808-1785G>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50681825 | ||||||
| chr17:50681913
|
C | T | 2 | a0007c0012t0003g0069a0007c0012t0003g0304 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3808-1697C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50681913 | ||||||
| chr17:50681992
|
T | C | 1 | a0017c0029t0001g0229 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3808-1618T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50681992 | ||||||
| chr17:50682096
|
G | A | 1 | a0016c0032t0001g0033 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3808-1514G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50682096 | ||||||
| chr17:50682192
|
G | A | 2 | a0007c0012t0003g0069a0007c0012t0003g0304 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3808-1418G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50682192 | ||||||
| chr17:50682345
|
T | TA | 42 | a0001c0001t0001g0091a0001c0001t0001g0178a0001c0001t0001g0185others(39): Show | 42 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.3808-1245dupA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr17 | 50682345 | |||||
| chr17:50682345
|
TA | T | 147 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0031others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.3808-1245delA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr17 | 50682345 | |||||
| chr17:50682345
|
TAA | T | 17 | a0001c0001t0001g0047a0001c0001t0001g0086a0001c0001t0001g0193others(14): Show | 17 | HG01891.hp2 HG01934.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.3808-1246_3808-124 others(6): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr17 | 50682345 | |||||
| chr17:50682346
|
A | T | 2 | a0001c0001t0003g0073a0001c0001t0003g0314 | 2 | HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.3808-1264A>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50682346 | ||||||
| chr17:50682498
|
C | T | 1 | a0001c0004t0003g0267 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3808-1112C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50682498 | ||||||
| chr17:50682769
|
C | G | 27 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0001g0042others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.3808-841C>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50682769 | ||||||
| chr17:50682969
|
C | T | 1 | a0001c0004t0003g0267 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3808-641C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50682969 | ||||||
| chr17:50683024
|
C | T | 2 | a0001c0004t0001g0117a0023c0020t0001g0063 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3808-586C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50683024 | ||||||
| chr17:50683246
|
CTGT | C | 26 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0001g0042others(23): Show | 26 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.3808-360_3808-358d others(5): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr17 | 50683246 | |||||
| chr17:50683259
|
A | C | 1 | a0001c0001t0001g0285 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3808-351A>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50683259 | ||||||
| chr17:50683288
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3808-322C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50683288 | ||||||
| chr17:50683350
|
TA | T | 28 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0039others(25): Show | 28 | HG00544.hp1 HG01169.hp2 HG01928.hp1 others(25): Show |
intron_variant | MODIFIER | c.3808-243delA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr17 | 50683350 | |||||
| chr17:50683448
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3808-162G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50683448 | ||||||
| chr17:50683471
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3808-139G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | chr17 | 50683471 | ||||||
| chr17:50683535
|
T | TG | 10 | a0001c0001t0001g0041a0001c0001t0001g0053a0001c0001t0001g0077others(7): Show | 10 | HG00733.hp1 HG00735.hp1 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.3808-70dupG | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr17 | 50683535 | |||||
| chr17:50683827
|
C | T | 1 | a0023c0020t0001g0063 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3954+71C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 27/30 | chr17 | 50683827 | ||||||
| chr17:50683862
|
A | T | 1 | a0001c0001t0001g0162 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3955-87A>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 27/30 | chr17 | 50683862 | ||||||
| chr17:50683943
|
G | A | 1 | a0002c0010t0001g0247 | 1 | NA20300.hp1 | splice_region_variant&intron_variant | LOW | c.3955-6G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 27/30 | chr17 | 50683943 | ||||||
| chr17:50684519
|
T | C | 51 | a0001c0001t0001g0136a0001c0003t0001g0070a0001c0003t0001g0153others(48): Show | 51 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.4114-190T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 28/30 | chr17 | 50684519 | ||||||
| chr17:50684899
|
C | T | 1 | a0001c0004t0001g0145 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.4280+24C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/30 | chr17 | 50684899 | ||||||
| chr17:50684919
|
G | C | 1 | a0003c0005t0002g0302 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4280+44G>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/30 | chr17 | 50684919 | ||||||
| chr17:50684948
|
G | A | 1 | a0001c0004t0003g0267 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4280+73G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/30 | chr17 | 50684948 | ||||||
| chr17:50685272
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.4280+397C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/30 | chr17 | 50685272 | ||||||
| chr17:50685291
|
C | T | 1 | a0002c0010t0001g0247 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4280+416C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/30 | chr17 | 50685291 | ||||||
| chr17:50685417
|
A | T | 140 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.4280+542A>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/30 | chr17 | 50685417 | ||||||
| chr17:50685624
|
A | C | 25 | a0001c0001t0002g0093a0001c0001t0002g0096a0001c0001t0002g0099others(22): Show | 25 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.4280+749A>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/30 | chr17 | 50685624 | ||||||
| chr17:50685748
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.4280+873G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/30 | chr17 | 50685748 | ||||||
| chr17:50685767
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.4280+892G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/30 | chr17 | 50685767 | ||||||
| chr17:50685831
|
T | C | 1 | a0001c0001t0001g0200 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.4280+956T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/30 | chr17 | 50685831 | ||||||
| chr17:50685832
|
C | T | 1 | a0001c0001t0001g0265 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.4280+957C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/30 | chr17 | 50685832 | ||||||
| chr17:50685833
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.4280+958C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/30 | chr17 | 50685833 | ||||||
| chr17:50685964
|
G | C | 1 | a0001c0003t0001g0070 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4280+1089G>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/30 | chr17 | 50685964 | ||||||
| chr17:50686156
|
T | G | 81 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0031others(78): Show | 81 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.4280+1281T>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/30 | chr17 | 50686156 | ||||||
| chr17:50686157
|
GCA | G | 81 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0031others(78): Show | 81 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.4280+1284_4280+128 others(6): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/30 | INFO_REALIGN_3_PRIME | chr17 | 50686157 | |||||
| chr17:50686162
|
C | A | 81 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0031others(78): Show | 81 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.4280+1287C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/30 | chr17 | 50686162 | ||||||
| chr17:50686163
|
T | G | 81 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0031others(78): Show | 81 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.4280+1288T>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/30 | chr17 | 50686163 | ||||||
| chr17:50686354
|
G | A | 44 | a0001c0002t0001g0009a0001c0002t0001g0021a0001c0002t0001g0032others(41): Show | 44 | HG00642.hp1 HG00733.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.4281-1182G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/30 | chr17 | 50686354 | ||||||
| chr17:50686521
|
C | T | 1 | a0001c0001t0001g0315 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4281-1015C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/30 | chr17 | 50686521 | ||||||
| chr17:50686529
|
G | A | 1 | a0001c0013t0001g0098 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4281-1007G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/30 | chr17 | 50686529 | ||||||
| chr17:50686537
|
G | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0206 | 2 | HG00423.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.4281-999G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/30 | chr17 | 50686537 | ||||||
| chr17:50686645
|
C | T | 1 | a0002c0006t0001g0334 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4281-891C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/30 | chr17 | 50686645 | ||||||
| chr17:50686929
|
C | T | 2 | a0001c0003t0001g0295a0001c0003t0001g0321 | 2 | HG02738.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.4281-607C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/30 | chr17 | 50686929 | ||||||
| chr17:50687075
|
C | A | 1 | a0002c0006t0001g0334 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4281-461C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 29/30 | chr17 | 50687075 | ||||||
| chr17:50687779
|
G | A | 2 | a0001c0004t0001g0117a0023c0020t0001g0063 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4475+49G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 30/30 | chr17 | 50687779 | ||||||
| chr17:50687850
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4475+120G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 30/30 | chr17 | 50687850 | ||||||
| chr17:50688014
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4475+284G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 30/30 | chr17 | 50688014 | ||||||
| chr17:50688024
|
G | A | 340 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(337): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.4475+294G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 30/30 | chr17 | 50688024 | ||||||
| chr17:50688025
|
C | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0248 | 2 | NA19007.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.4475+295C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 30/30 | chr17 | 50688025 | ||||||
| chr17:50688073
|
G | A | 2 | a0001c0001t0001g0053a0025c0015t0001g0328 | 2 | HG00733.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.4475+343G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 30/30 | chr17 | 50688073 | ||||||
| chr17:50688158
|
T | C | 61 | a0001c0001t0001g0136a0001c0001t0001g0178a0001c0001t0001g0275others(58): Show | 61 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.4475+428T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 30/30 | chr17 | 50688158 | ||||||
| chr17:50688201
|
C | T | 50 | a0001c0001t0001g0136a0001c0001t0001g0178a0001c0001t0001g0275others(47): Show | 50 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.4475+471C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 30/30 | chr17 | 50688201 | ||||||
| chr17:50688232
|
C | A | 1 | a0001c0001t0001g0317 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4475+502C>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 30/30 | chr17 | 50688232 | ||||||
| chr17:50688530
|
T | C | 14 | a0001c0001t0002g0093a0001c0001t0002g0099a0001c0001t0002g0281others(11): Show | 14 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(11): Show |
intron_variant | MODIFIER | c.4475+800T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 30/30 | chr17 | 50688530 | ||||||
| chr17:50688707
|
A | C | 1 | a0001c0002t0001g0294 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.4475+977A>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 30/30 | chr17 | 50688707 | ||||||
| chr17:50688763
|
G | A | 92 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(89): Show | 92 | HG00323.hp2 HG00438.hp2 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.4475+1033G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 30/30 | chr17 | 50688763 | ||||||
| chr17:50688860
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4475+1130G>A | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 30/30 | chr17 | 50688860 | ||||||
| chr17:50688902
|
CA | C | 80 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0016others(77): Show | 80 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.4475+1187delA | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr17 | 50688902 | |||||
| chr17:50689142
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.4475+1412C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 30/30 | chr17 | 50689142 | ||||||
| chr17:50689258
|
C | T | 35 | a0001c0002t0001g0009a0001c0002t0001g0021a0001c0002t0001g0032others(32): Show | 35 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.4475+1528C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 30/30 | chr17 | 50689258 | ||||||
| chr17:50689277
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4475+1547C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 30/30 | chr17 | 50689277 | ||||||
| chr17:50689351
|
T | G | 5 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0120others(2): Show | 5 | HG02622.hp1 HG02818.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.4475+1621T>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 30/30 | chr17 | 50689351 | ||||||
| chr17:50689376
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.4475+1646T>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 30/30 | chr17 | 50689376 | ||||||
| chr17:50689669
|
C | T | 3 | a0001c0001t0001g0132a0001c0001t0001g0135a0001c0001t0001g0137 | 3 | NA18974.hp2 NA19054.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.4476-1423C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 30/30 | chr17 | 50689669 | ||||||
| chr17:50689709
|
C | G | 12 | a0001c0001t0001g0167a0001c0003t0001g0217a0001c0003t0001g0218others(9): Show | 12 | HG00544.hp1 HG01346.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.4476-1383C>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 30/30 | chr17 | 50689709 | ||||||
| chr17:50690070
|
A | C | 77 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0031others(74): Show | 77 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.4476-1022A>C | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 30/30 | chr17 | 50690070 | ||||||
| chr17:50690730
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0139 | 2 | NA18969.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.4476-362C>T | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 30/30 | chr17 | 50690730 | ||||||
| chr17:50690747
|
A | G | 12 | a0001c0001t0001g0167a0001c0003t0001g0217a0001c0003t0001g0218others(9): Show | 12 | HG00544.hp1 HG01346.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.4476-345A>G | ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 30/30 | chr17 | 50690747 |