Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 10057 |
|---|---|
| ensemblid | ENSG00000114770.17 |
| hgncid | 56 |
| symbol | ABCC5 |
| name | ATP binding cassette subfamily C member 5 |
| refseq_nuc | NM_005688.4 |
| refseq_prot | NP_005679.2 |
| ensembl_nuc | ENST00000334444.11 |
| ensembl_prot | ENSP00000333926.6 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 183919934 |
| end | 184017884 |
| strand | - |
| ver | v1.2 |
| region | chr3:183919934-184017884 |
| region5000 | chr3:183914934-184022884 |
| regionname0 | ABCC5_chr3_183919934_184017884 |
| regionname5000 | ABCC5_chr3_183914934_184022884 |
| 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 | 1437 | 370 | 88 | 63 | 164 | 14 | 39 | 124 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0002 | 0/0 | 1437 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0003 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0004 | 0/0 | 1437 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0005 | 0/0 | 1437 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0006 | 0/0 | 1016 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0007 | 0/0 | 1437 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0008 | 0/0 | 1437 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0009 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 4314 | 136 | 16 | 23 | 74 | 5 | 17 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| c0002 | 0/0 | 4314 | 106 | 21 | 16 | 61 | 1 | 7 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| c0003 | 1/0 | 4314 | 79 | 17 | 18 | 23 | 6 | 14 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| c0004 | 0/0 | 4314 | 29 | 26 | 3 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| c0005 | 0/0 | 4314 | 6 | 5 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| c0006 | 0/0 | 4314 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| c0007 | 0/0 | 4314 | 2 | 1 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| c0008 | 0/0 | 4314 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| c0009 | 0/0 | 4314 | 2 | 0 | 0 | 0 | 2 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| c0010 | 0/0 | 4314 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| c0011 | 0/0 | 4314 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| c0012 | 0/0 | 4314 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| c0013 | 0/0 | 4314 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| c0014 | 0/0 | 4314 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| c0015 | 0/0 | 4314 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| c0016 | 0/0 | 4314 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| c0017 | 0/0 | 4314 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| c0018 | 0/0 | 4314 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| c0019 | 0/0 | 4346 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| c0020 | 0/0 | 4314 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| c0021 | 0/0 | 4314 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| c0022 | 0/0 | 4314 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| c0023 | 0/0 | 4314 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| 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 | 0/1 | 1477 | 140 | 14 | 34 | 73 | 5 | 13 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| t0002 | 1/0 | 1477 | 84 | 22 | 15 | 26 | 6 | 14 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| t0003 | 0/0 | 1477 | 56 | 1 | 3 | 41 | 1 | 10 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| t0004 | 0/0 | 1477 | 27 | 24 | 3 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| t0005 | 0/0 | 1473 | 26 | 0 | 0 | 25 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| t0006 | 0/0 | 1477 | 13 | 8 | 5 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| t0007 | 0/0 | 1473 | 8 | 7 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| t0008 | 0/0 | 1477 | 6 | 5 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| t0009 | 0/0 | 1477 | 3 | 2 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| t0010 | 0/0 | 1477 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| t0011 | 0/0 | 1477 | 3 | 0 | 1 | 0 | 0 | 2 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| t0012 | 0/0 | 1477 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| t0013 | 0/0 | 1477 | 2 | 0 | 0 | 0 | 2 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| t0014 | 0/0 | 1477 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| t0015 | 0/0 | 1477 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| t0016 | 0/0 | 1477 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| t0017 | 0/0 | 1477 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| t0018 | 0/0 | 1473 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0159 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0335 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0349 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 4314 | 136 | 16 | 23 | 74 | 5 | 17 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0002 | 0/0 | 4314 | 106 | 21 | 16 | 61 | 1 | 7 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0003 | 1/0 | 4314 | 79 | 17 | 18 | 23 | 6 | 14 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0004 | 0/0 | 4314 | 29 | 26 | 3 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0005 | 0/0 | 4314 | 6 | 5 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0006 | 0/0 | 4314 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0007 | 0/0 | 4314 | 2 | 1 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0008 | 0/0 | 4314 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0009 | 0/0 | 4314 | 2 | 0 | 0 | 0 | 2 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0013 | 0/0 | 4314 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0016 | 0/0 | 4314 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0018 | 0/0 | 4314 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0020 | 0/0 | 4314 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0022 | 0/0 | 4314 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0023 | 0/0 | 4314 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0002c0011 | 0/0 | 4314 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0003c0017 | 0/0 | 4314 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0004c0021 | 0/0 | 4314 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0005c0014 | 0/0 | 4314 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0006c0019 | 0/0 | 4346 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0007c0012 | 0/0 | 4314 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0008c0015 | 0/0 | 4314 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0009c0010 | 0/0 | 4314 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5790 | 35 | 0 | 15 | 9 | 4 | 6 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0001t0003 | 0/0 | 5790 | 53 | 1 | 2 | 39 | 1 | 10 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0001t0005 | 0/0 | 5786 | 26 | 0 | 0 | 25 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0001t0006 | 0/0 | 5790 | 13 | 8 | 5 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0001t0007 | 0/0 | 5786 | 8 | 7 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0001t0016 | 0/0 | 5790 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0002t0001 | 0/0 | 5790 | 97 | 13 | 15 | 61 | 1 | 7 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0002t0008 | 0/0 | 5790 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0002t0009 | 0/0 | 5790 | 3 | 2 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0002t0012 | 0/0 | 5790 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0003t0002 | 1/0 | 5790 | 74 | 17 | 15 | 23 | 6 | 12 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0003t0011 | 0/0 | 5790 | 3 | 0 | 1 | 0 | 0 | 2 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0003t0015 | 0/0 | 5790 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0003t0017 | 0/0 | 5790 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0004t0002 | 0/0 | 5790 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0004t0004 | 0/0 | 5790 | 27 | 24 | 3 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0005t0002 | 0/0 | 5790 | 3 | 2 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0005t0010 | 0/0 | 5790 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0006t0002 | 0/0 | 5790 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0007t0008 | 0/0 | 5790 | 2 | 1 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0008t0001 | 0/0 | 5790 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0009t0013 | 0/0 | 5790 | 2 | 0 | 0 | 0 | 2 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0013t0003 | 0/0 | 5790 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0016t0014 | 0/0 | 5790 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0018t0002 | 0/0 | 5790 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0020t0001 | 0/0 | 5790 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0022t0003 | 0/0 | 5790 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0001c0023t0001 | 0/0 | 5790 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0002c0011t0001 | 0/0 | 5790 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0003c0017t0002 | 0/0 | 5790 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0004c0021t0003 | 0/0 | 5790 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0005c0014t0001 | 0/0 | 5790 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0006c0019t0002 | 0/0 | 5822 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0007c0012t0001 | 0/0 | 5790 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0008c0015t0001 | 0/0 | 5790 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| a0009c0010t0018 | 0/0 | 5786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | copy fasta | chr3 | 183914934 | 184022884 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0159 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0006g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0006g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0006g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0006g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0006g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0006g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0006g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0006g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0007g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0007g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0007g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0007g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0007g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0007g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0001t0016g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0008g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0008g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0008g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0008g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0009g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0009g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0009g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0012g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0002t0012g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0335 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0349 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0002g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0011g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0011g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0011g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0015g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0003t0017g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0004t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0005t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0005t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0005t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0005t0010g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0005t0010g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0005t0010g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0006t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0006t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0007t0008g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0007t0008g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0008t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0008t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0009t0013g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0009t0013g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0013t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0016t0014g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0018t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0020t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0022t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0001c0023t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0002c0011t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0003c0017t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0004c0021t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0005c0014t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0006c0019t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0007c0012t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0008c0015t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| a0009c0010t0018g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0003 | t0002 | g0300 | EUR | FIN | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00280 | hp2 | a0001 | c0003 | t0002 | g0328 | EUR | FIN | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | FIN | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00323 | hp2 | a0001 | c0003 | t0002 | g0309 | EUR | FIN | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00408 | hp1 | a0001 | c0001 | t0005 | g0187 | EAS | CHS | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | CHS | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0157 | EAS | CHS | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | CHS | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00438 | hp1 | a0001 | c0001 | t0005 | g0167 | EAS | CHS | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | CHS | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | CHS | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00558 | hp1 | a0001 | c0001 | t0005 | g0162 | EAS | CHS | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00558 | hp2 | a0001 | c0003 | t0002 | g0008 | EAS | CHS | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | CHS | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00621 | hp1 | a0001 | c0005 | t0002 | g0274 | EAS | CHS | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | CHS | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00639 | hp1 | a0001 | c0004 | t0004 | g0123 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00639 | hp2 | a0001 | c0003 | t0002 | g0348 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0158 | EAS | CHS | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00673 | hp2 | a0001 | c0003 | t0002 | g0337 | EAS | CHS | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0358 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00735 | hp2 | a0001 | c0013 | t0003 | g0090 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG00741 | hp2 | a0001 | c0003 | t0002 | g0325 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01069 | hp1 | a0001 | c0001 | t0006 | g0054 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01070 | hp1 | a0001 | c0003 | t0002 | g0357 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0053 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01071 | hp2 | a0001 | c0003 | t0002 | g0354 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01074 | hp1 | a0001 | c0003 | t0015 | g0322 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01106 | hp1 | a0001 | c0003 | t0002 | g0299 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01106 | hp2 | a0008 | c0015 | t0001 | g0043 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01109 | hp2 | a0001 | c0001 | t0007 | g0195 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01167 | hp2 | a0001 | c0004 | t0004 | g0133 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01169 | hp1 | a0001 | c0003 | t0002 | g0302 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01169 | hp2 | a0001 | c0004 | t0004 | g0134 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01175 | hp2 | a0001 | c0001 | t0006 | g0051 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0248 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0252 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0083 | AMR | PUR | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01256 | hp1 | a0001 | c0003 | t0002 | g0346 | AMR | CLM | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0351 | AMR | CLM | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01261 | hp1 | a0001 | c0001 | t0006 | g0052 | AMR | CLM | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01261 | hp2 | a0001 | c0003 | t0002 | g0316 | AMR | CLM | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01358 | hp2 | a0001 | c0002 | t0009 | g0268 | AMR | CLM | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01361 | hp2 | a0001 | c0003 | t0002 | g0347 | AMR | CLM | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01433 | hp1 | a0001 | c0007 | t0008 | g0253 | AMR | CLM | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01433 | hp2 | a0001 | c0003 | t0011 | g0368 | AMR | CLM | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01496 | hp1 | a0001 | c0003 | t0002 | g0321 | AMR | CLM | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | IBS | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01515 | hp2 | a0001 | c0003 | t0002 | g0308 | EUR | IBS | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01516 | hp1 | a0001 | c0009 | t0013 | g0237 | EUR | IBS | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | IBS | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01517 | hp2 | a0001 | c0009 | t0013 | g0236 | EUR | IBS | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01884 | hp1 | a0001 | c0003 | t0002 | g0356 | AFR | ACB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01884 | hp2 | a0001 | c0007 | t0008 | g0254 | AFR | ACB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01891 | hp1 | a0001 | c0003 | t0002 | g0009 | AFR | ACB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01891 | hp2 | a0001 | c0004 | t0004 | g0136 | AFR | ACB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01934 | hp1 | a0001 | c0003 | t0002 | g0342 | AMR | PEL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0050 | AMR | PEL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0071 | AMR | PEL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01943 | hp2 | a0001 | c0003 | t0002 | g0305 | AMR | PEL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01975 | hp1 | a0001 | c0003 | t0002 | g0341 | AMR | PEL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0080 | AMR | PEL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0075 | AMR | PEL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01978 | hp2 | a0001 | c0020 | t0001 | g0163 | AMR | PEL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0093 | AMR | PEL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01981 | hp2 | a0001 | c0003 | t0002 | g0319 | AMR | PEL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0234 | AMR | PEL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01993 | hp2 | a0002 | c0011 | t0001 | g0077 | AMR | PEL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | KHV | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02027 | hp2 | a0001 | c0001 | t0005 | g0094 | EAS | KHV | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02055 | hp1 | a0001 | c0003 | t0002 | g0028 | AFR | ACB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02055 | hp2 | a0001 | c0004 | t0004 | g0129 | AFR | ACB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02056 | hp1 | a0001 | c0001 | t0005 | g0198 | EAS | KHV | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02056 | hp2 | a0001 | c0003 | t0002 | g0336 | EAS | KHV | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02071 | hp2 | a0001 | c0003 | t0002 | g0301 | EAS | KHV | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | KHV | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02074 | hp2 | a0001 | c0001 | t0005 | g0191 | EAS | KHV | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | KHV | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | KHV | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | KHV | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | KHV | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | KHV | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | KHV | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | KHV | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | KHV | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | KHV | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02135 | hp2 | a0001 | c0003 | t0002 | g0279 | EAS | KHV | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | ACB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02145 | hp2 | a0001 | c0004 | t0004 | g0117 | AFR | ACB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02257 | hp1 | a0001 | c0003 | t0002 | g0291 | AFR | ACB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | ACB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02258 | hp1 | a0001 | c0002 | t0008 | g0261 | AFR | ACB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02258 | hp2 | a0001 | c0004 | t0004 | g0120 | AFR | ACB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0076 | AFR | ACB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02280 | hp2 | a0001 | c0004 | t0004 | g0135 | AFR | ACB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02293 | hp1 | a0001 | c0003 | t0002 | g0278 | AMR | PEL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02293 | hp2 | a0007 | c0012 | t0001 | g0099 | AMR | PEL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02451 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | ACB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0059 | AFR | ACB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | KHV | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02523 | hp2 | a0001 | c0001 | t0005 | g0189 | EAS | KHV | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02572 | hp1 | a0001 | c0004 | t0004 | g0290 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02572 | hp2 | a0001 | c0003 | t0002 | g0355 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0040 | SAS | PJL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0249 | SAS | PJL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02615 | hp1 | a0001 | c0004 | t0004 | g0119 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02615 | hp2 | a0001 | c0002 | t0009 | g0267 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0362 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0296 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0365 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02630 | hp2 | a0001 | c0003 | t0002 | g0293 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02647 | hp1 | a0001 | c0004 | t0004 | g0126 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02717 | hp1 | a0001 | c0005 | t0002 | g0058 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02717 | hp2 | a0001 | c0004 | t0004 | g0128 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02723 | hp1 | a0001 | c0002 | t0008 | g0264 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02723 | hp2 | a0001 | c0003 | t0002 | g0294 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02735 | hp1 | a0001 | c0003 | t0002 | g0297 | SAS | PJL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0069 | SAS | PJL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0067 | SAS | PJL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02809 | hp1 | a0001 | c0002 | t0012 | g0269 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0359 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02818 | hp1 | a0001 | c0004 | t0004 | g0138 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02886 | hp1 | a0001 | c0004 | t0004 | g0116 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02886 | hp2 | a0001 | c0002 | t0012 | g0270 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02895 | hp1 | a0001 | c0003 | t0002 | g0056 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02895 | hp2 | a0001 | c0004 | t0004 | g0118 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02965 | hp1 | a0001 | c0004 | t0004 | g0122 | AFR | ESN | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0200 | AFR | ESN | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02976 | hp1 | a0001 | c0004 | t0004 | g0121 | AFR | ESN | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0194 | AFR | ESN | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0042 | SAS | PJL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03017 | hp2 | a0001 | c0003 | t0002 | g0344 | SAS | PJL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03041 | hp1 | a0001 | c0004 | t0004 | g0115 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03098 | hp1 | a0001 | c0005 | t0010 | g0110 | AFR | MSL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0055 | AFR | MSL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03130 | hp1 | a0001 | c0005 | t0002 | g0057 | AFR | ESN | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0288 | AFR | ESN | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0199 | AFR | ESN | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03139 | hp2 | a0001 | c0004 | t0004 | g0125 | AFR | ESN | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | ESN | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03195 | hp2 | a0001 | c0004 | t0004 | g0112 | AFR | ESN | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03209 | hp1 | a0001 | c0003 | t0002 | g0331 | AFR | MSL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | MSL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0196 | AFR | MSL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03225 | hp2 | a0001 | c0003 | t0002 | g0352 | AFR | MSL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03239 | hp1 | a0001 | c0003 | t0011 | g0367 | SAS | PJL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03239 | hp2 | a0001 | c0003 | t0002 | g0339 | SAS | PJL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0131 | AFR | MSL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03453 | hp2 | a0003 | c0017 | t0002 | g0327 | AFR | MSL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03486 | hp1 | a0001 | c0004 | t0004 | g0260 | AFR | MSL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0027 | AFR | MSL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0245 | SAS | PJL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03491 | hp2 | a0001 | c0003 | t0011 | g0366 | SAS | PJL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0246 | SAS | PJL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03492 | hp2 | a0001 | c0003 | t0002 | g0323 | SAS | PJL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03516 | hp1 | a0001 | c0004 | t0002 | g0070 | AFR | ESN | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03516 | hp2 | a0001 | c0004 | t0004 | g0137 | AFR | ESN | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03540 | hp1 | a0001 | c0003 | t0002 | g0201 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0360 | AFR | GWD | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03579 | hp1 | a0001 | c0003 | t0002 | g0009 | AFR | MSL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03579 | hp2 | a0001 | c0004 | t0004 | g0124 | AFR | MSL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03654 | hp1 | a0006 | c0019 | t0002 | g0320 | SAS | PJL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0247 | SAS | PJL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03688 | hp1 | a0001 | c0003 | t0002 | g0332 | SAS | STU | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0226 | SAS | STU | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0078 | SAS | PJL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03710 | hp2 | a0001 | c0018 | t0002 | g0277 | SAS | PJL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03831 | hp1 | a0001 | c0003 | t0002 | g0326 | SAS | BEB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0186 | SAS | BEB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0235 | SAS | BEB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03834 | hp2 | a0001 | c0003 | t0002 | g0312 | SAS | BEB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0243 | SAS | BEB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0259 | SAS | BEB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0098 | SAS | BEB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0091 | SAS | STU | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG04115 | hp2 | a0001 | c0003 | t0002 | g0324 | SAS | STU | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG04184 | hp2 | a0001 | c0003 | t0002 | g0292 | SAS | BEB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0251 | SAS | STU | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG04199 | hp2 | a0001 | c0003 | t0002 | g0295 | SAS | STU | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0219 | SAS | STU | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG04228 | hp2 | a0001 | c0003 | t0002 | g0340 | SAS | STU | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0010 | EAS | CHB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | CHB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0287 | EAS | CHB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | CHB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18906 | hp1 | a0001 | c0004 | t0004 | g0127 | AFR | YRI | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18906 | hp2 | a0001 | c0002 | t0008 | g0262 | AFR | YRI | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18941 | hp1 | a0001 | c0008 | t0001 | g0181 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18948 | hp2 | a0001 | c0003 | t0002 | g0280 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0168 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18951 | hp1 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18952 | hp1 | a0001 | c0001 | t0005 | g0180 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0143 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18956 | hp2 | a0001 | c0003 | t0002 | g0298 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18957 | hp1 | a0001 | c0006 | t0002 | g0311 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18959 | hp1 | a0001 | c0003 | t0002 | g0275 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18960 | hp1 | a0001 | c0001 | t0005 | g0161 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18963 | hp1 | a0001 | c0008 | t0001 | g0155 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18965 | hp2 | a0001 | c0001 | t0016 | g0023 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18966 | hp2 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18967 | hp2 | a0001 | c0003 | t0002 | g0285 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18968 | hp1 | a0001 | c0003 | t0002 | g0281 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18969 | hp2 | a0001 | c0001 | t0005 | g0160 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18970 | hp2 | a0001 | c0003 | t0002 | g0313 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18973 | hp1 | a0001 | c0003 | t0002 | g0303 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18977 | hp1 | a0001 | c0003 | t0002 | g0350 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18980 | hp1 | a0004 | c0021 | t0003 | g0212 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18981 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18982 | hp2 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18985 | hp1 | a0001 | c0003 | t0002 | g0310 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18992 | hp2 | a0001 | c0022 | t0003 | g0024 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18993 | hp2 | a0001 | c0001 | t0005 | g0178 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18994 | hp2 | a0001 | c0003 | t0002 | g0283 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18995 | hp1 | a0001 | c0003 | t0002 | g0282 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18998 | hp1 | a0005 | c0014 | t0001 | g0107 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18998 | hp2 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA18999 | hp2 | a0001 | c0003 | t0002 | g0284 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19001 | hp2 | a0001 | c0003 | t0002 | g0276 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19009 | hp1 | a0001 | c0003 | t0002 | g0286 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0289 | AFR | LWK | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19030 | hp2 | a0001 | c0023 | t0001 | g0140 | AFR | LWK | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19043 | hp1 | a0001 | c0004 | t0002 | g0304 | AFR | LWK | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19043 | hp2 | a0009 | c0010 | t0018 | g0353 | AFR | LWK | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19056 | hp1 | a0001 | c0003 | t0002 | g0343 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19062 | hp2 | a0001 | c0001 | t0005 | g0182 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19064 | hp1 | a0001 | c0001 | t0005 | g0190 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19067 | hp2 | a0001 | c0001 | t0005 | g0144 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19079 | hp1 | a0001 | c0001 | t0005 | g0151 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19080 | hp2 | a0001 | c0003 | t0002 | g0314 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19086 | hp2 | a0001 | c0003 | t0002 | g0315 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19088 | hp2 | a0001 | c0001 | t0005 | g0169 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19090 | hp1 | a0001 | c0006 | t0002 | g0338 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19240 | hp1 | a0001 | c0002 | t0008 | g0263 | AFR | YRI | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA19240 | hp2 | a0001 | c0016 | t0014 | g0265 | AFR | YRI | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0363 | AFR | ASW | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | ASW | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA20752 | hp1 | a0001 | c0003 | t0002 | g0349 | EUR | TSI | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA20752 | hp2 | a0001 | c0003 | t0002 | g0329 | EUR | TSI | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0073 | EUR | TSI | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0223 | EUR | TSI | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | GIH | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA20905 | hp2 | a0001 | c0003 | t0002 | g0345 | SAS | GIH | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01123 | hp1 | a0001 | c0003 | t0017 | g0330 | AMR | CLM | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02109 | hp1 | a0001 | c0004 | t0004 | g0130 | AFR | ACB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02109 | hp2 | a0001 | c0005 | t0010 | g0193 | AFR | ACB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02486 | hp1 | a0001 | c0004 | t0004 | g0255 | AFR | ACB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0364 | AFR | ACB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02559 | hp1 | a0001 | c0003 | t0002 | g0333 | AFR | ACB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG02559 | hp2 | a0001 | c0004 | t0004 | g0132 | AFR | ACB | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03471 | hp1 | a0001 | c0005 | t0010 | g0192 | AFR | MSL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG03471 | hp2 | a0001 | c0003 | t0002 | g0334 | AFR | MSL | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | USA | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| HG06807 | hp2 | a0001 | c0003 | t0002 | g0318 | AFR | USA | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA20300 | hp1 | a0001 | c0003 | t0002 | g0317 | AFR | USA | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0361 | AFR | USA | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA21309 | hp1 | a0001 | c0002 | t0009 | g0266 | AFR | LWK | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0139 | AFR | LWK | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0159 | REF | REF | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0002 | g0335 | REF | REF | ABCC5_chr3_183914934_184022884 | ABCC5 | chr3 | 183914934 | 184022884 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:183919934
|
T | G | 2 | a0001a0004 | 65 | HG00597.hp2 HG00735.hp2 HG01192.hp2 others(62): Show |
splice_region_variant | LOW | c.*1366A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 30/30 | chr3 | 183919934 | ||||||
| chr3:183942868
|
G | A | 1 | a0005 | 1 | NA18998.hp1 | missense_variant | MODERATE | c.3553C>T | p.Pro1185Ser | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/30 | 3663/5790 | 3553/4314 | 1185/1437 | chr3 | 183942868 | ||
| chr3:183950088
|
G | GATGAACA others(25): Show |
1 | a0006 | 1 | HG03654.hp1 | frameshift_variant | HIGH | c.2950_2981dupGTGCGG others(26): Show |
p.Ile994fs | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 21/30 | 3091/5790 | 2981/4314 | 994/1437 | chr3 | 183950088 | ||
| chr3:183950120
|
C | T | 1 | a0004 | 1 | NA18980.hp1 | missense_variant | MODERATE | c.2950G>A | p.Val984Met | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 21/30 | 3060/5790 | 2950/4314 | 984/1437 | chr3 | 183950120 | ||
| chr3:183953210
|
A | G | 1 | a0003 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.2543T>C | p.Val848Ala | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 18/30 | 2653/5790 | 2543/4314 | 848/1437 | chr3 | 183953210 | ||
| chr3:183963516
|
C | T | 1 | a0007 | 1 | HG02293.hp2 | missense_variant | MODERATE | c.2104G>A | p.Asp702Asn | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/30 | 2214/5790 | 2104/4314 | 702/1437 | chr3 | 183963516 | ||
| chr3:183971720
|
C | T | 1 | a0002 | 1 | HG01993.hp2 | missense_variant | MODERATE | c.1604G>A | p.Arg535His | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/30 | 1714/5790 | 1604/4314 | 535/1437 | chr3 | 183971720 | ||
| chr3:183971894
|
T | C | 1 | a0008 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.1430A>G | p.His477Arg | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/30 | 1540/5790 | 1430/4314 | 477/1437 | chr3 | 183971894 | ||
| chr3:183987843
|
A | T | 1 | a0009 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.518T>A | p.Ile173Asn | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/30 | 628/5790 | 518/4314 | 173/1437 | chr3 | 183987843 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:183921363
|
G | A | 1 | a0001c0016 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.4251C>T | p.Asn1417Asn | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 30/30 | 4361/5790 | 4251/4314 | 1417/1437 | chr3 | 183921363 | ||
| chr3:183921381
|
T | G | 1 | a0001c0022 | 1 | NA18992.hp2 | synonymous_variant | LOW | c.4233A>C | p.Pro1411Pro | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 30/30 | 4343/5790 | 4233/4314 | 1411/1437 | chr3 | 183921381 | ||
| chr3:183925585
|
G | A | 1 | a0009c0010 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.4182C>T | p.Ser1394Ser | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/30 | 4292/5790 | 4182/4314 | 1394/1437 | chr3 | 183925585 | ||
| chr3:183925651
|
G | A | 1 | a0001c0009 | 2 | HG01516.hp1 HG01517.hp2 |
synonymous_variant | LOW | c.4116C>T | p.Ile1372Ile | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/30 | 4226/5790 | 4116/4314 | 1372/1437 | chr3 | 183925651 | ||
| chr3:183942797
|
G | A | 6 | a0001c0002a0001c0023a0002c0011others(3): Show | 111 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(108): Show |
synonymous_variant | LOW | c.3624C>T | p.Leu1208Leu | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/30 | 3734/5790 | 3624/4314 | 1208/1437 | chr3 | 183942797 | ||
| chr3:183949767
|
C | T | 1 | a0001c0008 | 2 | NA18941.hp1 NA18963.hp1 |
synonymous_variant | LOW | c.3213G>A | p.Gln1071Gln | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 22/30 | 3323/5790 | 3213/4314 | 1071/1437 | chr3 | 183949767 | ||
| chr3:183949815
|
C | T | 1 | a0001c0018 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.3165G>A | p.Thr1055Thr | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 22/30 | 3275/5790 | 3165/4314 | 1055/1437 | chr3 | 183949815 | ||
| chr3:183951454
|
T | C | 1 | a0001c0007 | 2 | HG01433.hp1 HG01884.hp2 |
synonymous_variant | LOW | c.2931A>G | p.Lys977Lys | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 20/30 | 3041/5790 | 2931/4314 | 977/1437 | chr3 | 183951454 | ||
| chr3:183951971
|
C | T | 1 | a0001c0020 | 1 | HG01978.hp2 | synonymous_variant | LOW | c.2700G>A | p.Ser900Ser | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 19/30 | 2810/5790 | 2700/4314 | 900/1437 | chr3 | 183951971 | ||
| chr3:183967746
|
A | G | 17 | a0001c0001a0001c0002a0001c0004others(14): Show | 293 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(290): Show |
synonymous_variant | LOW | c.1782T>C | p.Cys594Cys | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/30 | 1892/5790 | 1782/4314 | 594/1437 | chr3 | 183967746 | ||
| chr3:183978599
|
G | A | 1 | a0001c0004 | 29 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(26): Show |
synonymous_variant | LOW | c.1200C>T | p.Ser400Ser | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 9/30 | 1310/5790 | 1200/4314 | 400/1437 | chr3 | 183978599 | ||
| chr3:183978614
|
A | G | 14 | a0001c0001a0001c0002a0001c0004others(11): Show | 284 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
synonymous_variant | LOW | c.1185T>C | p.Ala395Ala | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 9/30 | 1295/5790 | 1185/4314 | 395/1437 | chr3 | 183978614 | ||
| chr3:183981728
|
T | C | 6 | a0001c0001a0001c0008a0001c0009others(3): Show | 143 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(140): Show |
splice_region_variant&synonymous_variant | LOW | c.1146A>G | p.Gln382Gln | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/30 | 1256/5790 | 1146/4314 | 382/1437 | chr3 | 183981728 | ||
| chr3:183989291
|
C | T | 1 | a0001c0006 | 2 | NA18957.hp1 NA19090.hp1 |
synonymous_variant | LOW | c.222G>A | p.Glu74Glu | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 3/30 | 332/5790 | 222/4314 | 74/1437 | chr3 | 183989291 | ||
| chr3:184014345
|
C | A | 1 | a0001c0023 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.48G>T | p.Gly16Gly | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/30 | 158/5790 | 48/4314 | 16/1437 | chr3 | 184014345 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:183920057
|
T | C | 17 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(14): Show | 200 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*1243A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 30/30 | 1243 | chr3 | 183920057 | |||||
| chr3:183920110
|
G | C | 1 | a0001c0003t0015 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1190C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 30/30 | 1190 | chr3 | 183920110 | |||||
| chr3:183920241
|
GGAGA | G | 3 | a0001c0001t0005a0001c0001t0007a0009c0010t0018 | 35 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1055_*1058delTCTC | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 30/30 | 1055 | chr3 | 183920241 | |||||
| chr3:183920273
|
G | A | 1 | a0001c0016t0014 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1027C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 30/30 | 1027 | chr3 | 183920273 | |||||
| chr3:183920278
|
G | T | 2 | a0001c0005t0010a0001c0016t0014 | 4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1022C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 30/30 | 1022 | chr3 | 183920278 | |||||
| chr3:183920581
|
G | A | 1 | a0001c0002t0012 | 2 | HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*719C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 30/30 | 719 | chr3 | 183920581 | |||||
| chr3:183920711
|
G | A | 1 | a0001c0001t0016 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*589C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 30/30 | 589 | chr3 | 183920711 | |||||
| chr3:183920718
|
C | T | 11 | a0001c0001t0001a0001c0002t0001a0001c0002t0009others(8): Show | 145 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*582G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 30/30 | 582 | chr3 | 183920718 | |||||
| chr3:183920719
|
G | A | 1 | a0001c0004t0004 | 27 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*581C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 30/30 | 581 | chr3 | 183920719 | |||||
| chr3:183920757
|
A | G | 1 | a0001c0009t0013 | 2 | HG01516.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*543T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 30/30 | 543 | chr3 | 183920757 | |||||
| chr3:183920991
|
T | C | 1 | a0001c0003t0017 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*309A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 30/30 | 309 | chr3 | 183920991 | |||||
| chr3:183921221
|
G | A | 1 | a0009c0010t0018 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*79C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 30/30 | 79 | chr3 | 183921221 | |||||
| chr3:184014421
|
C | T | 2 | a0001c0002t0009a0001c0002t0012 | 5 | HG01358.hp2 HG02615.hp2 HG02809.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-29G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/30 | chr3 | 184014421 | ||||||
| chr3:184017856
|
G | A | 1 | a0001c0003t0011 | 3 | HG01433.hp2 HG03239.hp1 HG03491.hp2 |
5_prime_UTR_variant | MODIFIER | c.-82C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/30 | 3464 | chr3 | 184017856 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:183921462
|
A | C | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4213-61T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183921462 | ||||||
| chr3:183921522
|
G | A | 2 | a0001c0002t0001g0016a0001c0002t0001g0083 | 2 | HG01074.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.4213-121C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183921522 | ||||||
| chr3:183921535
|
C | T | 31 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(28): Show | 31 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.4213-134G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183921535 | ||||||
| chr3:183921668
|
G | A | 1 | a0001c0001t0003g0233 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.4213-267C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183921668 | ||||||
| chr3:183921698
|
A | G | 1 | a0001c0004t0004g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4213-297T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183921698 | ||||||
| chr3:183921804
|
C | A | 1 | a0001c0003t0002g0284 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.4213-403G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183921804 | ||||||
| chr3:183921998
|
G | A | 3 | a0001c0002t0001g0016a0001c0002t0001g0066a0001c0002t0001g0083 | 3 | HG01074.hp2 HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.4213-597C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183921998 | ||||||
| chr3:183922009
|
C | T | 1 | a0001c0003t0002g0337 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.4213-608G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922009 | ||||||
| chr3:183922017
|
C | T | 16 | a0001c0001t0006g0015a0001c0001t0006g0027a0001c0001t0006g0051others(13): Show | 16 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.4213-616G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922017 | ||||||
| chr3:183922018
|
G | A | 5 | a0001c0001t0006g0002a0001c0001t0006g0059a0001c0001t0006g0288others(2): Show | 6 | HG01257.hp2 HG02451.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.4213-617C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922018 | ||||||
| chr3:183922035
|
T | TAATA | 41 | a0001c0001t0003g0006a0001c0001t0003g0202a0001c0001t0003g0205others(38): Show | 42 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(39): Show |
intron_variant | MODIFIER | c.4213-638_4213-635d others(6): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922035 | ||||||
| chr3:183922035
|
T | TAATAAAT others(1): Show |
15 | a0001c0001t0003g0007a0001c0001t0003g0022a0001c0001t0003g0203others(12): Show | 16 | HG00735.hp2 HG02080.hp1 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.4213-642_4213-635d others(10): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922035 | ||||||
| chr3:183922035
|
T | TAATAAAT others(5): Show |
1 | a0001c0001t0003g0206 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.4213-646_4213-635d others(14): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922035 | ||||||
| chr3:183922035
|
TAATA | T | 31 | a0001c0001t0006g0002a0001c0001t0006g0288a0001c0001t0006g0289others(28): Show | 34 | HG00280.hp1 HG00280.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.4213-638_4213-635d others(6): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922035 | ||||||
| chr3:183922035
|
TAATAAAT others(1): Show |
T | 3 | a0001c0001t0003g0228a0001c0005t0002g0057a0001c0016t0014g0265 | 3 | HG00597.hp2 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4213-642_4213-635d others(10): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922035 | ||||||
| chr3:183922035
|
TAATAAAT others(5): Show |
T | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4213-646_4213-635d others(14): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922035 | ||||||
| chr3:183922035
|
TAATAAAT others(9): Show |
T | 26 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(23): Show | 26 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.4213-650_4213-635d others(18): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922035 | ||||||
| chr3:183922035
|
TAATAAAT others(13): Show |
T | 136 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(133): Show | 139 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.4213-654_4213-635d others(22): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922035 | ||||||
| chr3:183922057
|
ATAAATAA others(14): Show |
A | 8 | a0001c0002t0001g0001a0001c0002t0001g0050a0001c0002t0001g0071others(5): Show | 10 | HG01346.hp1 HG01496.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.4213-677_4213-657d others(23): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922057 | ||||||
| chr3:183922099
|
C | T | 28 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0031others(25): Show | 28 | HG00408.hp2 HG00544.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.4213-698G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922099 | ||||||
| chr3:183922124
|
C | T | 2 | a0001c0004t0002g0070a0001c0004t0002g0304 | 2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4213-723G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922124 | ||||||
| chr3:183922146
|
C | T | 11 | a0001c0001t0007g0013a0001c0001t0007g0014a0001c0001t0007g0139others(8): Show | 11 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.4213-745G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922146 | ||||||
| chr3:183922230
|
G | T | 59 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(56): Show | 61 | HG00597.hp2 HG00735.hp2 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.4213-829C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922230 | ||||||
| chr3:183922303
|
C | T | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4213-902G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922303 | ||||||
| chr3:183922327
|
G | A | 3 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193 | 3 | HG02109.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4213-926C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922327 | ||||||
| chr3:183922361
|
GA | G | 144 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(141): Show | 149 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.4213-961delT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922361 | ||||||
| chr3:183922368
|
C | T | 1 | a0001c0001t0003g0259 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4213-967G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922368 | ||||||
| chr3:183922527
|
G | C | 1 | a0001c0002t0001g0097 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.4213-1126C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922527 | ||||||
| chr3:183922596
|
T | C | 26 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(23): Show | 26 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.4213-1195A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922596 | ||||||
| chr3:183922821
|
G | GCGTGTCC others(12): Show |
75 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(72): Show | 79 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.4213-1439_4213-142 others(23): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922821 | ||||||
| chr3:183922821
|
G | GCGTGTCC others(31): Show |
4 | a0001c0002t0001g0068a0001c0002t0001g0085a0001c0002t0001g0087others(1): Show | 4 | NA18988.hp2 NA18995.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.4213-1421_4213-142 others(42): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922821 | ||||||
| chr3:183922841
|
C | T | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4213-1440G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922841 | ||||||
| chr3:183922990
|
C | T | 7 | a0001c0001t0003g0218a0001c0001t0003g0223a0001c0001t0003g0234others(4): Show | 7 | HG01192.hp2 HG01516.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.4213-1589G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183922990 | ||||||
| chr3:183923016
|
G | A | 2 | a0001c0003t0002g0317a0001c0003t0002g0319 | 2 | HG01981.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4213-1615C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183923016 | ||||||
| chr3:183923077
|
G | T | 183 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(180): Show | 189 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.4213-1676C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183923077 | ||||||
| chr3:183923101
|
G | A | 1 | a0001c0001t0003g0220 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.4213-1700C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183923101 | ||||||
| chr3:183923411
|
T | C | 1 | a0001c0018t0002g0277 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4213-2010A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183923411 | ||||||
| chr3:183923549
|
G | A | 59 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(56): Show | 61 | HG00597.hp2 HG00735.hp2 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.4212+2006C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183923549 | ||||||
| chr3:183923610
|
G | A | 1 | a0001c0002t0001g0306 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.4212+1945C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183923610 | ||||||
| chr3:183923879
|
G | A | 61 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(58): Show | 63 | HG00597.hp2 HG00735.hp2 HG01192.hp2 others(60): Show |
intron_variant | MODIFIER | c.4212+1676C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183923879 | ||||||
| chr3:183923881
|
G | C | 281 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(278): Show | 289 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(286): Show |
intron_variant | MODIFIER | c.4212+1674C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183923881 | ||||||
| chr3:183924010
|
C | CT | 59 | a0001c0001t0005g0012a0001c0001t0005g0018a0001c0001t0005g0157others(56): Show | 60 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.4212+1544dupA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183924010 | ||||||
| chr3:183924010
|
C | CTT | 12 | a0001c0001t0003g0203a0001c0001t0003g0227a0001c0003t0002g0282others(9): Show | 12 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.4212+1543_4212+154 others(6): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183924010 | ||||||
| chr3:183924010
|
C | CTTT | 52 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(49): Show | 54 | HG00597.hp2 HG00735.hp2 HG01192.hp2 others(51): Show |
intron_variant | MODIFIER | c.4212+1542_4212+154 others(7): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183924010 | ||||||
| chr3:183924010
|
CTTTTTTT others(3): Show |
C | 143 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(140): Show | 148 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.4212+1535_4212+154 others(14): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183924010 | ||||||
| chr3:183924110
|
C | T | 26 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(23): Show | 26 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.4212+1445G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183924110 | ||||||
| chr3:183924315
|
C | T | 26 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(23): Show | 26 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.4212+1240G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183924315 | ||||||
| chr3:183924334
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.4212+1221A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183924334 | ||||||
| chr3:183924364
|
G | C | 183 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(180): Show | 189 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.4212+1191C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183924364 | ||||||
| chr3:183924444
|
A | G | 1 | a0001c0001t0005g0169 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.4212+1111T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183924444 | ||||||
| chr3:183924515
|
G | A | 57 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(54): Show | 59 | HG00597.hp2 HG00735.hp2 HG01192.hp2 others(56): Show |
intron_variant | MODIFIER | c.4212+1040C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183924515 | ||||||
| chr3:183924553
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0174 | 2 | HG00741.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.4212+1002G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183924553 | ||||||
| chr3:183924849
|
T | C | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.4212+706A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183924849 | ||||||
| chr3:183924871
|
G | C | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4212+684C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183924871 | ||||||
| chr3:183924963
|
A | G | 144 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(141): Show | 149 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.4212+592T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183924963 | ||||||
| chr3:183925006
|
A | G | 281 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(278): Show | 289 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(286): Show |
intron_variant | MODIFIER | c.4212+549T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183925006 | ||||||
| chr3:183925012
|
A | T | 1 | a0001c0001t0001g0184 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.4212+543T>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183925012 | ||||||
| chr3:183925044
|
G | A | 1 | a0001c0004t0004g0125 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4212+511C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183925044 | ||||||
| chr3:183925091
|
G | A | 281 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(278): Show | 289 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(286): Show |
intron_variant | MODIFIER | c.4212+464C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183925091 | ||||||
| chr3:183925184
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.4212+371A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183925184 | ||||||
| chr3:183925347
|
T | C | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4212+208A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183925347 | ||||||
| chr3:183925357
|
A | C | 1 | a0001c0002t0001g0069 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4212+198T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183925357 | ||||||
| chr3:183925467
|
C | T | 2 | a0001c0004t0002g0070a0001c0004t0002g0304 | 2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4212+88G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 29/29 | chr3 | 183925467 | ||||||
| chr3:183925797
|
T | C | 37 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(34): Show | 38 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.4048-78A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 28/29 | chr3 | 183925797 | ||||||
| chr3:183925840
|
C | CT | 43 | a0001c0001t0001g0145a0001c0001t0006g0002a0001c0001t0006g0015others(40): Show | 44 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.4048-122dupA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 28/29 | chr3 | 183925840 | ||||||
| chr3:183925931
|
C | T | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4048-212G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 28/29 | chr3 | 183925931 | ||||||
| chr3:183925939
|
C | T | 34 | a0001c0002t0001g0004a0001c0002t0001g0029a0001c0002t0001g0030others(31): Show | 35 | HG00408.hp2 HG00544.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.4048-220G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 28/29 | chr3 | 183925939 | ||||||
| chr3:183926000
|
A | G | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4048-281T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 28/29 | chr3 | 183926000 | ||||||
| chr3:183926142
|
G | GT | 7 | a0001c0001t0005g0169a0001c0001t0005g0178a0001c0003t0002g0286others(4): Show | 7 | HG01433.hp1 HG02717.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.4048-424dupA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 28/29 | chr3 | 183926142 | ||||||
| chr3:183926142
|
G | GTT | 101 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(98): Show | 103 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.4048-425_4048-424d others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 28/29 | chr3 | 183926142 | ||||||
| chr3:183926142
|
G | GTTT | 81 | a0001c0001t0001g0145a0001c0001t0001g0175a0001c0002t0001g0001others(78): Show | 85 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.4048-426_4048-424d others(5): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 28/29 | chr3 | 183926142 | ||||||
| chr3:183926142
|
GT | G | 17 | a0001c0001t0003g0227a0001c0001t0005g0190a0001c0001t0005g0191others(14): Show | 17 | HG01109.hp2 HG01496.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.4048-424delA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 28/29 | chr3 | 183926142 | ||||||
| chr3:183926158
|
T | C | 9 | a0001c0001t0007g0013a0001c0001t0007g0014a0001c0001t0007g0139others(6): Show | 9 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.4048-439A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 28/29 | chr3 | 183926158 | ||||||
| chr3:183926256
|
A | G | 4 | a0001c0001t0003g0240a0001c0001t0003g0241a0001c0001t0003g0242others(1): Show | 4 | NA18948.hp1 NA18960.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.4048-537T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 28/29 | chr3 | 183926256 | ||||||
| chr3:183926349
|
A | T | 1 | a0001c0003t0002g0276 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.4048-630T>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 28/29 | chr3 | 183926349 | ||||||
| chr3:183926375
|
A | C | 282 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(279): Show | 290 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(287): Show |
intron_variant | MODIFIER | c.4048-656T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 28/29 | chr3 | 183926375 | ||||||
| chr3:183926406
|
C | T | 38 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(35): Show | 38 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.4048-687G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 28/29 | chr3 | 183926406 | ||||||
| chr3:183926449
|
C | T | 1 | a0001c0007t0008g0254 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4048-730G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 28/29 | chr3 | 183926449 | ||||||
| chr3:183926499
|
G | A | 2 | a0001c0001t0005g0169a0001c0003t0002g0325 | 2 | HG00741.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.4048-780C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 28/29 | chr3 | 183926499 | ||||||
| chr3:183926550
|
A | AAAAAC | 6 | a0001c0002t0001g0039a0001c0002t0001g0044a0001c0002t0001g0045others(3): Show | 6 | HG00408.hp2 HG02132.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.4047+775_4047+779d others(7): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 28/29 | chr3 | 183926550 | ||||||
| chr3:183926608
|
C | A | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4047+722G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 28/29 | chr3 | 183926608 | ||||||
| chr3:183926842
|
C | T | 12 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(9): Show | 13 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.4047+488G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 28/29 | chr3 | 183926842 | ||||||
| chr3:183926861
|
A | G | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4047+469T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 28/29 | chr3 | 183926861 | ||||||
| chr3:183926913
|
C | T | 59 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(56): Show | 61 | HG00597.hp2 HG00735.hp2 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.4047+417G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 28/29 | chr3 | 183926913 | ||||||
| chr3:183926935
|
C | T | 9 | a0001c0001t0007g0013a0001c0001t0007g0014a0001c0001t0007g0139others(6): Show | 9 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.4047+395G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 28/29 | chr3 | 183926935 | ||||||
| chr3:183927065
|
T | C | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4047+265A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 28/29 | chr3 | 183927065 | ||||||
| chr3:183927578
|
G | A | 1 | a0001c0004t0004g0120 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3934-135C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 27/29 | chr3 | 183927578 | ||||||
| chr3:183927653
|
G | A | 1 | a0001c0002t0001g0029 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3934-210C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 27/29 | chr3 | 183927653 | ||||||
| chr3:183927687
|
C | T | 3 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193 | 3 | HG02109.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3934-244G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 27/29 | chr3 | 183927687 | ||||||
| chr3:183927770
|
T | G | 1 | a0001c0004t0004g0255 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3934-327A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 27/29 | chr3 | 183927770 | ||||||
| chr3:183927874
|
C | T | 144 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(141): Show | 149 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.3934-431G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 27/29 | chr3 | 183927874 | ||||||
| chr3:183928079
|
G | C | 1 | a0001c0002t0001g0079 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3934-636C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 27/29 | chr3 | 183928079 | ||||||
| chr3:183928109
|
T | A | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.3933+638A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 27/29 | chr3 | 183928109 | ||||||
| chr3:183928112
|
CT | C | 181 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(178): Show | 186 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.3933+634delA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 27/29 | chr3 | 183928112 | ||||||
| chr3:183928135
|
A | T | 144 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(141): Show | 149 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.3933+612T>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 27/29 | chr3 | 183928135 | ||||||
| chr3:183928375
|
G | T | 9 | a0001c0001t0007g0013a0001c0001t0007g0014a0001c0001t0007g0139others(6): Show | 9 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.3933+372C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 27/29 | chr3 | 183928375 | ||||||
| chr3:183928434
|
A | G | 144 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(141): Show | 149 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.3933+313T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 27/29 | chr3 | 183928434 | ||||||
| chr3:183928441
|
C | T | 3 | a0001c0002t0001g0040a0001c0002t0001g0042a0001c0003t0015g0322 | 3 | HG01074.hp1 HG02602.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.3933+306G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 27/29 | chr3 | 183928441 | ||||||
| chr3:183928489
|
C | T | 2 | a0001c0004t0002g0070a0001c0004t0002g0304 | 2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3933+258G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 27/29 | chr3 | 183928489 | ||||||
| chr3:183928552
|
G | A | 1 | a0001c0004t0004g0112 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3933+195C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 27/29 | chr3 | 183928552 | ||||||
| chr3:183929085
|
T | A | 37 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(34): Show | 38 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.3855-260A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183929085 | ||||||
| chr3:183929293
|
T | C | 107 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(104): Show | 111 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.3855-468A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183929293 | ||||||
| chr3:183929705
|
C | G | 59 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(56): Show | 61 | HG00597.hp2 HG00735.hp2 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.3855-880G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183929705 | ||||||
| chr3:183929740
|
G | A | 1 | a0001c0003t0002g0312 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3855-915C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183929740 | ||||||
| chr3:183929913
|
C | T | 12 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(9): Show | 13 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.3855-1088G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183929913 | ||||||
| chr3:183930074
|
A | C | 1 | a0001c0001t0003g0227 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.3855-1249T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183930074 | ||||||
| chr3:183930196
|
A | G | 4 | a0001c0001t0005g0144a0001c0001t0005g0167a0001c0001t0005g0168others(1): Show | 4 | HG00438.hp1 HG02056.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.3855-1371T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183930196 | ||||||
| chr3:183930232
|
T | A | 1 | a0001c0005t0002g0274 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3855-1407A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183930232 | ||||||
| chr3:183930297
|
C | T | 2 | a0001c0003t0002g0297a0001c0003t0002g0339 | 2 | HG02735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.3855-1472G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183930297 | ||||||
| chr3:183930319
|
C | T | 1 | a0001c0001t0006g0002 | 2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3855-1494G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183930319 | ||||||
| chr3:183930354
|
G | A | 1 | a0001c0003t0002g0334 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3855-1529C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183930354 | ||||||
| chr3:183930465
|
A | C | 9 | a0001c0001t0007g0013a0001c0001t0007g0014a0001c0001t0007g0139others(6): Show | 9 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.3855-1640T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183930465 | ||||||
| chr3:183930619
|
T | C | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3855-1794A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183930619 | ||||||
| chr3:183930887
|
T | C | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.3855-2062A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183930887 | ||||||
| chr3:183930914
|
A | T | 1 | a0001c0004t0004g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3855-2089T>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183930914 | ||||||
| chr3:183930943
|
C | T | 1 | a0009c0010t0018g0353 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3855-2118G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183930943 | ||||||
| chr3:183931070
|
C | T | 57 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(54): Show | 59 | HG00597.hp2 HG00735.hp2 HG01192.hp2 others(56): Show |
intron_variant | MODIFIER | c.3855-2245G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183931070 | ||||||
| chr3:183931324
|
C | CT | 24 | a0001c0001t0003g0221a0001c0001t0003g0233a0001c0001t0005g0189others(21): Show | 24 | HG00738.hp2 HG01358.hp2 HG01934.hp1 others(21): Show |
intron_variant | MODIFIER | c.3855-2500dupA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183931324 | ||||||
| chr3:183931346
|
A | G | 39 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(36): Show | 40 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.3855-2521T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183931346 | ||||||
| chr3:183931396
|
A | C | 1 | a0001c0001t0003g0202 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.3855-2571T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183931396 | ||||||
| chr3:183931737
|
G | A | 1 | a0001c0002t0001g0068 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.3855-2912C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183931737 | ||||||
| chr3:183932082
|
A | G | 172 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(169): Show | 176 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.3855-3257T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183932082 | ||||||
| chr3:183932153
|
G | C | 27 | a0001c0004t0004g0112a0001c0004t0004g0115a0001c0004t0004g0116others(24): Show | 27 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.3855-3328C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183932153 | ||||||
| chr3:183932258
|
C | T | 2 | a0001c0006t0002g0311a0001c0006t0002g0338 | 2 | NA18957.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.3855-3433G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183932258 | ||||||
| chr3:183932542
|
T | C | 286 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(283): Show | 294 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(291): Show |
intron_variant | MODIFIER | c.3855-3717A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183932542 | ||||||
| chr3:183932599
|
G | T | 37 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(34): Show | 38 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.3855-3774C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183932599 | ||||||
| chr3:183932863
|
C | T | 1 | a0001c0002t0001g0068 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.3855-4038G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183932863 | ||||||
| chr3:183932902
|
T | C | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3855-4077A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183932902 | ||||||
| chr3:183932986
|
T | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0147 | 2 | NA18940.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.3855-4161A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183932986 | ||||||
| chr3:183933154
|
C | T | 3 | a0001c0003t0002g0328a0001c0003t0002g0329a0001c0003t0017g0330 | 3 | HG00280.hp2 HG01123.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.3855-4329G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183933154 | ||||||
| chr3:183933164
|
T | C | 2 | a0001c0001t0007g0013a0001c0001t0007g0200 | 2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.3855-4339A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183933164 | ||||||
| chr3:183933165
|
C | CA | 90 | a0001c0001t0001g0165a0001c0001t0003g0217a0001c0001t0003g0218others(87): Show | 93 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.3855-4341dupT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183933165 | ||||||
| chr3:183933165
|
C | CAA | 24 | a0001c0001t0005g0144a0001c0001t0005g0158a0001c0001t0005g0167others(21): Show | 26 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.3855-4342_3855-434 others(6): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183933165 | ||||||
| chr3:183933165
|
CA | C | 22 | a0001c0001t0001g0171a0001c0001t0003g0239a0001c0001t0005g0189others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.3855-4341delT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183933165 | ||||||
| chr3:183933165
|
CAAAAAA | C | 27 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0031others(24): Show | 27 | HG00408.hp2 HG00544.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.3855-4346_3855-434 others(10): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183933165 | ||||||
| chr3:183933220
|
TGAA | T | 39 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(36): Show | 40 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.3855-4398_3855-439 others(7): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183933220 | ||||||
| chr3:183933231
|
A | C | 1 | a0001c0001t0001g0258 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3855-4406T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183933231 | ||||||
| chr3:183933252
|
C | T | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3855-4427G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183933252 | ||||||
| chr3:183933283
|
G | A | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3855-4458C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183933283 | ||||||
| chr3:183933375
|
G | A | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.3854+4526C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183933375 | ||||||
| chr3:183933432
|
C | T | 1 | a0001c0003t0002g0292 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3854+4469G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183933432 | ||||||
| chr3:183933795
|
A | G | 2 | a0001c0003t0002g0056a0003c0017t0002g0327 | 2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3854+4106T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183933795 | ||||||
| chr3:183933905
|
C | T | 2 | a0001c0003t0002g0294a0001c0003t0002g0331 | 2 | HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3854+3996G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183933905 | ||||||
| chr3:183933951
|
C | T | 9 | a0001c0001t0007g0013a0001c0001t0007g0014a0001c0001t0007g0139others(6): Show | 9 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.3854+3950G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183933951 | ||||||
| chr3:183934214
|
G | A | 1 | a0001c0002t0001g0067 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3854+3687C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183934214 | ||||||
| chr3:183934455
|
C | A | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3854+3446G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183934455 | ||||||
| chr3:183934623
|
G | A | 1 | a0001c0003t0002g0340 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3854+3278C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183934623 | ||||||
| chr3:183934639
|
C | G | 1 | a0001c0001t0006g0351 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3854+3262G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183934639 | ||||||
| chr3:183934649
|
C | T | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3854+3252G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183934649 | ||||||
| chr3:183934650
|
G | A | 4 | a0001c0003t0002g0009a0001c0003t0002g0201a0001c0003t0002g0333others(1): Show | 5 | HG01891.hp1 HG02559.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.3854+3251C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183934650 | ||||||
| chr3:183934777
|
A | G | 1 | a0001c0004t0004g0121 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3854+3124T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183934777 | ||||||
| chr3:183934948
|
G | A | 282 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(279): Show | 290 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(287): Show |
intron_variant | MODIFIER | c.3854+2953C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183934948 | ||||||
| chr3:183935039
|
C | T | 12 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(9): Show | 13 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.3854+2862G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183935039 | ||||||
| chr3:183935144
|
G | C | 133 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(130): Show | 136 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.3854+2757C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183935144 | ||||||
| chr3:183935148
|
G | A | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.3854+2753C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183935148 | ||||||
| chr3:183935219
|
C | T | 6 | a0001c0001t0007g0014a0001c0001t0007g0139a0001c0001t0007g0194others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.3854+2682G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183935219 | ||||||
| chr3:183935220
|
G | A | 6 | a0001c0002t0001g0017a0001c0002t0001g0074a0001c0002t0001g0111others(3): Show | 6 | HG00423.hp2 HG00544.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.3854+2681C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183935220 | ||||||
| chr3:183935250
|
G | A | 1 | a0001c0002t0001g0050 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3854+2651C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183935250 | ||||||
| chr3:183935263
|
C | T | 3 | a0001c0001t0006g0002a0001c0001t0006g0288a0001c0001t0006g0289 | 4 | HG03130.hp2 HG03195.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.3854+2638G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183935263 | ||||||
| chr3:183935285
|
A | C | 1 | a0001c0001t0003g0006 | 2 | NA18971.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.3854+2616T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183935285 | ||||||
| chr3:183935371
|
G | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(8): Show | 12 | HG00738.hp1 HG00741.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.3854+2530C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183935371 | ||||||
| chr3:183935394
|
C | G | 1 | a0001c0003t0002g0300 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3854+2507G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183935394 | ||||||
| chr3:183935413
|
C | T | 1 | a0001c0001t0003g0233 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3854+2488G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183935413 | ||||||
| chr3:183935466
|
C | T | 74 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(71): Show | 75 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.3854+2435G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183935466 | ||||||
| chr3:183935469
|
C | T | 1 | a0001c0001t0003g0244 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3854+2432G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183935469 | ||||||
| chr3:183935470
|
G | A | 6 | a0001c0001t0007g0014a0001c0001t0007g0139a0001c0001t0007g0194others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.3854+2431C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183935470 | ||||||
| chr3:183935590
|
G | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0174 | 2 | HG00741.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.3854+2311C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183935590 | ||||||
| chr3:183935730
|
G | A | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3854+2171C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183935730 | ||||||
| chr3:183935755
|
C | T | 3 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193 | 3 | HG02109.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3854+2146G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183935755 | ||||||
| chr3:183935788
|
C | T | 3 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193 | 3 | HG02109.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3854+2113G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183935788 | ||||||
| chr3:183935930
|
A | G | 172 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(169): Show | 176 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.3854+1971T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183935930 | ||||||
| chr3:183936058
|
T | C | 1 | a0001c0004t0004g0128 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3854+1843A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183936058 | ||||||
| chr3:183936081
|
A | G | 286 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(283): Show | 294 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(291): Show |
intron_variant | MODIFIER | c.3854+1820T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183936081 | ||||||
| chr3:183936149
|
G | T | 74 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(71): Show | 75 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.3854+1752C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183936149 | ||||||
| chr3:183936241
|
C | G | 286 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(283): Show | 294 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(291): Show |
intron_variant | MODIFIER | c.3854+1660G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183936241 | ||||||
| chr3:183936267
|
G | A | 6 | a0001c0002t0001g0131a0001c0002t0009g0266a0001c0002t0009g0267others(3): Show | 6 | HG01358.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.3854+1634C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183936267 | ||||||
| chr3:183936372
|
C | T | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3854+1529G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183936372 | ||||||
| chr3:183936511
|
GA | G | 19 | a0001c0003t0002g0008a0001c0003t0002g0275a0001c0003t0002g0276others(16): Show | 20 | HG00280.hp2 HG00558.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.3854+1389delT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183936511 | ||||||
| chr3:183936512
|
A | AT | 44 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(41): Show | 45 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.3854+1388dupA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183936512 | ||||||
| chr3:183936581
|
C | T | 3 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193 | 3 | HG02109.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3854+1320G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183936581 | ||||||
| chr3:183936630
|
C | T | 1 | a0009c0010t0018g0353 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3854+1271G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183936630 | ||||||
| chr3:183936977
|
T | G | 3 | a0001c0002t0001g0101a0001c0002t0001g0106a0005c0014t0001g0107 | 3 | NA18998.hp1 NA19009.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.3854+924A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183936977 | ||||||
| chr3:183936987
|
C | T | 1 | a0001c0003t0002g0328 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3854+914G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183936987 | ||||||
| chr3:183937022
|
G | A | 1 | a0001c0001t0003g0220 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3854+879C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183937022 | ||||||
| chr3:183937064
|
C | T | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3854+837G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183937064 | ||||||
| chr3:183937638
|
G | A | 26 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(23): Show | 26 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.3854+263C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183937638 | ||||||
| chr3:183937642
|
C | G | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3854+259G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 26/29 | chr3 | 183937642 | ||||||
| chr3:183938066
|
G | A | 1 | a0001c0002t0001g0035 | 1 | NA18954.hp1 | splice_region_variant&intron_variant | LOW | c.3695-6C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183938066 | ||||||
| chr3:183938157
|
T | C | 1 | a0001c0002t0001g0252 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3695-97A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183938157 | ||||||
| chr3:183938208
|
T | C | 39 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(36): Show | 40 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.3695-148A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183938208 | ||||||
| chr3:183938321
|
C | T | 107 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(104): Show | 111 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.3695-261G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183938321 | ||||||
| chr3:183938353
|
C | T | 1 | a0009c0010t0018g0353 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3695-293G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183938353 | ||||||
| chr3:183938489
|
G | A | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.3695-429C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183938489 | ||||||
| chr3:183938577
|
G | A | 107 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(104): Show | 111 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.3695-517C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183938577 | ||||||
| chr3:183938588
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG02683.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.3695-528G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183938588 | ||||||
| chr3:183938886
|
T | C | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3695-826A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183938886 | ||||||
| chr3:183939018
|
C | G | 79 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(76): Show | 83 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.3695-958G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183939018 | ||||||
| chr3:183939018
|
C | T | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3695-958G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183939018 | ||||||
| chr3:183939102
|
A | G | 2 | a0001c0001t0003g0210a0001c0001t0003g0222 | 2 | NA18968.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.3695-1042T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183939102 | ||||||
| chr3:183939122
|
T | A | 1 | a0001c0003t0002g0349 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3695-1062A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183939122 | ||||||
| chr3:183939140
|
A | G | 1 | a0001c0003t0002g0332 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3695-1080T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183939140 | ||||||
| chr3:183939203
|
C | T | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.3695-1143G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183939203 | ||||||
| chr3:183939230
|
C | T | 1 | a0001c0001t0006g0002 | 2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3695-1170G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183939230 | ||||||
| chr3:183939320
|
G | A | 1 | a0001c0001t0006g0351 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3695-1260C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183939320 | ||||||
| chr3:183939525
|
T | C | 2 | a0001c0001t0003g0231a0001c0002t0001g0108 | 2 | NA18946.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.3695-1465A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183939525 | ||||||
| chr3:183939531
|
T | C | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3695-1471A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183939531 | ||||||
| chr3:183939646
|
C | T | 2 | a0001c0001t0003g0243a0001c0001t0003g0251 | 2 | HG03927.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.3695-1586G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183939646 | ||||||
| chr3:183939823
|
T | G | 2 | a0001c0003t0002g0291a0001c0003t0002g0352 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3695-1763A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183939823 | ||||||
| chr3:183939834
|
A | G | 1 | a0001c0001t0001g0159 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3695-1774T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183939834 | ||||||
| chr3:183939849
|
C | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0146others(5): Show | 9 | HG00738.hp1 HG01109.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.3695-1789G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183939849 | ||||||
| chr3:183939919
|
T | C | 1 | a0001c0003t0002g0319 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3695-1859A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183939919 | ||||||
| chr3:183939946
|
C | T | 1 | a0001c0003t0002g0339 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3695-1886G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183939946 | ||||||
| chr3:183939982
|
C | T | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3695-1922G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183939982 | ||||||
| chr3:183940006
|
C | G | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.3695-1946G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183940006 | ||||||
| chr3:183940031
|
C | CTAAT | 4 | a0001c0001t0007g0014a0001c0001t0007g0194a0001c0001t0007g0195others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.3695-1975_3695-197 others(8): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183940031 | ||||||
| chr3:183940075
|
C | T | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3695-2015G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183940075 | ||||||
| chr3:183940217
|
G | A | 1 | a0001c0001t0005g0157 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3695-2157C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183940217 | ||||||
| chr3:183940255
|
T | C | 6 | a0001c0001t0005g0144a0001c0001t0005g0158a0001c0001t0005g0167others(3): Show | 6 | HG00438.hp1 HG00673.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.3695-2195A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183940255 | ||||||
| chr3:183940344
|
C | CA | 92 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(89): Show | 95 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.3695-2285dupT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183940344 | ||||||
| chr3:183940344
|
C | CAA | 76 | a0001c0001t0001g0179a0001c0001t0003g0240a0001c0002t0001g0001others(73): Show | 80 | HG00544.hp1 HG00621.hp2 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.3695-2286_3695-228 others(6): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183940344 | ||||||
| chr3:183940462
|
G | GA | 15 | a0001c0001t0007g0194a0001c0002t0012g0270a0001c0003t0002g0285others(12): Show | 15 | HG00621.hp1 HG00741.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.3694+2264dupT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183940462 | ||||||
| chr3:183940462
|
G | GAA | 18 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0051others(15): Show | 19 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.3694+2263_3694+226 others(6): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183940462 | ||||||
| chr3:183940462
|
G | GAAA | 11 | a0001c0001t0001g0164a0001c0001t0006g0027a0001c0001t0006g0055others(8): Show | 11 | HG01109.hp2 HG01361.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.3694+2262_3694+226 others(7): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183940462 | ||||||
| chr3:183940462
|
G | GAAAA | 45 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(42): Show | 46 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.3694+2261_3694+226 others(8): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183940462 | ||||||
| chr3:183940462
|
G | GAAAAA | 61 | a0001c0001t0001g0145a0001c0001t0001g0152a0001c0001t0001g0153others(58): Show | 63 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.3694+2260_3694+226 others(9): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183940462 | ||||||
| chr3:183940462
|
G | GAAAAAA | 14 | a0001c0001t0001g0179a0001c0001t0003g0208a0001c0001t0003g0213others(11): Show | 14 | HG02080.hp1 HG02129.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.3694+2259_3694+226 others(10): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183940462 | ||||||
| chr3:183940462
|
GA | G | 29 | a0001c0002t0001g0075a0001c0002t0001g0082a0001c0002t0001g0109others(26): Show | 29 | HG00639.hp1 HG01070.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.3694+2264delT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183940462 | ||||||
| chr3:183940462
|
GAA | G | 98 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(95): Show | 102 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.3694+2263_3694+226 others(6): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183940462 | ||||||
| chr3:183940485
|
A | G | 102 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(99): Show | 106 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.3694+2242T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183940485 | ||||||
| chr3:183940513
|
G | T | 1 | a0001c0001t0003g0248 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3694+2214C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183940513 | ||||||
| chr3:183940530
|
C | G | 1 | a0001c0001t0006g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3694+2197G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183940530 | ||||||
| chr3:183940530
|
C | T | 56 | a0001c0001t0001g0179a0001c0001t0003g0006a0001c0001t0003g0007others(53): Show | 58 | HG00735.hp2 HG01192.hp2 HG01516.hp1 others(55): Show |
intron_variant | MODIFIER | c.3694+2197G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183940530 | ||||||
| chr3:183940567
|
G | A | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3694+2160C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183940567 | ||||||
| chr3:183940613
|
C | T | 3 | a0001c0001t0003g0205a0001c0001t0003g0213a0001c0001t0003g0215 | 3 | NA18964.hp2 NA19012.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.3694+2114G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183940613 | ||||||
| chr3:183940848
|
G | GTTA | 16 | a0001c0001t0001g0145a0001c0001t0001g0148a0001c0001t0001g0149others(13): Show | 16 | HG00597.hp1 HG02055.hp1 HG02683.hp1 others(13): Show |
intron_variant | MODIFIER | c.3694+1876_3694+187 others(7): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183940848 | ||||||
| chr3:183940868
|
T | C | 1 | a0001c0002t0001g0095 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3694+1859A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183940868 | ||||||
| chr3:183941520
|
G | GT | 6 | a0001c0001t0005g0011a0001c0002t0001g0092a0001c0002t0001g0150others(3): Show | 6 | HG00621.hp2 HG02056.hp2 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.3694+1206dupA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183941520 | ||||||
| chr3:183941675
|
A | T | 285 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(282): Show | 293 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(290): Show |
intron_variant | MODIFIER | c.3694+1052T>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183941675 | ||||||
| chr3:183941703
|
G | A | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.3694+1024C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183941703 | ||||||
| chr3:183941860
|
G | A | 1 | a0001c0003t0011g0367 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3694+867C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183941860 | ||||||
| chr3:183941889
|
G | A | 107 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(104): Show | 111 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.3694+838C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183941889 | ||||||
| chr3:183941972
|
C | CA | 68 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(65): Show | 70 | HG00280.hp2 HG00597.hp2 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.3694+754dupT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183941972 | ||||||
| chr3:183942047
|
CT | C | 107 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(104): Show | 111 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.3694+679delA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183942047 | ||||||
| chr3:183942293
|
C | T | 57 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(54): Show | 59 | HG00597.hp2 HG00735.hp2 HG01192.hp2 others(56): Show |
intron_variant | MODIFIER | c.3694+434G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183942293 | ||||||
| chr3:183942447
|
T | G | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3694+280A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 25/29 | chr3 | 183942447 | ||||||
| chr3:183943018
|
C | G | 63 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(60): Show | 64 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.3505-102G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183943018 | ||||||
| chr3:183943121
|
C | G | 1 | a0001c0001t0006g0052 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3505-205G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183943121 | ||||||
| chr3:183943236
|
T | G | 26 | a0001c0004t0004g0112a0001c0004t0004g0115a0001c0004t0004g0116others(23): Show | 26 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.3505-320A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183943236 | ||||||
| chr3:183943287
|
T | C | 3 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193 | 3 | HG02109.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3505-371A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183943287 | ||||||
| chr3:183943546
|
C | T | 66 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(63): Show | 68 | HG00597.hp2 HG00735.hp2 HG01192.hp2 others(65): Show |
intron_variant | MODIFIER | c.3505-630G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183943546 | ||||||
| chr3:183943598
|
C | T | 1 | a0001c0004t0004g0126 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3505-682G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183943598 | ||||||
| chr3:183943630
|
G | C | 9 | a0001c0003t0002g0028a0001c0005t0002g0057a0001c0005t0002g0058others(6): Show | 9 | HG01433.hp1 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.3505-714C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183943630 | ||||||
| chr3:183943730
|
G | A | 2 | a0001c0001t0005g0011a0001c0001t0005g0012 | 2 | NA18981.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.3505-814C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183943730 | ||||||
| chr3:183943790
|
T | C | 66 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(63): Show | 68 | HG00597.hp2 HG00735.hp2 HG01192.hp2 others(65): Show |
intron_variant | MODIFIER | c.3505-874A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183943790 | ||||||
| chr3:183943820
|
G | A | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3505-904C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183943820 | ||||||
| chr3:183943943
|
G | C | 1 | a0001c0005t0010g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3505-1027C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183943943 | ||||||
| chr3:183944066
|
C | G | 1 | a0001c0001t0003g0233 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3505-1150G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183944066 | ||||||
| chr3:183944115
|
G | T | 1 | a0001c0003t0015g0322 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3505-1199C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183944115 | ||||||
| chr3:183944133
|
C | T | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3505-1217G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183944133 | ||||||
| chr3:183944467
|
T | A | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3504+1383A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183944467 | ||||||
| chr3:183944479
|
G | A | 1 | a0001c0005t0002g0274 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3504+1371C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183944479 | ||||||
| chr3:183944484
|
GAAC | G | 76 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(73): Show | 80 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.3504+1363_3504+136 others(7): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183944484 | ||||||
| chr3:183944507
|
T | C | 66 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(63): Show | 68 | HG00597.hp2 HG00735.hp2 HG01192.hp2 others(65): Show |
intron_variant | MODIFIER | c.3504+1343A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183944507 | ||||||
| chr3:183944564
|
C | T | 1 | a0001c0002t0001g0091 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3504+1286G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183944564 | ||||||
| chr3:183944691
|
C | T | 1 | a0001c0002t0001g0036 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.3504+1159G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183944691 | ||||||
| chr3:183944735
|
C | A | 173 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(170): Show | 179 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(176): Show |
intron_variant | MODIFIER | c.3504+1115G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183944735 | ||||||
| chr3:183944983
|
T | G | 3 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193 | 3 | HG02109.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3504+867A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183944983 | ||||||
| chr3:183945136
|
T | G | 285 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(282): Show | 293 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(290): Show |
intron_variant | MODIFIER | c.3504+714A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183945136 | ||||||
| chr3:183945137
|
C | T | 1 | a0001c0001t0003g0231 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.3504+713G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183945137 | ||||||
| chr3:183945138
|
G | A | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.3504+712C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183945138 | ||||||
| chr3:183945263
|
C | T | 1 | a0001c0002t0001g0108 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3504+587G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183945263 | ||||||
| chr3:183945385
|
C | T | 76 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(73): Show | 80 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.3504+465G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183945385 | ||||||
| chr3:183945546
|
A | G | 1 | a0001c0001t0003g0250 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.3504+304T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183945546 | ||||||
| chr3:183945579
|
A | G | 29 | a0001c0004t0002g0070a0001c0004t0002g0304a0001c0004t0004g0112others(26): Show | 29 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.3504+271T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183945579 | ||||||
| chr3:183945718
|
T | C | 107 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(104): Show | 111 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.3504+132A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183945718 | ||||||
| chr3:183945813
|
G | A | 7 | a0001c0001t0006g0015a0001c0001t0006g0027a0001c0001t0006g0051others(4): Show | 7 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.3504+37C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 24/29 | chr3 | 183945813 | ||||||
| chr3:183946040
|
G | T | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3415-101C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 23/29 | chr3 | 183946040 | ||||||
| chr3:183946045
|
T | C | 285 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(282): Show | 293 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(290): Show |
intron_variant | MODIFIER | c.3415-106A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 23/29 | chr3 | 183946045 | ||||||
| chr3:183946700
|
C | T | 107 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(104): Show | 111 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.3414+624G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 23/29 | chr3 | 183946700 | ||||||
| chr3:183946874
|
C | T | 1 | a0001c0001t0005g0186 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3414+450G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 23/29 | chr3 | 183946874 | ||||||
| chr3:183946890
|
T | G | 173 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(170): Show | 179 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(176): Show |
intron_variant | MODIFIER | c.3414+434A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 23/29 | chr3 | 183946890 | ||||||
| chr3:183946985
|
A | G | 4 | a0001c0002t0008g0261a0001c0002t0008g0262a0001c0002t0008g0263others(1): Show | 4 | HG02258.hp1 HG02723.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.3414+339T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 23/29 | chr3 | 183946985 | ||||||
| chr3:183947085
|
C | T | 340 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(337): Show | 350 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(347): Show |
intron_variant | MODIFIER | c.3414+239G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 23/29 | chr3 | 183947085 | ||||||
| chr3:183947199
|
C | T | 3 | a0001c0001t0007g0013a0001c0001t0007g0199a0001c0001t0007g0200 | 3 | HG02818.hp2 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3414+125G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 23/29 | chr3 | 183947199 | ||||||
| chr3:183947274
|
G | C | 312 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(309): Show | 322 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(319): Show |
intron_variant | MODIFIER | c.3414+50C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 23/29 | chr3 | 183947274 | ||||||
| chr3:183947707
|
T | C | 1 | a0001c0003t0002g0315 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.3228-197A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 22/29 | chr3 | 183947707 | ||||||
| chr3:183947823
|
G | C | 1 | a0001c0001t0001g0153 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3228-313C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 22/29 | chr3 | 183947823 | ||||||
| chr3:183947824
|
C | T | 2 | a0001c0003t0002g0346a0001c0003t0002g0347 | 2 | HG01256.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.3228-314G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 22/29 | chr3 | 183947824 | ||||||
| chr3:183947831
|
T | C | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.3228-321A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 22/29 | chr3 | 183947831 | ||||||
| chr3:183947954
|
A | G | 57 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(54): Show | 59 | HG00597.hp2 HG00735.hp2 HG01192.hp2 others(56): Show |
intron_variant | MODIFIER | c.3228-444T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 22/29 | chr3 | 183947954 | ||||||
| chr3:183948061
|
A | C | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.3228-551T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 22/29 | chr3 | 183948061 | ||||||
| chr3:183948091
|
C | G | 10 | a0001c0004t0004g0115a0001c0004t0004g0117a0001c0004t0004g0118others(7): Show | 10 | HG02145.hp2 HG02615.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.3228-581G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 22/29 | chr3 | 183948091 | ||||||
| chr3:183948157
|
G | A | 3 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193 | 3 | HG02109.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3228-647C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 22/29 | chr3 | 183948157 | ||||||
| chr3:183948310
|
C | T | 3 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0196 | 3 | HG01109.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3228-800G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 22/29 | chr3 | 183948310 | ||||||
| chr3:183948328
|
G | GAT | 107 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(104): Show | 111 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.3228-820_3228-819d others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 22/29 | chr3 | 183948328 | ||||||
| chr3:183948365
|
A | G | 10 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0358others(7): Show | 10 | HG00735.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.3228-855T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 22/29 | chr3 | 183948365 | ||||||
| chr3:183948665
|
G | C | 1 | a0001c0004t0004g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3227+1088C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 22/29 | chr3 | 183948665 | ||||||
| chr3:183948924
|
G | C | 7 | a0001c0003t0002g0298a0001c0003t0002g0303a0001c0003t0002g0310others(4): Show | 7 | NA18956.hp2 NA18957.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3227+829C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 22/29 | chr3 | 183948924 | ||||||
| chr3:183949074
|
G | A | 63 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(60): Show | 64 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.3227+679C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 22/29 | chr3 | 183949074 | ||||||
| chr3:183949415
|
T | C | 1 | a0001c0002t0001g0098 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3227+338A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 22/29 | chr3 | 183949415 | ||||||
| chr3:183949729
|
C | T | 1 | a0001c0002t0001g0252 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3227+24G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 22/29 | chr3 | 183949729 | ||||||
| chr3:183950187
|
A | G | 1 | a0001c0001t0003g0243 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2945-62T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 20/29 | chr3 | 183950187 | ||||||
| chr3:183950298
|
C | T | 1 | a0001c0002t0001g0047 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2945-173G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 20/29 | chr3 | 183950298 | ||||||
| chr3:183950350
|
C | A | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2945-225G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 20/29 | chr3 | 183950350 | ||||||
| chr3:183950595
|
C | A | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.2945-470G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 20/29 | chr3 | 183950595 | ||||||
| chr3:183950595
|
C | T | 62 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(59): Show | 66 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.2945-470G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 20/29 | chr3 | 183950595 | ||||||
| chr3:183950598
|
C | G | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2945-473G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 20/29 | chr3 | 183950598 | ||||||
| chr3:183950985
|
T | C | 4 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2944+456A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 20/29 | chr3 | 183950985 | ||||||
| chr3:183951098
|
G | C | 1 | a0001c0002t0001g0045 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2944+343C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 20/29 | chr3 | 183951098 | ||||||
| chr3:183951106
|
G | C | 4 | a0001c0001t0003g0240a0001c0001t0003g0241a0001c0001t0003g0242others(1): Show | 4 | NA18948.hp1 NA18960.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.2944+335C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 20/29 | chr3 | 183951106 | ||||||
| chr3:183951155
|
G | A | 1 | a0001c0002t0001g0080 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2944+286C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 20/29 | chr3 | 183951155 | ||||||
| chr3:183951198
|
C | T | 1 | a0001c0002t0001g0093 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2944+243G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 20/29 | chr3 | 183951198 | ||||||
| chr3:183951608
|
C | T | 64 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(61): Show | 65 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.2815-38G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 19/29 | chr3 | 183951608 | ||||||
| chr3:183951723
|
G | A | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2814+134C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 19/29 | chr3 | 183951723 | ||||||
| chr3:183951800
|
C | G | 1 | a0001c0001t0003g0219 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2814+57G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 19/29 | chr3 | 183951800 | ||||||
| chr3:183951808
|
G | A | 1 | a0001c0001t0003g0219 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2814+49C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 19/29 | chr3 | 183951808 | ||||||
| chr3:183952144
|
C | CT | 36 | a0001c0001t0003g0240a0001c0002t0001g0364a0001c0003t0002g0297others(33): Show | 36 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.2668-142dupA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 18/29 | chr3 | 183952144 | ||||||
| chr3:183952144
|
CT | C | 103 | a0001c0001t0003g0245a0001c0001t0005g0143a0001c0001t0007g0014others(100): Show | 106 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.2668-142delA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 18/29 | chr3 | 183952144 | ||||||
| chr3:183952144
|
CTT | C | 80 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(77): Show | 82 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.2668-143_2668-142d others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 18/29 | chr3 | 183952144 | ||||||
| chr3:183952207
|
C | T | 3 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0196 | 3 | HG01109.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2668-204G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 18/29 | chr3 | 183952207 | ||||||
| chr3:183952303
|
T | C | 1 | a0001c0002t0001g0307 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2668-300A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 18/29 | chr3 | 183952303 | ||||||
| chr3:183952338
|
G | C | 107 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(104): Show | 111 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.2668-335C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 18/29 | chr3 | 183952338 | ||||||
| chr3:183952415
|
G | A | 1 | a0001c0001t0003g0218 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2668-412C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 18/29 | chr3 | 183952415 | ||||||
| chr3:183952593
|
G | A | 7 | a0001c0001t0003g0218a0001c0001t0003g0223a0001c0001t0003g0234others(4): Show | 7 | HG01192.hp2 HG01516.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.2667+493C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 18/29 | chr3 | 183952593 | ||||||
| chr3:183952840
|
C | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG02683.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2667+246G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 18/29 | chr3 | 183952840 | ||||||
| chr3:183952845
|
C | T | 64 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(61): Show | 65 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.2667+241G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 18/29 | chr3 | 183952845 | ||||||
| chr3:183952854
|
A | G | 286 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(283): Show | 294 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(291): Show |
intron_variant | MODIFIER | c.2667+232T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 18/29 | chr3 | 183952854 | ||||||
| chr3:183952884
|
C | A | 84 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(81): Show | 86 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.2667+202G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 18/29 | chr3 | 183952884 | ||||||
| chr3:183952909
|
C | T | 1 | a0001c0001t0006g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2667+177G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 18/29 | chr3 | 183952909 | ||||||
| chr3:183953304
|
G | A | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.2483-34C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183953304 | ||||||
| chr3:183953360
|
C | T | 1 | a0001c0001t0003g0239 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2483-90G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183953360 | ||||||
| chr3:183953420
|
T | C | 6 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193others(3): Show | 6 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2483-150A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183953420 | ||||||
| chr3:183953458
|
G | A | 1 | a0001c0004t0004g0255 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2483-188C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183953458 | ||||||
| chr3:183953514
|
C | A | 2 | a0001c0004t0002g0070a0001c0004t0002g0304 | 2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2483-244G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183953514 | ||||||
| chr3:183953552
|
G | T | 64 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(61): Show | 65 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.2483-282C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183953552 | ||||||
| chr3:183953814
|
C | T | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2483-544G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183953814 | ||||||
| chr3:183953937
|
T | C | 1 | a0001c0003t0002g0279 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2483-667A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183953937 | ||||||
| chr3:183953940
|
C | G | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2483-670G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183953940 | ||||||
| chr3:183953960
|
T | G | 4 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2483-690A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183953960 | ||||||
| chr3:183953968
|
G | A | 2 | a0001c0003t0002g0056a0003c0017t0002g0327 | 2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2483-698C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183953968 | ||||||
| chr3:183953979
|
G | C | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2483-709C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183953979 | ||||||
| chr3:183953996
|
C | T | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.2483-726G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183953996 | ||||||
| chr3:183954156
|
G | GT | 170 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(167): Show | 174 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.2483-887dupA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183954156 | ||||||
| chr3:183954297
|
C | T | 1 | a0001c0003t0017g0330 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2483-1027G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183954297 | ||||||
| chr3:183954305
|
C | A | 1 | a0001c0003t0002g0284 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2483-1035G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183954305 | ||||||
| chr3:183954342
|
T | G | 1 | a0001c0003t0011g0367 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2483-1072A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183954342 | ||||||
| chr3:183954395
|
T | C | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2483-1125A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183954395 | ||||||
| chr3:183954483
|
C | T | 10 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0358others(7): Show | 10 | HG00735.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2483-1213G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183954483 | ||||||
| chr3:183954492
|
G | A | 107 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(104): Show | 111 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.2483-1222C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183954492 | ||||||
| chr3:183954579
|
G | A | 1 | a0001c0001t0006g0055 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2483-1309C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183954579 | ||||||
| chr3:183954695
|
T | C | 3 | a0001c0003t0002g0328a0001c0003t0002g0329a0001c0003t0017g0330 | 3 | HG00280.hp2 HG01123.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2483-1425A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183954695 | ||||||
| chr3:183955041
|
G | C | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2483-1771C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183955041 | ||||||
| chr3:183955045
|
G | T | 11 | a0001c0002t0001g0001a0001c0002t0001g0050a0001c0002t0001g0071others(8): Show | 13 | HG00621.hp2 HG01346.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.2483-1775C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183955045 | ||||||
| chr3:183955058
|
C | T | 64 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(61): Show | 65 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.2483-1788G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183955058 | ||||||
| chr3:183955113
|
C | T | 6 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193others(3): Show | 6 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2483-1843G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183955113 | ||||||
| chr3:183955300
|
T | C | 6 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193others(3): Show | 6 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2483-2030A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183955300 | ||||||
| chr3:183955624
|
TGTTACAT others(505): Show |
T | 102 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(99): Show | 106 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.2483-2866_2483-235 others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183955624 | ||||||
| chr3:183955624
|
TGTTACAT others(537): Show |
T | 6 | a0001c0002t0001g0131a0001c0002t0009g0266a0001c0002t0009g0267others(3): Show | 6 | HG01358.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2483-2898_2483-235 others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183955624 | ||||||
| chr3:183955687
|
C | T | 3 | a0001c0001t0001g0177a0001c0001t0005g0144a0001c0001t0005g0167 | 3 | HG00438.hp1 NA18999.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.2483-2417G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183955687 | ||||||
| chr3:183955896
|
A | G | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2483-2626T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183955896 | ||||||
| chr3:183955992
|
A | G | 178 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(175): Show | 182 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.2483-2722T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183955992 | ||||||
| chr3:183956095
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2483-2825A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956095 | ||||||
| chr3:183956116
|
CTCCGTGT others(25): Show |
C | 71 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(68): Show | 72 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.2483-2878_2483-284 others(36): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956116 | ||||||
| chr3:183956127
|
T | C | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.2483-2857A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956127 | ||||||
| chr3:183956127
|
T | TATCACAT others(25): Show |
1 | a0001c0003t0002g0319 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2483-2889_2483-285 others(36): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956127 | ||||||
| chr3:183956127
|
TATCACAT others(25): Show |
T | 59 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(56): Show | 61 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(58): Show |
intron_variant | MODIFIER | c.2483-2889_2483-285 others(36): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956127 | ||||||
| chr3:183956136
|
G | A | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.2483-2866C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956136 | ||||||
| chr3:183956159
|
A | C | 71 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(68): Show | 72 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.2483-2889T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956159 | ||||||
| chr3:183956255
|
A | T | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.2483-2985T>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956255 | ||||||
| chr3:183956264
|
G | T | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.2483-2994C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956264 | ||||||
| chr3:183956286
|
A | C | 56 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(53): Show | 58 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(55): Show |
intron_variant | MODIFIER | c.2483-3016T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956286 | ||||||
| chr3:183956287
|
T | A | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.2483-3017A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956287 | ||||||
| chr3:183956296
|
T | C | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2483-3026A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956296 | ||||||
| chr3:183956296
|
T | G | 15 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(12): Show | 16 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.2483-3026A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956296 | ||||||
| chr3:183956319
|
A | T | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.2483-3049T>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956319 | ||||||
| chr3:183956340
|
A | C | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.2483-3070T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956340 | ||||||
| chr3:183956351
|
T | A | 16 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(13): Show | 17 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.2483-3081A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956351 | ||||||
| chr3:183956359
|
C | A | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.2483-3089G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956359 | ||||||
| chr3:183956372
|
C | A | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.2483-3102G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956372 | ||||||
| chr3:183956383
|
A | T | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.2483-3113T>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956383 | ||||||
| chr3:183956388
|
C | T | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.2483-3118G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956388 | ||||||
| chr3:183956391
|
A | C | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.2483-3121T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956391 | ||||||
| chr3:183956415
|
T | A | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.2483-3145A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956415 | ||||||
| chr3:183956420
|
T | C | 25 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(22): Show | 26 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.2483-3150A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956420 | ||||||
| chr3:183956420
|
TATCGGTT others(25): Show |
T | 1 | a0001c0003t0002g0318 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2483-3182_2483-315 others(36): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956420 | ||||||
| chr3:183956423
|
C | A | 10 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0358others(7): Show | 10 | HG00735.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2483-3153G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956423 | ||||||
| chr3:183956434
|
A | G | 19 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(16): Show | 20 | HG00423.hp2 HG00544.hp1 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.2483-3164T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956434 | ||||||
| chr3:183956440
|
G | A | 3 | a0001c0001t0006g0002a0001c0001t0006g0288a0001c0001t0006g0289 | 4 | HG03130.hp2 HG03195.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2483-3170C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956440 | ||||||
| chr3:183956447
|
A | T | 14 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(11): Show | 15 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.2483-3177T>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956447 | ||||||
| chr3:183956447
|
AATCACAT others(57): Show |
A | 10 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0358others(7): Show | 10 | HG00735.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2482+3222_2483-317 others(68): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956447 | ||||||
| chr3:183956456
|
G | T | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.2483-3186C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956456 | ||||||
| chr3:183956469
|
T | G | 1 | a0001c0003t0002g0314 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2483-3199A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956469 | ||||||
| chr3:183956479
|
T | A | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.2483-3209A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956479 | ||||||
| chr3:183956488
|
T | G | 99 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(96): Show | 103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.2483-3218A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956488 | ||||||
| chr3:183956503
|
CGTGTGTA others(25): Show |
C | 56 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(53): Show | 58 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(55): Show |
intron_variant | MODIFIER | c.2482+3198_2482+322 others(36): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956503 | ||||||
| chr3:183956511
|
T | A | 1 | a0001c0007t0008g0254 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2482+3222A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956511 | ||||||
| chr3:183956520
|
G | T | 1 | a0001c0007t0008g0254 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2482+3213C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956520 | ||||||
| chr3:183956530
|
A | G | 7 | a0001c0001t0001g0156a0001c0001t0006g0351a0001c0001t0007g0139others(4): Show | 7 | HG00323.hp2 HG01192.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2482+3203T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956530 | ||||||
| chr3:183956535
|
A | C | 5 | a0001c0002t0001g0060a0001c0002t0001g0061a0001c0002t0001g0062others(2): Show | 5 | NA18954.hp2 NA18993.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.2482+3198T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956535 | ||||||
| chr3:183956551
|
C | A | 1 | a0001c0003t0002g0337 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2482+3182G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956551 | ||||||
| chr3:183956552
|
G | T | 5 | a0001c0002t0001g0060a0001c0002t0001g0061a0001c0002t0001g0062others(2): Show | 5 | NA18954.hp2 NA18993.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.2482+3181C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956552 | ||||||
| chr3:183956562
|
AGATCAGT others(217): Show |
A | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2482+2947_2482+317 others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956562 | ||||||
| chr3:183956567
|
A | C | 108 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(105): Show | 112 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.2482+3166T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956567 | ||||||
| chr3:183956594
|
AGATCCGT others(185): Show |
A | 30 | a0001c0003t0002g0028a0001c0004t0002g0070a0001c0004t0002g0304others(27): Show | 30 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.2482+2947_2482+313 others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956594 | ||||||
| chr3:183956605
|
T | C | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG02683.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2482+3128A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956605 | ||||||
| chr3:183956616
|
T | G | 19 | a0001c0003t0002g0008a0001c0003t0002g0275a0001c0003t0002g0276others(16): Show | 20 | HG00280.hp2 HG00558.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2482+3117A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956616 | ||||||
| chr3:183956632
|
G | C | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.2482+3101C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956632 | ||||||
| chr3:183956648
|
G | A | 105 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(102): Show | 109 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.2482+3085C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956648 | ||||||
| chr3:183956664
|
G | A | 1 | a0001c0001t0006g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2482+3069C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956664 | ||||||
| chr3:183956664
|
G | C | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.2482+3069C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956664 | ||||||
| chr3:183956677
|
A | C | 1 | a0001c0003t0002g0276 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2482+3056T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956677 | ||||||
| chr3:183956735
|
A | C | 10 | a0001c0002t0001g0004a0001c0002t0001g0096a0001c0002t0001g0101others(7): Show | 11 | HG01257.hp1 HG01258.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.2482+2998T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956735 | ||||||
| chr3:183956760
|
G | A | 3 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193 | 3 | HG02109.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2482+2973C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956760 | ||||||
| chr3:183956767
|
CATCACAT others(153): Show |
C | 70 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(67): Show | 73 | HG00423.hp2 HG00544.hp1 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.2482+2806_2482+296 others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956767 | ||||||
| chr3:183956785
|
C | T | 2 | a0001c0003t0002g0354a0001c0003t0002g0357 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2482+2948G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956785 | ||||||
| chr3:183956786
|
GGATCCGT others(121): Show |
G | 113 | a0001c0001t0003g0224a0001c0001t0003g0225a0001c0001t0003g0227others(110): Show | 117 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.2482+2819_2482+294 others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956786 | ||||||
| chr3:183956791
|
C | CGTGTGTA others(1017): Show |
1 | a0001c0001t0007g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2482+2941_2482+294 others(1028): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956791 | ||||||
| chr3:183956799
|
T | C | 74 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(71): Show | 76 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.2482+2934A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956799 | ||||||
| chr3:183956807
|
CTGTTACA others(89): Show |
C | 1 | a0001c0002t0001g0131 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2482+2830_2482+292 others(100): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956807 | ||||||
| chr3:183956808
|
T | G | 70 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(67): Show | 71 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.2482+2925A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956808 | ||||||
| chr3:183956818
|
A | G | 71 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(68): Show | 72 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.2482+2915T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956818 | ||||||
| chr3:183956831
|
A | C | 69 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(66): Show | 70 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2482+2902T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956831 | ||||||
| chr3:183956831
|
A | T | 1 | a0001c0001t0007g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2482+2902T>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956831 | ||||||
| chr3:183956840
|
G | T | 1 | a0001c0001t0007g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2482+2893C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956840 | ||||||
| chr3:183956850
|
A | G | 69 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(66): Show | 70 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2482+2883T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956850 | ||||||
| chr3:183956852
|
A | G | 69 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(66): Show | 70 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2482+2881T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956852 | ||||||
| chr3:183956863
|
T | A | 1 | a0001c0001t0007g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2482+2870A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956863 | ||||||
| chr3:183956863
|
T | C | 69 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(66): Show | 70 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2482+2870A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956863 | ||||||
| chr3:183956868
|
T | C | 70 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(67): Show | 71 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.2482+2865A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956868 | ||||||
| chr3:183956871
|
A | C | 70 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(67): Show | 71 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.2482+2862T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956871 | ||||||
| chr3:183956882
|
A | G | 69 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(66): Show | 70 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2482+2851T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956882 | ||||||
| chr3:183956884
|
A | G | 63 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(60): Show | 64 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.2482+2849T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956884 | ||||||
| chr3:183956895
|
T | C | 63 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(60): Show | 64 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.2482+2838A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956895 | ||||||
| chr3:183956900
|
T | C | 69 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(66): Show | 70 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2482+2833A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956900 | ||||||
| chr3:183956902
|
T | A | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2482+2831A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956902 | ||||||
| chr3:183956903
|
A | C | 69 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(66): Show | 70 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2482+2830T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956903 | ||||||
| chr3:183956911
|
T | C | 7 | a0001c0001t0001g0173a0001c0001t0007g0013a0001c0001t0007g0194others(4): Show | 7 | HG01109.hp2 HG01346.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2482+2822A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956911 | ||||||
| chr3:183956913
|
C | T | 6 | a0001c0001t0007g0013a0001c0001t0007g0194a0001c0001t0007g0195others(3): Show | 6 | HG01109.hp2 HG02818.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2482+2820G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956913 | ||||||
| chr3:183956914
|
A | G | 64 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(61): Show | 65 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.2482+2819T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956914 | ||||||
| chr3:183956915
|
G | A | 6 | a0001c0001t0007g0013a0001c0001t0007g0194a0001c0001t0007g0195others(3): Show | 6 | HG01109.hp2 HG02818.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2482+2818C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956915 | ||||||
| chr3:183956919
|
C | T | 1 | a0001c0005t0002g0274 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2482+2814G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956919 | ||||||
| chr3:183956920
|
G | A | 3 | a0001c0001t0003g0240a0001c0001t0003g0242a0001c0022t0003g0024 | 3 | NA18948.hp1 NA18985.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.2482+2813C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956920 | ||||||
| chr3:183956927
|
A | C | 178 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(175): Show | 183 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.2482+2806T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956927 | ||||||
| chr3:183956927
|
A | T | 7 | a0001c0001t0007g0013a0001c0001t0007g0014a0001c0001t0007g0194others(4): Show | 7 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2482+2806T>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956927 | ||||||
| chr3:183956932
|
C | T | 1 | a0001c0001t0007g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2482+2801G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956932 | ||||||
| chr3:183956935
|
C | A | 1 | a0001c0001t0007g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2482+2798G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956935 | ||||||
| chr3:183956943
|
T | C | 69 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(66): Show | 70 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2482+2790A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956943 | ||||||
| chr3:183956945
|
C | T | 63 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(60): Show | 64 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.2482+2788G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956945 | ||||||
| chr3:183956946
|
G | A | 70 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(67): Show | 71 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.2482+2787C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956946 | ||||||
| chr3:183956947
|
G | A | 63 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(60): Show | 64 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.2482+2786C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956947 | ||||||
| chr3:183956948
|
A | G | 12 | a0001c0001t0003g0224a0001c0001t0003g0225a0001c0001t0003g0227others(9): Show | 12 | HG00597.hp2 HG03834.hp1 NA18948.hp1 others(9): Show |
intron_variant | MODIFIER | c.2482+2785T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956948 | ||||||
| chr3:183956959
|
C | A | 1 | a0001c0001t0007g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2482+2774G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956959 | ||||||
| chr3:183956959
|
C | T | 69 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(66): Show | 70 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2482+2774G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956959 | ||||||
| chr3:183956968
|
G | T | 6 | a0001c0001t0007g0013a0001c0001t0007g0194a0001c0001t0007g0195others(3): Show | 6 | HG01109.hp2 HG02818.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2482+2765C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956968 | ||||||
| chr3:183956975
|
T | C | 63 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(60): Show | 64 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.2482+2758A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956975 | ||||||
| chr3:183956978
|
G | A | 63 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(60): Show | 64 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.2482+2755C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956978 | ||||||
| chr3:183956980
|
A | G | 57 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(54): Show | 59 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(56): Show |
intron_variant | MODIFIER | c.2482+2753T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956980 | ||||||
| chr3:183956980
|
ATCCGTGT others(57): Show |
A | 1 | a0001c0003t0002g0009 | 2 | HG01891.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2482+2689_2482+275 others(68): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956980 | ||||||
| chr3:183956983
|
C | T | 1 | a0001c0001t0003g0249 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2482+2750G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956983 | ||||||
| chr3:183956991
|
C | T | 69 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(66): Show | 70 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2482+2742G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183956991 | ||||||
| chr3:183957000
|
G | T | 63 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(60): Show | 64 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.2482+2733C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957000 | ||||||
| chr3:183957007
|
T | C | 3 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0184 | 3 | HG02683.hp1 NA18957.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2482+2726A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957007 | ||||||
| chr3:183957009
|
C | T | 1 | a0001c0001t0003g0249 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2482+2724G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957009 | ||||||
| chr3:183957012
|
A | G | 80 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(77): Show | 83 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(80): Show |
intron_variant | MODIFIER | c.2482+2721T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957012 | ||||||
| chr3:183957012
|
ATCCGTGT others(25): Show |
A | 3 | a0001c0003t0011g0366a0001c0003t0011g0367a0001c0003t0011g0368 | 3 | HG01433.hp2 HG03239.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.2482+2689_2482+272 others(36): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957012 | ||||||
| chr3:183957023
|
C | T | 62 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(59): Show | 63 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.2482+2710G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957023 | ||||||
| chr3:183957044
|
G | A | 78 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(75): Show | 79 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.2482+2689C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957044 | ||||||
| chr3:183957052
|
G | T | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.2482+2681C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957052 | ||||||
| chr3:183957074
|
G | A | 3 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0196 | 3 | HG01109.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2482+2659C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957074 | ||||||
| chr3:183957076
|
G | A | 70 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(67): Show | 71 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.2482+2657C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957076 | ||||||
| chr3:183957103
|
T | C | 1 | a0001c0001t0005g0190 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2482+2630A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957103 | ||||||
| chr3:183957105
|
C | T | 1 | a0001c0001t0005g0190 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2482+2628G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957105 | ||||||
| chr3:183957106
|
G | A | 70 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(67): Show | 71 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.2482+2627C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957106 | ||||||
| chr3:183957107
|
G | A | 1 | a0001c0001t0005g0190 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2482+2626C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957107 | ||||||
| chr3:183957108
|
G | A | 84 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(81): Show | 86 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.2482+2625C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957108 | ||||||
| chr3:183957110
|
C | T | 6 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193others(3): Show | 6 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2482+2623G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957110 | ||||||
| chr3:183957111
|
C | T | 6 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193others(3): Show | 6 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2482+2622G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957111 | ||||||
| chr3:183957119
|
C | T | 20 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(17): Show | 21 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.2482+2614G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957119 | ||||||
| chr3:183957127
|
C | T | 1 | a0001c0002t0001g0306 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2482+2606G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957127 | ||||||
| chr3:183957128
|
G | T | 6 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193others(3): Show | 6 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2482+2605C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957128 | ||||||
| chr3:183957130
|
T | G | 6 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193others(3): Show | 6 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2482+2603A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957130 | ||||||
| chr3:183957135
|
T | C | 15 | a0001c0001t0005g0190a0001c0001t0006g0002a0001c0001t0006g0015others(12): Show | 16 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.2482+2598A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957135 | ||||||
| chr3:183957137
|
C | T | 15 | a0001c0001t0005g0190a0001c0001t0006g0002a0001c0001t0006g0015others(12): Show | 16 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.2482+2596G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957137 | ||||||
| chr3:183957137
|
CGGGTCCG others(25): Show |
C | 6 | a0001c0001t0007g0013a0001c0001t0007g0194a0001c0001t0007g0195others(3): Show | 6 | HG01109.hp2 HG02818.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2482+2564_2482+259 others(36): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957137 | ||||||
| chr3:183957138
|
G | A | 15 | a0001c0001t0005g0190a0001c0001t0006g0002a0001c0001t0006g0015others(12): Show | 16 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.2482+2595C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957138 | ||||||
| chr3:183957138
|
G | T | 6 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193others(3): Show | 6 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2482+2595C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957138 | ||||||
| chr3:183957139
|
G | A | 15 | a0001c0001t0005g0190a0001c0001t0006g0002a0001c0001t0006g0015others(12): Show | 16 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.2482+2594C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957139 | ||||||
| chr3:183957139
|
G | T | 6 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193others(3): Show | 6 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2482+2594C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957139 | ||||||
| chr3:183957140
|
G | A | 21 | a0001c0001t0005g0190a0001c0001t0006g0002a0001c0001t0006g0015others(18): Show | 22 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2482+2593C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957140 | ||||||
| chr3:183957151
|
C | T | 15 | a0001c0001t0005g0190a0001c0001t0006g0002a0001c0001t0006g0015others(12): Show | 16 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.2482+2582G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957151 | ||||||
| chr3:183957151
|
CATCACAT others(153): Show |
C | 47 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0029others(44): Show | 47 | HG00408.hp2 HG00544.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.2482+2422_2482+258 others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957151 | ||||||
| chr3:183957160
|
GGTTACAT others(121): Show |
G | 2 | a0001c0002t0001g0131a0001c0002t0001g0360 | 2 | HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2482+2445_2482+257 others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957160 | ||||||
| chr3:183957167
|
T | C | 15 | a0001c0001t0005g0190a0001c0001t0006g0002a0001c0001t0006g0015others(12): Show | 16 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.2482+2566A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957167 | ||||||
| chr3:183957169
|
T | C | 137 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(134): Show | 143 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.2482+2564A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957169 | ||||||
| chr3:183957170
|
G | A | 15 | a0001c0001t0005g0190a0001c0001t0006g0002a0001c0001t0006g0015others(12): Show | 16 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.2482+2563C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957170 | ||||||
| chr3:183957172
|
G | A | 15 | a0001c0001t0005g0190a0001c0001t0006g0002a0001c0001t0006g0015others(12): Show | 16 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.2482+2561C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957172 | ||||||
| chr3:183957175
|
C | T | 59 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(56): Show | 61 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(58): Show |
intron_variant | MODIFIER | c.2482+2558G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957175 | ||||||
| chr3:183957192
|
G | T | 15 | a0001c0001t0005g0190a0001c0001t0006g0002a0001c0001t0006g0015others(12): Show | 16 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.2482+2541C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957192 | ||||||
| chr3:183957202
|
T | G | 15 | a0001c0001t0005g0190a0001c0001t0006g0002a0001c0001t0006g0015others(12): Show | 16 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.2482+2531A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957202 | ||||||
| chr3:183957203
|
T | G | 15 | a0001c0001t0005g0190a0001c0001t0006g0002a0001c0001t0006g0015others(12): Show | 16 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.2482+2530A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957203 | ||||||
| chr3:183957212
|
G | A | 1 | a0001c0003t0011g0368 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2482+2521C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957212 | ||||||
| chr3:183957234
|
A | G | 15 | a0001c0001t0005g0190a0001c0001t0006g0002a0001c0001t0006g0015others(12): Show | 16 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.2482+2499T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957234 | ||||||
| chr3:183957240
|
G | A | 69 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(66): Show | 70 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2482+2493C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957240 | ||||||
| chr3:183957247
|
T | C | 15 | a0001c0001t0005g0190a0001c0001t0006g0002a0001c0001t0006g0015others(12): Show | 16 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.2482+2486A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957247 | ||||||
| chr3:183957256
|
T | G | 16 | a0001c0001t0005g0190a0001c0001t0006g0002a0001c0001t0006g0015others(13): Show | 17 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.2482+2477A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957256 | ||||||
| chr3:183957271
|
C | T | 1 | a0001c0001t0006g0351 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2482+2462G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957271 | ||||||
| chr3:183957279
|
T | C | 15 | a0001c0001t0005g0190a0001c0001t0006g0002a0001c0001t0006g0015others(12): Show | 16 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.2482+2454A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957279 | ||||||
| chr3:183957282
|
G | C | 15 | a0001c0001t0005g0190a0001c0001t0006g0002a0001c0001t0006g0015others(12): Show | 16 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.2482+2451C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957282 | ||||||
| chr3:183957288
|
A | G | 15 | a0001c0001t0005g0190a0001c0001t0006g0002a0001c0001t0006g0015others(12): Show | 16 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.2482+2445T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957288 | ||||||
| chr3:183957288
|
A | T | 1 | a0001c0002t0001g0095 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2482+2445T>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957288 | ||||||
| chr3:183957298
|
G | A | 11 | a0001c0001t0006g0015a0001c0001t0006g0027a0001c0001t0006g0051others(8): Show | 11 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.2482+2435C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957298 | ||||||
| chr3:183957300
|
A | G | 2 | a0001c0002t0001g0131a0001c0002t0001g0360 | 2 | HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2482+2433T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957300 | ||||||
| chr3:183957311
|
A | C | 17 | a0001c0001t0005g0190a0001c0001t0006g0002a0001c0001t0006g0015others(14): Show | 18 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.2482+2422T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957311 | ||||||
| chr3:183957330
|
G | A | 59 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(56): Show | 63 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.2482+2403C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957330 | ||||||
| chr3:183957330
|
G | T | 69 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(66): Show | 70 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2482+2403C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957330 | ||||||
| chr3:183957331
|
G | T | 69 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(66): Show | 70 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2482+2402C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957331 | ||||||
| chr3:183957331
|
GGTCCGTG others(185): Show |
G | 59 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(56): Show | 63 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.2482+2210_2482+240 others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957331 | ||||||
| chr3:183957332
|
G | A | 69 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(66): Show | 70 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2482+2401C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957332 | ||||||
| chr3:183957352
|
G | A | 69 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(66): Show | 70 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2482+2381C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957352 | ||||||
| chr3:183957364
|
G | A | 69 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(66): Show | 70 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2482+2369C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957364 | ||||||
| chr3:183957375
|
T | C | 69 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(66): Show | 70 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2482+2358A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957375 | ||||||
| chr3:183957384
|
G | A | 6 | a0001c0002t0001g0131a0001c0002t0009g0266a0001c0002t0009g0267others(3): Show | 6 | HG01358.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2482+2349C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957384 | ||||||
| chr3:183957395
|
TATCCGTG others(153): Show |
T | 69 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(66): Show | 70 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2482+2178_2482+233 others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957395 | ||||||
| chr3:183957432
|
A | G | 51 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0029others(48): Show | 51 | HG00408.hp2 HG00544.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.2482+2301T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957432 | ||||||
| chr3:183957488
|
G | C | 56 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(53): Show | 58 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(55): Show |
intron_variant | MODIFIER | c.2482+2245C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957488 | ||||||
| chr3:183957522
|
T | A | 49 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0029others(46): Show | 49 | HG00408.hp2 HG00544.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.2482+2211A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957522 | ||||||
| chr3:183957523
|
T | G | 49 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0029others(46): Show | 49 | HG00408.hp2 HG00544.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.2482+2210A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957523 | ||||||
| chr3:183957527
|
T | C | 188 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(185): Show | 195 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(192): Show |
intron_variant | MODIFIER | c.2482+2206A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957527 | ||||||
| chr3:183957528
|
G | A | 108 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(105): Show | 112 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.2482+2205C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957528 | ||||||
| chr3:183957544
|
A | G | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2482+2189T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957544 | ||||||
| chr3:183957555
|
G | GATCCGTG others(25): Show |
15 | a0001c0001t0005g0190a0001c0001t0006g0002a0001c0001t0006g0015others(12): Show | 16 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.2482+2146_2482+217 others(36): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957555 | ||||||
| chr3:183957570
|
C | G | 2 | a0001c0003t0002g0291a0001c0003t0002g0352 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2482+2163G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957570 | ||||||
| chr3:183957596
|
G | C | 1 | a0001c0004t0004g0255 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2482+2137C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957596 | ||||||
| chr3:183957624
|
A | G | 2 | a0001c0004t0002g0070a0001c0004t0002g0304 | 2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2482+2109T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957624 | ||||||
| chr3:183957672
|
G | A | 10 | a0001c0004t0004g0120a0001c0004t0004g0121a0001c0004t0004g0122others(7): Show | 10 | HG00639.hp1 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.2482+2061C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957672 | ||||||
| chr3:183957687
|
C | T | 1 | a0001c0002t0009g0268 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2482+2046G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957687 | ||||||
| chr3:183957727
|
C | CATCACAT others(25): Show |
26 | a0001c0004t0002g0070a0001c0004t0002g0304a0001c0004t0004g0112others(23): Show | 26 | HG00639.hp1 HG01891.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.2482+1974_2482+200 others(36): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957727 | ||||||
| chr3:183957743
|
T | C | 6 | a0001c0002t0001g0271a0001c0002t0001g0272a0001c0002t0001g0273others(3): Show | 6 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.2482+1990A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957743 | ||||||
| chr3:183957743
|
T | TGCGGATC others(25): Show |
3 | a0001c0004t0004g0132a0001c0004t0004g0133a0001c0004t0004g0134 | 3 | HG01167.hp2 HG01169.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2482+1958_2482+198 others(36): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957743 | ||||||
| chr3:183957746
|
G | A | 108 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(105): Show | 112 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.2482+1987C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957746 | ||||||
| chr3:183957774
|
A | C | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2482+1959T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957774 | ||||||
| chr3:183957775
|
C | T | 114 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(111): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.2482+1958G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957775 | ||||||
| chr3:183957777
|
T | C | 262 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(259): Show | 271 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(268): Show |
intron_variant | MODIFIER | c.2482+1956A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957777 | ||||||
| chr3:183957778
|
A | G | 256 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(253): Show | 264 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(261): Show |
intron_variant | MODIFIER | c.2482+1955T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957778 | ||||||
| chr3:183957779
|
A | G | 256 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(253): Show | 264 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(261): Show |
intron_variant | MODIFIER | c.2482+1954T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957779 | ||||||
| chr3:183957783
|
C | T | 1 | a0001c0004t0004g0255 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2482+1950G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957783 | ||||||
| chr3:183957807
|
C | T | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2482+1926G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957807 | ||||||
| chr3:183957807
|
CGCAGATC others(25): Show |
C | 1 | a0001c0001t0003g0022 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2482+1894_2482+192 others(36): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957807 | ||||||
| chr3:183957808
|
G | A | 2 | a0001c0003t0002g0300a0001c0003t0002g0316 | 2 | HG00280.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2482+1925C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957808 | ||||||
| chr3:183957809
|
C | T | 256 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(253): Show | 264 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(261): Show |
intron_variant | MODIFIER | c.2482+1924G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957809 | ||||||
| chr3:183957811
|
G | A | 256 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(253): Show | 264 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(261): Show |
intron_variant | MODIFIER | c.2482+1922C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957811 | ||||||
| chr3:183957832
|
T | G | 256 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(253): Show | 264 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(261): Show |
intron_variant | MODIFIER | c.2482+1901A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957832 | ||||||
| chr3:183957839
|
T | C | 256 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(253): Show | 264 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(261): Show |
intron_variant | MODIFIER | c.2482+1894A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957839 | ||||||
| chr3:183957842
|
G | A | 198 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(195): Show | 204 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.2482+1891C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957842 | ||||||
| chr3:183957864
|
TGTTACAT others(25): Show |
T | 1 | a0001c0001t0005g0158 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2482+1837_2482+186 others(36): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957864 | ||||||
| chr3:183957874
|
G | A | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2482+1859C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957874 | ||||||
| chr3:183957887
|
T | C | 26 | a0001c0004t0004g0112a0001c0004t0004g0115a0001c0004t0004g0116others(23): Show | 26 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.2482+1846A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957887 | ||||||
| chr3:183957896
|
G | T | 251 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(248): Show | 259 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(256): Show |
intron_variant | MODIFIER | c.2482+1837C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957896 | ||||||
| chr3:183957908
|
A | G | 26 | a0001c0004t0004g0112a0001c0004t0004g0115a0001c0004t0004g0116others(23): Show | 26 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.2482+1825T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957908 | ||||||
| chr3:183957912
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2482+1821C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957912 | ||||||
| chr3:183957919
|
T | C | 31 | a0001c0001t0003g0259a0001c0003t0002g0302a0001c0003t0002g0317others(28): Show | 31 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.2482+1814A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957919 | ||||||
| chr3:183957919
|
TATCACAT others(25): Show |
T | 6 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(3): Show | 6 | HG00408.hp1 HG02523.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.2482+1782_2482+181 others(36): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957919 | ||||||
| chr3:183957951
|
C | T | 107 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(104): Show | 111 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.2482+1782G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957951 | ||||||
| chr3:183957970
|
G | A | 1 | a0001c0002t0001g0101 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2482+1763C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957970 | ||||||
| chr3:183957970
|
GGATCCGT others(25): Show |
G | 1 | a0001c0002t0001g0032 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2482+1731_2482+176 others(36): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957970 | ||||||
| chr3:183957984
|
A | G | 1 | a0001c0002t0001g0080 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2482+1749T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183957984 | ||||||
| chr3:183958002
|
A | G | 114 | a0001c0001t0001g0159a0001c0001t0001g0164a0001c0001t0001g0166others(111): Show | 118 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.2482+1731T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183958002 | ||||||
| chr3:183958008
|
G | A | 1 | a0001c0002t0008g0262 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2482+1725C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183958008 | ||||||
| chr3:183958015
|
CATCACAT others(25): Show |
C | 4 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2482+1686_2482+171 others(36): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183958015 | ||||||
| chr3:183958020
|
C | T | 1 | a0001c0002t0001g0091 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2482+1713G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183958020 | ||||||
| chr3:183958039
|
C | T | 1 | a0001c0003t0002g0301 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2482+1694G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183958039 | ||||||
| chr3:183958088
|
T | C | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2482+1645A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183958088 | ||||||
| chr3:183958145
|
T | A | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2482+1588A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183958145 | ||||||
| chr3:183958167
|
C | T | 7 | a0001c0001t0007g0013a0001c0001t0007g0014a0001c0001t0007g0194others(4): Show | 7 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2482+1566G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183958167 | ||||||
| chr3:183958408
|
A | G | 1 | a0001c0001t0003g0207 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2482+1325T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183958408 | ||||||
| chr3:183958554
|
C | T | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2482+1179G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183958554 | ||||||
| chr3:183958605
|
A | C | 2 | a0001c0003t0002g0291a0001c0003t0002g0352 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2482+1128T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183958605 | ||||||
| chr3:183958839
|
A | G | 1 | a0009c0010t0018g0353 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2482+894T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183958839 | ||||||
| chr3:183959052
|
T | TAC | 68 | a0001c0001t0006g0015a0001c0001t0006g0051a0001c0001t0006g0052others(65): Show | 70 | HG00280.hp1 HG00323.hp2 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.2482+679_2482+680d others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183959052 | ||||||
| chr3:183959052
|
T | TACAC | 16 | a0001c0001t0006g0002a0001c0001t0006g0027a0001c0001t0006g0059others(13): Show | 17 | HG00639.hp2 HG01074.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.2482+677_2482+680d others(6): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183959052 | ||||||
| chr3:183959052
|
T | TACACAC | 119 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(116): Show | 122 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.2482+675_2482+680d others(8): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183959052 | ||||||
| chr3:183959052
|
T | TACACACA others(1): Show |
44 | a0001c0001t0003g0259a0001c0002t0001g0004a0001c0002t0001g0040others(41): Show | 45 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.2482+673_2482+680d others(10): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183959052 | ||||||
| chr3:183959052
|
T | TACACACA others(3): Show |
5 | a0001c0002t0001g0042a0001c0002t0001g0060a0001c0004t0004g0116others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2482+671_2482+680d others(12): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183959052 | ||||||
| chr3:183959052
|
T | TACACACA others(5): Show |
2 | a0001c0002t0001g0307a0001c0004t0004g0130 | 2 | HG02109.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.2482+669_2482+680d others(14): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183959052 | ||||||
| chr3:183959052
|
T | TACACACA others(7): Show |
1 | a0001c0002t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2482+667_2482+680d others(16): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183959052 | ||||||
| chr3:183959052
|
TAC | T | 17 | a0001c0001t0001g0145a0001c0001t0001g0183a0001c0001t0005g0190others(14): Show | 17 | HG00408.hp2 HG00597.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2482+679_2482+680d others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183959052 | ||||||
| chr3:183959052
|
TACAC | T | 61 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(58): Show | 62 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.2482+677_2482+680d others(6): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183959052 | ||||||
| chr3:183959589
|
A | G | 9 | a0001c0001t0003g0205a0001c0001t0003g0210a0001c0001t0003g0211others(6): Show | 9 | NA18747.hp2 NA18962.hp1 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.2482+144T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183959589 | ||||||
| chr3:183959700
|
G | A | 1 | a0001c0002t0001g0038 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2482+33C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183959700 | ||||||
| chr3:183959713
|
A | C | 31 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0031others(28): Show | 31 | HG00408.hp2 HG00544.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.2482+20T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 17/29 | chr3 | 183959713 | ||||||
| chr3:183959847
|
T | A | 56 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(53): Show | 58 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(55): Show |
intron_variant | MODIFIER | c.2380-12A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 16/29 | chr3 | 183959847 | ||||||
| chr3:183959978
|
C | G | 3 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193 | 3 | HG02109.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2380-143G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 16/29 | chr3 | 183959978 | ||||||
| chr3:183960277
|
C | T | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.2380-442G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 16/29 | chr3 | 183960277 | ||||||
| chr3:183960386
|
C | T | 1 | a0001c0003t0011g0368 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2380-551G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 16/29 | chr3 | 183960386 | ||||||
| chr3:183960396
|
C | T | 3 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193 | 3 | HG02109.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2380-561G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 16/29 | chr3 | 183960396 | ||||||
| chr3:183960554
|
C | G | 286 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(283): Show | 294 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(291): Show |
intron_variant | MODIFIER | c.2380-719G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 16/29 | chr3 | 183960554 | ||||||
| chr3:183960598
|
C | T | 1 | a0001c0001t0003g0226 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2380-763G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 16/29 | chr3 | 183960598 | ||||||
| chr3:183960607
|
C | G | 56 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(53): Show | 58 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(55): Show |
intron_variant | MODIFIER | c.2380-772G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 16/29 | chr3 | 183960607 | ||||||
| chr3:183960779
|
T | C | 2 | a0001c0004t0002g0070a0001c0004t0002g0304 | 2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2379+732A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 16/29 | chr3 | 183960779 | ||||||
| chr3:183960790
|
C | CT | 281 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(278): Show | 289 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(286): Show |
intron_variant | MODIFIER | c.2379+720dupA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 16/29 | chr3 | 183960790 | ||||||
| chr3:183960815
|
A | G | 7 | a0001c0001t0007g0013a0001c0001t0007g0014a0001c0001t0007g0194others(4): Show | 7 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2379+696T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 16/29 | chr3 | 183960815 | ||||||
| chr3:183960969
|
T | G | 1 | a0001c0001t0005g0158 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2379+542A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 16/29 | chr3 | 183960969 | ||||||
| chr3:183961004
|
G | T | 4 | a0001c0001t0003g0007a0001c0001t0003g0208a0001c0001t0003g0209others(1): Show | 5 | NA18945.hp1 NA18963.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.2379+507C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 16/29 | chr3 | 183961004 | ||||||
| chr3:183961022
|
C | T | 1 | a0001c0003t0002g0328 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2379+489G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 16/29 | chr3 | 183961022 | ||||||
| chr3:183961061
|
T | C | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.2379+450A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 16/29 | chr3 | 183961061 | ||||||
| chr3:183961397
|
C | G | 1 | a0001c0003t0011g0367 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2379+114G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 16/29 | chr3 | 183961397 | ||||||
| chr3:183961744
|
A | G | 285 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(282): Show | 293 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(290): Show |
intron_variant | MODIFIER | c.2236-90T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183961744 | ||||||
| chr3:183961827
|
T | C | 1 | a0001c0001t0003g0215 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2236-173A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183961827 | ||||||
| chr3:183961849
|
G | A | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2236-195C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183961849 | ||||||
| chr3:183961904
|
C | T | 108 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(105): Show | 112 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.2236-250G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183961904 | ||||||
| chr3:183961957
|
T | G | 1 | a0001c0003t0002g0309 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2236-303A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183961957 | ||||||
| chr3:183961966
|
G | C | 114 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(111): Show | 116 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.2236-312C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183961966 | ||||||
| chr3:183961970
|
C | T | 1 | a0001c0002t0001g0095 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2236-316G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183961970 | ||||||
| chr3:183962043
|
C | T | 108 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(105): Show | 112 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.2236-389G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183962043 | ||||||
| chr3:183962090
|
C | T | 2 | a0001c0003t0002g0294a0001c0003t0002g0331 | 2 | HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2236-436G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183962090 | ||||||
| chr3:183962138
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2236-484G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183962138 | ||||||
| chr3:183962165
|
C | T | 3 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193 | 3 | HG02109.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2236-511G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183962165 | ||||||
| chr3:183962268
|
C | T | 3 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193 | 3 | HG02109.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2236-614G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183962268 | ||||||
| chr3:183962283
|
C | T | 1 | a0001c0005t0002g0058 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2236-629G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183962283 | ||||||
| chr3:183962314
|
G | A | 285 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(282): Show | 293 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(290): Show |
intron_variant | MODIFIER | c.2236-660C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183962314 | ||||||
| chr3:183962321
|
C | T | 29 | a0001c0004t0002g0070a0001c0004t0002g0304a0001c0004t0004g0112others(26): Show | 29 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.2236-667G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183962321 | ||||||
| chr3:183962352
|
C | A | 29 | a0001c0004t0002g0070a0001c0004t0002g0304a0001c0004t0004g0112others(26): Show | 29 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.2236-698G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183962352 | ||||||
| chr3:183962364
|
G | T | 56 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(53): Show | 58 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(55): Show |
intron_variant | MODIFIER | c.2236-710C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183962364 | ||||||
| chr3:183962365
|
A | G | 56 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(53): Show | 58 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(55): Show |
intron_variant | MODIFIER | c.2236-711T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183962365 | ||||||
| chr3:183962366
|
C | G | 56 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(53): Show | 58 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(55): Show |
intron_variant | MODIFIER | c.2236-712G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183962366 | ||||||
| chr3:183962367
|
T | TATCTA | 56 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(53): Show | 58 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(55): Show |
intron_variant | MODIFIER | c.2236-714_2236-713i others(7): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183962367 | ||||||
| chr3:183962368
|
G | A | 2 | a0001c0001t0007g0013a0001c0001t0007g0200 | 2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2236-714C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183962368 | ||||||
| chr3:183962473
|
C | T | 1 | a0001c0003t0015g0322 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2236-819G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183962473 | ||||||
| chr3:183962532
|
C | CT | 14 | a0001c0001t0005g0158a0001c0002t0001g0098a0001c0003t0017g0330others(11): Show | 14 | HG00673.hp1 HG01123.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2235+852dupA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183962532 | ||||||
| chr3:183962539
|
T | C | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2235+846A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183962539 | ||||||
| chr3:183962579
|
C | T | 1 | a0001c0001t0005g0182 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2235+806G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183962579 | ||||||
| chr3:183962580
|
G | A | 108 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(105): Show | 112 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.2235+805C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183962580 | ||||||
| chr3:183962831
|
C | T | 2 | a0001c0002t0001g0096a0001c0002t0001g0114 | 2 | NA18939.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.2235+554G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183962831 | ||||||
| chr3:183962832
|
G | A | 29 | a0001c0004t0002g0070a0001c0004t0002g0304a0001c0004t0004g0112others(26): Show | 29 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.2235+553C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183962832 | ||||||
| chr3:183962963
|
C | A | 1 | a0001c0002t0001g0067 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2235+422G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183962963 | ||||||
| chr3:183963152
|
A | G | 1 | a0001c0003t0002g0315 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2235+233T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183963152 | ||||||
| chr3:183963213
|
T | C | 1 | a0001c0001t0001g0149 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2235+172A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183963213 | ||||||
| chr3:183963268
|
T | G | 56 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(53): Show | 58 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(55): Show |
intron_variant | MODIFIER | c.2235+117A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183963268 | ||||||
| chr3:183963316
|
A | G | 7 | a0001c0001t0007g0013a0001c0001t0007g0014a0001c0001t0007g0194others(4): Show | 7 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2235+69T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 15/29 | chr3 | 183963316 | ||||||
| chr3:183963655
|
A | G | 4 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2032-67T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 14/29 | chr3 | 183963655 | ||||||
| chr3:183963697
|
AATTCCCC others(20): Show |
A | 33 | a0001c0004t0002g0070a0001c0004t0002g0304a0001c0004t0004g0112others(30): Show | 33 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.2032-136_2032-110d others(29): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 14/29 | chr3 | 183963697 | ||||||
| chr3:183964180
|
C | T | 4 | a0001c0002t0008g0261a0001c0002t0008g0262a0001c0002t0008g0263others(1): Show | 4 | HG02258.hp1 HG02723.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2032-592G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 14/29 | chr3 | 183964180 | ||||||
| chr3:183964482
|
C | A | 2 | a0001c0002t0001g0033a0001c0002t0001g0034 | 2 | HG02135.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.2031+703G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 14/29 | chr3 | 183964482 | ||||||
| chr3:183964482
|
C | T | 1 | a0001c0001t0005g0160 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2031+703G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 14/29 | chr3 | 183964482 | ||||||
| chr3:183964703
|
G | A | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2031+482C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 14/29 | chr3 | 183964703 | ||||||
| chr3:183964737
|
C | A | 3 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0196 | 3 | HG01109.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2031+448G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 14/29 | chr3 | 183964737 | ||||||
| chr3:183964899
|
C | T | 3 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0196 | 3 | HG01109.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2031+286G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 14/29 | chr3 | 183964899 | ||||||
| chr3:183964907
|
T | C | 64 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(61): Show | 65 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.2031+278A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 14/29 | chr3 | 183964907 | ||||||
| chr3:183964922
|
A | G | 2 | a0001c0002t0001g0036a0001c0002t0001g0038 | 2 | NA18972.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.2031+263T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 14/29 | chr3 | 183964922 | ||||||
| chr3:183964927
|
A | T | 1 | a0009c0010t0018g0353 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2031+258T>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 14/29 | chr3 | 183964927 | ||||||
| chr3:183965109
|
G | A | 108 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(105): Show | 112 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.2031+76C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 14/29 | chr3 | 183965109 | ||||||
| chr3:183965172
|
G | A | 56 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(53): Show | 58 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(55): Show |
intron_variant | MODIFIER | c.2031+13C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 14/29 | chr3 | 183965172 | ||||||
| chr3:183965334
|
G | A | 1 | a0001c0001t0005g0162 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1958+43C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 13/29 | chr3 | 183965334 | ||||||
| chr3:183965336
|
G | A | 7 | a0001c0002t0001g0016a0001c0002t0001g0066a0001c0002t0001g0069others(4): Show | 7 | HG01074.hp2 HG01243.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1958+41C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 13/29 | chr3 | 183965336 | ||||||
| chr3:183965357
|
A | G | 23 | a0001c0001t0003g0203a0001c0001t0003g0204a0001c0001t0003g0221others(20): Show | 23 | HG00597.hp2 HG02074.hp1 HG02083.hp2 others(20): Show |
intron_variant | MODIFIER | c.1958+20T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 13/29 | chr3 | 183965357 | ||||||
| chr3:183965580
|
A | G | 1 | a0001c0006t0002g0311 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1834-79T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183965580 | ||||||
| chr3:183965581
|
T | C | 6 | a0001c0002t0001g0131a0001c0002t0009g0266a0001c0002t0009g0267others(3): Show | 6 | HG01358.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1834-80A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183965581 | ||||||
| chr3:183965657
|
C | T | 4 | a0001c0002t0008g0261a0001c0002t0008g0262a0001c0002t0008g0263others(1): Show | 4 | HG02258.hp1 HG02723.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1834-156G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183965657 | ||||||
| chr3:183965660
|
A | G | 5 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193others(2): Show | 5 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1834-159T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183965660 | ||||||
| chr3:183965837
|
G | A | 4 | a0001c0002t0001g0068a0001c0002t0001g0085a0001c0002t0001g0087others(1): Show | 4 | NA18988.hp2 NA18995.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.1834-336C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183965837 | ||||||
| chr3:183966092
|
C | T | 3 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0196 | 3 | HG01109.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1834-591G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183966092 | ||||||
| chr3:183966096
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1834-595A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183966096 | ||||||
| chr3:183966122
|
T | C | 17 | a0001c0001t0003g0007a0001c0001t0003g0202a0001c0001t0003g0205others(14): Show | 18 | HG02129.hp2 HG02523.hp1 NA18747.hp2 others(15): Show |
intron_variant | MODIFIER | c.1834-621A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183966122 | ||||||
| chr3:183966141
|
T | C | 2 | a0001c0001t0006g0052a0001c0001t0006g0055 | 2 | HG01261.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1834-640A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183966141 | ||||||
| chr3:183966150
|
G | A | 108 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(105): Show | 112 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1834-649C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183966150 | ||||||
| chr3:183966244
|
C | T | 1 | a0001c0001t0003g0206 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1834-743G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183966244 | ||||||
| chr3:183966251
|
C | T | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1834-750G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183966251 | ||||||
| chr3:183966341
|
A | G | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1834-840T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183966341 | ||||||
| chr3:183966465
|
T | C | 1 | a0001c0001t0007g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1834-964A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183966465 | ||||||
| chr3:183966591
|
C | T | 29 | a0001c0004t0002g0070a0001c0004t0002g0304a0001c0004t0004g0112others(26): Show | 29 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1834-1090G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183966591 | ||||||
| chr3:183966672
|
G | A | 2 | a0001c0002t0001g0084a0001c0002t0001g0256 | 2 | NA19077.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1833+1023C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183966672 | ||||||
| chr3:183966835
|
C | T | 1 | a0001c0003t0002g0325 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1833+860G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183966835 | ||||||
| chr3:183966857
|
G | A | 5 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193others(2): Show | 5 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1833+838C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183966857 | ||||||
| chr3:183966858
|
G | A | 2 | a0001c0001t0003g0245a0001c0001t0003g0246 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1833+837C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183966858 | ||||||
| chr3:183967009
|
G | GT | 7 | a0001c0002t0001g0029a0001c0002t0001g0031a0001c0002t0001g0032others(4): Show | 7 | NA18952.hp2 NA18964.hp1 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.1833+685dupA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183967009 | ||||||
| chr3:183967009
|
GT | G | 176 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(173): Show | 180 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.1833+685delA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183967009 | ||||||
| chr3:183967040
|
T | C | 7 | a0001c0001t0007g0013a0001c0001t0007g0014a0001c0001t0007g0194others(4): Show | 7 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1833+655A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183967040 | ||||||
| chr3:183967118
|
G | A | 29 | a0001c0004t0002g0070a0001c0004t0002g0304a0001c0004t0004g0112others(26): Show | 29 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1833+577C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183967118 | ||||||
| chr3:183967201
|
T | G | 1 | a0009c0010t0018g0353 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1833+494A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183967201 | ||||||
| chr3:183967264
|
G | T | 6 | a0001c0002t0001g0131a0001c0002t0009g0266a0001c0002t0009g0267others(3): Show | 6 | HG01358.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1833+431C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183967264 | ||||||
| chr3:183967377
|
T | C | 64 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(61): Show | 65 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.1833+318A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183967377 | ||||||
| chr3:183967395
|
T | C | 63 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(60): Show | 67 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.1833+300A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183967395 | ||||||
| chr3:183967436
|
T | C | 1 | a0001c0002t0008g0263 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1833+259A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183967436 | ||||||
| chr3:183967441
|
G | A | 1 | a0001c0003t0002g0201 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1833+254C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183967441 | ||||||
| chr3:183967461
|
T | C | 286 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(283): Show | 294 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(291): Show |
intron_variant | MODIFIER | c.1833+234A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183967461 | ||||||
| chr3:183967480
|
C | T | 5 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193others(2): Show | 5 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1833+215G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183967480 | ||||||
| chr3:183967495
|
C | T | 1 | a0001c0001t0003g0233 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1833+200G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 12/29 | chr3 | 183967495 | ||||||
| chr3:183967809
|
A | G | 7 | a0001c0001t0007g0013a0001c0001t0007g0014a0001c0001t0007g0194others(4): Show | 7 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1762-43T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183967809 | ||||||
| chr3:183968105
|
T | C | 285 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(282): Show | 293 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(290): Show |
intron_variant | MODIFIER | c.1762-339A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183968105 | ||||||
| chr3:183968129
|
T | TATC | 63 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(60): Show | 67 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.1762-364_1762-363i others(5): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183968129 | ||||||
| chr3:183968191
|
C | A | 108 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(105): Show | 112 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1762-425G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183968191 | ||||||
| chr3:183968358
|
C | T | 1 | a0001c0004t0004g0120 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1762-592G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183968358 | ||||||
| chr3:183968401
|
C | T | 77 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(74): Show | 81 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.1762-635G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183968401 | ||||||
| chr3:183968414
|
A | G | 1 | a0001c0003t0002g0302 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1762-648T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183968414 | ||||||
| chr3:183968507
|
A | T | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1762-741T>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183968507 | ||||||
| chr3:183968650
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1762-884C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183968650 | ||||||
| chr3:183969137
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1762-1371T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183969137 | ||||||
| chr3:183969220
|
G | A | 1 | a0001c0002t0001g0034 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1762-1454C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183969220 | ||||||
| chr3:183969420
|
C | T | 1 | a0001c0002t0001g0079 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1762-1654G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183969420 | ||||||
| chr3:183969559
|
G | A | 1 | a0001c0003t0015g0322 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1762-1793C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183969559 | ||||||
| chr3:183969570
|
T | A | 1 | a0001c0002t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1762-1804A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183969570 | ||||||
| chr3:183969574
|
C | T | 1 | a0001c0001t0005g0157 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1762-1808G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183969574 | ||||||
| chr3:183969641
|
G | A | 108 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(105): Show | 112 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1762-1875C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183969641 | ||||||
| chr3:183969691
|
C | CA | 13 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0179others(10): Show | 13 | HG01123.hp1 HG01175.hp2 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1761+1871dupT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183969691 | ||||||
| chr3:183969691
|
C | CAA | 29 | a0001c0004t0002g0070a0001c0004t0002g0304a0001c0004t0004g0112others(26): Show | 29 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1761+1870_1761+187 others(6): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183969691 | ||||||
| chr3:183969691
|
CA | C | 49 | a0001c0001t0003g0007a0001c0001t0003g0204a0001c0001t0003g0205others(46): Show | 50 | HG00408.hp2 HG00544.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.1761+1871delT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183969691 | ||||||
| chr3:183970125
|
C | T | 5 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193others(2): Show | 5 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1761+1438G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183970125 | ||||||
| chr3:183970439
|
CT | C | 6 | a0001c0004t0004g0133a0001c0005t0010g0110a0001c0005t0010g0192others(3): Show | 6 | HG01167.hp2 HG01433.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1761+1123delA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183970439 | ||||||
| chr3:183970439
|
CTTTTT | C | 108 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(105): Show | 112 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1761+1119_1761+112 others(9): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183970439 | ||||||
| chr3:183970506
|
G | A | 1 | a0001c0002t0001g0084 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1761+1057C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183970506 | ||||||
| chr3:183970839
|
C | T | 113 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(110): Show | 117 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.1761+724G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183970839 | ||||||
| chr3:183970841
|
G | A | 5 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193others(2): Show | 5 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1761+722C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183970841 | ||||||
| chr3:183970879
|
A | T | 62 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(59): Show | 66 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.1761+684T>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183970879 | ||||||
| chr3:183970896
|
T | G | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1761+667A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183970896 | ||||||
| chr3:183970954
|
G | A | 6 | a0001c0001t0001g0156a0001c0001t0001g0159a0001c0001t0001g0164others(3): Show | 6 | HG01192.hp1 HG01358.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1761+609C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183970954 | ||||||
| chr3:183971085
|
T | C | 1 | a0001c0002t0001g0306 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1761+478A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183971085 | ||||||
| chr3:183971228
|
C | T | 1 | a0001c0003t0002g0305 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1761+335G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183971228 | ||||||
| chr3:183971229
|
G | A | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1761+334C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183971229 | ||||||
| chr3:183971350
|
T | C | 285 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(282): Show | 293 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(290): Show |
intron_variant | MODIFIER | c.1761+213A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183971350 | ||||||
| chr3:183971544
|
C | G | 5 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193others(2): Show | 5 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1761+19G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183971544 | ||||||
| chr3:183971552
|
G | A | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1761+11C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 11/29 | chr3 | 183971552 | ||||||
| chr3:183972201
|
G | A | 31 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0031others(28): Show | 31 | HG00408.hp2 HG00544.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1405-282C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183972201 | ||||||
| chr3:183972204
|
C | T | 5 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193others(2): Show | 5 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1405-285G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183972204 | ||||||
| chr3:183972229
|
C | A | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1405-310G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183972229 | ||||||
| chr3:183972405
|
C | T | 1 | a0005c0014t0001g0107 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1405-486G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183972405 | ||||||
| chr3:183972455
|
G | A | 56 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(53): Show | 58 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(55): Show |
intron_variant | MODIFIER | c.1405-536C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183972455 | ||||||
| chr3:183972460
|
G | T | 2 | a0001c0003t0002g0291a0001c0003t0002g0352 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1405-541C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183972460 | ||||||
| chr3:183972477
|
G | A | 27 | a0001c0001t0001g0147a0001c0001t0005g0010a0001c0001t0005g0011others(24): Show | 27 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.1405-558C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183972477 | ||||||
| chr3:183972578
|
C | A | 29 | a0001c0004t0002g0070a0001c0004t0002g0304a0001c0004t0004g0112others(26): Show | 29 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1405-659G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183972578 | ||||||
| chr3:183972653
|
T | G | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.1405-734A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183972653 | ||||||
| chr3:183972920
|
A | G | 1 | a0001c0001t0003g0206 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1405-1001T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183972920 | ||||||
| chr3:183973049
|
C | CT | 160 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(157): Show | 164 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.1405-1131dupA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183973049 | ||||||
| chr3:183973049
|
C | CTT | 6 | a0001c0001t0001g0179a0001c0001t0003g0206a0001c0001t0003g0208others(3): Show | 6 | HG01175.hp2 HG02738.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1405-1132_1405-113 others(6): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183973049 | ||||||
| chr3:183973049
|
CT | C | 105 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(102): Show | 109 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.1405-1131delA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183973049 | ||||||
| chr3:183973091
|
G | A | 1 | a0001c0001t0007g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1405-1172C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183973091 | ||||||
| chr3:183973123
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1405-1204G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183973123 | ||||||
| chr3:183973124
|
G | A | 4 | a0001c0002t0008g0261a0001c0002t0008g0262a0001c0002t0008g0263others(1): Show | 4 | HG02258.hp1 HG02723.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1405-1205C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183973124 | ||||||
| chr3:183973157
|
C | T | 140 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(137): Show | 144 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.1405-1238G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183973157 | ||||||
| chr3:183973203
|
C | T | 1 | a0001c0002t0001g0047 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1405-1284G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183973203 | ||||||
| chr3:183973455
|
A | G | 31 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0031others(28): Show | 31 | HG00408.hp2 HG00544.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1405-1536T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183973455 | ||||||
| chr3:183973577
|
C | A | 31 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0031others(28): Show | 31 | HG00408.hp2 HG00544.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1405-1658G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183973577 | ||||||
| chr3:183973584
|
T | C | 1 | a0001c0004t0002g0070 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1405-1665A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183973584 | ||||||
| chr3:183973663
|
A | G | 108 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(105): Show | 112 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1405-1744T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183973663 | ||||||
| chr3:183973679
|
A | C | 1 | a0001c0002t0001g0060 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1405-1760T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183973679 | ||||||
| chr3:183973862
|
T | C | 276 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(273): Show | 284 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.1405-1943A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183973862 | ||||||
| chr3:183973877
|
A | G | 1 | a0001c0001t0003g0222 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1405-1958T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183973877 | ||||||
| chr3:183973937
|
T | C | 56 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(53): Show | 58 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(55): Show |
intron_variant | MODIFIER | c.1405-2018A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183973937 | ||||||
| chr3:183974045
|
A | G | 2 | a0001c0003t0002g0278a0001c0003t0002g0299 | 2 | HG01106.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1405-2126T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183974045 | ||||||
| chr3:183974160
|
C | T | 5 | a0001c0002t0001g0039a0001c0002t0001g0044a0001c0002t0001g0045others(2): Show | 5 | HG00408.hp2 HG02132.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.1405-2241G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183974160 | ||||||
| chr3:183974497
|
C | T | 1 | a0001c0001t0006g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1405-2578G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183974497 | ||||||
| chr3:183974574
|
C | T | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1405-2655G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183974574 | ||||||
| chr3:183974603
|
C | T | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1405-2684G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183974603 | ||||||
| chr3:183974653
|
T | C | 4 | a0001c0002t0001g0068a0001c0002t0001g0085a0001c0002t0001g0087others(1): Show | 4 | NA18988.hp2 NA18995.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.1405-2734A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183974653 | ||||||
| chr3:183974832
|
T | C | 3 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193 | 3 | HG02109.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1404+2685A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183974832 | ||||||
| chr3:183974867
|
T | C | 29 | a0001c0004t0002g0070a0001c0004t0002g0304a0001c0004t0004g0112others(26): Show | 29 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1404+2650A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183974867 | ||||||
| chr3:183974978
|
G | A | 1 | a0001c0002t0001g0073 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1404+2539C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183974978 | ||||||
| chr3:183975036
|
C | A | 1 | a0001c0003t0002g0350 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1404+2481G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183975036 | ||||||
| chr3:183975306
|
G | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0146others(5): Show | 9 | HG00738.hp1 HG01109.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.1404+2211C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183975306 | ||||||
| chr3:183975372
|
C | G | 3 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193 | 3 | HG02109.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1404+2145G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183975372 | ||||||
| chr3:183975383
|
C | T | 3 | a0001c0002t0001g0101a0001c0002t0001g0106a0005c0014t0001g0107 | 3 | NA18998.hp1 NA19009.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1404+2134G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183975383 | ||||||
| chr3:183975551
|
C | T | 4 | a0001c0003t0002g0009a0001c0003t0002g0201a0001c0003t0002g0333others(1): Show | 5 | HG01891.hp1 HG02559.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1404+1966G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183975551 | ||||||
| chr3:183975622
|
C | T | 168 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(165): Show | 172 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.1404+1895G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183975622 | ||||||
| chr3:183975731
|
T | C | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1404+1786A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183975731 | ||||||
| chr3:183976119
|
G | A | 2 | a0001c0004t0002g0070a0001c0004t0002g0304 | 2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1404+1398C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183976119 | ||||||
| chr3:183976212
|
T | C | 3 | a0001c0001t0003g0224a0001c0001t0003g0225a0001c0001t0003g0232 | 3 | NA18969.hp1 NA18972.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1404+1305A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183976212 | ||||||
| chr3:183976263
|
A | C | 2 | a0001c0003t0002g0294a0001c0003t0002g0331 | 2 | HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1404+1254T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183976263 | ||||||
| chr3:183976300
|
G | C | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1404+1217C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183976300 | ||||||
| chr3:183976330
|
C | CT | 29 | a0001c0004t0002g0070a0001c0004t0002g0304a0001c0004t0004g0112others(26): Show | 29 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1404+1186dupA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183976330 | ||||||
| chr3:183976400
|
G | A | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1404+1117C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183976400 | ||||||
| chr3:183976427
|
T | A | 63 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(60): Show | 64 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1404+1090A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183976427 | ||||||
| chr3:183976631
|
T | C | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1404+886A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183976631 | ||||||
| chr3:183976711
|
A | C | 1 | a0001c0002t0001g0031 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1404+806T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183976711 | ||||||
| chr3:183976730
|
A | C | 2 | a0001c0003t0002g0345a0001c0003t0002g0348 | 2 | HG00639.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1404+787T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183976730 | ||||||
| chr3:183976814
|
A | G | 63 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(60): Show | 64 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1404+703T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183976814 | ||||||
| chr3:183976891
|
C | T | 1 | a0001c0003t0002g0291 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1404+626G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183976891 | ||||||
| chr3:183977030
|
G | C | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1404+487C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183977030 | ||||||
| chr3:183977114
|
T | C | 1 | a0001c0003t0002g0280 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1404+403A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183977114 | ||||||
| chr3:183977449
|
G | A | 3 | a0001c0001t0003g0006a0001c0001t0003g0022a0001c0001t0003g0206 | 4 | NA18966.hp1 NA18971.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1404+68C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183977449 | ||||||
| chr3:183977491
|
C | T | 1 | a0001c0002t0001g0067 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1404+26G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 10/29 | chr3 | 183977491 | ||||||
| chr3:183977720
|
G | A | 6 | a0001c0001t0001g0156a0001c0001t0001g0159a0001c0001t0001g0164others(3): Show | 6 | HG01192.hp1 HG01358.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1297-96C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 9/29 | chr3 | 183977720 | ||||||
| chr3:183977779
|
G | A | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1297-155C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 9/29 | chr3 | 183977779 | ||||||
| chr3:183977866
|
C | T | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1297-242G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 9/29 | chr3 | 183977866 | ||||||
| chr3:183977979
|
C | T | 2 | a0001c0001t0003g0245a0001c0001t0003g0246 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1297-355G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 9/29 | chr3 | 183977979 | ||||||
| chr3:183977995
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1297-371G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 9/29 | chr3 | 183977995 | ||||||
| chr3:183977996
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1297-372C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 9/29 | chr3 | 183977996 | ||||||
| chr3:183978024
|
AT | A | 10 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0358others(7): Show | 10 | HG00735.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1297-401delA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 9/29 | chr3 | 183978024 | ||||||
| chr3:183978082
|
C | A | 108 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(105): Show | 112 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1296+421G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 9/29 | chr3 | 183978082 | ||||||
| chr3:183978100
|
A | G | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1296+403T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 9/29 | chr3 | 183978100 | ||||||
| chr3:183978173
|
T | C | 1 | a0001c0003t0002g0336 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1296+330A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 9/29 | chr3 | 183978173 | ||||||
| chr3:183978214
|
T | A | 29 | a0001c0004t0002g0070a0001c0004t0002g0304a0001c0004t0004g0112others(26): Show | 29 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1296+289A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 9/29 | chr3 | 183978214 | ||||||
| chr3:183978289
|
C | A | 108 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(105): Show | 112 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1296+214G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 9/29 | chr3 | 183978289 | ||||||
| chr3:183978314
|
AT | A | 275 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(272): Show | 283 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(280): Show |
intron_variant | MODIFIER | c.1296+188delA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 9/29 | chr3 | 183978314 | ||||||
| chr3:183978321
|
T | G | 22 | a0001c0003t0002g0008a0001c0003t0002g0275a0001c0003t0002g0276others(19): Show | 23 | HG00280.hp2 HG00558.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1296+182A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 9/29 | chr3 | 183978321 | ||||||
| chr3:183978325
|
G | T | 1 | a0001c0007t0008g0253 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1296+178C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 9/29 | chr3 | 183978325 | ||||||
| chr3:183978327
|
T | C | 108 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(105): Show | 112 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1296+176A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 9/29 | chr3 | 183978327 | ||||||
| chr3:183978779
|
C | T | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1148-128G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183978779 | ||||||
| chr3:183978882
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1148-231A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183978882 | ||||||
| chr3:183978891
|
T | C | 1 | a0001c0003t0002g0298 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1148-240A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183978891 | ||||||
| chr3:183979001
|
A | C | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1148-350T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183979001 | ||||||
| chr3:183979129
|
G | A | 2 | a0001c0002t0001g0025a0001c0002t0001g0026 | 2 | HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1148-478C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183979129 | ||||||
| chr3:183979173
|
C | T | 1 | a0001c0002t0001g0093 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1148-522G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183979173 | ||||||
| chr3:183979202
|
G | A | 111 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(108): Show | 115 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.1148-551C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183979202 | ||||||
| chr3:183979305
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1148-654C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183979305 | ||||||
| chr3:183979344
|
C | CA | 72 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(69): Show | 76 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1148-694dupT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183979344 | ||||||
| chr3:183979359
|
A | G | 1 | a0001c0001t0003g0202 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1148-708T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183979359 | ||||||
| chr3:183979360
|
A | G | 17 | a0001c0001t0003g0007a0001c0001t0003g0202a0001c0001t0003g0205others(14): Show | 18 | HG02129.hp2 HG02523.hp1 NA18747.hp2 others(15): Show |
intron_variant | MODIFIER | c.1148-709T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183979360 | ||||||
| chr3:183979424
|
A | C | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.1148-773T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183979424 | ||||||
| chr3:183979523
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1148-872G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183979523 | ||||||
| chr3:183979658
|
G | A | 1 | a0001c0002t0001g0103 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1148-1007C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183979658 | ||||||
| chr3:183979820
|
C | T | 1 | a0001c0002t0009g0268 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1148-1169G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183979820 | ||||||
| chr3:183979840
|
G | A | 63 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(60): Show | 64 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1148-1189C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183979840 | ||||||
| chr3:183979866
|
C | T | 2 | a0001c0002t0001g0046a0001c0003t0002g0028 | 2 | HG02055.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1148-1215G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183979866 | ||||||
| chr3:183979873
|
C | G | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1148-1222G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183979873 | ||||||
| chr3:183979918
|
G | A | 10 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0358others(7): Show | 10 | HG00735.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1148-1267C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183979918 | ||||||
| chr3:183979964
|
C | T | 10 | a0001c0002t0001g0004a0001c0002t0001g0096a0001c0002t0001g0101others(7): Show | 11 | HG01257.hp1 HG01258.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.1148-1313G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183979964 | ||||||
| chr3:183979988
|
G | A | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1148-1337C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183979988 | ||||||
| chr3:183979993
|
G | A | 1 | a0001c0003t0002g0323 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1148-1342C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183979993 | ||||||
| chr3:183980065
|
G | A | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1148-1414C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183980065 | ||||||
| chr3:183980388
|
T | A | 1 | a0001c0003t0002g0315 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1147+1339A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183980388 | ||||||
| chr3:183980431
|
G | A | 108 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(105): Show | 112 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1147+1296C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183980431 | ||||||
| chr3:183980553
|
C | T | 63 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(60): Show | 64 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1147+1174G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183980553 | ||||||
| chr3:183980705
|
C | G | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1147+1022G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183980705 | ||||||
| chr3:183980714
|
G | T | 1 | a0001c0003t0002g0337 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1147+1013C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183980714 | ||||||
| chr3:183980714
|
GT | G | 110 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(107): Show | 114 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.1147+1012delA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183980714 | ||||||
| chr3:183980717
|
T | TTG | 28 | a0001c0004t0002g0070a0001c0004t0002g0304a0001c0004t0004g0112others(25): Show | 28 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.1147+1009_1147+101 others(6): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183980717 | ||||||
| chr3:183980718
|
T | TG | 5 | a0001c0001t0003g0202a0001c0001t0003g0213a0001c0001t0003g0226others(2): Show | 5 | HG02486.hp1 HG03688.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.1147+1008_1147+100 others(5): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183980718 | ||||||
| chr3:183980719
|
T | G | 140 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(137): Show | 144 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.1147+1008A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183980719 | ||||||
| chr3:183980720
|
T | G | 103 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(100): Show | 107 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.1147+1007A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183980720 | ||||||
| chr3:183980724
|
T | G | 1 | a0001c0005t0010g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1147+1003A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183980724 | ||||||
| chr3:183980804
|
T | C | 276 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(273): Show | 284 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.1147+923A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183980804 | ||||||
| chr3:183980838
|
G | A | 63 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(60): Show | 64 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1147+889C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183980838 | ||||||
| chr3:183980995
|
G | A | 3 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193 | 3 | HG02109.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1147+732C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183980995 | ||||||
| chr3:183980997
|
G | A | 4 | a0001c0004t0004g0118a0001c0004t0004g0119a0001c0004t0004g0126others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1147+730C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183980997 | ||||||
| chr3:183981006
|
G | A | 4 | a0001c0001t0005g0144a0001c0001t0005g0167a0001c0001t0005g0168others(1): Show | 4 | HG00438.hp1 HG02056.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.1147+721C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183981006 | ||||||
| chr3:183981097
|
C | G | 7 | a0001c0001t0006g0015a0001c0001t0006g0027a0001c0001t0006g0051others(4): Show | 7 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1147+630G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183981097 | ||||||
| chr3:183981155
|
A | C | 285 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(282): Show | 293 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(290): Show |
intron_variant | MODIFIER | c.1147+572T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183981155 | ||||||
| chr3:183981170
|
C | A | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1147+557G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183981170 | ||||||
| chr3:183981300
|
C | T | 1 | a0001c0003t0002g0324 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1147+427G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183981300 | ||||||
| chr3:183981339
|
A | G | 2 | a0001c0009t0013g0236a0001c0009t0013g0237 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1147+388T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183981339 | ||||||
| chr3:183981573
|
C | T | 1 | a0001c0003t0011g0367 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1147+154G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183981573 | ||||||
| chr3:183981633
|
C | T | 77 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(74): Show | 81 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.1147+94G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 8/29 | chr3 | 183981633 | ||||||
| chr3:183981993
|
A | C | 63 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(60): Show | 64 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1000-119T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 7/29 | chr3 | 183981993 | ||||||
| chr3:183982008
|
G | A | 3 | a0001c0002t0001g0046a0001c0004t0004g0127a0001c0004t0004g0128 | 3 | HG02717.hp2 NA18612.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1000-134C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 7/29 | chr3 | 183982008 | ||||||
| chr3:183982102
|
T | A | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.1000-228A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 7/29 | chr3 | 183982102 | ||||||
| chr3:183982141
|
G | A | 1 | a0009c0010t0018g0353 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1000-267C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 7/29 | chr3 | 183982141 | ||||||
| chr3:183982423
|
C | T | 168 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(165): Show | 172 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.999+28G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 7/29 | chr3 | 183982423 | ||||||
| chr3:183982714
|
A | G | 1 | a0001c0003t0002g0292 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.825+60T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 6/29 | chr3 | 183982714 | ||||||
| chr3:183982764
|
C | T | 7 | a0001c0001t0006g0015a0001c0001t0006g0027a0001c0001t0006g0051others(4): Show | 7 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.825+10G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 6/29 | chr3 | 183982764 | ||||||
| chr3:183983117
|
C | T | 2 | a0001c0003t0002g0278a0001c0003t0002g0299 | 2 | HG01106.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.592-110G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183983117 | ||||||
| chr3:183983140
|
A | G | 284 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(281): Show | 292 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(289): Show |
intron_variant | MODIFIER | c.592-133T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183983140 | ||||||
| chr3:183983199
|
G | A | 3 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193 | 3 | HG02109.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.592-192C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183983199 | ||||||
| chr3:183983225
|
A | C | 1 | a0001c0003t0002g0291 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.592-218T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183983225 | ||||||
| chr3:183983278
|
G | T | 3 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193 | 3 | HG02109.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.592-271C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183983278 | ||||||
| chr3:183983359
|
G | C | 285 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(282): Show | 293 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(290): Show |
intron_variant | MODIFIER | c.592-352C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183983359 | ||||||
| chr3:183984047
|
C | T | 10 | a0001c0004t0004g0120a0001c0004t0004g0121a0001c0004t0004g0122others(7): Show | 10 | HG00639.hp1 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.592-1040G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183984047 | ||||||
| chr3:183984130
|
G | C | 1 | a0001c0001t0003g0248 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.592-1123C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183984130 | ||||||
| chr3:183984301
|
A | G | 168 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(165): Show | 172 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.592-1294T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183984301 | ||||||
| chr3:183984487
|
A | G | 276 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(273): Show | 284 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.592-1480T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183984487 | ||||||
| chr3:183984759
|
T | C | 1 | a0001c0003t0002g0281 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.592-1752A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183984759 | ||||||
| chr3:183985401
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.591+2369C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183985401 | ||||||
| chr3:183985541
|
G | A | 7 | a0001c0001t0003g0218a0001c0001t0003g0223a0001c0001t0003g0234others(4): Show | 7 | HG01192.hp2 HG01516.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.591+2229C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183985541 | ||||||
| chr3:183985753
|
C | T | 29 | a0001c0004t0002g0070a0001c0004t0002g0304a0001c0004t0004g0112others(26): Show | 29 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.591+2017G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183985753 | ||||||
| chr3:183985763
|
C | T | 1 | a0001c0003t0002g0339 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.591+2007G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183985763 | ||||||
| chr3:183986032
|
T | C | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.591+1738A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183986032 | ||||||
| chr3:183986103
|
A | G | 1 | a0001c0002t0001g0067 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.591+1667T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183986103 | ||||||
| chr3:183986280
|
G | A | 285 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(282): Show | 293 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(290): Show |
intron_variant | MODIFIER | c.591+1490C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183986280 | ||||||
| chr3:183986396
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.591+1374G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183986396 | ||||||
| chr3:183986486
|
G | A | 1 | a0001c0008t0001g0181 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.591+1284C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183986486 | ||||||
| chr3:183987031
|
C | G | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.591+739G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183987031 | ||||||
| chr3:183987050
|
C | T | 29 | a0001c0004t0002g0070a0001c0004t0002g0304a0001c0004t0004g0112others(26): Show | 29 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.591+720G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183987050 | ||||||
| chr3:183987218
|
T | C | 1 | a0001c0003t0002g0056 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.591+552A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183987218 | ||||||
| chr3:183987396
|
G | A | 139 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(136): Show | 143 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.591+374C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183987396 | ||||||
| chr3:183987426
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.591+344G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183987426 | ||||||
| chr3:183987440
|
C | G | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.591+330G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183987440 | ||||||
| chr3:183987452
|
C | G | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.591+318G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 5/29 | chr3 | 183987452 | ||||||
| chr3:183988205
|
C | T | 3 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193 | 3 | HG02109.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.444-288G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 4/29 | chr3 | 183988205 | ||||||
| chr3:183988412
|
G | T | 1 | a0001c0001t0006g0289 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.443+160C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 4/29 | chr3 | 183988412 | ||||||
| chr3:183988842
|
A | C | 276 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(273): Show | 284 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.288-115T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 3/29 | chr3 | 183988842 | ||||||
| chr3:183988893
|
C | T | 10 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0358others(7): Show | 10 | HG00735.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.288-166G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 3/29 | chr3 | 183988893 | ||||||
| chr3:183989104
|
G | T | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.287+122C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 3/29 | chr3 | 183989104 | ||||||
| chr3:183989157
|
C | CA | 13 | a0001c0003t0002g0276a0001c0003t0002g0279a0001c0003t0002g0282others(10): Show | 13 | HG00741.hp2 HG01123.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.287+68dupT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 3/29 | chr3 | 183989157 | ||||||
| chr3:183989157
|
CA | C | 53 | a0001c0001t0001g0175a0001c0001t0001g0179a0001c0001t0003g0205others(50): Show | 53 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(50): Show |
intron_variant | MODIFIER | c.287+68delT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 3/29 | chr3 | 183989157 | ||||||
| chr3:183989157
|
CAA | C | 143 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(140): Show | 147 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.287+67_287+68delTT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 3/29 | chr3 | 183989157 | ||||||
| chr3:183989157
|
CAAAAAA | C | 7 | a0001c0002t0001g0026a0001c0002t0001g0086a0001c0002t0001g0093others(4): Show | 7 | HG00621.hp2 HG01981.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.287+63_287+68delTT others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 3/29 | chr3 | 183989157 | ||||||
| chr3:183989157
|
CAAAAAAA | C | 70 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(67): Show | 74 | HG00423.hp2 HG00544.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.287+62_287+68delTT others(5): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 3/29 | chr3 | 183989157 | ||||||
| chr3:183989157
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0003t0002g0302 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.287+55_287+68delTT others(12): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 3/29 | chr3 | 183989157 | ||||||
| chr3:183989172
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.287+54T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 3/29 | chr3 | 183989172 | ||||||
| chr3:183989548
|
T | C | 1 | a0001c0001t0003g0233 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.130-165A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183989548 | ||||||
| chr3:183989569
|
A | G | 29 | a0001c0004t0002g0070a0001c0004t0002g0304a0001c0004t0004g0112others(26): Show | 29 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.130-186T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183989569 | ||||||
| chr3:183989592
|
C | CT | 83 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(80): Show | 85 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.130-210dupA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183989592 | ||||||
| chr3:183989592
|
C | CTT | 189 | a0001c0001t0001g0153a0001c0001t0003g0006a0001c0001t0003g0007others(186): Show | 195 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(192): Show |
intron_variant | MODIFIER | c.130-211_130-210dup others(2): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183989592 | ||||||
| chr3:183989641
|
T | C | 1 | a0001c0005t0010g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.130-258A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183989641 | ||||||
| chr3:183989669
|
T | C | 1 | a0001c0001t0003g0216 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.130-286A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183989669 | ||||||
| chr3:183989836
|
C | G | 282 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(279): Show | 290 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(287): Show |
intron_variant | MODIFIER | c.130-453G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183989836 | ||||||
| chr3:183989949
|
G | C | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.130-566C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183989949 | ||||||
| chr3:183990096
|
C | G | 3 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0184 | 3 | HG02683.hp1 NA18957.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.130-713G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183990096 | ||||||
| chr3:183990157
|
G | A | 1 | a0007c0012t0001g0099 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.130-774C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183990157 | ||||||
| chr3:183990213
|
A | G | 1 | a0001c0003t0002g0328 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.130-830T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183990213 | ||||||
| chr3:183990215
|
T | C | 2 | a0001c0004t0002g0070a0001c0004t0002g0304 | 2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.130-832A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183990215 | ||||||
| chr3:183990539
|
G | A | 110 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(107): Show | 114 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.130-1156C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183990539 | ||||||
| chr3:183990603
|
G | A | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.130-1220C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183990603 | ||||||
| chr3:183990617
|
A | G | 168 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(165): Show | 172 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.130-1234T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183990617 | ||||||
| chr3:183990651
|
T | C | 278 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(275): Show | 286 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(283): Show |
intron_variant | MODIFIER | c.130-1268A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183990651 | ||||||
| chr3:183990780
|
ACAAAAGT others(5): Show |
A | 29 | a0001c0004t0002g0070a0001c0004t0002g0304a0001c0004t0004g0112others(26): Show | 29 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.130-1409_130-1398d others(14): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183990780 | ||||||
| chr3:183991043
|
G | A | 1 | a0001c0001t0006g0288 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.130-1660C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183991043 | ||||||
| chr3:183991054
|
T | G | 3 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0196 | 3 | HG01109.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.130-1671A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183991054 | ||||||
| chr3:183991158
|
A | G | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.130-1775T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183991158 | ||||||
| chr3:183991251
|
C | T | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.130-1868G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183991251 | ||||||
| chr3:183991306
|
G | GA | 168 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(165): Show | 172 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.130-1924dupT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183991306 | ||||||
| chr3:183991493
|
A | G | 7 | a0001c0001t0007g0013a0001c0001t0007g0014a0001c0001t0007g0194others(4): Show | 7 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.130-2110T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183991493 | ||||||
| chr3:183991725
|
T | C | 1 | a0001c0005t0002g0274 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.130-2342A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183991725 | ||||||
| chr3:183991779
|
T | G | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.130-2396A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183991779 | ||||||
| chr3:183991787
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.130-2404C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183991787 | ||||||
| chr3:183991870
|
T | C | 4 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-2487A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183991870 | ||||||
| chr3:183992113
|
C | T | 4 | a0001c0002t0001g0003a0001c0002t0001g0017a0001c0002t0001g0074others(1): Show | 5 | HG00423.hp2 HG00544.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.130-2730G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183992113 | ||||||
| chr3:183992125
|
T | G | 8 | a0001c0003t0002g0009a0001c0003t0002g0056a0001c0003t0002g0201others(5): Show | 9 | HG01891.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.130-2742A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183992125 | ||||||
| chr3:183992265
|
A | T | 278 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(275): Show | 286 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(283): Show |
intron_variant | MODIFIER | c.130-2882T>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183992265 | ||||||
| chr3:183992357
|
C | T | 3 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193 | 3 | HG02109.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.130-2974G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183992357 | ||||||
| chr3:183992399
|
G | C | 1 | a0001c0004t0004g0112 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.130-3016C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183992399 | ||||||
| chr3:183992493
|
G | A | 3 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193 | 3 | HG02109.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.130-3110C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183992493 | ||||||
| chr3:183992600
|
A | G | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.130-3217T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183992600 | ||||||
| chr3:183992692
|
A | G | 279 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(276): Show | 287 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(284): Show |
intron_variant | MODIFIER | c.130-3309T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183992692 | ||||||
| chr3:183992759
|
G | A | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.130-3376C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183992759 | ||||||
| chr3:183992996
|
T | C | 56 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(53): Show | 58 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(55): Show |
intron_variant | MODIFIER | c.130-3613A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183992996 | ||||||
| chr3:183993000
|
A | C | 1 | a0001c0001t0007g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.130-3617T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183993000 | ||||||
| chr3:183993103
|
C | T | 1 | a0009c0010t0018g0353 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.130-3720G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183993103 | ||||||
| chr3:183993203
|
G | T | 1 | a0001c0001t0003g0207 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.130-3820C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183993203 | ||||||
| chr3:183993362
|
T | C | 63 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(60): Show | 64 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.130-3979A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183993362 | ||||||
| chr3:183993483
|
C | CA | 139 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(136): Show | 142 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.130-4101dupT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183993483 | ||||||
| chr3:183993483
|
C | CAA | 68 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(65): Show | 69 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.130-4102_130-4101d others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183993483 | ||||||
| chr3:183993483
|
CAAAAAAA others(3): Show |
C | 77 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(74): Show | 81 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.130-4110_130-4101d others(12): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183993483 | ||||||
| chr3:183993840
|
C | T | 63 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(60): Show | 64 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.130-4457G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183993840 | ||||||
| chr3:183993841
|
G | A | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.130-4458C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183993841 | ||||||
| chr3:183993892
|
A | G | 67 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(64): Show | 71 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.130-4509T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183993892 | ||||||
| chr3:183993923
|
T | C | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.130-4540A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183993923 | ||||||
| chr3:183993961
|
C | CT | 9 | a0001c0001t0003g0225a0001c0001t0005g0157a0001c0001t0005g0158others(6): Show | 9 | HG00423.hp1 HG00673.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.130-4579dupA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183993961 | ||||||
| chr3:183993961
|
CT | C | 10 | a0001c0001t0005g0020a0001c0001t0005g0143a0001c0001t0007g0013others(7): Show | 10 | HG02258.hp1 HG02723.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.130-4579delA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183993961 | ||||||
| chr3:183994299
|
A | C | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.130-4916T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183994299 | ||||||
| chr3:183994331
|
G | C | 4 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-4948C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183994331 | ||||||
| chr3:183994376
|
AT | A | 276 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(273): Show | 284 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.130-4994delA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183994376 | ||||||
| chr3:183994405
|
T | C | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.130-5022A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183994405 | ||||||
| chr3:183994411
|
T | C | 1 | a0001c0005t0010g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.130-5028A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183994411 | ||||||
| chr3:183994414
|
C | T | 4 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-5031G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183994414 | ||||||
| chr3:183994444
|
C | T | 1 | a0001c0003t0002g0308 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.130-5061G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183994444 | ||||||
| chr3:183994471
|
G | A | 2 | a0001c0003t0002g0291a0001c0003t0002g0352 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.130-5088C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183994471 | ||||||
| chr3:183994617
|
G | A | 1 | a0001c0002t0001g0091 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.130-5234C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183994617 | ||||||
| chr3:183994664
|
G | A | 1 | a0001c0001t0005g0182 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.130-5281C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183994664 | ||||||
| chr3:183994764
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.130-5381G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183994764 | ||||||
| chr3:183994853
|
ATG | A | 30 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0031others(27): Show | 30 | HG00408.hp2 HG00544.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.130-5472_130-5471d others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183994853 | ||||||
| chr3:183994855
|
G | GT | 15 | a0001c0001t0001g0147a0001c0001t0001g0188a0001c0001t0003g0243others(12): Show | 15 | HG00423.hp1 HG01175.hp1 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.130-5473dupA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183994855 | ||||||
| chr3:183994855
|
GT | G | 8 | a0001c0001t0001g0021a0001c0001t0001g0149a0001c0001t0003g0238others(5): Show | 8 | HG01256.hp2 HG02129.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.130-5473delA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183994855 | ||||||
| chr3:183994925
|
A | G | 1 | a0001c0003t0002g0344 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.130-5542T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183994925 | ||||||
| chr3:183995281
|
TTG | T | 3 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193 | 3 | HG02109.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.130-5900_130-5899d others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183995281 | ||||||
| chr3:183995298
|
A | G | 1 | a0001c0001t0007g0195 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.130-5915T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183995298 | ||||||
| chr3:183995435
|
C | G | 1 | a0001c0001t0007g0194 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.130-6052G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183995435 | ||||||
| chr3:183995513
|
G | T | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.130-6130C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183995513 | ||||||
| chr3:183995593
|
G | A | 1 | a0001c0001t0003g0238 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.130-6210C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183995593 | ||||||
| chr3:183995595
|
C | A | 1 | a0001c0001t0003g0238 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.130-6212G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183995595 | ||||||
| chr3:183995598
|
T | A | 1 | a0001c0001t0003g0238 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.130-6215A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183995598 | ||||||
| chr3:183995603
|
G | T | 1 | a0001c0001t0003g0238 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.130-6220C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183995603 | ||||||
| chr3:183995604
|
T | G | 1 | a0001c0001t0003g0238 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.130-6221A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183995604 | ||||||
| chr3:183995605
|
C | T | 1 | a0001c0001t0003g0238 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.130-6222G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183995605 | ||||||
| chr3:183995634
|
T | C | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.130-6251A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183995634 | ||||||
| chr3:183995754
|
C | T | 4 | a0001c0001t0007g0014a0001c0001t0007g0194a0001c0001t0007g0195others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-6371G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183995754 | ||||||
| chr3:183995802
|
G | C | 3 | a0001c0004t0004g0132a0001c0004t0004g0133a0001c0004t0004g0134 | 3 | HG01167.hp2 HG01169.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.130-6419C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183995802 | ||||||
| chr3:183995819
|
T | G | 2 | a0001c0001t0003g0245a0001c0001t0003g0246 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.130-6436A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183995819 | ||||||
| chr3:183995890
|
C | A | 1 | a0001c0003t0002g0340 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.130-6507G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183995890 | ||||||
| chr3:183995895
|
C | T | 67 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(64): Show | 71 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.130-6512G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183995895 | ||||||
| chr3:183995939
|
C | A | 29 | a0001c0004t0002g0070a0001c0004t0002g0304a0001c0004t0004g0112others(26): Show | 29 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.130-6556G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183995939 | ||||||
| chr3:183995957
|
G | A | 1 | a0001c0002t0001g0095 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.130-6574C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183995957 | ||||||
| chr3:183996028
|
C | T | 106 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(103): Show | 110 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(107): Show |
intron_variant | MODIFIER | c.130-6645G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183996028 | ||||||
| chr3:183996089
|
A | G | 285 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(282): Show | 293 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(290): Show |
intron_variant | MODIFIER | c.130-6706T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183996089 | ||||||
| chr3:183996275
|
C | T | 67 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(64): Show | 71 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.130-6892G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183996275 | ||||||
| chr3:183996542
|
C | A | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.130-7159G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183996542 | ||||||
| chr3:183996679
|
G | A | 56 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(53): Show | 58 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(55): Show |
intron_variant | MODIFIER | c.130-7296C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183996679 | ||||||
| chr3:183996854
|
C | T | 1 | a0001c0001t0003g0222 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.130-7471G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183996854 | ||||||
| chr3:183997333
|
T | A | 1 | a0001c0004t0002g0070 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.130-7950A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183997333 | ||||||
| chr3:183997334
|
G | T | 1 | a0001c0004t0002g0070 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.130-7951C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183997334 | ||||||
| chr3:183997335
|
A | G | 1 | a0001c0004t0002g0070 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.130-7952T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183997335 | ||||||
| chr3:183997925
|
G | C | 1 | a0005c0014t0001g0107 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.130-8542C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183997925 | ||||||
| chr3:183998119
|
T | A | 3 | a0001c0003t0002g0028a0001c0007t0008g0253a0001c0007t0008g0254 | 3 | HG01433.hp1 HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.130-8736A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183998119 | ||||||
| chr3:183998173
|
G | A | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.130-8790C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183998173 | ||||||
| chr3:183998397
|
G | A | 3 | a0001c0005t0010g0110a0001c0005t0010g0192a0001c0005t0010g0193 | 3 | HG02109.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.130-9014C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183998397 | ||||||
| chr3:183998475
|
C | G | 32 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0031others(29): Show | 32 | HG00408.hp2 HG00544.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.130-9092G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183998475 | ||||||
| chr3:183998620
|
A | T | 23 | a0001c0003t0002g0294a0001c0003t0002g0298a0001c0003t0002g0303others(20): Show | 23 | HG01070.hp1 HG01071.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.130-9237T>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183998620 | ||||||
| chr3:183998680
|
A | C | 1 | a0001c0004t0004g0119 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.130-9297T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183998680 | ||||||
| chr3:183998681
|
C | CA | 241 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(238): Show | 249 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.130-9299dupT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183998681 | ||||||
| chr3:183998744
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.130-9361G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183998744 | ||||||
| chr3:183998816
|
G | A | 106 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(103): Show | 110 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(107): Show |
intron_variant | MODIFIER | c.130-9433C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183998816 | ||||||
| chr3:183998821
|
G | T | 245 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(242): Show | 253 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.130-9438C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183998821 | ||||||
| chr3:183998863
|
G | A | 1 | a0001c0013t0003g0090 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.130-9480C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183998863 | ||||||
| chr3:183999102
|
GAA | G | 244 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(241): Show | 252 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(249): Show |
intron_variant | MODIFIER | c.130-9721_130-9720d others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183999102 | ||||||
| chr3:183999104
|
A | G | 1 | a0001c0002t0001g0113 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.130-9721T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183999104 | ||||||
| chr3:183999415
|
T | C | 3 | a0001c0003t0002g0328a0001c0003t0002g0329a0001c0003t0017g0330 | 3 | HG00280.hp2 HG01123.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.130-10032A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183999415 | ||||||
| chr3:183999711
|
C | T | 3 | a0001c0002t0001g0271a0001c0002t0001g0272a0001c0002t0001g0273 | 3 | NA18946.hp1 NA19056.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.130-10328G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183999711 | ||||||
| chr3:183999998
|
A | C | 31 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0031others(28): Show | 31 | HG00408.hp2 HG00544.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.130-10615T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 183999998 | ||||||
| chr3:184000022
|
C | T | 29 | a0001c0004t0002g0070a0001c0004t0002g0304a0001c0004t0004g0112others(26): Show | 29 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.130-10639G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184000022 | ||||||
| chr3:184000087
|
G | A | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.130-10704C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184000087 | ||||||
| chr3:184000097
|
A | T | 62 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(59): Show | 66 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.130-10714T>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184000097 | ||||||
| chr3:184000169
|
G | C | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.130-10786C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184000169 | ||||||
| chr3:184000187
|
C | T | 4 | a0001c0002t0008g0261a0001c0002t0008g0262a0001c0002t0008g0263others(1): Show | 4 | HG02258.hp1 HG02723.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-10804G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184000187 | ||||||
| chr3:184000188
|
G | A | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.130-10805C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184000188 | ||||||
| chr3:184000546
|
G | A | 26 | a0001c0004t0004g0112a0001c0004t0004g0115a0001c0004t0004g0116others(23): Show | 26 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.130-11163C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184000546 | ||||||
| chr3:184000591
|
A | G | 25 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0031others(22): Show | 25 | HG00408.hp2 HG00544.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-11208T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184000591 | ||||||
| chr3:184000678
|
T | C | 5 | a0001c0002t0001g0060a0001c0002t0001g0061a0001c0002t0001g0062others(2): Show | 5 | NA18954.hp2 NA18993.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.130-11295A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184000678 | ||||||
| chr3:184000971
|
G | C | 1 | a0001c0003t0002g0348 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.130-11588C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184000971 | ||||||
| chr3:184001076
|
A | G | 278 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(275): Show | 286 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(283): Show |
intron_variant | MODIFIER | c.130-11693T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184001076 | ||||||
| chr3:184001164
|
G | C | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.130-11781C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184001164 | ||||||
| chr3:184001189
|
G | A | 1 | a0001c0001t0005g0178 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.130-11806C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184001189 | ||||||
| chr3:184001189
|
G | C | 17 | a0001c0001t0003g0007a0001c0001t0003g0202a0001c0001t0003g0205others(14): Show | 18 | HG02129.hp2 HG02523.hp1 NA18747.hp2 others(15): Show |
intron_variant | MODIFIER | c.130-11806C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184001189 | ||||||
| chr3:184001299
|
T | C | 10 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0358others(7): Show | 10 | HG00735.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.130-11916A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184001299 | ||||||
| chr3:184001374
|
G | A | 1 | a0001c0002t0001g0095 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.130-11991C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184001374 | ||||||
| chr3:184001387
|
C | T | 77 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0004others(74): Show | 81 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.130-12004G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184001387 | ||||||
| chr3:184001417
|
T | A | 1 | a0001c0002t0001g0069 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.130-12034A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184001417 | ||||||
| chr3:184001544
|
G | A | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.130-12161C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184001544 | ||||||
| chr3:184002082
|
G | A | 2 | a0001c0009t0013g0236a0001c0009t0013g0237 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.129+12182C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184002082 | ||||||
| chr3:184002090
|
A | G | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.129+12174T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184002090 | ||||||
| chr3:184002190
|
G | C | 1 | a0001c0003t0002g0349 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.129+12074C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184002190 | ||||||
| chr3:184002226
|
C | T | 1 | a0001c0002t0001g0072 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.129+12038G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184002226 | ||||||
| chr3:184002312
|
T | C | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.129+11952A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184002312 | ||||||
| chr3:184002398
|
C | CA | 7 | a0001c0001t0001g0197a0001c0002t0001g0091a0001c0002t0001g0092others(4): Show | 7 | HG01981.hp1 HG02145.hp2 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.129+11865dupT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184002398 | ||||||
| chr3:184002411
|
AAG | A | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.129+11851_129+1185 others(6): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184002411 | ||||||
| chr3:184002460
|
A | C | 1 | a0001c0001t0005g0180 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.129+11804T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184002460 | ||||||
| chr3:184002525
|
T | A | 138 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(135): Show | 142 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.129+11739A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184002525 | ||||||
| chr3:184002547
|
C | A | 3 | a0001c0001t0003g0218a0001c0001t0003g0223a0001c0001t0003g0234 | 3 | HG01993.hp1 HG03041.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.129+11717G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184002547 | ||||||
| chr3:184002572
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.129+11692C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184002572 | ||||||
| chr3:184002581
|
C | T | 1 | a0001c0004t0004g0137 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.129+11683G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184002581 | ||||||
| chr3:184002593
|
G | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG02683.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.129+11671C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184002593 | ||||||
| chr3:184002711
|
C | G | 64 | a0001c0001t0003g0221a0001c0002t0001g0001a0001c0002t0001g0003others(61): Show | 68 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.129+11553G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184002711 | ||||||
| chr3:184002713
|
C | T | 1 | a0001c0002t0001g0030 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.129+11551G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184002713 | ||||||
| chr3:184002788
|
A | C | 278 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(275): Show | 286 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(283): Show |
intron_variant | MODIFIER | c.129+11476T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184002788 | ||||||
| chr3:184002797
|
A | G | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.129+11467T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184002797 | ||||||
| chr3:184002883
|
C | A | 1 | a0001c0003t0002g0331 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.129+11381G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184002883 | ||||||
| chr3:184002899
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.129+11365G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184002899 | ||||||
| chr3:184002900
|
G | A | 1 | a0001c0003t0002g0331 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.129+11364C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184002900 | ||||||
| chr3:184002957
|
C | T | 64 | a0001c0001t0003g0221a0001c0002t0001g0001a0001c0002t0001g0003others(61): Show | 68 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.129+11307G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184002957 | ||||||
| chr3:184003016
|
T | G | 11 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(8): Show | 12 | HG00738.hp1 HG00741.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.129+11248A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184003016 | ||||||
| chr3:184003020
|
C | T | 1 | a0001c0002t0009g0267 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.129+11244G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184003020 | ||||||
| chr3:184003058
|
G | T | 26 | a0001c0004t0004g0112a0001c0004t0004g0115a0001c0004t0004g0116others(23): Show | 26 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.129+11206C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184003058 | ||||||
| chr3:184003161
|
G | A | 33 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0031others(30): Show | 33 | HG00408.hp2 HG00544.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.129+11103C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184003161 | ||||||
| chr3:184003181
|
G | A | 31 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0031others(28): Show | 31 | HG00408.hp2 HG00544.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.129+11083C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184003181 | ||||||
| chr3:184003303
|
C | T | 2 | a0001c0003t0002g0308a0001c0003t0002g0309 | 2 | HG00323.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.129+10961G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184003303 | ||||||
| chr3:184004013
|
A | G | 1 | a0001c0005t0002g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.129+10251T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184004013 | ||||||
| chr3:184004151
|
G | C | 1 | a0001c0003t0002g0337 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.129+10113C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184004151 | ||||||
| chr3:184004187
|
C | A | 7 | a0001c0003t0002g0009a0001c0003t0002g0201a0001c0003t0002g0293others(4): Show | 8 | HG01891.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.129+10077G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184004187 | ||||||
| chr3:184004213
|
TA | T | 275 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(272): Show | 283 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(280): Show |
intron_variant | MODIFIER | c.129+10050delT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184004213 | ||||||
| chr3:184004253
|
A | AT | 63 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(60): Show | 64 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.129+10010dupA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184004253 | ||||||
| chr3:184004476
|
A | C | 1 | a0001c0001t0001g0197 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.129+9788T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184004476 | ||||||
| chr3:184004506
|
C | CA | 16 | a0001c0001t0003g0243a0001c0001t0003g0251a0001c0002t0001g0029others(13): Show | 17 | HG01106.hp2 HG01891.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.129+9757dupT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184004506 | ||||||
| chr3:184004506
|
CA | C | 222 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(219): Show | 230 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.129+9757delT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184004506 | ||||||
| chr3:184004506
|
CAA | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0003g0022others(11): Show | 14 | HG01433.hp1 HG01884.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.129+9756_129+9757d others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184004506 | ||||||
| chr3:184004576
|
T | A | 63 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(60): Show | 64 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.129+9688A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184004576 | ||||||
| chr3:184004625
|
A | G | 1 | a0001c0003t0002g0305 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.129+9639T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184004625 | ||||||
| chr3:184004628
|
A | C | 1 | a0001c0001t0001g0197 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.129+9636T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184004628 | ||||||
| chr3:184004629
|
T | C | 65 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(62): Show | 66 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.129+9635A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184004629 | ||||||
| chr3:184004803
|
A | C | 367 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(364): Show | 377 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(374): Show |
intron_variant | MODIFIER | c.129+9461T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184004803 | ||||||
| chr3:184004824
|
A | T | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.129+9440T>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184004824 | ||||||
| chr3:184004991
|
G | A | 55 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(52): Show | 57 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(54): Show |
intron_variant | MODIFIER | c.129+9273C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184004991 | ||||||
| chr3:184004999
|
C | G | 1 | a0001c0007t0008g0254 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.129+9265G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184004999 | ||||||
| chr3:184005112
|
C | A | 1 | a0001c0002t0001g0095 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.129+9152G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184005112 | ||||||
| chr3:184005136
|
T | C | 7 | a0001c0004t0004g0116a0001c0004t0004g0132a0001c0004t0004g0133others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.129+9128A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184005136 | ||||||
| chr3:184005233
|
C | T | 55 | a0001c0001t0001g0197a0001c0001t0005g0094a0001c0002t0001g0001others(52): Show | 58 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.129+9031G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184005233 | ||||||
| chr3:184005287
|
A | G | 276 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(273): Show | 285 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(282): Show |
intron_variant | MODIFIER | c.129+8977T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184005287 | ||||||
| chr3:184005533
|
T | C | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | HG00438.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.129+8731A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184005533 | ||||||
| chr3:184005556
|
G | A | 2 | a0001c0007t0008g0253a0001c0007t0008g0254 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.129+8708C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184005556 | ||||||
| chr3:184005581
|
T | G | 27 | a0001c0002t0001g0131a0001c0004t0004g0112a0001c0004t0004g0115others(24): Show | 27 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.129+8683A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184005581 | ||||||
| chr3:184005631
|
G | C | 5 | a0001c0002t0008g0261a0001c0002t0008g0262a0001c0002t0008g0263others(2): Show | 5 | HG02258.hp1 HG02723.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+8633C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184005631 | ||||||
| chr3:184005651
|
G | A | 1 | a0001c0008t0001g0155 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.129+8613C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184005651 | ||||||
| chr3:184005673
|
C | A | 27 | a0001c0002t0001g0131a0001c0004t0004g0112a0001c0004t0004g0115others(24): Show | 27 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.129+8591G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184005673 | ||||||
| chr3:184005733
|
A | G | 1 | a0001c0001t0006g0289 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.129+8531T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184005733 | ||||||
| chr3:184005762
|
C | G | 54 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(51): Show | 56 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(53): Show |
intron_variant | MODIFIER | c.129+8502G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184005762 | ||||||
| chr3:184005780
|
T | A | 3 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0196 | 3 | HG01109.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.129+8484A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184005780 | ||||||
| chr3:184005908
|
T | A | 1 | a0001c0002t0001g0100 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.129+8356A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184005908 | ||||||
| chr3:184005908
|
T | TA | 259 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(256): Show | 267 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(264): Show |
intron_variant | MODIFIER | c.129+8355dupT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184005908 | ||||||
| chr3:184005908
|
T | TAA | 19 | a0001c0002t0001g0030a0001c0002t0001g0033a0001c0002t0001g0034others(16): Show | 19 | HG00408.hp2 HG00544.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.129+8354_129+8355d others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184005908 | ||||||
| chr3:184006028
|
C | T | 7 | a0001c0001t0006g0015a0001c0001t0006g0027a0001c0001t0006g0051others(4): Show | 7 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.129+8236G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184006028 | ||||||
| chr3:184006072
|
G | A | 1 | a0001c0003t0002g0336 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.129+8192C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184006072 | ||||||
| chr3:184006168
|
C | T | 282 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(279): Show | 290 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(287): Show |
intron_variant | MODIFIER | c.129+8096G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184006168 | ||||||
| chr3:184006284
|
G | A | 74 | a0001c0001t0005g0094a0001c0002t0001g0001a0001c0002t0001g0003others(71): Show | 78 | HG00423.hp2 HG00544.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.129+7980C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184006284 | ||||||
| chr3:184006300
|
GA | G | 208 | a0001c0001t0001g0147a0001c0001t0003g0006a0001c0001t0003g0007others(205): Show | 215 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(212): Show |
intron_variant | MODIFIER | c.129+7963delT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184006300 | ||||||
| chr3:184006300
|
GAA | G | 73 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0141others(70): Show | 74 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.129+7962_129+7963d others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184006300 | ||||||
| chr3:184006428
|
C | T | 20 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(17): Show | 21 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.129+7836G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184006428 | ||||||
| chr3:184006486
|
C | A | 1 | a0001c0003t0002g0337 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.129+7778G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184006486 | ||||||
| chr3:184006569
|
A | G | 1 | a0001c0003t0002g0341 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.129+7695T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184006569 | ||||||
| chr3:184006670
|
G | A | 7 | a0001c0001t0007g0013a0001c0001t0007g0194a0001c0001t0007g0195others(4): Show | 7 | HG01109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.129+7594C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184006670 | ||||||
| chr3:184006674
|
A | T | 1 | a0001c0001t0003g0249 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.129+7590T>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184006674 | ||||||
| chr3:184007016
|
C | CT | 177 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0179others(174): Show | 182 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(179): Show |
intron_variant | MODIFIER | c.129+7247dupA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184007016 | ||||||
| chr3:184007016
|
C | CTT | 27 | a0001c0001t0003g0022a0001c0001t0003g0220a0001c0001t0003g0239others(24): Show | 28 | HG00423.hp2 HG00544.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.129+7246_129+7247d others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184007016 | ||||||
| chr3:184007016
|
CT | C | 6 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0176others(3): Show | 6 | HG01070.hp1 HG01070.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+7247delA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184007016 | ||||||
| chr3:184007113
|
C | T | 5 | a0001c0002t0008g0261a0001c0002t0008g0262a0001c0002t0008g0263others(2): Show | 5 | HG02258.hp1 HG02723.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+7151G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184007113 | ||||||
| chr3:184007124
|
G | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0177 | 2 | NA18940.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.129+7140C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184007124 | ||||||
| chr3:184007186
|
A | C | 63 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(60): Show | 64 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.129+7078T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184007186 | ||||||
| chr3:184007208
|
G | C | 25 | a0001c0002t0001g0131a0001c0004t0004g0115a0001c0004t0004g0116others(22): Show | 25 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.129+7056C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184007208 | ||||||
| chr3:184007312
|
G | A | 2 | a0001c0005t0010g0192a0001c0005t0010g0193 | 2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.129+6952C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184007312 | ||||||
| chr3:184007319
|
C | T | 10 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0358others(7): Show | 10 | HG00735.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.129+6945G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184007319 | ||||||
| chr3:184007415
|
A | T | 5 | a0001c0002t0009g0266a0001c0002t0009g0267a0001c0002t0009g0268others(2): Show | 5 | HG01358.hp2 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+6849T>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184007415 | ||||||
| chr3:184007473
|
G | C | 1 | a0001c0001t0005g0178 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.129+6791C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184007473 | ||||||
| chr3:184007515
|
T | G | 2 | a0001c0002t0001g0048a0001c0002t0001g0049 | 2 | NA18979.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.129+6749A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184007515 | ||||||
| chr3:184007543
|
T | C | 1 | a0001c0001t0007g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.129+6721A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184007543 | ||||||
| chr3:184007551
|
C | T | 7 | a0001c0002t0009g0266a0001c0002t0009g0267a0001c0002t0009g0268others(4): Show | 7 | HG01358.hp2 HG02109.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.129+6713G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184007551 | ||||||
| chr3:184007756
|
G | A | 2 | a0001c0005t0002g0057a0001c0005t0002g0058 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.129+6508C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184007756 | ||||||
| chr3:184007901
|
A | T | 4 | a0001c0002t0008g0261a0001c0002t0008g0262a0001c0002t0008g0263others(1): Show | 4 | HG02258.hp1 HG02723.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+6363T>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184007901 | ||||||
| chr3:184007944
|
C | T | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.129+6320G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184007944 | ||||||
| chr3:184008121
|
G | GT | 282 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(279): Show | 290 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(287): Show |
intron_variant | MODIFIER | c.129+6142dupA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184008121 | ||||||
| chr3:184008194
|
C | T | 277 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(274): Show | 285 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(282): Show |
intron_variant | MODIFIER | c.129+6070G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184008194 | ||||||
| chr3:184008211
|
T | C | 266 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(263): Show | 274 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(271): Show |
intron_variant | MODIFIER | c.129+6053A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184008211 | ||||||
| chr3:184008430
|
C | T | 22 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0031others(19): Show | 22 | HG00408.hp2 HG00544.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.129+5834G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184008430 | ||||||
| chr3:184008531
|
A | G | 1 | a0001c0001t0003g0205 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.129+5733T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184008531 | ||||||
| chr3:184008591
|
A | G | 269 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(266): Show | 277 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(274): Show |
intron_variant | MODIFIER | c.129+5673T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184008591 | ||||||
| chr3:184008628
|
A | G | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.129+5636T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184008628 | ||||||
| chr3:184008719
|
C | T | 1 | a0001c0003t0002g0278 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.129+5545G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184008719 | ||||||
| chr3:184008856
|
T | C | 256 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(253): Show | 264 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(261): Show |
intron_variant | MODIFIER | c.129+5408A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184008856 | ||||||
| chr3:184008862
|
A | AT | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.129+5401dupA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184008862 | ||||||
| chr3:184008862
|
A | C | 10 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0358others(7): Show | 10 | HG00735.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.129+5402T>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184008862 | ||||||
| chr3:184009057
|
G | T | 13 | a0001c0001t0006g0002a0001c0001t0006g0015a0001c0001t0006g0027others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.129+5207C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184009057 | ||||||
| chr3:184009179
|
G | A | 4 | a0001c0001t0007g0013a0001c0001t0007g0199a0001c0001t0007g0200others(1): Show | 4 | HG02818.hp2 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+5085C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184009179 | ||||||
| chr3:184009235
|
A | G | 10 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0358others(7): Show | 10 | HG00735.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.129+5029T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184009235 | ||||||
| chr3:184009324
|
C | T | 1 | a0001c0002t0009g0268 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.129+4940G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184009324 | ||||||
| chr3:184009341
|
T | C | 1 | a0001c0005t0010g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.129+4923A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184009341 | ||||||
| chr3:184009456
|
A | G | 10 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0358others(7): Show | 10 | HG00735.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.129+4808T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184009456 | ||||||
| chr3:184009573
|
A | G | 1 | a0001c0004t0004g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.129+4691T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184009573 | ||||||
| chr3:184009612
|
G | T | 7 | a0001c0002t0009g0266a0001c0002t0009g0267a0001c0002t0009g0268others(4): Show | 7 | HG01358.hp2 HG02109.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.129+4652C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184009612 | ||||||
| chr3:184009639
|
A | G | 3 | a0001c0004t0004g0255a0001c0007t0008g0253a0001c0007t0008g0254 | 3 | HG01433.hp1 HG01884.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.129+4625T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184009639 | ||||||
| chr3:184009647
|
T | A | 56 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(53): Show | 58 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(55): Show |
intron_variant | MODIFIER | c.129+4617A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184009647 | ||||||
| chr3:184009667
|
A | G | 56 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(53): Show | 58 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(55): Show |
intron_variant | MODIFIER | c.129+4597T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184009667 | ||||||
| chr3:184009955
|
C | T | 10 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0358others(7): Show | 10 | HG00735.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.129+4309G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184009955 | ||||||
| chr3:184010044
|
C | T | 1 | a0001c0004t0004g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.129+4220G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184010044 | ||||||
| chr3:184010081
|
C | T | 3 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035 | 3 | HG02135.hp1 NA18954.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.129+4183G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184010081 | ||||||
| chr3:184010082
|
G | A | 4 | a0001c0002t0008g0261a0001c0002t0008g0262a0001c0002t0008g0263others(1): Show | 4 | HG02258.hp1 HG02723.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+4182C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184010082 | ||||||
| chr3:184010192
|
G | A | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.129+4072C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184010192 | ||||||
| chr3:184010266
|
C | CA | 13 | a0001c0002t0001g0358a0001c0002t0008g0261a0001c0002t0008g0262others(10): Show | 13 | HG00735.hp1 HG02055.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.129+3997dupT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184010266 | ||||||
| chr3:184010266
|
CA | C | 203 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(200): Show | 209 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.129+3997delT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184010266 | ||||||
| chr3:184010266
|
CAA | C | 39 | a0001c0001t0001g0152a0001c0001t0006g0015a0001c0001t0006g0027others(36): Show | 40 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.129+3996_129+3997d others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184010266 | ||||||
| chr3:184010266
|
CAAA | C | 6 | a0001c0001t0006g0002a0001c0001t0006g0059a0001c0001t0006g0288others(3): Show | 7 | HG02451.hp2 HG02615.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.129+3995_129+3997d others(5): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184010266 | ||||||
| chr3:184010377
|
A | G | 2 | a0001c0002t0001g0358a0001c0002t0001g0364 | 2 | HG00735.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.129+3887T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184010377 | ||||||
| chr3:184010483
|
T | C | 10 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0358others(7): Show | 10 | HG00735.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.129+3781A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184010483 | ||||||
| chr3:184010494
|
T | A | 1 | a0001c0001t0006g0055 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.129+3770A>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184010494 | ||||||
| chr3:184010552
|
C | A | 1 | a0001c0002t0001g0114 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.129+3712G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184010552 | ||||||
| chr3:184010798
|
C | CTT | 220 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(217): Show | 228 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(225): Show |
intron_variant | MODIFIER | c.129+3464_129+3465d others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184010798 | ||||||
| chr3:184010798
|
C | CTTT | 11 | a0001c0001t0005g0018a0001c0001t0005g0020a0001c0001t0005g0143others(8): Show | 11 | HG02074.hp2 HG02818.hp2 NA18951.hp1 others(8): Show |
intron_variant | MODIFIER | c.129+3463_129+3465d others(5): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184010798 | ||||||
| chr3:184010799
|
T | TTC | 22 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0031others(19): Show | 22 | HG00408.hp2 HG00544.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.129+3464_129+3465i others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184010799 | ||||||
| chr3:184010827
|
T | C | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.129+3437A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184010827 | ||||||
| chr3:184010854
|
A | G | 1 | a0001c0001t0007g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.129+3410T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184010854 | ||||||
| chr3:184010860
|
C | T | 3 | a0001c0004t0004g0255a0001c0007t0008g0253a0001c0007t0008g0254 | 3 | HG01433.hp1 HG01884.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.129+3404G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184010860 | ||||||
| chr3:184011041
|
C | A | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.129+3223G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184011041 | ||||||
| chr3:184011056
|
A | AT | 22 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0031others(19): Show | 22 | HG00408.hp2 HG00544.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.129+3207dupA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184011056 | ||||||
| chr3:184011323
|
G | A | 141 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(138): Show | 145 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.129+2941C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184011323 | ||||||
| chr3:184011416
|
G | A | 1 | a0001c0001t0007g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.129+2848C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184011416 | ||||||
| chr3:184011500
|
C | CA | 266 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(263): Show | 274 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(271): Show |
intron_variant | MODIFIER | c.129+2763dupT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184011500 | ||||||
| chr3:184011565
|
A | G | 1 | a0001c0001t0006g0288 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.129+2699T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184011565 | ||||||
| chr3:184011698
|
A | G | 3 | a0001c0001t0006g0002a0001c0001t0006g0288a0001c0001t0006g0289 | 4 | HG03130.hp2 HG03195.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+2566T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184011698 | ||||||
| chr3:184011699
|
C | T | 266 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(263): Show | 274 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(271): Show |
intron_variant | MODIFIER | c.129+2565G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184011699 | ||||||
| chr3:184011876
|
C | G | 91 | a0001c0001t0005g0094a0001c0002t0001g0001a0001c0002t0001g0003others(88): Show | 95 | HG00423.hp2 HG00544.hp1 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.129+2388G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184011876 | ||||||
| chr3:184012014
|
A | AAC | 25 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(22): Show | 25 | HG00408.hp2 HG00738.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.129+2248_129+2249d others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184012014 | ||||||
| chr3:184012014
|
A | AACAC | 10 | a0001c0001t0006g0059a0001c0001t0007g0014a0001c0001t0007g0139others(7): Show | 10 | HG00544.hp2 HG01433.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.129+2246_129+2249d others(6): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184012014 | ||||||
| chr3:184012014
|
A | AACACAC | 15 | a0001c0001t0003g0244a0001c0001t0003g0245a0001c0001t0003g0246others(12): Show | 16 | HG01109.hp2 HG01192.hp2 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.129+2244_129+2249d others(8): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184012014 | ||||||
| chr3:184012014
|
A | AACACACA others(1): Show |
17 | a0001c0001t0001g0188a0001c0001t0003g0239a0001c0001t0003g0240others(14): Show | 17 | HG00408.hp1 HG01175.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.129+2242_129+2249d others(10): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184012014 | ||||||
| chr3:184012014
|
A | AACACACA others(3): Show |
26 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(23): Show | 26 | HG00597.hp1 HG00597.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.129+2240_129+2249d others(12): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184012014 | ||||||
| chr3:184012014
|
A | AACACACA others(5): Show |
65 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0141others(62): Show | 67 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.129+2238_129+2249d others(14): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184012014 | ||||||
| chr3:184012014
|
A | AACACACA others(7): Show |
8 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(5): Show | 9 | HG00621.hp2 HG00738.hp1 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.129+2236_129+2249d others(16): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184012014 | ||||||
| chr3:184012014
|
A | AACACACA others(9): Show |
4 | a0001c0001t0001g0019a0001c0001t0001g0197a0001c0001t0003g0203others(1): Show | 4 | HG01167.hp1 NA18994.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+2234_129+2249d others(18): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184012014 | ||||||
| chr3:184012014
|
AAC | A | 29 | a0001c0001t0005g0191a0001c0002t0001g0025a0001c0002t0001g0026others(26): Show | 29 | HG00639.hp2 HG00735.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.129+2248_129+2249d others(4): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184012014 | ||||||
| chr3:184012014
|
AACACACA others(1): Show |
A | 90 | a0001c0001t0005g0094a0001c0002t0001g0001a0001c0002t0001g0003others(87): Show | 94 | HG00423.hp2 HG00544.hp1 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.129+2242_129+2249d others(10): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184012014 | ||||||
| chr3:184012014
|
AACACACA others(7): Show |
A | 5 | a0001c0002t0008g0261a0001c0002t0008g0262a0001c0002t0008g0263others(2): Show | 5 | HG02258.hp1 HG02723.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+2236_129+2249d others(16): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184012014 | ||||||
| chr3:184012047
|
A | ACACACAC others(6): Show |
1 | a0001c0001t0005g0018 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.129+2216_129+2217i others(15): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184012047 | ||||||
| chr3:184012047
|
A | ACACACAC others(8): Show |
1 | a0001c0001t0003g0202 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.129+2216_129+2217i others(17): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184012047 | ||||||
| chr3:184012047
|
A | ACACACAC others(10): Show |
1 | a0001c0001t0001g0145 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.129+2216_129+2217i others(19): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184012047 | ||||||
| chr3:184012058
|
T | C | 1 | a0001c0003t0011g0367 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.129+2206A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184012058 | ||||||
| chr3:184012241
|
G | GT | 13 | a0001c0001t0005g0143a0001c0001t0005g0144a0001c0002t0001g0025others(10): Show | 13 | HG00735.hp1 HG02486.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.129+2022dupA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184012241 | ||||||
| chr3:184012241
|
GT | G | 23 | a0001c0001t0007g0013a0001c0002t0001g0029a0001c0002t0001g0030others(20): Show | 23 | HG00408.hp2 HG00544.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.129+2022delA | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184012241 | ||||||
| chr3:184012303
|
T | C | 56 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(53): Show | 58 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(55): Show |
intron_variant | MODIFIER | c.129+1961A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184012303 | ||||||
| chr3:184012313
|
T | C | 7 | a0001c0002t0009g0266a0001c0002t0009g0267a0001c0002t0009g0268others(4): Show | 7 | HG01358.hp2 HG02109.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.129+1951A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184012313 | ||||||
| chr3:184012328
|
G | A | 27 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0131others(24): Show | 27 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.129+1936C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184012328 | ||||||
| chr3:184012354
|
T | C | 1 | a0001c0003t0002g0350 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.129+1910A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184012354 | ||||||
| chr3:184012393
|
G | C | 10 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0358others(7): Show | 10 | HG00735.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.129+1871C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184012393 | ||||||
| chr3:184012507
|
C | T | 142 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(139): Show | 146 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.129+1757G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184012507 | ||||||
| chr3:184012869
|
G | A | 7 | a0001c0001t0007g0013a0001c0001t0007g0194a0001c0001t0007g0195others(4): Show | 7 | HG01109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.129+1395C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184012869 | ||||||
| chr3:184013036
|
T | C | 5 | a0001c0002t0009g0266a0001c0002t0009g0267a0001c0002t0009g0268others(2): Show | 5 | HG01358.hp2 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+1228A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184013036 | ||||||
| chr3:184013107
|
C | A | 1 | a0001c0002t0001g0364 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.129+1157G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184013107 | ||||||
| chr3:184013107
|
C | T | 5 | a0001c0002t0009g0266a0001c0002t0009g0267a0001c0002t0009g0268others(2): Show | 5 | HG01358.hp2 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+1157G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184013107 | ||||||
| chr3:184013115
|
C | T | 1 | a0001c0002t0009g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.129+1149G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184013115 | ||||||
| chr3:184013412
|
C | T | 22 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0031others(19): Show | 22 | HG00408.hp2 HG00544.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.129+852G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184013412 | ||||||
| chr3:184013534
|
A | G | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG02683.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.129+730T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184013534 | ||||||
| chr3:184013538
|
G | C | 10 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0358others(7): Show | 10 | HG00735.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.129+726C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184013538 | ||||||
| chr3:184013574
|
C | G | 270 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(267): Show | 278 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(275): Show |
intron_variant | MODIFIER | c.129+690G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184013574 | ||||||
| chr3:184013576
|
T | C | 1 | a0001c0002t0001g0050 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.129+688A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184013576 | ||||||
| chr3:184013583
|
A | T | 1 | a0001c0002t0001g0050 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.129+681T>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184013583 | ||||||
| chr3:184013584
|
A | G | 1 | a0001c0002t0001g0050 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.129+680T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184013584 | ||||||
| chr3:184013585
|
G | T | 1 | a0001c0002t0001g0050 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.129+679C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184013585 | ||||||
| chr3:184013606
|
G | A | 1 | a0001c0004t0004g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.129+658C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184013606 | ||||||
| chr3:184013682
|
G | A | 56 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(53): Show | 58 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(55): Show |
intron_variant | MODIFIER | c.129+582C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184013682 | ||||||
| chr3:184013814
|
A | G | 1 | a0001c0005t0002g0274 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.129+450T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184013814 | ||||||
| chr3:184013824
|
G | A | 1 | a0001c0001t0007g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.129+440C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184013824 | ||||||
| chr3:184013929
|
G | A | 1 | a0001c0003t0011g0368 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.129+335C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184013929 | ||||||
| chr3:184013959
|
G | A | 4 | a0001c0001t0006g0351a0001c0003t0002g0291a0001c0003t0002g0352others(1): Show | 4 | HG01257.hp2 HG02257.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+305C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184013959 | ||||||
| chr3:184013975
|
C | A | 1 | a0001c0001t0006g0027 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.129+289G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184013975 | ||||||
| chr3:184014018
|
G | A | 5 | a0001c0002t0009g0266a0001c0002t0009g0267a0001c0002t0009g0268others(2): Show | 5 | HG01358.hp2 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+246C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 2/29 | chr3 | 184014018 | ||||||
| chr3:184014526
|
G | GA | 124 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(121): Show | 127 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.-55-80dupT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184014526 | ||||||
| chr3:184014526
|
G | GAA | 9 | a0001c0001t0001g0197a0001c0001t0003g0250a0001c0001t0003g0251others(6): Show | 9 | HG02056.hp1 HG02818.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.-55-81_-55-80dupTT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184014526 | ||||||
| chr3:184014526
|
GA | G | 35 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0031others(32): Show | 35 | HG00408.hp2 HG00544.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.-55-80delT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184014526 | ||||||
| chr3:184014665
|
C | T | 3 | a0001c0004t0004g0255a0001c0007t0008g0253a0001c0007t0008g0254 | 3 | HG01433.hp1 HG01884.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-55-218G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184014665 | ||||||
| chr3:184014697
|
A | G | 1 | a0001c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-55-250T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184014697 | ||||||
| chr3:184014829
|
A | T | 1 | a0001c0001t0006g0027 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-55-382T>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184014829 | ||||||
| chr3:184014946
|
T | G | 56 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0022others(53): Show | 58 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(55): Show |
intron_variant | MODIFIER | c.-55-499A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184014946 | ||||||
| chr3:184015253
|
C | T | 10 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0358others(7): Show | 10 | HG00735.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-55-806G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184015253 | ||||||
| chr3:184015345
|
C | G | 1 | a0001c0003t0002g0291 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-55-898G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184015345 | ||||||
| chr3:184015346
|
C | T | 3 | a0001c0004t0004g0255a0001c0007t0008g0253a0001c0007t0008g0254 | 3 | HG01433.hp1 HG01884.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-55-899G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184015346 | ||||||
| chr3:184015467
|
T | C | 1 | a0001c0016t0014g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-55-1020A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184015467 | ||||||
| chr3:184015655
|
G | A | 2 | a0001c0001t0005g0011a0001c0001t0005g0012 | 2 | NA18981.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.-55-1208C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184015655 | ||||||
| chr3:184015688
|
TA | T | 10 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0003g0022others(7): Show | 10 | HG01074.hp2 HG01167.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.-55-1242delT | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184015688 | ||||||
| chr3:184015863
|
CCTT | C | 4 | a0001c0003t0002g0354a0001c0003t0002g0355a0001c0003t0002g0356others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.-55-1419_-55-1417d others(5): Show |
ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184015863 | ||||||
| chr3:184015874
|
G | C | 1 | a0001c0002t0001g0252 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-55-1427C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184015874 | ||||||
| chr3:184015936
|
G | C | 1 | a0001c0002t0001g0252 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-55-1489C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184015936 | ||||||
| chr3:184015996
|
A | G | 268 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(265): Show | 276 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(273): Show |
intron_variant | MODIFIER | c.-55-1549T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184015996 | ||||||
| chr3:184015997
|
G | C | 1 | a0001c0002t0001g0256 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-55-1550C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184015997 | ||||||
| chr3:184016386
|
C | T | 1 | a0001c0001t0007g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-56+1444G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184016386 | ||||||
| chr3:184016400
|
A | G | 1 | a0001c0002t0001g0287 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-56+1430T>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184016400 | ||||||
| chr3:184016553
|
T | C | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | HG00438.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.-56+1277A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184016553 | ||||||
| chr3:184016826
|
T | C | 1 | a0001c0001t0003g0259 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-56+1004A>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184016826 | ||||||
| chr3:184016993
|
G | C | 6 | a0001c0002t0001g0365a0001c0002t0009g0266a0001c0002t0009g0267others(3): Show | 6 | HG01358.hp2 HG02615.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-56+837C>G | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184016993 | ||||||
| chr3:184017035
|
T | G | 11 | a0001c0002t0008g0261a0001c0002t0008g0262a0001c0002t0008g0263others(8): Show | 11 | HG01358.hp2 HG02258.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-56+795A>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184017035 | ||||||
| chr3:184017202
|
C | G | 14 | a0001c0003t0002g0008a0001c0003t0002g0275a0001c0003t0002g0276others(11): Show | 15 | HG00558.hp2 HG00621.hp1 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.-56+628G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184017202 | ||||||
| chr3:184017406
|
G | A | 3 | a0001c0002t0001g0271a0001c0002t0001g0272a0001c0002t0001g0273 | 3 | NA18946.hp1 NA19056.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-56+424C>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184017406 | ||||||
| chr3:184017498
|
C | G | 279 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0021others(276): Show | 287 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(284): Show |
intron_variant | MODIFIER | c.-56+332G>C | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184017498 | ||||||
| chr3:184017570
|
C | T | 1 | a0001c0001t0007g0013 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-56+260G>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184017570 | ||||||
| chr3:184017664
|
C | A | 8 | a0001c0002t0001g0358a0001c0002t0001g0359a0001c0002t0001g0360others(5): Show | 8 | HG00735.hp1 HG02486.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56+166G>T | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184017664 | ||||||
| chr3:184017731
|
G | T | 3 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012 | 3 | NA18612.hp1 NA18981.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.-56+99C>A | ABCC5 | ENSG00000114770.17 | transcript | ENST00000334444.11 | protein_coding | 1/29 | chr3 | 184017731 |