| geneid | 81671 |
|---|---|
| ensemblid | ENSG00000062716.13 |
| hgncid | 29559 |
| symbol | VMP1 |
| name | vacuole membrane protein 1 |
| refseq_nuc | NM_030938.5 |
| refseq_prot | NP_112200.2 |
| ensembl_nuc | ENST00000262291.9 |
| ensembl_prot | ENSP00000262291.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 59707654 |
| end | 59842255 |
| strand | + |
| ver | v1.2 |
| region | chr17:59707654-59842255 |
| region5000 | chr17:59702654-59847255 |
| regionname0 | VMP1_chr17_59707654_59842255 |
| regionname5000 | VMP1_chr17_59702654_59847255 |
| 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 | 406 | 285 | 86 | 49 | 112 | 6 | 30 | 84 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| a0002 | 0/0 | 406 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1221 | 283 | 86 | 49 | 111 | 5 | 30 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| c0002 | 0/0 | 1221 | 2 | 0 | 0 | 1 | 1 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| c0003 | 0/0 | 1221 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 2466 | 133 | 45 | 27 | 42 | 5 | 13 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| t0002 | 0/1 | 2466 | 71 | 3 | 12 | 46 | 1 | 8 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| t0003 | 0/0 | 2466 | 52 | 20 | 9 | 21 | 0 | 2 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| t0004 | 0/0 | 2466 | 11 | 10 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| t0005 | 0/0 | 2466 | 5 | 0 | 0 | 1 | 0 | 4 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| t0006 | 0/0 | 2466 | 4 | 4 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| t0007 | 0/0 | 2466 | 2 | 0 | 0 | 0 | 0 | 2 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| t0008 | 0/0 | 2466 | 2 | 2 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| t0009 | 0/0 | 2466 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| t0010 | 0/0 | 2466 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| t0011 | 0/0 | 2466 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| t0012 | 0/0 | 2466 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| t0013 | 0/0 | 2466 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| t0014 | 0/0 | 2466 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| 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 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0196 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1221 | 283 | 86 | 49 | 111 | 5 | 30 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| a0001c0002 | 0/0 | 1221 | 2 | 0 | 0 | 1 | 1 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| a0002c0003 | 0/0 | 1221 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3686 | 131 | 45 | 27 | 41 | 4 | 13 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| a0001c0001t0002 | 0/1 | 3686 | 70 | 3 | 11 | 46 | 1 | 8 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| a0001c0001t0003 | 0/0 | 3686 | 52 | 20 | 9 | 21 | 0 | 2 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| a0001c0001t0004 | 0/0 | 3686 | 11 | 10 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| a0001c0001t0005 | 0/0 | 3686 | 5 | 0 | 0 | 1 | 0 | 4 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| a0001c0001t0006 | 0/0 | 3686 | 4 | 4 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| a0001c0001t0007 | 0/0 | 3686 | 2 | 0 | 0 | 0 | 0 | 2 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| a0001c0001t0008 | 0/0 | 3686 | 2 | 2 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| a0001c0001t0009 | 0/0 | 3686 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| a0001c0001t0010 | 0/0 | 3686 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| a0001c0001t0011 | 0/0 | 3686 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| a0001c0001t0012 | 0/0 | 3686 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| a0001c0001t0013 | 0/0 | 3686 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| a0001c0001t0014 | 0/0 | 3686 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| a0001c0002t0001 | 0/0 | 3686 | 2 | 0 | 0 | 1 | 1 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| a0002c0003t0002 | 0/0 | 3686 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | copy fasta | chr17 | 59702654 | 59847255 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0196 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0005g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0006g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0006g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0006g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0007g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0007g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0008g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0008g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0009g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0010g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0011g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0012g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0013g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0014g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0002c0003t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0168 | EUR | GBR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0229 | EUR | GBR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0224 | EUR | FIN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | FIN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | CHS | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | CHS | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | CHS | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | CHS | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | CHS | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00639 | hp2 | a0002 | c0003 | t0002 | g0030 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0113 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | CHS | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | CHS | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0125 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00741 | hp2 | a0001 | c0001 | t0010 | g0230 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0127 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0111 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0262 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0156 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0124 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0129 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0281 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | CDX | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | CDX | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0273 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0105 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0059 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0002 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0267 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0259 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02965 | hp1 | a0001 | c0001 | t0014 | g0191 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0268 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0265 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0264 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0270 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0137 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0284 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0151 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0154 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0266 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0263 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03491 | hp2 | a0001 | c0001 | t0007 | g0274 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03492 | hp1 | a0001 | c0001 | t0007 | g0275 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0271 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0134 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | STU | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | STU | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0237 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03831 | hp2 | a0001 | c0001 | t0009 | g0109 | SAS | BEB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0112 | SAS | BEB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0027 | SAS | BEB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0058 | SAS | BEB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0108 | SAS | BEB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03942 | hp2 | a0001 | c0001 | t0005 | g0018 | SAS | BEB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | STU | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | STU | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | YRI | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0269 | AFR | YRI | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0279 | AFR | YRI | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0272 | AFR | YRI | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18942 | hp1 | a0001 | c0001 | t0005 | g0061 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18961 | hp2 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0258 | AFR | LWK | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0285 | AFR | LWK | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | LWK | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | LWK | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19085 | hp2 | a0001 | c0001 | t0011 | g0021 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | TSI | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0071 | EUR | TSI | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02109 | hp1 | a0001 | c0001 | t0013 | g0218 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0286 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0157 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0261 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | USA | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0283 | AFR | USA | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | USA | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0131 | AFR | USA | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0260 | AFR | LWK | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | LWK | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0196 | REF | REF | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0164 | REF | REF | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:59738847
|
G | A | 1 | a0002 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.314G>A | p.Arg105His | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/12 | 435/3686 | 314/1221 | 105/406 | chr17 | 59738847 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:59773765
|
A | G | 1 | a0001c0002 | 2 | HG00140.hp2 HG00544.hp2 |
synonymous_variant | LOW | c.594A>G | p.Thr198Thr | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/12 | 715/3686 | 594/1221 | 198/406 | chr17 | 59773765 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:59839982
|
G | A | 1 | a0001c0001t0009 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*71G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 71 | chr17 | 59839982 | |||||
| chr17:59840859
|
G | A | 1 | a0001c0001t0010 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*948G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 948 | chr17 | 59840859 | |||||
| chr17:59840891
|
C | T | 1 | a0001c0001t0014 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*980C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 980 | chr17 | 59840891 | |||||
| chr17:59841009
|
T | C | 1 | a0001c0001t0004 | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1098T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 1098 | chr17 | 59841009 | |||||
| chr17:59841136
|
G | A | 1 | a0001c0001t0011 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1225G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 1225 | chr17 | 59841136 | |||||
| chr17:59841221
|
G | C | 2 | a0001c0001t0005a0001c0001t0007 | 7 | HG02698.hp2 HG02738.hp1 HG03491.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1310G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 1310 | chr17 | 59841221 | |||||
| chr17:59841547
|
T | C | 5 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(2): Show | 79 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1636T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 1636 | chr17 | 59841547 | |||||
| chr17:59841648
|
C | G | 1 | a0001c0001t0007 | 2 | HG03491.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1737C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 1737 | chr17 | 59841648 | |||||
| chr17:59841670
|
A | T | 5 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(2): Show | 79 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1759A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 1759 | chr17 | 59841670 | |||||
| chr17:59841705
|
G | A | 1 | a0001c0001t0012 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1794G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 1794 | chr17 | 59841705 | |||||
| chr17:59841938
|
C | T | 1 | a0001c0001t0013 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2027C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 2027 | chr17 | 59841938 | |||||
| chr17:59842094
|
T | G | 2 | a0001c0001t0003a0001c0001t0009 | 53 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*2183T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 2183 | chr17 | 59842094 | |||||
| chr17:59842105
|
A | G | 1 | a0001c0001t0006 | 4 | HG02109.hp2 HG03130.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2194A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 2194 | chr17 | 59842105 | |||||
| chr17:59842174
|
A | G | 1 | a0001c0001t0008 | 2 | HG02145.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2263A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 2263 | chr17 | 59842174 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:59707926
|
G | C | 1 | a0001c0001t0012g0001 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-27+178G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59707926 | ||||||
| chr17:59707966
|
C | T | 4 | a0001c0001t0006g0283a0001c0001t0006g0284a0001c0001t0006g0285others(1): Show | 4 | HG02109.hp2 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27+218C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59707966 | ||||||
| chr17:59708356
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-27+608A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59708356 | ||||||
| chr17:59708408
|
C | G | 4 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0008g0279others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27+660C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59708408 | ||||||
| chr17:59708500
|
C | A | 4 | a0001c0001t0006g0283a0001c0001t0006g0284a0001c0001t0006g0285others(1): Show | 4 | HG02109.hp2 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27+752C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59708500 | ||||||
| chr17:59708809
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-27+1061A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59708809 | ||||||
| chr17:59709061
|
C | A | 1 | a0001c0001t0005g0002 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-27+1313C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59709061 | ||||||
| chr17:59709142
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-27+1394C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59709142 | ||||||
| chr17:59709387
|
G | T | 2 | a0001c0001t0007g0274a0001c0001t0007g0275 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-27+1639G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59709387 | ||||||
| chr17:59709633
|
C | T | 12 | a0001c0001t0003g0264a0001c0001t0004g0262a0001c0001t0004g0263others(9): Show | 12 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.-27+1885C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59709633 | ||||||
| chr17:59709682
|
A | G | 4 | a0001c0001t0003g0258a0001c0001t0003g0259a0001c0001t0003g0260others(1): Show | 4 | HG02896.hp2 HG03471.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27+1934A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59709682 | ||||||
| chr17:59709907
|
T | C | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-27+2159T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59709907 | ||||||
| chr17:59709956
|
G | C | 1 | a0001c0001t0001g0003 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-27+2208G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59709956 | ||||||
| chr17:59710006
|
G | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.-27+2258G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59710006 | ||||||
| chr17:59710070
|
G | C | 93 | a0001c0001t0001g0003a0001c0001t0001g0069a0001c0001t0001g0070others(90): Show | 93 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.-27+2322G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59710070 | ||||||
| chr17:59710094
|
G | C | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG01261.hp2 HG01358.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27+2346G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59710094 | ||||||
| chr17:59710128
|
C | T | 2 | a0001c0001t0002g0098a0001c0001t0002g0099 | 2 | NA18973.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.-27+2380C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59710128 | ||||||
| chr17:59710129
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-27+2381G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59710129 | ||||||
| chr17:59710403
|
C | A | 3 | a0001c0001t0003g0264a0001c0001t0004g0262a0001c0001t0004g0263 | 3 | HG01109.hp2 HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-27+2655C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59710403 | ||||||
| chr17:59710449
|
C | T | 1 | a0001c0001t0003g0257 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-27+2701C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59710449 | ||||||
| chr17:59710672
|
T | A | 1 | a0001c0001t0003g0105 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-27+2924T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59710672 | ||||||
| chr17:59710836
|
C | T | 2 | a0001c0001t0002g0096a0001c0001t0002g0097 | 2 | HG02683.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.-27+3088C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59710836 | ||||||
| chr17:59711011
|
T | G | 1 | a0001c0001t0001g0106 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-27+3263T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59711011 | ||||||
| chr17:59711072
|
C | CA | 91 | a0001c0001t0001g0003a0001c0001t0001g0069a0001c0001t0001g0070others(88): Show | 91 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.-27+3334dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59711072 | |||||
| chr17:59711135
|
C | CA | 94 | a0001c0001t0001g0003a0001c0001t0001g0069a0001c0001t0001g0070others(91): Show | 94 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.-27+3398dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59711135 | |||||
| chr17:59711201
|
T | C | 1 | a0001c0001t0002g0012 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-27+3453T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59711201 | ||||||
| chr17:59711247
|
G | A | 22 | a0001c0001t0003g0110a0001c0001t0003g0111a0001c0001t0003g0112others(19): Show | 22 | HG00642.hp1 HG00673.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+3499G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59711247 | ||||||
| chr17:59711419
|
AACT | A | 95 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(92): Show | 95 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.-27+3672_-27+3674d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59711419 | ||||||
| chr17:59711423
|
C | T | 95 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(92): Show | 95 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.-27+3675C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59711423 | ||||||
| chr17:59712845
|
T | C | 251 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(248): Show | 251 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.-27+5097T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59712845 | ||||||
| chr17:59713266
|
A | G | 93 | a0001c0001t0001g0003a0001c0001t0001g0069a0001c0001t0001g0070others(90): Show | 93 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.-27+5518A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59713266 | ||||||
| chr17:59713479
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-27+5731G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59713479 | ||||||
| chr17:59713683
|
CT | C | 64 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(61): Show | 64 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.-27+5954delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59713683 | |||||
| chr17:59713683
|
CTTT | C | 71 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0002g0012others(68): Show | 71 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.-27+5952_-27+5954d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59713683 | |||||
| chr17:59713683
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-27+5945_-27+5954d others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59713683 | |||||
| chr17:59713685
|
T | C | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG02071.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.-27+5937T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59713685 | ||||||
| chr17:59713797
|
C | T | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02451.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-27+6049C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59713797 | ||||||
| chr17:59713834
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-27+6086A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59713834 | ||||||
| chr17:59713841
|
G | A | 19 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(16): Show | 19 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.-27+6093G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59713841 | ||||||
| chr17:59714035
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-27+6287C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59714035 | ||||||
| chr17:59714046
|
G | GA | 24 | a0001c0001t0001g0011a0001c0001t0001g0076a0001c0001t0001g0104others(21): Show | 24 | HG00423.hp1 HG00438.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.-27+6319dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59714046 | |||||
| chr17:59714046
|
GA | G | 20 | a0001c0001t0001g0103a0001c0001t0001g0253a0001c0001t0001g0254others(17): Show | 20 | HG01109.hp2 HG02109.hp2 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.-27+6319delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59714046 | |||||
| chr17:59714386
|
C | T | 1 | a0001c0001t0006g0286 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-27+6638C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59714386 | ||||||
| chr17:59714483
|
A | G | 95 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(92): Show | 95 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.-27+6735A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59714483 | ||||||
| chr17:59714582
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-27+6834T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59714582 | ||||||
| chr17:59714611
|
C | A | 12 | a0001c0001t0003g0264a0001c0001t0004g0262a0001c0001t0004g0263others(9): Show | 12 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.-27+6863C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59714611 | ||||||
| chr17:59714670
|
A | G | 262 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(259): Show | 262 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.-27+6922A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59714670 | ||||||
| chr17:59715218
|
C | T | 1 | a0001c0001t0004g0273 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-27+7470C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59715218 | ||||||
| chr17:59715432
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-27+7684A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59715432 | ||||||
| chr17:59715560
|
G | A | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | HG02602.hp1 HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-27+7812G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59715560 | ||||||
| chr17:59715986
|
T | G | 1 | a0001c0001t0002g0096 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-27+8238T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59715986 | ||||||
| chr17:59716623
|
A | T | 1 | a0001c0001t0003g0257 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-27+8875A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59716623 | ||||||
| chr17:59716710
|
T | G | 4 | a0001c0001t0006g0283a0001c0001t0006g0284a0001c0001t0006g0285others(1): Show | 4 | HG02109.hp2 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27+8962T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59716710 | ||||||
| chr17:59716784
|
A | AT | 101 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(98): Show | 101 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.-27+9045dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59716784 | |||||
| chr17:59716978
|
A | T | 24 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(21): Show | 24 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.-27+9230A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59716978 | ||||||
| chr17:59716985
|
T | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-27+9237T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59716985 | ||||||
| chr17:59717192
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-27+9444G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59717192 | ||||||
| chr17:59717254
|
G | A | 1 | a0001c0001t0014g0191 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-27+9506G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59717254 | ||||||
| chr17:59717747
|
T | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG01261.hp2 HG01358.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-27+9999T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59717747 | ||||||
| chr17:59717904
|
A | T | 1 | a0001c0001t0001g0091 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-27+10156A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59717904 | ||||||
| chr17:59718081
|
G | A | 4 | a0001c0001t0003g0111a0001c0001t0003g0112a0001c0001t0003g0113others(1): Show | 4 | HG00642.hp1 HG01071.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27+10333G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59718081 | ||||||
| chr17:59718099
|
A | T | 1 | a0001c0001t0001g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-27+10351A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59718099 | ||||||
| chr17:59718122
|
T | G | 50 | a0001c0001t0001g0132a0001c0001t0001g0139a0001c0001t0001g0277others(47): Show | 50 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.-27+10374T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59718122 | ||||||
| chr17:59718162
|
T | G | 1 | a0001c0001t0003g0114 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-27+10414T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59718162 | ||||||
| chr17:59718163
|
C | A | 1 | a0001c0001t0003g0114 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-27+10415C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59718163 | ||||||
| chr17:59718184
|
C | CT | 114 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.-27+10464dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59718184 | |||||
| chr17:59718184
|
C | CTT | 31 | a0001c0001t0001g0010a0001c0001t0001g0100a0001c0001t0001g0101others(28): Show | 31 | HG00423.hp1 HG01123.hp2 HG01256.hp2 others(28): Show |
intron_variant | MODIFIER | c.-27+10463_-27+1046 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59718184 | |||||
| chr17:59718307
|
C | T | 4 | a0001c0001t0003g0258a0001c0001t0003g0259a0001c0001t0003g0260others(1): Show | 4 | HG02896.hp2 HG03471.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27+10559C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59718307 | ||||||
| chr17:59718334
|
T | C | 50 | a0001c0001t0001g0132a0001c0001t0001g0139a0001c0001t0001g0150others(47): Show | 50 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.-27+10586T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59718334 | ||||||
| chr17:59718357
|
C | T | 5 | a0001c0001t0003g0151a0001c0001t0003g0258a0001c0001t0003g0259others(2): Show | 5 | HG02896.hp2 HG03195.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27+10609C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59718357 | ||||||
| chr17:59718593
|
T | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG01243.hp1 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-27+10845T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59718593 | ||||||
| chr17:59718862
|
A | C | 1 | a0001c0001t0001g0173 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-27+11114A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59718862 | ||||||
| chr17:59719022
|
A | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | NA18968.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-27+11274A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59719022 | ||||||
| chr17:59719079
|
C | T | 1 | a0001c0001t0002g0074 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-27+11331C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59719079 | ||||||
| chr17:59719080
|
G | A | 2 | a0001c0001t0006g0285a0001c0001t0006g0286 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-27+11332G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59719080 | ||||||
| chr17:59719080
|
G | T | 2 | a0001c0001t0007g0274a0001c0001t0007g0275 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-27+11332G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59719080 | ||||||
| chr17:59719164
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-27+11416T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59719164 | ||||||
| chr17:59719284
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-27+11536A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59719284 | ||||||
| chr17:59719316
|
C | CACAA | 98 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(95): Show | 98 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.-27+11590_-27+1159 others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59719316 | |||||
| chr17:59719316
|
C | CACAAACA others(1): Show |
158 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 158 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.-27+11586_-27+1159 others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59719316 | |||||
| chr17:59719316
|
C | CACAAACA others(5): Show |
2 | a0001c0001t0001g0200a0001c0001t0003g0116 | 2 | NA18949.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.-27+11582_-27+1159 others(16): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59719316 | |||||
| chr17:59719316
|
C | CACAAACA others(9): Show |
1 | a0001c0001t0001g0199 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-27+11578_-27+1159 others(20): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59719316 | |||||
| chr17:59719493
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-27+11745T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59719493 | ||||||
| chr17:59719675
|
T | G | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | NA19001.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-26-11746T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59719675 | ||||||
| chr17:59719690
|
A | G | 2 | a0001c0001t0003g0134a0001c0001t0003g0146 | 2 | HG02895.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-26-11731A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59719690 | ||||||
| chr17:59719805
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-26-11616T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59719805 | ||||||
| chr17:59719849
|
A | C | 2 | a0001c0001t0005g0058a0001c0001t0005g0059 | 2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-26-11572A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59719849 | ||||||
| chr17:59720026
|
G | C | 2 | a0001c0001t0001g0187a0001c0001t0001g0189 | 2 | NA18963.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.-26-11395G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59720026 | ||||||
| chr17:59720804
|
T | C | 162 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(159): Show | 162 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.-26-10617T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59720804 | ||||||
| chr17:59720822
|
C | A | 261 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(258): Show | 261 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.-26-10599C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59720822 | ||||||
| chr17:59720871
|
G | A | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-26-10550G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59720871 | ||||||
| chr17:59720973
|
C | CA | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.-26-10436dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59720973 | |||||
| chr17:59721072
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-26-10349G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59721072 | ||||||
| chr17:59721073
|
C | T | 1 | a0001c0001t0003g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-26-10348C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59721073 | ||||||
| chr17:59721100
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-26-10321C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59721100 | ||||||
| chr17:59721333
|
C | T | 2 | a0001c0001t0004g0269a0001c0001t0004g0270 | 2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-26-10088C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59721333 | ||||||
| chr17:59721715
|
C | CAAACA | 99 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(96): Show | 99 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.-26-9674_-26-9670d others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59721715 | |||||
| chr17:59721715
|
C | CAAACAAA others(3): Show |
10 | a0001c0001t0001g0081a0001c0001t0001g0153a0001c0001t0002g0071others(7): Show | 10 | HG01168.hp2 HG02027.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26-9679_-26-9670d others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59721715 | |||||
| chr17:59721715
|
CAAACA | C | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(55): Show | 58 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.-26-9674_-26-9670d others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59721715 | |||||
| chr17:59721715
|
CAAACAAA others(3): Show |
C | 5 | a0001c0001t0001g0252a0001c0001t0001g0280a0001c0001t0004g0268others(2): Show | 5 | HG01123.hp2 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26-9679_-26-9670d others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59721715 | |||||
| chr17:59721799
|
T | C | 11 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0082others(8): Show | 11 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-26-9622T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59721799 | ||||||
| chr17:59721843
|
A | G | 262 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(259): Show | 262 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.-26-9578A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59721843 | ||||||
| chr17:59722127
|
A | G | 1 | a0001c0001t0001g0234 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-26-9294A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59722127 | ||||||
| chr17:59722169
|
G | C | 3 | a0001c0001t0001g0280a0001c0001t0008g0279a0001c0001t0008g0281 | 3 | HG02145.hp2 HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-26-9252G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59722169 | ||||||
| chr17:59722467
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-26-8954A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59722467 | ||||||
| chr17:59722536
|
A | G | 1 | a0001c0001t0004g0263 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-26-8885A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59722536 | ||||||
| chr17:59722580
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.-26-8841C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59722580 | ||||||
| chr17:59722613
|
AGCAGAT | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.-26-8807_-26-8802d others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59722613 | ||||||
| chr17:59722620
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.-26-8801C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59722620 | ||||||
| chr17:59722700
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-26-8721C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59722700 | ||||||
| chr17:59722748
|
G | T | 1 | a0001c0001t0001g0203 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-26-8673G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59722748 | ||||||
| chr17:59722938
|
A | T | 1 | a0001c0001t0001g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-26-8483A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59722938 | ||||||
| chr17:59722997
|
C | T | 261 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(258): Show | 261 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.-26-8424C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59722997 | ||||||
| chr17:59723027
|
G | A | 261 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(258): Show | 261 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.-26-8394G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59723027 | ||||||
| chr17:59723049
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-26-8372T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59723049 | ||||||
| chr17:59723189
|
A | G | 2 | a0001c0001t0003g0259a0001c0001t0003g0260 | 2 | HG02896.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-26-8232A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59723189 | ||||||
| chr17:59723420
|
A | G | 4 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0056others(1): Show | 4 | NA18950.hp1 NA18967.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26-8001A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59723420 | ||||||
| chr17:59723605
|
G | A | 79 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.-26-7816G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59723605 | ||||||
| chr17:59723611
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-26-7810T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59723611 | ||||||
| chr17:59723747
|
C | T | 1 | a0001c0001t0003g0128 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-26-7674C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59723747 | ||||||
| chr17:59724061
|
A | C | 101 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(98): Show | 101 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.-26-7360A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59724061 | ||||||
| chr17:59724127
|
A | G | 51 | a0001c0001t0001g0132a0001c0001t0001g0139a0001c0001t0001g0150others(48): Show | 51 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.-26-7294A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59724127 | ||||||
| chr17:59724211
|
C | CA | 15 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(12): Show | 15 | HG01099.hp1 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-26-7195dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59724211 | |||||
| chr17:59724224
|
AAAG | A | 47 | a0001c0001t0001g0132a0001c0001t0001g0139a0001c0001t0001g0277others(44): Show | 47 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.-26-7194_-26-7192d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59724224 | |||||
| chr17:59724236
|
G | T | 87 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.-26-7185G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59724236 | ||||||
| chr17:59724380
|
T | C | 2 | a0001c0001t0001g0088a0001c0001t0001g0090 | 2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-26-7041T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59724380 | ||||||
| chr17:59724400
|
G | A | 87 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.-26-7021G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59724400 | ||||||
| chr17:59724516
|
A | C | 21 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(18): Show | 21 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-26-6905A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59724516 | ||||||
| chr17:59724596
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-26-6825C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59724596 | ||||||
| chr17:59724686
|
G | T | 162 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(159): Show | 162 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.-26-6735G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59724686 | ||||||
| chr17:59724735
|
G | A | 1 | a0001c0001t0004g0271 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-26-6686G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59724735 | ||||||
| chr17:59724791
|
A | C | 174 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(171): Show | 174 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.-26-6630A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59724791 | ||||||
| chr17:59724823
|
G | A | 1 | a0001c0001t0003g0148 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-26-6598G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59724823 | ||||||
| chr17:59724965
|
CA | C | 174 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(171): Show | 174 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.-26-6445delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59724965 | |||||
| chr17:59724990
|
C | CA | 97 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(94): Show | 97 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.-26-6423dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59724990 | |||||
| chr17:59725551
|
C | CA | 163 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(160): Show | 163 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.-26-5854dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59725551 | |||||
| chr17:59725602
|
A | G | 1 | a0001c0001t0002g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-26-5819A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59725602 | ||||||
| chr17:59725605
|
C | T | 45 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(42): Show | 45 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.-26-5816C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59725605 | ||||||
| chr17:59725635
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-26-5786A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59725635 | ||||||
| chr17:59725802
|
A | C | 1 | a0001c0001t0001g0170 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-26-5619A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59725802 | ||||||
| chr17:59726291
|
G | GT | 88 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(85): Show | 88 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.-26-5119dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59726291 | |||||
| chr17:59726366
|
T | G | 1 | a0001c0001t0001g0239 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-26-5055T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59726366 | ||||||
| chr17:59726422
|
T | G | 1 | a0001c0001t0001g0207 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-26-4999T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59726422 | ||||||
| chr17:59726514
|
G | A | 1 | a0001c0001t0003g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-26-4907G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59726514 | ||||||
| chr17:59726529
|
G | T | 1 | a0001c0001t0001g0185 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-26-4892G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59726529 | ||||||
| chr17:59726678
|
T | A | 2 | a0001c0001t0006g0283a0001c0001t0006g0284 | 2 | HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-26-4743T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59726678 | ||||||
| chr17:59726804
|
T | G | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-26-4617T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59726804 | ||||||
| chr17:59727125
|
C | A | 1 | a0001c0001t0001g0159 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-26-4296C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59727125 | ||||||
| chr17:59727125
|
CTTTTTGT others(3): Show |
C | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-26-4279_-26-4270d others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59727125 | |||||
| chr17:59727558
|
A | T | 1 | a0001c0001t0001g0186 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-26-3863A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59727558 | ||||||
| chr17:59727775
|
C | G | 1 | a0001c0001t0001g0180 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-26-3646C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59727775 | ||||||
| chr17:59727872
|
G | T | 1 | a0001c0001t0001g0158 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-26-3549G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59727872 | ||||||
| chr17:59727889
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-26-3532G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59727889 | ||||||
| chr17:59728020
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-26-3401T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59728020 | ||||||
| chr17:59728159
|
G | C | 282 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(279): Show | 282 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.-26-3262G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59728159 | ||||||
| chr17:59728318
|
T | C | 1 | a0001c0001t0001g0200 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-26-3103T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59728318 | ||||||
| chr17:59728366
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-26-3055A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59728366 | ||||||
| chr17:59728439
|
C | CAT | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-26-2977_-26-2976d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59728439 | |||||
| chr17:59728544
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-26-2877A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59728544 | ||||||
| chr17:59728650
|
G | T | 79 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.-26-2771G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59728650 | ||||||
| chr17:59728684
|
A | ATTAT | 58 | a0001c0001t0001g0132a0001c0001t0001g0139a0001c0001t0003g0105others(55): Show | 58 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.-26-2716_-26-2713d others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59728684 | |||||
| chr17:59728876
|
A | G | 1 | a0001c0001t0004g0273 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-26-2545A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59728876 | ||||||
| chr17:59729197
|
G | A | 1 | a0001c0001t0003g0257 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-26-2224G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59729197 | ||||||
| chr17:59729279
|
A | T | 261 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(258): Show | 261 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.-26-2142A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59729279 | ||||||
| chr17:59729318
|
A | G | 1 | a0001c0001t0005g0002 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-26-2103A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59729318 | ||||||
| chr17:59729408
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-26-2013G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59729408 | ||||||
| chr17:59729478
|
C | CA | 26 | a0001c0001t0001g0078a0001c0001t0001g0088a0001c0001t0001g0103others(23): Show | 26 | HG00438.hp2 HG00621.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.-26-1924dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59729478 | |||||
| chr17:59729491
|
A | C | 7 | a0001c0001t0001g0174a0001c0001t0001g0202a0001c0001t0001g0233others(4): Show | 7 | NA18942.hp2 NA18943.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.-26-1930A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59729491 | ||||||
| chr17:59729673
|
C | A | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-26-1748C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59729673 | ||||||
| chr17:59729686
|
C | CT | 105 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(102): Show | 105 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.-26-1719dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59729686 | |||||
| chr17:59729738
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-26-1683C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59729738 | ||||||
| chr17:59729790
|
A | T | 3 | a0001c0001t0001g0190a0001c0001t0001g0232a0001c0001t0001g0249 | 3 | HG01074.hp2 HG01361.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-26-1631A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59729790 | ||||||
| chr17:59729795
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-26-1626C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59729795 | ||||||
| chr17:59729810
|
C | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0080 | 2 | HG01243.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-26-1611C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59729810 | ||||||
| chr17:59730131
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-26-1290G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59730131 | ||||||
| chr17:59730259
|
A | G | 2 | a0001c0001t0004g0265a0001c0001t0004g0266 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-26-1162A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59730259 | ||||||
| chr17:59731244
|
G | A | 1 | a0001c0001t0003g0137 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-26-177G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59731244 | ||||||
| chr17:59731249
|
A | G | 1 | a0001c0001t0006g0284 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-26-172A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59731249 | ||||||
| chr17:59731555
|
A | T | 1 | a0001c0001t0001g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.76+33A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59731555 | ||||||
| chr17:59732092
|
A | T | 261 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(258): Show | 261 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.76+570A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59732092 | ||||||
| chr17:59732104
|
A | G | 1 | a0001c0001t0003g0127 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.76+582A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59732104 | ||||||
| chr17:59732154
|
C | A | 1 | a0001c0001t0005g0061 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.76+632C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59732154 | ||||||
| chr17:59732269
|
C | T | 1 | a0001c0001t0003g0156 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.76+747C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59732269 | ||||||
| chr17:59732392
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.76+870G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59732392 | ||||||
| chr17:59732492
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.76+970C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59732492 | ||||||
| chr17:59732532
|
C | T | 2 | a0001c0001t0007g0274a0001c0001t0007g0275 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.76+1010C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59732532 | ||||||
| chr17:59732534
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.76+1012C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59732534 | ||||||
| chr17:59732552
|
TGTTA | T | 87 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.76+1031_76+1034del others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59732552 | ||||||
| chr17:59732673
|
T | C | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.76+1151T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59732673 | ||||||
| chr17:59732795
|
A | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0092 | 2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.76+1273A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59732795 | ||||||
| chr17:59732809
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.76+1287A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59732809 | ||||||
| chr17:59733188
|
A | C | 53 | a0001c0001t0001g0132a0001c0001t0001g0139a0001c0001t0001g0205others(50): Show | 53 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.76+1666A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59733188 | ||||||
| chr17:59733189
|
A | C | 1 | a0001c0001t0003g0114 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.76+1667A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59733189 | ||||||
| chr17:59733199
|
T | A | 1 | a0001c0001t0001g0251 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.76+1677T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59733199 | ||||||
| chr17:59733284
|
A | G | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG01255.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.76+1762A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59733284 | ||||||
| chr17:59733472
|
T | TG | 5 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0267others(2): Show | 5 | HG01109.hp2 HG02896.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.77-1864dupG | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 59733472 | |||||
| chr17:59733524
|
C | G | 1 | a0001c0001t0001g0231 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.77-1814C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59733524 | ||||||
| chr17:59733620
|
T | A | 1 | a0001c0001t0003g0134 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.77-1718T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59733620 | ||||||
| chr17:59734046
|
A | C | 104 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(101): Show | 104 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.77-1292A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59734046 | ||||||
| chr17:59734246
|
AG | A | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.77-1091delG | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59734246 | ||||||
| chr17:59734448
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.77-890G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59734448 | ||||||
| chr17:59734706
|
T | C | 105 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(102): Show | 105 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.77-632T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59734706 | ||||||
| chr17:59734772
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.77-566T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59734772 | ||||||
| chr17:59734902
|
C | CT | 81 | a0001c0001t0001g0010a0001c0001t0001g0069a0001c0001t0001g0070others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.77-413dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 59734902 | |||||
| chr17:59734902
|
C | CTT | 95 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0082others(92): Show | 95 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.77-414_77-413dupTT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 59734902 | |||||
| chr17:59734902
|
C | CTTT | 17 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0079others(14): Show | 17 | HG00673.hp1 HG00741.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.77-415_77-413dupTT others(1): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 59734902 | |||||
| chr17:59735013
|
G | A | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.77-325G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59735013 | ||||||
| chr17:59735574
|
G | T | 1 | a0001c0001t0001g0242 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.212+101G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 3/11 | chr17 | 59735574 | ||||||
| chr17:59735807
|
A | G | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(55): Show | 58 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.212+334A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 3/11 | chr17 | 59735807 | ||||||
| chr17:59736323
|
A | C | 1 | a0001c0001t0010g0230 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.212+850A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 3/11 | chr17 | 59736323 | ||||||
| chr17:59736402
|
CA | C | 271 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(268): Show | 271 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.212+943delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 59736402 | |||||
| chr17:59736463
|
A | G | 261 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(258): Show | 261 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.212+990A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 3/11 | chr17 | 59736463 | ||||||
| chr17:59736765
|
G | A | 2 | a0001c0001t0002g0074a0001c0001t0002g0075 | 2 | HG01981.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.213-688G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 3/11 | chr17 | 59736765 | ||||||
| chr17:59737067
|
T | C | 21 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(18): Show | 21 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.213-386T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 3/11 | chr17 | 59737067 | ||||||
| chr17:59737280
|
A | G | 79 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.213-173A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 3/11 | chr17 | 59737280 | ||||||
| chr17:59737335
|
A | C | 2 | a0001c0002t0001g0228a0001c0002t0001g0229 | 2 | HG00140.hp2 HG00544.hp2 |
intron_variant | MODIFIER | c.213-118A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 3/11 | chr17 | 59737335 | ||||||
| chr17:59737579
|
C | G | 1 | a0001c0001t0003g0116 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.303+36C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 4/11 | chr17 | 59737579 | ||||||
| chr17:59738060
|
C | T | 2 | a0001c0001t0007g0274a0001c0001t0007g0275 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.303+517C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 4/11 | chr17 | 59738060 | ||||||
| chr17:59738102
|
G | A | 1 | a0001c0001t0002g0071 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.303+559G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 4/11 | chr17 | 59738102 | ||||||
| chr17:59738247
|
G | C | 87 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.304-590G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 4/11 | chr17 | 59738247 | ||||||
| chr17:59739217
|
T | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(100): Show | 103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.414+270T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59739217 | ||||||
| chr17:59739309
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.414+362A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59739309 | ||||||
| chr17:59739396
|
T | C | 89 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(86): Show | 89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.414+449T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59739396 | ||||||
| chr17:59739478
|
A | G | 1 | a0002c0003t0002g0030 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.414+531A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59739478 | ||||||
| chr17:59739581
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.414+634G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59739581 | ||||||
| chr17:59739655
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.414+708C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59739655 | ||||||
| chr17:59739723
|
C | CA | 10 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(7): Show | 10 | HG01109.hp2 HG02615.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.414+798dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59739723 | |||||
| chr17:59739723
|
CA | C | 240 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(237): Show | 240 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.414+798delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59739723 | |||||
| chr17:59739801
|
T | C | 261 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(258): Show | 261 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.414+854T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59739801 | ||||||
| chr17:59739833
|
T | C | 2 | a0001c0001t0001g0077a0001c0001t0001g0278 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.414+886T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59739833 | ||||||
| chr17:59740019
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.414+1072G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59740019 | ||||||
| chr17:59740076
|
CA | C | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+1142delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59740076 | |||||
| chr17:59740312
|
G | A | 1 | a0001c0001t0002g0237 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.414+1365G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59740312 | ||||||
| chr17:59740336
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.414+1389A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59740336 | ||||||
| chr17:59740450
|
C | T | 10 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0133others(7): Show | 10 | HG00438.hp2 HG02071.hp2 HG03927.hp2 others(7): Show |
intron_variant | MODIFIER | c.414+1503C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59740450 | ||||||
| chr17:59740793
|
G | A | 7 | a0001c0001t0001g0203a0001c0001t0001g0206a0001c0001t0001g0210others(4): Show | 7 | HG02145.hp2 HG02818.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.414+1846G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59740793 | ||||||
| chr17:59740852
|
A | G | 52 | a0001c0001t0001g0087a0001c0001t0001g0132a0001c0001t0001g0139others(49): Show | 52 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.414+1905A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59740852 | ||||||
| chr17:59740980
|
T | C | 1 | a0001c0001t0003g0138 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.414+2033T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59740980 | ||||||
| chr17:59741206
|
T | A | 1 | a0001c0001t0002g0098 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.414+2259T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59741206 | ||||||
| chr17:59741207
|
A | T | 1 | a0001c0001t0002g0098 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.414+2260A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59741207 | ||||||
| chr17:59741345
|
A | G | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+2398A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59741345 | ||||||
| chr17:59741532
|
C | G | 1 | a0001c0001t0002g0034 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.414+2585C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59741532 | ||||||
| chr17:59741621
|
G | T | 1 | a0001c0001t0003g0113 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.414+2674G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59741621 | ||||||
| chr17:59741742
|
C | G | 1 | a0001c0001t0001g0241 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.414+2795C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59741742 | ||||||
| chr17:59742428
|
G | A | 1 | a0001c0001t0003g0141 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.414+3481G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59742428 | ||||||
| chr17:59742477
|
A | C | 1 | a0001c0001t0003g0105 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.414+3530A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59742477 | ||||||
| chr17:59742488
|
A | G | 270 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(267): Show | 270 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.414+3541A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59742488 | ||||||
| chr17:59742522
|
C | CAAT | 25 | a0001c0001t0001g0080a0001c0001t0001g0091a0001c0001t0001g0166others(22): Show | 25 | HG00423.hp2 HG01109.hp2 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.414+3607_414+3609d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59742522 | |||||
| chr17:59742522
|
C | CAATAAT | 13 | a0001c0001t0001g0070a0001c0001t0001g0178a0001c0001t0001g0199others(10): Show | 13 | HG01243.hp2 HG01884.hp2 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.414+3604_414+3609d others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59742522 | |||||
| chr17:59742522
|
C | CAATAATA others(2): Show |
67 | a0001c0001t0001g0069a0001c0001t0001g0100a0001c0001t0001g0101others(64): Show | 67 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.414+3601_414+3609d others(11): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59742522 | |||||
| chr17:59742522
|
C | CAATAATA others(5): Show |
1 | a0001c0001t0001g0211 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.414+3598_414+3609d others(14): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59742522 | |||||
| chr17:59742522
|
CAAT | C | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(55): Show | 58 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.414+3607_414+3609d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59742522 | |||||
| chr17:59742688
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.414+3741G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59742688 | ||||||
| chr17:59742871
|
A | C | 1 | a0001c0001t0001g0224 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.414+3924A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59742871 | ||||||
| chr17:59742995
|
G | A | 50 | a0001c0001t0001g0132a0001c0001t0001g0139a0001c0001t0001g0277others(47): Show | 50 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.414+4048G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59742995 | ||||||
| chr17:59743011
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.414+4064A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59743011 | ||||||
| chr17:59743082
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.414+4135A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59743082 | ||||||
| chr17:59743373
|
C | T | 1 | a0001c0001t0001g0223 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.414+4426C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59743373 | ||||||
| chr17:59743537
|
T | G | 1 | a0001c0001t0003g0118 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.414+4590T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59743537 | ||||||
| chr17:59743559
|
GCTCTCTC others(3): Show |
G | 4 | a0001c0001t0003g0111a0001c0001t0003g0112a0001c0001t0003g0113others(1): Show | 4 | HG00642.hp1 HG01071.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+4625_414+4634d others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59743559 | |||||
| chr17:59743576
|
C | A | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.414+4629C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59743576 | ||||||
| chr17:59743578
|
C | A | 8 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0104others(5): Show | 8 | HG01123.hp2 HG01361.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.414+4631C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59743578 | ||||||
| chr17:59743580
|
C | A | 43 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(40): Show | 43 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.414+4633C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59743580 | ||||||
| chr17:59743582
|
A | C | 44 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(41): Show | 44 | HG00408.hp2 HG01099.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.414+4635A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59743582 | ||||||
| chr17:59743941
|
G | T | 1 | a0001c0001t0001g0153 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.414+4994G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59743941 | ||||||
| chr17:59744069
|
G | A | 174 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(171): Show | 174 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.414+5122G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59744069 | ||||||
| chr17:59744092
|
G | GT | 105 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0076others(102): Show | 105 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.414+5157dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59744092 | |||||
| chr17:59744092
|
G | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0086 | 2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.414+5145G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59744092 | ||||||
| chr17:59744322
|
C | T | 1 | a0001c0001t0003g0143 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.414+5375C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59744322 | ||||||
| chr17:59744330
|
C | A | 1 | a0001c0001t0001g0185 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.414+5383C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59744330 | ||||||
| chr17:59744462
|
C | CA | 20 | a0001c0001t0001g0207a0001c0001t0001g0231a0001c0001t0001g0244others(17): Show | 20 | HG01109.hp2 HG01243.hp2 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.414+5536dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59744462 | |||||
| chr17:59744462
|
CA | C | 17 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0087others(14): Show | 17 | HG01884.hp1 HG02257.hp2 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.414+5536delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59744462 | |||||
| chr17:59744462
|
CAA | C | 37 | a0001c0001t0001g0132a0001c0001t0001g0139a0001c0001t0003g0107others(34): Show | 37 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.414+5535_414+5536d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59744462 | |||||
| chr17:59744764
|
C | T | 105 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(102): Show | 105 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.414+5817C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59744764 | ||||||
| chr17:59744771
|
A | G | 4 | a0001c0001t0001g0177a0001c0001t0001g0222a0001c0001t0001g0227others(1): Show | 4 | HG00642.hp2 HG01978.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+5824A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59744771 | ||||||
| chr17:59744993
|
A | G | 105 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(102): Show | 105 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.414+6046A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59744993 | ||||||
| chr17:59745017
|
G | T | 1 | a0001c0001t0001g0239 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.414+6070G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59745017 | ||||||
| chr17:59745247
|
G | T | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(55): Show | 58 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.414+6300G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59745247 | ||||||
| chr17:59745386
|
G | A | 4 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(1): Show | 4 | NA19057.hp2 NA19060.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+6439G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59745386 | ||||||
| chr17:59745533
|
A | T | 1 | a0001c0001t0001g0185 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.414+6586A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59745533 | ||||||
| chr17:59745552
|
T | G | 2 | a0001c0001t0007g0274a0001c0001t0007g0275 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.414+6605T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59745552 | ||||||
| chr17:59746192
|
A | T | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+7245A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59746192 | ||||||
| chr17:59746324
|
G | A | 174 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(171): Show | 174 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.414+7377G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59746324 | ||||||
| chr17:59746401
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.414+7454G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59746401 | ||||||
| chr17:59746418
|
C | T | 1 | a0001c0001t0001g0254 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.414+7471C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59746418 | ||||||
| chr17:59746973
|
G | A | 25 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(22): Show | 25 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.414+8026G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59746973 | ||||||
| chr17:59747284
|
T | C | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+8337T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59747284 | ||||||
| chr17:59747388
|
G | A | 2 | a0001c0001t0002g0027a0001c0001t0002g0094 | 2 | HG01975.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.414+8441G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59747388 | ||||||
| chr17:59747410
|
TTTC | T | 13 | a0001c0001t0002g0015a0001c0001t0002g0033a0001c0001t0002g0035others(10): Show | 13 | HG00423.hp2 HG02083.hp2 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.414+8466_414+8468d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59747410 | |||||
| chr17:59747413
|
C | CT | 87 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(84): Show | 87 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.414+8480dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59747413 | |||||
| chr17:59747566
|
C | T | 104 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(101): Show | 104 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.414+8619C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59747566 | ||||||
| chr17:59747615
|
TG | T | 6 | a0001c0001t0003g0149a0001c0001t0003g0151a0001c0001t0003g0258others(3): Show | 6 | HG02896.hp2 HG03195.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.414+8670delG | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59747615 | |||||
| chr17:59747760
|
G | A | 5 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156others(2): Show | 5 | HG01168.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.414+8813G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59747760 | ||||||
| chr17:59747951
|
C | G | 1 | a0001c0001t0003g0151 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.414+9004C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59747951 | ||||||
| chr17:59747993
|
G | A | 4 | a0001c0001t0006g0283a0001c0001t0006g0284a0001c0001t0006g0285others(1): Show | 4 | HG02109.hp2 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+9046G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59747993 | ||||||
| chr17:59748127
|
C | G | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+9180C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59748127 | ||||||
| chr17:59748195
|
CA | C | 229 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(226): Show | 229 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.414+9270delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59748195 | |||||
| chr17:59748195
|
CAA | C | 9 | a0001c0001t0001g0081a0001c0001t0001g0084a0001c0001t0001g0085others(6): Show | 9 | HG00673.hp2 HG01168.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.414+9269_414+9270d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59748195 | |||||
| chr17:59748211
|
A | C | 79 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(76): Show | 79 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.414+9264A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59748211 | ||||||
| chr17:59748214
|
A | C | 2 | a0001c0001t0004g0268a0001c0001t0004g0273 | 2 | HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.414+9267A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59748214 | ||||||
| chr17:59748890
|
A | AT | 42 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0132others(39): Show | 42 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.414+9946dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59748890 | |||||
| chr17:59748890
|
A | ATT | 3 | a0001c0001t0003g0116a0001c0001t0003g0135a0001c0001t0003g0147 | 3 | NA18949.hp2 NA18967.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.414+9945_414+9946d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59748890 | |||||
| chr17:59748890
|
A | T | 4 | a0001c0001t0001g0086a0001c0001t0001g0186a0001c0001t0001g0233others(1): Show | 4 | HG02280.hp2 HG02615.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+9943A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59748890 | ||||||
| chr17:59748892
|
T | TA | 15 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(12): Show | 15 | HG00642.hp1 HG00673.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.414+9945_414+9946i others(3): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59748892 | ||||||
| chr17:59748893
|
T | A | 152 | a0001c0001t0001g0003a0001c0001t0001g0069a0001c0001t0001g0070others(149): Show | 152 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.414+9946T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59748893 | ||||||
| chr17:59748893
|
TA | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0092a0001c0001t0001g0095 | 3 | HG02622.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.414+9947delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59748893 | ||||||
| chr17:59748894
|
A | T | 279 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(276): Show | 279 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.414+9947A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59748894 | ||||||
| chr17:59748895
|
T | A | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.414+9948T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59748895 | ||||||
| chr17:59748896
|
T | A | 9 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(6): Show | 9 | HG00639.hp1 HG01243.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.414+9949T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59748896 | ||||||
| chr17:59749062
|
G | C | 5 | a0001c0001t0001g0174a0001c0001t0001g0202a0001c0001t0001g0233others(2): Show | 5 | NA18942.hp2 NA18943.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.414+10115G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59749062 | ||||||
| chr17:59749115
|
A | AT | 8 | a0001c0001t0001g0106a0001c0001t0001g0189a0001c0001t0001g0207others(5): Show | 8 | HG00408.hp1 HG01074.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.414+10183dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59749115 | |||||
| chr17:59749169
|
T | G | 174 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(171): Show | 174 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.414+10222T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59749169 | ||||||
| chr17:59749244
|
A | G | 79 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.414+10297A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59749244 | ||||||
| chr17:59749370
|
C | A | 87 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.414+10423C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59749370 | ||||||
| chr17:59749430
|
A | T | 1 | a0001c0001t0001g0240 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.414+10483A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59749430 | ||||||
| chr17:59749470
|
TATAAATC | T | 21 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(18): Show | 21 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.414+10525_414+1053 others(11): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59749470 | |||||
| chr17:59749610
|
A | G | 18 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(15): Show | 18 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.414+10663A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59749610 | ||||||
| chr17:59749793
|
A | G | 49 | a0001c0001t0001g0132a0001c0001t0001g0139a0001c0001t0003g0105others(46): Show | 49 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.414+10846A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59749793 | ||||||
| chr17:59749860
|
C | T | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+10913C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59749860 | ||||||
| chr17:59750057
|
G | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.414+11110G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59750057 | ||||||
| chr17:59750217
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.414+11270A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59750217 | ||||||
| chr17:59750290
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.414+11343G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59750290 | ||||||
| chr17:59750302
|
A | AT | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(169): Show | 172 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.414+11371dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59750302 | |||||
| chr17:59750338
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.414+11391G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59750338 | ||||||
| chr17:59750351
|
T | G | 282 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(279): Show | 282 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.414+11404T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59750351 | ||||||
| chr17:59750423
|
T | G | 4 | a0001c0001t0001g0209a0001c0001t0001g0213a0001c0001t0001g0220others(1): Show | 4 | HG00280.hp2 HG00639.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+11476T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59750423 | ||||||
| chr17:59750729
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.414+11782A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59750729 | ||||||
| chr17:59750901
|
C | A | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+11954C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59750901 | ||||||
| chr17:59750926
|
C | CT | 122 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.414+12002dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59750926 | |||||
| chr17:59750926
|
C | CTT | 18 | a0001c0001t0001g0152a0001c0001t0001g0278a0001c0001t0002g0014others(15): Show | 18 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.414+12001_414+1200 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59750926 | |||||
| chr17:59750926
|
CT | C | 11 | a0001c0001t0003g0127a0001c0001t0004g0262a0001c0001t0004g0263others(8): Show | 11 | HG01069.hp1 HG01109.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+12002delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59750926 | |||||
| chr17:59751058
|
G | A | 1 | a0001c0001t0003g0131 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.414+12111G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59751058 | ||||||
| chr17:59751355
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.414+12408A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59751355 | ||||||
| chr17:59751387
|
C | T | 1 | a0001c0001t0002g0037 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.414+12440C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59751387 | ||||||
| chr17:59751603
|
G | A | 104 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(101): Show | 104 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.414+12656G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59751603 | ||||||
| chr17:59751607
|
T | G | 1 | a0001c0001t0002g0035 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.414+12660T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59751607 | ||||||
| chr17:59751607
|
T | TG | 93 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(90): Show | 93 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.414+12668dupG | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59751607 | |||||
| chr17:59751607
|
T | TGG | 17 | a0001c0001t0001g0081a0001c0001t0001g0095a0001c0001t0002g0017others(14): Show | 17 | HG00408.hp2 HG00544.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.414+12667_414+1266 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59751607 | |||||
| chr17:59751608
|
G | T | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+12661G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59751608 | ||||||
| chr17:59751643
|
C | CTGAGG | 105 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(102): Show | 105 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.414+12701_414+1270 others(9): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59751643 | |||||
| chr17:59751744
|
C | CA | 95 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0089others(92): Show | 95 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.414+12821dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59751744 | |||||
| chr17:59751744
|
C | CAA | 13 | a0001c0001t0001g0101a0001c0001t0002g0017a0001c0001t0002g0034others(10): Show | 13 | HG00673.hp1 HG01358.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.414+12820_414+1282 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59751744 | |||||
| chr17:59751744
|
CA | C | 6 | a0001c0001t0001g0070a0001c0001t0001g0163a0001c0001t0001g0184others(3): Show | 6 | HG01256.hp1 HG02004.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.414+12821delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59751744 | |||||
| chr17:59751768
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.414+12821A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59751768 | ||||||
| chr17:59751777
|
T | G | 1 | a0001c0001t0001g0252 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.414+12830T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59751777 | ||||||
| chr17:59752041
|
C | T | 6 | a0001c0001t0002g0033a0001c0001t0002g0042a0001c0001t0002g0043others(3): Show | 6 | NA18956.hp1 NA18973.hp2 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-12930C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59752041 | ||||||
| chr17:59752227
|
A | C | 2 | a0001c0001t0007g0274a0001c0001t0007g0275 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.415-12744A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59752227 | ||||||
| chr17:59752278
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.415-12693G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59752278 | ||||||
| chr17:59752631
|
G | A | 105 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(102): Show | 105 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.415-12340G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59752631 | ||||||
| chr17:59753061
|
G | A | 1 | a0001c0001t0001g0254 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.415-11910G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59753061 | ||||||
| chr17:59753065
|
G | A | 87 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.415-11906G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59753065 | ||||||
| chr17:59753112
|
C | A | 87 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.415-11859C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59753112 | ||||||
| chr17:59753121
|
T | A | 3 | a0001c0001t0002g0041a0001c0001t0002g0046a0001c0001t0002g0093 | 3 | HG00621.hp1 NA18962.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.415-11850T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59753121 | ||||||
| chr17:59753560
|
A | G | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.415-11411A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59753560 | ||||||
| chr17:59753671
|
T | C | 2 | a0001c0001t0006g0285a0001c0001t0006g0286 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.415-11300T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59753671 | ||||||
| chr17:59753672
|
A | T | 2 | a0001c0001t0006g0285a0001c0001t0006g0286 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.415-11299A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59753672 | ||||||
| chr17:59753827
|
A | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0216 | 2 | NA19057.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.415-11144A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59753827 | ||||||
| chr17:59754199
|
A | T | 1 | a0001c0001t0001g0199 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.415-10772A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59754199 | ||||||
| chr17:59754241
|
A | G | 3 | a0001c0001t0001g0280a0001c0001t0008g0279a0001c0001t0008g0281 | 3 | HG02145.hp2 HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.415-10730A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59754241 | ||||||
| chr17:59754428
|
T | C | 1 | a0001c0001t0002g0037 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.415-10543T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59754428 | ||||||
| chr17:59754483
|
T | A | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG01261.hp2 HG01358.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.415-10488T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59754483 | ||||||
| chr17:59754829
|
A | G | 107 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(104): Show | 107 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.415-10142A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59754829 | ||||||
| chr17:59754978
|
G | GC | 30 | a0001c0001t0001g0095a0001c0001t0001g0150a0001c0001t0001g0153others(27): Show | 30 | HG00140.hp1 HG01109.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.415-9985dupC | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59754978 | |||||
| chr17:59754978
|
G | GCC | 220 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 220 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.415-9986_415-9985d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59754978 | |||||
| chr17:59754978
|
G | GCCC | 27 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0078others(24): Show | 27 | HG00621.hp1 HG01243.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.415-9987_415-9985d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59754978 | |||||
| chr17:59754995
|
T | G | 1 | a0001c0001t0002g0063 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.415-9976T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59754995 | ||||||
| chr17:59755030
|
T | G | 87 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.415-9941T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59755030 | ||||||
| chr17:59755095
|
CTTCTTTT others(5): Show |
C | 1 | a0001c0001t0001g0207 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.415-9861_415-9850d others(14): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59755095 | |||||
| chr17:59755140
|
C | G | 49 | a0001c0001t0001g0132a0001c0001t0001g0139a0001c0001t0003g0105others(46): Show | 49 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.415-9831C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59755140 | ||||||
| chr17:59755523
|
G | A | 13 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(10): Show | 13 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.415-9448G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59755523 | ||||||
| chr17:59755556
|
A | T | 64 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(61): Show | 64 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.415-9415A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59755556 | ||||||
| chr17:59755742
|
G | GT | 18 | a0001c0001t0001g0103a0001c0001t0001g0150a0001c0001t0001g0192others(15): Show | 18 | HG00621.hp1 HG01109.hp2 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.415-9215dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59755742 | |||||
| chr17:59755742
|
G | GTT | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01099.hp1 HG01168.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.415-9216_415-9215d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59755742 | |||||
| chr17:59755742
|
G | GTTT | 43 | a0001c0001t0001g0132a0001c0001t0001g0139a0001c0001t0003g0105others(40): Show | 43 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.415-9217_415-9215d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59755742 | |||||
| chr17:59755742
|
G | GTTTT | 11 | a0001c0001t0003g0117a0001c0001t0003g0120a0001c0001t0003g0133others(8): Show | 11 | HG02027.hp2 HG02071.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.415-9218_415-9215d others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59755742 | |||||
| chr17:59755745
|
T | G | 4 | a0001c0001t0001g0177a0001c0001t0001g0222a0001c0001t0001g0227others(1): Show | 4 | HG00642.hp2 HG01978.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-9226T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59755745 | ||||||
| chr17:59755986
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.415-8985C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59755986 | ||||||
| chr17:59756115
|
T | C | 64 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(61): Show | 64 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.415-8856T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59756115 | ||||||
| chr17:59756181
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.415-8790C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59756181 | ||||||
| chr17:59756270
|
T | C | 1 | a0001c0001t0002g0039 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.415-8701T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59756270 | ||||||
| chr17:59756334
|
A | G | 5 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0267others(2): Show | 5 | HG01109.hp2 HG02896.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.415-8637A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59756334 | ||||||
| chr17:59756585
|
A | G | 267 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(264): Show | 267 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.415-8386A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59756585 | ||||||
| chr17:59756685
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.415-8286C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59756685 | ||||||
| chr17:59757157
|
G | C | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.415-7814G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59757157 | ||||||
| chr17:59757238
|
G | GAGAT | 24 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0091others(21): Show | 24 | HG00544.hp2 HG00741.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.415-7680_415-7677d others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59757238 | |||||
| chr17:59757238
|
G | GAGATAGA others(1): Show |
6 | a0001c0001t0001g0189a0001c0001t0002g0054a0001c0001t0002g0097others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.415-7684_415-7677d others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59757238 | |||||
| chr17:59757238
|
GAGAT | G | 108 | a0001c0001t0001g0008a0001c0001t0001g0070a0001c0001t0001g0076others(105): Show | 108 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.415-7680_415-7677d others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59757238 | |||||
| chr17:59757238
|
GAGATAGA others(1): Show |
G | 62 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(59): Show | 62 | HG00642.hp1 HG00673.hp2 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.415-7684_415-7677d others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59757238 | |||||
| chr17:59757238
|
GAGATAGA others(5): Show |
G | 5 | a0001c0001t0001g0213a0001c0001t0003g0131a0001c0001t0003g0155others(2): Show | 5 | HG00639.hp1 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.415-7688_415-7677d others(14): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59757238 | |||||
| chr17:59757238
|
GAGATAGA others(9): Show |
G | 9 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(6): Show | 9 | HG01109.hp2 HG02896.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.415-7692_415-7677d others(18): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59757238 | |||||
| chr17:59757241
|
A | C | 1 | a0001c0001t0003g0147 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.415-7730A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59757241 | ||||||
| chr17:59757245
|
A | C | 11 | a0001c0001t0003g0108a0001c0001t0003g0121a0001c0001t0003g0122others(8): Show | 11 | HG00438.hp2 HG01069.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.415-7726A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59757245 | ||||||
| chr17:59757249
|
A | C | 41 | a0001c0001t0001g0132a0001c0001t0001g0139a0001c0001t0001g0277others(38): Show | 41 | HG00642.hp1 HG00673.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.415-7722A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59757249 | ||||||
| chr17:59757253
|
A | C | 2 | a0001c0001t0003g0131a0001c0001t0003g0155 | 2 | HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.415-7718A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59757253 | ||||||
| chr17:59757277
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.415-7694A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59757277 | ||||||
| chr17:59757610
|
T | A | 1 | a0001c0001t0002g0054 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.415-7361T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59757610 | ||||||
| chr17:59757803
|
T | C | 1 | a0001c0001t0002g0049 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.415-7168T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59757803 | ||||||
| chr17:59757855
|
G | GC | 87 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(84): Show | 87 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.415-7114dupC | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59757855 | |||||
| chr17:59757858
|
A | C | 168 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(165): Show | 168 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.415-7113A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59757858 | ||||||
| chr17:59757859
|
C | CCT | 9 | a0001c0001t0001g0090a0001c0001t0001g0276a0001c0001t0002g0014others(6): Show | 9 | HG00741.hp1 HG02027.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.415-7112_415-7111i others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59757859 | ||||||
| chr17:59757859
|
C | CTTT | 31 | a0001c0001t0001g0106a0001c0001t0001g0179a0001c0001t0001g0180others(28): Show | 31 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.415-7089_415-7087d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59757859 | |||||
| chr17:59757859
|
C | CTTTT | 85 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(82): Show | 85 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.415-7090_415-7087d others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59757859 | |||||
| chr17:59757859
|
C | CTTTTT | 21 | a0001c0001t0001g0095a0001c0001t0001g0101a0001c0001t0001g0103others(18): Show | 21 | HG00423.hp1 HG00438.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.415-7091_415-7087d others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59757859 | |||||
| chr17:59757859
|
CTT | C | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.415-7088_415-7087d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59757859 | |||||
| chr17:59757859
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0003g0133 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.415-7099_415-7087d others(15): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59757859 | |||||
| chr17:59757860
|
T | C | 10 | a0001c0001t0001g0079a0001c0001t0001g0089a0001c0001t0002g0027others(7): Show | 10 | HG02015.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.415-7111T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59757860 | ||||||
| chr17:59757861
|
T | C | 1 | a0001c0001t0005g0061 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.415-7110T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59757861 | ||||||
| chr17:59758035
|
C | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0090 | 2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.415-6936C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59758035 | ||||||
| chr17:59758073
|
C | G | 1 | a0001c0001t0001g0152 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.415-6898C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59758073 | ||||||
| chr17:59758189
|
A | G | 2 | a0001c0001t0001g0176a0001c0001t0001g0214 | 2 | NA18977.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.415-6782A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59758189 | ||||||
| chr17:59758390
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.415-6581G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59758390 | ||||||
| chr17:59758429
|
C | A | 17 | a0001c0001t0003g0110a0001c0001t0003g0115a0001c0001t0003g0116others(14): Show | 17 | HG00673.hp2 HG00738.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.415-6542C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59758429 | ||||||
| chr17:59758773
|
C | T | 261 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(258): Show | 261 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.415-6198C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59758773 | ||||||
| chr17:59758946
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.415-6025C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59758946 | ||||||
| chr17:59759010
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.415-5961C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759010 | ||||||
| chr17:59759192
|
G | A | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(55): Show | 58 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.415-5779G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759192 | ||||||
| chr17:59759242
|
C | T | 1 | a0001c0001t0004g0262 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.415-5729C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759242 | ||||||
| chr17:59759243
|
G | A | 1 | a0001c0001t0003g0157 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.415-5728G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759243 | ||||||
| chr17:59759296
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.415-5675C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759296 | ||||||
| chr17:59759377
|
AAAAAT | A | 87 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.415-5585_415-5581d others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59759377 | |||||
| chr17:59759406
|
A | G | 79 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.415-5565A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759406 | ||||||
| chr17:59759563
|
A | G | 180 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 180 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.415-5408A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759563 | ||||||
| chr17:59759745
|
G | C | 2 | a0001c0001t0004g0269a0001c0001t0004g0270 | 2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.415-5226G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759745 | ||||||
| chr17:59759842
|
C | T | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.415-5129C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759842 | ||||||
| chr17:59759903
|
GT | G | 103 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0082others(100): Show | 103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.415-5048delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59759903 | |||||
| chr17:59759903
|
GTT | G | 16 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(13): Show | 16 | HG00741.hp1 HG01099.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.415-5049_415-5048d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59759903 | |||||
| chr17:59759908
|
T | TG | 85 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(82): Show | 85 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.415-5063_415-5062i others(3): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759908 | ||||||
| chr17:59759909
|
T | G | 59 | a0001c0001t0001g0089a0001c0001t0001g0132a0001c0001t0001g0139others(56): Show | 59 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.415-5062T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759909 | ||||||
| chr17:59759910
|
T | G | 104 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0082others(101): Show | 104 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.415-5061T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759910 | ||||||
| chr17:59759911
|
T | G | 18 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(15): Show | 18 | HG00741.hp1 HG01099.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.415-5060T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759911 | ||||||
| chr17:59759912
|
T | G | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.415-5059T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759912 | ||||||
| chr17:59760122
|
CA | C | 179 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(176): Show | 179 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.415-4837delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59760122 | |||||
| chr17:59760136
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.415-4835A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59760136 | ||||||
| chr17:59760262
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.415-4709C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59760262 | ||||||
| chr17:59760500
|
A | G | 1 | a0001c0001t0003g0115 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.415-4471A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59760500 | ||||||
| chr17:59760520
|
C | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0282 | 2 | HG01099.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.415-4451C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59760520 | ||||||
| chr17:59760524
|
T | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.415-4447T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59760524 | ||||||
| chr17:59760679
|
G | A | 56 | a0001c0001t0001g0132a0001c0001t0001g0139a0001c0001t0001g0277others(53): Show | 56 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.415-4292G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59760679 | ||||||
| chr17:59760714
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.415-4257G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59760714 | ||||||
| chr17:59760920
|
A | G | 1 | a0001c0001t0002g0065 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.415-4051A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59760920 | ||||||
| chr17:59761006
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.415-3965G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59761006 | ||||||
| chr17:59761063
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.415-3908C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59761063 | ||||||
| chr17:59761064
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.415-3907G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59761064 | ||||||
| chr17:59761342
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.415-3629G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59761342 | ||||||
| chr17:59761362
|
T | C | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.415-3609T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59761362 | ||||||
| chr17:59761470
|
G | A | 56 | a0001c0001t0001g0132a0001c0001t0001g0139a0001c0001t0001g0277others(53): Show | 56 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.415-3501G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59761470 | ||||||
| chr17:59761823
|
T | C | 1 | a0001c0001t0002g0031 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.415-3148T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59761823 | ||||||
| chr17:59761823
|
T | TTC | 266 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(263): Show | 266 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.415-3144_415-3143d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59761823 | |||||
| chr17:59761901
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.415-3070G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59761901 | ||||||
| chr17:59761926
|
C | T | 1 | a0001c0001t0002g0072 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.415-3045C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59761926 | ||||||
| chr17:59761948
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.415-3023T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59761948 | ||||||
| chr17:59762178
|
G | A | 3 | a0001c0001t0002g0195a0001c0001t0002g0198a0001c0001t0002g0235 | 3 | HG01069.hp2 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.415-2793G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59762178 | ||||||
| chr17:59762207
|
A | G | 180 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 180 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.415-2764A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59762207 | ||||||
| chr17:59762243
|
C | T | 79 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.415-2728C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59762243 | ||||||
| chr17:59762549
|
G | A | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.415-2422G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59762549 | ||||||
| chr17:59762762
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.415-2209A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59762762 | ||||||
| chr17:59762856
|
AT | A | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.415-2113delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59762856 | |||||
| chr17:59762903
|
G | T | 1 | a0001c0001t0002g0056 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.415-2068G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59762903 | ||||||
| chr17:59763172
|
C | T | 2 | a0001c0001t0004g0265a0001c0001t0004g0266 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.415-1799C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59763172 | ||||||
| chr17:59763480
|
G | A | 55 | a0001c0001t0001g0132a0001c0001t0001g0139a0001c0001t0003g0105others(52): Show | 55 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.415-1491G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59763480 | ||||||
| chr17:59763546
|
A | G | 4 | a0001c0001t0001g0178a0001c0001t0001g0190a0001c0001t0001g0232others(1): Show | 4 | HG01074.hp2 HG01361.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-1425A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59763546 | ||||||
| chr17:59763961
|
A | G | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.415-1010A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59763961 | ||||||
| chr17:59763996
|
A | G | 79 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.415-975A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59763996 | ||||||
| chr17:59764484
|
T | C | 1 | a0001c0001t0003g0134 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.415-487T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59764484 | ||||||
| chr17:59764694
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.415-277C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59764694 | ||||||
| chr17:59764766
|
A | G | 2 | a0001c0001t0003g0111a0001c0001t0003g0112 | 2 | HG01071.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.415-205A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59764766 | ||||||
| chr17:59764906
|
A | T | 1 | a0001c0001t0002g0036 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.415-65A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59764906 | ||||||
| chr17:59765375
|
G | T | 64 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(61): Show | 64 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.582+237G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59765375 | ||||||
| chr17:59765398
|
T | C | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.582+260T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59765398 | ||||||
| chr17:59765404
|
C | T | 270 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(267): Show | 270 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.582+266C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59765404 | ||||||
| chr17:59765648
|
A | G | 4 | a0001c0001t0006g0283a0001c0001t0006g0284a0001c0001t0006g0285others(1): Show | 4 | HG02109.hp2 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.582+510A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59765648 | ||||||
| chr17:59765947
|
T | TA | 6 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156others(3): Show | 6 | HG01168.hp2 HG02027.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.582+810dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59765947 | |||||
| chr17:59766291
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.582+1153G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59766291 | ||||||
| chr17:59766340
|
C | A | 1 | a0001c0001t0001g0282 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.582+1202C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59766340 | ||||||
| chr17:59766452
|
C | T | 1 | a0001c0001t0002g0062 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.582+1314C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59766452 | ||||||
| chr17:59766465
|
C | T | 2 | a0001c0001t0006g0283a0001c0001t0006g0284 | 2 | HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.582+1327C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59766465 | ||||||
| chr17:59766843
|
A | G | 267 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(264): Show | 267 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.582+1705A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59766843 | ||||||
| chr17:59766970
|
C | T | 1 | a0001c0001t0002g0064 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.582+1832C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59766970 | ||||||
| chr17:59767025
|
A | C | 1 | a0001c0001t0001g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.582+1887A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59767025 | ||||||
| chr17:59767123
|
G | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.582+1985G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59767123 | ||||||
| chr17:59767337
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.582+2199T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59767337 | ||||||
| chr17:59767698
|
G | A | 1 | a0001c0001t0010g0230 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.582+2560G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59767698 | ||||||
| chr17:59767919
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.582+2781G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59767919 | ||||||
| chr17:59767960
|
A | G | 104 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(101): Show | 104 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.582+2822A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59767960 | ||||||
| chr17:59768109
|
CA | C | 180 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 180 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.582+2981delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59768109 | |||||
| chr17:59768225
|
G | A | 1 | a0001c0001t0002g0034 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.582+3087G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59768225 | ||||||
| chr17:59768263
|
A | C | 87 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.582+3125A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59768263 | ||||||
| chr17:59768576
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.582+3438C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59768576 | ||||||
| chr17:59768649
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.582+3511T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59768649 | ||||||
| chr17:59768706
|
G | C | 2 | a0001c0001t0001g0181a0001c0001t0001g0204 | 2 | HG00423.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.582+3568G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59768706 | ||||||
| chr17:59768908
|
G | A | 49 | a0001c0001t0001g0132a0001c0001t0001g0139a0001c0001t0003g0105others(46): Show | 49 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.582+3770G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59768908 | ||||||
| chr17:59768940
|
G | T | 1 | a0001c0001t0001g0256 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.582+3802G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59768940 | ||||||
| chr17:59769018
|
C | T | 1 | a0001c0001t0009g0109 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.582+3880C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59769018 | ||||||
| chr17:59769154
|
CT | C | 259 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(256): Show | 259 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.582+4033delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59769154 | |||||
| chr17:59769154
|
CTT | C | 6 | a0001c0001t0001g0139a0001c0001t0001g0248a0001c0001t0001g0254others(3): Show | 6 | HG01256.hp2 HG02698.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.582+4032_582+4033d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59769154 | |||||
| chr17:59769525
|
GTCTTTGA others(5): Show |
G | 1 | a0001c0001t0002g0050 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.583-4219_583-4208d others(14): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59769525 | |||||
| chr17:59769714
|
C | T | 2 | a0001c0001t0007g0274a0001c0001t0007g0275 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.583-4040C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59769714 | ||||||
| chr17:59769923
|
T | G | 1 | a0001c0001t0001g0256 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.583-3831T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59769923 | ||||||
| chr17:59770262
|
T | C | 1 | a0001c0001t0002g0041 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.583-3492T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59770262 | ||||||
| chr17:59770645
|
A | G | 180 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 180 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.583-3109A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59770645 | ||||||
| chr17:59770673
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.583-3081C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59770673 | ||||||
| chr17:59770823
|
T | G | 180 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 180 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.583-2931T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59770823 | ||||||
| chr17:59770990
|
G | GT | 12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(9): Show | 12 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.583-2752dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59770990 | |||||
| chr17:59771044
|
C | T | 1 | a0001c0001t0002g0050 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.583-2710C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59771044 | ||||||
| chr17:59771166
|
C | CT | 181 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(178): Show | 181 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.583-2576dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59771166 | |||||
| chr17:59771226
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.583-2528G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59771226 | ||||||
| chr17:59771237
|
A | G | 7 | a0001c0001t0002g0194a0001c0001t0002g0195a0001c0001t0002g0196others(4): Show | 7 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.583-2517A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59771237 | ||||||
| chr17:59771378
|
C | T | 2 | a0001c0001t0003g0105a0001c0001t0003g0148 | 2 | HG02257.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.583-2376C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59771378 | ||||||
| chr17:59771379
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.583-2375G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59771379 | ||||||
| chr17:59771606
|
G | GT | 47 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(44): Show | 47 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.583-2129dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59771606 | |||||
| chr17:59771606
|
GT | G | 7 | a0001c0001t0001g0095a0001c0001t0001g0165a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp1 HG02559.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.583-2129delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59771606 | |||||
| chr17:59771899
|
A | C | 1 | a0001c0001t0006g0285 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.583-1855A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59771899 | ||||||
| chr17:59772095
|
G | A | 180 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 180 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.583-1659G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59772095 | ||||||
| chr17:59772325
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.583-1429T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59772325 | ||||||
| chr17:59772335
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.583-1419C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59772335 | ||||||
| chr17:59772674
|
C | CA | 7 | a0001c0001t0002g0194a0001c0001t0002g0195a0001c0001t0002g0196others(4): Show | 7 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.583-1079dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772674 | |||||
| chr17:59772890
|
C | T | 87 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.583-864C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59772890 | ||||||
| chr17:59772950
|
C | CT | 58 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(55): Show | 58 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.583-774dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | |||||
| chr17:59772950
|
C | CTT | 35 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(32): Show | 35 | HG00140.hp2 HG00642.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.583-775_583-774dup others(2): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | |||||
| chr17:59772950
|
C | CTTT | 7 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0208others(4): Show | 7 | HG00621.hp2 HG01952.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.583-776_583-774dup others(3): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | |||||
| chr17:59772950
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0003g0111 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.583-783_583-774dup others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | |||||
| chr17:59772950
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0095a0001c0001t0003g0112 | 2 | HG03471.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.583-784_583-774dup others(11): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | |||||
| chr17:59772950
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0003g0118 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.583-787_583-774dup others(14): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | |||||
| chr17:59772950
|
C | CTTTTTTT others(8): Show |
8 | a0001c0001t0001g0139a0001c0001t0003g0110a0001c0001t0003g0121others(5): Show | 8 | HG00673.hp2 HG01978.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.583-788_583-774dup others(15): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | |||||
| chr17:59772950
|
C | CTTTTTTT others(9): Show |
9 | a0001c0001t0001g0132a0001c0001t0003g0114a0001c0001t0003g0115others(6): Show | 9 | HG00738.hp2 HG01069.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.583-789_583-774dup others(16): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | |||||
| chr17:59772950
|
C | CTTTTTTT others(10): Show |
4 | a0001c0001t0003g0105a0001c0001t0003g0117a0001c0001t0003g0128others(1): Show | 4 | HG02647.hp1 HG02717.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.583-790_583-774dup others(17): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | |||||
| chr17:59772950
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0003g0138 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.583-791_583-774dup others(18): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | |||||
| chr17:59772950
|
C | CTTTTTTT others(12): Show |
2 | a0001c0001t0003g0136a0001c0001t0003g0141 | 2 | HG00438.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.583-792_583-774dup others(19): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | |||||
| chr17:59772950
|
C | CTTTTTTT others(13): Show |
2 | a0001c0001t0003g0135a0001c0001t0003g0147 | 2 | NA18967.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.583-793_583-774dup others(20): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | |||||
| chr17:59772950
|
C | CTTTTTTT others(15): Show |
2 | a0001c0001t0003g0108a0001c0001t0003g0126 | 2 | HG03927.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.583-795_583-774dup others(22): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | |||||
| chr17:59772950
|
C | CTTTTTTT others(16): Show |
4 | a0001c0001t0003g0122a0001c0001t0003g0142a0001c0001t0003g0259others(1): Show | 4 | HG02896.hp2 NA18987.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.583-796_583-774dup others(23): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | |||||
| chr17:59772950
|
C | CTTTTTTT others(18): Show |
1 | a0001c0001t0003g0143 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.583-798_583-774dup others(25): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | |||||
| chr17:59772950
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0003g0116 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.583-799_583-774dup others(26): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | |||||
| chr17:59772950
|
C | CTTTTTTT others(21): Show |
1 | a0001c0001t0003g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.583-801_583-774dup others(28): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | |||||
| chr17:59772950
|
C | CTTTTTTT others(23): Show |
1 | a0001c0001t0003g0151 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.583-803_583-774dup others(30): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | |||||
| chr17:59772950
|
C | CTTTTTTT others(24): Show |
1 | a0001c0001t0003g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.583-774_583-773ins others(31): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | |||||
| chr17:59772950
|
CTTTTTTT | C | 12 | a0001c0001t0001g0277a0001c0001t0002g0026a0001c0001t0002g0034others(9): Show | 12 | HG00621.hp1 HG01168.hp2 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.583-780_583-774del others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | |||||
| chr17:59772950
|
CTTTTTTT others(1): Show |
C | 97 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(94): Show | 97 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.583-781_583-774del others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | |||||
| chr17:59772950
|
CTTTTTTT others(16): Show |
C | 1 | a0001c0001t0003g0133 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.583-796_583-774del others(23): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | |||||
| chr17:59772993
|
T | G | 1 | a0001c0001t0004g0272 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.583-761T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59772993 | ||||||
| chr17:59773047
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0181 | 2 | HG00423.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.583-707C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59773047 | ||||||
| chr17:59773048
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.583-706G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59773048 | ||||||
| chr17:59773181
|
C | T | 3 | a0001c0001t0002g0013a0001c0001t0002g0023a0001c0001t0002g0071 | 3 | HG02735.hp1 HG03688.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.583-573C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59773181 | ||||||
| chr17:59773190
|
G | A | 21 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(18): Show | 21 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.583-564G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59773190 | ||||||
| chr17:59773304
|
T | TG | 27 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(24): Show | 27 | HG01099.hp1 HG01109.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.583-441dupG | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59773304 | |||||
| chr17:59773402
|
A | AT | 102 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(99): Show | 102 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.583-339dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59773402 | |||||
| chr17:59773427
|
A | C | 1 | a0001c0001t0001g0240 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.583-327A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59773427 | ||||||
| chr17:59773520
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.583-234C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59773520 | ||||||
| chr17:59773606
|
T | C | 1 | a0001c0001t0003g0118 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.583-148T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59773606 | ||||||
| chr17:59774379
|
C | T | 1 | a0001c0001t0002g0043 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.714+494C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59774379 | ||||||
| chr17:59774412
|
TA | T | 87 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.714+539delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59774412 | |||||
| chr17:59774420
|
A | T | 87 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.714+535A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59774420 | ||||||
| chr17:59774421
|
AAAAGAAA others(1): Show |
A | 79 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.714+552_714+559del others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59774421 | |||||
| chr17:59774933
|
CA | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.714+1056delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59774933 | |||||
| chr17:59774941
|
AT | A | 149 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0095others(146): Show | 149 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.714+1074delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59774941 | |||||
| chr17:59774942
|
T | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(98): Show | 101 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.714+1057T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59774942 | ||||||
| chr17:59774943
|
T | A | 3 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0002g0053 | 3 | HG02486.hp2 HG06807.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.714+1058T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59774943 | ||||||
| chr17:59775087
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.714+1202G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59775087 | ||||||
| chr17:59775224
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.714+1339G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59775224 | ||||||
| chr17:59775278
|
A | T | 1 | a0001c0001t0001g0220 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.714+1393A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59775278 | ||||||
| chr17:59775283
|
C | T | 3 | a0001c0001t0003g0131a0001c0001t0003g0134a0001c0001t0003g0146 | 3 | HG02895.hp1 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.714+1398C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59775283 | ||||||
| chr17:59775306
|
T | C | 1 | a0001c0001t0003g0259 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.714+1421T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59775306 | ||||||
| chr17:59775369
|
T | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.714+1484T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59775369 | ||||||
| chr17:59775796
|
A | G | 1 | a0001c0001t0004g0268 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.714+1911A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59775796 | ||||||
| chr17:59775853
|
A | C | 166 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(163): Show | 166 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.714+1968A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59775853 | ||||||
| chr17:59775854
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.714+1969G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59775854 | ||||||
| chr17:59776210
|
TAAAA | T | 62 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(59): Show | 62 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.714+2331_714+2334d others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59776210 | |||||
| chr17:59776314
|
A | C | 1 | a0001c0001t0003g0107 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.714+2429A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59776314 | ||||||
| chr17:59776341
|
T | C | 267 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(264): Show | 267 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.714+2456T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59776341 | ||||||
| chr17:59776796
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.714+2911G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59776796 | ||||||
| chr17:59776905
|
T | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.714+3020T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59776905 | ||||||
| chr17:59777059
|
G | A | 267 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(264): Show | 267 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.714+3174G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59777059 | ||||||
| chr17:59777249
|
G | A | 2 | a0001c0001t0001g0077a0001c0001t0001g0278 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.714+3364G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59777249 | ||||||
| chr17:59777422
|
C | T | 104 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(101): Show | 104 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.714+3537C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59777422 | ||||||
| chr17:59777494
|
A | G | 53 | a0001c0001t0003g0105a0001c0001t0003g0107a0001c0001t0003g0108others(50): Show | 53 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.714+3609A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59777494 | ||||||
| chr17:59777731
|
G | A | 21 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(18): Show | 21 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.714+3846G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59777731 | ||||||
| chr17:59777788
|
T | G | 6 | a0001c0001t0003g0115a0001c0001t0003g0123a0001c0001t0003g0124others(3): Show | 6 | HG00738.hp2 HG01069.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+3903T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59777788 | ||||||
| chr17:59777812
|
T | TCAAAA | 62 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0188others(59): Show | 62 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.714+3968_714+3972d others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59777812 | |||||
| chr17:59777812
|
T | TCAAAACA others(3): Show |
16 | a0001c0001t0002g0033a0001c0001t0002g0035a0001c0001t0002g0042others(13): Show | 16 | HG00423.hp2 HG00741.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.714+3963_714+3972d others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59777812 | |||||
| chr17:59777812
|
TCAAAA | T | 61 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(58): Show | 61 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.714+3968_714+3972d others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59777812 | |||||
| chr17:59777812
|
TCAAAACA others(3): Show |
T | 10 | a0001c0001t0001g0009a0001c0001t0001g0242a0001c0001t0001g0255others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.714+3963_714+3972d others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59777812 | |||||
| chr17:59777812
|
TCAAAACA others(8): Show |
T | 1 | a0001c0001t0001g0202 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.714+3958_714+3972d others(17): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59777812 | |||||
| chr17:59777812
|
TCAAAACA others(13): Show |
T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.714+3953_714+3972d others(22): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59777812 | |||||
| chr17:59777955
|
C | G | 2 | a0001c0001t0007g0274a0001c0001t0007g0275 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.714+4070C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59777955 | ||||||
| chr17:59778250
|
A | C | 1 | a0001c0001t0002g0068 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.714+4365A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59778250 | ||||||
| chr17:59778263
|
C | T | 4 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0058others(1): Show | 4 | HG02698.hp2 HG02738.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+4378C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59778263 | ||||||
| chr17:59778289
|
C | A | 2 | a0001c0001t0006g0285a0001c0001t0006g0286 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.714+4404C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59778289 | ||||||
| chr17:59778498
|
G | A | 1 | a0001c0001t0002g0049 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.714+4613G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59778498 | ||||||
| chr17:59778540
|
CA | C | 174 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(171): Show | 174 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.714+4671delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59778540 | |||||
| chr17:59778549
|
A | G | 5 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156others(2): Show | 5 | HG01168.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.714+4664A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59778549 | ||||||
| chr17:59779268
|
A | G | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.714+5383A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59779268 | ||||||
| chr17:59779398
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.714+5513G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59779398 | ||||||
| chr17:59779918
|
G | C | 2 | a0001c0001t0001g0132a0001c0001t0001g0139 | 2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.714+6033G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59779918 | ||||||
| chr17:59779926
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.714+6041T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59779926 | ||||||
| chr17:59780113
|
T | G | 2 | a0001c0001t0002g0012a0001c0001t0002g0019 | 2 | HG00738.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.714+6228T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59780113 | ||||||
| chr17:59780329
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.714+6444G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59780329 | ||||||
| chr17:59780779
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.714+6894G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59780779 | ||||||
| chr17:59780824
|
G | T | 1 | a0001c0001t0001g0240 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.714+6939G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59780824 | ||||||
| chr17:59781013
|
A | T | 79 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.714+7128A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59781013 | ||||||
| chr17:59781345
|
C | T | 4 | a0001c0001t0001g0209a0001c0001t0001g0213a0001c0001t0001g0220others(1): Show | 4 | HG00280.hp2 HG00639.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+7460C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59781345 | ||||||
| chr17:59781445
|
A | G | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.714+7560A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59781445 | ||||||
| chr17:59781615
|
T | A | 5 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156others(2): Show | 5 | HG01168.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.714+7730T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59781615 | ||||||
| chr17:59781637
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.714+7752C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59781637 | ||||||
| chr17:59781763
|
A | T | 1 | a0001c0001t0001g0210 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.714+7878A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59781763 | ||||||
| chr17:59781849
|
G | A | 89 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(86): Show | 89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.714+7964G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59781849 | ||||||
| chr17:59782096
|
A | G | 2 | a0001c0001t0001g0076a0001c0001t0001g0082 | 2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.714+8211A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59782096 | ||||||
| chr17:59782300
|
CTTTT | C | 54 | a0001c0001t0001g0277a0001c0001t0003g0105a0001c0001t0003g0107others(51): Show | 54 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.714+8418_714+8421d others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59782300 | |||||
| chr17:59782344
|
C | T | 79 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.714+8459C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59782344 | ||||||
| chr17:59782598
|
C | T | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.714+8713C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59782598 | ||||||
| chr17:59782599
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.714+8714G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59782599 | ||||||
| chr17:59782681
|
G | A | 2 | a0001c0001t0001g0077a0001c0001t0001g0278 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.714+8796G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59782681 | ||||||
| chr17:59782789
|
G | T | 178 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.714+8904G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59782789 | ||||||
| chr17:59782792
|
G | A | 1 | a0001c0001t0003g0113 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.714+8907G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59782792 | ||||||
| chr17:59782796
|
AG | A | 104 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(101): Show | 104 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.714+8912delG | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59782796 | ||||||
| chr17:59782867
|
T | C | 4 | a0001c0001t0006g0283a0001c0001t0006g0284a0001c0001t0006g0285others(1): Show | 4 | HG02109.hp2 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+8982T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59782867 | ||||||
| chr17:59782989
|
A | T | 1 | a0001c0001t0001g0202 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.714+9104A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59782989 | ||||||
| chr17:59783001
|
C | G | 1 | a0001c0001t0004g0273 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.714+9116C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59783001 | ||||||
| chr17:59783020
|
C | T | 18 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(15): Show | 18 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.714+9135C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59783020 | ||||||
| chr17:59783064
|
C | T | 1 | a0001c0001t0003g0120 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.714+9179C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59783064 | ||||||
| chr17:59783089
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.714+9204C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59783089 | ||||||
| chr17:59783153
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.714+9268G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59783153 | ||||||
| chr17:59783322
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0232 | 2 | HG01074.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.714+9437G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59783322 | ||||||
| chr17:59783690
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.714+9805C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59783690 | ||||||
| chr17:59783748
|
C | T | 2 | a0001c0001t0003g0134a0001c0001t0003g0146 | 2 | HG02895.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.714+9863C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59783748 | ||||||
| chr17:59783893
|
A | C | 1 | a0001c0001t0001g0006 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.714+10008A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59783893 | ||||||
| chr17:59784100
|
AGT | A | 45 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0162others(42): Show | 45 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.714+10257_714+1025 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784100 | |||||
| chr17:59784100
|
AGTGT | A | 18 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0153others(15): Show | 18 | HG00438.hp2 HG01071.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.714+10255_714+1025 others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784100 | |||||
| chr17:59784100
|
AGTGTGTG others(9): Show |
A | 1 | a0001c0001t0003g0260 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.714+10243_714+1025 others(20): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784100 | |||||
| chr17:59784136
|
T | A | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.714+10251T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784136 | ||||||
| chr17:59784138
|
T | A | 8 | a0001c0001t0001g0011a0001c0001t0001g0106a0001c0001t0001g0227others(5): Show | 8 | HG00408.hp1 HG00673.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.714+10253T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784138 | ||||||
| chr17:59784138
|
T | TGAGA | 7 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(4): Show | 7 | HG01099.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.714+10254_714+1025 others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784138 | |||||
| chr17:59784138
|
TGTGTGA | T | 3 | a0001c0001t0001g0280a0001c0001t0008g0279a0001c0001t0008g0281 | 3 | HG02145.hp2 HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.714+10255_714+1026 others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784138 | |||||
| chr17:59784140
|
T | A | 130 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(127): Show | 130 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.714+10255T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784140 | ||||||
| chr17:59784140
|
T | TGA | 8 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0132others(5): Show | 8 | HG00621.hp2 HG01069.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.714+10256_714+1025 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784140 | |||||
| chr17:59784140
|
T | TGAGAGAG others(1): Show |
5 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0269others(2): Show | 5 | HG01109.hp2 HG03041.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.714+10256_714+1025 others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784140 | |||||
| chr17:59784142
|
T | A | 164 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.714+10257T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784142 | ||||||
| chr17:59784142
|
T | TGA | 11 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0088others(8): Show | 11 | HG00544.hp1 HG01358.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.714+10272_714+1027 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784142 | |||||
| chr17:59784142
|
T | TGAGA | 6 | a0001c0001t0001g0178a0001c0001t0001g0183a0001c0001t0001g0221others(3): Show | 6 | HG02083.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+10270_714+1027 others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784142 | |||||
| chr17:59784142
|
T | TGAGAGAG others(1): Show |
5 | a0001c0001t0001g0009a0001c0001t0004g0265a0001c0001t0004g0266others(2): Show | 5 | HG02615.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.714+10266_714+1027 others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784142 | |||||
| chr17:59784142
|
T | TGTGA | 26 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(23): Show | 26 | HG00423.hp2 HG00741.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.714+10258_714+1025 others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784142 | |||||
| chr17:59784142
|
T | TGTGAGAG others(5): Show |
1 | a0001c0001t0004g0267 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.714+10258_714+1025 others(16): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784142 | |||||
| chr17:59784142
|
T | TGTGTGA | 20 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(17): Show | 20 | HG00408.hp2 HG00738.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.714+10258_714+1025 others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784142 | |||||
| chr17:59784142
|
T | TGTGTGTG others(1): Show |
17 | a0001c0001t0002g0023a0001c0001t0002g0033a0001c0001t0002g0034others(14): Show | 17 | HG00621.hp1 HG00639.hp2 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.714+10258_714+1025 others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784142 | |||||
| chr17:59784142
|
T | TGTGTGTG others(3): Show |
1 | a0001c0001t0005g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.714+10258_714+1025 others(14): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784142 | |||||
| chr17:59784142
|
T | TGTGTGTG others(7): Show |
1 | a0001c0001t0002g0022 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.714+10258_714+1025 others(18): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784142 | |||||
| chr17:59784144
|
A | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.714+10259A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784144 | ||||||
| chr17:59784146
|
A | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.714+10261A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784146 | ||||||
| chr17:59784247
|
T | G | 1 | a0001c0001t0003g0110 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.714+10362T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784247 | ||||||
| chr17:59784280
|
C | T | 1 | a0001c0001t0002g0237 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.714+10395C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784280 | ||||||
| chr17:59784380
|
C | A | 1 | a0001c0001t0003g0110 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.714+10495C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784380 | ||||||
| chr17:59784405
|
C | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0239 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.714+10520C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784405 | ||||||
| chr17:59784425
|
C | T | 18 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(15): Show | 18 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.714+10540C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784425 | ||||||
| chr17:59784433
|
A | C | 53 | a0001c0001t0003g0105a0001c0001t0003g0107a0001c0001t0003g0108others(50): Show | 53 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.714+10548A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784433 | ||||||
| chr17:59784621
|
C | G | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.714+10736C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784621 | ||||||
| chr17:59784634
|
G | A | 62 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(59): Show | 62 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.714+10749G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784634 | ||||||
| chr17:59785159
|
A | G | 3 | a0001c0001t0003g0154a0001c0001t0003g0156a0001c0001t0003g0264 | 3 | HG01168.hp2 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.714+11274A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59785159 | ||||||
| chr17:59785231
|
T | C | 267 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(264): Show | 267 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.714+11346T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59785231 | ||||||
| chr17:59785597
|
C | T | 1 | a0001c0001t0002g0072 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.714+11712C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59785597 | ||||||
| chr17:59785598
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.714+11713G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59785598 | ||||||
| chr17:59785613
|
C | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.714+11728C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59785613 | ||||||
| chr17:59785622
|
A | G | 1 | a0001c0001t0003g0121 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.714+11737A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59785622 | ||||||
| chr17:59785689
|
C | CA | 11 | a0001c0001t0001g0150a0001c0001t0001g0163a0001c0001t0001g0178others(8): Show | 11 | HG01256.hp1 HG02109.hp2 HG03130.hp2 others(8): Show |
intron_variant | MODIFIER | c.714+11822dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59785689 | |||||
| chr17:59785689
|
CA | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0103a0001c0001t0001g0205others(3): Show | 6 | HG01099.hp1 HG01884.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.714+11822delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59785689 | |||||
| chr17:59786099
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.714+12214A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59786099 | ||||||
| chr17:59786136
|
A | G | 5 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(2): Show | 5 | NA18977.hp2 NA19057.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.714+12251A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59786136 | ||||||
| chr17:59786351
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.714+12466C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59786351 | ||||||
| chr17:59786732
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.714+12847G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59786732 | ||||||
| chr17:59787391
|
T | G | 2 | a0001c0001t0002g0020a0001c0001t0002g0028 | 2 | HG01123.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.714+13506T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59787391 | ||||||
| chr17:59787459
|
G | A | 2 | a0001c0001t0004g0269a0001c0001t0004g0270 | 2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.714+13574G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59787459 | ||||||
| chr17:59787479
|
G | T | 5 | a0001c0001t0002g0194a0001c0001t0002g0195a0001c0001t0002g0198others(2): Show | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.714+13594G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59787479 | ||||||
| chr17:59787584
|
G | T | 2 | a0001c0001t0004g0269a0001c0001t0004g0270 | 2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.714+13699G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59787584 | ||||||
| chr17:59787710
|
A | G | 18 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(15): Show | 18 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.714+13825A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59787710 | ||||||
| chr17:59787747
|
G | A | 1 | a0001c0001t0001g0254 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.714+13862G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59787747 | ||||||
| chr17:59787757
|
G | T | 19 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(16): Show | 19 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.714+13872G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59787757 | ||||||
| chr17:59787870
|
ACT | A | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.714+13987_714+1398 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59787870 | |||||
| chr17:59787906
|
A | G | 1 | a0001c0001t0002g0063 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.714+14021A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59787906 | ||||||
| chr17:59788131
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.714+14246G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59788131 | ||||||
| chr17:59788267
|
T | C | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.714+14382T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59788267 | ||||||
| chr17:59788558
|
C | CT | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.714+14676dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59788558 | |||||
| chr17:59788777
|
G | T | 6 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156others(3): Show | 6 | HG01168.hp2 HG02027.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+14892G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59788777 | ||||||
| chr17:59788804
|
T | TA | 74 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(71): Show | 74 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(71): Show |
intron_variant | MODIFIER | c.714+14934dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59788804 | |||||
| chr17:59788804
|
T | TAA | 99 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(96): Show | 99 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.714+14933_714+1493 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59788804 | |||||
| chr17:59788820
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.714+14935G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59788820 | ||||||
| chr17:59788941
|
C | CT | 20 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(17): Show | 20 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.714+15069dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59788941 | |||||
| chr17:59789027
|
A | ATGCCTGT others(13): Show |
1 | a0001c0001t0001g0174 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.714+15145_714+1516 others(24): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59789027 | |||||
| chr17:59789061
|
A | C | 265 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(262): Show | 265 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.714+15176A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59789061 | ||||||
| chr17:59789167
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.714+15282G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59789167 | ||||||
| chr17:59789305
|
C | T | 7 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0267others(4): Show | 7 | HG01109.hp2 HG02896.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.714+15420C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59789305 | ||||||
| chr17:59789361
|
C | T | 4 | a0001c0001t0001g0177a0001c0001t0001g0222a0001c0001t0001g0227others(1): Show | 4 | HG00642.hp2 HG01978.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+15476C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59789361 | ||||||
| chr17:59789575
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.714+15690A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59789575 | ||||||
| chr17:59789585
|
T | C | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.714+15700T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59789585 | ||||||
| chr17:59789610
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.714+15725A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59789610 | ||||||
| chr17:59789644
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.714+15759G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59789644 | ||||||
| chr17:59789645
|
T | A | 1 | a0001c0001t0001g0169 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.714+15760T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59789645 | ||||||
| chr17:59789835
|
C | CT | 68 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(65): Show | 68 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.714+15972dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59789835 | |||||
| chr17:59789835
|
C | CTT | 19 | a0001c0001t0001g0103a0001c0001t0001g0132a0001c0001t0001g0177others(16): Show | 19 | HG00642.hp2 HG01978.hp2 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.714+15971_714+1597 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59789835 | |||||
| chr17:59789835
|
C | CTTTTT | 14 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(11): Show | 14 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.714+15968_714+1597 others(9): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59789835 | |||||
| chr17:59789835
|
C | CTTTTTT | 7 | a0001c0001t0001g0003a0001c0001t0001g0078a0001c0001t0001g0087others(4): Show | 7 | HG01243.hp1 HG03098.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.714+15967_714+1597 others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59789835 | |||||
| chr17:59789835
|
C | CTTTTTTT | 23 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0020others(20): Show | 23 | HG00639.hp2 HG00741.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.714+15966_714+1597 others(11): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59789835 | |||||
| chr17:59789835
|
C | CTTTTTTT others(1): Show |
39 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0019others(36): Show | 39 | HG00423.hp2 HG00544.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.714+15965_714+1597 others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59789835 | |||||
| chr17:59789835
|
C | CTTTTTTT others(2): Show |
16 | a0001c0001t0001g0089a0001c0001t0002g0015a0001c0001t0002g0032others(13): Show | 16 | HG00408.hp2 HG00621.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.714+15964_714+1597 others(13): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59789835 | |||||
| chr17:59789835
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0002g0017 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.714+15963_714+1597 others(14): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59789835 | |||||
| chr17:59789835
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.714+15960_714+1597 others(17): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59789835 | |||||
| chr17:59789835
|
CTT | C | 26 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(23): Show | 26 | HG00642.hp1 HG00738.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.714+15971_714+1597 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59789835 | |||||
| chr17:59789835
|
CTTT | C | 47 | a0001c0001t0001g0277a0001c0001t0003g0105a0001c0001t0003g0107others(44): Show | 47 | HG00438.hp2 HG00673.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.714+15970_714+1597 others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59789835 | |||||
| chr17:59789932
|
C | T | 3 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0087 | 3 | HG02559.hp1 HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.714+16047C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59789932 | ||||||
| chr17:59789949
|
C | T | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.714+16064C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59789949 | ||||||
| chr17:59790083
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0001g0090 | 2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.714+16198C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59790083 | ||||||
| chr17:59790263
|
G | C | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.714+16378G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59790263 | ||||||
| chr17:59790444
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.714+16559G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59790444 | ||||||
| chr17:59790647
|
G | A | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.714+16762G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59790647 | ||||||
| chr17:59791184
|
C | CT | 102 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(99): Show | 102 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.714+17320dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59791184 | |||||
| chr17:59791184
|
C | CTT | 6 | a0001c0001t0001g0080a0001c0001t0002g0017a0001c0001t0002g0032others(3): Show | 6 | HG03209.hp1 NA18949.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+17319_714+1732 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59791184 | |||||
| chr17:59791184
|
CTTTTTTT | C | 85 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(82): Show | 85 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.714+17314_714+1732 others(11): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59791184 | |||||
| chr17:59791240
|
G | A | 104 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(101): Show | 104 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.714+17355G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59791240 | ||||||
| chr17:59791481
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0170 | 2 | HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.715-17315G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59791481 | ||||||
| chr17:59791491
|
C | CT | 18 | a0001c0001t0001g0008a0001c0001t0001g0103a0001c0001t0001g0150others(15): Show | 18 | HG00423.hp1 HG00621.hp2 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.715-17287dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59791491 | |||||
| chr17:59791491
|
CT | C | 12 | a0001c0001t0002g0062a0001c0001t0004g0262a0001c0001t0004g0263others(9): Show | 12 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.715-17287delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59791491 | |||||
| chr17:59791812
|
G | A | 2 | a0001c0001t0003g0113a0001c0001t0009g0109 | 2 | HG00642.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.715-16984G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59791812 | ||||||
| chr17:59792042
|
T | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.715-16754T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59792042 | ||||||
| chr17:59792303
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.715-16493C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59792303 | ||||||
| chr17:59792414
|
A | G | 1 | a0001c0001t0003g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.715-16382A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59792414 | ||||||
| chr17:59792455
|
T | A | 2 | a0001c0001t0001g0227a0001c0001t0001g0242 | 2 | HG01978.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.715-16341T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59792455 | ||||||
| chr17:59792603
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0090 | 2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.715-16193G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59792603 | ||||||
| chr17:59792619
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.715-16177C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59792619 | ||||||
| chr17:59792854
|
A | AAAT | 35 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(32): Show | 35 | HG00738.hp2 HG01069.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.715-15920_715-1591 others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59792854 | |||||
| chr17:59792854
|
A | AAATAAT | 4 | a0001c0001t0003g0146a0001c0001t0004g0269a0001c0001t0004g0270others(1): Show | 4 | HG02615.hp1 HG02895.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-15923_715-1591 others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59792854 | |||||
| chr17:59792854
|
A | AAATAATA others(2): Show |
15 | a0001c0001t0001g0277a0001c0001t0003g0110a0001c0001t0003g0112others(12): Show | 15 | HG00673.hp2 HG02027.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.715-15926_715-1591 others(13): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59792854 | |||||
| chr17:59792854
|
A | AAATAATA others(5): Show |
15 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0111others(12): Show | 15 | HG00438.hp2 HG01071.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.715-15929_715-1591 others(16): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59792854 | |||||
| chr17:59792854
|
A | AAATAATA others(8): Show |
9 | a0001c0001t0003g0105a0001c0001t0003g0113a0001c0001t0003g0134others(6): Show | 9 | HG00642.hp1 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.715-15932_715-1591 others(19): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59792854 | |||||
| chr17:59792854
|
A | AAATAATA others(11): Show |
1 | a0001c0001t0003g0141 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.715-15935_715-1591 others(22): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59792854 | |||||
| chr17:59792854
|
AAATAATA others(962): Show |
A | 87 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.715-15940_715-1497 others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59792854 | |||||
| chr17:59792876
|
A | T | 5 | a0001c0001t0001g0153a0001c0001t0001g0165a0001c0001t0001g0170others(2): Show | 5 | HG01891.hp1 HG02559.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.715-15920A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59792876 | ||||||
| chr17:59792876
|
AATTATT | A | 22 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(19): Show | 22 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.715-15908_715-1590 others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59792876 | |||||
| chr17:59792879
|
T | A | 154 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 154 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.715-15917T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59792879 | ||||||
| chr17:59792882
|
T | A | 156 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 156 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.715-15914T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59792882 | ||||||
| chr17:59792885
|
T | A | 178 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.715-15911T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59792885 | ||||||
| chr17:59792888
|
T | A | 178 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.715-15908T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59792888 | ||||||
| chr17:59792891
|
T | A | 1 | a0001c0001t0001g0004 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.715-15905T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59792891 | ||||||
| chr17:59793419
|
G | C | 178 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.715-15377G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59793419 | ||||||
| chr17:59793605
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.715-15191C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59793605 | ||||||
| chr17:59793645
|
G | T | 4 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(1): Show | 4 | HG01243.hp1 HG02451.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-15151G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59793645 | ||||||
| chr17:59793761
|
A | G | 178 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.715-15035A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59793761 | ||||||
| chr17:59793859
|
T | G | 1 | a0001c0001t0001g0160 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.715-14937T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59793859 | ||||||
| chr17:59794018
|
T | C | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-14778T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59794018 | ||||||
| chr17:59794077
|
C | T | 2 | a0001c0001t0003g0131a0001c0001t0011g0021 | 2 | NA19085.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.715-14719C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59794077 | ||||||
| chr17:59794219
|
C | CT | 39 | a0001c0001t0001g0166a0001c0001t0001g0173a0001c0001t0002g0062others(36): Show | 39 | HG00642.hp1 HG00673.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.715-14556dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794219 | |||||
| chr17:59794219
|
C | CTT | 17 | a0001c0001t0003g0120a0001c0001t0003g0124a0001c0001t0003g0130others(14): Show | 17 | HG01109.hp2 HG01934.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.715-14557_715-1455 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794219 | |||||
| chr17:59794219
|
CT | C | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(116): Show | 119 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.715-14556delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794219 | |||||
| chr17:59794219
|
CTT | C | 70 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.715-14557_715-1455 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794219 | |||||
| chr17:59794368
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.715-14428C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59794368 | ||||||
| chr17:59794376
|
C | T | 54 | a0001c0001t0001g0277a0001c0001t0003g0105a0001c0001t0003g0107others(51): Show | 54 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.715-14420C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59794376 | ||||||
| chr17:59794425
|
G | C | 3 | a0001c0001t0001g0208a0001c0001t0001g0211a0001c0001t0001g0226 | 3 | HG00621.hp2 HG02040.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.715-14371G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59794425 | ||||||
| chr17:59794507
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.715-14289C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59794507 | ||||||
| chr17:59794509
|
C | T | 1 | a0002c0003t0002g0030 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.715-14287C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59794509 | ||||||
| chr17:59794517
|
AT | A | 13 | a0001c0001t0001g0069a0001c0001t0001g0150a0001c0001t0001g0153others(10): Show | 13 | HG00140.hp1 HG01255.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.715-14245delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794517 | |||||
| chr17:59794517
|
ATTT | A | 25 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(22): Show | 25 | HG00673.hp2 HG00741.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.715-14247_715-1424 others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794517 | |||||
| chr17:59794517
|
ATTTT | A | 55 | a0001c0001t0001g0089a0001c0001t0002g0013a0001c0001t0002g0014others(52): Show | 55 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.715-14248_715-1424 others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794517 | |||||
| chr17:59794517
|
ATTTTT | A | 69 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0092others(66): Show | 69 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.715-14249_715-1424 others(9): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794517 | |||||
| chr17:59794517
|
ATTTTTT | A | 48 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(45): Show | 48 | HG00621.hp2 HG00741.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.715-14250_715-1424 others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794517 | |||||
| chr17:59794517
|
ATTTTTTT | A | 59 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(56): Show | 59 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.715-14251_715-1424 others(11): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794517 | |||||
| chr17:59794517
|
ATTTTTTT others(1): Show |
A | 7 | a0001c0001t0001g0139a0001c0001t0001g0177a0001c0001t0001g0222others(4): Show | 7 | HG00642.hp2 HG01256.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.715-14252_715-1424 others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794517 | |||||
| chr17:59794551
|
T | A | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG01261.hp2 HG01358.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-14245T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59794551 | ||||||
| chr17:59794597
|
A | G | 1 | a0001c0001t0003g0105 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.715-14199A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59794597 | ||||||
| chr17:59794726
|
T | A | 3 | a0001c0001t0002g0049a0001c0001t0002g0096a0001c0001t0002g0097 | 3 | HG00544.hp1 HG02683.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.715-14070T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59794726 | ||||||
| chr17:59794879
|
C | T | 5 | a0001c0001t0003g0151a0001c0001t0003g0258a0001c0001t0003g0259others(2): Show | 5 | HG02896.hp2 HG03195.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.715-13917C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59794879 | ||||||
| chr17:59794927
|
C | T | 3 | a0001c0001t0001g0206a0001c0001t0001g0239a0001c0001t0014g0191 | 3 | HG02922.hp2 HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.715-13869C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59794927 | ||||||
| chr17:59794995
|
C | CT | 155 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.715-13782dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794995 | |||||
| chr17:59794995
|
C | CTT | 27 | a0001c0001t0001g0004a0001c0001t0001g0081a0001c0001t0001g0084others(24): Show | 27 | HG00642.hp1 HG01258.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.715-13783_715-1378 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794995 | |||||
| chr17:59794995
|
C | CTTT | 71 | a0001c0001t0001g0092a0001c0001t0001g0100a0001c0001t0001g0101others(68): Show | 71 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.715-13784_715-1378 others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794995 | |||||
| chr17:59794995
|
C | CTTTT | 7 | a0001c0001t0001g0103a0001c0001t0001g0175a0001c0001t0001g0188others(4): Show | 7 | HG00741.hp2 HG02071.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.715-13785_715-1378 others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794995 | |||||
| chr17:59795133
|
G | A | 105 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(102): Show | 105 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.715-13663G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795133 | ||||||
| chr17:59795146
|
C | T | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-13650C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795146 | ||||||
| chr17:59795408
|
T | C | 3 | a0001c0001t0002g0049a0001c0001t0002g0096a0001c0001t0002g0097 | 3 | HG00544.hp1 HG02683.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.715-13388T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795408 | ||||||
| chr17:59795412
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.715-13384T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795412 | ||||||
| chr17:59795477
|
C | G | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13319C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795477 | ||||||
| chr17:59795479
|
T | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13317T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795479 | ||||||
| chr17:59795481
|
C | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13315C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795481 | ||||||
| chr17:59795484
|
C | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13312C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795484 | ||||||
| chr17:59795485
|
T | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13311T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795485 | ||||||
| chr17:59795486
|
T | G | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13310T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795486 | ||||||
| chr17:59795487
|
T | G | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13309T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795487 | ||||||
| chr17:59795490
|
T | G | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13306T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795490 | ||||||
| chr17:59795492
|
T | G | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13304T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795492 | ||||||
| chr17:59795493
|
G | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13303G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795493 | ||||||
| chr17:59795496
|
C | G | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13300C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795496 | ||||||
| chr17:59795498
|
T | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13298T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795498 | ||||||
| chr17:59795500
|
T | G | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13296T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795500 | ||||||
| chr17:59795501
|
T | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13295T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795501 | ||||||
| chr17:59795502
|
T | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13294T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795502 | ||||||
| chr17:59795503
|
C | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13293C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795503 | ||||||
| chr17:59795504
|
T | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13292T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795504 | ||||||
| chr17:59795506
|
T | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13290T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795506 | ||||||
| chr17:59795508
|
G | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13288G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795508 | ||||||
| chr17:59795510
|
T | C | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13286T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795510 | ||||||
| chr17:59795512
|
T | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13284T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795512 | ||||||
| chr17:59795513
|
T | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13283T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795513 | ||||||
| chr17:59795514
|
T | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13282T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795514 | ||||||
| chr17:59795517
|
A | T | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13279A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795517 | ||||||
| chr17:59795518
|
A | C | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13278A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795518 | ||||||
| chr17:59795520
|
T | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13276T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795520 | ||||||
| chr17:59795526
|
C | T | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13270C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795526 | ||||||
| chr17:59795527
|
A | T | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13269A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795527 | ||||||
| chr17:59795532
|
T | C | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13264T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795532 | ||||||
| chr17:59795534
|
G | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13262G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795534 | ||||||
| chr17:59795545
|
C | T | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13251C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795545 | ||||||
| chr17:59795713
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.715-13083C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795713 | ||||||
| chr17:59796301
|
C | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0221 | 2 | HG02083.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.715-12495C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59796301 | ||||||
| chr17:59796355
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.715-12441G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59796355 | ||||||
| chr17:59796652
|
T | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0216 | 2 | NA19057.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.715-12144T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59796652 | ||||||
| chr17:59796956
|
A | T | 1 | a0001c0001t0002g0028 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.715-11840A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59796956 | ||||||
| chr17:59797069
|
C | G | 1 | a0001c0001t0002g0024 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.715-11727C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59797069 | ||||||
| chr17:59797156
|
AC | A | 121 | a0001c0001t0001g0095a0001c0001t0001g0277a0001c0001t0002g0012others(118): Show | 121 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.715-11630delC | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59797156 | |||||
| chr17:59797156
|
ACC | A | 21 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(18): Show | 21 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.715-11631_715-1163 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59797156 | |||||
| chr17:59797650
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.715-11146G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59797650 | ||||||
| chr17:59797709
|
G | A | 4 | a0001c0001t0001g0177a0001c0001t0001g0222a0001c0001t0001g0227others(1): Show | 4 | HG00642.hp2 HG01978.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-11087G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59797709 | ||||||
| chr17:59797833
|
C | T | 1 | a0001c0001t0003g0257 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.715-10963C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59797833 | ||||||
| chr17:59797838
|
C | T | 1 | a0001c0001t0002g0064 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.715-10958C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59797838 | ||||||
| chr17:59797913
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.715-10883A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59797913 | ||||||
| chr17:59797931
|
G | A | 76 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(73): Show | 76 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.715-10865G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59797931 | ||||||
| chr17:59797940
|
A | G | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-10856A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59797940 | ||||||
| chr17:59798035
|
C | T | 87 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.715-10761C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59798035 | ||||||
| chr17:59798078
|
T | C | 1 | a0001c0001t0002g0041 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.715-10718T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59798078 | ||||||
| chr17:59798193
|
G | A | 79 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.715-10603G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59798193 | ||||||
| chr17:59798546
|
A | G | 104 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(101): Show | 104 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.715-10250A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59798546 | ||||||
| chr17:59798594
|
A | G | 2 | a0001c0001t0003g0136a0001c0001t0003g0147 | 2 | HG00438.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.715-10202A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59798594 | ||||||
| chr17:59798608
|
C | A | 1 | a0001c0001t0002g0042 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.715-10188C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59798608 | ||||||
| chr17:59798747
|
G | A | 4 | a0001c0001t0006g0283a0001c0001t0006g0284a0001c0001t0006g0285others(1): Show | 4 | HG02109.hp2 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-10049G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59798747 | ||||||
| chr17:59798846
|
A | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.715-9950A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59798846 | ||||||
| chr17:59798905
|
G | T | 1 | a0001c0001t0002g0060 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.715-9891G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59798905 | ||||||
| chr17:59799114
|
G | C | 1 | a0001c0001t0003g0122 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.715-9682G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59799114 | ||||||
| chr17:59799688
|
C | T | 104 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(101): Show | 104 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.715-9108C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59799688 | ||||||
| chr17:59799820
|
A | T | 1 | a0001c0001t0001g0177 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.715-8976A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59799820 | ||||||
| chr17:59799843
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.715-8953G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59799843 | ||||||
| chr17:59799852
|
A | G | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-8944A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59799852 | ||||||
| chr17:59799855
|
C | T | 1 | a0001c0001t0002g0039 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.715-8941C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59799855 | ||||||
| chr17:59799894
|
C | T | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-8902C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59799894 | ||||||
| chr17:59799895
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.715-8901G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59799895 | ||||||
| chr17:59799945
|
CA | C | 257 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(254): Show | 257 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.715-8834delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59799945 | |||||
| chr17:59800045
|
A | T | 1 | a0001c0001t0011g0021 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.715-8751A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59800045 | ||||||
| chr17:59800118
|
A | G | 1 | a0001c0001t0005g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.715-8678A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59800118 | ||||||
| chr17:59800243
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.715-8553A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59800243 | ||||||
| chr17:59800375
|
T | G | 4 | a0001c0001t0006g0283a0001c0001t0006g0284a0001c0001t0006g0285others(1): Show | 4 | HG02109.hp2 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-8421T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59800375 | ||||||
| chr17:59800418
|
G | A | 2 | a0001c0001t0004g0262a0001c0001t0004g0263 | 2 | HG01109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.715-8378G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59800418 | ||||||
| chr17:59800700
|
A | G | 1 | a0001c0001t0001g0199 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.715-8096A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59800700 | ||||||
| chr17:59800788
|
A | G | 53 | a0001c0001t0003g0105a0001c0001t0003g0107a0001c0001t0003g0108others(50): Show | 53 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.715-8008A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59800788 | ||||||
| chr17:59800807
|
C | G | 3 | a0001c0001t0003g0140a0001c0001t0003g0144a0001c0001t0003g0145 | 3 | HG02717.hp1 HG02895.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.715-7989C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59800807 | ||||||
| chr17:59801080
|
G | GA | 62 | a0001c0001t0001g0095a0001c0001t0001g0162a0001c0001t0001g0170others(59): Show | 62 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.715-7704dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801080 | |||||
| chr17:59801080
|
G | GAA | 48 | a0001c0001t0001g0132a0001c0001t0001g0139a0001c0001t0001g0168others(45): Show | 48 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.715-7705_715-7704d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801080 | |||||
| chr17:59801080
|
G | GAAA | 10 | a0001c0001t0001g0104a0001c0001t0001g0153a0001c0001t0001g0249others(7): Show | 10 | HG01361.hp1 HG01361.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.715-7706_715-7704d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801080 | |||||
| chr17:59801080
|
GAA | G | 17 | a0001c0001t0003g0111a0001c0001t0003g0116a0001c0001t0003g0117others(14): Show | 17 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.715-7705_715-7704d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801080 | |||||
| chr17:59801081
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.715-7715A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801081 | ||||||
| chr17:59801089
|
A | T | 1 | a0001c0001t0003g0105 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.715-7707A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801089 | ||||||
| chr17:59801091
|
A | AAAAT | 13 | a0001c0001t0001g0174a0001c0001t0001g0176a0001c0001t0001g0179others(10): Show | 13 | HG00438.hp1 HG01978.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.715-7704_715-7703i others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801091 | |||||
| chr17:59801091
|
A | AT | 9 | a0001c0001t0001g0200a0001c0001t0002g0035a0001c0001t0002g0042others(6): Show | 9 | NA18952.hp2 NA18956.hp1 NA18956.hp2 others(6): Show |
intron_variant | MODIFIER | c.715-7705_715-7704i others(3): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801091 | ||||||
| chr17:59801091
|
A | T | 32 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(29): Show | 32 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.715-7705A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801091 | ||||||
| chr17:59801092
|
AT | A | 17 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0089others(14): Show | 17 | HG01123.hp1 HG01168.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.715-7703delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801092 | ||||||
| chr17:59801093
|
T | A | 103 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(100): Show | 103 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.715-7703T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801093 | ||||||
| chr17:59801095
|
T | A | 33 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0078others(30): Show | 33 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.715-7701T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801095 | ||||||
| chr17:59801097
|
T | A | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-7699T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801097 | ||||||
| chr17:59801099
|
T | A | 9 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(6): Show | 9 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.715-7697T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801099 | ||||||
| chr17:59801106
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.715-7690A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801106 | ||||||
| chr17:59801108
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.715-7688A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801108 | ||||||
| chr17:59801108
|
ATATATGT others(11): Show |
A | 8 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0084others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.715-7686_715-7669d others(20): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801108 | |||||
| chr17:59801110
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.715-7686A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801110 | ||||||
| chr17:59801110
|
ATATGTGT others(5): Show |
A | 7 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG01243.hp1 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.715-7684_715-7673d others(14): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801110 | |||||
| chr17:59801110
|
ATATGTGT others(9): Show |
A | 2 | a0001c0001t0001g0082a0001c0001t0001g0087 | 2 | HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.715-7684_715-7669d others(18): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801110 | |||||
| chr17:59801112
|
A | ATATATGT others(1): Show |
3 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0234 | 3 | HG02886.hp2 HG03516.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.715-7683_715-7682i others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801112 | |||||
| chr17:59801112
|
A | ATATGTG | 6 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.715-7683_715-7682i others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801112 | |||||
| chr17:59801112
|
A | G | 8 | a0001c0001t0001g0095a0001c0001t0001g0168a0001c0001t0001g0186others(5): Show | 8 | HG00140.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.715-7684A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801112 | ||||||
| chr17:59801112
|
ATG | A | 5 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0002g0050others(2): Show | 5 | HG02109.hp1 HG02622.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.715-7648_715-7647d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801112 | |||||
| chr17:59801112
|
ATGTGTG | A | 10 | a0001c0001t0004g0262a0001c0001t0004g0265a0001c0001t0004g0266others(7): Show | 10 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.715-7652_715-7647d others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801112 | |||||
| chr17:59801112
|
ATGTGTGT others(3): Show |
A | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.715-7656_715-7647d others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801112 | |||||
| chr17:59801112
|
ATGTGTGT others(7): Show |
A | 1 | a0001c0001t0001g0076 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.715-7660_715-7647d others(16): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801112 | |||||
| chr17:59801112
|
ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0003g0147 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.715-7662_715-7647d others(18): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801112 | |||||
| chr17:59801114
|
G | A | 164 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(161): Show | 164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.715-7682G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801114 | ||||||
| chr17:59801116
|
G | A | 3 | a0001c0001t0001g0204a0001c0001t0002g0020a0001c0001t0013g0218 | 3 | HG01168.hp1 HG02109.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.715-7680G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801116 | ||||||
| chr17:59801118
|
G | A | 1 | a0001c0001t0013g0218 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.715-7678G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801118 | ||||||
| chr17:59801141
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.715-7655T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801141 | ||||||
| chr17:59801146
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.715-7650G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801146 | ||||||
| chr17:59801148
|
G | A | 141 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(138): Show | 141 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.715-7648G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801148 | ||||||
| chr17:59801148
|
G | GTA | 11 | a0001c0001t0001g0277a0001c0001t0003g0108a0001c0001t0003g0110others(8): Show | 11 | HG00438.hp2 HG00673.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.715-7646_715-7645d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801148 | |||||
| chr17:59801355
|
C | T | 25 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(22): Show | 25 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.715-7441C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801355 | ||||||
| chr17:59801367
|
T | G | 1 | a0001c0001t0002g0060 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.715-7429T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801367 | ||||||
| chr17:59801415
|
G | GT | 78 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(75): Show | 78 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.715-7370dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801415 | |||||
| chr17:59801544
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.715-7252G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801544 | ||||||
| chr17:59801669
|
C | T | 18 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(15): Show | 18 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.715-7127C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801669 | ||||||
| chr17:59801938
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.715-6858C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801938 | ||||||
| chr17:59802022
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.715-6774G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59802022 | ||||||
| chr17:59802249
|
A | G | 87 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.715-6547A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59802249 | ||||||
| chr17:59802840
|
G | A | 104 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(101): Show | 104 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.715-5956G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59802840 | ||||||
| chr17:59802913
|
AT | A | 87 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.715-5879delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59802913 | |||||
| chr17:59802974
|
G | A | 1 | a0001c0001t0002g0063 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.715-5822G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59802974 | ||||||
| chr17:59803064
|
A | G | 1 | a0001c0001t0003g0125 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.715-5732A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59803064 | ||||||
| chr17:59803510
|
T | C | 1 | a0001c0001t0003g0257 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.715-5286T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59803510 | ||||||
| chr17:59803949
|
A | AT | 87 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.715-4839dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59803949 | |||||
| chr17:59803983
|
T | A | 1 | a0001c0001t0001g0166 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.715-4813T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59803983 | ||||||
| chr17:59803983
|
T | G | 1 | a0001c0001t0003g0257 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.715-4813T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59803983 | ||||||
| chr17:59804339
|
C | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0216 | 2 | NA19057.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.715-4457C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59804339 | ||||||
| chr17:59804443
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.715-4353A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59804443 | ||||||
| chr17:59804476
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.715-4320G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59804476 | ||||||
| chr17:59804615
|
T | TA | 154 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 154 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.715-4159dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59804615 | |||||
| chr17:59804615
|
T | TAA | 6 | a0001c0001t0001g0103a0001c0001t0001g0186a0001c0001t0001g0200others(3): Show | 6 | HG02145.hp1 HG02738.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.715-4160_715-4159d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59804615 | |||||
| chr17:59804615
|
TA | T | 7 | a0001c0001t0001g0079a0001c0001t0002g0020a0001c0001t0002g0023others(4): Show | 7 | HG01168.hp1 HG02451.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.715-4159delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59804615 | |||||
| chr17:59804639
|
T | G | 3 | a0001c0001t0002g0195a0001c0001t0002g0198a0001c0001t0002g0235 | 3 | HG01069.hp2 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.715-4157T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59804639 | ||||||
| chr17:59804676
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.715-4120C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59804676 | ||||||
| chr17:59805150
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.715-3646G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59805150 | ||||||
| chr17:59805156
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.715-3640G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59805156 | ||||||
| chr17:59805313
|
T | C | 62 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(59): Show | 62 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.715-3483T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59805313 | ||||||
| chr17:59805318
|
C | A | 4 | a0001c0001t0001g0177a0001c0001t0001g0222a0001c0001t0001g0227others(1): Show | 4 | HG00642.hp2 HG01978.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-3478C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59805318 | ||||||
| chr17:59805388
|
C | T | 2 | a0001c0001t0003g0113a0001c0001t0009g0109 | 2 | HG00642.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.715-3408C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59805388 | ||||||
| chr17:59806010
|
T | G | 104 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(101): Show | 104 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.715-2786T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59806010 | ||||||
| chr17:59806153
|
G | T | 1 | a0001c0001t0003g0137 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.715-2643G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59806153 | ||||||
| chr17:59806266
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.715-2530A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59806266 | ||||||
| chr17:59806285
|
T | C | 87 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.715-2511T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59806285 | ||||||
| chr17:59806452
|
G | T | 1 | a0001c0001t0003g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.715-2344G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59806452 | ||||||
| chr17:59806461
|
C | T | 1 | a0001c0001t0002g0075 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.715-2335C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59806461 | ||||||
| chr17:59806561
|
A | C | 1 | a0001c0001t0001g0088 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.715-2235A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59806561 | ||||||
| chr17:59806600
|
A | G | 1 | a0001c0001t0002g0098 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.715-2196A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59806600 | ||||||
| chr17:59806715
|
C | CA | 124 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(121): Show | 124 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.715-2064dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59806715 | |||||
| chr17:59806715
|
CA | C | 9 | a0001c0001t0001g0158a0001c0001t0001g0165a0001c0001t0001g0171others(6): Show | 9 | HG00639.hp2 HG01891.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.715-2064delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59806715 | |||||
| chr17:59806895
|
T | C | 1 | a0001c0001t0003g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.715-1901T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59806895 | ||||||
| chr17:59806899
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.715-1897T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59806899 | ||||||
| chr17:59807036
|
T | A | 178 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.715-1760T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807036 | ||||||
| chr17:59807199
|
G | GT | 32 | a0001c0001t0001g0069a0001c0001t0001g0080a0001c0001t0001g0090others(29): Show | 32 | HG00741.hp1 HG01243.hp2 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.715-1582dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59807199 | |||||
| chr17:59807199
|
G | T | 6 | a0001c0001t0001g0206a0001c0001t0001g0239a0001c0001t0001g0280others(3): Show | 6 | HG02145.hp2 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.715-1597G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807199 | ||||||
| chr17:59807207
|
T | G | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.715-1589T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807207 | ||||||
| chr17:59807223
|
G | A | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-1573G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807223 | ||||||
| chr17:59807227
|
C | T | 21 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(18): Show | 21 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.715-1569C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807227 | ||||||
| chr17:59807232
|
T | C | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-1564T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807232 | ||||||
| chr17:59807290
|
C | A | 1 | a0001c0001t0003g0157 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.715-1506C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807290 | ||||||
| chr17:59807291
|
G | T | 1 | a0001c0001t0003g0157 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.715-1505G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807291 | ||||||
| chr17:59807302
|
A | G | 62 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(59): Show | 62 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.715-1494A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807302 | ||||||
| chr17:59807497
|
G | A | 1 | a0001c0001t0003g0108 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.715-1299G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807497 | ||||||
| chr17:59807507
|
A | G | 62 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(59): Show | 62 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.715-1289A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807507 | ||||||
| chr17:59807736
|
G | A | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-1060G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807736 | ||||||
| chr17:59807741
|
A | C | 25 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(22): Show | 25 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.715-1055A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807741 | ||||||
| chr17:59807781
|
A | G | 265 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(262): Show | 265 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.715-1015A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807781 | ||||||
| chr17:59807832
|
C | CA | 76 | a0001c0001t0001g0007a0001c0001t0001g0152a0001c0001t0002g0012others(73): Show | 76 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.715-945dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59807832 | |||||
| chr17:59807832
|
CA | C | 11 | a0001c0001t0001g0069a0001c0001t0001g0206a0001c0001t0001g0219others(8): Show | 11 | HG01256.hp2 HG02145.hp2 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.715-945delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59807832 | |||||
| chr17:59807832
|
CAAAAA | C | 51 | a0001c0001t0003g0105a0001c0001t0003g0107a0001c0001t0003g0108others(48): Show | 51 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.715-949_715-945del others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59807832 | |||||
| chr17:59808080
|
A | T | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-716A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59808080 | ||||||
| chr17:59808348
|
C | T | 62 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(59): Show | 62 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.715-448C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59808348 | ||||||
| chr17:59808467
|
T | C | 53 | a0001c0001t0003g0105a0001c0001t0003g0107a0001c0001t0003g0108others(50): Show | 53 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.715-329T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59808467 | ||||||
| chr17:59808475
|
C | T | 2 | a0001c0001t0001g0175a0001c0001t0002g0196 | 2 | HG02071.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.715-321C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59808475 | ||||||
| chr17:59808540
|
T | A | 104 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(101): Show | 104 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.715-256T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59808540 | ||||||
| chr17:59808764
|
T | G | 104 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(101): Show | 104 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.715-32T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59808764 | ||||||
| chr17:59808766
|
A | G | 11 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0082others(8): Show | 11 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.715-30A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59808766 | ||||||
| chr17:59808977
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.795+101G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | chr17 | 59808977 | ||||||
| chr17:59809014
|
T | C | 21 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(18): Show | 21 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.795+138T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | chr17 | 59809014 | ||||||
| chr17:59809304
|
C | CTT | 56 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(53): Show | 56 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.795+455_795+456dup others(2): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809304 | |||||
| chr17:59809304
|
C | CTTT | 27 | a0001c0001t0001g0103a0001c0001t0001g0132a0001c0001t0001g0175others(24): Show | 27 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.795+454_795+456dup others(3): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809304 | |||||
| chr17:59809304
|
CT | C | 51 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0081others(48): Show | 51 | HG00423.hp2 HG00438.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.795+456delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809304 | |||||
| chr17:59809304
|
CTT | C | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 135 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.795+455_795+456del others(2): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809304 | |||||
| chr17:59809332
|
T | C | 1 | a0002c0003t0002g0030 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.795+456T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | chr17 | 59809332 | ||||||
| chr17:59809484
|
A | AT | 45 | a0001c0001t0001g0070a0001c0001t0001g0158a0001c0001t0001g0159others(42): Show | 45 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.795+648dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | |||||
| chr17:59809484
|
A | ATT | 13 | a0001c0001t0002g0012a0001c0001t0002g0015a0001c0001t0002g0017others(10): Show | 13 | HG01123.hp1 HG01981.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.795+647_795+648dup others(2): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | |||||
| chr17:59809484
|
A | ATTTT | 6 | a0001c0001t0001g0089a0001c0001t0002g0014a0001c0001t0006g0283others(3): Show | 6 | HG00639.hp2 HG02486.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.795+645_795+648dup others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | |||||
| chr17:59809484
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0007g0274 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.795+639_795+648dup others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | |||||
| chr17:59809484
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0007g0275 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.795+638_795+648dup others(11): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | |||||
| chr17:59809484
|
A | ATTTTTTT others(6): Show |
1 | a0001c0001t0001g0076 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.795+636_795+648dup others(13): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | |||||
| chr17:59809484
|
A | ATTTTTTT others(7): Show |
2 | a0001c0001t0001g0003a0001c0001t0001g0278 | 2 | HG02258.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.795+635_795+648dup others(14): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | |||||
| chr17:59809484
|
A | ATTTTTTT others(8): Show |
2 | a0001c0001t0001g0082a0001c0001t0001g0087 | 2 | HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.795+634_795+648dup others(15): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | |||||
| chr17:59809484
|
ATTT | A | 13 | a0001c0001t0001g0277a0001c0001t0003g0107a0001c0001t0003g0113others(10): Show | 13 | HG00438.hp2 HG00642.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.795+646_795+648del others(3): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | |||||
| chr17:59809484
|
ATTTT | A | 23 | a0001c0001t0003g0105a0001c0001t0003g0110a0001c0001t0003g0114others(20): Show | 23 | HG00673.hp2 HG01261.hp1 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.795+645_795+648del others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | |||||
| chr17:59809484
|
ATTTTT | A | 18 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(15): Show | 18 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.795+644_795+648del others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | |||||
| chr17:59809484
|
ATTTTTTT others(1): Show |
A | 10 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0080others(7): Show | 10 | HG01243.hp1 HG02615.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.795+641_795+648del others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | |||||
| chr17:59809484
|
ATTTTTTT others(2): Show |
A | 6 | a0001c0001t0001g0079a0001c0001t0004g0262a0001c0001t0004g0263others(3): Show | 6 | HG01109.hp2 HG02451.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.795+640_795+648del others(9): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | |||||
| chr17:59809484
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.795+639_795+648del others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | |||||
| chr17:59809484
|
ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0001g0088a0001c0001t0001g0165 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.795+637_795+648del others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | |||||
| chr17:59809484
|
ATTTTTTT others(6): Show |
A | 3 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0002g0196 | 3 | HG01891.hp1 HG03540.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.795+636_795+648del others(13): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | |||||
| chr17:59809484
|
ATTTTTTT others(11): Show |
A | 12 | a0001c0001t0001g0103a0001c0001t0001g0186a0001c0001t0001g0200others(9): Show | 12 | HG00544.hp2 HG00621.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.795+631_795+648del others(18): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | |||||
| chr17:59809484
|
ATTTTTTT others(12): Show |
A | 74 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(71): Show | 74 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.795+630_795+648del others(19): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | |||||
| chr17:59809484
|
ATTTTTTT others(13): Show |
A | 1 | a0001c0001t0001g0203 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.795+629_795+648del others(20): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | |||||
| chr17:59809530
|
G | A | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.795+654G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | chr17 | 59809530 | ||||||
| chr17:59809554
|
G | T | 178 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.795+678G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | chr17 | 59809554 | ||||||
| chr17:59809737
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.795+861A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | chr17 | 59809737 | ||||||
| chr17:59809851
|
A | C | 1 | a0001c0001t0002g0237 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.795+975A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | chr17 | 59809851 | ||||||
| chr17:59810210
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.795+1334G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | chr17 | 59810210 | ||||||
| chr17:59810406
|
G | A | 1 | a0001c0001t0001g0250 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.796-1264G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | chr17 | 59810406 | ||||||
| chr17:59810591
|
G | A | 79 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.796-1079G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | chr17 | 59810591 | ||||||
| chr17:59811065
|
G | A | 2 | a0001c0001t0003g0140a0001c0001t0003g0145 | 2 | HG02717.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.796-605G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | chr17 | 59811065 | ||||||
| chr17:59811405
|
G | A | 1 | a0001c0001t0014g0191 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.796-265G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | chr17 | 59811405 | ||||||
| chr17:59811831
|
T | G | 78 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.912+45T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59811831 | ||||||
| chr17:59812044
|
T | G | 178 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.912+258T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59812044 | ||||||
| chr17:59812045
|
T | A | 178 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.912+259T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59812045 | ||||||
| chr17:59812322
|
G | T | 1 | a0001c0001t0003g0113 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.912+536G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59812322 | ||||||
| chr17:59812460
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0170 | 2 | HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.912+674G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59812460 | ||||||
| chr17:59812624
|
G | A | 79 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.912+838G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59812624 | ||||||
| chr17:59812888
|
G | A | 1 | a0001c0001t0002g0094 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.912+1102G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59812888 | ||||||
| chr17:59813007
|
A | G | 1 | a0001c0001t0002g0063 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.912+1221A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59813007 | ||||||
| chr17:59813133
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.912+1347C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59813133 | ||||||
| chr17:59813215
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.912+1429T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59813215 | ||||||
| chr17:59813268
|
C | T | 53 | a0001c0001t0003g0105a0001c0001t0003g0107a0001c0001t0003g0108others(50): Show | 53 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.912+1482C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59813268 | ||||||
| chr17:59813571
|
C | CA | 98 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(95): Show | 98 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.912+1800dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59813571 | |||||
| chr17:59813789
|
A | G | 1 | a0001c0001t0004g0267 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.912+2003A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59813789 | ||||||
| chr17:59813846
|
T | C | 53 | a0001c0001t0003g0105a0001c0001t0003g0107a0001c0001t0003g0108others(50): Show | 53 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.912+2060T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59813846 | ||||||
| chr17:59813943
|
T | G | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.912+2157T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59813943 | ||||||
| chr17:59813974
|
A | ATGATTGA others(1): Show |
265 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(262): Show | 265 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.912+2202_912+2209d others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59813974 | |||||
| chr17:59813974
|
A | ATGATTGA others(5): Show |
2 | a0001c0001t0001g0254a0001c0001t0003g0131 | 2 | NA18959.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.912+2198_912+2209d others(14): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59813974 | |||||
| chr17:59814215
|
G | A | 1 | a0001c0001t0003g0157 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.912+2429G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59814215 | ||||||
| chr17:59814236
|
C | T | 1 | a0001c0001t0004g0273 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.912+2450C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59814236 | ||||||
| chr17:59814267
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.912+2481G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59814267 | ||||||
| chr17:59814278
|
A | C | 1 | a0001c0001t0004g0268 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.912+2492A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59814278 | ||||||
| chr17:59815259
|
T | TTAGAAAA others(322): Show |
1 | a0001c0001t0006g0284 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.913-2438_913-2437i others(331): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59815259 | |||||
| chr17:59815259
|
T | TTAGAAAA others(323): Show |
1 | a0001c0001t0006g0283 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.913-2438_913-2437i others(332): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59815259 | |||||
| chr17:59815279
|
A | T | 79 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.913-2433A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59815279 | ||||||
| chr17:59815464
|
ATTT | A | 104 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(101): Show | 104 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.913-2245_913-2243d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59815464 | |||||
| chr17:59815468
|
T | A | 104 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(101): Show | 104 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.913-2244T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59815468 | ||||||
| chr17:59815573
|
G | A | 1 | a0001c0001t0003g0121 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.913-2139G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59815573 | ||||||
| chr17:59815689
|
TA | T | 178 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.913-2015delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59815689 | |||||
| chr17:59815788
|
G | A | 63 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(60): Show | 63 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.913-1924G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59815788 | ||||||
| chr17:59815804
|
C | G | 1 | a0001c0001t0001g0077 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.913-1908C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59815804 | ||||||
| chr17:59815850
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.913-1862C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59815850 | ||||||
| chr17:59815855
|
C | CA | 63 | a0001c0001t0001g0069a0001c0001t0001g0150a0001c0001t0001g0212others(60): Show | 63 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.913-1836dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59815855 | |||||
| chr17:59815855
|
C | CAA | 82 | a0001c0001t0001g0070a0001c0001t0001g0095a0001c0001t0001g0100others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.913-1837_913-1836d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59815855 | |||||
| chr17:59815855
|
C | CAAA | 8 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0175others(5): Show | 8 | HG00408.hp1 HG00438.hp1 HG00639.hp1 others(5): Show |
intron_variant | MODIFIER | c.913-1838_913-1836d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59815855 | |||||
| chr17:59815855
|
CAAAAAAA others(5): Show |
C | 79 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.913-1847_913-1836d others(14): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59815855 | |||||
| chr17:59815934
|
A | G | 5 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(2): Show | 5 | NA18977.hp2 NA19057.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.913-1778A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59815934 | ||||||
| chr17:59816305
|
T | G | 1 | a0001c0001t0005g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.913-1407T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59816305 | ||||||
| chr17:59816599
|
A | T | 1 | a0001c0001t0002g0036 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.913-1113A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59816599 | ||||||
| chr17:59816660
|
C | T | 1 | a0001c0001t0003g0118 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.913-1052C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59816660 | ||||||
| chr17:59816661
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.913-1051C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59816661 | ||||||
| chr17:59816815
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.913-897G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59816815 | ||||||
| chr17:59816869
|
C | G | 54 | a0001c0001t0001g0277a0001c0001t0003g0105a0001c0001t0003g0107others(51): Show | 54 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.913-843C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59816869 | ||||||
| chr17:59816902
|
C | A | 1 | a0001c0001t0004g0273 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.913-810C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59816902 | ||||||
| chr17:59816945
|
CA | C | 52 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0110others(49): Show | 52 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.913-754delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59816945 | |||||
| chr17:59816974
|
G | GA | 6 | a0001c0001t0002g0014a0001c0001t0003g0138a0001c0001t0006g0283others(3): Show | 6 | HG02109.hp2 HG03130.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.913-727dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59816974 | |||||
| chr17:59816974
|
GA | G | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.913-727delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59816974 | |||||
| chr17:59817098
|
A | G | 119 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0095others(116): Show | 119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.913-614A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59817098 | ||||||
| chr17:59817231
|
G | T | 1 | a0001c0001t0003g0120 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.913-481G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59817231 | ||||||
| chr17:59817246
|
CCTGGGCA others(1): Show |
C | 181 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.913-457_913-450del others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59817246 | |||||
| chr17:59817282
|
C | CA | 11 | a0001c0001t0001g0103a0001c0001t0001g0247a0001c0001t0001g0254others(8): Show | 11 | HG01123.hp1 HG02145.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.913-408dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59817282 | |||||
| chr17:59817282
|
CA | C | 65 | a0001c0001t0001g0150a0001c0001t0002g0020a0001c0001t0002g0037others(62): Show | 65 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.913-408delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59817282 | |||||
| chr17:59817282
|
CAA | C | 24 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(21): Show | 24 | HG00140.hp1 HG01099.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.913-409_913-408del others(2): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59817282 | |||||
| chr17:59817342
|
C | CTTTTA | 107 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(104): Show | 107 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.913-350_913-346dup others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59817342 | |||||
| chr17:59817434
|
C | T | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.913-278C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59817434 | ||||||
| chr17:59817459
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.913-253C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59817459 | ||||||
| chr17:59817524
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.913-188G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59817524 | ||||||
| chr17:59817660
|
GTTGGTTT | G | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.913-49_913-43delGG others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59817660 | |||||
| chr17:59817664
|
G | T | 15 | a0001c0001t0001g0150a0001c0001t0001g0153a0001c0001t0001g0158others(12): Show | 15 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.913-48G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59817664 | ||||||
| chr17:59818303
|
G | T | 1 | a0001c0001t0001g0221 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.974+530G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59818303 | ||||||
| chr17:59818549
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.974+776T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59818549 | ||||||
| chr17:59818580
|
C | G | 119 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0095others(116): Show | 119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.974+807C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59818580 | ||||||
| chr17:59818595
|
A | C | 62 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(59): Show | 62 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.974+822A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59818595 | ||||||
| chr17:59818661
|
G | T | 181 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.974+888G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59818661 | ||||||
| chr17:59818667
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.974+894G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59818667 | ||||||
| chr17:59818859
|
T | A | 119 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0095others(116): Show | 119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.974+1086T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59818859 | ||||||
| chr17:59818977
|
C | T | 119 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0095others(116): Show | 119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.974+1204C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59818977 | ||||||
| chr17:59819024
|
T | G | 3 | a0001c0001t0001g0208a0001c0001t0001g0211a0001c0001t0001g0226 | 3 | HG00621.hp2 HG02040.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.974+1251T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59819024 | ||||||
| chr17:59819372
|
G | A | 1 | a0001c0001t0004g0271 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.974+1599G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59819372 | ||||||
| chr17:59819464
|
TTTG | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.974+1700_974+1702d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59819464 | |||||
| chr17:59819528
|
A | G | 1 | a0001c0001t0002g0074 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.974+1755A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59819528 | ||||||
| chr17:59819546
|
C | G | 18 | a0001c0001t0001g0150a0001c0001t0001g0153a0001c0001t0001g0158others(15): Show | 18 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.974+1773C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59819546 | ||||||
| chr17:59819602
|
C | T | 2 | a0001c0001t0003g0111a0001c0001t0003g0112 | 2 | HG01071.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.974+1829C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59819602 | ||||||
| chr17:59819742
|
G | A | 7 | a0001c0001t0001g0203a0001c0001t0001g0206a0001c0001t0001g0239others(4): Show | 7 | HG02145.hp2 HG02818.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.974+1969G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59819742 | ||||||
| chr17:59820248
|
C | T | 53 | a0001c0001t0003g0105a0001c0001t0003g0107a0001c0001t0003g0108others(50): Show | 53 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.974+2475C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59820248 | ||||||
| chr17:59820624
|
T | C | 1 | a0001c0001t0002g0063 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.974+2851T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59820624 | ||||||
| chr17:59820974
|
G | GT | 17 | a0001c0001t0001g0089a0001c0001t0001g0175a0001c0001t0001g0177others(14): Show | 17 | HG00280.hp2 HG01884.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.974+3215dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59820974 | |||||
| chr17:59820974
|
G | T | 12 | a0001c0001t0002g0237a0001c0001t0004g0262a0001c0001t0004g0263others(9): Show | 12 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.974+3201G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59820974 | ||||||
| chr17:59821430
|
T | C | 1 | a0001c0001t0002g0037 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.974+3657T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59821430 | ||||||
| chr17:59821539
|
C | CT | 15 | a0001c0001t0001g0087a0001c0001t0002g0015a0001c0001t0002g0017others(12): Show | 15 | HG00741.hp1 HG01069.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.974+3789dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59821539 | |||||
| chr17:59821539
|
C | CTTTTTT | 9 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(6): Show | 9 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.974+3784_974+3789d others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59821539 | |||||
| chr17:59821539
|
CT | C | 16 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0078others(13): Show | 16 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.974+3789delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59821539 | |||||
| chr17:59821539
|
CTTTTTT | C | 103 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(100): Show | 103 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.974+3784_974+3789d others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59821539 | |||||
| chr17:59821539
|
CTTTTTTT | C | 62 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(59): Show | 62 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.974+3783_974+3789d others(9): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59821539 | |||||
| chr17:59822326
|
C | CT | 28 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(25): Show | 28 | HG00438.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.974+4571dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59822326 | |||||
| chr17:59822326
|
C | CTT | 76 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(73): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.974+4570_974+4571d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59822326 | |||||
| chr17:59822326
|
C | CTTT | 7 | a0001c0001t0001g0103a0001c0001t0001g0177a0001c0001t0001g0178others(4): Show | 7 | HG01074.hp2 HG01361.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.974+4569_974+4571d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59822326 | |||||
| chr17:59822415
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.974+4642G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59822415 | ||||||
| chr17:59822784
|
A | T | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | HG02602.hp1 HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.974+5011A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59822784 | ||||||
| chr17:59822965
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.974+5192A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59822965 | ||||||
| chr17:59823300
|
A | C | 1 | a0001c0001t0001g0201 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.974+5527A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59823300 | ||||||
| chr17:59823447
|
CA | C | 112 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0095others(109): Show | 112 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.974+5691delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59823447 | |||||
| chr17:59823524
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.974+5751C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59823524 | ||||||
| chr17:59823562
|
A | C | 1 | a0001c0001t0003g0117 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.974+5789A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59823562 | ||||||
| chr17:59823608
|
C | T | 10 | a0001c0001t0002g0014a0001c0001t0002g0031a0001c0001t0002g0040others(7): Show | 10 | NA18949.hp1 NA18963.hp1 NA18964.hp2 others(7): Show |
intron_variant | MODIFIER | c.974+5835C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59823608 | ||||||
| chr17:59823609
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.974+5836G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59823609 | ||||||
| chr17:59823682
|
C | T | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.974+5909C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59823682 | ||||||
| chr17:59823754
|
A | C | 1 | a0001c0001t0001g0103 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.974+5981A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59823754 | ||||||
| chr17:59823990
|
G | A | 1 | a0001c0001t0001g0250 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.974+6217G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59823990 | ||||||
| chr17:59824131
|
G | A | 1 | a0001c0001t0001g0250 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.974+6358G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824131 | ||||||
| chr17:59824251
|
C | CA | 15 | a0001c0001t0001g0088a0001c0001t0001g0150a0001c0001t0002g0049others(12): Show | 15 | HG00544.hp1 HG00741.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.974+6492dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59824251 | |||||
| chr17:59824251
|
CA | C | 55 | a0001c0001t0001g0095a0001c0001t0001g0216a0001c0001t0001g0277others(52): Show | 55 | HG00642.hp1 HG00673.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.974+6492delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59824251 | |||||
| chr17:59824253
|
A | G | 5 | a0001c0001t0001g0153a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 5 | HG00140.hp1 HG01109.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.974+6480A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824253 | ||||||
| chr17:59824264
|
A | G | 2 | a0001c0001t0006g0285a0001c0001t0006g0286 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.974+6491A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824264 | ||||||
| chr17:59824265
|
A | G | 3 | a0001c0001t0006g0284a0001c0001t0006g0285a0001c0001t0006g0286 | 3 | HG02109.hp2 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.974+6492A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824265 | ||||||
| chr17:59824291
|
G | A | 89 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(86): Show | 89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.974+6518G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824291 | ||||||
| chr17:59824398
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.974+6625C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824398 | ||||||
| chr17:59824466
|
G | A | 1 | a0001c0001t0005g0002 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.974+6693G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824466 | ||||||
| chr17:59824571
|
T | TA | 26 | a0001c0001t0001g0089a0001c0001t0001g0153a0001c0001t0001g0158others(23): Show | 26 | HG00140.hp1 HG00423.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.974+6816dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59824571 | |||||
| chr17:59824581
|
A | C | 1 | a0001c0001t0001g0087 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.974+6808A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824581 | ||||||
| chr17:59824621
|
C | A | 1 | a0001c0001t0001g0224 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.974+6848C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824621 | ||||||
| chr17:59824851
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7078T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824851 | ||||||
| chr17:59824852
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7079G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824852 | ||||||
| chr17:59824854
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7081C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824854 | ||||||
| chr17:59824858
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7085G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824858 | ||||||
| chr17:59824862
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7089G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824862 | ||||||
| chr17:59824867
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7094C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824867 | ||||||
| chr17:59824872
|
C | CA | 122 | a0001c0001t0001g0003a0001c0001t0001g0069a0001c0001t0001g0070others(119): Show | 122 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.974+7121dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59824872 | |||||
| chr17:59824872
|
C | CAA | 34 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0278others(31): Show | 34 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.974+7120_974+7121d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59824872 | |||||
| chr17:59824901
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.974+7128A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824901 | ||||||
| chr17:59824904
|
C | A | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7131C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824904 | ||||||
| chr17:59824907
|
G | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7134G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824907 | ||||||
| chr17:59824908
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7135G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824908 | ||||||
| chr17:59824909
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7136T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824909 | ||||||
| chr17:59824910
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7137G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824910 | ||||||
| chr17:59824911
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7138G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824911 | ||||||
| chr17:59824914
|
C | A | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7141C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824914 | ||||||
| chr17:59824921
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7148G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824921 | ||||||
| chr17:59824926
|
C | G | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7153C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824926 | ||||||
| chr17:59824937
|
G | T | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7164G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824937 | ||||||
| chr17:59824938
|
G | T | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7165G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824938 | ||||||
| chr17:59824942
|
G | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7169G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824942 | ||||||
| chr17:59824943
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7170C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824943 | ||||||
| chr17:59824944
|
C | A | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7171C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824944 | ||||||
| chr17:59824947
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7174G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824947 | ||||||
| chr17:59824950
|
A | T | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7177A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824950 | ||||||
| chr17:59824951
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7178G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824951 | ||||||
| chr17:59824952
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7179A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824952 | ||||||
| chr17:59824954
|
G | T | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7181G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824954 | ||||||
| chr17:59824955
|
G | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7182G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824955 | ||||||
| chr17:59824956
|
A | T | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7183A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824956 | ||||||
| chr17:59824963
|
G | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7190G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824963 | ||||||
| chr17:59824964
|
A | T | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7191A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824964 | ||||||
| chr17:59824969
|
T | A | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7196T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824969 | ||||||
| chr17:59824971
|
A | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7198A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824971 | ||||||
| chr17:59824972
|
G | T | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7199G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824972 | ||||||
| chr17:59824975
|
A | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7202A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824975 | ||||||
| chr17:59824980
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7207A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824980 | ||||||
| chr17:59824984
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7211C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824984 | ||||||
| chr17:59824985
|
A | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7212A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824985 | ||||||
| chr17:59824989
|
T | A | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7216T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824989 | ||||||
| chr17:59824990
|
G | T | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7217G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824990 | ||||||
| chr17:59825000
|
A | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7227A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825000 | ||||||
| chr17:59825001
|
T | A | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7228T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825001 | ||||||
| chr17:59825005
|
G | T | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7232G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825005 | ||||||
| chr17:59825006
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7233A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825006 | ||||||
| chr17:59825010
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7237C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825010 | ||||||
| chr17:59825015
|
G | T | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7242G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825015 | ||||||
| chr17:59825018
|
A | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7245A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825018 | ||||||
| chr17:59825019
|
G | T | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7246G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825019 | ||||||
| chr17:59825021
|
T | A | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7248T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825021 | ||||||
| chr17:59825025
|
A | T | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7252A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825025 | ||||||
| chr17:59825026
|
G | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7253G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825026 | ||||||
| chr17:59825033
|
A | T | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7260A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825033 | ||||||
| chr17:59825034
|
G | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7261G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825034 | ||||||
| chr17:59825035
|
A | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7262A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825035 | ||||||
| chr17:59825037
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7264C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825037 | ||||||
| chr17:59825038
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7265T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825038 | ||||||
| chr17:59825039
|
A | T | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7266A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825039 | ||||||
| chr17:59825046
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7273T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825046 | ||||||
| chr17:59825049
|
T | G | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7276T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825049 | ||||||
| chr17:59825050
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7277A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825050 | ||||||
| chr17:59825051
|
G | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7278G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825051 | ||||||
| chr17:59825055
|
A | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7282A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825055 | ||||||
| chr17:59825056
|
A | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7283A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825056 | ||||||
| chr17:59825061
|
C | G | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7288C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825061 | ||||||
| chr17:59825066
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7293T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825066 | ||||||
| chr17:59825069
|
T | G | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7296T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825069 | ||||||
| chr17:59825072
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7299T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825072 | ||||||
| chr17:59825073
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7300T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825073 | ||||||
| chr17:59825074
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7301G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825074 | ||||||
| chr17:59825075
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7302T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825075 | ||||||
| chr17:59825076
|
G | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7303G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825076 | ||||||
| chr17:59825077
|
A | AT | 50 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0084others(47): Show | 50 | HG00438.hp2 HG00621.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.974+7331dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59825077 | |||||
| chr17:59825077
|
AT | A | 33 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(30): Show | 33 | HG00140.hp1 HG01099.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.974+7331delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59825077 | |||||
| chr17:59825077
|
ATT | A | 24 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0158others(21): Show | 24 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.974+7330_974+7331d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59825077 | |||||
| chr17:59825077
|
ATTT | A | 69 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0095others(66): Show | 69 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.974+7329_974+7331d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59825077 | |||||
| chr17:59825077
|
ATTTT | A | 8 | a0001c0001t0001g0192a0001c0001t0001g0205a0001c0001t0001g0214others(5): Show | 8 | HG01109.hp2 HG01884.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.974+7328_974+7331d others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59825077 | |||||
| chr17:59825079
|
T | G | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7306T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825079 | ||||||
| chr17:59825080
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7307T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825080 | ||||||
| chr17:59825081
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7308T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825081 | ||||||
| chr17:59825110
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7337A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825110 | ||||||
| chr17:59825115
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7342T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825115 | ||||||
| chr17:59825119
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7346T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825119 | ||||||
| chr17:59825123
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7350A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825123 | ||||||
| chr17:59825125
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7352T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825125 | ||||||
| chr17:59825126
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7353G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825126 | ||||||
| chr17:59825139
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7366C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825139 | ||||||
| chr17:59825142
|
T | A | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7369T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825142 | ||||||
| chr17:59825147
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7374T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825147 | ||||||
| chr17:59825157
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7384A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825157 | ||||||
| chr17:59825159
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7386C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825159 | ||||||
| chr17:59825164
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7391G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825164 | ||||||
| chr17:59825181
|
T | G | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7408T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825181 | ||||||
| chr17:59825219
|
A | T | 2 | a0001c0001t0003g0108a0001c0001t0003g0133 | 2 | HG02071.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.974+7446A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825219 | ||||||
| chr17:59825680
|
G | C | 53 | a0001c0001t0003g0105a0001c0001t0003g0107a0001c0001t0003g0108others(50): Show | 53 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.974+7907G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825680 | ||||||
| chr17:59825986
|
T | A | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+8213T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825986 | ||||||
| chr17:59826196
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.974+8423A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59826196 | ||||||
| chr17:59826595
|
G | A | 2 | a0001c0001t0003g0113a0001c0001t0009g0109 | 2 | HG00642.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.974+8822G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59826595 | ||||||
| chr17:59826941
|
A | C | 4 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(1): Show | 4 | HG01243.hp1 HG02451.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.974+9168A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59826941 | ||||||
| chr17:59827383
|
C | G | 18 | a0001c0001t0001g0150a0001c0001t0001g0153a0001c0001t0001g0158others(15): Show | 18 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.974+9610C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59827383 | ||||||
| chr17:59827415
|
C | T | 1 | a0001c0001t0004g0267 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.974+9642C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59827415 | ||||||
| chr17:59827462
|
A | G | 181 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.974+9689A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59827462 | ||||||
| chr17:59827519
|
A | G | 1 | a0001c0001t0002g0196 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.974+9746A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59827519 | ||||||
| chr17:59827831
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.974+10058G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59827831 | ||||||
| chr17:59827873
|
G | T | 21 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(18): Show | 21 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.974+10100G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59827873 | ||||||
| chr17:59828024
|
TA | T | 7 | a0001c0001t0001g0095a0001c0001t0001g0160a0001c0001t0002g0020others(4): Show | 7 | HG01168.hp1 HG01975.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.975-10255delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59828024 | |||||
| chr17:59828040
|
A | G | 1 | a0001c0001t0006g0286 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.975-10255A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59828040 | ||||||
| chr17:59828403
|
A | C | 1 | a0001c0001t0002g0093 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.975-9892A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59828403 | ||||||
| chr17:59828927
|
C | G | 107 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(104): Show | 107 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.975-9368C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59828927 | ||||||
| chr17:59828957
|
A | C | 89 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(86): Show | 89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.975-9338A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59828957 | ||||||
| chr17:59828962
|
A | G | 1 | a0001c0001t0002g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.975-9333A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59828962 | ||||||
| chr17:59828967
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.975-9328C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59828967 | ||||||
| chr17:59829215
|
TC | T | 89 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(86): Show | 89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.975-9078delC | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59829215 | |||||
| chr17:59829378
|
C | T | 1 | a0001c0001t0002g0066 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.975-8917C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59829378 | ||||||
| chr17:59829383
|
A | T | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.975-8912A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59829383 | ||||||
| chr17:59829502
|
C | G | 1 | a0001c0001t0001g0249 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.975-8793C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59829502 | ||||||
| chr17:59829577
|
G | A | 3 | a0001c0001t0001g0280a0001c0001t0008g0279a0001c0001t0008g0281 | 3 | HG02145.hp2 HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.975-8718G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59829577 | ||||||
| chr17:59830064
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.975-8231A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59830064 | ||||||
| chr17:59830407
|
T | A | 181 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.975-7888T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59830407 | ||||||
| chr17:59830428
|
T | G | 1 | a0001c0001t0001g0248 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.975-7867T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59830428 | ||||||
| chr17:59830465
|
A | C | 1 | a0001c0001t0002g0029 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.975-7830A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59830465 | ||||||
| chr17:59830589
|
A | G | 62 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(59): Show | 62 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.975-7706A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59830589 | ||||||
| chr17:59830598
|
T | G | 1 | a0001c0001t0001g0088 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.975-7697T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59830598 | ||||||
| chr17:59830735
|
T | C | 62 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(59): Show | 62 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.975-7560T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59830735 | ||||||
| chr17:59831049
|
C | T | 2 | a0001c0001t0003g0136a0001c0001t0003g0147 | 2 | HG00438.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.975-7246C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59831049 | ||||||
| chr17:59831094
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.975-7201C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59831094 | ||||||
| chr17:59831576
|
C | T | 2 | a0001c0001t0006g0285a0001c0001t0006g0286 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.975-6719C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59831576 | ||||||
| chr17:59831612
|
A | AT | 39 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(36): Show | 39 | HG01243.hp1 HG01361.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.975-6663dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59831612 | |||||
| chr17:59831612
|
A | ATT | 8 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0091others(5): Show | 8 | HG01109.hp2 HG01891.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.975-6664_975-6663d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59831612 | |||||
| chr17:59831612
|
A | ATTT | 14 | a0001c0001t0001g0150a0001c0001t0001g0153a0001c0001t0001g0158others(11): Show | 14 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.975-6665_975-6663d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59831612 | |||||
| chr17:59831612
|
AT | A | 63 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(60): Show | 63 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.975-6663delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59831612 | |||||
| chr17:59831772
|
A | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.975-6523A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59831772 | ||||||
| chr17:59831801
|
G | GT | 266 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(263): Show | 266 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.975-6484dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59831801 | |||||
| chr17:59831801
|
G | GTT | 18 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0159others(15): Show | 18 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.975-6485_975-6484d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59831801 | |||||
| chr17:59832012
|
A | G | 89 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(86): Show | 89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.975-6283A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59832012 | ||||||
| chr17:59832068
|
A | T | 89 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(86): Show | 89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.975-6227A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59832068 | ||||||
| chr17:59832121
|
A | G | 1 | a0001c0001t0003g0121 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.975-6174A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59832121 | ||||||
| chr17:59832182
|
C | CT | 80 | a0001c0001t0001g0069a0001c0001t0001g0104a0001c0001t0001g0153others(77): Show | 80 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.975-6089dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59832182 | |||||
| chr17:59832182
|
C | CTT | 12 | a0001c0001t0001g0070a0001c0001t0001g0150a0001c0001t0001g0161others(9): Show | 12 | HG00673.hp2 HG01255.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.975-6090_975-6089d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59832182 | |||||
| chr17:59832182
|
C | CTTT | 20 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(17): Show | 20 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.975-6091_975-6089d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59832182 | |||||
| chr17:59832182
|
CT | C | 14 | a0001c0001t0001g0203a0001c0001t0001g0206a0001c0001t0001g0212others(11): Show | 14 | HG02004.hp2 HG02145.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.975-6089delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59832182 | |||||
| chr17:59832182
|
CTTT | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.975-6091_975-6089d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59832182 | |||||
| chr17:59832348
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.975-5947A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59832348 | ||||||
| chr17:59832573
|
A | ATTTGT | 6 | a0001c0001t0001g0084a0001c0001t0001g0090a0001c0001t0003g0108others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.975-5687_975-5683d others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59832573 | |||||
| chr17:59832573
|
A | ATTTGTTT others(3): Show |
46 | a0001c0001t0002g0050a0001c0001t0003g0110a0001c0001t0003g0111others(43): Show | 46 | HG00642.hp1 HG00673.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.975-5692_975-5683d others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59832573 | |||||
| chr17:59832573
|
A | ATTTGTTT others(8): Show |
4 | a0001c0001t0001g0277a0001c0001t0003g0105a0001c0001t0003g0107others(1): Show | 4 | HG01261.hp1 HG02647.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.975-5697_975-5683d others(17): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59832573 | |||||
| chr17:59832573
|
ATTTGT | A | 119 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(116): Show | 119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.975-5687_975-5683d others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59832573 | |||||
| chr17:59832633
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.975-5662G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59832633 | ||||||
| chr17:59832761
|
A | AT | 106 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0081others(103): Show | 106 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.975-5513dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59832761 | |||||
| chr17:59832761
|
A | ATT | 60 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(57): Show | 60 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.975-5514_975-5513d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59832761 | |||||
| chr17:59832761
|
A | T | 1 | a0001c0001t0003g0115 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.975-5534A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59832761 | ||||||
| chr17:59832763
|
T | A | 1 | a0001c0001t0001g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.975-5532T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59832763 | ||||||
| chr17:59832902
|
T | C | 119 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0095others(116): Show | 119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.975-5393T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59832902 | ||||||
| chr17:59833858
|
C | T | 3 | a0001c0001t0003g0131a0001c0001t0003g0134a0001c0001t0003g0146 | 3 | HG02895.hp1 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.975-4437C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59833858 | ||||||
| chr17:59833869
|
A | G | 89 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100others(86): Show | 89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.975-4426A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59833869 | ||||||
| chr17:59834403
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.975-3892T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59834403 | ||||||
| chr17:59834483
|
G | A | 3 | a0001c0001t0001g0224a0001c0001t0006g0283a0001c0001t0006g0284 | 3 | HG00280.hp1 HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.975-3812G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59834483 | ||||||
| chr17:59834626
|
A | AT | 104 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0090others(101): Show | 104 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.975-3653dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59834626 | |||||
| chr17:59834626
|
A | ATT | 14 | a0001c0001t0001g0132a0001c0001t0001g0189a0001c0001t0001g0212others(11): Show | 14 | HG01109.hp2 HG02004.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.975-3654_975-3653d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59834626 | |||||
| chr17:59834978
|
T | C | 1 | a0001c0001t0001g0233 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.975-3317T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59834978 | ||||||
| chr17:59835030
|
G | A | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.975-3265G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59835030 | ||||||
| chr17:59835080
|
G | A | 1 | a0001c0001t0002g0014 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.975-3215G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59835080 | ||||||
| chr17:59835135
|
G | GT | 29 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0031others(26): Show | 29 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.975-3149dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59835135 | |||||
| chr17:59835168
|
G | A | 1 | a0001c0001t0005g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.975-3127G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59835168 | ||||||
| chr17:59835232
|
G | A | 7 | a0001c0001t0001g0203a0001c0001t0001g0206a0001c0001t0001g0239others(4): Show | 7 | HG02145.hp2 HG02818.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.975-3063G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59835232 | ||||||
| chr17:59835474
|
T | C | 1 | a0001c0001t0003g0111 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.975-2821T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59835474 | ||||||
| chr17:59835493
|
G | GT | 18 | a0001c0001t0001g0132a0001c0001t0001g0193a0001c0001t0001g0240others(15): Show | 18 | HG00673.hp2 HG01109.hp2 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.975-2788dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59835493 | |||||
| chr17:59835493
|
G | T | 7 | a0001c0001t0001g0203a0001c0001t0001g0206a0001c0001t0001g0239others(4): Show | 7 | HG02145.hp2 HG02818.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.975-2802G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59835493 | ||||||
| chr17:59835560
|
G | A | 1 | a0001c0001t0003g0145 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.975-2735G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59835560 | ||||||
| chr17:59835742
|
G | A | 1 | a0001c0001t0004g0270 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.975-2553G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59835742 | ||||||
| chr17:59835928
|
T | G | 18 | a0001c0001t0001g0150a0001c0001t0001g0153a0001c0001t0001g0158others(15): Show | 18 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.975-2367T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59835928 | ||||||
| chr17:59836012
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.975-2283T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59836012 | ||||||
| chr17:59836196
|
G | T | 3 | a0001c0001t0001g0165a0001c0001t0001g0171a0001c0001t0001g0172 | 3 | HG01891.hp1 HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.975-2099G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59836196 | ||||||
| chr17:59836245
|
T | A | 9 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(6): Show | 9 | HG01109.hp2 HG02896.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.975-2050T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59836245 | ||||||
| chr17:59836268
|
C | T | 1 | a0001c0001t0003g0148 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.975-2027C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59836268 | ||||||
| chr17:59836288
|
G | T | 1 | a0001c0001t0001g0203 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.975-2007G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59836288 | ||||||
| chr17:59836290
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.975-2005C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59836290 | ||||||
| chr17:59836488
|
A | G | 178 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.975-1807A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59836488 | ||||||
| chr17:59836592
|
T | C | 2 | a0001c0001t0003g0105a0001c0001t0003g0148 | 2 | HG02257.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.975-1703T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59836592 | ||||||
| chr17:59836646
|
C | T | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.975-1649C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59836646 | ||||||
| chr17:59836719
|
G | GT | 126 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(123): Show | 126 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.975-1562dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59836719 | |||||
| chr17:59836719
|
GT | G | 10 | a0001c0001t0003g0146a0001c0001t0004g0265a0001c0001t0004g0266others(7): Show | 10 | HG02615.hp1 HG02895.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.975-1562delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59836719 | |||||
| chr17:59836960
|
G | T | 18 | a0001c0001t0001g0150a0001c0001t0001g0153a0001c0001t0001g0158others(15): Show | 18 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.975-1335G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59836960 | ||||||
| chr17:59837020
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG01358.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.975-1275T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59837020 | ||||||
| chr17:59837195
|
T | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.975-1100T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59837195 | ||||||
| chr17:59837233
|
G | T | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0265others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.975-1062G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59837233 | ||||||
| chr17:59837366
|
G | T | 1 | a0001c0001t0001g0213 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.975-929G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59837366 | ||||||
| chr17:59837402
|
C | T | 1 | a0001c0001t0003g0148 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.975-893C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59837402 | ||||||
| chr17:59837522
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.975-773G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59837522 | ||||||
| chr17:59837908
|
G | T | 1 | a0001c0001t0001g0212 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.975-387G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59837908 | ||||||
| chr17:59838063
|
T | G | 5 | a0001c0001t0001g0153a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 5 | HG00140.hp1 HG01109.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.975-232T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59838063 | ||||||
| chr17:59838100
|
C | CT | 31 | a0001c0001t0001g0150a0001c0001t0001g0158a0001c0001t0001g0159others(28): Show | 31 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.975-174dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59838100 | |||||
| chr17:59838100
|
CT | C | 34 | a0001c0001t0001g0190a0001c0001t0001g0205a0001c0001t0001g0225others(31): Show | 34 | HG00639.hp2 HG00642.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.975-174delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59838100 | |||||
| chr17:59838100
|
CTT | C | 21 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(18): Show | 21 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.975-175_975-174del others(2): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59838100 | |||||
| chr17:59838104
|
T | C | 1 | a0001c0001t0003g0137 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.975-191T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59838104 | ||||||
| chr17:59838105
|
T | C | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.975-190T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59838105 | ||||||
| chr17:59838461
|
C | A | 1 | a0001c0001t0002g0067 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1077+64C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 11/11 | chr17 | 59838461 | ||||||
| chr17:59838652
|
G | T | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1077+255G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 11/11 | chr17 | 59838652 | ||||||
| chr17:59838804
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0232 | 2 | HG01074.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1077+407G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 11/11 | chr17 | 59838804 | ||||||
| chr17:59838871
|
T | C | 2 | a0001c0001t0007g0274a0001c0001t0007g0275 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1077+474T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 11/11 | chr17 | 59838871 | ||||||
| chr17:59839182
|
C | T | 1 | a0001c0001t0002g0023 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1078-586C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 11/11 | chr17 | 59839182 |