| geneid | 55914 |
|---|---|
| ensemblid | ENSG00000112851.16 |
| hgncid | 15842 |
| symbol | ERBIN |
| name | erbb2 interacting protein |
| refseq_nuc | NM_001253697.2 |
| refseq_prot | NP_001240626.1 |
| ensembl_nuc | ENST00000284037.10 |
| ensembl_prot | ENSP00000284037.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 65926575 |
| end | 66082546 |
| strand | + |
| ver | v1.2 |
| region | chr5:65926575-66082546 |
| region5000 | chr5:65921575-66087546 |
| regionname0 | ERBIN_chr5_65926575_66082546 |
| regionname5000 | ERBIN_chr5_65921575_66087546 |
| 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 | 1412 | 182 | 53 | 26 | 86 | 3 | 12 | 67 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0002 | 0/0 | 1412 | 46 | 1 | 9 | 32 | 1 | 3 | 30 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0003 | 0/0 | 1412 | 31 | 0 | 6 | 18 | 2 | 5 | 15 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0004 | 0/0 | 1412 | 16 | 15 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0005 | 0/0 | 1412 | 12 | 10 | 2 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0006 | 0/0 | 1412 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0007 | 0/0 | 1412 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0008 | 0/0 | 1412 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0009 | 0/0 | 1412 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0010 | 0/0 | 1412 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0011 | 0/0 | 1412 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0012 | 0/0 | 1412 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0013 | 0/0 | 1412 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0014 | 0/0 | 1412 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0015 | 0/0 | 1412 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0016 | 0/0 | 1412 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| 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 | 4239 | 115 | 35 | 17 | 50 | 3 | 9 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| c0002 | 0/0 | 4239 | 53 | 9 | 8 | 33 | 0 | 3 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| c0003 | 0/0 | 4239 | 46 | 1 | 9 | 32 | 1 | 3 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| c0004 | 0/0 | 4239 | 30 | 0 | 6 | 17 | 2 | 5 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| c0005 | 0/0 | 4239 | 14 | 13 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| c0006 | 0/0 | 4239 | 12 | 10 | 2 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| c0007 | 1/0 | 4239 | 10 | 9 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| c0008 | 0/0 | 4239 | 5 | 0 | 0 | 5 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| c0009 | 0/0 | 4239 | 2 | 0 | 0 | 2 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| c0010 | 0/0 | 4239 | 2 | 0 | 0 | 2 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| c0011 | 0/0 | 4239 | 2 | 2 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| c0012 | 0/0 | 4239 | 2 | 2 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| c0013 | 0/0 | 4239 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| c0014 | 0/0 | 4239 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| c0015 | 0/0 | 4239 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| c0016 | 0/0 | 4239 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| c0017 | 0/0 | 4239 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| c0018 | 0/0 | 4239 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| c0019 | 0/0 | 4239 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| c0020 | 0/0 | 4239 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| c0021 | 0/0 | 4239 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| c0022 | 0/0 | 4239 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| c0023 | 0/0 | 4239 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| c0024 | 0/0 | 4239 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| c0025 | 0/0 | 4239 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 4306 | 123 | 25 | 19 | 63 | 5 | 9 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0002 | 0/0 | 4306 | 64 | 11 | 9 | 39 | 1 | 4 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0003 | 0/0 | 4306 | 24 | 2 | 3 | 17 | 0 | 2 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0004 | 0/0 | 4306 | 15 | 14 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0005 | 0/0 | 4306 | 13 | 0 | 5 | 8 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0006 | 0/0 | 4306 | 11 | 10 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0007 | 0/0 | 4306 | 9 | 7 | 2 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0008 | 0/0 | 4306 | 8 | 0 | 0 | 8 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0009 | 0/0 | 4311 | 6 | 0 | 0 | 5 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0010 | 0/0 | 4306 | 6 | 6 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0011 | 0/0 | 4302 | 4 | 4 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0012 | 0/0 | 4307 | 3 | 3 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0013 | 0/0 | 4306 | 3 | 0 | 1 | 0 | 0 | 2 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0014 | 0/0 | 4306 | 2 | 0 | 0 | 2 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0015 | 0/0 | 4306 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0016 | 0/0 | 4306 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0017 | 0/0 | 4306 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0018 | 0/0 | 4306 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0019 | 0/0 | 4306 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0020 | 0/0 | 4306 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0021 | 0/0 | 4306 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0022 | 0/0 | 4306 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0023 | 0/0 | 4306 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0024 | 0/0 | 4306 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0025 | 0/0 | 4306 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0026 | 0/0 | 4306 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0027 | 0/0 | 4306 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0028 | 0/0 | 4306 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| t0029 | 0/0 | 4306 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0247 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| 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 | 4239 | 115 | 35 | 17 | 50 | 3 | 9 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0001c0002 | 0/0 | 4239 | 53 | 9 | 8 | 33 | 0 | 3 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0001c0007 | 1/0 | 4239 | 10 | 9 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0001c0015 | 0/0 | 4239 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0001c0020 | 0/0 | 4239 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0001c0021 | 0/0 | 4239 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0001c0022 | 0/0 | 4239 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0002c0003 | 0/0 | 4239 | 46 | 1 | 9 | 32 | 1 | 3 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0003c0004 | 0/0 | 4239 | 30 | 0 | 6 | 17 | 2 | 5 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0003c0025 | 0/0 | 4239 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0004c0005 | 0/0 | 4239 | 14 | 13 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0004c0014 | 0/0 | 4239 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0004c0017 | 0/0 | 4239 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0005c0006 | 0/0 | 4239 | 12 | 10 | 2 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0006c0008 | 0/0 | 4239 | 5 | 0 | 0 | 5 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0007c0012 | 0/0 | 4239 | 2 | 2 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0008c0011 | 0/0 | 4239 | 2 | 2 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0009c0010 | 0/0 | 4239 | 2 | 0 | 0 | 2 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0010c0009 | 0/0 | 4239 | 2 | 0 | 0 | 2 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0011c0019 | 0/0 | 4239 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0012c0016 | 0/0 | 4239 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0013c0018 | 0/0 | 4239 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0014c0023 | 0/0 | 4239 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0015c0024 | 0/0 | 4239 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0016c0013 | 0/0 | 4239 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 8544 | 90 | 22 | 14 | 44 | 3 | 6 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0001c0001t0003 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0001c0001t0006 | 0/0 | 8544 | 11 | 10 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0001c0001t0009 | 0/0 | 8549 | 5 | 0 | 0 | 4 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0001c0001t0013 | 0/0 | 8544 | 3 | 0 | 1 | 0 | 0 | 2 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0001c0001t0014 | 0/0 | 8544 | 2 | 0 | 0 | 2 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0001c0001t0020 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0001c0001t0024 | 0/0 | 8544 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0001c0001t0028 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0001c0002t0002 | 0/0 | 8544 | 52 | 9 | 8 | 32 | 0 | 3 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0001c0002t0019 | 0/0 | 8544 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0001c0007t0001 | 1/0 | 8544 | 1 | 0 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0001c0007t0010 | 0/0 | 8544 | 6 | 6 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0001c0007t0012 | 0/0 | 8545 | 3 | 3 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0001c0015t0029 | 0/0 | 8544 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0001c0020t0001 | 0/0 | 8544 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0001c0021t0001 | 0/0 | 8544 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0001c0022t0009 | 0/0 | 8549 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0002c0003t0002 | 0/0 | 8544 | 6 | 0 | 1 | 3 | 1 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0002c0003t0003 | 0/0 | 8544 | 19 | 1 | 3 | 13 | 0 | 2 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0002c0003t0005 | 0/0 | 8544 | 13 | 0 | 5 | 8 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0002c0003t0008 | 0/0 | 8544 | 8 | 0 | 0 | 8 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0003c0004t0001 | 0/0 | 8544 | 25 | 0 | 4 | 16 | 2 | 3 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0003c0004t0017 | 0/0 | 8544 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0003c0004t0021 | 0/0 | 8544 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0003c0004t0023 | 0/0 | 8544 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0003c0004t0026 | 0/0 | 8544 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0003c0004t0027 | 0/0 | 8544 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0003c0025t0001 | 0/0 | 8544 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0004c0005t0004 | 0/0 | 8544 | 13 | 12 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0004c0005t0025 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0004c0014t0004 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0004c0017t0004 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0005c0006t0002 | 0/0 | 8544 | 2 | 2 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0005c0006t0007 | 0/0 | 8544 | 8 | 6 | 2 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0005c0006t0015 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0005c0006t0016 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0006c0008t0003 | 0/0 | 8544 | 4 | 0 | 0 | 4 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0006c0008t0018 | 0/0 | 8544 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0007c0012t0011 | 0/0 | 8540 | 2 | 2 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0008c0011t0011 | 0/0 | 8540 | 2 | 2 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0009c0010t0002 | 0/0 | 8544 | 2 | 0 | 0 | 2 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0010c0009t0002 | 0/0 | 8544 | 2 | 0 | 0 | 2 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0011c0019t0001 | 0/0 | 8544 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0012c0016t0007 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0013c0018t0001 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0014c0023t0001 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0015c0024t0022 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| a0016c0013t0001 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | copy fasta | chr5 | 65921575 | 66087546 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0009g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0009g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0009g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0009g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0009g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0013g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0013g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0013g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0014g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0014g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0020g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0024g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0001t0028g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0002t0019g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0007t0001g0247 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0007t0010g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0007t0010g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0007t0010g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0007t0010g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0007t0010g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0007t0010g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0007t0012g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0007t0012g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0007t0012g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0015t0029g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0020t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0021t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0001c0022t0009g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0003g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0003g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0005g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0005g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0005g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0005g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0005g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0008g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0008g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0008g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0008g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0008g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0008g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0008g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0002c0003t0008g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0017g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0021g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0023g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0026g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0004t0027g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0003c0025t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0004c0005t0004g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0004c0005t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0004c0005t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0004c0005t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0004c0005t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0004c0005t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0004c0005t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0004c0005t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0004c0005t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0004c0005t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0004c0005t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0004c0005t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0004c0005t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0004c0005t0025g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0004c0014t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0004c0017t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0005c0006t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0005c0006t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0005c0006t0007g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0005c0006t0007g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0005c0006t0007g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0005c0006t0007g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0005c0006t0007g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0005c0006t0007g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0005c0006t0007g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0005c0006t0007g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0005c0006t0015g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0005c0006t0016g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0006c0008t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0006c0008t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0006c0008t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0006c0008t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0006c0008t0018g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0007c0012t0011g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0007c0012t0011g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0008c0011t0011g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0008c0011t0011g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0009c0010t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0009c0010t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0010c0009t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0010c0009t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0011c0019t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0012c0016t0007g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0013c0018t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0014c0023t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0015c0024t0022g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| a0016c0013t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0004 | t0001 | g0131 | EUR | GBR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | GBR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | FIN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG00280 | hp2 | a0002 | c0003 | t0002 | g0216 | EUR | FIN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0290 | EAS | CHS | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG00408 | hp2 | a0002 | c0003 | t0008 | g0280 | EAS | CHS | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0296 | EAS | CHS | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | CHS | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG00621 | hp1 | a0001 | c0001 | t0014 | g0071 | EAS | CHS | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG00621 | hp2 | a0003 | c0004 | t0001 | g0134 | EAS | CHS | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG00642 | hp1 | a0003 | c0004 | t0001 | g0136 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0286 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0256 | EAS | CHS | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0287 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG00738 | hp2 | a0001 | c0001 | t0006 | g0154 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0260 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0255 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01081 | hp1 | a0002 | c0003 | t0005 | g0186 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01109 | hp1 | a0002 | c0003 | t0003 | g0300 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01109 | hp2 | a0005 | c0006 | t0007 | g0224 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01167 | hp1 | a0003 | c0004 | t0001 | g0305 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01167 | hp2 | a0004 | c0005 | t0004 | g0007 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01243 | hp1 | a0001 | c0001 | t0024 | g0158 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01243 | hp2 | a0005 | c0006 | t0007 | g0222 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0236 | AMR | CLM | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01257 | hp1 | a0002 | c0003 | t0005 | g0176 | AMR | CLM | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01261 | hp2 | a0001 | c0001 | t0013 | g0124 | AMR | CLM | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01433 | hp1 | a0002 | c0003 | t0003 | g0166 | AMR | CLM | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01433 | hp2 | a0002 | c0003 | t0002 | g0202 | AMR | CLM | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | IBS | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01515 | hp2 | a0003 | c0004 | t0001 | g0140 | EUR | IBS | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01884 | hp1 | a0012 | c0016 | t0007 | g0228 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0155 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0153 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01934 | hp1 | a0002 | c0003 | t0005 | g0185 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01943 | hp1 | a0002 | c0003 | t0005 | g0172 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01943 | hp2 | a0003 | c0004 | t0027 | g0139 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01952 | hp2 | a0003 | c0004 | t0001 | g0306 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0261 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01981 | hp2 | a0001 | c0021 | t0001 | g0101 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01993 | hp1 | a0002 | c0003 | t0003 | g0200 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG01993 | hp2 | a0003 | c0004 | t0001 | g0132 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0244 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02055 | hp2 | a0001 | c0007 | t0010 | g0275 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0239 | EAS | KHV | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02071 | hp1 | a0002 | c0003 | t0008 | g0257 | EAS | KHV | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0279 | EAS | KHV | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0246 | EAS | KHV | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02132 | hp1 | a0003 | c0004 | t0001 | g0001 | EAS | KHV | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0156 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02148 | hp1 | a0002 | c0003 | t0005 | g0177 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02165 | hp1 | a0001 | c0002 | t0019 | g0298 | EAS | CDX | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CDX | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02257 | hp1 | a0005 | c0006 | t0002 | g0263 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02258 | hp1 | a0004 | c0005 | t0004 | g0013 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02258 | hp2 | a0005 | c0006 | t0007 | g0223 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02273 | hp1 | a0003 | c0004 | t0023 | g0304 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0243 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0212 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02451 | hp1 | a0005 | c0006 | t0015 | g0225 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02451 | hp2 | a0004 | c0005 | t0004 | g0019 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02572 | hp1 | a0004 | c0005 | t0004 | g0027 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02602 | hp2 | a0003 | c0004 | t0001 | g0137 | SAS | PJL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02615 | hp1 | a0001 | c0007 | t0012 | g0218 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0214 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02622 | hp1 | a0001 | c0007 | t0012 | g0220 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0211 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02647 | hp1 | a0005 | c0006 | t0002 | g0229 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0209 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02723 | hp1 | a0008 | c0011 | t0011 | g0025 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02723 | hp2 | a0004 | c0014 | t0004 | g0018 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02738 | hp1 | a0002 | c0003 | t0003 | g0198 | SAS | PJL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02738 | hp2 | a0003 | c0004 | t0001 | g0141 | SAS | PJL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02818 | hp1 | a0004 | c0017 | t0004 | g0011 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02886 | hp1 | a0001 | c0007 | t0010 | g0165 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0215 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02895 | hp1 | a0004 | c0005 | t0004 | g0020 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0217 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02896 | hp1 | a0005 | c0006 | t0007 | g0026 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02896 | hp2 | a0001 | c0007 | t0010 | g0164 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02897 | hp1 | a0004 | c0005 | t0004 | g0014 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02897 | hp2 | a0001 | c0007 | t0010 | g0163 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02922 | hp1 | a0007 | c0012 | t0011 | g0022 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02922 | hp2 | a0004 | c0005 | t0004 | g0016 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02965 | hp1 | a0005 | c0006 | t0016 | g0299 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0157 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02976 | hp1 | a0005 | c0006 | t0007 | g0227 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0034 | SAS | PJL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03017 | hp2 | a0003 | c0004 | t0026 | g0301 | SAS | PJL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03041 | hp1 | a0004 | c0005 | t0004 | g0009 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0149 | AFR | MSL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03098 | hp2 | a0015 | c0024 | t0022 | g0146 | AFR | MSL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03139 | hp2 | a0004 | c0005 | t0025 | g0012 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0173 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03195 | hp2 | a0007 | c0012 | t0011 | g0023 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03209 | hp2 | a0004 | c0005 | t0004 | g0015 | AFR | MSL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03225 | hp2 | a0005 | c0006 | t0007 | g0221 | AFR | MSL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03239 | hp1 | a0002 | c0003 | t0002 | g0203 | SAS | PJL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03239 | hp2 | a0003 | c0004 | t0021 | g0303 | SAS | PJL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0147 | AFR | MSL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03486 | hp2 | a0004 | c0005 | t0004 | g0021 | AFR | MSL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03516 | hp1 | a0008 | c0011 | t0011 | g0024 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0152 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03540 | hp1 | a0013 | c0018 | t0001 | g0049 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03540 | hp2 | a0005 | c0006 | t0007 | g0226 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0148 | AFR | MSL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03579 | hp2 | a0004 | c0005 | t0004 | g0008 | AFR | MSL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03704 | hp1 | a0002 | c0003 | t0003 | g0283 | SAS | PJL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0032 | SAS | PJL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03710 | hp1 | a0001 | c0001 | t0009 | g0036 | SAS | PJL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03710 | hp2 | a0003 | c0004 | t0001 | g0302 | SAS | PJL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0033 | SAS | BEB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | BEB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | STU | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG04115 | hp2 | a0001 | c0001 | t0013 | g0100 | SAS | STU | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | STU | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG04228 | hp2 | a0001 | c0001 | t0013 | g0125 | SAS | STU | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0150 | AFR | YRI | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0251 | EAS | CHB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18747 | hp1 | a0003 | c0004 | t0001 | g0115 | EAS | CHB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18747 | hp2 | a0001 | c0015 | t0029 | g0258 | EAS | CHB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18940 | hp1 | a0002 | c0003 | t0003 | g0196 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18942 | hp2 | a0003 | c0004 | t0001 | g0108 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18943 | hp1 | a0002 | c0003 | t0008 | g0179 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18944 | hp1 | a0002 | c0003 | t0005 | g0278 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18944 | hp2 | a0003 | c0025 | t0001 | g0143 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18946 | hp2 | a0002 | c0003 | t0003 | g0170 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18948 | hp1 | a0003 | c0004 | t0001 | g0128 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18948 | hp2 | a0002 | c0003 | t0003 | g0183 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18949 | hp1 | a0003 | c0004 | t0001 | g0127 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0235 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18950 | hp1 | a0002 | c0003 | t0008 | g0197 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18950 | hp2 | a0006 | c0008 | t0003 | g0084 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18951 | hp1 | a0010 | c0009 | t0002 | g0169 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18951 | hp2 | a0002 | c0003 | t0003 | g0206 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18954 | hp1 | a0002 | c0003 | t0003 | g0181 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18956 | hp2 | a0006 | c0008 | t0003 | g0189 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18957 | hp2 | a0002 | c0003 | t0003 | g0167 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18961 | hp1 | a0001 | c0001 | t0009 | g0039 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0297 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18963 | hp1 | a0003 | c0004 | t0001 | g0269 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18968 | hp1 | a0002 | c0003 | t0008 | g0241 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0293 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18970 | hp1 | a0009 | c0010 | t0002 | g0292 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18970 | hp2 | a0003 | c0004 | t0001 | g0114 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18971 | hp2 | a0006 | c0008 | t0018 | g0190 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18972 | hp1 | a0002 | c0003 | t0008 | g0175 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18972 | hp2 | a0003 | c0004 | t0001 | g0130 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0288 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18977 | hp1 | a0003 | c0004 | t0001 | g0271 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18977 | hp2 | a0002 | c0003 | t0005 | g0180 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18978 | hp1 | a0002 | c0003 | t0003 | g0282 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18981 | hp1 | a0006 | c0008 | t0003 | g0194 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0253 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18982 | hp2 | a0003 | c0004 | t0001 | g0089 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18985 | hp1 | a0002 | c0003 | t0005 | g0201 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18985 | hp2 | a0001 | c0001 | t0009 | g0038 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0284 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0245 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18991 | hp2 | a0002 | c0003 | t0003 | g0281 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18992 | hp1 | a0003 | c0004 | t0001 | g0122 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18992 | hp2 | a0010 | c0009 | t0002 | g0205 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18994 | hp1 | a0001 | c0001 | t0009 | g0037 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0254 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18999 | hp1 | a0002 | c0003 | t0003 | g0193 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0259 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19001 | hp2 | a0002 | c0003 | t0002 | g0204 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19003 | hp1 | a0003 | c0004 | t0001 | g0107 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19004 | hp1 | a0003 | c0004 | t0001 | g0270 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0289 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19009 | hp2 | a0002 | c0003 | t0003 | g0276 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19010 | hp1 | a0003 | c0004 | t0001 | g0094 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0294 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19012 | hp2 | a0002 | c0003 | t0005 | g0187 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19030 | hp1 | a0016 | c0013 | t0001 | g0062 | AFR | LWK | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19030 | hp2 | a0001 | c0001 | t0020 | g0142 | AFR | LWK | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | LWK | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0213 | AFR | LWK | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19057 | hp2 | a0003 | c0004 | t0017 | g0121 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19060 | hp1 | a0002 | c0003 | t0003 | g0182 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19063 | hp2 | a0002 | c0003 | t0005 | g0199 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19064 | hp1 | a0001 | c0020 | t0001 | g0117 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19064 | hp2 | a0006 | c0008 | t0003 | g0191 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19066 | hp2 | a0009 | c0010 | t0002 | g0291 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19067 | hp2 | a0002 | c0003 | t0005 | g0188 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19068 | hp1 | a0002 | c0003 | t0005 | g0178 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19070 | hp1 | a0001 | c0001 | t0014 | g0070 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19070 | hp2 | a0002 | c0003 | t0008 | g0174 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19076 | hp1 | a0011 | c0019 | t0001 | g0088 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19076 | hp2 | a0002 | c0003 | t0002 | g0208 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19079 | hp2 | a0002 | c0003 | t0003 | g0195 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19080 | hp1 | a0002 | c0003 | t0002 | g0207 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19083 | hp1 | a0002 | c0003 | t0008 | g0277 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19084 | hp2 | a0001 | c0001 | t0009 | g0040 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19087 | hp1 | a0001 | c0022 | t0009 | g0035 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19088 | hp1 | a0003 | c0004 | t0001 | g0105 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19088 | hp2 | a0002 | c0003 | t0003 | g0192 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19090 | hp2 | a0002 | c0003 | t0005 | g0184 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0285 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0151 | AFR | YRI | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | YRI | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA20129 | hp1 | a0001 | c0007 | t0010 | g0161 | AFR | ASW | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA20129 | hp2 | a0002 | c0003 | t0003 | g0168 | AFR | ASW | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02109 | hp1 | a0004 | c0005 | t0004 | g0010 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02109 | hp2 | a0001 | c0007 | t0010 | g0162 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02559 | hp1 | a0014 | c0023 | t0001 | g0087 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG02559 | hp2 | a0001 | c0007 | t0012 | g0219 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03471 | hp1 | a0004 | c0005 | t0004 | g0017 | AFR | MSL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG06807 | hp1 | a0005 | c0006 | t0007 | g0230 | AFR | USA | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0113 | AFR | USA | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0210 | AFR | USA | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| NA20300 | hp2 | a0001 | c0001 | t0028 | g0092 | AFR | USA | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0112 | REF | REF | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| homoSapiens_grch38 | hp1 | a0001 | c0007 | t0001 | g0247 | REF | REF | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:65992840
|
T | C | 1 | a0016 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.122T>C | p.Ile41Thr | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/26 | 411/8544 | 122/4239 | 41/1412 | chr5 | 65992840 | ||
| chr5:66025483
|
C | T | 1 | a0003 | 31 | HG00099.hp1 HG00621.hp2 HG00642.hp1 others(28): Show |
missense_variant | MODERATE | c.821C>T | p.Ser274Leu | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 11/26 | 1110/8544 | 821/4239 | 274/1412 | chr5 | 66025483 | ||
| chr5:66025496
|
A | G | 1 | a0015 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.834A>G | p.Ile278Met | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 11/26 | 1123/8544 | 834/4239 | 278/1412 | chr5 | 66025496 | ||
| chr5:66025867
|
C | G | 1 | a0014 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.910C>G | p.Leu304Val | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 12/26 | 1199/8544 | 910/4239 | 304/1412 | chr5 | 66025867 | ||
| chr5:66025922
|
C | T | 2 | a0007a0008 | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
missense_variant | MODERATE | c.965C>T | p.Thr322Ile | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 12/26 | 1254/8544 | 965/4239 | 322/1412 | chr5 | 66025922 | ||
| chr5:66048704
|
T | C | 1 | a0013 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.1826T>C | p.Met609Thr | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/26 | 2115/8544 | 1826/4239 | 609/1412 | chr5 | 66048704 | ||
| chr5:66050951
|
T | C | 1 | a0015 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.2072T>C | p.Ile691Thr | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/26 | 2361/8544 | 2072/4239 | 691/1412 | chr5 | 66050951 | ||
| chr5:66053554
|
A | G | 1 | a0004 | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
missense_variant | MODERATE | c.2236A>G | p.Lys746Glu | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 2525/8544 | 2236/4239 | 746/1412 | chr5 | 66053554 | ||
| chr5:66054059
|
A | G | 1 | a0012 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.2741A>G | p.Lys914Arg | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3030/8544 | 2741/4239 | 914/1412 | chr5 | 66054059 | ||
| chr5:66054287
|
C | G | 1 | a0007 | 2 | HG02922.hp1 HG03195.hp2 |
missense_variant | MODERATE | c.2969C>G | p.Thr990Ser | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3258/8544 | 2969/4239 | 990/1412 | chr5 | 66054287 | ||
| chr5:66054515
|
T | C | 1 | a0010 | 2 | NA18951.hp1 NA18992.hp2 |
missense_variant | MODERATE | c.3197T>C | p.Ile1066Thr | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3486/8544 | 3197/4239 | 1066/1412 | chr5 | 66054515 | ||
| chr5:66054578
|
A | G | 1 | a0006 | 5 | NA18950.hp2 NA18956.hp2 NA18971.hp2 others(2): Show |
missense_variant | MODERATE | c.3260A>G | p.Asn1087Ser | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3549/8544 | 3260/4239 | 1087/1412 | chr5 | 66054578 | ||
| chr5:66054584
|
G | T | 1 | a0005 | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
missense_variant | MODERATE | c.3266G>T | p.Gly1089Val | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3555/8544 | 3266/4239 | 1089/1412 | chr5 | 66054584 | ||
| chr5:66054613
|
A | G | 1 | a0009 | 2 | NA18970.hp1 NA19066.hp2 |
missense_variant | MODERATE | c.3295A>G | p.Ile1099Val | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3584/8544 | 3295/4239 | 1099/1412 | chr5 | 66054613 | ||
| chr5:66054653
|
C | T | 3 | a0002a0006a0010 | 53 | HG00280.hp2 HG00408.hp2 HG01081.hp1 others(50): Show |
missense_variant | MODERATE | c.3335C>T | p.Ser1112Leu | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3624/8544 | 3335/4239 | 1112/1412 | chr5 | 66054653 | ||
| chr5:66054707
|
G | T | 1 | a0011 | 1 | NA19076.hp1 | missense_variant | MODERATE | c.3389G>T | p.Arg1130Leu | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3678/8544 | 3389/4239 | 1130/1412 | chr5 | 66054707 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:66021353
|
C | T | 11 | a0001c0001a0001c0020a0001c0021others(8): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
synonymous_variant | LOW | c.565C>T | p.Leu189Leu | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/26 | 854/8544 | 565/4239 | 189/1412 | chr5 | 66021353 | ||
| chr5:66025484
|
G | A | 1 | a0004c0014 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.822G>A | p.Ser274Ser | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 11/26 | 1111/8544 | 822/4239 | 274/1412 | chr5 | 66025484 | ||
| chr5:66046418
|
C | T | 1 | a0001c0022 | 1 | NA19087.hp1 | synonymous_variant | LOW | c.1668C>T | p.Asn556Asn | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/26 | 1957/8544 | 1668/4239 | 556/1412 | chr5 | 66046418 | ||
| chr5:66054036
|
T | C | 1 | a0003c0025 | 1 | NA18944.hp2 | synonymous_variant | LOW | c.2718T>C | p.Asp906Asp | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3007/8544 | 2718/4239 | 906/1412 | chr5 | 66054036 | ||
| chr5:66054051
|
C | T | 1 | a0001c0021 | 1 | HG01981.hp2 | synonymous_variant | LOW | c.2733C>T | p.Val911Val | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3022/8544 | 2733/4239 | 911/1412 | chr5 | 66054051 | ||
| chr5:66054174
|
C | T | 1 | a0004c0017 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.2856C>T | p.Pro952Pro | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3145/8544 | 2856/4239 | 952/1412 | chr5 | 66054174 | ||
| chr5:66054345
|
C | T | 1 | a0001c0020 | 1 | NA19064.hp1 | synonymous_variant | LOW | c.3027C>T | p.Leu1009Leu | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3316/8544 | 3027/4239 | 1009/1412 | chr5 | 66054345 | ||
| chr5:66054546
|
A | G | 6 | a0001c0002a0001c0015a0002c0003others(3): Show | 109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
synonymous_variant | LOW | c.3228A>G | p.Arg1076Arg | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3517/8544 | 3228/4239 | 1076/1412 | chr5 | 66054546 | ||
| chr5:66054631
|
T | C | 2 | a0007c0012a0008c0011 | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
synonymous_variant | LOW | c.3313T>C | p.Leu1105Leu | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3602/8544 | 3313/4239 | 1105/1412 | chr5 | 66054631 | ||
| chr5:66076920
|
T | C | 1 | a0001c0015 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.4102T>C | p.Leu1368Leu | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/26 | 4391/8544 | 4102/4239 | 1368/1412 | chr5 | 66076920 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:65926656
|
G | C | 1 | a0002c0003t0005 | 13 | HG01081.hp1 HG01257.hp1 HG01934.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-208G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/26 | 66063 | chr5 | 65926656 | |||||
| chr5:65926682
|
C | T | 1 | a0001c0015t0029 | 1 | NA18747.hp2 | 5_prime_UTR_variant | MODIFIER | c.-182C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/26 | 66037 | chr5 | 65926682 | |||||
| chr5:65926689
|
A | C | 1 | a0001c0001t0028 | 1 | NA20300.hp2 | 5_prime_UTR_variant | MODIFIER | c.-175A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/26 | 66030 | chr5 | 65926689 | |||||
| chr5:65926713
|
T | G | 4 | a0005c0006t0007a0005c0006t0015a0005c0006t0016others(1): Show | 11 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-151T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/26 | 66006 | chr5 | 65926713 | |||||
| chr5:65926728
|
A | C | 1 | a0005c0006t0016 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-136A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/26 | 65991 | chr5 | 65926728 | |||||
| chr5:65926791
|
G | GAAAAA | 2 | a0001c0001t0009a0001c0022t0009 | 6 | HG03710.hp1 NA18961.hp1 NA18985.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-73_-72insAAAAA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/26 | 65927 | chr5 | 65926791 | |||||
| chr5:65926792
|
G | A | 1 | a0003c0004t0017 | 1 | NA19057.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-72G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/26 | chr5 | 65926792 | ||||||
| chr5:65926793
|
T | C | 2 | a0001c0001t0009a0001c0022t0009 | 6 | HG03710.hp1 NA18961.hp1 NA18985.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-71T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/26 | 65926 | chr5 | 65926793 | |||||
| chr5:65926794
|
G | T | 2 | a0001c0001t0009a0001c0022t0009 | 6 | HG03710.hp1 NA18961.hp1 NA18985.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-70G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/26 | 65925 | chr5 | 65926794 | |||||
| chr5:65926795
|
T | G | 2 | a0001c0001t0009a0001c0022t0009 | 6 | HG03710.hp1 NA18961.hp1 NA18985.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-69T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/26 | 65924 | chr5 | 65926795 | |||||
| chr5:65926798
|
C | G | 1 | a0003c0004t0027 | 1 | HG01943.hp2 | 5_prime_UTR_variant | MODIFIER | c.-66C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/26 | 65921 | chr5 | 65926798 | |||||
| chr5:65926801
|
C | T | 1 | a0003c0004t0026 | 1 | HG03017.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-63C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/26 | chr5 | 65926801 | ||||||
| chr5:66078665
|
A | G | 5 | a0001c0007t0010a0004c0005t0004a0004c0005t0025others(2): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*135A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 135 | chr5 | 66078665 | |||||
| chr5:66078691
|
A | G | 2 | a0001c0001t0006a0001c0001t0024 | 12 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*161A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 161 | chr5 | 66078691 | |||||
| chr5:66078808
|
T | C | 1 | a0006c0008t0018 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*278T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 278 | chr5 | 66078808 | |||||
| chr5:66078969
|
C | A | 1 | a0001c0002t0019 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*439C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 439 | chr5 | 66078969 | |||||
| chr5:66079213
|
A | G | 1 | a0001c0007t0010 | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*683A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 683 | chr5 | 66079213 | |||||
| chr5:66079540
|
CT | C | 5 | a0001c0007t0010a0004c0005t0004a0004c0005t0025others(2): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1013delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 1013 | INFO_REALIGN_3_PRIME | chr5 | 66079540 | ||||
| chr5:66079585
|
A | C | 1 | a0004c0005t0025 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1055A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 1055 | chr5 | 66079585 | |||||
| chr5:66080359
|
T | C | 1 | a0001c0007t0012 | 3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1829T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 1829 | chr5 | 66080359 | |||||
| chr5:66080478
|
T | TA | 6 | a0001c0007t0010a0001c0007t0012a0004c0005t0004others(3): Show | 25 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1959dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 1960 | INFO_REALIGN_3_PRIME | chr5 | 66080478 | ||||
| chr5:66080647
|
T | C | 1 | a0001c0001t0020 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2117T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 2117 | chr5 | 66080647 | |||||
| chr5:66080779
|
T | C | 1 | a0003c0004t0021 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2249T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 2249 | chr5 | 66080779 | |||||
| chr5:66080813
|
A | G | 1 | a0003c0004t0023 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2283A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 2283 | chr5 | 66080813 | |||||
| chr5:66080818
|
C | T | 5 | a0001c0007t0010a0004c0005t0004a0004c0005t0025others(2): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2288C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 2288 | chr5 | 66080818 | |||||
| chr5:66080878
|
G | A | 1 | a0001c0007t0010 | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2348G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 2348 | chr5 | 66080878 | |||||
| chr5:66080927
|
T | C | 1 | a0001c0007t0010 | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2397T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 2397 | chr5 | 66080927 | |||||
| chr5:66081024
|
A | C | 1 | a0001c0007t0010 | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2494A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 2494 | chr5 | 66081024 | |||||
| chr5:66081213
|
C | T | 1 | a0001c0007t0010 | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2683C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 2683 | chr5 | 66081213 | |||||
| chr5:66081364
|
A | G | 6 | a0001c0001t0003a0002c0003t0003a0002c0003t0005others(3): Show | 46 | HG00408.hp2 HG01081.hp1 HG01109.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2834A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 2834 | chr5 | 66081364 | |||||
| chr5:66081393
|
C | G | 1 | a0002c0003t0008 | 8 | HG00408.hp2 HG02071.hp1 NA18943.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2863C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 2863 | chr5 | 66081393 | |||||
| chr5:66081430
|
G | A | 6 | a0001c0001t0003a0002c0003t0003a0002c0003t0005others(3): Show | 46 | HG00408.hp2 HG01081.hp1 HG01109.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2900G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 2900 | chr5 | 66081430 | |||||
| chr5:66081500
|
G | T | 1 | a0001c0001t0014 | 2 | HG00621.hp1 NA19070.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2970G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 2970 | chr5 | 66081500 | |||||
| chr5:66081604
|
T | C | 2 | a0001c0001t0006a0001c0001t0024 | 12 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3074T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 3074 | chr5 | 66081604 | |||||
| chr5:66081636
|
ATATC | A | 2 | a0007c0012t0011a0008c0011t0011 | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3109_*3112delTCTA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 3109 | INFO_REALIGN_3_PRIME | chr5 | 66081636 | ||||
| chr5:66081698
|
G | C | 28 | a0001c0001t0003a0001c0001t0006a0001c0001t0024others(25): Show | 165 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*3168G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 3168 | chr5 | 66081698 | |||||
| chr5:66081713
|
A | T | 1 | a0001c0001t0024 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3183A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 3183 | chr5 | 66081713 | |||||
| chr5:66081843
|
A | G | 2 | a0007c0012t0011a0008c0011t0011 | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3313A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 3313 | chr5 | 66081843 | |||||
| chr5:66082042
|
G | A | 1 | a0001c0001t0013 | 3 | HG01261.hp2 HG04115.hp2 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3512G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 3512 | chr5 | 66082042 | |||||
| chr5:66082111
|
G | A | 4 | a0004c0005t0004a0004c0005t0025a0004c0014t0004others(1): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3581G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 3581 | chr5 | 66082111 | |||||
| chr5:66082148
|
C | T | 5 | a0001c0007t0010a0004c0005t0004a0004c0005t0025others(2): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3618C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 3618 | chr5 | 66082148 | |||||
| chr5:66082394
|
C | T | 1 | a0005c0006t0015 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3864C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 3864 | chr5 | 66082394 | |||||
| chr5:66082425
|
C | T | 1 | a0015c0024t0022 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3895C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 3895 | chr5 | 66082425 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:65926870
|
G | T | 6 | a0003c0004t0001g0302a0003c0004t0001g0305a0003c0004t0001g0306others(3): Show | 6 | HG01167.hp1 HG01952.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+64G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65926870 | ||||||
| chr5:65926876
|
T | A | 1 | a0003c0004t0001g0001 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-58+70T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65926876 | ||||||
| chr5:65926880
|
T | C | 2 | a0001c0002t0002g0002a0001c0002t0002g0003 | 2 | NA19057.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-58+74T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65926880 | ||||||
| chr5:65926897
|
C | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006 | 3 | HG02280.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-58+91C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65926897 | ||||||
| chr5:65926902
|
A | T | 1 | a0002c0003t0003g0300 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-58+96A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65926902 | ||||||
| chr5:65926917
|
T | C | 21 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(18): Show | 21 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-58+111T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65926917 | ||||||
| chr5:65926990
|
C | G | 1 | a0005c0006t0016g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-58+184C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65926990 | ||||||
| chr5:65926997
|
G | GC | 27 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(24): Show | 27 | HG00408.hp2 HG00438.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.-58+199dupC | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65926997 | |||||
| chr5:65927005
|
C | G | 10 | a0001c0002t0002g0289a0001c0002t0002g0290a0001c0002t0002g0293others(7): Show | 10 | HG00408.hp1 HG00438.hp2 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.-58+199C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927005 | ||||||
| chr5:65927070
|
T | C | 180 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.-58+264T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927070 | ||||||
| chr5:65927104
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-58+298G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927104 | ||||||
| chr5:65927201
|
A | C | 1 | a0005c0006t0002g0263 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-58+395A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927201 | ||||||
| chr5:65927227
|
G | A | 1 | a0003c0004t0026g0301 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-58+421G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927227 | ||||||
| chr5:65927275
|
T | C | 257 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(254): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.-58+469T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927275 | ||||||
| chr5:65927288
|
A | T | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+482A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927288 | ||||||
| chr5:65927359
|
G | C | 6 | a0002c0003t0003g0166a0002c0003t0003g0167a0002c0003t0003g0168others(3): Show | 6 | HG01433.hp1 NA18946.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+553G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927359 | ||||||
| chr5:65927392
|
T | C | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+586T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927392 | ||||||
| chr5:65927429
|
G | T | 1 | a0005c0006t0007g0230 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-58+623G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927429 | ||||||
| chr5:65927646
|
A | G | 2 | a0005c0006t0002g0229a0005c0006t0002g0263 | 2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-58+840A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927646 | ||||||
| chr5:65927679
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-58+873T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927679 | ||||||
| chr5:65927693
|
C | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+887C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927693 | ||||||
| chr5:65927725
|
G | T | 2 | a0005c0006t0002g0229a0005c0006t0002g0263 | 2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-58+919G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927725 | ||||||
| chr5:65927873
|
T | C | 6 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0231others(3): Show | 6 | NA18954.hp2 NA18999.hp2 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58+1067T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927873 | ||||||
| chr5:65927902
|
C | G | 188 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.-58+1096C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927902 | ||||||
| chr5:65928010
|
T | C | 6 | a0001c0001t0009g0036a0001c0001t0009g0037a0001c0001t0009g0038others(3): Show | 6 | HG03710.hp1 NA18961.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58+1204T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65928010 | ||||||
| chr5:65928067
|
A | T | 1 | a0001c0001t0001g0160 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-58+1261A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65928067 | ||||||
| chr5:65928068
|
G | T | 1 | a0001c0001t0001g0160 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-58+1262G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65928068 | ||||||
| chr5:65928170
|
C | G | 17 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(14): Show | 17 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-58+1364C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65928170 | ||||||
| chr5:65928246
|
C | CT | 7 | a0001c0001t0001g0159a0003c0004t0001g0302a0003c0004t0001g0305others(4): Show | 7 | HG01167.hp1 HG01952.hp2 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.-58+1451dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65928246 | |||||
| chr5:65928311
|
C | G | 1 | a0001c0001t0001g0234 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-58+1505C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65928311 | ||||||
| chr5:65928384
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-58+1578G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65928384 | ||||||
| chr5:65928428
|
T | C | 1 | a0001c0002t0002g0171 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-58+1622T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65928428 | ||||||
| chr5:65928648
|
G | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG02572.hp2 HG02717.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+1842G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65928648 | ||||||
| chr5:65928678
|
T | C | 1 | a0001c0002t0002g0235 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-58+1872T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65928678 | ||||||
| chr5:65929478
|
C | T | 2 | a0005c0006t0002g0229a0005c0006t0002g0263 | 2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-58+2672C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65929478 | ||||||
| chr5:65929490
|
C | A | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+2684C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65929490 | ||||||
| chr5:65929557
|
T | G | 1 | a0001c0001t0001g0047 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-58+2751T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65929557 | ||||||
| chr5:65929608
|
A | C | 12 | a0001c0001t0006g0147a0001c0001t0006g0148a0001c0001t0006g0149others(9): Show | 12 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+2802A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65929608 | ||||||
| chr5:65929610
|
C | T | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-58+2804C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65929610 | ||||||
| chr5:65929637
|
C | CT | 12 | a0001c0001t0001g0145a0001c0002t0002g0261a0001c0002t0002g0262others(9): Show | 12 | HG01981.hp1 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+2851dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65929637 | |||||
| chr5:65929637
|
CT | C | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG01256.hp1 HG01515.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.-58+2851delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65929637 | |||||
| chr5:65929639
|
T | TG | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+2833_-58+2834i others(3): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65929639 | ||||||
| chr5:65929657
|
T | C | 105 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(102): Show | 105 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.-58+2851T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65929657 | ||||||
| chr5:65929657
|
T | TC | 3 | a0001c0001t0001g0031a0001c0001t0001g0126a0003c0004t0001g0127 | 3 | NA18949.hp1 NA18954.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-58+2852dupC | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65929657 | |||||
| chr5:65929741
|
A | T | 3 | a0001c0001t0001g0272a0001c0001t0013g0124a0001c0001t0013g0125 | 3 | HG01261.hp2 HG04115.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-58+2935A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65929741 | ||||||
| chr5:65930035
|
C | T | 3 | a0001c0007t0012g0218a0001c0007t0012g0219a0001c0007t0012g0220 | 3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-58+3229C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930035 | ||||||
| chr5:65930045
|
C | T | 1 | a0002c0003t0003g0283 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-58+3239C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930045 | ||||||
| chr5:65930171
|
C | G | 1 | a0005c0006t0007g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-58+3365C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930171 | ||||||
| chr5:65930213
|
G | T | 1 | a0001c0001t0001g0234 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-58+3407G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930213 | ||||||
| chr5:65930227
|
A | G | 2 | a0001c0007t0012g0218a0001c0007t0012g0220 | 2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-58+3421A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930227 | ||||||
| chr5:65930460
|
A | G | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+3654A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930460 | ||||||
| chr5:65930470
|
G | A | 6 | a0005c0006t0007g0223a0005c0006t0007g0224a0005c0006t0007g0226others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+3664G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930470 | ||||||
| chr5:65930485
|
T | G | 1 | a0002c0003t0003g0166 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-58+3679T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930485 | ||||||
| chr5:65930621
|
T | C | 1 | a0001c0002t0002g0237 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-58+3815T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930621 | ||||||
| chr5:65930689
|
G | A | 1 | a0013c0018t0001g0049 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-58+3883G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930689 | ||||||
| chr5:65930705
|
A | G | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-58+3899A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930705 | ||||||
| chr5:65930823
|
C | T | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+4017C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930823 | ||||||
| chr5:65930849
|
A | C | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | NA18999.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.-58+4043A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930849 | ||||||
| chr5:65930937
|
A | C | 1 | a0003c0004t0001g0306 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-58+4131A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930937 | ||||||
| chr5:65930989
|
GTGTGGAA others(35): Show |
G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+4226_-58+4267d others(44): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65930989 | |||||
| chr5:65931275
|
C | G | 10 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(7): Show | 10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-58+4469C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65931275 | ||||||
| chr5:65931640
|
A | G | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-58+4834A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65931640 | ||||||
| chr5:65931692
|
G | A | 1 | a0001c0022t0009g0035 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-58+4886G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65931692 | ||||||
| chr5:65931698
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-58+4892C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65931698 | ||||||
| chr5:65931819
|
C | CT | 43 | a0001c0001t0001g0028a0001c0001t0001g0041a0001c0001t0001g0048others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.-58+5030dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65931819 | |||||
| chr5:65931819
|
CT | C | 14 | a0001c0001t0001g0129a0001c0001t0001g0144a0001c0001t0001g0159others(11): Show | 14 | HG01256.hp1 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-58+5030delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65931819 | |||||
| chr5:65931823
|
T | C | 43 | a0001c0002t0002g0171a0001c0002t0002g0279a0002c0003t0003g0166others(40): Show | 43 | HG00408.hp2 HG01081.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.-58+5017T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65931823 | ||||||
| chr5:65931895
|
C | A | 1 | a0001c0001t0001g0272 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-58+5089C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65931895 | ||||||
| chr5:65931922
|
G | A | 1 | a0001c0001t0006g0152 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-58+5116G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65931922 | ||||||
| chr5:65932020
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-58+5214G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65932020 | ||||||
| chr5:65932033
|
G | A | 1 | a0002c0003t0002g0202 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-58+5227G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65932033 | ||||||
| chr5:65932055
|
T | C | 1 | a0001c0001t0006g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-58+5249T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65932055 | ||||||
| chr5:65932108
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+5302G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65932108 | ||||||
| chr5:65932157
|
A | G | 6 | a0001c0001t0001g0123a0003c0004t0001g0089a0003c0004t0001g0122others(3): Show | 6 | NA18955.hp2 NA18977.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58+5351A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65932157 | ||||||
| chr5:65932337
|
C | CA | 7 | a0001c0001t0009g0036a0003c0004t0001g0130a0003c0004t0001g0302others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-58+5550dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65932337 | |||||
| chr5:65932337
|
CA | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0119others(17): Show | 20 | HG00438.hp1 HG01069.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.-58+5550delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65932337 | |||||
| chr5:65932423
|
G | C | 138 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-58+5617G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65932423 | ||||||
| chr5:65932585
|
A | G | 1 | a0001c0001t0020g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-58+5779A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65932585 | ||||||
| chr5:65932639
|
A | G | 2 | a0001c0002t0002g0296a0001c0002t0002g0297 | 2 | HG00438.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.-58+5833A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65932639 | ||||||
| chr5:65932712
|
A | G | 2 | a0004c0005t0004g0019a0004c0014t0004g0018 | 2 | HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-58+5906A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65932712 | ||||||
| chr5:65932866
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | NA18962.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.-58+6060G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65932866 | ||||||
| chr5:65932963
|
T | A | 1 | a0001c0001t0001g0144 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-58+6157T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65932963 | ||||||
| chr5:65933067
|
A | G | 1 | a0014c0023t0001g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-58+6261A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65933067 | ||||||
| chr5:65933072
|
A | G | 1 | a0013c0018t0001g0049 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-58+6266A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65933072 | ||||||
| chr5:65933491
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-58+6685A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65933491 | ||||||
| chr5:65933575
|
C | T | 1 | a0002c0003t0002g0216 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-58+6769C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65933575 | ||||||
| chr5:65933616
|
C | T | 1 | a0001c0001t0001g0031 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-58+6810C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65933616 | ||||||
| chr5:65933618
|
C | T | 2 | a0005c0006t0002g0229a0005c0006t0002g0263 | 2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-58+6812C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65933618 | ||||||
| chr5:65933707
|
A | T | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 4 | HG02572.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+6901A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65933707 | ||||||
| chr5:65933911
|
T | A | 19 | a0001c0001t0001g0232a0003c0004t0001g0131a0005c0006t0002g0229others(16): Show | 19 | HG00099.hp1 HG01109.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.-58+7105T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65933911 | ||||||
| chr5:65934042
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | NA18991.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-58+7236G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65934042 | ||||||
| chr5:65934175
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+7369C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65934175 | ||||||
| chr5:65934176
|
G | A | 1 | a0001c0001t0028g0092 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-58+7370G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65934176 | ||||||
| chr5:65934253
|
A | T | 1 | a0001c0001t0001g0118 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-58+7447A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65934253 | ||||||
| chr5:65934421
|
T | TTCTCTTT others(195): Show |
1 | a0001c0001t0001g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-58+7616_-58+7817d others(204): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65934421 | |||||
| chr5:65934425
|
CT | C | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+7627delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65934425 | |||||
| chr5:65935028
|
C | A | 44 | a0001c0002t0002g0171a0001c0002t0002g0279a0002c0003t0003g0166others(41): Show | 44 | HG00408.hp2 HG01081.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.-58+8222C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935028 | ||||||
| chr5:65935140
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-58+8334T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935140 | ||||||
| chr5:65935230
|
C | T | 138 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-58+8424C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935230 | ||||||
| chr5:65935233
|
G | A | 193 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.-58+8427G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935233 | ||||||
| chr5:65935252
|
T | G | 1 | a0003c0004t0001g0132 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-58+8446T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935252 | ||||||
| chr5:65935336
|
A | G | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-58+8530A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935336 | ||||||
| chr5:65935376
|
G | GT | 17 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(14): Show | 17 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-58+8571dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65935376 | |||||
| chr5:65935399
|
A | G | 6 | a0001c0002t0002g0173a0001c0002t0002g0212a0001c0002t0002g0213others(3): Show | 6 | HG02280.hp2 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58+8593A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935399 | ||||||
| chr5:65935436
|
T | A | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+8630T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935436 | ||||||
| chr5:65935552
|
C | T | 2 | a0001c0001t0001g0129a0001c0020t0001g0117 | 2 | HG01891.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-58+8746C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935552 | ||||||
| chr5:65935617
|
A | G | 17 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(14): Show | 17 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-58+8811A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935617 | ||||||
| chr5:65935816
|
A | G | 17 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(14): Show | 17 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-58+9010A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935816 | ||||||
| chr5:65935820
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-58+9014C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935820 | ||||||
| chr5:65935924
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0085 | 3 | NA18954.hp2 NA18955.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-58+9118C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935924 | ||||||
| chr5:65935985
|
C | G | 92 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0031others(89): Show | 92 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.-58+9179C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935985 | ||||||
| chr5:65936130
|
C | G | 2 | a0001c0001t0009g0039a0001c0001t0009g0040 | 2 | NA18961.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-58+9324C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65936130 | ||||||
| chr5:65936175
|
G | C | 1 | a0002c0003t0002g0203 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-58+9369G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65936175 | ||||||
| chr5:65936252
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+9446A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65936252 | ||||||
| chr5:65936672
|
G | A | 1 | a0003c0004t0001g0094 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-58+9866G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65936672 | ||||||
| chr5:65936724
|
T | A | 2 | a0001c0002t0002g0239a0001c0002t0002g0240 | 2 | HG02056.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.-58+9918T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65936724 | ||||||
| chr5:65936832
|
G | A | 5 | a0001c0001t0006g0147a0001c0001t0006g0148a0001c0001t0006g0149others(2): Show | 5 | HG03098.hp1 HG03486.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+10026G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65936832 | ||||||
| chr5:65937016
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-58+10210C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65937016 | ||||||
| chr5:65937055
|
G | A | 26 | a0001c0002t0002g0171a0001c0002t0002g0279a0002c0003t0003g0181others(23): Show | 26 | HG00408.hp2 HG01081.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.-58+10249G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65937055 | ||||||
| chr5:65937111
|
T | TA | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0011c0019t0001g0088 | 3 | NA18957.hp1 NA18990.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.-58+10306dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65937111 | |||||
| chr5:65937343
|
C | T | 21 | a0001c0001t0001g0135a0001c0001t0001g0138a0001c0001t0001g0274others(18): Show | 21 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.-58+10537C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65937343 | ||||||
| chr5:65937765
|
G | C | 184 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(181): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.-58+10959G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65937765 | ||||||
| chr5:65937863
|
C | T | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+11057C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65937863 | ||||||
| chr5:65937943
|
T | G | 6 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(3): Show | 6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+11137T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65937943 | ||||||
| chr5:65937983
|
C | T | 1 | a0002c0003t0003g0198 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-58+11177C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65937983 | ||||||
| chr5:65937986
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-58+11180T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65937986 | ||||||
| chr5:65938044
|
G | A | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0265 | 3 | NA18940.hp2 NA18978.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.-58+11238G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65938044 | ||||||
| chr5:65938294
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+11488G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65938294 | ||||||
| chr5:65938371
|
C | CT | 15 | a0001c0002t0002g0032a0001c0002t0002g0033a0001c0002t0002g0034others(12): Show | 15 | HG02055.hp2 HG02109.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-58+11583dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65938371 | |||||
| chr5:65938371
|
CT | C | 154 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-58+11583delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65938371 | |||||
| chr5:65938371
|
CTT | C | 7 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(4): Show | 7 | HG00735.hp1 HG01069.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.-58+11582_-58+1158 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65938371 | |||||
| chr5:65938529
|
C | T | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+11723C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65938529 | ||||||
| chr5:65938552
|
C | CTGTTT | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+11753_-58+1175 others(9): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65938552 | |||||
| chr5:65938585
|
C | T | 1 | a0015c0024t0022g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-58+11779C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65938585 | ||||||
| chr5:65938773
|
G | C | 1 | a0001c0001t0006g0154 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-58+11967G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65938773 | ||||||
| chr5:65938796
|
C | T | 5 | a0001c0002t0002g0289a0001c0002t0002g0293a0001c0002t0002g0294others(2): Show | 5 | HG02165.hp1 NA18969.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+11990C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65938796 | ||||||
| chr5:65938802
|
C | T | 2 | a0001c0002t0002g0259a0002c0003t0008g0257 | 2 | HG02071.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-58+11996C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65938802 | ||||||
| chr5:65939158
|
G | A | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-58+12352G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65939158 | ||||||
| chr5:65939383
|
G | A | 1 | a0001c0002t0002g0261 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-58+12577G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65939383 | ||||||
| chr5:65939394
|
G | A | 1 | a0004c0005t0004g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-58+12588G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65939394 | ||||||
| chr5:65939482
|
T | C | 197 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-58+12676T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65939482 | ||||||
| chr5:65939491
|
A | C | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+12685A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65939491 | ||||||
| chr5:65939507
|
TCCCTCTC others(20): Show |
T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+12717_-58+1274 others(31): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65939507 | |||||
| chr5:65939524
|
T | TTCCCTCT others(8): Show |
4 | a0001c0001t0001g0123a0001c0001t0001g0126a0001c0001t0001g0160others(1): Show | 4 | HG00609.hp1 NA18950.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+12730_-58+1274 others(19): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65939524 | |||||
| chr5:65939531
|
TC | T | 8 | a0001c0002t0002g0173a0001c0002t0002g0210a0001c0002t0002g0211others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-58+12731delC | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65939531 | |||||
| chr5:65939536
|
C | G | 1 | a0003c0004t0001g0132 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-58+12730C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65939536 | ||||||
| chr5:65939627
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-58+12821G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65939627 | ||||||
| chr5:65939664
|
AGCCTGCC others(4): Show |
A | 151 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.-58+12865_-58+1287 others(15): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65939664 | |||||
| chr5:65939706
|
C | T | 1 | a0004c0005t0004g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-58+12900C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65939706 | ||||||
| chr5:65939808
|
C | T | 3 | a0001c0001t0006g0152a0001c0001t0006g0153a0001c0001t0006g0157 | 3 | HG01891.hp1 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-58+13002C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65939808 | ||||||
| chr5:65939836
|
G | C | 3 | a0001c0001t0006g0152a0001c0001t0006g0153a0001c0001t0006g0157 | 3 | HG01891.hp1 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-58+13030G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65939836 | ||||||
| chr5:65939864
|
G | C | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-58+13058G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65939864 | ||||||
| chr5:65939926
|
G | T | 1 | a0001c0001t0001g0272 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-58+13120G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65939926 | ||||||
| chr5:65940020
|
G | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+13214G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940020 | ||||||
| chr5:65940056
|
A | G | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-58+13250A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940056 | ||||||
| chr5:65940080
|
G | A | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+13274G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940080 | ||||||
| chr5:65940156
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+13350G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940156 | ||||||
| chr5:65940199
|
G | A | 2 | a0005c0006t0007g0221a0005c0006t0007g0222 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-58+13393G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940199 | ||||||
| chr5:65940313
|
A | G | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-58+13507A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940313 | ||||||
| chr5:65940341
|
C | T | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-58+13535C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940341 | ||||||
| chr5:65940379
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+13573A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940379 | ||||||
| chr5:65940384
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+13578C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940384 | ||||||
| chr5:65940396
|
A | ACCCCATC others(39): Show |
11 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(8): Show | 11 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.-58+13592_-58+1359 others(50): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940396 | |||||
| chr5:65940399
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+13593T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940399 | ||||||
| chr5:65940399
|
TCGTCCGG others(42): Show |
T | 1 | a0001c0001t0001g0091 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-58+13621_-58+1366 others(53): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940399 | |||||
| chr5:65940401
|
G | A | 5 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(2): Show | 5 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+13595G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940401 | ||||||
| chr5:65940426
|
GC | G | 5 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(2): Show | 5 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+13626delC | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940426 | |||||
| chr5:65940427
|
C | A | 6 | a0002c0003t0003g0166a0002c0003t0003g0167a0002c0003t0003g0168others(3): Show | 6 | HG01433.hp1 NA18946.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+13621C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940427 | ||||||
| chr5:65940427
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-58+13621C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940427 | ||||||
| chr5:65940428
|
CCCCCGCC others(41): Show |
C | 1 | a0001c0001t0001g0090 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-58+13627_-58+1367 others(52): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940428 | |||||
| chr5:65940432
|
C | A | 11 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(8): Show | 11 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.-58+13626C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940432 | ||||||
| chr5:65940432
|
C | G | 1 | a0001c0001t0001g0083 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-58+13626C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940432 | ||||||
| chr5:65940433
|
G | A | 11 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(8): Show | 11 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.-58+13627G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940433 | ||||||
| chr5:65940436
|
C | A | 5 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(2): Show | 5 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+13630C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940436 | ||||||
| chr5:65940436
|
C | T | 2 | a0009c0010t0002g0291a0009c0010t0002g0292 | 2 | NA18970.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-58+13630C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940436 | ||||||
| chr5:65940444
|
T | C | 195 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.-58+13638T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940444 | ||||||
| chr5:65940447
|
C | A | 11 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(8): Show | 11 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.-58+13641C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940447 | ||||||
| chr5:65940449
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-58+13643C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940449 | ||||||
| chr5:65940450
|
G | A | 11 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(8): Show | 11 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.-58+13644G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940450 | ||||||
| chr5:65940464
|
T | TG | 17 | a0002c0003t0003g0198a0003c0004t0001g0134a0004c0005t0004g0013others(14): Show | 17 | HG00621.hp2 HG02258.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.-58+13665dupG | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940464 | |||||
| chr5:65940466
|
GGGGGGTC others(171): Show |
G | 1 | a0001c0001t0001g0083 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-58+13666_-58+1384 others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940466 | |||||
| chr5:65940475
|
G | GCCCCCAA others(49): Show |
3 | a0004c0005t0004g0009a0004c0005t0004g0010a0004c0005t0004g0027 | 3 | HG02109.hp1 HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-58+13669_-58+1367 others(60): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940475 | ||||||
| chr5:65940475
|
G | GCCCCCAA others(50): Show |
1 | a0004c0005t0004g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-58+13669_-58+1367 others(61): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940475 | ||||||
| chr5:65940475
|
G | GCCCCCAA others(51): Show |
1 | a0004c0005t0004g0007 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-58+13669_-58+1367 others(62): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940475 | ||||||
| chr5:65940476
|
T | C | 5 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(2): Show | 5 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+13670T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940476 | ||||||
| chr5:65940476
|
T | TC | 85 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0048others(82): Show | 85 | HG00609.hp1 HG00621.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.-58+13682dupC | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940476 | |||||
| chr5:65940476
|
T | TCC | 29 | a0001c0001t0001g0047a0001c0001t0001g0057a0001c0001t0001g0099others(26): Show | 29 | HG00099.hp2 HG00408.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-58+13681_-58+1368 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940476 | |||||
| chr5:65940476
|
T | TCCC | 19 | a0001c0001t0006g0147a0001c0001t0006g0148a0001c0001t0006g0149others(16): Show | 19 | HG00408.hp2 HG01109.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-58+13680_-58+1368 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940476 | |||||
| chr5:65940476
|
T | TCCCCCCC others(3): Show |
1 | a0001c0001t0006g0154 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-58+13673_-58+1368 others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940476 | |||||
| chr5:65940488
|
CG | C | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0133others(2): Show | 5 | HG01071.hp2 HG01934.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+13684delG | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940488 | |||||
| chr5:65940489
|
G | C | 14 | a0001c0001t0001g0004a0001c0001t0001g0144a0001c0007t0010g0275others(11): Show | 14 | HG02055.hp2 HG02258.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-58+13683G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940489 | ||||||
| chr5:65940516
|
T | TG | 26 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0272others(23): Show | 26 | HG00099.hp1 HG00738.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.-58+13718dupG | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940516 | |||||
| chr5:65940516
|
TG | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+13718delG | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940516 | |||||
| chr5:65940534
|
T | TGCCCGGC others(168): Show |
1 | a0001c0002t0002g0245 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-58+13811_-58+1398 others(179): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940534 | |||||
| chr5:65940558
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+13752G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940558 | ||||||
| chr5:65940568
|
GCGCCTCT others(12): Show |
G | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-58+13764_-58+1378 others(23): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940568 | |||||
| chr5:65940590
|
A | G | 141 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-58+13784A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940590 | ||||||
| chr5:65940605
|
G | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+13799G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940605 | ||||||
| chr5:65940606
|
C | A | 1 | a0001c0001t0001g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-58+13800C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940606 | ||||||
| chr5:65940617
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-58+13811G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940617 | ||||||
| chr5:65940617
|
GGCCA | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+13815_-58+1381 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940617 | |||||
| chr5:65940624
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+13818C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940624 | ||||||
| chr5:65940644
|
T | TG | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+13844dupG | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940644 | |||||
| chr5:65940644
|
T | TGGGGGGT others(43): Show |
1 | a0001c0001t0001g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-58+13853_-58+1385 others(54): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940644 | |||||
| chr5:65940644
|
T | TGGGGGGT others(43): Show |
145 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.-58+13853_-58+1385 others(54): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940644 | |||||
| chr5:65940644
|
T | TGGGGGGT others(43): Show |
3 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026 | 3 | HG02257.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-58+13853_-58+1385 others(54): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940644 | |||||
| chr5:65940644
|
T | TGGGGGGT others(43): Show |
4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+13853_-58+1385 others(54): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940644 | |||||
| chr5:65940645
|
G | GGGGGGTC others(43): Show |
1 | a0005c0006t0007g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-58+13853_-58+1385 others(54): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940645 | |||||
| chr5:65940655
|
C | CCCCCGGC others(43): Show |
4 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(1): Show | 4 | HG02970.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+13853_-58+1385 others(54): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940655 | |||||
| chr5:65940660
|
C | CGCCCGCC others(73): Show |
4 | a0004c0005t0004g0013a0004c0005t0004g0015a0004c0005t0004g0016others(1): Show | 4 | HG02258.hp1 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+13859_-58+1386 others(84): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940660 | |||||
| chr5:65940660
|
C | CGCCCGGC others(73): Show |
12 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(9): Show | 12 | HG01167.hp2 HG02109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+13869_-58+1387 others(84): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940660 | |||||
| chr5:65940660
|
C | G | 13 | a0001c0001t0006g0147a0001c0001t0006g0148a0001c0001t0006g0149others(10): Show | 13 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-58+13854C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940660 | ||||||
| chr5:65940676
|
C | G | 2 | a0001c0001t0006g0149a0001c0001t0006g0151 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-58+13870C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940676 | ||||||
| chr5:65940677
|
G | T | 1 | a0003c0004t0001g0141 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-58+13871G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940677 | ||||||
| chr5:65940726
|
C | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+13920C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940726 | ||||||
| chr5:65940726
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-58+13920C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940726 | ||||||
| chr5:65940730
|
C | G | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+13924C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940730 | ||||||
| chr5:65940830
|
T | C | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-58+14024T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940830 | ||||||
| chr5:65940876
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-58+14070G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940876 | ||||||
| chr5:65940906
|
T | C | 3 | a0001c0007t0012g0218a0001c0007t0012g0219a0001c0007t0012g0220 | 3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-58+14100T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940906 | ||||||
| chr5:65940992
|
T | G | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+14186T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940992 | ||||||
| chr5:65941257
|
A | G | 5 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(2): Show | 5 | HG01884.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+14451A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941257 | ||||||
| chr5:65941313
|
TA | T | 103 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0032others(100): Show | 103 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.-58+14526delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65941313 | |||||
| chr5:65941313
|
TAAA | T | 17 | a0001c0002t0002g0209a0004c0005t0004g0007a0004c0005t0004g0008others(14): Show | 17 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-58+14524_-58+1452 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65941313 | |||||
| chr5:65941314
|
A | T | 3 | a0001c0001t0001g0029a0001c0001t0001g0054a0001c0001t0001g0145 | 3 | HG02055.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-58+14508A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941314 | ||||||
| chr5:65941329
|
AAAAG | A | 13 | a0001c0015t0029g0258a0003c0004t0001g0137a0005c0006t0002g0229others(10): Show | 13 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-58+14526_-58+1452 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65941329 | |||||
| chr5:65941331
|
AAG | A | 126 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 126 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.-58+14527_-58+1452 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65941331 | |||||
| chr5:65941332
|
AG | A | 3 | a0001c0001t0001g0065a0001c0001t0001g0231a0001c0001t0001g0234 | 3 | NA19003.hp2 NA19066.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-58+14527delG | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941332 | ||||||
| chr5:65941333
|
GAAC | G | 30 | a0001c0001t0001g0082a0001c0001t0001g0135a0001c0001t0001g0138others(27): Show | 30 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.-58+14530_-58+1453 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65941333 | |||||
| chr5:65941336
|
C | G | 142 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 142 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.-58+14530C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941336 | ||||||
| chr5:65941345
|
TAAC | T | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-58+14545_-58+1454 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65941345 | |||||
| chr5:65941357
|
A | G | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-58+14551A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941357 | ||||||
| chr5:65941432
|
A | G | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+14626A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941432 | ||||||
| chr5:65941524
|
C | T | 1 | a0001c0002t0002g0290 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-58+14718C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941524 | ||||||
| chr5:65941606
|
TGTA | T | 10 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(7): Show | 10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-58+14805_-58+1480 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65941606 | |||||
| chr5:65941607
|
G | A | 178 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.-58+14801G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941607 | ||||||
| chr5:65941680
|
A | G | 1 | a0015c0024t0022g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-58+14874A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941680 | ||||||
| chr5:65941689
|
C | G | 8 | a0001c0002t0002g0173a0001c0002t0002g0210a0001c0002t0002g0211others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-58+14883C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941689 | ||||||
| chr5:65941694
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-58+14888G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941694 | ||||||
| chr5:65941827
|
G | A | 2 | a0001c0002t0002g0286a0001c0002t0002g0287 | 2 | HG00642.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-58+15021G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941827 | ||||||
| chr5:65941842
|
T | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+15036T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941842 | ||||||
| chr5:65941955
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-58+15149T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941955 | ||||||
| chr5:65941982
|
C | T | 18 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(15): Show | 18 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-58+15176C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941982 | ||||||
| chr5:65942039
|
C | CGAAA | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+15233_-58+1523 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942039 | ||||||
| chr5:65942134
|
C | T | 5 | a0001c0001t0001g0061a0001c0001t0001g0077a0001c0001t0001g0078others(2): Show | 5 | HG00673.hp1 NA18946.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+15328C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942134 | ||||||
| chr5:65942197
|
T | C | 2 | a0005c0006t0007g0223a0005c0006t0016g0299 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-58+15391T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942197 | ||||||
| chr5:65942302
|
G | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+15496G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942302 | ||||||
| chr5:65942312
|
C | G | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+15506C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942312 | ||||||
| chr5:65942457
|
A | G | 127 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0031others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.-58+15651A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942457 | ||||||
| chr5:65942471
|
G | A | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-58+15665G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942471 | ||||||
| chr5:65942471
|
G | T | 3 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0010 | 3 | HG01167.hp2 HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-58+15665G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942471 | ||||||
| chr5:65942529
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+15723T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942529 | ||||||
| chr5:65942744
|
G | A | 1 | a0001c0020t0001g0117 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-58+15938G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942744 | ||||||
| chr5:65942753
|
T | C | 188 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.-58+15947T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942753 | ||||||
| chr5:65942757
|
T | A | 1 | a0001c0020t0001g0117 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-58+15951T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942757 | ||||||
| chr5:65942838
|
G | C | 1 | a0001c0020t0001g0117 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-58+16032G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942838 | ||||||
| chr5:65942908
|
CA | C | 14 | a0001c0001t0001g0029a0001c0001t0001g0054a0001c0001t0001g0061others(11): Show | 14 | HG00673.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-58+16119delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65942908 | |||||
| chr5:65942908
|
CAA | C | 184 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(181): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.-58+16118_-58+1611 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65942908 | |||||
| chr5:65942930
|
CTT | C | 154 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-58+16126_-58+1612 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65942930 | |||||
| chr5:65943001
|
C | T | 2 | a0003c0004t0001g0136a0003c0004t0001g0140 | 2 | HG00642.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.-58+16195C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65943001 | ||||||
| chr5:65943521
|
C | G | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+16715C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65943521 | ||||||
| chr5:65943579
|
T | G | 1 | a0001c0001t0001g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-58+16773T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65943579 | ||||||
| chr5:65943640
|
A | G | 142 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.-58+16834A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65943640 | ||||||
| chr5:65943641
|
A | G | 4 | a0001c0007t0010g0162a0001c0007t0010g0163a0001c0007t0010g0164others(1): Show | 4 | HG02109.hp2 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+16835A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65943641 | ||||||
| chr5:65943861
|
C | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0267 | 2 | HG02056.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.-58+17055C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65943861 | ||||||
| chr5:65943862
|
T | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0011c0019t0001g0088 | 3 | NA18957.hp1 NA18990.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.-58+17056T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65943862 | ||||||
| chr5:65943907
|
T | C | 2 | a0001c0002t0002g0296a0001c0002t0002g0297 | 2 | HG00438.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.-58+17101T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65943907 | ||||||
| chr5:65944204
|
A | AT | 42 | a0001c0002t0002g0235a0001c0002t0002g0237a0001c0002t0002g0259others(39): Show | 42 | HG00408.hp2 HG00609.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.-58+17419dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65944204 | |||||
| chr5:65944204
|
AT | A | 13 | a0001c0002t0002g0003a0001c0002t0002g0033a0001c0002t0002g0173others(10): Show | 13 | HG02055.hp2 HG02109.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-58+17419delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65944204 | |||||
| chr5:65944222
|
TTTTA | T | 8 | a0001c0001t0001g0052a0001c0001t0001g0106a0001c0001t0009g0038others(5): Show | 8 | HG01257.hp2 HG01515.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.-58+17417_-58+1742 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65944222 | ||||||
| chr5:65944223
|
TTTA | T | 162 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.-58+17418_-58+1742 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65944223 | ||||||
| chr5:65944224
|
TTA | T | 17 | a0001c0001t0001g0075a0001c0001t0001g0091a0001c0001t0001g0116others(14): Show | 17 | HG01109.hp2 HG02004.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-58+17419_-58+1742 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65944224 | ||||||
| chr5:65944278
|
C | T | 2 | a0001c0007t0010g0161a0001c0007t0010g0275 | 2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-58+17472C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65944278 | ||||||
| chr5:65944393
|
G | A | 5 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(2): Show | 5 | HG01884.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+17587G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65944393 | ||||||
| chr5:65944416
|
G | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+17610G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65944416 | ||||||
| chr5:65944450
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+17644A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65944450 | ||||||
| chr5:65944503
|
C | G | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+17697C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65944503 | ||||||
| chr5:65944635
|
G | A | 2 | a0005c0006t0007g0223a0005c0006t0016g0299 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-58+17829G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65944635 | ||||||
| chr5:65944850
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+18044T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65944850 | ||||||
| chr5:65945220
|
A | T | 2 | a0001c0007t0012g0218a0001c0007t0012g0220 | 2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-58+18414A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65945220 | ||||||
| chr5:65945285
|
A | G | 1 | a0001c0002t0002g0237 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-58+18479A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65945285 | ||||||
| chr5:65945350
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+18544T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65945350 | ||||||
| chr5:65945369
|
C | T | 1 | a0001c0002t0002g0262 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-58+18563C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65945369 | ||||||
| chr5:65945486
|
A | G | 6 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(3): Show | 6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+18680A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65945486 | ||||||
| chr5:65945537
|
G | C | 2 | a0001c0007t0012g0218a0001c0007t0012g0220 | 2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-58+18731G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65945537 | ||||||
| chr5:65945618
|
A | G | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-58+18812A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65945618 | ||||||
| chr5:65945684
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+18878T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65945684 | ||||||
| chr5:65946179
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+19373A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65946179 | ||||||
| chr5:65946193
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+19387C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65946193 | ||||||
| chr5:65946272
|
A | G | 188 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.-58+19466A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65946272 | ||||||
| chr5:65946366
|
A | AAATG | 16 | a0003c0004t0001g0107a0003c0004t0001g0108a0004c0005t0004g0013others(13): Show | 16 | HG02258.hp1 HG02451.hp2 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+19585_-58+1958 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65946366 | |||||
| chr5:65946422
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+19616T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65946422 | ||||||
| chr5:65946688
|
C | T | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+19882C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65946688 | ||||||
| chr5:65946739
|
G | A | 6 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(3): Show | 6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+19933G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65946739 | ||||||
| chr5:65946787
|
C | CT | 24 | a0001c0001t0001g0047a0001c0001t0001g0074a0001c0001t0006g0154others(21): Show | 24 | HG00738.hp2 HG01167.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.-58+19998dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65946787 | |||||
| chr5:65946787
|
CT | C | 6 | a0001c0007t0012g0218a0001c0007t0012g0219a0001c0007t0012g0220others(3): Show | 6 | HG01167.hp1 HG01943.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58+19998delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65946787 | |||||
| chr5:65946902
|
C | T | 13 | a0003c0004t0001g0089a0003c0004t0001g0094a0003c0004t0001g0105others(10): Show | 13 | NA18747.hp1 NA18942.hp2 NA18949.hp1 others(10): Show |
intron_variant | MODIFIER | c.-58+20096C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65946902 | ||||||
| chr5:65946957
|
A | AT | 18 | a0001c0001t0009g0040a0001c0002t0002g0286a0004c0005t0004g0007others(15): Show | 18 | HG00642.hp2 HG01167.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-58+20161dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65946957 | |||||
| chr5:65947028
|
G | C | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-58+20222G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65947028 | ||||||
| chr5:65947095
|
A | G | 1 | a0003c0004t0001g0134 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-58+20289A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65947095 | ||||||
| chr5:65947755
|
C | A | 1 | a0015c0024t0022g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-58+20949C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65947755 | ||||||
| chr5:65947756
|
C | T | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+20950C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65947756 | ||||||
| chr5:65947956
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+21150G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65947956 | ||||||
| chr5:65948010
|
C | CA | 139 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-58+21220dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65948010 | |||||
| chr5:65948023
|
A | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+21217A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65948023 | ||||||
| chr5:65948062
|
A | G | 1 | a0001c0001t0024g0158 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-58+21256A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65948062 | ||||||
| chr5:65948153
|
TTTTG | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+21359_-58+2136 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65948153 | |||||
| chr5:65948321
|
C | T | 5 | a0001c0001t0001g0061a0001c0001t0001g0077a0001c0001t0001g0078others(2): Show | 5 | HG00673.hp1 NA18946.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+21515C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65948321 | ||||||
| chr5:65948341
|
A | AT | 7 | a0001c0001t0001g0104a0001c0001t0001g0116a0001c0001t0009g0040others(4): Show | 7 | HG01256.hp1 HG01256.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.-58+21549dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65948341 | |||||
| chr5:65948429
|
A | T | 1 | a0001c0001t0001g0074 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-58+21623A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65948429 | ||||||
| chr5:65948464
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-58+21658G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65948464 | ||||||
| chr5:65948479
|
G | T | 4 | a0005c0006t0007g0224a0005c0006t0007g0226a0005c0006t0007g0230others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+21673G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65948479 | ||||||
| chr5:65948762
|
G | GT | 21 | a0001c0002t0002g0245a0001c0002t0002g0255a0001c0002t0002g0256others(18): Show | 21 | HG00673.hp2 HG01071.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.-58+21975dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65948762 | |||||
| chr5:65948762
|
G | GTT | 21 | a0001c0022t0009g0035a0003c0004t0001g0128a0004c0005t0004g0007others(18): Show | 21 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.-58+21974_-58+2197 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65948762 | |||||
| chr5:65948762
|
G | GTTT | 110 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.-58+21973_-58+2197 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65948762 | |||||
| chr5:65948762
|
G | GTTTT | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0031others(28): Show | 31 | HG01071.hp2 HG01257.hp2 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.-58+21972_-58+2197 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65948762 | |||||
| chr5:65948771
|
T | TTTG | 12 | a0001c0001t0006g0147a0001c0001t0006g0148a0001c0001t0006g0149others(9): Show | 12 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+21967_-58+2196 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65948771 | |||||
| chr5:65948782
|
G | T | 1 | a0005c0006t0007g0026 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-58+21976G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65948782 | ||||||
| chr5:65948783
|
A | T | 1 | a0005c0006t0007g0026 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-58+21977A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65948783 | ||||||
| chr5:65948786
|
C | G | 1 | a0005c0006t0007g0026 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-58+21980C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65948786 | ||||||
| chr5:65948786
|
CAG | C | 3 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0227 | 3 | HG02257.hp1 HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-58+21983_-58+2198 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65948786 | |||||
| chr5:65948788
|
G | C | 1 | a0005c0006t0007g0026 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-58+21982G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65948788 | ||||||
| chr5:65948835
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-58+22029C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65948835 | ||||||
| chr5:65949030
|
C | G | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | NA18991.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-58+22224C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65949030 | ||||||
| chr5:65949305
|
C | A | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-58+22499C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65949305 | ||||||
| chr5:65949345
|
T | G | 1 | a0001c0001t0001g0159 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-58+22539T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65949345 | ||||||
| chr5:65949363
|
A | G | 1 | a0001c0002t0002g0033 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-58+22557A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65949363 | ||||||
| chr5:65949579
|
T | A | 1 | a0001c0001t0006g0147 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-58+22773T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65949579 | ||||||
| chr5:65949594
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-58+22788A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65949594 | ||||||
| chr5:65949719
|
A | G | 1 | a0001c0001t0013g0125 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-58+22913A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65949719 | ||||||
| chr5:65949770
|
A | G | 1 | a0001c0001t0001g0268 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-58+22964A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65949770 | ||||||
| chr5:65949794
|
C | T | 1 | a0013c0018t0001g0049 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-58+22988C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65949794 | ||||||
| chr5:65949977
|
C | G | 2 | a0005c0006t0002g0229a0005c0006t0002g0263 | 2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-58+23171C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65949977 | ||||||
| chr5:65949993
|
G | A | 1 | a0005c0006t0007g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-58+23187G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65949993 | ||||||
| chr5:65950216
|
A | G | 1 | a0001c0002t0002g0238 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-58+23410A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65950216 | ||||||
| chr5:65950219
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+23413A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65950219 | ||||||
| chr5:65950463
|
C | T | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-58+23657C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65950463 | ||||||
| chr5:65950736
|
C | T | 1 | a0005c0006t0007g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-58+23930C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65950736 | ||||||
| chr5:65950737
|
T | G | 1 | a0004c0005t0004g0017 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-58+23931T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65950737 | ||||||
| chr5:65951155
|
C | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+24349C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65951155 | ||||||
| chr5:65951168
|
G | A | 1 | a0001c0002t0002g0242 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-58+24362G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65951168 | ||||||
| chr5:65951290
|
T | C | 5 | a0002c0003t0002g0204a0002c0003t0002g0207a0002c0003t0002g0208others(2): Show | 5 | NA18951.hp2 NA18992.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+24484T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65951290 | ||||||
| chr5:65951354
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-58+24548G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65951354 | ||||||
| chr5:65951382
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+24576A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65951382 | ||||||
| chr5:65951654
|
A | G | 1 | a0002c0003t0002g0202 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-58+24848A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65951654 | ||||||
| chr5:65951802
|
A | G | 1 | a0005c0006t0016g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-58+24996A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65951802 | ||||||
| chr5:65951848
|
T | C | 1 | a0002c0003t0002g0216 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-58+25042T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65951848 | ||||||
| chr5:65952065
|
C | T | 142 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.-58+25259C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952065 | ||||||
| chr5:65952202
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+25396C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952202 | ||||||
| chr5:65952221
|
G | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+25415G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952221 | ||||||
| chr5:65952282
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-58+25476A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952282 | ||||||
| chr5:65952338
|
T | G | 1 | a0002c0003t0008g0174 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-58+25532T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952338 | ||||||
| chr5:65952380
|
A | G | 1 | a0005c0006t0007g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-58+25574A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952380 | ||||||
| chr5:65952435
|
T | TGAGGCC | 7 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(4): Show | 7 | HG02258.hp1 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-58+25629_-58+2563 others(10): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952435 | ||||||
| chr5:65952436
|
T | A | 7 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(4): Show | 7 | HG02258.hp1 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-58+25630T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952436 | ||||||
| chr5:65952437
|
G | T | 7 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(4): Show | 7 | HG02258.hp1 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-58+25631G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952437 | ||||||
| chr5:65952474
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+25668C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952474 | ||||||
| chr5:65952549
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-58+25743T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952549 | ||||||
| chr5:65952551
|
CT | C | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0085others(4): Show | 7 | NA18954.hp2 NA18955.hp1 NA18999.hp2 others(4): Show |
intron_variant | MODIFIER | c.-58+25756delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65952551 | |||||
| chr5:65952663
|
T | G | 1 | a0001c0001t0001g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-58+25857T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952663 | ||||||
| chr5:65952737
|
T | G | 1 | a0003c0004t0001g0105 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-58+25931T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952737 | ||||||
| chr5:65952925
|
A | C | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-58+26119A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952925 | ||||||
| chr5:65952969
|
T | G | 2 | a0003c0004t0001g0306a0003c0004t0023g0304 | 2 | HG01952.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.-58+26163T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952969 | ||||||
| chr5:65952978
|
T | A | 1 | a0001c0001t0013g0100 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-58+26172T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952978 | ||||||
| chr5:65953081
|
T | A | 1 | a0003c0004t0001g0305 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-58+26275T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65953081 | ||||||
| chr5:65953142
|
A | G | 4 | a0002c0003t0005g0178a0002c0003t0005g0180a0002c0003t0005g0187others(1): Show | 4 | NA18977.hp2 NA18985.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+26336A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65953142 | ||||||
| chr5:65953152
|
G | A | 1 | a0001c0001t0006g0148 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-58+26346G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65953152 | ||||||
| chr5:65953576
|
G | C | 1 | a0003c0004t0001g0001 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-58+26770G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65953576 | ||||||
| chr5:65953872
|
A | G | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-58+27066A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65953872 | ||||||
| chr5:65953882
|
C | T | 10 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(7): Show | 10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-58+27076C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65953882 | ||||||
| chr5:65953922
|
C | T | 1 | a0001c0015t0029g0258 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-58+27116C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65953922 | ||||||
| chr5:65953982
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+27176G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65953982 | ||||||
| chr5:65954002
|
T | A | 4 | a0005c0006t0007g0224a0005c0006t0007g0226a0005c0006t0007g0230others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+27196T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954002 | ||||||
| chr5:65954026
|
C | T | 2 | a0001c0001t0001g0274a0001c0001t0013g0100 | 2 | HG00438.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-58+27220C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954026 | ||||||
| chr5:65954031
|
C | T | 142 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.-58+27225C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954031 | ||||||
| chr5:65954135
|
T | G | 1 | a0001c0001t0001g0159 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-58+27329T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954135 | ||||||
| chr5:65954160
|
C | T | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+27354C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954160 | ||||||
| chr5:65954238
|
A | C | 2 | a0008c0011t0011g0024a0008c0011t0011g0025 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-58+27432A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954238 | ||||||
| chr5:65954280
|
A | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+27474A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954280 | ||||||
| chr5:65954284
|
C | T | 1 | a0001c0001t0006g0148 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-58+27478C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954284 | ||||||
| chr5:65954304
|
T | G | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-58+27498T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954304 | ||||||
| chr5:65954357
|
A | G | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0085others(4): Show | 7 | NA18954.hp2 NA18955.hp1 NA18999.hp2 others(4): Show |
intron_variant | MODIFIER | c.-58+27551A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954357 | ||||||
| chr5:65954485
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+27679G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954485 | ||||||
| chr5:65954646
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+27840A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954646 | ||||||
| chr5:65954687
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+27881C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954687 | ||||||
| chr5:65954724
|
G | A | 2 | a0004c0005t0004g0014a0004c0005t0004g0020 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-58+27918G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954724 | ||||||
| chr5:65954762
|
GA | G | 21 | a0001c0001t0013g0100a0004c0005t0004g0007a0004c0005t0004g0008others(18): Show | 21 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-58+27968delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65954762 | |||||
| chr5:65954805
|
C | T | 1 | a0004c0005t0004g0009 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-58+27999C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954805 | ||||||
| chr5:65954825
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0054 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-58+28019G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954825 | ||||||
| chr5:65954882
|
T | A | 1 | a0002c0003t0003g0206 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-58+28076T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954882 | ||||||
| chr5:65954894
|
G | A | 1 | a0015c0024t0022g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-58+28088G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954894 | ||||||
| chr5:65955030
|
C | T | 1 | a0001c0007t0012g0219 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-58+28224C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65955030 | ||||||
| chr5:65955082
|
A | C | 2 | a0002c0003t0003g0276a0010c0009t0002g0169 | 2 | NA18951.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-58+28276A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65955082 | ||||||
| chr5:65955173
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+28367A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65955173 | ||||||
| chr5:65955310
|
C | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+28504C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65955310 | ||||||
| chr5:65955405
|
G | A | 7 | a0001c0001t0001g0043a0001c0007t0010g0161a0001c0007t0010g0162others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-58+28599G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65955405 | ||||||
| chr5:65955431
|
A | T | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+28625A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65955431 | ||||||
| chr5:65955544
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+28738C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65955544 | ||||||
| chr5:65955602
|
C | G | 1 | a0015c0024t0022g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-58+28796C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65955602 | ||||||
| chr5:65955717
|
A | G | 1 | a0001c0002t0002g0286 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-58+28911A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65955717 | ||||||
| chr5:65955913
|
G | A | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+29107G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65955913 | ||||||
| chr5:65955918
|
A | G | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+29112A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65955918 | ||||||
| chr5:65956006
|
A | C | 1 | a0001c0001t0001g0264 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-58+29200A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65956006 | ||||||
| chr5:65956047
|
A | C | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+29241A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65956047 | ||||||
| chr5:65956217
|
T | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | NA18612.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.-58+29411T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65956217 | ||||||
| chr5:65956372
|
A | AT | 6 | a0001c0001t0001g0030a0001c0001t0001g0056a0001c0001t0001g0232others(3): Show | 6 | HG06807.hp2 NA18949.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+29585dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65956372 | |||||
| chr5:65956372
|
AT | A | 9 | a0001c0001t0001g0058a0001c0001t0001g0090a0001c0001t0020g0142others(6): Show | 9 | NA18949.hp2 NA18954.hp1 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.-58+29585delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65956372 | |||||
| chr5:65956372
|
ATT | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+29584_-58+2958 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65956372 | |||||
| chr5:65956406
|
CT | C | 197 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-58+29602delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65956406 | |||||
| chr5:65956444
|
T | G | 2 | a0005c0006t0007g0221a0005c0006t0007g0222 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-58+29638T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65956444 | ||||||
| chr5:65956450
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-58+29644C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65956450 | ||||||
| chr5:65956457
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+29651A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65956457 | ||||||
| chr5:65956505
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+29699G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65956505 | ||||||
| chr5:65956526
|
C | T | 3 | a0001c0001t0001g0103a0001c0001t0001g0112a0001c0001t0013g0100 | 3 | HG01952.hp1 HG04115.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-58+29720C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65956526 | ||||||
| chr5:65956545
|
C | CT | 12 | a0001c0007t0010g0161a0001c0007t0010g0275a0004c0005t0004g0013others(9): Show | 12 | HG02055.hp2 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+29754dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65956545 | |||||
| chr5:65956545
|
CT | C | 9 | a0001c0002t0002g0173a0001c0002t0002g0210a0001c0002t0002g0211others(6): Show | 9 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-58+29754delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65956545 | |||||
| chr5:65956625
|
C | T | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-58+29819C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65956625 | ||||||
| chr5:65956626
|
T | G | 12 | a0001c0001t0006g0147a0001c0001t0006g0148a0001c0001t0006g0149others(9): Show | 12 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+29820T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65956626 | ||||||
| chr5:65956673
|
C | T | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-58+29867C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65956673 | ||||||
| chr5:65956821
|
T | C | 1 | a0004c0005t0004g0009 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-58+30015T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65956821 | ||||||
| chr5:65956986
|
TG | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+30182delG | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65956986 | |||||
| chr5:65957017
|
A | G | 2 | a0001c0001t0009g0039a0001c0001t0009g0040 | 2 | NA18961.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-58+30211A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957017 | ||||||
| chr5:65957205
|
T | A | 4 | a0001c0007t0010g0162a0001c0007t0010g0163a0001c0007t0010g0164others(1): Show | 4 | HG02109.hp2 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+30399T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957205 | ||||||
| chr5:65957206
|
A | T | 17 | a0001c0001t0006g0155a0004c0005t0004g0007a0004c0005t0004g0008others(14): Show | 17 | HG01167.hp2 HG01884.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-58+30400A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957206 | ||||||
| chr5:65957209
|
TTTTTA | T | 7 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(4): Show | 7 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-58+30423_-58+3042 others(9): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65957209 | |||||
| chr5:65957223
|
TATTTTA | T | 8 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(5): Show | 8 | HG02258.hp1 HG02451.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.-58+30418_-58+3042 others(10): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957223 | ||||||
| chr5:65957229
|
A | T | 2 | a0001c0001t0001g0060a0004c0005t0004g0016 | 2 | HG02145.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-58+30423A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957229 | ||||||
| chr5:65957243
|
T | A | 1 | a0001c0001t0001g0109 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-58+30437T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957243 | ||||||
| chr5:65957280
|
G | T | 1 | a0001c0001t0001g0274 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-58+30474G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957280 | ||||||
| chr5:65957397
|
G | C | 2 | a0007c0012t0011g0022a0007c0012t0011g0023 | 2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-58+30591G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957397 | ||||||
| chr5:65957472
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+30666C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957472 | ||||||
| chr5:65957636
|
A | C | 1 | a0001c0001t0001g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-58+30830A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957636 | ||||||
| chr5:65957737
|
C | G | 1 | a0003c0004t0023g0304 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-57-30898C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957737 | ||||||
| chr5:65957739
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-30896A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957739 | ||||||
| chr5:65957815
|
C | G | 1 | a0002c0003t0003g0198 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-57-30820C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957815 | ||||||
| chr5:65957860
|
C | T | 1 | a0001c0001t0020g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-57-30775C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957860 | ||||||
| chr5:65957883
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-30752A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957883 | ||||||
| chr5:65957912
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-30723C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957912 | ||||||
| chr5:65957913
|
G | A | 1 | a0005c0006t0016g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-57-30722G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957913 | ||||||
| chr5:65957954
|
G | A | 8 | a0001c0002t0002g0173a0001c0002t0002g0210a0001c0002t0002g0211others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57-30681G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957954 | ||||||
| chr5:65957978
|
G | C | 1 | a0015c0024t0022g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-57-30657G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957978 | ||||||
| chr5:65957986
|
C | T | 1 | a0001c0007t0010g0161 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-57-30649C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957986 | ||||||
| chr5:65958090
|
C | T | 1 | a0001c0002t0002g0209 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-57-30545C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958090 | ||||||
| chr5:65958194
|
C | T | 1 | a0002c0003t0003g0181 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-57-30441C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958194 | ||||||
| chr5:65958212
|
T | C | 186 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-57-30423T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958212 | ||||||
| chr5:65958212
|
T | G | 2 | a0001c0001t0020g0142a0004c0005t0004g0010 | 2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-57-30423T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958212 | ||||||
| chr5:65958243
|
C | T | 4 | a0005c0006t0007g0224a0005c0006t0007g0226a0005c0006t0007g0230others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-30392C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958243 | ||||||
| chr5:65958291
|
C | T | 5 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(2): Show | 5 | HG01884.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57-30344C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958291 | ||||||
| chr5:65958292
|
A | G | 188 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.-57-30343A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958292 | ||||||
| chr5:65958383
|
C | T | 1 | a0001c0001t0020g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-57-30252C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958383 | ||||||
| chr5:65958410
|
G | A | 1 | a0003c0004t0021g0303 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-57-30225G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958410 | ||||||
| chr5:65958445
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-30190C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958445 | ||||||
| chr5:65958466
|
C | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-30169C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958466 | ||||||
| chr5:65958487
|
G | A | 12 | a0001c0001t0006g0147a0001c0001t0006g0148a0001c0001t0006g0149others(9): Show | 12 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-57-30148G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958487 | ||||||
| chr5:65958501
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-57-30134A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958501 | ||||||
| chr5:65958596
|
C | CAGAGGGA others(12): Show |
1 | a0002c0003t0008g0277 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-57-30023_-57-3000 others(23): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65958596 | |||||
| chr5:65958596
|
CAGAGGGA others(12): Show |
C | 1 | a0001c0001t0028g0092 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-57-30023_-57-3000 others(23): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65958596 | |||||
| chr5:65958613
|
A | AAGAGAG | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-30022_-57-3002 others(10): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958613 | ||||||
| chr5:65958636
|
G | C | 8 | a0002c0003t0002g0202a0002c0003t0002g0203a0002c0003t0002g0204others(5): Show | 8 | HG00280.hp2 HG01433.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57-29999G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958636 | ||||||
| chr5:65958639
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-29996G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958639 | ||||||
| chr5:65958836
|
G | C | 1 | a0001c0001t0001g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-57-29799G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958836 | ||||||
| chr5:65959029
|
A | T | 1 | a0001c0002t0002g0209 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-57-29606A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65959029 | ||||||
| chr5:65959663
|
C | G | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-57-28972C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65959663 | ||||||
| chr5:65959669
|
C | T | 1 | a0001c0001t0009g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-57-28966C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65959669 | ||||||
| chr5:65959727
|
A | G | 1 | a0003c0004t0026g0301 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-57-28908A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65959727 | ||||||
| chr5:65959809
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-28826G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65959809 | ||||||
| chr5:65959842
|
C | T | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-28793C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65959842 | ||||||
| chr5:65959844
|
C | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0098a0001c0001t0001g0102others(2): Show | 5 | HG00280.hp1 HG00738.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57-28791C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65959844 | ||||||
| chr5:65959859
|
T | C | 1 | a0001c0002t0002g0250 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-57-28776T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65959859 | ||||||
| chr5:65959909
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-57-28726C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65959909 | ||||||
| chr5:65959988
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-57-28647C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65959988 | ||||||
| chr5:65960207
|
G | C | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-28428G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65960207 | ||||||
| chr5:65960427
|
C | T | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-57-28208C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65960427 | ||||||
| chr5:65960455
|
G | A | 298 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(295): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-57-28180G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65960455 | ||||||
| chr5:65960491
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-57-28144C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65960491 | ||||||
| chr5:65960678
|
A | G | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-57-27957A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65960678 | ||||||
| chr5:65960709
|
AT | A | 6 | a0001c0002t0002g0242a0002c0003t0003g0181a0002c0003t0003g0182others(3): Show | 6 | NA18948.hp2 NA18954.hp1 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-27920delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65960709 | |||||
| chr5:65960963
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-57-27672T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65960963 | ||||||
| chr5:65961095
|
A | G | 2 | a0005c0006t0007g0223a0005c0006t0016g0299 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-57-27540A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65961095 | ||||||
| chr5:65961265
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-27370T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65961265 | ||||||
| chr5:65961600
|
G | T | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-27035G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65961600 | ||||||
| chr5:65961810
|
C | CT | 6 | a0005c0006t0007g0223a0005c0006t0007g0224a0005c0006t0007g0226others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-26820dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65961810 | |||||
| chr5:65961912
|
A | G | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-26723A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65961912 | ||||||
| chr5:65962086
|
A | G | 1 | a0003c0004t0027g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-57-26549A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65962086 | ||||||
| chr5:65962188
|
A | G | 1 | a0002c0003t0005g0172 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-57-26447A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65962188 | ||||||
| chr5:65962416
|
G | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-26219G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65962416 | ||||||
| chr5:65962469
|
C | CAG | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-26166_-57-2616 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65962469 | ||||||
| chr5:65962499
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-26136T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65962499 | ||||||
| chr5:65962639
|
C | T | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0119 | 3 | HG00735.hp1 HG01069.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-57-25996C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65962639 | ||||||
| chr5:65962787
|
C | A | 1 | a0001c0002t0002g0290 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-57-25848C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65962787 | ||||||
| chr5:65962845
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0054 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-57-25790G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65962845 | ||||||
| chr5:65963160
|
TAAC | T | 3 | a0001c0001t0006g0152a0001c0001t0006g0153a0001c0001t0006g0157 | 3 | HG01891.hp1 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-57-25472_-57-2547 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65963160 | |||||
| chr5:65963197
|
A | T | 6 | a0005c0006t0007g0223a0005c0006t0007g0224a0005c0006t0007g0226others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-25438A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65963197 | ||||||
| chr5:65963257
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-57-25378G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65963257 | ||||||
| chr5:65963322
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-57-25313A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65963322 | ||||||
| chr5:65963344
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-25291T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65963344 | ||||||
| chr5:65963414
|
C | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-25221C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65963414 | ||||||
| chr5:65963443
|
A | C | 6 | a0005c0006t0007g0223a0005c0006t0007g0224a0005c0006t0007g0226others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-25192A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65963443 | ||||||
| chr5:65963463
|
T | G | 1 | a0001c0007t0010g0275 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-57-25172T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65963463 | ||||||
| chr5:65963499
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-25136G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65963499 | ||||||
| chr5:65963792
|
C | CT | 10 | a0001c0007t0010g0162a0001c0007t0010g0163a0001c0007t0010g0164others(7): Show | 10 | HG01884.hp1 HG02109.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-57-24828dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65963792 | |||||
| chr5:65963792
|
CT | C | 140 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.-57-24828delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65963792 | |||||
| chr5:65963829
|
G | A | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-24806G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65963829 | ||||||
| chr5:65963839
|
G | GAGTGC | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-24791_-57-2478 others(9): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65963839 | |||||
| chr5:65963939
|
A | G | 6 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(3): Show | 6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-24696A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65963939 | ||||||
| chr5:65963990
|
G | A | 17 | a0001c0001t0001g0098a0004c0005t0004g0007a0004c0005t0004g0008others(14): Show | 17 | HG00738.hp1 HG01167.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-57-24645G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65963990 | ||||||
| chr5:65964056
|
C | T | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-24579C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964056 | ||||||
| chr5:65964270
|
G | A | 1 | a0013c0018t0001g0049 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-57-24365G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964270 | ||||||
| chr5:65964270
|
G | T | 1 | a0001c0002t0002g0003 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-57-24365G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964270 | ||||||
| chr5:65964531
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-24104A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964531 | ||||||
| chr5:65964741
|
C | CT | 156 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-57-23875dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964741 | |||||
| chr5:65964741
|
C | CTT | 8 | a0001c0001t0001g0065a0001c0001t0001g0090a0001c0001t0001g0138others(5): Show | 8 | HG01109.hp2 HG02451.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57-23876_-57-2387 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964741 | |||||
| chr5:65964741
|
CT | C | 18 | a0001c0002t0002g0293a0004c0005t0004g0007a0004c0005t0004g0008others(15): Show | 18 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-57-23875delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964741 | |||||
| chr5:65964894
|
C | A | 4 | a0005c0006t0007g0224a0005c0006t0007g0226a0005c0006t0007g0230others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-23741C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964894 | ||||||
| chr5:65964908
|
T | TTG | 19 | a0001c0002t0002g0034a0001c0002t0002g0237a0001c0002t0002g0248others(16): Show | 19 | HG00438.hp2 HG00609.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-57-23691_-57-2369 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | |||||
| chr5:65964908
|
T | TTGTG | 12 | a0001c0002t0002g0249a0001c0007t0012g0220a0002c0003t0002g0216others(9): Show | 12 | HG00280.hp2 HG02451.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-57-23693_-57-2369 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | |||||
| chr5:65964908
|
T | TTGTGTGT others(3): Show |
3 | a0007c0012t0011g0022a0007c0012t0011g0023a0012c0016t0007g0228 | 3 | HG01884.hp1 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-57-23699_-57-2369 others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | |||||
| chr5:65964908
|
T | TTGTGTGT others(5): Show |
2 | a0005c0006t0002g0229a0005c0006t0002g0263 | 2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-57-23701_-57-2369 others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | |||||
| chr5:65964908
|
T | TTGTGTGT others(7): Show |
1 | a0005c0006t0007g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-57-23703_-57-2369 others(18): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | |||||
| chr5:65964908
|
TTG | T | 3 | a0001c0002t0002g0033a0001c0002t0002g0287a0001c0002t0002g0290 | 3 | HG00408.hp1 HG00735.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-57-23691_-57-2369 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | |||||
| chr5:65964908
|
TTGTG | T | 13 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0054others(10): Show | 13 | HG02280.hp1 HG03209.hp1 HG03225.hp1 others(10): Show |
intron_variant | MODIFIER | c.-57-23693_-57-2369 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | |||||
| chr5:65964908
|
TTGTGTG | T | 22 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0041others(19): Show | 22 | HG01071.hp2 HG01256.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.-57-23695_-57-2369 others(10): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | |||||
| chr5:65964908
|
TTGTGTGT others(1): Show |
T | 114 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0031others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.-57-23697_-57-2369 others(12): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | |||||
| chr5:65964908
|
TTGTGTGT others(3): Show |
T | 1 | a0001c0007t0012g0219 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-57-23699_-57-2369 others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | |||||
| chr5:65964908
|
TTGTGTGT others(5): Show |
T | 1 | a0014c0023t0001g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-57-23701_-57-2369 others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | |||||
| chr5:65964908
|
TTGTGTGT others(9): Show |
T | 1 | a0001c0001t0001g0266 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-57-23705_-57-2369 others(20): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | |||||
| chr5:65964908
|
TTGTGTGT others(13): Show |
T | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-57-23709_-57-2369 others(24): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | |||||
| chr5:65964937
|
TGTGTGTG | T | 8 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0065others(5): Show | 8 | HG00642.hp1 HG02970.hp2 HG04228.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57-23697_-57-2369 others(11): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964937 | ||||||
| chr5:65964941
|
T | TGTGTGTG others(5): Show |
2 | a0008c0011t0011g0024a0008c0011t0011g0025 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-57-23690_-57-2368 others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964941 | |||||
| chr5:65964944
|
GTAAT | G | 9 | a0004c0005t0004g0009a0004c0005t0004g0013a0004c0005t0004g0014others(6): Show | 9 | HG02258.hp1 HG02572.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57-23689_-57-2368 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964944 | |||||
| chr5:65964945
|
T | A | 10 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0065others(7): Show | 10 | HG00642.hp1 HG02970.hp2 HG04228.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57-23690T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964945 | ||||||
| chr5:65964945
|
T | TGTA | 7 | a0001c0002t0002g0173a0001c0002t0002g0210a0001c0002t0002g0211others(4): Show | 7 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57-23690_-57-2368 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964945 | ||||||
| chr5:65964945
|
T | TGTGTGTG others(4): Show |
2 | a0001c0007t0010g0163a0001c0007t0010g0164 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-57-23690_-57-2368 others(15): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964945 | ||||||
| chr5:65964945
|
T | TGTGTGTG others(8): Show |
1 | a0001c0007t0010g0275 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-57-23690_-57-2368 others(19): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964945 | ||||||
| chr5:65964945
|
TAA | T | 4 | a0004c0005t0004g0007a0004c0005t0004g0010a0004c0005t0004g0019others(1): Show | 4 | HG01167.hp2 HG02109.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-23689_-57-2368 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964945 | ||||||
| chr5:65964946
|
A | G | 3 | a0004c0005t0004g0008a0004c0005t0004g0017a0004c0017t0004g0011 | 3 | HG02818.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-57-23689A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964946 | ||||||
| chr5:65964946
|
A | T | 7 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-57-23689A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964946 | ||||||
| chr5:65964947
|
A | T | 23 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0065others(20): Show | 23 | HG00642.hp1 HG01109.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.-57-23688A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964947 | ||||||
| chr5:65964948
|
T | A | 7 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-57-23687T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964948 | ||||||
| chr5:65964948
|
T | G | 7 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0010others(4): Show | 7 | HG01167.hp2 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57-23687T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964948 | ||||||
| chr5:65964950
|
T | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-23685T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964950 | ||||||
| chr5:65964952
|
T | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-23683T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964952 | ||||||
| chr5:65964954
|
T | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-23681T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964954 | ||||||
| chr5:65964956
|
T | A | 15 | a0004c0005t0004g0007a0004c0005t0004g0009a0004c0005t0004g0010others(12): Show | 15 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-57-23679T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964956 | ||||||
| chr5:65964956
|
T | G | 1 | a0004c0005t0004g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-57-23679T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964956 | ||||||
| chr5:65964957
|
T | A | 15 | a0004c0005t0004g0007a0004c0005t0004g0009a0004c0005t0004g0010others(12): Show | 15 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-57-23678T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964957 | ||||||
| chr5:65964969
|
TA | T | 3 | a0001c0001t0001g0031a0003c0004t0001g0132a0003c0004t0001g0140 | 3 | HG01515.hp2 HG01993.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.-57-23664delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964969 | |||||
| chr5:65964970
|
A | T | 185 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.-57-23665A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964970 | ||||||
| chr5:65965095
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-23540C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965095 | ||||||
| chr5:65965170
|
A | ATAAAATG others(9): Show |
172 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.-57-23462_-57-2344 others(20): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965170 | |||||
| chr5:65965372
|
GTTTTTTG others(19): Show |
G | 3 | a0004c0005t0004g0009a0004c0005t0004g0027a0004c0005t0025g0012 | 3 | HG02572.hp1 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-57-23256_-57-2323 others(30): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965372 | |||||
| chr5:65965372
|
GTTTTTTG others(20): Show |
G | 13 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0010others(10): Show | 13 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-57-23256_-57-2323 others(31): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965372 | |||||
| chr5:65965379
|
G | GTTTTTTT others(5): Show |
1 | a0010c0009t0002g0205 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-57-23254_-57-2325 others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965379 | |||||
| chr5:65965379
|
G | GTTTTTTT others(10): Show |
1 | a0002c0003t0003g0206 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-57-23254_-57-2325 others(21): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965379 | |||||
| chr5:65965379
|
G | T | 1 | a0002c0003t0008g0257 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-57-23256G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965379 | ||||||
| chr5:65965379
|
GTTGTTTT others(12): Show |
G | 1 | a0001c0002t0002g0209 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-57-23253_-57-2323 others(23): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965379 | |||||
| chr5:65965382
|
G | GT | 9 | a0001c0002t0002g0002a0001c0002t0002g0211a0001c0002t0002g0240others(6): Show | 9 | HG00408.hp1 HG02071.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57-23212dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | |||||
| chr5:65965382
|
G | GTTGTTTT others(7): Show |
1 | a0001c0002t0002g0253 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-57-23251_-57-2325 others(18): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | |||||
| chr5:65965382
|
G | GTTTTTTT others(4): Show |
2 | a0002c0003t0008g0175a0002c0003t0008g0280 | 2 | HG00408.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.-57-23222_-57-2321 others(15): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | |||||
| chr5:65965382
|
G | GTTTTTTT others(5): Show |
1 | a0002c0003t0005g0176 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-57-23223_-57-2321 others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | |||||
| chr5:65965382
|
G | GTTTTTTT others(6): Show |
2 | a0002c0003t0005g0185a0002c0003t0005g0186 | 2 | HG01081.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.-57-23224_-57-2321 others(17): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | |||||
| chr5:65965382
|
G | GTTTTTTT others(9): Show |
1 | a0002c0003t0002g0208 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-57-23227_-57-2321 others(20): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | |||||
| chr5:65965382
|
G | GTTTTTTT others(11): Show |
1 | a0002c0003t0002g0204 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-57-23229_-57-2321 others(22): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | |||||
| chr5:65965382
|
G | GTTTTTTT others(12): Show |
1 | a0002c0003t0005g0188 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-57-23230_-57-2321 others(23): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | |||||
| chr5:65965382
|
G | GTTTTTTT others(13): Show |
1 | a0002c0003t0005g0199 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-57-23231_-57-2321 others(24): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | |||||
| chr5:65965382
|
G | GTTTTTTT others(17): Show |
1 | a0002c0003t0008g0179 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-57-23235_-57-2321 others(28): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | |||||
| chr5:65965382
|
G | GTTTTTTT others(47): Show |
1 | a0002c0003t0005g0177 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-57-23212_-57-2321 others(58): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | |||||
| chr5:65965382
|
G | T | 4 | a0002c0003t0003g0166a0002c0003t0003g0168a0002c0003t0003g0206others(1): Show | 4 | HG01433.hp1 NA18951.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-23253G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965382 | ||||||
| chr5:65965382
|
GT | G | 14 | a0001c0002t0002g0032a0001c0002t0002g0033a0001c0002t0002g0034others(11): Show | 14 | HG02004.hp2 HG02056.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-57-23212delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | |||||
| chr5:65965382
|
GTT | G | 11 | a0001c0002t0002g0173a0001c0002t0002g0210a0001c0002t0002g0215others(8): Show | 11 | HG00438.hp2 HG00609.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57-23213_-57-2321 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | |||||
| chr5:65965382
|
GTTTTTTT others(3): Show |
G | 5 | a0001c0007t0012g0220a0002c0003t0003g0181a0002c0003t0003g0183others(2): Show | 5 | HG02622.hp1 NA18940.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57-23221_-57-2321 others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | |||||
| chr5:65965382
|
GTTTTTTT others(5): Show |
G | 3 | a0002c0003t0002g0203a0002c0003t0005g0184a0002c0003t0005g0278 | 3 | HG03239.hp1 NA18944.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-57-23223_-57-2321 others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | |||||
| chr5:65965382
|
GTTTTTTT others(8): Show |
G | 1 | a0001c0002t0019g0298 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-57-23226_-57-2321 others(19): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | |||||
| chr5:65965382
|
GTTTTTTT others(9): Show |
G | 3 | a0001c0002t0002g0255a0001c0002t0002g0260a0002c0003t0003g0198 | 3 | HG01069.hp1 HG01071.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-57-23227_-57-2321 others(20): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | |||||
| chr5:65965382
|
GTTTTTTT others(10): Show |
G | 1 | a0002c0003t0003g0200 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-57-23228_-57-2321 others(21): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | |||||
| chr5:65965382
|
GTTTTTTT others(11): Show |
G | 1 | a0002c0003t0003g0283 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-57-23229_-57-2321 others(22): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | |||||
| chr5:65965382
|
GTTTTTTT others(12): Show |
G | 1 | a0002c0003t0005g0172 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-57-23230_-57-2321 others(23): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | |||||
| chr5:65965382
|
GTTTTTTT others(15): Show |
G | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-23233_-57-2321 others(26): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | |||||
| chr5:65965382
|
GTTTTTTT others(16): Show |
G | 14 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(11): Show | 14 | HG00673.hp1 HG01891.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-57-23234_-57-2321 others(27): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | |||||
| chr5:65965382
|
GTTTTTTT others(17): Show |
G | 154 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-57-23235_-57-2321 others(28): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | |||||
| chr5:65965382
|
GTTTTTTT others(20): Show |
G | 2 | a0006c0008t0003g0194a0006c0008t0018g0190 | 2 | NA18971.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.-57-23238_-57-2321 others(31): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | |||||
| chr5:65965384
|
T | TG | 4 | a0001c0002t0002g0235a0001c0002t0002g0245a0001c0002t0002g0252others(1): Show | 4 | NA18949.hp2 NA18975.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-23251_-57-2325 others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965384 | ||||||
| chr5:65965385
|
T | G | 2 | a0001c0002t0002g0251a0006c0008t0003g0189 | 2 | NA18612.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.-57-23250T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965385 | ||||||
| chr5:65965386
|
T | G | 2 | a0001c0002t0002g0242a0002c0003t0003g0182 | 2 | NA19060.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-57-23249T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965386 | ||||||
| chr5:65965389
|
T | G | 1 | a0001c0002t0002g0288 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-57-23246T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965389 | ||||||
| chr5:65965399
|
T | G | 3 | a0004c0005t0004g0009a0004c0005t0004g0027a0004c0005t0025g0012 | 3 | HG02572.hp1 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-57-23236T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965399 | ||||||
| chr5:65965400
|
T | G | 13 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0010others(10): Show | 13 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-57-23235T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965400 | ||||||
| chr5:65965429
|
G | A | 1 | a0001c0001t0024g0158 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-57-23206G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965429 | ||||||
| chr5:65965545
|
C | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-23090C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965545 | ||||||
| chr5:65965559
|
C | CATGCCTG others(4): Show |
188 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.-57-23074_-57-2307 others(15): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965559 | |||||
| chr5:65965569
|
T | G | 1 | a0004c0005t0004g0009 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-57-23066T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965569 | ||||||
| chr5:65965607
|
A | C | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-23028A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965607 | ||||||
| chr5:65965631
|
G | T | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-57-23004G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965631 | ||||||
| chr5:65965732
|
G | A | 1 | a0005c0006t0002g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-57-22903G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965732 | ||||||
| chr5:65965841
|
T | C | 1 | a0002c0003t0003g0283 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-57-22794T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965841 | ||||||
| chr5:65965895
|
A | C | 1 | a0001c0001t0001g0144 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-57-22740A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965895 | ||||||
| chr5:65965998
|
G | T | 6 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(3): Show | 6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-22637G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965998 | ||||||
| chr5:65966020
|
A | G | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-57-22615A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65966020 | ||||||
| chr5:65966107
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-57-22528A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65966107 | ||||||
| chr5:65966112
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-57-22523A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65966112 | ||||||
| chr5:65966115
|
CTG | C | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-57-22518_-57-2251 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65966115 | |||||
| chr5:65966183
|
G | C | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-57-22452G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65966183 | ||||||
| chr5:65966245
|
A | G | 4 | a0005c0006t0007g0224a0005c0006t0007g0226a0005c0006t0007g0230others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-22390A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65966245 | ||||||
| chr5:65966311
|
A | G | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-22324A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65966311 | ||||||
| chr5:65966349
|
A | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-22286A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65966349 | ||||||
| chr5:65966378
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-57-22257G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65966378 | ||||||
| chr5:65966461
|
A | T | 2 | a0005c0006t0007g0221a0005c0006t0007g0222 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-57-22174A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65966461 | ||||||
| chr5:65966468
|
G | T | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-57-22167G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65966468 | ||||||
| chr5:65966680
|
C | CA | 33 | a0001c0001t0001g0046a0001c0002t0002g0032a0001c0002t0002g0210others(30): Show | 33 | HG00609.hp2 HG00735.hp2 HG02056.hp2 others(30): Show |
intron_variant | MODIFIER | c.-57-21926dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65966680 | |||||
| chr5:65966680
|
CA | C | 7 | a0001c0001t0001g0006a0001c0001t0001g0144a0001c0001t0001g0272others(4): Show | 7 | HG01257.hp1 HG02280.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.-57-21926delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65966680 | |||||
| chr5:65966680
|
CAA | C | 42 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0030others(39): Show | 42 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.-57-21927_-57-2192 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65966680 | |||||
| chr5:65966680
|
CAAA | C | 113 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(110): Show | 113 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.-57-21928_-57-2192 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65966680 | |||||
| chr5:65966680
|
CAAAA | C | 10 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0001g0120others(7): Show | 10 | HG01243.hp2 HG02165.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-57-21929_-57-2192 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65966680 | |||||
| chr5:65966680
|
CAAAAAAA | C | 15 | a0004c0005t0004g0008a0004c0005t0004g0009a0004c0005t0004g0010others(12): Show | 15 | HG02109.hp1 HG02258.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57-21932_-57-2192 others(11): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65966680 | |||||
| chr5:65966790
|
C | G | 1 | a0001c0001t0001g0159 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-57-21845C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65966790 | ||||||
| chr5:65966792
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-21843G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65966792 | ||||||
| chr5:65967014
|
G | C | 1 | a0001c0001t0003g0113 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-57-21621G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967014 | ||||||
| chr5:65967036
|
C | T | 1 | a0003c0004t0001g0001 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-57-21599C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967036 | ||||||
| chr5:65967140
|
A | T | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-57-21495A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967140 | ||||||
| chr5:65967161
|
A | G | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-57-21474A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967161 | ||||||
| chr5:65967170
|
C | A | 1 | a0014c0023t0001g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-57-21465C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967170 | ||||||
| chr5:65967262
|
C | T | 1 | a0001c0001t0013g0100 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-57-21373C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967262 | ||||||
| chr5:65967290
|
G | A | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-21345G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967290 | ||||||
| chr5:65967313
|
C | T | 1 | a0003c0004t0001g0122 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-57-21322C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967313 | ||||||
| chr5:65967403
|
T | A | 1 | a0003c0004t0001g0130 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-57-21232T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967403 | ||||||
| chr5:65967566
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-57-21069T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967566 | ||||||
| chr5:65967598
|
G | A | 4 | a0005c0006t0007g0224a0005c0006t0007g0226a0005c0006t0007g0230others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-21037G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967598 | ||||||
| chr5:65967802
|
T | C | 2 | a0005c0006t0007g0221a0005c0006t0007g0222 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-57-20833T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967802 | ||||||
| chr5:65967846
|
A | C | 10 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(7): Show | 10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57-20789A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967846 | ||||||
| chr5:65967988
|
C | T | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-57-20647C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967988 | ||||||
| chr5:65968072
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-20563G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65968072 | ||||||
| chr5:65968262
|
A | G | 42 | a0001c0001t0001g0028a0001c0001t0001g0041a0001c0001t0001g0048others(39): Show | 42 | HG00280.hp1 HG00735.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.-57-20373A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65968262 | ||||||
| chr5:65968367
|
G | C | 1 | a0001c0001t0001g0112 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-57-20268G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65968367 | ||||||
| chr5:65968380
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-20255G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65968380 | ||||||
| chr5:65968386
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-57-20249A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65968386 | ||||||
| chr5:65968587
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-20048G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65968587 | ||||||
| chr5:65968616
|
A | G | 1 | a0005c0006t0002g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-57-20019A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65968616 | ||||||
| chr5:65968660
|
A | G | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-57-19975A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65968660 | ||||||
| chr5:65968751
|
G | C | 2 | a0001c0001t0001g0133a0001c0001t0001g0273 | 2 | HG01071.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-57-19884G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65968751 | ||||||
| chr5:65968853
|
G | A | 1 | a0001c0001t0006g0148 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-57-19782G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65968853 | ||||||
| chr5:65968925
|
A | T | 1 | a0015c0024t0022g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-57-19710A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65968925 | ||||||
| chr5:65968990
|
T | A | 1 | a0001c0001t0013g0100 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-57-19645T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65968990 | ||||||
| chr5:65969020
|
A | G | 2 | a0005c0006t0002g0229a0005c0006t0002g0263 | 2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-57-19615A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65969020 | ||||||
| chr5:65969027
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-19608C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65969027 | ||||||
| chr5:65969041
|
T | G | 1 | a0001c0001t0001g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-57-19594T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65969041 | ||||||
| chr5:65969143
|
A | G | 1 | a0002c0003t0003g0196 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-57-19492A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65969143 | ||||||
| chr5:65969372
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-19263C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65969372 | ||||||
| chr5:65970007
|
G | A | 1 | a0001c0001t0028g0092 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-57-18628G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65970007 | ||||||
| chr5:65970093
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-18542G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65970093 | ||||||
| chr5:65970126
|
TA | T | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-57-18508delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65970126 | ||||||
| chr5:65970130
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-57-18505C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65970130 | ||||||
| chr5:65970142
|
T | C | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-18493T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65970142 | ||||||
| chr5:65970150
|
T | A | 1 | a0005c0006t0016g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-57-18485T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65970150 | ||||||
| chr5:65970297
|
A | G | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-57-18338A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65970297 | ||||||
| chr5:65970463
|
CACTA | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-18167_-57-1816 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65970463 | |||||
| chr5:65970474
|
A | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-18161A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65970474 | ||||||
| chr5:65970489
|
G | A | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-57-18146G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65970489 | ||||||
| chr5:65970649
|
G | C | 34 | a0001c0001t0001g0135a0001c0001t0001g0138a0001c0001t0001g0274others(31): Show | 34 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.-57-17986G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65970649 | ||||||
| chr5:65970694
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-17941T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65970694 | ||||||
| chr5:65970744
|
A | G | 6 | a0001c0001t0009g0036a0001c0001t0009g0037a0001c0001t0009g0038others(3): Show | 6 | HG03710.hp1 NA18961.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57-17891A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65970744 | ||||||
| chr5:65971008
|
A | G | 2 | a0002c0003t0008g0174a0002c0003t0008g0175 | 2 | NA18972.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.-57-17627A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65971008 | ||||||
| chr5:65971102
|
G | A | 10 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(7): Show | 10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57-17533G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65971102 | ||||||
| chr5:65971217
|
T | C | 3 | a0001c0001t0001g0133a0001c0001t0001g0144a0001c0001t0001g0273 | 3 | HG01071.hp2 HG01934.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-57-17418T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65971217 | ||||||
| chr5:65971270
|
G | C | 1 | a0001c0001t0001g0159 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-57-17365G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65971270 | ||||||
| chr5:65971396
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-57-17239A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65971396 | ||||||
| chr5:65971512
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-17123A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65971512 | ||||||
| chr5:65971778
|
A | G | 1 | a0003c0004t0001g0134 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-57-16857A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65971778 | ||||||
| chr5:65971780
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-57-16855C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65971780 | ||||||
| chr5:65971821
|
TTGAC | T | 4 | a0004c0005t0004g0013a0004c0005t0004g0015a0004c0005t0004g0016others(1): Show | 4 | HG02258.hp1 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-16811_-57-1680 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65971821 | |||||
| chr5:65972066
|
C | A | 8 | a0002c0003t0002g0202a0002c0003t0002g0203a0002c0003t0002g0204others(5): Show | 8 | HG00280.hp2 HG01433.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57-16569C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65972066 | ||||||
| chr5:65972112
|
G | A | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-16523G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65972112 | ||||||
| chr5:65972197
|
CACCCTTG others(1934): Show |
C | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-57-16347_-57-1440 others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65972197 | |||||
| chr5:65972364
|
A | G | 6 | a0002c0003t0002g0204a0002c0003t0002g0207a0002c0003t0002g0208others(3): Show | 6 | HG00280.hp2 NA18951.hp2 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57-16271A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65972364 | ||||||
| chr5:65972684
|
G | C | 1 | a0001c0001t0001g0029 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-57-15951G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65972684 | ||||||
| chr5:65972762
|
T | C | 3 | a0001c0007t0012g0218a0001c0007t0012g0219a0001c0007t0012g0220 | 3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-57-15873T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65972762 | ||||||
| chr5:65972842
|
T | G | 45 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0050others(42): Show | 45 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.-57-15793T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65972842 | ||||||
| chr5:65972857
|
T | C | 2 | a0007c0012t0011g0022a0007c0012t0011g0023 | 2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-57-15778T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65972857 | ||||||
| chr5:65972936
|
A | G | 1 | a0001c0002t0002g0217 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-57-15699A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65972936 | ||||||
| chr5:65973028
|
C | T | 2 | a0001c0002t0002g0255a0001c0002t0002g0260 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-57-15607C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973028 | ||||||
| chr5:65973039
|
T | G | 1 | a0001c0001t0024g0158 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-57-15596T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973039 | ||||||
| chr5:65973046
|
T | C | 15 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(12): Show | 15 | HG01071.hp2 HG01934.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-57-15589T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973046 | ||||||
| chr5:65973073
|
T | C | 1 | a0003c0004t0001g0134 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-57-15562T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973073 | ||||||
| chr5:65973094
|
A | C | 1 | a0003c0004t0001g0134 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-57-15541A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973094 | ||||||
| chr5:65973393
|
A | G | 6 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(3): Show | 6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-15242A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973393 | ||||||
| chr5:65973485
|
G | A | 1 | a0015c0024t0022g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-57-15150G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973485 | ||||||
| chr5:65973636
|
A | G | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-57-14999A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973636 | ||||||
| chr5:65973732
|
G | T | 1 | a0001c0001t0009g0039 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-57-14903G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973732 | ||||||
| chr5:65973750
|
G | A | 275 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(272): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.-57-14885G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973750 | ||||||
| chr5:65973790
|
A | G | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-57-14845A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973790 | ||||||
| chr5:65973822
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-14813T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973822 | ||||||
| chr5:65973918
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-14717A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973918 | ||||||
| chr5:65973925
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-57-14710A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973925 | ||||||
| chr5:65973928
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-57-14707G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973928 | ||||||
| chr5:65974084
|
A | T | 1 | a0002c0003t0002g0202 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-57-14551A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65974084 | ||||||
| chr5:65974173
|
C | G | 6 | a0001c0001t0009g0036a0001c0001t0009g0037a0001c0001t0009g0038others(3): Show | 6 | HG03710.hp1 NA18961.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57-14462C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65974173 | ||||||
| chr5:65974184
|
A | C | 142 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.-57-14451A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65974184 | ||||||
| chr5:65974519
|
G | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-14116G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65974519 | ||||||
| chr5:65974524
|
CCTGTTAT | C | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-14108_-57-1410 others(11): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65974524 | |||||
| chr5:65974956
|
G | T | 2 | a0001c0007t0010g0161a0001c0007t0010g0275 | 2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-57-13679G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65974956 | ||||||
| chr5:65974981
|
G | A | 2 | a0008c0011t0011g0024a0008c0011t0011g0025 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-57-13654G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65974981 | ||||||
| chr5:65975128
|
C | G | 1 | a0002c0003t0002g0202 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-57-13507C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65975128 | ||||||
| chr5:65975160
|
A | AC | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-13474dupC | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65975160 | |||||
| chr5:65975278
|
G | T | 1 | a0014c0023t0001g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-57-13357G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65975278 | ||||||
| chr5:65975602
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-57-13033G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65975602 | ||||||
| chr5:65975634
|
A | G | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-57-13001A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65975634 | ||||||
| chr5:65975839
|
C | G | 1 | a0001c0001t0013g0125 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-57-12796C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65975839 | ||||||
| chr5:65976150
|
C | T | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-57-12485C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976150 | ||||||
| chr5:65976203
|
G | A | 1 | a0002c0003t0003g0192 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-57-12432G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976203 | ||||||
| chr5:65976262
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-12373C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976262 | ||||||
| chr5:65976263
|
C | T | 2 | a0005c0006t0007g0223a0005c0006t0016g0299 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-57-12372C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976263 | ||||||
| chr5:65976397
|
C | T | 10 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0235others(7): Show | 10 | NA18612.hp1 NA18949.hp2 NA18975.hp1 others(7): Show |
intron_variant | MODIFIER | c.-57-12238C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976397 | ||||||
| chr5:65976520
|
CT | C | 19 | a0003c0004t0001g0089a0003c0004t0017g0121a0004c0005t0004g0007others(16): Show | 19 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-57-12100delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65976520 | |||||
| chr5:65976542
|
C | T | 2 | a0002c0003t0003g0206a0010c0009t0002g0205 | 2 | NA18951.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.-57-12093C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976542 | ||||||
| chr5:65976597
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-12038A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976597 | ||||||
| chr5:65976631
|
G | T | 2 | a0002c0003t0003g0206a0010c0009t0002g0205 | 2 | NA18951.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.-57-12004G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976631 | ||||||
| chr5:65976711
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-11924G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976711 | ||||||
| chr5:65976718
|
C | CTTA | 4 | a0005c0006t0007g0224a0005c0006t0007g0226a0005c0006t0007g0230others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-11916_-57-1191 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65976718 | |||||
| chr5:65976722
|
C | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-57-11913C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976722 | ||||||
| chr5:65976723
|
G | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-57-11912G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976723 | ||||||
| chr5:65976771
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-57-11864G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976771 | ||||||
| chr5:65976774
|
C | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-57-11861C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976774 | ||||||
| chr5:65976785
|
C | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-57-11850C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976785 | ||||||
| chr5:65976799
|
T | C | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-57-11836T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976799 | ||||||
| chr5:65976818
|
A | G | 1 | a0001c0001t0006g0154 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-57-11817A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976818 | ||||||
| chr5:65976836
|
A | G | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-57-11799A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976836 | ||||||
| chr5:65976843
|
A | C | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-57-11792A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976843 | ||||||
| chr5:65976880
|
A | G | 197 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-57-11755A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976880 | ||||||
| chr5:65976944
|
A | C | 2 | a0005c0006t0007g0221a0005c0006t0007g0222 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-57-11691A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976944 | ||||||
| chr5:65977039
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-57-11596C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977039 | ||||||
| chr5:65977118
|
C | T | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-11517C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977118 | ||||||
| chr5:65977127
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-11508C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977127 | ||||||
| chr5:65977144
|
G | A | 5 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(2): Show | 5 | HG01884.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57-11491G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977144 | ||||||
| chr5:65977161
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-57-11474C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977161 | ||||||
| chr5:65977163
|
CTCCCGGA others(339): Show |
C | 1 | a0001c0001t0001g0112 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-57-11455_-57-1111 others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65977163 | |||||
| chr5:65977198
|
AC | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-11428delC | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65977198 | |||||
| chr5:65977200
|
CCCCCCCC others(42): Show |
C | 8 | a0003c0004t0001g0134a0005c0006t0007g0221a0005c0006t0007g0222others(5): Show | 8 | HG00621.hp2 HG01109.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57-11364_-57-1131 others(53): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65977200 | |||||
| chr5:65977201
|
CCCCCCCA others(41): Show |
C | 1 | a0005c0006t0007g0223 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-57-11427_-57-1138 others(52): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65977201 | |||||
| chr5:65977205
|
C | T | 2 | a0002c0003t0003g0166a0002c0003t0003g0168 | 2 | HG01433.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-57-11430C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977205 | ||||||
| chr5:65977240
|
G | A | 11 | a0001c0001t0006g0147a0001c0001t0006g0148a0001c0001t0006g0149others(8): Show | 11 | HG00738.hp2 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57-11395G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977240 | ||||||
| chr5:65977245
|
G | A | 1 | a0001c0002t0002g0173 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-57-11390G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977245 | ||||||
| chr5:65977271
|
T | C | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11364T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977271 | ||||||
| chr5:65977273
|
G | A | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11362G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977273 | ||||||
| chr5:65977276
|
C | T | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11359C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977276 | ||||||
| chr5:65977280
|
TG | T | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11353delG | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65977280 | |||||
| chr5:65977293
|
G | A | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11342G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977293 | ||||||
| chr5:65977295
|
C | A | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11340C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977295 | ||||||
| chr5:65977297
|
GAC | G | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11337_-57-1133 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977297 | ||||||
| chr5:65977301
|
C | T | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11334C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977301 | ||||||
| chr5:65977304
|
C | T | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11331C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977304 | ||||||
| chr5:65977308
|
C | T | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11327C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977308 | ||||||
| chr5:65977312
|
C | CAGACGGG others(29): Show |
4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11323_-57-1132 others(40): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977312 | ||||||
| chr5:65977315
|
C | T | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11320C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977315 | ||||||
| chr5:65977317
|
G | A | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11318G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977317 | ||||||
| chr5:65977322
|
A | G | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11313A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977322 | ||||||
| chr5:65977325
|
T | C | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11310T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977325 | ||||||
| chr5:65977368
|
C | T | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-11267C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977368 | ||||||
| chr5:65977376
|
C | T | 10 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(7): Show | 10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57-11259C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977376 | ||||||
| chr5:65977416
|
C | G | 2 | a0004c0005t0004g0019a0004c0014t0004g0018 | 2 | HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-57-11219C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977416 | ||||||
| chr5:65977439
|
A | G | 38 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0123others(35): Show | 38 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.-57-11196A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977439 | ||||||
| chr5:65977445
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-11190T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977445 | ||||||
| chr5:65977481
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-57-11154G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977481 | ||||||
| chr5:65977490
|
G | A | 1 | a0002c0003t0003g0300 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-57-11145G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977490 | ||||||
| chr5:65977500
|
G | A | 1 | a0001c0002t0002g0033 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-57-11135G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977500 | ||||||
| chr5:65977553
|
A | G | 1 | a0001c0002t0002g0209 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-57-11082A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977553 | ||||||
| chr5:65977579
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-11056C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977579 | ||||||
| chr5:65977749
|
C | CG | 7 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0273others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57-10882dupG | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65977749 | |||||
| chr5:65977762
|
G | C | 1 | a0003c0004t0001g0131 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-57-10873G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977762 | ||||||
| chr5:65977788
|
C | T | 2 | a0004c0005t0004g0009a0004c0005t0004g0027 | 2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-57-10847C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977788 | ||||||
| chr5:65977794
|
G | T | 1 | a0001c0001t0001g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-57-10841G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977794 | ||||||
| chr5:65977892
|
C | T | 2 | a0002c0003t0003g0192a0002c0003t0003g0193 | 2 | NA18999.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-57-10743C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977892 | ||||||
| chr5:65977904
|
C | T | 2 | a0005c0006t0007g0223a0005c0006t0016g0299 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-57-10731C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977904 | ||||||
| chr5:65977913
|
A | G | 1 | a0003c0004t0026g0301 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-57-10722A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977913 | ||||||
| chr5:65977919
|
C | CCGAGGCT others(7): Show |
1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-57-10714_-57-1070 others(18): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65977919 | |||||
| chr5:65977958
|
G | GGGGAGA | 80 | a0001c0001t0001g0093a0001c0001t0003g0113a0001c0001t0006g0147others(77): Show | 80 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.-57-10653_-57-1064 others(10): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65977958 | |||||
| chr5:65977958
|
G | GGGGAGAG others(5): Show |
196 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(193): Show | 196 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.-57-10659_-57-1064 others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65977958 | |||||
| chr5:65977958
|
G | GGGGAGAG others(11): Show |
13 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(10): Show | 13 | HG01071.hp2 HG01261.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.-57-10665_-57-1064 others(22): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65977958 | |||||
| chr5:65977958
|
G | GGGGAGAG others(17): Show |
6 | a0005c0006t0007g0221a0005c0006t0007g0222a0005c0006t0007g0224others(3): Show | 6 | HG01109.hp2 HG01243.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-10671_-57-1064 others(28): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65977958 | |||||
| chr5:65977958
|
G | GGGGAGAG others(23): Show |
1 | a0005c0006t0016g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-57-10648_-57-1064 others(34): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65977958 | |||||
| chr5:65977958
|
G | GGGGAGAG others(35): Show |
1 | a0005c0006t0007g0223 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-57-10648_-57-1064 others(46): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65977958 | |||||
| chr5:65978093
|
A | G | 1 | a0002c0003t0003g0193 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-57-10542A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65978093 | ||||||
| chr5:65978472
|
A | T | 10 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(7): Show | 10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57-10163A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65978472 | ||||||
| chr5:65978483
|
G | A | 188 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.-57-10152G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65978483 | ||||||
| chr5:65978585
|
G | T | 1 | a0001c0001t0001g0041 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-57-10050G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65978585 | ||||||
| chr5:65978927
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-9708C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65978927 | ||||||
| chr5:65979135
|
A | T | 38 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0123others(35): Show | 38 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.-57-9500A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65979135 | ||||||
| chr5:65979195
|
G | A | 197 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-57-9440G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65979195 | ||||||
| chr5:65979285
|
TGTG | T | 142 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.-57-9340_-57-9338d others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65979285 | |||||
| chr5:65979666
|
A | G | 2 | a0001c0002t0002g0255a0001c0002t0002g0260 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-57-8969A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65979666 | ||||||
| chr5:65979812
|
T | A | 1 | a0002c0003t0005g0172 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-57-8823T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65979812 | ||||||
| chr5:65979817
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-8818C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65979817 | ||||||
| chr5:65979818
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-57-8817G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65979818 | ||||||
| chr5:65980030
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-8605T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65980030 | ||||||
| chr5:65980241
|
C | A | 142 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.-57-8394C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65980241 | ||||||
| chr5:65980274
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-8361G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65980274 | ||||||
| chr5:65980583
|
A | G | 1 | a0001c0007t0012g0219 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-57-8052A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65980583 | ||||||
| chr5:65980587
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-8048G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65980587 | ||||||
| chr5:65980644
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-57-7991A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65980644 | ||||||
| chr5:65980650
|
A | G | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-57-7985A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65980650 | ||||||
| chr5:65980722
|
G | GA | 14 | a0002c0003t0002g0208a0002c0003t0005g0199a0005c0006t0002g0229others(11): Show | 14 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-57-7903dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65980722 | |||||
| chr5:65980779
|
A | G | 2 | a0001c0001t0014g0070a0001c0001t0014g0071 | 2 | HG00621.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-57-7856A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65980779 | ||||||
| chr5:65980797
|
T | A | 1 | a0001c0001t0001g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-57-7838T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65980797 | ||||||
| chr5:65980842
|
A | G | 2 | a0001c0001t0028g0092a0004c0005t0004g0017 | 2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-57-7793A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65980842 | ||||||
| chr5:65980929
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-7706T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65980929 | ||||||
| chr5:65981011
|
G | A | 3 | a0001c0007t0012g0218a0001c0007t0012g0219a0001c0007t0012g0220 | 3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-57-7624G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65981011 | ||||||
| chr5:65981034
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-7601C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65981034 | ||||||
| chr5:65981150
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-7485A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65981150 | ||||||
| chr5:65981458
|
A | G | 1 | a0003c0004t0001g0132 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-57-7177A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65981458 | ||||||
| chr5:65981651
|
C | CA | 18 | a0001c0001t0001g0096a0001c0001t0009g0036a0001c0001t0009g0037others(15): Show | 18 | HG01109.hp2 HG01243.hp2 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.-57-6974dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65981651 | |||||
| chr5:65981652
|
A | AAC | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-6982_-57-6981i others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65981652 | |||||
| chr5:65981654
|
A | C | 1 | a0001c0001t0001g0272 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-57-6981A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65981654 | ||||||
| chr5:65981986
|
C | T | 42 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0050others(39): Show | 42 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.-57-6649C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65981986 | ||||||
| chr5:65982170
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-57-6465C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65982170 | ||||||
| chr5:65982282
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-6353G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65982282 | ||||||
| chr5:65982307
|
G | A | 3 | a0003c0004t0001g0132a0003c0004t0001g0141a0003c0004t0027g0139 | 3 | HG01943.hp2 HG01993.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-57-6328G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65982307 | ||||||
| chr5:65982379
|
A | T | 5 | a0001c0001t0006g0147a0001c0001t0006g0148a0001c0001t0006g0149others(2): Show | 5 | HG03098.hp1 HG03486.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57-6256A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65982379 | ||||||
| chr5:65982385
|
A | G | 4 | a0005c0006t0007g0224a0005c0006t0007g0226a0005c0006t0007g0230others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-6250A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65982385 | ||||||
| chr5:65982590
|
G | C | 1 | a0005c0006t0016g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-57-6045G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65982590 | ||||||
| chr5:65982653
|
T | G | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-57-5982T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65982653 | ||||||
| chr5:65982680
|
A | AGACTG | 188 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.-57-5955_-57-5954i others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65982680 | ||||||
| chr5:65982791
|
G | A | 1 | a0003c0004t0001g0271 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-57-5844G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65982791 | ||||||
| chr5:65982872
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-5763G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65982872 | ||||||
| chr5:65982909
|
T | G | 1 | a0004c0005t0004g0009 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-57-5726T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65982909 | ||||||
| chr5:65983159
|
T | C | 1 | a0002c0003t0005g0185 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-57-5476T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65983159 | ||||||
| chr5:65983176
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-57-5459A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65983176 | ||||||
| chr5:65983284
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-5351A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65983284 | ||||||
| chr5:65983602
|
CAACCACT others(13): Show |
C | 3 | a0001c0002t0002g0032a0001c0002t0002g0033a0001c0002t0002g0034 | 3 | HG03017.hp1 HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-57-5032_-57-5013d others(22): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65983602 | ||||||
| chr5:65983613
|
T | G | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-57-5022T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65983613 | ||||||
| chr5:65983709
|
C | G | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-4926C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65983709 | ||||||
| chr5:65983795
|
C | A | 1 | a0001c0007t0012g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-57-4840C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65983795 | ||||||
| chr5:65983795
|
C | T | 1 | a0003c0004t0001g0137 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-57-4840C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65983795 | ||||||
| chr5:65983817
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-4818A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65983817 | ||||||
| chr5:65983927
|
A | G | 2 | a0005c0006t0007g0221a0005c0006t0007g0222 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-57-4708A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65983927 | ||||||
| chr5:65983974
|
C | T | 4 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(1): Show | 4 | HG00735.hp1 HG01069.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-4661C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65983974 | ||||||
| chr5:65983977
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-4658G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65983977 | ||||||
| chr5:65984091
|
A | G | 1 | a0001c0001t0001g0268 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-57-4544A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984091 | ||||||
| chr5:65984094
|
G | T | 3 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0073 | 3 | HG02145.hp1 HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-57-4541G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984094 | ||||||
| chr5:65984140
|
A | ACTGACGT others(24): Show |
16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-4490_-57-4489i others(33): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65984140 | |||||
| chr5:65984293
|
G | A | 2 | a0007c0012t0011g0022a0007c0012t0011g0023 | 2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-57-4342G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984293 | ||||||
| chr5:65984320
|
A | G | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-57-4315A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984320 | ||||||
| chr5:65984377
|
C | T | 3 | a0001c0007t0012g0218a0001c0007t0012g0219a0001c0007t0012g0220 | 3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-57-4258C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984377 | ||||||
| chr5:65984495
|
C | A | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-4140C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984495 | ||||||
| chr5:65984574
|
C | T | 3 | a0001c0007t0012g0218a0001c0007t0012g0219a0001c0007t0012g0220 | 3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-57-4061C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984574 | ||||||
| chr5:65984657
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-57-3978A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984657 | ||||||
| chr5:65984737
|
A | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-3898A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984737 | ||||||
| chr5:65984869
|
C | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-3766C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984869 | ||||||
| chr5:65984900
|
T | TA | 20 | a0001c0001t0001g0069a0001c0001t0001g0076a0001c0001t0001g0266others(17): Show | 20 | HG01167.hp2 HG02056.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-57-3722dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65984900 | |||||
| chr5:65984900
|
TA | T | 6 | a0005c0006t0007g0223a0005c0006t0007g0224a0005c0006t0007g0226others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-3722delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65984900 | |||||
| chr5:65984901
|
A | T | 1 | a0001c0022t0009g0035 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-57-3734A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984901 | ||||||
| chr5:65984912
|
A | C | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-57-3723A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984912 | ||||||
| chr5:65984913
|
A | C | 1 | a0001c0001t0009g0038 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-57-3722A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984913 | ||||||
| chr5:65984915
|
C | T | 1 | a0001c0001t0009g0038 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-57-3720C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984915 | ||||||
| chr5:65984984
|
A | G | 1 | a0001c0001t0024g0158 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-57-3651A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984984 | ||||||
| chr5:65985077
|
A | G | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-57-3558A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985077 | ||||||
| chr5:65985093
|
A | G | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-57-3542A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985093 | ||||||
| chr5:65985098
|
T | G | 6 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(3): Show | 6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-3537T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985098 | ||||||
| chr5:65985124
|
C | T | 1 | a0015c0024t0022g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-57-3511C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985124 | ||||||
| chr5:65985178
|
G | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-3457G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985178 | ||||||
| chr5:65985206
|
G | A | 1 | a0001c0002t0002g0252 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-57-3429G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985206 | ||||||
| chr5:65985241
|
C | T | 3 | a0001c0001t0006g0152a0001c0001t0006g0153a0001c0001t0006g0157 | 3 | HG01891.hp1 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-57-3394C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985241 | ||||||
| chr5:65985422
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-3213T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985422 | ||||||
| chr5:65985620
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-3015C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985620 | ||||||
| chr5:65985670
|
A | G | 12 | a0001c0001t0006g0147a0001c0001t0006g0148a0001c0001t0006g0149others(9): Show | 12 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-57-2965A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985670 | ||||||
| chr5:65985810
|
T | C | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-2825T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985810 | ||||||
| chr5:65985839
|
T | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-2796T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985839 | ||||||
| chr5:65985958
|
A | G | 1 | a0001c0007t0012g0219 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-57-2677A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985958 | ||||||
| chr5:65986231
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-57-2404A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65986231 | ||||||
| chr5:65986512
|
A | T | 6 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(3): Show | 6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-2123A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65986512 | ||||||
| chr5:65986608
|
G | T | 1 | a0001c0007t0012g0219 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-57-2027G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65986608 | ||||||
| chr5:65987105
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-1530C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65987105 | ||||||
| chr5:65987195
|
A | G | 1 | a0015c0024t0022g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-57-1440A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65987195 | ||||||
| chr5:65987367
|
T | TAC | 3 | a0001c0002t0002g0171a0001c0002t0002g0242a0001c0002t0002g0297 | 3 | NA18962.hp1 NA18968.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-57-1241_-57-1240d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987367 | |||||
| chr5:65987367
|
T | TACACAC | 50 | a0001c0001t0024g0158a0002c0003t0002g0202a0002c0003t0002g0203others(47): Show | 50 | HG00280.hp2 HG00408.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.-57-1245_-57-1240d others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987367 | |||||
| chr5:65987367
|
T | TACACACA others(1): Show |
8 | a0001c0002t0002g0296a0002c0003t0003g0196a0002c0003t0003g0282others(5): Show | 8 | HG00438.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57-1247_-57-1240d others(10): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987367 | |||||
| chr5:65987367
|
T | TACACACA others(3): Show |
14 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(11): Show | 14 | HG00738.hp2 HG01081.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-57-1249_-57-1240d others(12): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987367 | |||||
| chr5:65987367
|
T | TACACACA others(5): Show |
10 | a0001c0001t0006g0151a0001c0001t0006g0153a0001c0001t0013g0125others(7): Show | 10 | HG01167.hp2 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-57-1251_-57-1240d others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987367 | |||||
| chr5:65987367
|
T | TACACACA others(7): Show |
59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(56): Show | 59 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.-57-1253_-57-1240d others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987367 | |||||
| chr5:65987367
|
T | TACACACA others(9): Show |
36 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(33): Show | 36 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.-57-1255_-57-1240d others(18): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987367 | |||||
| chr5:65987367
|
T | TACACACA others(11): Show |
31 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(28): Show | 31 | HG00280.hp1 HG00735.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.-57-1257_-57-1240d others(20): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987367 | |||||
| chr5:65987367
|
T | TACACACA others(13): Show |
30 | a0001c0001t0001g0030a0001c0001t0001g0051a0001c0001t0001g0067others(27): Show | 30 | HG00438.hp1 HG01069.hp2 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.-57-1259_-57-1240d others(22): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987367 | |||||
| chr5:65987367
|
T | TACACACA others(15): Show |
5 | a0001c0001t0001g0090a0001c0007t0010g0275a0003c0004t0001g0114others(2): Show | 5 | HG00621.hp2 HG02055.hp2 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57-1261_-57-1240d others(24): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987367 | |||||
| chr5:65987367
|
T | TACACACA others(17): Show |
4 | a0001c0001t0001g0085a0001c0001t0001g0118a0001c0001t0009g0036others(1): Show | 4 | HG03710.hp1 HG03834.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-1263_-57-1240d others(26): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987367 | |||||
| chr5:65987367
|
T | TACACACA others(19): Show |
2 | a0001c0001t0001g0104a0003c0004t0001g0269 | 2 | HG01256.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.-57-1265_-57-1240d others(28): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987367 | |||||
| chr5:65987394
|
A | ACACACAC others(4): Show |
1 | a0001c0001t0001g0266 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-57-1240_-57-1239i others(13): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987394 | |||||
| chr5:65987439
|
A | G | 45 | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0001t0001g0053others(42): Show | 45 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.-57-1196A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65987439 | ||||||
| chr5:65987487
|
A | G | 1 | a0003c0004t0001g0306 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-57-1148A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65987487 | ||||||
| chr5:65987590
|
G | A | 1 | a0015c0024t0022g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-57-1045G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65987590 | ||||||
| chr5:65987610
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-57-1025C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65987610 | ||||||
| chr5:65987722
|
G | A | 1 | a0001c0001t0009g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-57-913G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65987722 | ||||||
| chr5:65987842
|
C | CA | 14 | a0001c0001t0003g0113a0001c0001t0006g0147a0001c0001t0006g0148others(11): Show | 14 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-57-776dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987842 | |||||
| chr5:65987842
|
CAAAA | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-779_-57-776del others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987842 | |||||
| chr5:65988183
|
C | T | 9 | a0001c0002t0002g0289a0001c0002t0002g0290a0001c0002t0002g0293others(6): Show | 9 | HG00408.hp1 HG02165.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57-452C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65988183 | ||||||
| chr5:65988211
|
AG | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-423delG | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65988211 | ||||||
| chr5:65988290
|
T | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0126 | 2 | NA18955.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-57-345T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65988290 | ||||||
| chr5:65988334
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-57-301T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65988334 | ||||||
| chr5:65988374
|
T | TA | 17 | a0002c0003t0003g0282a0004c0005t0004g0007a0004c0005t0004g0008others(14): Show | 17 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-57-248dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65988374 | |||||
| chr5:65988417
|
A | ATG | 10 | a0002c0003t0003g0195a0002c0003t0003g0196a0004c0005t0004g0013others(7): Show | 10 | HG02258.hp1 HG02895.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.-57-201_-57-200dup others(2): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65988417 | |||||
| chr5:65988451
|
A | G | 188 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.-57-184A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65988451 | ||||||
| chr5:65988465
|
CT | C | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-169delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65988465 | ||||||
| chr5:65988557
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-78G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65988557 | ||||||
| chr5:65988605
|
T | G | 1 | a0003c0004t0001g0302 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-57-30T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65988605 | ||||||
| chr5:65988696
|
A | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0111 | 2 | HG00738.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-10+14A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65988696 | ||||||
| chr5:65988931
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0112 | 2 | HG01952.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-10+249C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65988931 | ||||||
| chr5:65988983
|
C | CA | 27 | a0001c0002t0002g0211a0001c0002t0002g0248a0001c0007t0010g0161others(24): Show | 27 | HG01167.hp2 HG01243.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.-10+323dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 65988983 | |||||
| chr5:65988983
|
CA | C | 142 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.-10+323delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 65988983 | |||||
| chr5:65989016
|
G | A | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+334G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65989016 | ||||||
| chr5:65989033
|
C | G | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+351C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65989033 | ||||||
| chr5:65989040
|
TTCTTCTT others(19): Show |
T | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-10+360_-10+385del others(26): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 65989040 | |||||
| chr5:65989471
|
C | T | 1 | a0001c0002t0002g0173 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-10+789C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65989471 | ||||||
| chr5:65989539
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-10+857G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65989539 | ||||||
| chr5:65989648
|
T | C | 3 | a0001c0002t0002g0032a0001c0002t0002g0033a0001c0002t0002g0034 | 3 | HG03017.hp1 HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-10+966T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65989648 | ||||||
| chr5:65989862
|
CCTAA | C | 41 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0050others(38): Show | 41 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-10+1183_-10+1186d others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 65989862 | |||||
| chr5:65990019
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-10+1337T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65990019 | ||||||
| chr5:65990440
|
A | G | 197 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-10+1758A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65990440 | ||||||
| chr5:65990533
|
G | C | 1 | a0001c0002t0002g0286 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-10+1851G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65990533 | ||||||
| chr5:65990540
|
G | GGCACCTG others(5): Show |
16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-10+1861_-10+1862i others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 65990540 | |||||
| chr5:65990582
|
C | T | 3 | a0001c0002t0002g0236a0001c0002t0002g0243a0001c0002t0002g0244 | 3 | HG01256.hp1 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.-10+1900C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65990582 | ||||||
| chr5:65990627
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-10+1945C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65990627 | ||||||
| chr5:65990765
|
A | AT | 9 | a0001c0001t0001g0056a0001c0001t0001g0091a0001c0001t0014g0071others(6): Show | 9 | HG00621.hp1 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9-1932dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 65990765 | |||||
| chr5:65990765
|
AT | A | 17 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(14): Show | 17 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-9-1932delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 65990765 | |||||
| chr5:65990868
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-9-1842A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65990868 | ||||||
| chr5:65990912
|
C | A | 8 | a0001c0002t0002g0173a0001c0002t0002g0210a0001c0002t0002g0211others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9-1798C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65990912 | ||||||
| chr5:65990927
|
A | G | 2 | a0001c0002t0002g0286a0001c0002t0002g0287 | 2 | HG00642.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-9-1783A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65990927 | ||||||
| chr5:65990978
|
A | T | 1 | a0003c0004t0001g0140 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-9-1732A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65990978 | ||||||
| chr5:65990998
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-9-1712T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65990998 | ||||||
| chr5:65991066
|
A | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | NA18954.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-9-1644A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65991066 | ||||||
| chr5:65991114
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-9-1596C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65991114 | ||||||
| chr5:65991432
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-9-1278T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65991432 | ||||||
| chr5:65991509
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-9-1201A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65991509 | ||||||
| chr5:65991670
|
ATAATCTT others(32): Show |
A | 1 | a0003c0004t0027g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-9-1038_-9-1000del others(39): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 65991670 | |||||
| chr5:65991852
|
C | G | 8 | a0001c0002t0002g0173a0001c0002t0002g0210a0001c0002t0002g0211others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9-858C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65991852 | ||||||
| chr5:65991947
|
G | C | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-763G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65991947 | ||||||
| chr5:65992001
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-9-709C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65992001 | ||||||
| chr5:65992028
|
C | T | 1 | a0003c0004t0001g0131 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-9-682C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65992028 | ||||||
| chr5:65992180
|
C | G | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-530C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65992180 | ||||||
| chr5:65992218
|
C | T | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-9-492C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65992218 | ||||||
| chr5:65992243
|
G | A | 1 | a0001c0002t0002g0279 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-9-467G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65992243 | ||||||
| chr5:65992274
|
C | T | 1 | a0001c0021t0001g0101 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-9-436C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65992274 | ||||||
| chr5:65992416
|
G | A | 1 | a0015c0024t0022g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-9-294G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65992416 | ||||||
| chr5:65992963
|
A | G | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.189+56A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65992963 | ||||||
| chr5:65992999
|
A | G | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.189+92A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65992999 | ||||||
| chr5:65993005
|
G | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0085others(4): Show | 7 | NA18954.hp2 NA18955.hp1 NA18999.hp2 others(4): Show |
intron_variant | MODIFIER | c.189+98G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65993005 | ||||||
| chr5:65993232
|
A | T | 6 | a0005c0006t0007g0223a0005c0006t0007g0224a0005c0006t0007g0226others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.189+325A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65993232 | ||||||
| chr5:65993285
|
G | C | 4 | a0005c0006t0007g0224a0005c0006t0007g0226a0005c0006t0007g0230others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+378G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65993285 | ||||||
| chr5:65993377
|
T | C | 5 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(2): Show | 5 | HG01884.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.189+470T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65993377 | ||||||
| chr5:65993589
|
ATATTTAA others(16): Show |
A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.189+683_189+705del others(23): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65993589 | ||||||
| chr5:65993851
|
A | C | 5 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(2): Show | 5 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-896A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65993851 | ||||||
| chr5:65993945
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.190-802T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65993945 | ||||||
| chr5:65994239
|
T | C | 2 | a0005c0006t0007g0221a0005c0006t0007g0222 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.190-508T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65994239 | ||||||
| chr5:65994297
|
G | T | 1 | a0001c0020t0001g0117 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.190-450G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65994297 | ||||||
| chr5:65994404
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.190-343T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65994404 | ||||||
| chr5:65994602
|
G | A | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-145G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65994602 | ||||||
| chr5:65994715
|
A | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.190-32A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65994715 | ||||||
| chr5:65994716
|
A | G | 3 | a0001c0007t0012g0218a0001c0007t0012g0219a0001c0007t0012g0220 | 3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.190-31A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65994716 | ||||||
| chr5:65994885
|
A | G | 6 | a0002c0003t0002g0204a0002c0003t0002g0207a0002c0003t0002g0208others(3): Show | 6 | HG00280.hp2 NA18951.hp2 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.307+21A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65994885 | ||||||
| chr5:65994949
|
TA | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+86delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65994949 | ||||||
| chr5:65995253
|
C | A | 3 | a0001c0001t0001g0272a0001c0001t0013g0124a0001c0001t0013g0125 | 3 | HG01261.hp2 HG04115.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.307+389C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65995253 | ||||||
| chr5:65995267
|
T | A | 4 | a0005c0006t0007g0224a0005c0006t0007g0226a0005c0006t0007g0230others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.307+403T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65995267 | ||||||
| chr5:65995373
|
AT | A | 20 | a0001c0001t0001g0093a0002c0003t0003g0195a0002c0003t0008g0179others(17): Show | 20 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.307+525delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65995373 | |||||
| chr5:65995373
|
ATT | A | 152 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.307+524_307+525del others(2): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65995373 | |||||
| chr5:65995373
|
ATTTT | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+522_307+525del others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65995373 | |||||
| chr5:65995517
|
C | G | 2 | a0005c0006t0007g0221a0005c0006t0007g0222 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.307+653C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65995517 | ||||||
| chr5:65995581
|
T | C | 2 | a0009c0010t0002g0291a0009c0010t0002g0292 | 2 | NA18970.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.307+717T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65995581 | ||||||
| chr5:65995974
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+1110T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65995974 | ||||||
| chr5:65996011
|
A | T | 19 | a0002c0003t0003g0181a0002c0003t0003g0182a0002c0003t0003g0183others(16): Show | 19 | HG01081.hp1 HG01257.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.307+1147A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65996011 | ||||||
| chr5:65996226
|
A | AT | 45 | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0001t0001g0053others(42): Show | 45 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.307+1372dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65996226 | |||||
| chr5:65996244
|
G | GT | 12 | a0001c0002t0002g0209a0001c0002t0002g0235a0001c0002t0002g0288others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.307+1401dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65996244 | |||||
| chr5:65996244
|
GT | G | 40 | a0001c0001t0001g0028a0001c0001t0001g0041a0001c0001t0001g0042others(37): Show | 40 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.307+1401delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65996244 | |||||
| chr5:65996244
|
GTT | G | 124 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.307+1400_307+1401d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65996244 | |||||
| chr5:65996244
|
GTTT | G | 7 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(4): Show | 7 | HG02080.hp2 NA18940.hp2 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.307+1399_307+1401d others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65996244 | |||||
| chr5:65996255
|
T | TTTG | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+1393_307+1394i others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65996255 | |||||
| chr5:65996260
|
T | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+1396T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65996260 | ||||||
| chr5:65996473
|
G | C | 1 | a0001c0002t0019g0298 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.307+1609G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65996473 | ||||||
| chr5:65996519
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.307+1655A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65996519 | ||||||
| chr5:65996797
|
T | C | 6 | a0005c0006t0007g0223a0005c0006t0007g0224a0005c0006t0007g0226others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.307+1933T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65996797 | ||||||
| chr5:65996840
|
A | C | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.307+1976A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65996840 | ||||||
| chr5:65997013
|
A | AT | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+2153dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65997013 | |||||
| chr5:65997050
|
G | A | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.307+2186G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997050 | ||||||
| chr5:65997295
|
G | A | 1 | a0005c0006t0007g0026 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.307+2431G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997295 | ||||||
| chr5:65997426
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+2562G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997426 | ||||||
| chr5:65997477
|
C | T | 1 | a0001c0002t0002g0237 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.307+2613C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997477 | ||||||
| chr5:65997598
|
T | C | 2 | a0005c0006t0007g0221a0005c0006t0007g0222 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.307+2734T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997598 | ||||||
| chr5:65997621
|
A | G | 1 | a0001c0001t0001g0112 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.307+2757A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997621 | ||||||
| chr5:65997633
|
C | T | 2 | a0001c0002t0002g0032a0015c0024t0022g0146 | 2 | HG03098.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.307+2769C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997633 | ||||||
| chr5:65997634
|
G | A | 141 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.307+2770G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997634 | ||||||
| chr5:65997717
|
G | A | 2 | a0005c0006t0007g0221a0005c0006t0007g0222 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.307+2853G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997717 | ||||||
| chr5:65997721
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+2857G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997721 | ||||||
| chr5:65997779
|
A | G | 1 | a0004c0005t0004g0019 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.307+2915A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997779 | ||||||
| chr5:65997841
|
A | G | 1 | a0005c0006t0007g0222 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307+2977A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997841 | ||||||
| chr5:65997927
|
T | TAC | 7 | a0001c0001t0001g0054a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 7 | HG00735.hp2 HG02257.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.307+3083_307+3084d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65997927 | |||||
| chr5:65997927
|
T | TACAC | 3 | a0005c0006t0007g0221a0005c0006t0007g0222a0012c0016t0007g0228 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.307+3081_307+3084d others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65997927 | |||||
| chr5:65997927
|
TACACAC | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+3079_307+3084d others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65997927 | |||||
| chr5:65997965
|
C | T | 1 | a0001c0007t0012g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.307+3101C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997965 | ||||||
| chr5:65997966
|
G | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+3102G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997966 | ||||||
| chr5:65998086
|
G | A | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.307+3222G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65998086 | ||||||
| chr5:65998214
|
C | G | 4 | a0005c0006t0007g0224a0005c0006t0007g0226a0005c0006t0007g0230others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.307+3350C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65998214 | ||||||
| chr5:65998223
|
C | CA | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+3368dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65998223 | |||||
| chr5:65998231
|
A | T | 27 | a0001c0001t0001g0103a0001c0001t0006g0147a0001c0001t0006g0148others(24): Show | 27 | HG01884.hp1 HG01952.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.307+3367A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65998231 | ||||||
| chr5:65998232
|
A | T | 1 | a0001c0002t0002g0296 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.307+3368A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65998232 | ||||||
| chr5:65998233
|
T | A | 16 | a0001c0001t0001g0135a0002c0003t0008g0174a0002c0003t0008g0175others(13): Show | 16 | HG00408.hp2 HG01109.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+3369T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65998233 | ||||||
| chr5:65998411
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+3547T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65998411 | ||||||
| chr5:65998522
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+3658A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65998522 | ||||||
| chr5:65998698
|
A | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+3834A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65998698 | ||||||
| chr5:65998710
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+3846G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65998710 | ||||||
| chr5:65998781
|
C | T | 20 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(17): Show | 20 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.307+3917C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65998781 | ||||||
| chr5:65998894
|
C | CA | 12 | a0001c0002t0002g0244a0001c0002t0002g0246a0001c0002t0002g0256others(9): Show | 12 | HG00673.hp2 HG02004.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.307+4055dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65998894 | |||||
| chr5:65998894
|
CA | C | 129 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0042others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.307+4055delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65998894 | |||||
| chr5:65998894
|
CAA | C | 15 | a0001c0001t0001g0031a0001c0001t0001g0051a0001c0001t0001g0079others(12): Show | 15 | HG01943.hp2 HG02273.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.307+4054_307+4055d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65998894 | |||||
| chr5:65998894
|
CAAAA | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+4052_307+4055d others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65998894 | |||||
| chr5:65999188
|
G | GTGAA | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+4324_307+4325i others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65999188 | ||||||
| chr5:65999258
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.307+4394C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65999258 | ||||||
| chr5:65999420
|
G | A | 1 | a0001c0001t0001g0112 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.307+4556G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65999420 | ||||||
| chr5:65999456
|
G | T | 10 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(7): Show | 10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.307+4592G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65999456 | ||||||
| chr5:65999508
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+4644T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65999508 | ||||||
| chr5:65999527
|
A | G | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.307+4663A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65999527 | ||||||
| chr5:65999726
|
A | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+4862A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65999726 | ||||||
| chr5:65999830
|
T | C | 1 | a0001c0001t0001g0159 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.307+4966T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65999830 | ||||||
| chr5:65999934
|
T | C | 3 | a0001c0001t0001g0272a0001c0001t0013g0124a0001c0001t0013g0125 | 3 | HG01261.hp2 HG04115.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.307+5070T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65999934 | ||||||
| chr5:65999966
|
T | C | 4 | a0005c0006t0007g0224a0005c0006t0007g0226a0005c0006t0007g0230others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.307+5102T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65999966 | ||||||
| chr5:66000487
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+5623T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66000487 | ||||||
| chr5:66000789
|
C | G | 5 | a0001c0002t0002g0289a0001c0002t0002g0293a0001c0002t0002g0294others(2): Show | 5 | HG02165.hp1 NA18969.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.307+5925C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66000789 | ||||||
| chr5:66000930
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+6066C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66000930 | ||||||
| chr5:66000933
|
A | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+6069A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66000933 | ||||||
| chr5:66001000
|
A | G | 1 | a0002c0003t0002g0202 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.307+6136A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66001000 | ||||||
| chr5:66001052
|
C | G | 1 | a0003c0004t0027g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.307+6188C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66001052 | ||||||
| chr5:66001122
|
A | G | 1 | a0001c0001t0020g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.307+6258A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66001122 | ||||||
| chr5:66001148
|
T | A | 3 | a0001c0007t0012g0218a0001c0007t0012g0219a0001c0007t0012g0220 | 3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.307+6284T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66001148 | ||||||
| chr5:66001185
|
T | A | 1 | a0002c0003t0002g0207 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.307+6321T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66001185 | ||||||
| chr5:66001217
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+6353C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66001217 | ||||||
| chr5:66001229
|
A | C | 1 | a0005c0006t0007g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.307+6365A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66001229 | ||||||
| chr5:66001515
|
A | G | 8 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(5): Show | 8 | HG02258.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.307+6651A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66001515 | ||||||
| chr5:66001642
|
A | T | 1 | a0005c0006t0007g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.307+6778A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66001642 | ||||||
| chr5:66001855
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+6991A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66001855 | ||||||
| chr5:66002012
|
C | T | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.307+7148C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66002012 | ||||||
| chr5:66002205
|
C | T | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.307+7341C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66002205 | ||||||
| chr5:66002429
|
TTC | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+7567_307+7568d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66002429 | |||||
| chr5:66002501
|
C | A | 1 | a0001c0002t0002g0295 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.307+7637C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66002501 | ||||||
| chr5:66002698
|
G | GA | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+7838dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66002698 | |||||
| chr5:66002932
|
T | C | 2 | a0008c0011t0011g0024a0008c0011t0011g0025 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.307+8068T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66002932 | ||||||
| chr5:66003027
|
C | T | 2 | a0004c0005t0004g0019a0004c0014t0004g0018 | 2 | HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.307+8163C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66003027 | ||||||
| chr5:66003136
|
C | T | 1 | a0003c0004t0001g0134 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.307+8272C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66003136 | ||||||
| chr5:66003356
|
T | TA | 16 | a0001c0001t0001g0274a0004c0005t0004g0007a0004c0005t0004g0008others(13): Show | 16 | HG00438.hp1 HG01167.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+8502dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66003356 | |||||
| chr5:66003662
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.308-8387G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66003662 | ||||||
| chr5:66003798
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-8251G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66003798 | ||||||
| chr5:66003887
|
C | G | 154 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.308-8162C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66003887 | ||||||
| chr5:66003923
|
C | CT | 22 | a0001c0001t0001g0111a0001c0002t0002g0032a0001c0002t0002g0033others(19): Show | 22 | HG01167.hp2 HG01433.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.308-8101dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66003923 | |||||
| chr5:66003923
|
C | CTT | 7 | a0002c0003t0002g0204a0002c0003t0002g0216a0004c0005t0004g0008others(4): Show | 7 | HG00280.hp2 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.308-8102_308-8101d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66003923 | |||||
| chr5:66003923
|
CT | C | 93 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0030others(90): Show | 93 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.308-8101delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66003923 | |||||
| chr5:66003923
|
CTT | C | 22 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0059others(19): Show | 22 | HG00738.hp2 HG01109.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.308-8102_308-8101d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66003923 | |||||
| chr5:66003923
|
CTTT | C | 8 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(5): Show | 8 | HG01243.hp2 HG02257.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.308-8103_308-8101d others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66003923 | |||||
| chr5:66003923
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0007t0012g0219 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.308-8111_308-8101d others(13): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66003923 | |||||
| chr5:66003948
|
T | A | 1 | a0001c0001t0001g0096 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.308-8101T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66003948 | ||||||
| chr5:66003978
|
T | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-8071T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66003978 | ||||||
| chr5:66004070
|
T | C | 1 | a0002c0003t0005g0176 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.308-7979T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004070 | ||||||
| chr5:66004103
|
A | AT | 52 | a0001c0001t0001g0059a0001c0001t0013g0124a0001c0007t0010g0161others(49): Show | 52 | HG00408.hp2 HG01081.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.308-7926dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66004103 | |||||
| chr5:66004103
|
AT | A | 20 | a0001c0001t0001g0119a0001c0002t0002g0285a0001c0002t0002g0293others(17): Show | 20 | HG01069.hp2 HG01109.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.308-7926delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66004103 | |||||
| chr5:66004103
|
ATTTTTTT others(5): Show |
A | 1 | a0005c0006t0007g0026 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.308-7937_308-7926d others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66004103 | |||||
| chr5:66004139
|
G | A | 1 | a0001c0002t0002g0209 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.308-7910G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004139 | ||||||
| chr5:66004189
|
G | C | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.308-7860G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004189 | ||||||
| chr5:66004225
|
C | T | 8 | a0001c0002t0002g0173a0001c0002t0002g0210a0001c0002t0002g0211others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.308-7824C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004225 | ||||||
| chr5:66004379
|
CGT | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-7660_308-7659d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66004379 | |||||
| chr5:66004389
|
T | C | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.308-7660T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004389 | ||||||
| chr5:66004391
|
C | T | 1 | a0001c0002t0002g0211 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.308-7658C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004391 | ||||||
| chr5:66004395
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-7654C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004395 | ||||||
| chr5:66004399
|
T | C | 251 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.308-7650T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004399 | ||||||
| chr5:66004401
|
C | T | 2 | a0001c0001t0001g0086a0001c0007t0012g0219 | 2 | HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.308-7648C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004401 | ||||||
| chr5:66004402
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.308-7647G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004402 | ||||||
| chr5:66004434
|
C | T | 2 | a0001c0001t0006g0149a0001c0001t0006g0151 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.308-7615C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004434 | ||||||
| chr5:66004639
|
A | G | 3 | a0001c0002t0002g0032a0001c0002t0002g0033a0001c0002t0002g0034 | 3 | HG03017.hp1 HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.308-7410A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004639 | ||||||
| chr5:66004680
|
T | C | 1 | a0001c0020t0001g0117 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.308-7369T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004680 | ||||||
| chr5:66004689
|
C | T | 4 | a0005c0006t0007g0224a0005c0006t0007g0226a0005c0006t0007g0230others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.308-7360C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004689 | ||||||
| chr5:66004716
|
T | G | 1 | a0001c0002t0002g0256 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.308-7333T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004716 | ||||||
| chr5:66004790
|
T | A | 8 | a0001c0002t0002g0235a0001c0002t0002g0242a0001c0002t0002g0245others(5): Show | 8 | NA18612.hp1 NA18949.hp2 NA18975.hp1 others(5): Show |
intron_variant | MODIFIER | c.308-7259T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004790 | ||||||
| chr5:66005049
|
G | A | 2 | a0001c0007t0010g0162a0001c0007t0010g0165 | 2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.308-7000G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005049 | ||||||
| chr5:66005078
|
CTGT | C | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.308-6970_308-6968d others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005078 | ||||||
| chr5:66005084
|
A | G | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.308-6965A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005084 | ||||||
| chr5:66005085
|
TA | T | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.308-6963delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005085 | ||||||
| chr5:66005240
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-6809C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005240 | ||||||
| chr5:66005500
|
C | T | 1 | a0001c0002t0002g0239 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.308-6549C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005500 | ||||||
| chr5:66005643
|
G | A | 1 | a0001c0002t0002g0209 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.308-6406G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005643 | ||||||
| chr5:66005734
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-6315A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005734 | ||||||
| chr5:66005795
|
A | G | 1 | a0001c0001t0001g0234 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.308-6254A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005795 | ||||||
| chr5:66005835
|
C | A | 6 | a0005c0006t0007g0223a0005c0006t0007g0224a0005c0006t0007g0226others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.308-6214C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005835 | ||||||
| chr5:66005935
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-6114A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005935 | ||||||
| chr5:66005951
|
G | A | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.308-6098G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005951 | ||||||
| chr5:66005993
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-6056A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005993 | ||||||
| chr5:66006124
|
G | A | 10 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(7): Show | 10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.308-5925G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006124 | ||||||
| chr5:66006259
|
C | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-5790C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006259 | ||||||
| chr5:66006343
|
T | G | 1 | a0001c0002t0002g0209 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.308-5706T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006343 | ||||||
| chr5:66006381
|
C | T | 1 | a0005c0006t0007g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.308-5668C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006381 | ||||||
| chr5:66006518
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-5531A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006518 | ||||||
| chr5:66006534
|
T | C | 1 | a0001c0002t0002g0252 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.308-5515T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006534 | ||||||
| chr5:66006617
|
T | C | 1 | a0001c0001t0006g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.308-5432T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006617 | ||||||
| chr5:66006636
|
T | C | 1 | a0001c0001t0006g0154 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.308-5413T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006636 | ||||||
| chr5:66006642
|
T | C | 1 | a0001c0001t0006g0154 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.308-5407T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006642 | ||||||
| chr5:66006868
|
G | A | 23 | a0003c0004t0001g0132a0003c0004t0027g0139a0004c0005t0004g0007others(20): Show | 23 | HG01167.hp2 HG01884.hp1 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.308-5181G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006868 | ||||||
| chr5:66006903
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.308-5146A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006903 | ||||||
| chr5:66006917
|
T | C | 6 | a0005c0006t0007g0223a0005c0006t0007g0224a0005c0006t0007g0226others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.308-5132T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006917 | ||||||
| chr5:66006990
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-5059T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006990 | ||||||
| chr5:66006991
|
A | T | 53 | a0002c0003t0002g0202a0002c0003t0002g0203a0002c0003t0002g0204others(50): Show | 53 | HG00280.hp2 HG00408.hp2 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.308-5058A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006991 | ||||||
| chr5:66007000
|
G | C | 3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079 | 3 | NA18946.hp1 NA18969.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.308-5049G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66007000 | ||||||
| chr5:66007002
|
A | AC | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.308-5047_308-5046i others(3): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66007002 | ||||||
| chr5:66007009
|
T | TA | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-5039dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66007009 | |||||
| chr5:66007012
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.308-5037C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66007012 | ||||||
| chr5:66007056
|
G | T | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.308-4993G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66007056 | ||||||
| chr5:66007262
|
C | G | 1 | a0003c0004t0001g0306 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.308-4787C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66007262 | ||||||
| chr5:66007334
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-4715A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66007334 | ||||||
| chr5:66007361
|
G | T | 171 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.308-4688G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66007361 | ||||||
| chr5:66007403
|
C | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-4646C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66007403 | ||||||
| chr5:66007412
|
G | T | 1 | a0014c0023t0001g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.308-4637G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66007412 | ||||||
| chr5:66007426
|
ATATACC | A | 196 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.308-4614_308-4609d others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66007426 | |||||
| chr5:66007540
|
G | A | 6 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(3): Show | 6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.308-4509G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66007540 | ||||||
| chr5:66007546
|
T | TA | 11 | a0001c0001t0006g0147a0001c0001t0006g0148a0001c0001t0006g0149others(8): Show | 11 | HG01109.hp2 HG02451.hp1 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.308-4489dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66007546 | |||||
| chr5:66007546
|
TA | T | 92 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0041others(89): Show | 92 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.308-4489delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66007546 | |||||
| chr5:66007547
|
A | T | 1 | a0005c0006t0002g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.308-4502A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66007547 | ||||||
| chr5:66007549
|
A | T | 1 | a0003c0004t0001g0306 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.308-4500A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66007549 | ||||||
| chr5:66008185
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-3864G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66008185 | ||||||
| chr5:66008264
|
A | G | 1 | a0001c0001t0013g0124 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.308-3785A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66008264 | ||||||
| chr5:66008280
|
G | A | 1 | a0002c0003t0003g0300 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.308-3769G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66008280 | ||||||
| chr5:66008403
|
T | C | 2 | a0001c0002t0002g0255a0001c0002t0002g0260 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.308-3646T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66008403 | ||||||
| chr5:66008416
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.308-3633C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66008416 | ||||||
| chr5:66008488
|
AAAT | A | 3 | a0001c0001t0001g0093a0001c0001t0001g0104a0001c0001t0001g0116 | 3 | HG01256.hp2 HG02004.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.308-3556_308-3554d others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66008488 | |||||
| chr5:66008562
|
G | A | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.308-3487G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66008562 | ||||||
| chr5:66008833
|
G | A | 2 | a0002c0003t0003g0166a0002c0003t0003g0168 | 2 | HG01433.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.308-3216G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66008833 | ||||||
| chr5:66008869
|
A | G | 6 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(3): Show | 6 | HG02572.hp2 HG02717.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.308-3180A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66008869 | ||||||
| chr5:66008915
|
A | T | 3 | a0001c0001t0006g0154a0001c0001t0006g0155a0001c0001t0006g0156 | 3 | HG00738.hp2 HG01884.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.308-3134A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66008915 | ||||||
| chr5:66009178
|
C | T | 10 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(7): Show | 10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.308-2871C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66009178 | ||||||
| chr5:66009741
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-2308T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66009741 | ||||||
| chr5:66010068
|
A | G | 1 | a0014c0023t0001g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.308-1981A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66010068 | ||||||
| chr5:66010283
|
G | A | 1 | a0002c0003t0005g0172 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.308-1766G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66010283 | ||||||
| chr5:66010318
|
T | C | 18 | a0001c0007t0010g0163a0001c0007t0010g0164a0004c0005t0004g0007others(15): Show | 18 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.308-1731T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66010318 | ||||||
| chr5:66010350
|
C | CATG | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-1692_308-1690d others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66010350 | |||||
| chr5:66010627
|
T | TATATG | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-1417_308-1413d others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66010627 | |||||
| chr5:66010652
|
T | G | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.308-1397T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66010652 | ||||||
| chr5:66010777
|
T | C | 2 | a0005c0006t0002g0229a0005c0006t0002g0263 | 2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.308-1272T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66010777 | ||||||
| chr5:66010981
|
AT | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-1065delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66010981 | |||||
| chr5:66011172
|
A | G | 2 | a0005c0006t0007g0221a0005c0006t0007g0222 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.308-877A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66011172 | ||||||
| chr5:66011309
|
CTG | C | 4 | a0001c0007t0010g0162a0001c0007t0010g0163a0001c0007t0010g0164others(1): Show | 4 | HG02109.hp2 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.308-738_308-737del others(2): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66011309 | |||||
| chr5:66011371
|
T | A | 19 | a0002c0003t0003g0181a0002c0003t0003g0182a0002c0003t0003g0183others(16): Show | 19 | HG01081.hp1 HG01257.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.308-678T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66011371 | ||||||
| chr5:66011517
|
G | A | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.308-532G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66011517 | ||||||
| chr5:66011521
|
C | G | 6 | a0001c0001t0009g0036a0001c0001t0009g0037a0001c0001t0009g0038others(3): Show | 6 | HG03710.hp1 NA18961.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.308-528C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66011521 | ||||||
| chr5:66011522
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.308-527T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66011522 | ||||||
| chr5:66011660
|
G | C | 300 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(297): Show | 300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.308-389G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66011660 | ||||||
| chr5:66011717
|
CT | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-323delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66011717 | |||||
| chr5:66011726
|
T | A | 5 | a0001c0001t0001g0041a0001c0001t0001g0093a0001c0001t0001g0104others(2): Show | 5 | HG01256.hp2 HG02004.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.308-323T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66011726 | ||||||
| chr5:66011760
|
C | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-289C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66011760 | ||||||
| chr5:66012148
|
T | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | NA18991.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.386+21T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66012148 | ||||||
| chr5:66012227
|
C | G | 82 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0031others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.386+100C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66012227 | ||||||
| chr5:66012239
|
C | T | 7 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.386+112C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66012239 | ||||||
| chr5:66012481
|
T | TAAAG | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.386+354_386+355ins others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66012481 | ||||||
| chr5:66012639
|
C | T | 1 | a0002c0003t0003g0283 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.386+512C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66012639 | ||||||
| chr5:66012699
|
A | G | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.386+572A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66012699 | ||||||
| chr5:66012776
|
A | T | 6 | a0005c0006t0007g0223a0005c0006t0007g0224a0005c0006t0007g0226others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.386+649A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66012776 | ||||||
| chr5:66012856
|
C | T | 1 | a0001c0015t0029g0258 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.387-693C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66012856 | ||||||
| chr5:66012972
|
A | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0054 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.387-577A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66012972 | ||||||
| chr5:66013080
|
T | G | 1 | a0001c0001t0006g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.387-469T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66013080 | ||||||
| chr5:66013112
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.387-437T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66013112 | ||||||
| chr5:66013120
|
A | G | 8 | a0001c0002t0002g0173a0001c0002t0002g0210a0001c0002t0002g0211others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.387-429A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66013120 | ||||||
| chr5:66013311
|
T | G | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.387-238T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66013311 | ||||||
| chr5:66013433
|
A | T | 1 | a0001c0002t0002g0250 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.387-116A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66013433 | ||||||
| chr5:66013723
|
A | G | 1 | a0001c0001t0006g0148 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.476+85A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 6/25 | chr5 | 66013723 | ||||||
| chr5:66013781
|
G | C | 194 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.476+143G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 6/25 | chr5 | 66013781 | ||||||
| chr5:66014005
|
T | C | 2 | a0005c0006t0007g0221a0005c0006t0007g0222 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.476+367T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 6/25 | chr5 | 66014005 | ||||||
| chr5:66014014
|
G | A | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.476+376G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 6/25 | chr5 | 66014014 | ||||||
| chr5:66014176
|
A | G | 7 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.477-493A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 6/25 | chr5 | 66014176 | ||||||
| chr5:66014258
|
A | G | 3 | a0001c0007t0012g0218a0001c0007t0012g0219a0001c0007t0012g0220 | 3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.477-411A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 6/25 | chr5 | 66014258 | ||||||
| chr5:66014541
|
T | C | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.477-128T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 6/25 | chr5 | 66014541 | ||||||
| chr5:66014563
|
G | A | 1 | a0001c0001t0006g0155 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.477-106G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 6/25 | chr5 | 66014563 | ||||||
| chr5:66014577
|
A | T | 1 | a0003c0004t0001g0306 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.477-92A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 6/25 | chr5 | 66014577 | ||||||
| chr5:66014649
|
AT | A | 28 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(25): Show | 28 | HG01167.hp2 HG01243.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.477-10delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 66014649 | |||||
| chr5:66014886
|
G | T | 1 | a0014c0023t0001g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.533+161G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66014886 | ||||||
| chr5:66015026
|
A | G | 1 | a0001c0002t0002g0279 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.533+301A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66015026 | ||||||
| chr5:66015114
|
C | G | 1 | a0005c0006t0007g0223 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.533+389C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66015114 | ||||||
| chr5:66015143
|
A | G | 3 | a0001c0007t0012g0218a0001c0007t0012g0219a0001c0007t0012g0220 | 3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.533+418A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66015143 | ||||||
| chr5:66015389
|
C | CAA | 287 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.533+665_533+666dup others(2): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66015389 | |||||
| chr5:66015714
|
A | G | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.533+989A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66015714 | ||||||
| chr5:66015902
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.533+1177T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66015902 | ||||||
| chr5:66016157
|
T | C | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.533+1432T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016157 | ||||||
| chr5:66016254
|
A | G | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.533+1529A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016254 | ||||||
| chr5:66016300
|
G | C | 1 | a0001c0001t0001g0272 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.533+1575G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016300 | ||||||
| chr5:66016322
|
A | G | 1 | a0001c0001t0013g0124 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.533+1597A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016322 | ||||||
| chr5:66016353
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.533+1628C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016353 | ||||||
| chr5:66016359
|
T | G | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.533+1634T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016359 | ||||||
| chr5:66016449
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.533+1724C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016449 | ||||||
| chr5:66016582
|
C | G | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.533+1857C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016582 | ||||||
| chr5:66016615
|
C | CT | 12 | a0001c0002t0002g0215a0004c0005t0004g0013a0004c0005t0004g0014others(9): Show | 12 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.533+1906dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66016615 | |||||
| chr5:66016615
|
C | CTT | 6 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(3): Show | 6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.533+1905_533+1906d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66016615 | |||||
| chr5:66016615
|
CT | C | 139 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0028others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.533+1906delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66016615 | |||||
| chr5:66016637
|
G | A | 1 | a0001c0002t0002g0293 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.533+1912G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016637 | ||||||
| chr5:66016750
|
A | G | 1 | a0016c0013t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.533+2025A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016750 | ||||||
| chr5:66016821
|
G | A | 2 | a0001c0007t0010g0161a0001c0007t0010g0275 | 2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.533+2096G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016821 | ||||||
| chr5:66016835
|
G | A | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.533+2110G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016835 | ||||||
| chr5:66016845
|
C | T | 1 | a0001c0001t0024g0158 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.533+2120C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016845 | ||||||
| chr5:66016857
|
C | T | 1 | a0003c0004t0001g0141 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.533+2132C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016857 | ||||||
| chr5:66016866
|
C | T | 1 | a0004c0005t0004g0009 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.533+2141C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016866 | ||||||
| chr5:66016916
|
G | A | 1 | a0003c0004t0001g0136 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.533+2191G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016916 | ||||||
| chr5:66017098
|
C | T | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.533+2373C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66017098 | ||||||
| chr5:66017339
|
C | A | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.533+2614C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66017339 | ||||||
| chr5:66017436
|
A | AT | 12 | a0001c0001t0006g0147a0001c0001t0006g0148a0001c0001t0006g0149others(9): Show | 12 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.533+2717dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66017436 | |||||
| chr5:66017518
|
AT | A | 169 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.533+2810delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66017518 | |||||
| chr5:66017518
|
ATTT | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.533+2808_533+2810d others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66017518 | |||||
| chr5:66017562
|
A | G | 2 | a0005c0006t0007g0223a0005c0006t0016g0299 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.533+2837A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66017562 | ||||||
| chr5:66017654
|
G | GT | 6 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(3): Show | 6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.533+2935dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66017654 | |||||
| chr5:66017685
|
A | G | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.533+2960A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66017685 | ||||||
| chr5:66017779
|
A | G | 3 | a0001c0007t0012g0218a0001c0007t0012g0219a0001c0007t0012g0220 | 3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.533+3054A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66017779 | ||||||
| chr5:66017888
|
T | C | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.533+3163T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66017888 | ||||||
| chr5:66018061
|
G | A | 154 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.534-3261G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018061 | ||||||
| chr5:66018073
|
A | T | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.534-3249A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018073 | ||||||
| chr5:66018404
|
G | T | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.534-2918G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018404 | ||||||
| chr5:66018441
|
A | AATATAAT others(26): Show |
1 | a0001c0002t0002g0217 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.534-2875_534-2843d others(35): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018441 | |||||
| chr5:66018443
|
TATAATAT others(109): Show |
T | 1 | a0014c0023t0001g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.534-2875_534-2760d others(2): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018443 | |||||
| chr5:66018447
|
A | T | 1 | a0001c0002t0002g0254 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.534-2875A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018447 | ||||||
| chr5:66018447
|
ATATATAT others(26): Show |
A | 1 | a0001c0002t0002g0294 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.534-2835_534-2803d others(35): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018447 | |||||
| chr5:66018447
|
ATATATAT others(146): Show |
A | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.534-2867_534-2715d others(2): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018447 | |||||
| chr5:66018448
|
T | A | 1 | a0001c0002t0002g0254 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.534-2874T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018448 | ||||||
| chr5:66018449
|
A | T | 1 | a0001c0002t0002g0254 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.534-2873A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018449 | ||||||
| chr5:66018452
|
TATTATAT others(40): Show |
T | 1 | a0005c0006t0016g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.534-2869_534-2823d others(49): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018452 | ||||||
| chr5:66018454
|
T | TTATATTA others(80): Show |
1 | a0001c0001t0001g0109 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.534-2844_534-2843i others(89): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018454 | |||||
| chr5:66018459
|
T | TAATATAA others(116): Show |
1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.534-2863_534-2862i others(125): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018459 | ||||||
| chr5:66018460
|
TATATA | T | 4 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(1): Show | 4 | NA18999.hp2 NA19003.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.534-2856_534-2852d others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018460 | |||||
| chr5:66018466
|
A | ATATATAT | 69 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0032others(66): Show | 69 | HG00280.hp2 HG00408.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.534-2836_534-2830d others(9): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018466 | |||||
| chr5:66018466
|
A | ATATATAT others(7): Show |
6 | a0001c0002t0002g0290a0001c0002t0002g0293a0001c0002t0002g0295others(3): Show | 6 | HG00408.hp1 HG03704.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.534-2843_534-2830d others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018466 | |||||
| chr5:66018466
|
A | ATATATAT others(14): Show |
2 | a0001c0002t0002g0296a0001c0002t0002g0297 | 2 | HG00438.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.534-2850_534-2830d others(23): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018466 | |||||
| chr5:66018466
|
A | ATATATAT others(40): Show |
1 | a0001c0002t0002g0288 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.534-2830_534-2829i others(49): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018466 | |||||
| chr5:66018466
|
A | ATATATAT others(19): Show |
1 | a0002c0003t0003g0198 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.534-2844_534-2843i others(28): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018466 | |||||
| chr5:66018466
|
A | T | 3 | a0001c0002t0002g0254a0002c0003t0003g0167a0005c0006t0007g0223 | 3 | HG02258.hp2 NA18957.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.534-2856A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018466 | ||||||
| chr5:66018466
|
ATATATAT others(7): Show |
A | 2 | a0001c0001t0001g0085a0001c0001t0001g0118 | 2 | HG03834.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.534-2843_534-2830d others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018466 | |||||
| chr5:66018468
|
ATATATTA others(12): Show |
A | 1 | a0005c0006t0015g0225 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.534-2842_534-2824d others(21): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018468 | |||||
| chr5:66018468
|
ATATATTA others(52): Show |
A | 5 | a0005c0006t0007g0221a0005c0006t0007g0222a0005c0006t0007g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.534-2842_534-2784d others(61): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018468 | |||||
| chr5:66018473
|
T | TTATATAT others(45): Show |
3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046 | 3 | HG02572.hp2 HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.534-2836_534-2835i others(54): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018473 | |||||
| chr5:66018473
|
T | TTATATTA others(5): Show |
9 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0078others(6): Show | 9 | HG01978.hp1 HG03098.hp1 HG03540.hp1 others(6): Show |
intron_variant | MODIFIER | c.534-2844_534-2843i others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018473 | |||||
| chr5:66018473
|
T | TTATATTA others(31): Show |
1 | a0001c0001t0014g0071 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.534-2844_534-2843i others(40): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018473 | |||||
| chr5:66018473
|
T | TTATATTA others(40): Show |
1 | a0001c0001t0001g0082 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.534-2844_534-2843i others(49): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018473 | |||||
| chr5:66018473
|
T | TTATATTA others(31): Show |
27 | a0001c0001t0001g0030a0001c0001t0001g0050a0001c0001t0001g0051others(24): Show | 27 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.534-2844_534-2843i others(40): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018473 | |||||
| chr5:66018473
|
T | TTATATTA others(45): Show |
9 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(6): Show | 9 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.534-2844_534-2843i others(54): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018473 | |||||
| chr5:66018473
|
T | TTATATTA others(45): Show |
3 | a0001c0001t0001g0060a0001c0001t0013g0124a0001c0020t0001g0117 | 3 | HG01261.hp2 HG02145.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.534-2844_534-2843i others(54): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018473 | |||||
| chr5:66018473
|
T | TTATATTA others(57): Show |
1 | a0001c0001t0001g0041 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.534-2844_534-2843i others(66): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018473 | |||||
| chr5:66018473
|
T | TTATATTA others(59): Show |
9 | a0001c0001t0001g0055a0001c0001t0001g0080a0001c0001t0001g0081others(6): Show | 9 | HG01256.hp2 HG02647.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.534-2844_534-2843i others(68): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018473 | |||||
| chr5:66018473
|
T | TTATATTA others(66): Show |
3 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0267 | 3 | HG02056.hp1 NA18954.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.534-2844_534-2843i others(75): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018473 | |||||
| chr5:66018473
|
T | TTATATTA others(94): Show |
1 | a0001c0001t0001g0266 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.534-2844_534-2843i others(103): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018473 | |||||
| chr5:66018473
|
TTATATAT others(19): Show |
T | 1 | a0001c0002t0019g0298 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.534-2829_534-2804d others(28): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018473 | |||||
| chr5:66018475
|
ATATATTA others(5): Show |
A | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.534-2835_534-2824d others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018475 | |||||
| chr5:66018475
|
ATATATTA others(85): Show |
A | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.534-2835_534-2744d others(94): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018475 | |||||
| chr5:66018480
|
T | A | 12 | a0001c0001t0001g0048a0001c0001t0001g0055a0001c0001t0001g0145others(9): Show | 12 | HG01515.hp1 HG02055.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.534-2842T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018480 | ||||||
| chr5:66018480
|
T | TAATATAA | 3 | a0001c0007t0012g0218a0001c0007t0012g0219a0001c0007t0012g0220 | 3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.534-2842_534-2841i others(9): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018480 | ||||||
| chr5:66018480
|
T | TTATAATA others(33): Show |
1 | a0001c0001t0001g0073 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.534-2838_534-2837i others(42): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018480 | |||||
| chr5:66018480
|
T | TTATATAA | 45 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0123others(42): Show | 45 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.534-2836_534-2835i others(9): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018480 | |||||
| chr5:66018480
|
T | TTATATAA others(15): Show |
1 | a0001c0001t0001g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.534-2836_534-2835i others(24): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018480 | |||||
| chr5:66018480
|
T | TTATATAA others(19): Show |
3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0042 | 3 | HG02818.hp2 HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.534-2836_534-2835i others(28): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018480 | |||||
| chr5:66018480
|
T | TTATATAA others(38): Show |
2 | a0001c0001t0001g0029a0001c0001t0001g0054 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.534-2836_534-2835i others(47): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018480 | |||||
| chr5:66018480
|
T | TTATATAA others(19): Show |
1 | a0003c0004t0001g0128 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.534-2836_534-2835i others(28): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018480 | |||||
| chr5:66018480
|
T | TTATATAT others(40): Show |
1 | a0001c0002t0002g0250 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.534-2830_534-2829i others(49): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018480 | |||||
| chr5:66018480
|
T | TTATATAT others(33): Show |
1 | a0001c0002t0002g0211 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.534-2769_534-2730d others(42): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018480 | |||||
| chr5:66018480
|
T | TTATATTA others(17): Show |
1 | a0001c0001t0001g0006 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.534-2837_534-2836i others(26): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018480 | |||||
| chr5:66018480
|
TTATATAT others(7): Show |
T | 4 | a0001c0001t0006g0153a0001c0001t0006g0155a0001c0001t0006g0157others(1): Show | 4 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.534-2837_534-2824d others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018480 | |||||
| chr5:66018481
|
T | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0120 | 2 | HG00280.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.534-2841T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018481 | ||||||
| chr5:66018482
|
A | ATAATATA others(10): Show |
3 | a0001c0001t0006g0147a0001c0001t0006g0148a0001c0001t0006g0150 | 3 | HG03486.hp1 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.534-2838_534-2837i others(19): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018482 | |||||
| chr5:66018482
|
ATATAT | A | 4 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(1): Show | 4 | NA18999.hp2 NA19003.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.534-2829_534-2825d others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018482 | |||||
| chr5:66018483
|
T | TA | 3 | a0001c0001t0001g0066a0001c0001t0001g0103a0001c0001t0001g0112 | 3 | HG01952.hp1 HG03471.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.534-2838dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018483 | |||||
| chr5:66018485
|
T | A | 2 | a0001c0001t0006g0152a0001c0001t0006g0154 | 2 | HG00738.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.534-2837T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018485 | ||||||
| chr5:66018486
|
A | AAT | 53 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0041others(50): Show | 53 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.534-2836_534-2835i others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018486 | ||||||
| chr5:66018486
|
A | AATATATA others(85): Show |
1 | a0001c0001t0020g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.534-2836_534-2835i others(94): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018486 | ||||||
| chr5:66018486
|
A | AATATATA others(132): Show |
1 | a0001c0001t0001g0273 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.534-2836_534-2835i others(141): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018486 | ||||||
| chr5:66018486
|
A | AATATATA others(146): Show |
1 | a0001c0001t0001g0133 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.534-2836_534-2835i others(155): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018486 | ||||||
| chr5:66018486
|
A | AATATATA others(59): Show |
1 | a0001c0001t0001g0043 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.534-2836_534-2835i others(68): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018486 | ||||||
| chr5:66018486
|
A | T | 2 | a0001c0001t0006g0152a0001c0001t0006g0154 | 2 | HG00738.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.534-2836A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018486 | ||||||
| chr5:66018487
|
T | A | 62 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0041others(59): Show | 62 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.534-2835T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018487 | ||||||
| chr5:66018487
|
T | TAATA | 3 | a0001c0001t0006g0147a0001c0001t0006g0148a0001c0001t0006g0150 | 3 | HG03486.hp1 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.534-2835_534-2834i others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018487 | ||||||
| chr5:66018487
|
T | TATAATAT others(27): Show |
1 | a0001c0001t0001g0103 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.534-2835_534-2834i others(36): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018487 | ||||||
| chr5:66018487
|
T | TATAATAT others(41): Show |
2 | a0001c0001t0001g0066a0001c0001t0001g0112 | 2 | HG03471.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.534-2835_534-2834i others(50): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018487 | ||||||
| chr5:66018487
|
T | TATTATAT others(30): Show |
1 | a0001c0001t0001g0028 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.534-2835_534-2834i others(39): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018487 | ||||||
| chr5:66018487
|
T | TATTATAT others(49): Show |
1 | a0001c0001t0001g0120 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.534-2835_534-2834i others(58): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018487 | ||||||
| chr5:66018487
|
T | TTA | 3 | a0001c0001t0001g0109a0001c0001t0001g0264a0001c0001t0006g0156 | 3 | HG01978.hp2 HG02145.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.534-2831_534-2830d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018487 | |||||
| chr5:66018487
|
T | TTATAATA others(7): Show |
2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | NA18612.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.534-2831_534-2830i others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018487 | |||||
| chr5:66018487
|
T | TTATATAT others(21): Show |
1 | a0002c0003t0003g0183 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.534-2830_534-2829i others(30): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018487 | |||||
| chr5:66018487
|
TTATATTA others(5): Show |
T | 2 | a0002c0003t0005g0188a0002c0003t0005g0199 | 2 | NA19063.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.534-2829_534-2818d others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018487 | |||||
| chr5:66018492
|
T | A | 9 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(6): Show | 9 | HG01978.hp1 HG02572.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.534-2830T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018492 | ||||||
| chr5:66018492
|
T | TAA | 3 | a0001c0001t0001g0055a0001c0001t0001g0073a0001c0001t0013g0124 | 3 | HG01261.hp2 HG03139.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.534-2830_534-2829i others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018492 | ||||||
| chr5:66018492
|
T | TATTATAT others(52): Show |
1 | a0003c0004t0001g0306 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.534-2830_534-2829i others(61): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018492 | ||||||
| chr5:66018492
|
T | TATTATAT others(94): Show |
1 | a0003c0004t0001g0115 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.534-2830_534-2829i others(103): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018492 | ||||||
| chr5:66018493
|
T | A | 12 | a0001c0001t0001g0029a0001c0001t0001g0048a0001c0001t0001g0054others(9): Show | 12 | HG01515.hp1 HG02055.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.534-2829T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018493 | ||||||
| chr5:66018494
|
A | T | 9 | a0001c0001t0001g0048a0001c0001t0001g0272a0001c0001t0003g0113others(6): Show | 9 | HG01515.hp1 HG04115.hp1 HG04228.hp2 others(6): Show |
intron_variant | MODIFIER | c.534-2828A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018494 | ||||||
| chr5:66018498
|
A | T | 1 | a0001c0001t0001g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.534-2824A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018498 | ||||||
| chr5:66018499
|
A | T | 13 | a0001c0001t0001g0055a0001c0001t0001g0073a0001c0001t0001g0264others(10): Show | 13 | HG00738.hp2 HG01978.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.534-2823A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018499 | ||||||
| chr5:66018506
|
T | A | 55 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(52): Show | 55 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.534-2816T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018506 | ||||||
| chr5:66018506
|
T | TTATATAA | 4 | a0001c0001t0006g0156a0001c0001t0013g0100a0001c0001t0028g0092others(1): Show | 4 | HG02145.hp2 HG03540.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.534-2810_534-2809i others(9): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018506 | |||||
| chr5:66018506
|
T | TTATATAT others(61): Show |
1 | a0003c0004t0001g0305 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.534-2805_534-2804i others(70): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018506 | |||||
| chr5:66018506
|
T | TTATATTA others(59): Show |
1 | a0001c0001t0001g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.534-2811_534-2810i others(68): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018506 | |||||
| chr5:66018506
|
T | TTATATTA others(87): Show |
1 | a0001c0001t0001g0053 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.534-2811_534-2810i others(96): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018506 | |||||
| chr5:66018506
|
T | TTATATTA others(101): Show |
1 | a0001c0001t0001g0052 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.534-2811_534-2810i others(110): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018506 | |||||
| chr5:66018506
|
T | TTATATTA others(38): Show |
2 | a0003c0004t0001g0136a0003c0004t0001g0140 | 2 | HG00642.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.534-2811_534-2810i others(47): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018506 | |||||
| chr5:66018506
|
T | TTATATTA others(57): Show |
1 | a0015c0024t0022g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.534-2811_534-2810i others(66): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018506 | |||||
| chr5:66018506
|
TTA | T | 37 | a0001c0001t0001g0123a0001c0001t0001g0135a0001c0001t0001g0274others(34): Show | 37 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.534-2810_534-2809d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018506 | |||||
| chr5:66018507
|
T | A | 1 | a0001c0001t0001g0144 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.534-2815T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018507 | ||||||
| chr5:66018508
|
A | ATATAT | 3 | a0001c0001t0001g0129a0001c0002t0002g0261a0002c0003t0003g0198 | 3 | HG01891.hp2 HG01981.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.534-2808_534-2804d others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018508 | |||||
| chr5:66018508
|
A | T | 1 | a0001c0001t0001g0144 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.534-2814A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018508 | ||||||
| chr5:66018512
|
ATT | A | 5 | a0001c0001t0001g0266a0007c0012t0011g0022a0007c0012t0011g0023others(2): Show | 5 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.534-2809_534-2808d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018512 | ||||||
| chr5:66018513
|
T | A | 36 | a0001c0001t0001g0028a0001c0001t0001g0041a0001c0001t0001g0043others(33): Show | 36 | HG00280.hp1 HG00735.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.534-2809T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018513 | ||||||
| chr5:66018513
|
T | TTATAA | 3 | a0001c0001t0001g0042a0001c0001t0006g0152a0003c0004t0001g0128 | 3 | HG02976.hp2 HG03516.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.534-2805_534-2804i others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018513 | |||||
| chr5:66018518
|
T | A | 1 | a0001c0001t0001g0085 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.534-2804T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018518 | ||||||
| chr5:66018519
|
A | T | 2 | a0001c0001t0001g0085a0002c0003t0008g0277 | 2 | NA18955.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.534-2803A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018519 | ||||||
| chr5:66018519
|
AATATATA others(56): Show |
A | 1 | a0005c0006t0007g0223 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.534-2798_534-2736d others(65): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018519 | |||||
| chr5:66018520
|
A | T | 43 | a0001c0001t0001g0028a0001c0001t0001g0041a0001c0001t0001g0043others(40): Show | 43 | HG00280.hp1 HG00735.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.534-2802A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018520 | ||||||
| chr5:66018522
|
ATATAT | A | 9 | a0001c0001t0001g0118a0001c0001t0006g0155a0001c0001t0024g0158others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.534-2789_534-2785d others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018522 | |||||
| chr5:66018525
|
T | A | 1 | a0001c0001t0001g0085 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.534-2797T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018525 | ||||||
| chr5:66018526
|
A | AAT | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 4 | HG02572.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.534-2796_534-2795i others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018526 | ||||||
| chr5:66018526
|
A | T | 1 | a0001c0001t0001g0085 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.534-2796A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018526 | ||||||
| chr5:66018527
|
T | A | 10 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(7): Show | 10 | HG02572.hp2 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.534-2795T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018527 | ||||||
| chr5:66018527
|
T | TTA | 13 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0073others(10): Show | 13 | HG00642.hp1 HG01167.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.534-2791_534-2790d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018527 | |||||
| chr5:66018527
|
T | TTATATAA others(2): Show |
7 | a0001c0001t0001g0042a0001c0001t0006g0147a0001c0001t0006g0148others(4): Show | 7 | HG02976.hp2 HG03098.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.534-2790_534-2789i others(11): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018527 | |||||
| chr5:66018527
|
T | TTATATAA others(30): Show |
1 | a0001c0001t0013g0125 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.534-2790_534-2789i others(39): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018527 | |||||
| chr5:66018527
|
T | TTATATAT others(56): Show |
1 | a0001c0001t0001g0272 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.534-2790_534-2789i others(65): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018527 | |||||
| chr5:66018532
|
T | A | 5 | a0006c0008t0003g0084a0006c0008t0003g0189a0006c0008t0003g0191others(2): Show | 5 | NA18950.hp2 NA18956.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.534-2790T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018532 | ||||||
| chr5:66018532
|
T | TAA | 72 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(69): Show | 72 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.534-2790_534-2789i others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018532 | ||||||
| chr5:66018532
|
T | TAATATAT others(9): Show |
1 | a0001c0001t0001g0078 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.534-2790_534-2789i others(18): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018532 | ||||||
| chr5:66018532
|
T | TAATATAT others(44): Show |
1 | a0001c0001t0003g0113 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.534-2790_534-2789i others(53): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018532 | ||||||
| chr5:66018532
|
T | TAATATAT others(100): Show |
1 | a0001c0001t0001g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.534-2790_534-2789i others(109): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018532 | ||||||
| chr5:66018532
|
T | TAATATAT others(86): Show |
1 | a0001c0001t0001g0048 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.534-2790_534-2789i others(95): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018532 | ||||||
| chr5:66018532
|
T | TAATATAT others(30): Show |
1 | a0001c0001t0001g0096 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.534-2790_534-2789i others(39): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018532 | ||||||
| chr5:66018532
|
T | TAATATAT others(194): Show |
1 | a0001c0001t0001g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.534-2790_534-2789i others(203): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018532 | ||||||
| chr5:66018532
|
T | TAATATAT others(131): Show |
1 | a0001c0001t0001g0006 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.534-2790_534-2789i others(140): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018532 | ||||||
| chr5:66018532
|
T | TAATATAT others(299): Show |
1 | a0001c0001t0001g0005 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.534-2790_534-2789i others(308): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018532 | ||||||
| chr5:66018532
|
T | TATTATAT others(2): Show |
3 | a0001c0001t0001g0133a0001c0001t0006g0156a0013c0018t0001g0049 | 3 | HG01071.hp2 HG02145.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.534-2790_534-2789i others(11): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018532 | ||||||
| chr5:66018532
|
T | TTATATAA others(120): Show |
2 | a0001c0001t0009g0037a0001c0022t0009g0035 | 2 | NA18994.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.534-2771_534-2770i others(129): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018532 | |||||
| chr5:66018532
|
T | TTATATAA others(106): Show |
1 | a0001c0001t0009g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.534-2771_534-2770i others(115): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018532 | |||||
| chr5:66018533
|
T | A | 38 | a0001c0001t0001g0047a0001c0001t0001g0123a0001c0001t0001g0135others(35): Show | 38 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.534-2789T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018533 | ||||||
| chr5:66018534
|
A | T | 29 | a0001c0001t0001g0123a0001c0001t0001g0135a0001c0001t0001g0274others(26): Show | 29 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.534-2788A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018534 | ||||||
| chr5:66018539
|
A | T | 91 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.534-2783A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018539 | ||||||
| chr5:66018540
|
T | A | 1 | a0001c0001t0001g0047 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.534-2782T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018540 | ||||||
| chr5:66018541
|
A | T | 1 | a0001c0001t0001g0047 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.534-2781A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018541 | ||||||
| chr5:66018546
|
T | A | 40 | a0001c0001t0001g0054a0001c0001t0001g0110a0001c0001t0001g0123others(37): Show | 40 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.534-2776T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018546 | ||||||
| chr5:66018546
|
T | TTATATTA others(5): Show |
1 | a0001c0002t0002g0261 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.534-2771_534-2770i others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018546 | |||||
| chr5:66018546
|
TTA | T | 8 | a0001c0001t0009g0038a0001c0001t0009g0040a0006c0008t0003g0084others(5): Show | 8 | HG01884.hp1 NA18950.hp2 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.534-2770_534-2769d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018546 | |||||
| chr5:66018547
|
T | TATATTAT others(71): Show |
1 | a0001c0001t0009g0039 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.534-2771_534-2770i others(80): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018547 | |||||
| chr5:66018548
|
A | ATATAT | 10 | a0002c0003t0002g0203a0002c0003t0002g0204a0002c0003t0002g0207others(7): Show | 10 | HG00280.hp2 HG02738.hp1 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.534-2768_534-2764d others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018548 | |||||
| chr5:66018548
|
A | ATATATTA others(83): Show |
1 | a0002c0003t0003g0300 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.534-2730_534-2729i others(92): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018548 | |||||
| chr5:66018548
|
A | ATATATTA others(36): Show |
1 | a0002c0003t0003g0196 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.534-2764_534-2763i others(45): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018548 | |||||
| chr5:66018548
|
A | ATATATTA others(43): Show |
30 | a0002c0003t0003g0166a0002c0003t0003g0167a0002c0003t0003g0168others(27): Show | 30 | HG00408.hp2 HG01081.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.534-2764_534-2763i others(52): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018548 | |||||
| chr5:66018553
|
T | A | 26 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(23): Show | 26 | HG01891.hp2 HG02055.hp1 HG02273.hp1 others(23): Show |
intron_variant | MODIFIER | c.534-2769T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018553 | ||||||
| chr5:66018553
|
T | TTATATTA others(24): Show |
4 | a0002c0003t0003g0181a0002c0003t0003g0182a0002c0003t0003g0281others(1): Show | 4 | NA18954.hp1 NA18978.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.534-2764_534-2763i others(33): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018553 | |||||
| chr5:66018560
|
A | T | 7 | a0001c0001t0006g0155a0002c0003t0003g0181a0002c0003t0003g0182others(4): Show | 7 | HG01884.hp2 HG02965.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.534-2762A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018560 | ||||||
| chr5:66018566
|
A | AAT | 8 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(5): Show | 8 | HG02572.hp2 HG02717.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.534-2756_534-2755i others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018566 | ||||||
| chr5:66018566
|
A | AATATATA others(9): Show |
4 | a0003c0004t0001g0136a0003c0004t0001g0140a0003c0004t0001g0305others(1): Show | 4 | HG00642.hp1 HG01167.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.534-2756_534-2755i others(18): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018566 | ||||||
| chr5:66018566
|
A | T | 1 | a0014c0023t0001g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.534-2756A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018566 | ||||||
| chr5:66018567
|
T | A | 16 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(13): Show | 16 | HG00642.hp1 HG01071.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.534-2755T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018567 | ||||||
| chr5:66018567
|
T | TTA | 101 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(98): Show | 101 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.534-2751_534-2750d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018567 | |||||
| chr5:66018567
|
T | TTATATAA others(107): Show |
6 | a0001c0001t0001g0135a0001c0001t0001g0274a0003c0004t0001g0302others(3): Show | 6 | HG00438.hp1 HG02273.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.534-2750_534-2749i others(116): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018567 | |||||
| chr5:66018567
|
T | TTATATAA others(107): Show |
1 | a0011c0019t0001g0088 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.534-2750_534-2749i others(116): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018567 | |||||
| chr5:66018567
|
T | TTATATAA others(93): Show |
1 | a0003c0004t0001g0131 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.534-2750_534-2749i others(102): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018567 | |||||
| chr5:66018567
|
T | TTATATAA others(93): Show |
3 | a0003c0004t0001g0132a0003c0004t0001g0141a0003c0004t0027g0139 | 3 | HG01943.hp2 HG01993.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.534-2750_534-2749i others(102): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018567 | |||||
| chr5:66018567
|
T | TTATATAA others(58): Show |
4 | a0003c0004t0001g0094a0003c0004t0001g0105a0003c0004t0001g0114others(1): Show | 4 | NA18963.hp1 NA18970.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.534-2750_534-2749i others(67): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018567 | |||||
| chr5:66018567
|
T | TTATATAA others(100): Show |
1 | a0003c0004t0017g0121 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.534-2750_534-2749i others(109): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018567 | |||||
| chr5:66018567
|
T | TTATATAA others(100): Show |
9 | a0001c0001t0001g0123a0003c0004t0001g0089a0003c0004t0001g0107others(6): Show | 9 | NA18942.hp2 NA18944.hp2 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.534-2750_534-2749i others(109): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018567 | |||||
| chr5:66018567
|
T | TTATATAT others(147): Show |
1 | a0003c0004t0001g0137 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.534-2750_534-2749i others(156): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018567 | |||||
| chr5:66018567
|
TTATATTA others(5): Show |
T | 1 | a0008c0011t0011g0025 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.534-2749_534-2738d others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018567 | |||||
| chr5:66018567
|
TTATATTA others(9): Show |
T | 1 | a0005c0006t0016g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.534-2751_534-2736d others(18): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018567 | |||||
| chr5:66018569
|
A | ATATATTA others(3): Show |
1 | a0001c0001t0001g0273 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.534-2750_534-2749i others(12): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018569 | |||||
| chr5:66018572
|
T | A | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.534-2750T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018572 | ||||||
| chr5:66018572
|
T | TAA | 12 | a0001c0001t0001g0085a0001c0001t0001g0110a0001c0001t0001g0268others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.534-2750_534-2749i others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018572 | ||||||
| chr5:66018572
|
T | TTATATAA others(66): Show |
1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.534-2737_534-2736i others(75): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018572 | |||||
| chr5:66018573
|
T | A | 4 | a0001c0001t0001g0047a0001c0007t0012g0218a0001c0007t0012g0219others(1): Show | 4 | HG02559.hp2 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.534-2749T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018573 | ||||||
| chr5:66018574
|
A | T | 1 | a0001c0001t0001g0047 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.534-2748A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018574 | ||||||
| chr5:66018579
|
A | T | 18 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(15): Show | 18 | HG00738.hp2 HG01891.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.534-2743A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018579 | ||||||
| chr5:66018583
|
A | T | 1 | a0005c0006t0007g0223 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.534-2739A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018583 | ||||||
| chr5:66018586
|
T | A | 147 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.534-2736T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018586 | ||||||
| chr5:66018586
|
T | TTATATAT others(138): Show |
1 | a0003c0004t0001g0001 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.534-2730_534-2729i others(147): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018586 | |||||
| chr5:66018586
|
T | TTATATAT others(143): Show |
1 | a0001c0001t0009g0038 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.534-2730_534-2729i others(152): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018586 | |||||
| chr5:66018586
|
T | TTATATAT others(187): Show |
1 | a0001c0001t0001g0144 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.534-2730_534-2729i others(196): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018586 | |||||
| chr5:66018586
|
T | TTATATAT others(14): Show |
1 | a0001c0001t0028g0092 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.534-2730_534-2729i others(23): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018586 | |||||
| chr5:66018586
|
T | TTATATTA others(223): Show |
1 | a0001c0001t0009g0040 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.534-2731_534-2730i others(232): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018586 | |||||
| chr5:66018591
|
T | C | 1 | a0002c0003t0002g0202 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.534-2731T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018591 | ||||||
| chr5:66018592
|
A | T | 5 | a0002c0003t0003g0181a0002c0003t0003g0182a0002c0003t0003g0183others(2): Show | 5 | NA18948.hp2 NA18954.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.534-2730A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018592 | ||||||
| chr5:66018593
|
A | ATATATAT others(98): Show |
1 | a0003c0004t0001g0134 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.534-2716_534-2715i others(107): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018593 | |||||
| chr5:66018593
|
A | T | 166 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.534-2729A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018593 | ||||||
| chr5:66018600
|
T | A | 1 | a0003c0004t0001g0105 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.534-2722T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018600 | ||||||
| chr5:66018621
|
CAT | C | 5 | a0001c0001t0009g0037a0001c0001t0009g0038a0001c0001t0009g0039others(2): Show | 5 | NA18961.hp1 NA18985.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.534-2697_534-2696d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018621 | |||||
| chr5:66018634
|
T | A | 16 | a0001c0001t0028g0092a0004c0005t0004g0013a0004c0005t0004g0014others(13): Show | 16 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.534-2688T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018634 | ||||||
| chr5:66018637
|
T | A | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.534-2685T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018637 | ||||||
| chr5:66018647
|
T | G | 1 | a0001c0001t0001g0043 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.534-2675T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018647 | ||||||
| chr5:66018649
|
G | T | 8 | a0001c0002t0002g0235a0001c0002t0002g0242a0001c0002t0002g0245others(5): Show | 8 | NA18612.hp1 NA18949.hp2 NA18975.hp1 others(5): Show |
intron_variant | MODIFIER | c.534-2673G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018649 | ||||||
| chr5:66018698
|
A | G | 2 | a0005c0006t0007g0223a0005c0006t0016g0299 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.534-2624A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018698 | ||||||
| chr5:66018838
|
T | G | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.534-2484T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018838 | ||||||
| chr5:66018857
|
G | A | 2 | a0005c0006t0002g0229a0005c0006t0002g0263 | 2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.534-2465G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018857 | ||||||
| chr5:66018892
|
C | T | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.534-2430C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018892 | ||||||
| chr5:66018945
|
AT | A | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.534-2371delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018945 | |||||
| chr5:66019066
|
C | T | 196 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.534-2256C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66019066 | ||||||
| chr5:66019095
|
A | G | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.534-2227A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66019095 | ||||||
| chr5:66019165
|
T | C | 1 | a0001c0015t0029g0258 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.534-2157T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66019165 | ||||||
| chr5:66019470
|
C | G | 3 | a0001c0002t0002g0032a0001c0002t0002g0033a0001c0002t0002g0034 | 3 | HG03017.hp1 HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.534-1852C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66019470 | ||||||
| chr5:66019791
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.534-1531T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66019791 | ||||||
| chr5:66019814
|
A | G | 1 | a0005c0006t0007g0026 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.534-1508A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66019814 | ||||||
| chr5:66019897
|
C | G | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.534-1425C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66019897 | ||||||
| chr5:66019903
|
C | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(3): Show | 6 | HG01071.hp2 HG01934.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.534-1419C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66019903 | ||||||
| chr5:66019960
|
G | A | 6 | a0005c0006t0007g0223a0005c0006t0007g0224a0005c0006t0007g0226others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.534-1362G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66019960 | ||||||
| chr5:66020123
|
A | G | 40 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0050others(37): Show | 40 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.534-1199A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66020123 | ||||||
| chr5:66020131
|
G | C | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.534-1191G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66020131 | ||||||
| chr5:66020214
|
G | T | 15 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(12): Show | 15 | HG01071.hp2 HG01934.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.534-1108G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66020214 | ||||||
| chr5:66020360
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.534-962T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66020360 | ||||||
| chr5:66020377
|
G | A | 154 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.534-945G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66020377 | ||||||
| chr5:66020466
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.534-856A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66020466 | ||||||
| chr5:66020474
|
C | T | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.534-848C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66020474 | ||||||
| chr5:66020536
|
A | G | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.534-786A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66020536 | ||||||
| chr5:66020675
|
C | CA | 305 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.534-644dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66020675 | |||||
| chr5:66020861
|
G | C | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.534-461G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66020861 | ||||||
| chr5:66020891
|
G | A | 12 | a0001c0001t0006g0147a0001c0001t0006g0148a0001c0001t0006g0149others(9): Show | 12 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.534-431G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66020891 | ||||||
| chr5:66021113
|
T | C | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.534-209T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66021113 | ||||||
| chr5:66021169
|
T | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.534-153T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66021169 | ||||||
| chr5:66021169
|
TA | T | 154 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.534-149delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66021169 | |||||
| chr5:66021277
|
A | G | 2 | a0001c0002t0002g0239a0001c0002t0002g0240 | 2 | HG02056.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.534-45A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66021277 | ||||||
| chr5:66021504
|
A | T | 141 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.597+119A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66021504 | ||||||
| chr5:66021510
|
T | C | 154 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.597+125T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66021510 | ||||||
| chr5:66021618
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.597+233A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66021618 | ||||||
| chr5:66021624
|
A | AC | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.597+240dupC | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 66021624 | |||||
| chr5:66021646
|
A | G | 1 | a0013c0018t0001g0049 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.597+261A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66021646 | ||||||
| chr5:66022082
|
A | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.597+697A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66022082 | ||||||
| chr5:66022085
|
C | A | 193 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.597+700C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66022085 | ||||||
| chr5:66022416
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.598-874A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66022416 | ||||||
| chr5:66022447
|
T | G | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.598-843T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66022447 | ||||||
| chr5:66022493
|
A | G | 4 | a0005c0006t0007g0224a0005c0006t0007g0226a0005c0006t0007g0230others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.598-797A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66022493 | ||||||
| chr5:66022519
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.598-771A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66022519 | ||||||
| chr5:66022720
|
A | G | 5 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(2): Show | 5 | HG01884.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-570A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66022720 | ||||||
| chr5:66023041
|
C | G | 1 | a0001c0001t0001g0041 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.598-249C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66023041 | ||||||
| chr5:66023075
|
T | G | 4 | a0001c0007t0010g0162a0001c0007t0010g0163a0001c0007t0010g0164others(1): Show | 4 | HG02109.hp2 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.598-215T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66023075 | ||||||
| chr5:66023272
|
C | G | 1 | a0015c0024t0022g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.598-18C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66023272 | ||||||
| chr5:66023469
|
T | C | 1 | a0005c0006t0007g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.672+105T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 9/25 | chr5 | 66023469 | ||||||
| chr5:66023673
|
A | AT | 34 | a0001c0001t0001g0047a0001c0001t0001g0060a0001c0001t0001g0090others(31): Show | 34 | HG00621.hp2 HG01109.hp2 HG02056.hp2 others(31): Show |
intron_variant | MODIFIER | c.672+329dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr5 | 66023673 | |||||
| chr5:66023673
|
AT | A | 9 | a0001c0001t0001g0031a0001c0001t0001g0104a0001c0007t0010g0161others(6): Show | 9 | HG01256.hp2 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.672+329delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr5 | 66023673 | |||||
| chr5:66023868
|
G | A | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.673-438G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 9/25 | chr5 | 66023868 | ||||||
| chr5:66023879
|
G | A | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.673-427G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 9/25 | chr5 | 66023879 | ||||||
| chr5:66023934
|
A | C | 1 | a0002c0003t0003g0300 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.673-372A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 9/25 | chr5 | 66023934 | ||||||
| chr5:66024013
|
C | T | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.673-293C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 9/25 | chr5 | 66024013 | ||||||
| chr5:66024025
|
A | G | 154 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.673-281A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 9/25 | chr5 | 66024025 | ||||||
| chr5:66024497
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.817+47G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 10/25 | chr5 | 66024497 | ||||||
| chr5:66024542
|
T | C | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.817+92T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 10/25 | chr5 | 66024542 | ||||||
| chr5:66024618
|
A | G | 1 | a0002c0003t0008g0241 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.817+168A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 10/25 | chr5 | 66024618 | ||||||
| chr5:66024642
|
A | T | 1 | a0015c0024t0022g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.817+192A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 10/25 | chr5 | 66024642 | ||||||
| chr5:66024699
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.817+249T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 10/25 | chr5 | 66024699 | ||||||
| chr5:66024778
|
A | G | 1 | a0002c0003t0005g0172 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.817+328A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 10/25 | chr5 | 66024778 | ||||||
| chr5:66024825
|
A | G | 1 | a0001c0001t0024g0158 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.817+375A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 10/25 | chr5 | 66024825 | ||||||
| chr5:66024973
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.818-507T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 10/25 | chr5 | 66024973 | ||||||
| chr5:66024988
|
A | G | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.818-492A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 10/25 | chr5 | 66024988 | ||||||
| chr5:66025112
|
A | G | 6 | a0005c0006t0007g0223a0005c0006t0007g0224a0005c0006t0007g0226others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.818-368A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 10/25 | chr5 | 66025112 | ||||||
| chr5:66025133
|
A | G | 12 | a0001c0001t0006g0147a0001c0001t0006g0148a0001c0001t0006g0149others(9): Show | 12 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.818-347A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 10/25 | chr5 | 66025133 | ||||||
| chr5:66025651
|
T | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.890+99T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 11/25 | chr5 | 66025651 | ||||||
| chr5:66025687
|
T | A | 1 | a0015c0024t0022g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.890+135T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 11/25 | chr5 | 66025687 | ||||||
| chr5:66026025
|
T | C | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1020+48T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 12/25 | chr5 | 66026025 | ||||||
| chr5:66026050
|
G | A | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1020+73G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 12/25 | chr5 | 66026050 | ||||||
| chr5:66026169
|
A | T | 1 | a0001c0002t0002g0254 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1021-133A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 12/25 | chr5 | 66026169 | ||||||
| chr5:66026600
|
T | G | 6 | a0005c0006t0007g0223a0005c0006t0007g0224a0005c0006t0007g0226others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1136+183T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 13/25 | chr5 | 66026600 | ||||||
| chr5:66026611
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1136+194G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 13/25 | chr5 | 66026611 | ||||||
| chr5:66026650
|
C | T | 1 | a0001c0001t0024g0158 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1136+233C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 13/25 | chr5 | 66026650 | ||||||
| chr5:66027210
|
C | G | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1136+793C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 13/25 | chr5 | 66027210 | ||||||
| chr5:66027312
|
C | CT | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1136+895_1136+896i others(3): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 13/25 | chr5 | 66027312 | ||||||
| chr5:66027328
|
T | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1136+911T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 13/25 | chr5 | 66027328 | ||||||
| chr5:66027344
|
G | A | 193 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.1136+927G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 13/25 | chr5 | 66027344 | ||||||
| chr5:66027422
|
A | G | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1137-852A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 13/25 | chr5 | 66027422 | ||||||
| chr5:66027665
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1137-609G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 13/25 | chr5 | 66027665 | ||||||
| chr5:66028006
|
A | C | 1 | a0001c0007t0010g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1137-268A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 13/25 | chr5 | 66028006 | ||||||
| chr5:66028169
|
G | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG02572.hp2 HG02717.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1137-105G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 13/25 | chr5 | 66028169 | ||||||
| chr5:66029122
|
A | C | 1 | a0001c0001t0001g0233 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1206+779A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66029122 | ||||||
| chr5:66029289
|
G | A | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1206+946G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66029289 | ||||||
| chr5:66029512
|
G | A | 2 | a0001c0021t0001g0101a0004c0005t0004g0009 | 2 | HG01981.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1206+1169G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66029512 | ||||||
| chr5:66029539
|
G | C | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1206+1196G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66029539 | ||||||
| chr5:66029547
|
TTTCTG | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1206+1226_1206+123 others(9): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 66029547 | |||||
| chr5:66029569
|
T | C | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1206+1226T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66029569 | ||||||
| chr5:66029569
|
T | TCTGTC | 15 | a0002c0003t0005g0178a0002c0003t0005g0180a0002c0003t0005g0201others(12): Show | 15 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1206+1252_1206+125 others(9): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 66029569 | |||||
| chr5:66029574
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1206+1231C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66029574 | ||||||
| chr5:66029591
|
TG | T | 5 | a0002c0003t0002g0204a0002c0003t0002g0207a0002c0003t0002g0208others(2): Show | 5 | NA18951.hp1 NA18992.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.1206+1249delG | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66029591 | ||||||
| chr5:66029645
|
G | A | 1 | a0005c0006t0015g0225 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1206+1302G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66029645 | ||||||
| chr5:66029689
|
C | G | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1206+1346C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66029689 | ||||||
| chr5:66029707
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1206+1364C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66029707 | ||||||
| chr5:66029728
|
C | T | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1206+1385C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66029728 | ||||||
| chr5:66029824
|
C | T | 4 | a0005c0006t0007g0224a0005c0006t0007g0226a0005c0006t0007g0230others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1206+1481C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66029824 | ||||||
| chr5:66030200
|
G | A | 1 | a0001c0002t0002g0217 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1206+1857G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66030200 | ||||||
| chr5:66030204
|
A | G | 8 | a0001c0002t0002g0173a0001c0002t0002g0210a0001c0002t0002g0211others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1206+1861A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66030204 | ||||||
| chr5:66030438
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1206+2095T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66030438 | ||||||
| chr5:66030470
|
C | A | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1206+2127C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66030470 | ||||||
| chr5:66030523
|
C | T | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1206+2180C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66030523 | ||||||
| chr5:66030562
|
C | CT | 15 | a0001c0001t0001g0005a0001c0001t0001g0096a0001c0002t0002g0296others(12): Show | 15 | HG00438.hp2 HG01433.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1206+2237dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 66030562 | |||||
| chr5:66030588
|
G | A | 10 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(7): Show | 10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1206+2245G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66030588 | ||||||
| chr5:66030782
|
G | C | 1 | a0015c0024t0022g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1206+2439G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66030782 | ||||||
| chr5:66030784
|
T | A | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1206+2441T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66030784 | ||||||
| chr5:66030838
|
C | T | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1206+2495C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66030838 | ||||||
| chr5:66031043
|
C | T | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1206+2700C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031043 | ||||||
| chr5:66031050
|
G | A | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1206+2707G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031050 | ||||||
| chr5:66031141
|
A | T | 1 | a0001c0020t0001g0117 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1206+2798A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031141 | ||||||
| chr5:66031184
|
T | C | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1206+2841T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031184 | ||||||
| chr5:66031198
|
G | C | 1 | a0001c0001t0009g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1206+2855G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031198 | ||||||
| chr5:66031361
|
T | C | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1206+3018T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031361 | ||||||
| chr5:66031390
|
A | C | 10 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(7): Show | 10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1206+3047A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031390 | ||||||
| chr5:66031452
|
G | C | 4 | a0005c0006t0007g0224a0005c0006t0007g0226a0005c0006t0007g0230others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1206+3109G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031452 | ||||||
| chr5:66031608
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | NA18612.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1206+3265G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031608 | ||||||
| chr5:66031643
|
A | C | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1206+3300A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031643 | ||||||
| chr5:66031696
|
G | T | 1 | a0001c0001t0001g0118 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1206+3353G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031696 | ||||||
| chr5:66031701
|
A | T | 3 | a0001c0001t0006g0152a0001c0001t0006g0153a0001c0001t0006g0157 | 3 | HG01891.hp1 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1206+3358A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031701 | ||||||
| chr5:66031717
|
G | T | 3 | a0003c0004t0001g0302a0003c0004t0021g0303a0003c0004t0026g0301 | 3 | HG03017.hp2 HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1206+3374G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031717 | ||||||
| chr5:66032064
|
T | C | 6 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(3): Show | 6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1206+3721T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66032064 | ||||||
| chr5:66032282
|
T | C | 1 | a0001c0020t0001g0117 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1206+3939T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66032282 | ||||||
| chr5:66032330
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1206+3987T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66032330 | ||||||
| chr5:66032538
|
G | A | 1 | a0002c0003t0003g0283 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1206+4195G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66032538 | ||||||
| chr5:66032619
|
A | G | 44 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0050others(41): Show | 44 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1206+4276A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66032619 | ||||||
| chr5:66032820
|
A | G | 1 | a0001c0021t0001g0101 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1206+4477A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66032820 | ||||||
| chr5:66033029
|
G | A | 1 | a0015c0024t0022g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1206+4686G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66033029 | ||||||
| chr5:66033120
|
C | T | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1206+4777C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66033120 | ||||||
| chr5:66033166
|
A | G | 1 | a0001c0002t0002g0254 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1206+4823A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66033166 | ||||||
| chr5:66033506
|
A | G | 1 | a0001c0002t0002g0244 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1207-4877A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66033506 | ||||||
| chr5:66033677
|
T | A | 1 | a0001c0002t0002g0240 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1207-4706T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66033677 | ||||||
| chr5:66033678
|
C | G | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1207-4705C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66033678 | ||||||
| chr5:66033749
|
G | A | 8 | a0003c0004t0001g0094a0003c0004t0001g0105a0003c0004t0001g0107others(5): Show | 8 | NA18747.hp1 NA18942.hp2 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.1207-4634G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66033749 | ||||||
| chr5:66033874
|
C | T | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG02572.hp2 HG02717.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207-4509C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66033874 | ||||||
| chr5:66033938
|
G | A | 2 | a0001c0001t0009g0039a0001c0001t0009g0040 | 2 | NA18961.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1207-4445G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66033938 | ||||||
| chr5:66033970
|
G | A | 2 | a0005c0006t0007g0223a0005c0006t0016g0299 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1207-4413G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66033970 | ||||||
| chr5:66033978
|
G | A | 2 | a0008c0011t0011g0024a0008c0011t0011g0025 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1207-4405G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66033978 | ||||||
| chr5:66034115
|
C | CA | 150 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0028others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1207-4253dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 66034115 | |||||
| chr5:66034115
|
C | CAA | 8 | a0001c0001t0001g0004a0001c0001t0001g0086a0001c0001t0009g0037others(5): Show | 8 | HG02647.hp2 HG03098.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1207-4254_1207-425 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 66034115 | |||||
| chr5:66034115
|
CA | C | 15 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(12): Show | 15 | HG01167.hp2 HG02258.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1207-4253delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 66034115 | |||||
| chr5:66034115
|
CAA | C | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1207-4254_1207-425 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 66034115 | |||||
| chr5:66034181
|
A | G | 12 | a0001c0001t0006g0147a0001c0001t0006g0148a0001c0001t0006g0149others(9): Show | 12 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1207-4202A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66034181 | ||||||
| chr5:66034291
|
T | A | 1 | a0001c0001t0001g0112 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1207-4092T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66034291 | ||||||
| chr5:66034291
|
T | C | 1 | a0001c0002t0002g0236 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1207-4092T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66034291 | ||||||
| chr5:66034301
|
T | A | 1 | a0005c0006t0007g0223 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1207-4082T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66034301 | ||||||
| chr5:66034305
|
T | G | 1 | a0002c0003t0008g0179 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1207-4078T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66034305 | ||||||
| chr5:66034569
|
G | A | 1 | a0004c0017t0004g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1207-3814G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66034569 | ||||||
| chr5:66034606
|
C | CT | 23 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(20): Show | 23 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1207-3763dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 66034606 | |||||
| chr5:66034694
|
GTAT | G | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1207-3683_1207-368 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 66034694 | |||||
| chr5:66034980
|
C | A | 1 | a0005c0006t0007g0223 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1207-3403C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66034980 | ||||||
| chr5:66034994
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1207-3389C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66034994 | ||||||
| chr5:66034997
|
G | A | 45 | a0002c0003t0003g0166a0002c0003t0003g0167a0002c0003t0003g0168others(42): Show | 45 | HG00408.hp2 HG01081.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.1207-3386G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66034997 | ||||||
| chr5:66035014
|
G | A | 2 | a0005c0006t0007g0221a0005c0006t0007g0222 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1207-3369G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035014 | ||||||
| chr5:66035169
|
C | T | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1207-3214C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035169 | ||||||
| chr5:66035328
|
C | T | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1207-3055C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035328 | ||||||
| chr5:66035349
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1207-3034C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035349 | ||||||
| chr5:66035465
|
G | T | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1207-2918G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035465 | ||||||
| chr5:66035483
|
C | T | 3 | a0001c0007t0012g0218a0001c0007t0012g0219a0001c0007t0012g0220 | 3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1207-2900C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035483 | ||||||
| chr5:66035543
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1207-2840C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035543 | ||||||
| chr5:66035565
|
G | T | 1 | a0001c0001t0009g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1207-2818G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035565 | ||||||
| chr5:66035648
|
T | C | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1207-2735T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035648 | ||||||
| chr5:66035702
|
G | T | 2 | a0005c0006t0002g0229a0005c0006t0002g0263 | 2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1207-2681G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035702 | ||||||
| chr5:66035778
|
T | A | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1207-2605T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035778 | ||||||
| chr5:66035888
|
G | T | 1 | a0001c0001t0020g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1207-2495G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035888 | ||||||
| chr5:66035978
|
C | A | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1207-2405C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035978 | ||||||
| chr5:66036021
|
C | G | 1 | a0001c0002t0002g0002 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1207-2362C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66036021 | ||||||
| chr5:66036035
|
G | T | 2 | a0007c0012t0011g0022a0007c0012t0011g0023 | 2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1207-2348G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66036035 | ||||||
| chr5:66036144
|
TCTTAC | T | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1207-2233_1207-222 others(9): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 66036144 | |||||
| chr5:66036550
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1207-1833A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66036550 | ||||||
| chr5:66036607
|
A | T | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1207-1776A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66036607 | ||||||
| chr5:66036740
|
G | T | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1207-1643G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66036740 | ||||||
| chr5:66036791
|
G | A | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1207-1592G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66036791 | ||||||
| chr5:66036857
|
C | G | 1 | a0004c0005t0004g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1207-1526C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66036857 | ||||||
| chr5:66036870
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1207-1513G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66036870 | ||||||
| chr5:66036876
|
A | G | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1207-1507A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66036876 | ||||||
| chr5:66036976
|
G | T | 2 | a0005c0006t0002g0229a0005c0006t0002g0263 | 2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1207-1407G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66036976 | ||||||
| chr5:66037068
|
G | A | 1 | a0002c0003t0008g0257 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1207-1315G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037068 | ||||||
| chr5:66037126
|
T | C | 5 | a0002c0003t0002g0204a0002c0003t0002g0207a0002c0003t0002g0208others(2): Show | 5 | NA18951.hp1 NA18992.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207-1257T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037126 | ||||||
| chr5:66037227
|
G | T | 1 | a0001c0001t0001g0065 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1207-1156G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037227 | ||||||
| chr5:66037629
|
A | T | 5 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(2): Show | 5 | HG01884.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1207-754A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037629 | ||||||
| chr5:66037659
|
T | C | 2 | a0005c0006t0007g0221a0005c0006t0007g0222 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1207-724T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037659 | ||||||
| chr5:66037856
|
C | G | 1 | a0001c0002t0002g0034 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1207-527C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037856 | ||||||
| chr5:66037921
|
A | G | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1207-462A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037921 | ||||||
| chr5:66037928
|
T | G | 1 | a0002c0003t0003g0170 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1207-455T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037928 | ||||||
| chr5:66037929
|
T | A | 1 | a0002c0003t0003g0170 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1207-454T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037929 | ||||||
| chr5:66037931
|
C | A | 1 | a0002c0003t0003g0170 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1207-452C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037931 | ||||||
| chr5:66037933
|
G | A | 1 | a0002c0003t0003g0170 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1207-450G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037933 | ||||||
| chr5:66037936
|
G | T | 1 | a0002c0003t0003g0170 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1207-447G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037936 | ||||||
| chr5:66037979
|
C | A | 23 | a0001c0001t0006g0147a0001c0007t0010g0161a0001c0007t0010g0162others(20): Show | 23 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1207-404C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037979 | ||||||
| chr5:66038093
|
G | A | 2 | a0005c0006t0007g0224a0005c0006t0007g0230 | 2 | HG01109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1207-290G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66038093 | ||||||
| chr5:66038113
|
A | G | 1 | a0003c0004t0001g0094 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1207-270A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66038113 | ||||||
| chr5:66038144
|
G | A | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1207-239G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66038144 | ||||||
| chr5:66038488
|
A | G | 2 | a0005c0006t0002g0229a0005c0006t0002g0263 | 2 | HG02257.hp1 HG02647.hp1 |
splice_region_variant&intron_variant | LOW | c.1306+6A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66038488 | ||||||
| chr5:66038636
|
C | T | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1306+154C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66038636 | ||||||
| chr5:66038801
|
T | C | 1 | a0001c0001t0001g0268 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1306+319T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66038801 | ||||||
| chr5:66038807
|
T | C | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1306+325T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66038807 | ||||||
| chr5:66038951
|
G | A | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1306+469G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66038951 | ||||||
| chr5:66038990
|
G | A | 1 | a0004c0005t0004g0016 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1306+508G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66038990 | ||||||
| chr5:66039025
|
C | CGT | 19 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0109others(16): Show | 19 | HG01081.hp2 HG02165.hp1 HG02165.hp2 others(16): Show |
intron_variant | MODIFIER | c.1306+562_1306+563d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr5 | 66039025 | |||||
| chr5:66039025
|
C | CGTGTGTG others(3): Show |
14 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0010others(11): Show | 14 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1306+554_1306+563d others(12): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr5 | 66039025 | |||||
| chr5:66039044
|
G | T | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1306+562G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66039044 | ||||||
| chr5:66039087
|
C | A | 1 | a0001c0002t0002g0003 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1306+605C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66039087 | ||||||
| chr5:66039224
|
G | C | 1 | a0001c0001t0001g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1306+742G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66039224 | ||||||
| chr5:66039932
|
A | G | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1306+1450A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66039932 | ||||||
| chr5:66040036
|
G | C | 1 | a0003c0004t0001g0115 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1306+1554G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040036 | ||||||
| chr5:66040124
|
G | A | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1306+1642G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040124 | ||||||
| chr5:66040169
|
C | A | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1306+1687C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040169 | ||||||
| chr5:66040180
|
A | G | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306+1698A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040180 | ||||||
| chr5:66040185
|
C | T | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1306+1703C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040185 | ||||||
| chr5:66040210
|
T | C | 10 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(7): Show | 10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1306+1728T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040210 | ||||||
| chr5:66040227
|
A | G | 1 | a0003c0004t0001g0134 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1306+1745A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040227 | ||||||
| chr5:66040241
|
C | T | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1306+1759C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040241 | ||||||
| chr5:66040254
|
G | C | 1 | a0007c0012t0011g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1306+1772G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040254 | ||||||
| chr5:66040258
|
G | A | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1306+1776G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040258 | ||||||
| chr5:66040295
|
G | A | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1306+1813G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040295 | ||||||
| chr5:66040297
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1306+1815T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040297 | ||||||
| chr5:66040374
|
T | C | 1 | a0004c0005t0004g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1306+1892T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040374 | ||||||
| chr5:66040391
|
A | G | 2 | a0007c0012t0011g0022a0007c0012t0011g0023 | 2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1306+1909A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040391 | ||||||
| chr5:66040455
|
A | G | 4 | a0001c0002t0002g0290a0001c0015t0029g0258a0009c0010t0002g0291others(1): Show | 4 | HG00408.hp1 NA18747.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1306+1973A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040455 | ||||||
| chr5:66040571
|
TC | T | 9 | a0001c0002t0002g0289a0001c0002t0002g0290a0001c0002t0002g0293others(6): Show | 9 | HG00408.hp1 HG02165.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.1306+2092delC | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr5 | 66040571 | |||||
| chr5:66040573
|
C | T | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1306+2091C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040573 | ||||||
| chr5:66040579
|
G | A | 2 | a0005c0006t0007g0223a0005c0006t0016g0299 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1306+2097G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040579 | ||||||
| chr5:66040627
|
A | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0112 | 2 | HG01952.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1306+2145A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040627 | ||||||
| chr5:66040689
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1306+2207T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040689 | ||||||
| chr5:66040704
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1306+2222G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040704 | ||||||
| chr5:66040844
|
T | TA | 23 | a0001c0002t0002g0235a0001c0007t0010g0161a0001c0007t0010g0162others(20): Show | 23 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1307-2222dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr5 | 66040844 | |||||
| chr5:66040859
|
GA | G | 79 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0031others(76): Show | 79 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.1307-2211delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr5 | 66040859 | |||||
| chr5:66040877
|
A | G | 1 | a0001c0001t0003g0113 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1307-2200A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040877 | ||||||
| chr5:66041026
|
T | A | 1 | a0001c0001t0001g0118 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1307-2051T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66041026 | ||||||
| chr5:66041044
|
T | G | 1 | a0001c0001t0001g0264 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1307-2033T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66041044 | ||||||
| chr5:66041224
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1307-1853A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66041224 | ||||||
| chr5:66041593
|
G | C | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1307-1484G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66041593 | ||||||
| chr5:66041620
|
G | A | 1 | a0003c0004t0001g0131 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1307-1457G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66041620 | ||||||
| chr5:66041756
|
T | C | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1307-1321T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66041756 | ||||||
| chr5:66041913
|
A | T | 1 | a0001c0001t0006g0148 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1307-1164A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66041913 | ||||||
| chr5:66042347
|
C | T | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | NA18999.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1307-730C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66042347 | ||||||
| chr5:66042654
|
A | G | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1307-423A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66042654 | ||||||
| chr5:66042745
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1307-332T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66042745 | ||||||
| chr5:66042752
|
A | G | 1 | a0001c0001t0024g0158 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1307-325A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66042752 | ||||||
| chr5:66042850
|
C | T | 5 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(2): Show | 5 | HG01884.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1307-227C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66042850 | ||||||
| chr5:66042918
|
C | T | 3 | a0003c0004t0001g0302a0003c0004t0021g0303a0003c0004t0026g0301 | 3 | HG03017.hp2 HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1307-159C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66042918 | ||||||
| chr5:66042977
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1307-100T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66042977 | ||||||
| chr5:66043320
|
C | G | 6 | a0001c0001t0009g0036a0001c0001t0009g0037a0001c0001t0009g0038others(3): Show | 6 | HG03710.hp1 NA18961.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.1428+122C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 16/25 | chr5 | 66043320 | ||||||
| chr5:66043513
|
C | T | 3 | a0001c0007t0012g0218a0001c0007t0012g0219a0001c0007t0012g0220 | 3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1428+315C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 16/25 | chr5 | 66043513 | ||||||
| chr5:66043792
|
A | T | 1 | a0003c0004t0001g0001 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1429-345A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 16/25 | chr5 | 66043792 | ||||||
| chr5:66044072
|
A | C | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1429-65A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 16/25 | chr5 | 66044072 | ||||||
| chr5:66044339
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1602+29G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66044339 | ||||||
| chr5:66044342
|
T | C | 1 | a0001c0002t0002g0295 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1602+32T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66044342 | ||||||
| chr5:66044456
|
T | C | 1 | a0001c0002t0002g0212 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1602+146T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66044456 | ||||||
| chr5:66044480
|
A | T | 1 | a0001c0001t0001g0144 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1602+170A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66044480 | ||||||
| chr5:66044621
|
T | C | 2 | a0005c0006t0002g0229a0005c0006t0002g0263 | 2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1602+311T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66044621 | ||||||
| chr5:66044626
|
G | A | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1602+316G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66044626 | ||||||
| chr5:66044719
|
C | T | 6 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(3): Show | 6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1602+409C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66044719 | ||||||
| chr5:66044721
|
T | C | 193 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.1602+411T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66044721 | ||||||
| chr5:66044727
|
T | A | 1 | a0003c0004t0001g0140 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1602+417T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66044727 | ||||||
| chr5:66044759
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1602+449T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66044759 | ||||||
| chr5:66044782
|
G | A | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1602+472G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66044782 | ||||||
| chr5:66044887
|
T | C | 2 | a0002c0003t0005g0188a0002c0003t0005g0199 | 2 | NA19063.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1602+577T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66044887 | ||||||
| chr5:66045206
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1602+896G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045206 | ||||||
| chr5:66045235
|
T | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1602+925T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045235 | ||||||
| chr5:66045293
|
G | T | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1602+983G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045293 | ||||||
| chr5:66045398
|
TATATTAC others(71): Show |
T | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1603-936_1603-859d others(80): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr5 | 66045398 | |||||
| chr5:66045406
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1603-947A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045406 | ||||||
| chr5:66045407
|
T | G | 1 | a0003c0004t0001g0128 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1603-946T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045407 | ||||||
| chr5:66045481
|
T | A | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1603-872T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045481 | ||||||
| chr5:66045491
|
C | A | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1603-862C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045491 | ||||||
| chr5:66045537
|
CTG | C | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1603-813_1603-812d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr5 | 66045537 | |||||
| chr5:66045608
|
G | A | 1 | a0001c0001t0013g0125 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1603-745G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045608 | ||||||
| chr5:66045631
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1603-722G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045631 | ||||||
| chr5:66045689
|
A | G | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603-664A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045689 | ||||||
| chr5:66045754
|
A | C | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1603-599A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045754 | ||||||
| chr5:66045911
|
C | G | 1 | a0001c0001t0001g0029 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1603-442C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045911 | ||||||
| chr5:66045959
|
C | T | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | NA18999.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1603-394C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045959 | ||||||
| chr5:66045962
|
A | G | 1 | a0003c0004t0001g0306 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1603-391A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045962 | ||||||
| chr5:66045996
|
T | C | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1603-357T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045996 | ||||||
| chr5:66046073
|
G | A | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1603-280G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66046073 | ||||||
| chr5:66046091
|
T | TACAA | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1603-261_1603-258d others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr5 | 66046091 | |||||
| chr5:66046224
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1603-129T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66046224 | ||||||
| chr5:66046946
|
C | CT | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1788+415dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr5 | 66046946 | |||||
| chr5:66046961
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1788+423A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66046961 | ||||||
| chr5:66047062
|
C | T | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1788+524C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66047062 | ||||||
| chr5:66047207
|
A | C | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1788+669A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66047207 | ||||||
| chr5:66047227
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1788+689T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66047227 | ||||||
| chr5:66047498
|
A | G | 2 | a0006c0008t0003g0194a0006c0008t0018g0190 | 2 | NA18971.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.1788+960A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66047498 | ||||||
| chr5:66047585
|
C | A | 1 | a0003c0004t0001g0305 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1788+1047C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66047585 | ||||||
| chr5:66047645
|
A | G | 1 | a0005c0006t0007g0223 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1789-1022A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66047645 | ||||||
| chr5:66047825
|
G | C | 1 | a0001c0002t0002g0261 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1789-842G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66047825 | ||||||
| chr5:66047862
|
G | A | 4 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(1): Show | 4 | HG02970.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1789-805G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66047862 | ||||||
| chr5:66048038
|
G | A | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1789-629G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66048038 | ||||||
| chr5:66048127
|
T | C | 2 | a0001c0007t0010g0161a0001c0007t0010g0275 | 2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1789-540T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66048127 | ||||||
| chr5:66048194
|
A | G | 3 | a0001c0001t0013g0100a0001c0001t0013g0124a0001c0001t0013g0125 | 3 | HG01261.hp2 HG04115.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1789-473A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66048194 | ||||||
| chr5:66048267
|
C | T | 6 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(3): Show | 6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1789-400C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66048267 | ||||||
| chr5:66048281
|
T | G | 1 | a0004c0005t0004g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1789-386T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66048281 | ||||||
| chr5:66048354
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1789-313A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66048354 | ||||||
| chr5:66048541
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1789-126G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66048541 | ||||||
| chr5:66048541
|
G | T | 1 | a0015c0024t0022g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1789-126G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66048541 | ||||||
| chr5:66048559
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1789-108A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66048559 | ||||||
| chr5:66048578
|
G | A | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1789-89G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66048578 | ||||||
| chr5:66048795
|
G | A | 3 | a0001c0007t0012g0218a0001c0007t0012g0219a0001c0007t0012g0220 | 3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1903+14G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66048795 | ||||||
| chr5:66048834
|
A | G | 1 | a0015c0024t0022g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1903+53A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66048834 | ||||||
| chr5:66048836
|
A | G | 7 | a0003c0004t0001g0107a0003c0004t0001g0108a0006c0008t0003g0084others(4): Show | 7 | NA18942.hp2 NA18950.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.1903+55A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66048836 | ||||||
| chr5:66049023
|
T | C | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1903+242T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66049023 | ||||||
| chr5:66049164
|
A | G | 1 | a0010c0009t0002g0205 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1903+383A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66049164 | ||||||
| chr5:66049188
|
C | T | 1 | a0002c0003t0005g0172 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1903+407C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66049188 | ||||||
| chr5:66049194
|
T | G | 1 | a0001c0007t0012g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1903+413T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66049194 | ||||||
| chr5:66049397
|
T | C | 6 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(3): Show | 6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1903+616T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66049397 | ||||||
| chr5:66049479
|
C | G | 1 | a0001c0001t0001g0055 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1903+698C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66049479 | ||||||
| chr5:66049497
|
G | A | 2 | a0001c0007t0012g0218a0001c0007t0012g0220 | 2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1903+716G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66049497 | ||||||
| chr5:66049776
|
A | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1903+995A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66049776 | ||||||
| chr5:66049788
|
A | T | 1 | a0001c0001t0001g0058 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1904-995A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66049788 | ||||||
| chr5:66049830
|
T | C | 1 | a0013c0018t0001g0049 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1904-953T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66049830 | ||||||
| chr5:66050002
|
A | G | 141 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.1904-781A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66050002 | ||||||
| chr5:66050213
|
ACTAAATC others(323): Show |
A | 192 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.1904-554_1904-225d others(2): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050213 | |||||
| chr5:66050226
|
C | CT | 15 | a0001c0001t0001g0160a0001c0002t0002g0002a0001c0002t0002g0240others(12): Show | 15 | HG00609.hp1 HG02080.hp1 NA18943.hp1 others(12): Show |
intron_variant | MODIFIER | c.1904-521dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050226 | |||||
| chr5:66050226
|
C | CTT | 9 | a0001c0002t0002g0003a0001c0002t0002g0254a0002c0003t0002g0203others(6): Show | 9 | HG01257.hp1 HG01433.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1904-522_1904-521d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050226 | |||||
| chr5:66050226
|
C | CTTT | 8 | a0001c0002t0002g0209a0002c0003t0002g0202a0002c0003t0003g0200others(5): Show | 8 | HG01081.hp1 HG01433.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.1904-523_1904-521d others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050226 | |||||
| chr5:66050226
|
C | CTTTT | 6 | a0002c0003t0003g0182a0002c0003t0003g0183a0002c0003t0003g0192others(3): Show | 6 | HG01934.hp1 NA18948.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1904-524_1904-521d others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050226 | |||||
| chr5:66050226
|
C | CTTTTT | 6 | a0001c0002t0002g0256a0002c0003t0003g0181a0002c0003t0003g0281others(3): Show | 6 | HG00673.hp2 NA18944.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.1904-525_1904-521d others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050226 | |||||
| chr5:66050226
|
CT | C | 17 | a0001c0002t0002g0033a0001c0002t0002g0235a0001c0002t0002g0236others(14): Show | 17 | HG00408.hp1 HG01069.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.1904-521delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050226 | |||||
| chr5:66050226
|
CTT | C | 7 | a0001c0002t0002g0032a0001c0002t0002g0034a0001c0002t0002g0239others(4): Show | 7 | HG00642.hp2 HG02056.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.1904-522_1904-521d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050226 | |||||
| chr5:66050226
|
CTTTTTTT others(3): Show |
C | 3 | a0001c0007t0012g0218a0001c0007t0012g0219a0001c0007t0012g0220 | 3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1904-530_1904-521d others(12): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050226 | |||||
| chr5:66050226
|
CTTTTTTT others(4): Show |
C | 1 | a0002c0003t0002g0216 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1904-531_1904-521d others(13): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050226 | |||||
| chr5:66050226
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0002t0002g0289a0001c0002t0002g0294 | 2 | NA19004.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1904-533_1904-521d others(15): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050226 | |||||
| chr5:66050226
|
CTTTTTTT others(8): Show |
C | 2 | a0001c0002t0002g0261a0002c0003t0003g0300 | 2 | HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1904-535_1904-521d others(17): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050226 | |||||
| chr5:66050226
|
CTTTTTTT others(12): Show |
C | 8 | a0001c0002t0002g0173a0001c0002t0002g0210a0001c0002t0002g0211others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1904-539_1904-521d others(21): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050226 | |||||
| chr5:66050467
|
G | A | 8 | a0001c0002t0002g0235a0001c0002t0002g0242a0001c0002t0002g0245others(5): Show | 8 | NA18612.hp1 NA18949.hp2 NA18975.hp1 others(5): Show |
intron_variant | MODIFIER | c.1904-316G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66050467 | ||||||
| chr5:66050662
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1904-121A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66050662 | ||||||
| chr5:66050697
|
G | T | 1 | a0001c0001t0001g0264 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1904-86G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66050697 | ||||||
| chr5:66050771
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1904-12G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66050771 | ||||||
| chr5:66051061
|
T | C | 2 | a0005c0006t0007g0221a0005c0006t0007g0222 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2087+95T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66051061 | ||||||
| chr5:66051147
|
T | C | 3 | a0001c0001t0006g0154a0001c0001t0006g0155a0001c0001t0006g0156 | 3 | HG00738.hp2 HG01884.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2087+181T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66051147 | ||||||
| chr5:66051529
|
G | C | 153 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.2087+563G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66051529 | ||||||
| chr5:66051852
|
C | A | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.2087+886C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66051852 | ||||||
| chr5:66051894
|
C | CA | 171 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.2087+942dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | INFO_REALIGN_3_PRIME | chr5 | 66051894 | |||||
| chr5:66051907
|
A | AAAAAAAA others(14): Show |
1 | a0001c0007t0010g0275 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2087+942_2087+943i others(23): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | INFO_REALIGN_3_PRIME | chr5 | 66051907 | |||||
| chr5:66051907
|
A | AAAAAAAA others(12): Show |
1 | a0001c0007t0010g0161 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2087+942_2087+943i others(21): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | INFO_REALIGN_3_PRIME | chr5 | 66051907 | |||||
| chr5:66051907
|
A | AAAAAAAA others(11): Show |
4 | a0001c0007t0010g0162a0001c0007t0010g0163a0001c0007t0010g0164others(1): Show | 4 | HG02109.hp2 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2087+942_2087+943i others(20): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | INFO_REALIGN_3_PRIME | chr5 | 66051907 | |||||
| chr5:66051983
|
T | G | 3 | a0001c0001t0006g0154a0001c0001t0006g0155a0001c0001t0006g0156 | 3 | HG00738.hp2 HG01884.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2087+1017T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66051983 | ||||||
| chr5:66052177
|
A | G | 1 | a0004c0005t0004g0017 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2087+1211A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66052177 | ||||||
| chr5:66052292
|
G | T | 154 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.2088-1114G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66052292 | ||||||
| chr5:66052325
|
C | T | 193 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.2088-1081C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66052325 | ||||||
| chr5:66052326
|
G | A | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088-1080G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66052326 | ||||||
| chr5:66052495
|
A | C | 1 | a0001c0007t0012g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2088-911A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66052495 | ||||||
| chr5:66052544
|
A | G | 3 | a0001c0007t0012g0218a0001c0007t0012g0219a0001c0007t0012g0220 | 3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2088-862A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66052544 | ||||||
| chr5:66052600
|
T | C | 1 | a0001c0002t0002g0261 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2088-806T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66052600 | ||||||
| chr5:66053103
|
A | AATTCCAC | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.2088-303_2088-302i others(9): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66053103 | ||||||
| chr5:66053112
|
A | G | 154 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.2088-294A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66053112 | ||||||
| chr5:66053233
|
T | A | 196 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.2088-173T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66053233 | ||||||
| chr5:66053328
|
CAATT | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2088-77_2088-74del others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66053328 | ||||||
| chr5:66055124
|
A | G | 1 | a0014c0023t0001g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3633+173A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66055124 | ||||||
| chr5:66055137
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3633+186A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66055137 | ||||||
| chr5:66055312
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3633+361A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66055312 | ||||||
| chr5:66055369
|
T | A | 1 | a0001c0001t0001g0055 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3633+418T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66055369 | ||||||
| chr5:66055543
|
C | T | 1 | a0015c0024t0022g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3633+592C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66055543 | ||||||
| chr5:66055572
|
T | A | 1 | a0001c0001t0001g0055 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3633+621T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66055572 | ||||||
| chr5:66055780
|
C | A | 1 | a0001c0001t0013g0100 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3633+829C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66055780 | ||||||
| chr5:66055800
|
T | A | 1 | a0001c0001t0001g0055 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3633+849T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66055800 | ||||||
| chr5:66055825
|
A | T | 1 | a0001c0001t0001g0055 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3633+874A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66055825 | ||||||
| chr5:66055946
|
A | G | 3 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0010 | 3 | HG01167.hp2 HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3633+995A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66055946 | ||||||
| chr5:66056169
|
G | T | 1 | a0001c0001t0006g0149 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3633+1218G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66056169 | ||||||
| chr5:66056384
|
G | C | 1 | a0001c0002t0002g0261 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3633+1433G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66056384 | ||||||
| chr5:66056477
|
T | C | 1 | a0005c0006t0015g0225 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3633+1526T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66056477 | ||||||
| chr5:66056495
|
TAAG | T | 112 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0032others(109): Show | 112 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.3633+1548_3633+155 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66056495 | |||||
| chr5:66056585
|
C | T | 2 | a0005c0006t0007g0223a0005c0006t0016g0299 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3633+1634C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66056585 | ||||||
| chr5:66056719
|
A | T | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3633+1768A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66056719 | ||||||
| chr5:66056772
|
C | T | 8 | a0001c0002t0002g0173a0001c0002t0002g0210a0001c0002t0002g0211others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.3633+1821C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66056772 | ||||||
| chr5:66056842
|
TGTA | T | 112 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0032others(109): Show | 112 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.3633+1895_3633+189 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66056842 | |||||
| chr5:66056893
|
G | C | 3 | a0001c0007t0012g0218a0001c0007t0012g0219a0001c0007t0012g0220 | 3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.3633+1942G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66056893 | ||||||
| chr5:66056895
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3633+1944A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66056895 | ||||||
| chr5:66056919
|
C | G | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0119 | 3 | HG00735.hp1 HG01069.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.3633+1968C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66056919 | ||||||
| chr5:66057072
|
A | C | 2 | a0005c0006t0002g0229a0005c0006t0002g0263 | 2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.3633+2121A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057072 | ||||||
| chr5:66057123
|
T | A | 1 | a0001c0001t0001g0031 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3633+2172T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057123 | ||||||
| chr5:66057205
|
A | G | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+2254A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057205 | ||||||
| chr5:66057331
|
A | G | 1 | a0001c0002t0002g0252 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.3633+2380A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057331 | ||||||
| chr5:66057341
|
C | G | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+2390C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057341 | ||||||
| chr5:66057553
|
CT | C | 4 | a0001c0007t0012g0218a0001c0007t0012g0219a0001c0007t0012g0220others(1): Show | 4 | HG02559.hp2 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3633+2609delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66057553 | |||||
| chr5:66057593
|
C | T | 1 | a0002c0003t0003g0283 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3633+2642C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057593 | ||||||
| chr5:66057657
|
C | T | 109 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0032others(106): Show | 109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.3633+2706C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057657 | ||||||
| chr5:66057668
|
A | G | 1 | a0004c0017t0004g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3633+2717A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057668 | ||||||
| chr5:66057813
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3633+2862G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057813 | ||||||
| chr5:66057843
|
T | C | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3633+2892T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057843 | ||||||
| chr5:66057884
|
T | C | 2 | a0008c0011t0011g0024a0008c0011t0011g0025 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3633+2933T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057884 | ||||||
| chr5:66057908
|
T | TCCATGAT others(10): Show |
22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+2958_3633+295 others(21): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66057908 | |||||
| chr5:66057948
|
C | G | 1 | a0002c0003t0003g0192 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3633+2997C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057948 | ||||||
| chr5:66057977
|
G | T | 5 | a0003c0004t0001g0089a0003c0004t0001g0122a0003c0004t0001g0270others(2): Show | 5 | NA18977.hp1 NA18982.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.3633+3026G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057977 | ||||||
| chr5:66058047
|
C | A | 1 | a0001c0001t0001g0055 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3633+3096C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058047 | ||||||
| chr5:66058198
|
T | G | 2 | a0005c0006t0007g0221a0005c0006t0007g0222 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3633+3247T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058198 | ||||||
| chr5:66058244
|
GTATC | G | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3633+3299_3633+330 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66058244 | |||||
| chr5:66058272
|
T | C | 7 | a0001c0001t0014g0071a0001c0007t0010g0161a0001c0007t0010g0162others(4): Show | 7 | HG00621.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.3633+3321T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058272 | ||||||
| chr5:66058371
|
C | T | 1 | a0016c0013t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3633+3420C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058371 | ||||||
| chr5:66058397
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3633+3446G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058397 | ||||||
| chr5:66058417
|
T | C | 2 | a0002c0003t0003g0192a0002c0003t0003g0193 | 2 | NA18999.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.3633+3466T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058417 | ||||||
| chr5:66058445
|
A | G | 1 | a0001c0001t0001g0044 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3633+3494A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058445 | ||||||
| chr5:66058474
|
G | A | 23 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(20): Show | 23 | HG01109.hp1 HG01167.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.3633+3523G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058474 | ||||||
| chr5:66058532
|
T | G | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3633+3581T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058532 | ||||||
| chr5:66058573
|
C | T | 112 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0032others(109): Show | 112 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.3633+3622C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058573 | ||||||
| chr5:66058636
|
C | T | 1 | a0002c0003t0002g0216 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3633+3685C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058636 | ||||||
| chr5:66058691
|
G | C | 152 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0032others(149): Show | 152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.3633+3740G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058691 | ||||||
| chr5:66058709
|
A | T | 303 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.3633+3758A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058709 | ||||||
| chr5:66058717
|
G | C | 1 | a0001c0001t0003g0113 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3633+3766G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058717 | ||||||
| chr5:66058748
|
C | A | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+3797C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058748 | ||||||
| chr5:66058768
|
C | T | 2 | a0001c0002t0002g0255a0001c0002t0002g0260 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.3633+3817C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058768 | ||||||
| chr5:66058849
|
T | A | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+3898T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058849 | ||||||
| chr5:66058948
|
G | A | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3633+3997G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058948 | ||||||
| chr5:66058968
|
G | A | 2 | a0008c0011t0011g0024a0008c0011t0011g0025 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3633+4017G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058968 | ||||||
| chr5:66059006
|
T | A | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+4055T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059006 | ||||||
| chr5:66059010
|
G | T | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+4059G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059010 | ||||||
| chr5:66059014
|
A | G | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+4063A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059014 | ||||||
| chr5:66059060
|
C | A | 109 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0032others(106): Show | 109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.3633+4109C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059060 | ||||||
| chr5:66059063
|
A | G | 2 | a0009c0010t0002g0291a0009c0010t0002g0292 | 2 | NA18970.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.3633+4112A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059063 | ||||||
| chr5:66059159
|
C | T | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3633+4208C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059159 | ||||||
| chr5:66059168
|
A | T | 5 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(2): Show | 5 | HG01884.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.3633+4217A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059168 | ||||||
| chr5:66059337
|
TTGTC | T | 4 | a0005c0006t0007g0224a0005c0006t0007g0226a0005c0006t0007g0230others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3633+4390_3633+439 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66059337 | |||||
| chr5:66059383
|
A | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0011c0019t0001g0088 | 3 | NA18957.hp1 NA18990.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.3633+4432A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059383 | ||||||
| chr5:66059403
|
G | A | 1 | a0002c0003t0002g0208 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.3633+4452G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059403 | ||||||
| chr5:66059539
|
T | A | 6 | a0001c0001t0009g0036a0001c0001t0009g0037a0001c0001t0009g0038others(3): Show | 6 | HG03710.hp1 NA18961.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.3633+4588T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059539 | ||||||
| chr5:66059716
|
G | A | 13 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(10): Show | 13 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3633+4765G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059716 | ||||||
| chr5:66059741
|
C | G | 1 | a0005c0006t0007g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3633+4790C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059741 | ||||||
| chr5:66059790
|
G | C | 1 | a0015c0024t0022g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3633+4839G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059790 | ||||||
| chr5:66059893
|
T | C | 1 | a0004c0005t0004g0017 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3633+4942T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059893 | ||||||
| chr5:66059926
|
T | C | 1 | a0001c0001t0024g0158 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3633+4975T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059926 | ||||||
| chr5:66060028
|
C | G | 1 | a0001c0001t0001g0104 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.3633+5077C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060028 | ||||||
| chr5:66060037
|
A | T | 1 | a0001c0002t0002g0252 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.3633+5086A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060037 | ||||||
| chr5:66060060
|
G | A | 1 | a0001c0020t0001g0117 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.3633+5109G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060060 | ||||||
| chr5:66060136
|
T | G | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3633+5185T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060136 | ||||||
| chr5:66060159
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3633+5208A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060159 | ||||||
| chr5:66060215
|
A | C | 1 | a0002c0003t0002g0202 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3633+5264A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060215 | ||||||
| chr5:66060216
|
G | T | 1 | a0002c0003t0002g0202 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3633+5265G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060216 | ||||||
| chr5:66060337
|
T | A | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+5386T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060337 | ||||||
| chr5:66060409
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3633+5458G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060409 | ||||||
| chr5:66060582
|
T | C | 26 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(23): Show | 26 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.3633+5631T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060582 | ||||||
| chr5:66060614
|
G | T | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+5663G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060614 | ||||||
| chr5:66060722
|
A | C | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3633+5771A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060722 | ||||||
| chr5:66060769
|
C | G | 44 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0050others(41): Show | 44 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.3633+5818C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060769 | ||||||
| chr5:66060769
|
CT | C | 134 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0032others(131): Show | 134 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.3633+5826delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66060769 | |||||
| chr5:66060791
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3633+5840G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060791 | ||||||
| chr5:66060793
|
T | G | 1 | a0004c0005t0004g0017 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3633+5842T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060793 | ||||||
| chr5:66060795
|
G | T | 1 | a0004c0005t0004g0017 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3633+5844G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060795 | ||||||
| chr5:66061083
|
G | C | 152 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0032others(149): Show | 152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.3633+6132G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66061083 | ||||||
| chr5:66061120
|
G | A | 1 | a0002c0003t0002g0202 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3633+6169G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66061120 | ||||||
| chr5:66061218
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3633+6267T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66061218 | ||||||
| chr5:66061236
|
G | T | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3633+6285G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66061236 | ||||||
| chr5:66061260
|
TA | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3633+6310delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66061260 | ||||||
| chr5:66061262
|
G | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3633+6311G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66061262 | ||||||
| chr5:66061262
|
G | GTTC | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3633+6314_3633+631 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66061262 | |||||
| chr5:66061347
|
G | A | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3633+6396G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66061347 | ||||||
| chr5:66061414
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3633+6463G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66061414 | ||||||
| chr5:66061498
|
A | G | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+6547A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66061498 | ||||||
| chr5:66061682
|
C | T | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3633+6731C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66061682 | ||||||
| chr5:66061779
|
A | G | 1 | a0005c0006t0007g0223 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3633+6828A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66061779 | ||||||
| chr5:66062123
|
A | G | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+7172A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062123 | ||||||
| chr5:66062131
|
C | CAG | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+7181_3633+718 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66062131 | |||||
| chr5:66062158
|
C | T | 1 | a0001c0001t0009g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3633+7207C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062158 | ||||||
| chr5:66062181
|
G | A | 1 | a0001c0007t0012g0219 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3633+7230G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062181 | ||||||
| chr5:66062183
|
G | C | 1 | a0001c0007t0012g0219 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3633+7232G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062183 | ||||||
| chr5:66062237
|
G | A | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3633+7286G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062237 | ||||||
| chr5:66062247
|
A | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3633+7296A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062247 | ||||||
| chr5:66062275
|
G | A | 2 | a0001c0007t0010g0161a0001c0007t0010g0275 | 2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3633+7324G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062275 | ||||||
| chr5:66062280
|
A | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3633+7329A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062280 | ||||||
| chr5:66062293
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3633+7342C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062293 | ||||||
| chr5:66062304
|
G | A | 1 | a0002c0003t0005g0176 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3633+7353G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062304 | ||||||
| chr5:66062329
|
C | T | 1 | a0001c0001t0003g0113 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3633+7378C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062329 | ||||||
| chr5:66062415
|
G | A | 53 | a0002c0003t0002g0202a0002c0003t0002g0203a0002c0003t0002g0204others(50): Show | 53 | HG00280.hp2 HG00408.hp2 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.3633+7464G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062415 | ||||||
| chr5:66062530
|
CCT | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3633+7585_3633+758 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66062530 | |||||
| chr5:66062625
|
G | T | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+7674G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062625 | ||||||
| chr5:66062695
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3633+7744T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062695 | ||||||
| chr5:66062763
|
C | A | 1 | a0001c0001t0001g0272 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3633+7812C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062763 | ||||||
| chr5:66062765
|
A | G | 112 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0032others(109): Show | 112 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.3633+7814A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062765 | ||||||
| chr5:66062779
|
G | A | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.3633+7828G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062779 | ||||||
| chr5:66062979
|
T | A | 1 | a0010c0009t0002g0169 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3633+8028T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062979 | ||||||
| chr5:66062998
|
T | G | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3633+8047T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062998 | ||||||
| chr5:66063056
|
C | G | 1 | a0001c0001t0001g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3633+8105C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063056 | ||||||
| chr5:66063184
|
T | C | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+8233T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063184 | ||||||
| chr5:66063339
|
C | A | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3633+8388C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063339 | ||||||
| chr5:66063381
|
C | T | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3633+8430C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063381 | ||||||
| chr5:66063395
|
A | G | 8 | a0002c0003t0008g0174a0002c0003t0008g0175a0002c0003t0008g0179others(5): Show | 8 | HG00408.hp2 HG02071.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.3633+8444A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063395 | ||||||
| chr5:66063416
|
C | T | 3 | a0001c0001t0001g0080a0001c0001t0001g0082a0016c0013t0001g0062 | 3 | NA19030.hp1 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3633+8465C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063416 | ||||||
| chr5:66063538
|
C | T | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3633+8587C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063538 | ||||||
| chr5:66063586
|
G | A | 112 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0032others(109): Show | 112 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.3634-8583G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063586 | ||||||
| chr5:66063622
|
C | G | 2 | a0005c0006t0007g0221a0005c0006t0007g0222 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3634-8547C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063622 | ||||||
| chr5:66063625
|
C | T | 2 | a0007c0012t0011g0022a0007c0012t0011g0023 | 2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3634-8544C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063625 | ||||||
| chr5:66063653
|
G | T | 20 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0058others(17): Show | 20 | HG00609.hp1 HG00673.hp1 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.3634-8516G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063653 | ||||||
| chr5:66063702
|
A | G | 152 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0032others(149): Show | 152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.3634-8467A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063702 | ||||||
| chr5:66063766
|
A | G | 2 | a0005c0006t0007g0221a0005c0006t0007g0222 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3634-8403A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063766 | ||||||
| chr5:66063917
|
G | A | 304 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(301): Show | 304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.3634-8252G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063917 | ||||||
| chr5:66063993
|
A | G | 1 | a0001c0001t0006g0154 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3634-8176A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063993 | ||||||
| chr5:66064484
|
G | T | 13 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(10): Show | 13 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3634-7685G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66064484 | ||||||
| chr5:66064595
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3634-7574G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66064595 | ||||||
| chr5:66064743
|
G | C | 1 | a0005c0006t0002g0263 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3634-7426G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66064743 | ||||||
| chr5:66064898
|
C | G | 3 | a0006c0008t0003g0084a0006c0008t0003g0194a0006c0008t0018g0190 | 3 | NA18950.hp2 NA18971.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.3634-7271C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66064898 | ||||||
| chr5:66065039
|
G | A | 2 | a0003c0004t0001g0302a0003c0004t0021g0303 | 2 | HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.3634-7130G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065039 | ||||||
| chr5:66065236
|
A | C | 1 | a0001c0001t0013g0100 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3634-6933A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065236 | ||||||
| chr5:66065330
|
G | A | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3634-6839G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065330 | ||||||
| chr5:66065337
|
A | T | 1 | a0001c0001t0001g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3634-6832A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065337 | ||||||
| chr5:66065359
|
AC | A | 88 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0031others(85): Show | 88 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.3634-6807delC | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065359 | |||||
| chr5:66065425
|
T | C | 1 | a0001c0015t0029g0258 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3634-6744T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065425 | ||||||
| chr5:66065556
|
C | T | 1 | a0004c0005t0004g0009 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3634-6613C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065556 | ||||||
| chr5:66065559
|
G | A | 21 | a0001c0001t0001g0138a0001c0001t0001g0266a0001c0001t0001g0274others(18): Show | 21 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.3634-6610G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065559 | ||||||
| chr5:66065590
|
CCTGTGTG others(12): Show |
C | 6 | a0001c0002t0002g0173a0001c0002t0002g0211a0001c0002t0002g0212others(3): Show | 6 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3634-6578_3634-656 others(23): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065590 | ||||||
| chr5:66065590
|
CCTGTGTG others(14): Show |
C | 1 | a0001c0002t0002g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3634-6578_3634-655 others(25): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065590 | ||||||
| chr5:66065590
|
CCTGTGTG others(16): Show |
C | 1 | a0001c0002t0002g0210 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3634-6578_3634-655 others(27): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065590 | ||||||
| chr5:66065591
|
CTGTGTG | C | 6 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0009g0039others(3): Show | 6 | HG03041.hp2 NA18961.hp1 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-6514_3634-650 others(10): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | |||||
| chr5:66065591
|
CTGTGTGT others(1): Show |
C | 16 | a0001c0001t0001g0048a0001c0001t0001g0057a0001c0001t0001g0098others(13): Show | 16 | HG00738.hp1 HG01261.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.3634-6516_3634-650 others(12): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | |||||
| chr5:66065591
|
CTGTGTGT others(3): Show |
C | 21 | a0001c0001t0001g0031a0001c0001t0001g0043a0001c0001t0001g0067others(18): Show | 21 | HG00099.hp2 HG01256.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.3634-6518_3634-650 others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | |||||
| chr5:66065591
|
CTGTGTGT others(5): Show |
C | 21 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0056others(18): Show | 21 | HG00673.hp1 HG01069.hp2 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.3634-6520_3634-650 others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | |||||
| chr5:66065591
|
CTGTGTGT others(7): Show |
C | 25 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0045others(22): Show | 25 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.3634-6522_3634-650 others(18): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | |||||
| chr5:66065591
|
CTGTGTGT others(9): Show |
C | 14 | a0001c0001t0001g0042a0001c0001t0001g0058a0001c0001t0001g0073others(11): Show | 14 | HG00099.hp1 HG00438.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.3634-6524_3634-650 others(20): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | |||||
| chr5:66065591
|
CTGTGTGT others(11): Show |
C | 31 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(28): Show | 31 | HG00408.hp1 HG00621.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.3634-6526_3634-650 others(22): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | |||||
| chr5:66065591
|
CTGTGTGT others(13): Show |
C | 42 | a0001c0001t0001g0029a0001c0001t0001g0050a0001c0001t0001g0059others(39): Show | 42 | HG00438.hp2 HG00609.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.3634-6528_3634-650 others(24): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | |||||
| chr5:66065591
|
CTGTGTGT others(15): Show |
C | 55 | a0001c0002t0002g0032a0001c0002t0002g0242a0001c0002t0002g0251others(52): Show | 55 | HG00280.hp2 HG00408.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.3634-6530_3634-650 others(26): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | |||||
| chr5:66065591
|
CTGTGTGT others(17): Show |
C | 29 | a0001c0001t0001g0054a0001c0001t0001g0086a0001c0001t0001g0159others(26): Show | 29 | HG01167.hp2 HG02071.hp1 HG02165.hp1 others(26): Show |
intron_variant | MODIFIER | c.3634-6532_3634-650 others(28): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | |||||
| chr5:66065591
|
CTGTGTGT others(19): Show |
C | 10 | a0001c0001t0006g0147a0001c0001t0006g0148a0001c0007t0012g0218others(7): Show | 10 | HG02109.hp1 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.3634-6534_3634-650 others(30): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | |||||
| chr5:66065591
|
CTGTGTGT others(21): Show |
C | 6 | a0001c0001t0006g0149a0001c0001t0006g0150a0001c0001t0006g0151others(3): Show | 6 | HG02717.hp2 HG02922.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-6536_3634-650 others(32): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | |||||
| chr5:66065591
|
CTGTGTGT others(31): Show |
C | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-6546_3634-650 others(42): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | |||||
| chr5:66065637
|
G | A | 10 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(7): Show | 10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.3634-6532G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065637 | ||||||
| chr5:66065639
|
G | A | 6 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(3): Show | 6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-6530G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065639 | ||||||
| chr5:66065639
|
GTGTGTGT others(14): Show |
G | 1 | a0002c0003t0002g0202 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3634-6528_3634-650 others(25): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065639 | |||||
| chr5:66065641
|
GTGTGTGT others(12): Show |
G | 1 | a0001c0002t0002g0261 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3634-6526_3634-650 others(23): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065641 | |||||
| chr5:66065641
|
GTGTGTGT others(14): Show |
G | 1 | a0001c0001t0001g0044 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3634-6525_3634-650 others(25): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065641 | |||||
| chr5:66065647
|
GTGTGTGT others(6): Show |
G | 1 | a0001c0001t0001g0046 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3634-6520_3634-650 others(17): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065647 | |||||
| chr5:66065649
|
GTGTGTGT others(4): Show |
G | 1 | a0003c0004t0001g0137 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3634-6518_3634-650 others(15): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065649 | |||||
| chr5:66065655
|
G | T | 1 | a0001c0001t0001g0126 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.3634-6514G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065655 | ||||||
| chr5:66065753
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3634-6416G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065753 | ||||||
| chr5:66065803
|
T | C | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3634-6366T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065803 | ||||||
| chr5:66065942
|
C | T | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-6227C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065942 | ||||||
| chr5:66065949
|
A | G | 1 | a0001c0002t0002g0239 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3634-6220A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065949 | ||||||
| chr5:66065959
|
T | A | 1 | a0001c0002t0002g0237 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3634-6210T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065959 | ||||||
| chr5:66066038
|
T | G | 1 | a0001c0002t0002g0173 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3634-6131T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066038 | ||||||
| chr5:66066269
|
C | G | 1 | a0002c0003t0003g0198 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3634-5900C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066269 | ||||||
| chr5:66066275
|
G | A | 3 | a0001c0001t0006g0154a0001c0001t0006g0155a0001c0001t0006g0156 | 3 | HG00738.hp2 HG01884.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.3634-5894G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066275 | ||||||
| chr5:66066359
|
A | T | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3634-5810A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066359 | ||||||
| chr5:66066367
|
G | A | 1 | a0013c0018t0001g0049 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3634-5802G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066367 | ||||||
| chr5:66066493
|
C | T | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3634-5676C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066493 | ||||||
| chr5:66066502
|
TA | T | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3634-5665delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66066502 | |||||
| chr5:66066522
|
T | TA | 6 | a0002c0003t0003g0198a0003c0004t0001g0136a0003c0004t0001g0140others(3): Show | 6 | HG00642.hp1 HG01515.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-5634dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66066522 | |||||
| chr5:66066526
|
A | AAAAAAT | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-5638_3634-563 others(10): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66066526 | |||||
| chr5:66066530
|
A | AAT | 10 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(7): Show | 10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.3634-5638_3634-563 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66066530 | |||||
| chr5:66066534
|
A | T | 1 | a0001c0007t0010g0161 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3634-5635A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066534 | ||||||
| chr5:66066535
|
A | T | 4 | a0001c0007t0010g0162a0001c0007t0010g0163a0001c0007t0010g0164others(1): Show | 4 | HG02109.hp2 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3634-5634A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066535 | ||||||
| chr5:66066536
|
C | A | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3634-5633C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066536 | ||||||
| chr5:66066568
|
A | G | 13 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(10): Show | 13 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3634-5601A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066568 | ||||||
| chr5:66066714
|
C | A | 1 | a0001c0001t0001g0104 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.3634-5455C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066714 | ||||||
| chr5:66066773
|
C | T | 6 | a0002c0003t0002g0204a0002c0003t0002g0207a0002c0003t0002g0208others(3): Show | 6 | HG00280.hp2 NA18951.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.3634-5396C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066773 | ||||||
| chr5:66066834
|
C | G | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3634-5335C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066834 | ||||||
| chr5:66066835
|
T | C | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3634-5334T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066835 | ||||||
| chr5:66066841
|
G | T | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-5328G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066841 | ||||||
| chr5:66066857
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3634-5312C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066857 | ||||||
| chr5:66067204
|
C | T | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-4965C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66067204 | ||||||
| chr5:66067215
|
G | A | 1 | a0005c0006t0007g0026 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3634-4954G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66067215 | ||||||
| chr5:66067480
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3634-4689G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66067480 | ||||||
| chr5:66067595
|
A | G | 2 | a0001c0002t0002g0289a0001c0002t0002g0294 | 2 | NA19004.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.3634-4574A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66067595 | ||||||
| chr5:66067724
|
TTTC | T | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-4436_3634-443 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66067724 | |||||
| chr5:66067913
|
C | A | 1 | a0002c0003t0008g0241 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3634-4256C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66067913 | ||||||
| chr5:66067938
|
C | A | 3 | a0001c0001t0006g0152a0001c0001t0006g0153a0001c0001t0006g0157 | 3 | HG01891.hp1 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3634-4231C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66067938 | ||||||
| chr5:66067989
|
T | C | 4 | a0005c0006t0007g0224a0005c0006t0007g0226a0005c0006t0007g0230others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3634-4180T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66067989 | ||||||
| chr5:66068051
|
G | A | 12 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.3634-4118G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068051 | ||||||
| chr5:66068168
|
A | AAAT | 8 | a0001c0001t0001g0044a0001c0001t0006g0150a0001c0002t0002g0238others(5): Show | 8 | NA18522.hp1 NA18522.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.3634-3980_3634-397 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66068168 | |||||
| chr5:66068189
|
T | C | 7 | a0001c0002t0002g0242a0001c0007t0010g0161a0001c0007t0010g0162others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.3634-3980T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068189 | ||||||
| chr5:66068306
|
C | T | 1 | a0002c0003t0003g0200 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3634-3863C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068306 | ||||||
| chr5:66068326
|
T | TAAAAAAA others(324): Show |
1 | a0004c0005t0004g0014 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.3634-3831_3634-383 others(335): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66068326 | |||||
| chr5:66068326
|
T | TAAAAAAA others(325): Show |
1 | a0004c0005t0004g0020 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3634-3831_3634-383 others(336): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66068326 | |||||
| chr5:66068338
|
A | T | 1 | a0001c0007t0010g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3634-3831A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068338 | ||||||
| chr5:66068339
|
A | T | 20 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(17): Show | 20 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.3634-3830A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068339 | ||||||
| chr5:66068340
|
A | T | 31 | a0001c0001t0001g0057a0001c0001t0001g0086a0001c0001t0006g0147others(28): Show | 31 | HG01167.hp2 HG01261.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.3634-3829A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068340 | ||||||
| chr5:66068346
|
G | A | 1 | a0005c0006t0007g0026 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3634-3823G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068346 | ||||||
| chr5:66068352
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3634-3817G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068352 | ||||||
| chr5:66068381
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3634-3788G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068381 | ||||||
| chr5:66068423
|
A | G | 1 | a0014c0023t0001g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3634-3746A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068423 | ||||||
| chr5:66068679
|
G | A | 2 | a0002c0003t0003g0192a0002c0003t0003g0193 | 2 | NA18999.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.3634-3490G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068679 | ||||||
| chr5:66068707
|
C | A | 19 | a0002c0003t0003g0181a0002c0003t0003g0182a0002c0003t0003g0183others(16): Show | 19 | HG01081.hp1 HG01257.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.3634-3462C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068707 | ||||||
| chr5:66068726
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3634-3443T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068726 | ||||||
| chr5:66068823
|
G | A | 1 | a0003c0025t0001g0143 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3634-3346G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068823 | ||||||
| chr5:66068864
|
CCT | C | 26 | a0001c0001t0001g0028a0001c0001t0001g0041a0001c0001t0001g0048others(23): Show | 26 | HG00280.hp1 HG00735.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.3634-3302_3634-330 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66068864 | |||||
| chr5:66068898
|
A | T | 1 | a0001c0001t0001g0112 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3634-3271A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068898 | ||||||
| chr5:66069113
|
A | T | 1 | a0004c0014t0004g0018 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3634-3056A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66069113 | ||||||
| chr5:66069237
|
C | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3634-2932C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66069237 | ||||||
| chr5:66069264
|
T | C | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-2905T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66069264 | ||||||
| chr5:66069296
|
C | T | 1 | a0002c0003t0002g0207 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.3634-2873C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66069296 | ||||||
| chr5:66069302
|
A | G | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-2867A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66069302 | ||||||
| chr5:66069560
|
T | C | 1 | a0002c0003t0005g0185 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3634-2609T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66069560 | ||||||
| chr5:66069604
|
C | T | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3634-2565C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66069604 | ||||||
| chr5:66069675
|
C | A | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-2494C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66069675 | ||||||
| chr5:66069740
|
G | A | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3634-2429G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66069740 | ||||||
| chr5:66069776
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3634-2393C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66069776 | ||||||
| chr5:66069811
|
A | G | 2 | a0007c0012t0011g0022a0007c0012t0011g0023 | 2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3634-2358A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66069811 | ||||||
| chr5:66069840
|
G | A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3634-2329G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66069840 | ||||||
| chr5:66070067
|
G | A | 13 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(10): Show | 13 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3634-2102G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66070067 | ||||||
| chr5:66070084
|
G | A | 109 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0032others(106): Show | 109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.3634-2085G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66070084 | ||||||
| chr5:66070289
|
C | T | 1 | a0001c0002t0002g0296 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3634-1880C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66070289 | ||||||
| chr5:66070329
|
C | T | 1 | a0005c0006t0007g0026 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3634-1840C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66070329 | ||||||
| chr5:66070482
|
G | GT | 3 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0073 | 3 | HG02145.hp1 HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3634-1686dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66070482 | |||||
| chr5:66070520
|
GT | G | 12 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(9): Show | 12 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.3634-1640delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66070520 | |||||
| chr5:66070817
|
C | T | 113 | a0001c0001t0003g0113a0001c0002t0002g0002a0001c0002t0002g0003others(110): Show | 113 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.3634-1352C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66070817 | ||||||
| chr5:66070910
|
A | G | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-1259A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66070910 | ||||||
| chr5:66070920
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3634-1249C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66070920 | ||||||
| chr5:66070978
|
A | C | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-1191A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66070978 | ||||||
| chr5:66071223
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3634-946C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66071223 | ||||||
| chr5:66071351
|
AAAGT | A | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3634-817_3634-814d others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66071351 | ||||||
| chr5:66071369
|
AAAAG | A | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3634-780_3634-777d others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66071369 | |||||
| chr5:66071410
|
AT | A | 6 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(3): Show | 6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-757delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66071410 | |||||
| chr5:66071438
|
T | G | 13 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(10): Show | 13 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3634-731T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66071438 | ||||||
| chr5:66071580
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3634-589A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66071580 | ||||||
| chr5:66071676
|
GA | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3634-486delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66071676 | |||||
| chr5:66071722
|
A | AT | 31 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0060others(28): Show | 31 | HG00621.hp1 HG00621.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.3634-428dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66071722 | |||||
| chr5:66071722
|
A | T | 1 | a0002c0003t0005g0185 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3634-447A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66071722 | ||||||
| chr5:66071813
|
T | C | 1 | a0001c0001t0001g0268 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3634-356T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66071813 | ||||||
| chr5:66071973
|
A | C | 1 | a0003c0004t0001g0141 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3634-196A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66071973 | ||||||
| chr5:66072006
|
G | A | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-163G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66072006 | ||||||
| chr5:66072089
|
A | G | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3634-80A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66072089 | ||||||
| chr5:66072104
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3634-65G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66072104 | ||||||
| chr5:66072146
|
A | G | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-23A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66072146 | ||||||
| chr5:66072511
|
T | C | 1 | a0005c0006t0007g0026 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3756+220T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66072511 | ||||||
| chr5:66072659
|
A | G | 7 | a0004c0005t0004g0013a0004c0005t0004g0014a0004c0005t0004g0015others(4): Show | 7 | HG02258.hp1 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.3756+368A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66072659 | ||||||
| chr5:66072824
|
A | G | 1 | a0001c0007t0012g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3756+533A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66072824 | ||||||
| chr5:66073062
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3756+771T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66073062 | ||||||
| chr5:66073117
|
C | G | 1 | a0002c0003t0002g0203 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3756+826C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66073117 | ||||||
| chr5:66073318
|
G | A | 1 | a0001c0002t0002g0033 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3756+1027G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66073318 | ||||||
| chr5:66073352
|
A | C | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3756+1061A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66073352 | ||||||
| chr5:66073400
|
G | GT | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3756+1116dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 66073400 | |||||
| chr5:66073607
|
A | C | 1 | a0001c0002t0002g0214 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3756+1316A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66073607 | ||||||
| chr5:66073616
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3756+1325A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66073616 | ||||||
| chr5:66073791
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3757-1233A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66073791 | ||||||
| chr5:66073841
|
C | G | 1 | a0001c0001t0001g0081 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3757-1183C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66073841 | ||||||
| chr5:66073867
|
T | C | 1 | a0001c0002t0002g0259 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.3757-1157T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66073867 | ||||||
| chr5:66074045
|
A | AT | 138 | a0001c0001t0001g0028a0001c0001t0001g0047a0001c0001t0001g0050others(135): Show | 138 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.3757-952dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 66074045 | |||||
| chr5:66074045
|
A | ATT | 28 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(25): Show | 28 | HG00408.hp1 HG00642.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.3757-953_3757-952d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 66074045 | |||||
| chr5:66074045
|
AT | A | 8 | a0001c0001t0001g0106a0001c0001t0006g0147a0001c0001t0006g0148others(5): Show | 8 | HG00738.hp2 HG01257.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.3757-952delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 66074045 | |||||
| chr5:66074045
|
ATTT | A | 6 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(3): Show | 6 | HG01167.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3757-954_3757-952d others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 66074045 | |||||
| chr5:66074045
|
ATTTT | A | 15 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(12): Show | 15 | HG02055.hp2 HG02109.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.3757-955_3757-952d others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 66074045 | |||||
| chr5:66074045
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0014g0070 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3757-963_3757-952d others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 66074045 | |||||
| chr5:66074045
|
ATTTTTTT others(7): Show |
A | 1 | a0001c0002t0002g0254 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3757-965_3757-952d others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 66074045 | |||||
| chr5:66074072
|
T | TA | 3 | a0001c0001t0009g0037a0001c0001t0009g0038a0001c0022t0009g0035 | 3 | NA18985.hp2 NA18994.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.3757-951dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 66074072 | |||||
| chr5:66074135
|
C | T | 1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3757-889C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66074135 | ||||||
| chr5:66074147
|
C | T | 1 | a0001c0002t0002g0242 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3757-877C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66074147 | ||||||
| chr5:66074314
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3757-710A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66074314 | ||||||
| chr5:66074352
|
T | TACTTTAT others(7): Show |
1 | a0012c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3757-671_3757-658d others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 66074352 | |||||
| chr5:66074417
|
A | ATAT | 149 | a0001c0001t0003g0113a0001c0002t0002g0002a0001c0002t0002g0003others(146): Show | 149 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.3757-605_3757-604i others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 66074417 | |||||
| chr5:66074551
|
C | T | 113 | a0001c0001t0003g0113a0001c0002t0002g0002a0001c0002t0002g0003others(110): Show | 113 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.3757-473C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66074551 | ||||||
| chr5:66074745
|
AAAG | A | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.3757-278_3757-276d others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66074745 | ||||||
| chr5:66074832
|
T | C | 1 | a0001c0007t0012g0219 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3757-192T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66074832 | ||||||
| chr5:66075312
|
A | G | 1 | a0001c0001t0006g0155 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3963+82A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 23/25 | chr5 | 66075312 | ||||||
| chr5:66075326
|
C | T | 4 | a0007c0012t0011g0022a0007c0012t0011g0023a0008c0011t0011g0024others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3963+96C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 23/25 | chr5 | 66075326 | ||||||
| chr5:66075327
|
G | A | 2 | a0005c0006t0007g0221a0005c0006t0007g0222 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3963+97G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 23/25 | chr5 | 66075327 | ||||||
| chr5:66075929
|
T | C | 1 | a0015c0024t0022g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3964-387T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 23/25 | chr5 | 66075929 | ||||||
| chr5:66075974
|
G | A | 1 | a0004c0005t0004g0007 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3964-342G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 23/25 | chr5 | 66075974 | ||||||
| chr5:66075983
|
A | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0011c0019t0001g0088 | 3 | NA18957.hp1 NA18990.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.3964-333A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 23/25 | chr5 | 66075983 | ||||||
| chr5:66076059
|
T | C | 6 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(3): Show | 6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3964-257T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 23/25 | chr5 | 66076059 | ||||||
| chr5:66076069
|
T | C | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3964-247T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 23/25 | chr5 | 66076069 | ||||||
| chr5:66076458
|
G | A | 2 | a0003c0004t0001g0306a0003c0004t0023g0304 | 2 | HG01952.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.4056+50G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 24/25 | chr5 | 66076458 | ||||||
| chr5:66076623
|
A | G | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.4056+215A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 24/25 | chr5 | 66076623 | ||||||
| chr5:66076638
|
C | T | 1 | a0003c0004t0001g0131 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4056+230C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 24/25 | chr5 | 66076638 | ||||||
| chr5:66076708
|
A | T | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4057-167A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 24/25 | chr5 | 66076708 | ||||||
| chr5:66076964
|
T | C | 3 | a0001c0002t0002g0235a0001c0002t0002g0245a0001c0002t0002g0250 | 3 | NA18949.hp2 NA18990.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.4131+15T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66076964 | ||||||
| chr5:66076965
|
C | CT | 146 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0032others(143): Show | 146 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.4131+27dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66076965 | |||||
| chr5:66076977
|
C | T | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.4131+28C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66076977 | ||||||
| chr5:66077076
|
G | A | 1 | a0004c0005t0004g0017 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4131+127G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077076 | ||||||
| chr5:66077082
|
C | T | 3 | a0001c0001t0006g0154a0001c0001t0006g0155a0001c0001t0006g0156 | 3 | HG00738.hp2 HG01884.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.4131+133C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077082 | ||||||
| chr5:66077085
|
C | A | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4131+136C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077085 | ||||||
| chr5:66077086
|
A | G | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4131+137A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077086 | ||||||
| chr5:66077150
|
C | CA | 29 | a0001c0001t0001g0231a0001c0001t0001g0272a0001c0001t0006g0147others(26): Show | 29 | HG00642.hp2 HG00738.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.4131+220dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077150 | |||||
| chr5:66077150
|
CA | C | 20 | a0001c0001t0001g0048a0001c0001t0001g0076a0001c0002t0002g0251others(17): Show | 20 | HG01167.hp2 HG01515.hp1 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.4131+220delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077150 | |||||
| chr5:66077166
|
A | C | 2 | a0001c0007t0012g0218a0001c0007t0012g0220 | 2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.4131+217A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077166 | ||||||
| chr5:66077191
|
T | C | 1 | a0001c0001t0001g0068 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.4131+242T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077191 | ||||||
| chr5:66077391
|
A | G | 22 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(19): Show | 22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.4131+442A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077391 | ||||||
| chr5:66077395
|
A | T | 5 | a0006c0008t0003g0084a0006c0008t0003g0189a0006c0008t0003g0191others(2): Show | 5 | NA18950.hp2 NA18956.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.4131+446A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077395 | ||||||
| chr5:66077423
|
C | T | 1 | a0002c0003t0003g0170 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.4131+474C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077423 | ||||||
| chr5:66077481
|
C | CA | 113 | a0001c0001t0003g0113a0001c0002t0002g0002a0001c0002t0002g0003others(110): Show | 113 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.4131+541dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077481 | |||||
| chr5:66077591
|
C | T | 165 | a0001c0001t0003g0113a0001c0001t0006g0147a0001c0001t0006g0148others(162): Show | 165 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.4131+642C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077591 | ||||||
| chr5:66077604
|
A | T | 13 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(10): Show | 13 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.4131+655A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077604 | ||||||
| chr5:66077605
|
T | A | 1 | a0002c0003t0002g0203 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4131+656T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077605 | ||||||
| chr5:66077759
|
T | TAC | 53 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(50): Show | 53 | HG00438.hp2 HG00621.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.4132-630_4132-629d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077759 | |||||
| chr5:66077759
|
T | TACAC | 13 | a0001c0001t0001g0072a0001c0001t0001g0231a0001c0002t0002g0214others(10): Show | 13 | HG00408.hp1 HG02148.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.4132-632_4132-629d others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077759 | |||||
| chr5:66077759
|
T | TACACAC | 8 | a0001c0002t0002g0252a0002c0003t0002g0203a0002c0003t0002g0204others(5): Show | 8 | HG00280.hp2 HG03239.hp1 NA19001.hp2 others(5): Show |
intron_variant | MODIFIER | c.4132-634_4132-629d others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077759 | |||||
| chr5:66077759
|
T | TACACACA others(1): Show |
30 | a0002c0003t0002g0202a0002c0003t0003g0166a0002c0003t0003g0181others(27): Show | 30 | HG00408.hp2 HG01257.hp1 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.4132-636_4132-629d others(10): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077759 | |||||
| chr5:66077759
|
T | TACACACA others(3): Show |
8 | a0001c0001t0001g0090a0001c0001t0001g0091a0002c0003t0003g0198others(5): Show | 8 | HG01081.hp1 HG01934.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.4132-638_4132-629d others(12): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077759 | |||||
| chr5:66077759
|
T | TACACACA others(5): Show |
2 | a0002c0003t0003g0167a0002c0003t0003g0170 | 2 | NA18946.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.4132-640_4132-629d others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077759 | |||||
| chr5:66077759
|
T | TACACACA others(7): Show |
1 | a0002c0003t0003g0300 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4132-642_4132-629d others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077759 | |||||
| chr5:66077759
|
TAC | T | 12 | a0001c0001t0001g0047a0001c0001t0001g0159a0001c0001t0006g0148others(9): Show | 12 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.4132-630_4132-629d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077759 | |||||
| chr5:66077759
|
TACAC | T | 4 | a0001c0001t0006g0149a0003c0004t0001g0134a0005c0006t0016g0299others(1): Show | 4 | HG00621.hp2 HG01884.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.4132-632_4132-629d others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077759 | |||||
| chr5:66077759
|
TACACAC | T | 4 | a0005c0006t0002g0229a0005c0006t0002g0263a0005c0006t0007g0026others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4132-634_4132-629d others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077759 | |||||
| chr5:66077759
|
TACACACA others(3): Show |
T | 1 | a0005c0006t0007g0221 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4132-638_4132-629d others(12): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077759 | |||||
| chr5:66077759
|
TACACACA others(11): Show |
T | 1 | a0014c0023t0001g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4132-646_4132-629d others(20): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077759 | |||||
| chr5:66077771
|
CACACACA others(17): Show |
C | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(2): Show | 5 | HG01071.hp2 HG01934.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.4132-636_4132-613d others(26): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077771 | |||||
| chr5:66077773
|
CACACACA others(15): Show |
C | 1 | a0001c0001t0001g0144 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4132-634_4132-613d others(24): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077773 | |||||
| chr5:66077782
|
A | AGT | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4132-641_4132-640i others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077782 | ||||||
| chr5:66077785
|
CACACACA others(3): Show |
C | 3 | a0003c0004t0001g0122a0003c0004t0001g0271a0003c0004t0017g0121 | 3 | NA18977.hp1 NA18992.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.4132-628_4132-619d others(12): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077785 | |||||
| chr5:66077788
|
A | T | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4132-635A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077788 | ||||||
| chr5:66077792
|
A | T | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4132-631A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077792 | ||||||
| chr5:66077793
|
C | G | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.4132-630C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077793 | ||||||
| chr5:66077794
|
A | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.4132-629A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077794 | ||||||
| chr5:66077795
|
T | C | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.4132-628T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077795 | ||||||
| chr5:66077796
|
ACACACAC others(15): Show |
A | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4132-623_4132-602d others(24): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077796 | |||||
| chr5:66077797
|
C | T | 1 | a0005c0006t0007g0223 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4132-626C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077797 | ||||||
| chr5:66077800
|
A | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.4132-623A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077800 | ||||||
| chr5:66077804
|
A | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.4132-619A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077804 | ||||||
| chr5:66077807
|
C | T | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.4132-616C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077807 | ||||||
| chr5:66077808
|
ACAGTCAC others(3): Show |
A | 16 | a0004c0005t0004g0007a0004c0005t0004g0008a0004c0005t0004g0009others(13): Show | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.4132-612_4132-603d others(12): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077808 | |||||
| chr5:66077877
|
G | A | 1 | a0002c0003t0003g0281 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.4132-546G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077877 | ||||||
| chr5:66077883
|
G | GT | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4132-538dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077883 | |||||
| chr5:66078096
|
G | T | 3 | a0001c0007t0012g0218a0001c0007t0012g0219a0001c0007t0012g0220 | 3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.4132-327G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66078096 | ||||||
| chr5:66078307
|
GTTATT | G | 6 | a0001c0007t0010g0161a0001c0007t0010g0162a0001c0007t0010g0163others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4132-112_4132-108d others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66078307 | |||||
| chr5:66078414
|
C | T | 1 | a0001c0001t0006g0148 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4132-9C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66078414 |