Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 79679 |
|---|---|
| ensemblid | ENSG00000134258.18 |
| hgncid | 28873 |
| symbol | VTCN1 |
| name | V-set domain containing T cell activation inhibitor 1 |
| refseq_nuc | NM_024626.4 |
| refseq_prot | NP_078902.2 |
| ensembl_nuc | ENST00000369458.8 |
| ensembl_prot | ENSP00000358470.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 117143587 |
| end | 117210927 |
| strand | - |
| ver | v1.2 |
| region | chr1:117143587-117210927 |
| region5000 | chr1:117138587-117215927 |
| regionname0 | VTCN1_chr1_117143587_117210927 |
| regionname5000 | VTCN1_chr1_117138587_117215927 |
| 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 | 282 | 242 | 89 | 43 | 60 | 12 | 36 | 40 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| a0002 | 0/0 | 282 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| 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 | 849 | 242 | 89 | 43 | 60 | 12 | 36 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| c0002 | 0/0 | 849 | 6 | 5 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1757 | 106 | 22 | 25 | 30 | 7 | 22 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| t0002 | 1/0 | 1757 | 42 | 11 | 7 | 16 | 2 | 5 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| t0003 | 0/0 | 1757 | 36 | 33 | 2 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| t0004 | 0/1 | 1757 | 20 | 0 | 8 | 2 | 2 | 7 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| t0005 | 0/0 | 1755 | 12 | 12 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| t0006 | 0/0 | 1757 | 11 | 0 | 0 | 9 | 1 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| t0007 | 0/0 | 1757 | 7 | 7 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| t0008 | 0/0 | 1757 | 3 | 3 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| t0009 | 0/0 | 1757 | 3 | 0 | 0 | 3 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| t0010 | 0/0 | 1755 | 2 | 2 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| t0011 | 0/0 | 1757 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| t0012 | 0/0 | 1757 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| t0013 | 0/0 | 1757 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| t0014 | 0/0 | 1757 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| t0015 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| t0016 | 0/0 | 1757 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| 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 | 2 | 0 | 1 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0028 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| 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 | 849 | 242 | 89 | 43 | 60 | 12 | 36 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| a0002c0002 | 0/0 | 849 | 6 | 5 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2605 | 105 | 21 | 25 | 30 | 7 | 22 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| a0001c0001t0002 | 1/0 | 2605 | 40 | 9 | 7 | 16 | 2 | 5 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| a0001c0001t0003 | 0/0 | 2605 | 33 | 31 | 1 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| a0001c0001t0004 | 0/1 | 2605 | 20 | 0 | 8 | 2 | 2 | 7 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| a0001c0001t0005 | 0/0 | 2603 | 12 | 12 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| a0001c0001t0006 | 0/0 | 2605 | 11 | 0 | 0 | 9 | 1 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| a0001c0001t0007 | 0/0 | 2605 | 7 | 7 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| a0001c0001t0008 | 0/0 | 2605 | 3 | 3 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| a0001c0001t0009 | 0/0 | 2605 | 3 | 0 | 0 | 3 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| a0001c0001t0010 | 0/0 | 2603 | 2 | 2 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| a0001c0001t0011 | 0/0 | 2605 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| a0001c0001t0012 | 0/0 | 2605 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| a0001c0001t0013 | 0/0 | 2605 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| a0001c0001t0014 | 0/0 | 2605 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| a0001c0001t0015 | 0/0 | 2603 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| a0001c0001t0016 | 0/0 | 2605 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| a0002c0002t0001 | 0/0 | 2605 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| a0002c0002t0002 | 0/0 | 2605 | 2 | 2 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| a0002c0002t0003 | 0/0 | 2605 | 3 | 2 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | copy fasta | chr1 | 117138587 | 117215927 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0028 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0005g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0005g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0005g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0006g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0006g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0006g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0006g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0006g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0006g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0006g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0006g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0006g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0007g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0007g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0007g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0008g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0008g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0008g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0009g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0009g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0009g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0010g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0010g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0011g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0012g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0013g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0014g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0015g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0016g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0002c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0002c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0002c0002t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0002c0002t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0002c0002t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0098 | EUR | GBR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0108 | EUR | GBR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0058 | EUR | FIN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | FIN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | FIN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | CHS | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0035 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0134 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0147 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0154 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01361 | hp1 | a0001 | c0001 | t0014 | g0149 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0148 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01433 | hp1 | a0002 | c0002 | t0003 | g0214 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0074 | EUR | IBS | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01515 | hp2 | a0001 | c0001 | t0006 | g0235 | EUR | IBS | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0064 | EUR | IBS | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0075 | EUR | IBS | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01884 | hp2 | a0002 | c0002 | t0003 | g0173 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01891 | hp1 | a0001 | c0001 | t0013 | g0025 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0045 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0046 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02004 | hp2 | a0001 | c0001 | t0016 | g0240 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0126 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02056 | hp1 | a0001 | c0001 | t0006 | g0238 | EAS | KHV | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0119 | EAS | KHV | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | KHV | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0228 | EAS | KHV | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02145 | hp1 | a0001 | c0001 | t0012 | g0048 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CDX | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CDX | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02258 | hp1 | a0001 | c0001 | t0011 | g0015 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0203 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | KHV | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0187 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0047 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0207 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0182 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0118 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0190 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0142 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0127 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0189 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02895 | hp1 | a0001 | c0001 | t0010 | g0211 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02895 | hp2 | a0001 | c0001 | t0015 | g0239 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0197 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0137 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0212 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0184 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0192 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0196 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0007 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0103 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0013 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03195 | hp1 | a0001 | c0001 | t0008 | g0193 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0186 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0135 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0129 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0204 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0199 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0136 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0056 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0175 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0132 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0143 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0183 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0209 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0101 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0116 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0033 | SAS | BEB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | STU | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | STU | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG04204 | hp1 | a0001 | c0001 | t0006 | g0233 | SAS | STU | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | STU | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0117 | SAS | STU | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | STU | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0188 | AFR | YRI | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | YRI | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | CHB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | YRI | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0185 | AFR | YRI | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18945 | hp2 | a0001 | c0001 | t0006 | g0236 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18950 | hp1 | a0001 | c0001 | t0009 | g0225 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18950 | hp2 | a0001 | c0001 | t0009 | g0227 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18982 | hp2 | a0001 | c0001 | t0006 | g0237 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19000 | hp1 | a0001 | c0001 | t0006 | g0231 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19011 | hp1 | a0001 | c0001 | t0006 | g0229 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0195 | AFR | LWK | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | LWK | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19043 | hp1 | a0002 | c0002 | t0003 | g0172 | AFR | LWK | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19063 | hp1 | a0001 | c0001 | t0006 | g0230 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19063 | hp2 | a0001 | c0001 | t0009 | g0232 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19090 | hp2 | a0001 | c0001 | t0006 | g0234 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | YRI | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0007 | AFR | YRI | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0130 | EUR | TSI | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | TSI | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | GIH | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0036 | SAS | GIH | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0174 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0151 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0194 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0152 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | USA | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0221 | AFR | USA | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18955 | hp1 | a0001 | c0001 | t0006 | g0226 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | USA | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | USA | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | LWK | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0128 | REF | REF | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0028 | REF | REF | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:117170136
|
A | G | 1 | a0002 | 6 | HG01433.hp1 HG01884.hp2 HG03225.hp2 others(3): Show |
missense_variant | MODERATE | c.68T>C | p.Ile23Thr | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/6 | 140/2605 | 68/849 | 23/282 | chr1 | 117170136 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:117143870
|
C | A | 15 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(12): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*1401G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 6/6 | 3788 | chr1 | 117143870 | |||||
| chr1:117144205
|
C | T | 15 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(12): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*1066G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 6/6 | 3453 | chr1 | 117144205 | |||||
| chr1:117144216
|
T | C | 1 | a0001c0001t0008 | 3 | HG02055.hp1 HG02486.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1055A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 6/6 | 3442 | chr1 | 117144216 | |||||
| chr1:117144292
|
C | T | 15 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(12): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*979G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 6/6 | 3366 | chr1 | 117144292 | |||||
| chr1:117144415
|
T | C | 2 | a0001c0001t0007a0001c0001t0013 | 8 | HG01891.hp1 HG02451.hp2 HG02723.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*856A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 6/6 | 3243 | chr1 | 117144415 | |||||
| chr1:117144503
|
A | T | 15 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(12): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*768T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 6/6 | 3155 | chr1 | 117144503 | |||||
| chr1:117144535
|
C | T | 1 | a0001c0001t0012 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*736G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 6/6 | 3123 | chr1 | 117144535 | |||||
| chr1:117144928
|
C | T | 1 | a0001c0001t0011 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*343G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 6/6 | 2730 | chr1 | 117144928 | |||||
| chr1:117144958
|
G | C | 1 | a0001c0001t0014 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*313C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 6/6 | 2700 | chr1 | 117144958 | |||||
| chr1:117145130
|
CTT | C | 3 | a0001c0001t0005a0001c0001t0010a0001c0001t0015 | 15 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*139_*140delAA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 6/6 | 2526 | chr1 | 117145130 | |||||
| chr1:117147630
|
T | C | 1 | a0001c0001t0013 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*28A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/6 | 28 | chr1 | 117147630 | |||||
| chr1:117147650
|
G | A | 7 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(4): Show | 141 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*8C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/6 | 8 | chr1 | 117147650 | |||||
| chr1:117210906
|
G | A | 2 | a0001c0001t0006a0001c0001t0009 | 14 | HG01515.hp2 HG02056.hp1 HG02129.hp2 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-51C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/6 | 51 | chr1 | 117210906 | |||||
| chr1:117210911
|
C | A | 1 | a0001c0001t0015 | 1 | HG02895.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-56G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/6 | chr1 | 117210911 | ||||||
| chr1:117210921
|
G | A | 1 | a0001c0001t0016 | 1 | HG02004.hp2 | 5_prime_UTR_variant | MODIFIER | c.-66C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/6 | 66 | chr1 | 117210921 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:117145328
|
T | C | 1 | a0001c0001t0013g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.*46-103A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117145328 | ||||||
| chr1:117145431
|
C | G | 8 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0101others(5): Show | 8 | HG00741.hp1 HG01255.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.*46-206G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117145431 | ||||||
| chr1:117145437
|
A | T | 1 | a0001c0001t0002g0170 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.*46-212T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117145437 | ||||||
| chr1:117145530
|
G | A | 18 | a0001c0001t0003g0010a0001c0001t0003g0018a0001c0001t0003g0038others(15): Show | 18 | HG01099.hp1 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.*46-305C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117145530 | ||||||
| chr1:117145778
|
T | C | 32 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0037others(29): Show | 36 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(33): Show |
intron_variant | MODIFIER | c.*46-553A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117145778 | ||||||
| chr1:117145981
|
A | G | 1 | a0001c0001t0007g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.*46-756T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117145981 | ||||||
| chr1:117146231
|
T | TC | 14 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0037others(11): Show | 15 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.*46-1007dupG | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117146231 | ||||||
| chr1:117146233
|
A | C | 81 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(78): Show | 87 | HG00408.hp1 HG01099.hp1 HG01106.hp2 others(84): Show |
intron_variant | MODIFIER | c.*46-1008T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117146233 | ||||||
| chr1:117146307
|
G | A | 12 | a0001c0001t0003g0186a0001c0001t0003g0188a0001c0001t0003g0196others(9): Show | 12 | HG02055.hp1 HG02486.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.*46-1082C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117146307 | ||||||
| chr1:117146308
|
A | C | 12 | a0001c0001t0003g0186a0001c0001t0003g0188a0001c0001t0003g0196others(9): Show | 12 | HG02055.hp1 HG02486.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.*46-1083T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117146308 | ||||||
| chr1:117146315
|
C | T | 1 | a0001c0001t0004g0181 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.*46-1090G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117146315 | ||||||
| chr1:117146344
|
T | G | 14 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0037others(11): Show | 15 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.*46-1119A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117146344 | ||||||
| chr1:117146664
|
G | C | 1 | a0001c0001t0001g0084 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.*45+949C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117146664 | ||||||
| chr1:117146813
|
C | A | 1 | a0001c0001t0005g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.*45+800G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117146813 | ||||||
| chr1:117146853
|
A | G | 1 | a0001c0001t0005g0007 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.*45+760T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117146853 | ||||||
| chr1:117146869
|
A | G | 24 | a0001c0001t0003g0010a0001c0001t0003g0018a0001c0001t0003g0038others(21): Show | 24 | HG01099.hp1 HG02109.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.*45+744T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117146869 | ||||||
| chr1:117146886
|
C | T | 1 | a0001c0001t0004g0003 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.*45+727G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117146886 | ||||||
| chr1:117146954
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.*45+659C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117146954 | ||||||
| chr1:117147063
|
C | T | 14 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0037others(11): Show | 15 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.*45+550G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117147063 | ||||||
| chr1:117147086
|
C | G | 14 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0037others(11): Show | 15 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.*45+527G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117147086 | ||||||
| chr1:117147089
|
T | C | 14 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0037others(11): Show | 15 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.*45+524A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117147089 | ||||||
| chr1:117147243
|
G | T | 12 | a0001c0001t0003g0186a0001c0001t0003g0188a0001c0001t0003g0196others(9): Show | 12 | HG02055.hp1 HG02486.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.*45+370C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117147243 | ||||||
| chr1:117147291
|
G | C | 15 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0037others(12): Show | 16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.*45+322C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117147291 | ||||||
| chr1:117147300
|
C | G | 80 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(77): Show | 86 | HG00408.hp1 HG01099.hp1 HG01106.hp2 others(83): Show |
intron_variant | MODIFIER | c.*45+313G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117147300 | ||||||
| chr1:117147306
|
G | T | 1 | a0001c0001t0012g0048 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.*45+307C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117147306 | ||||||
| chr1:117147323
|
C | T | 15 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0037others(12): Show | 16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.*45+290G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117147323 | ||||||
| chr1:117147349
|
G | A | 2 | a0001c0001t0003g0137a0001c0001t0003g0139 | 2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.*45+264C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117147349 | ||||||
| chr1:117147402
|
T | C | 2 | a0001c0001t0007g0012a0001c0001t0013g0025 | 2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.*45+211A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117147402 | ||||||
| chr1:117147438
|
G | A | 1 | a0001c0001t0006g0226 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.*45+175C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117147438 | ||||||
| chr1:117147562
|
G | C | 4 | a0001c0001t0007g0013a0001c0001t0007g0127a0001c0001t0007g0136others(1): Show | 4 | HG02818.hp1 HG03098.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.*45+51C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117147562 | ||||||
| chr1:117147927
|
C | T | 1 | a0001c0001t0013g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.725-145G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117147927 | ||||||
| chr1:117148006
|
C | T | 2 | a0001c0001t0001g0069a0002c0002t0002g0204 | 2 | HG03225.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.725-224G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117148006 | ||||||
| chr1:117148136
|
C | T | 71 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(68): Show | 77 | HG01099.hp1 HG01106.hp2 HG01243.hp2 others(74): Show |
intron_variant | MODIFIER | c.725-354G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117148136 | ||||||
| chr1:117148316
|
T | C | 3 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0214 | 3 | HG01433.hp1 HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.725-534A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117148316 | ||||||
| chr1:117148578
|
T | C | 85 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0002g0002others(82): Show | 91 | HG00408.hp1 HG01099.hp1 HG01106.hp2 others(88): Show |
intron_variant | MODIFIER | c.725-796A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117148578 | ||||||
| chr1:117148622
|
T | C | 15 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0037others(12): Show | 16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.725-840A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117148622 | ||||||
| chr1:117148673
|
C | A | 23 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0011others(20): Show | 25 | HG02083.hp1 HG02523.hp2 HG02818.hp2 others(22): Show |
intron_variant | MODIFIER | c.725-891G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117148673 | ||||||
| chr1:117148816
|
T | G | 38 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0037others(35): Show | 39 | HG01099.hp1 HG01106.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.725-1034A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117148816 | ||||||
| chr1:117148914
|
G | A | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 13 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.725-1132C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117148914 | ||||||
| chr1:117148928
|
C | T | 5 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0134others(2): Show | 5 | HG01099.hp1 HG02257.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.725-1146G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117148928 | ||||||
| chr1:117149083
|
G | A | 38 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0037others(35): Show | 39 | HG01099.hp1 HG01106.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.725-1301C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117149083 | ||||||
| chr1:117149084
|
G | A | 3 | a0001c0001t0004g0035a0001c0001t0004g0147a0001c0001t0004g0148 | 3 | HG00741.hp1 HG01255.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.725-1302C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117149084 | ||||||
| chr1:117149290
|
T | TG | 47 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0041others(44): Show | 51 | HG01099.hp1 HG01106.hp2 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.725-1509dupC | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117149290 | ||||||
| chr1:117149294
|
T | G | 47 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0002g0002others(44): Show | 49 | HG01433.hp1 HG01884.hp2 HG01891.hp1 others(46): Show |
intron_variant | MODIFIER | c.725-1512A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117149294 | ||||||
| chr1:117149295
|
T | G | 1 | a0001c0001t0002g0165 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.725-1513A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117149295 | ||||||
| chr1:117149359
|
C | T | 38 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0037others(35): Show | 39 | HG01099.hp1 HG01106.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.725-1577G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117149359 | ||||||
| chr1:117149425
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.725-1643A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117149425 | ||||||
| chr1:117149662
|
C | T | 23 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0011others(20): Show | 25 | HG02083.hp1 HG02523.hp2 HG02818.hp2 others(22): Show |
intron_variant | MODIFIER | c.725-1880G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117149662 | ||||||
| chr1:117149801
|
C | G | 7 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0007g0012others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.725-2019G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117149801 | ||||||
| chr1:117150137
|
T | C | 12 | a0001c0001t0003g0024a0001c0001t0005g0006a0001c0001t0005g0007others(9): Show | 15 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.725-2355A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117150137 | ||||||
| chr1:117150160
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.725-2378G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117150160 | ||||||
| chr1:117150312
|
C | T | 15 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0037others(12): Show | 16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.725-2530G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117150312 | ||||||
| chr1:117150357
|
G | A | 1 | a0002c0002t0002g0204 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.725-2575C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117150357 | ||||||
| chr1:117150472
|
C | T | 34 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0037others(31): Show | 35 | HG01099.hp1 HG01106.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.724+2619G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117150472 | ||||||
| chr1:117150550
|
T | C | 2 | a0001c0001t0004g0119a0001c0001t0004g0181 | 2 | HG02056.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.724+2541A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117150550 | ||||||
| chr1:117150597
|
TTTAG | T | 15 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(12): Show | 18 | HG00642.hp2 HG01943.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.724+2490_724+2493d others(6): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117150597 | ||||||
| chr1:117150679
|
T | C | 5 | a0001c0001t0001g0092a0001c0001t0001g0097a0001c0001t0001g0107others(2): Show | 5 | HG01099.hp2 HG02735.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.724+2412A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117150679 | ||||||
| chr1:117150773
|
C | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0034 | 2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.724+2318G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117150773 | ||||||
| chr1:117150911
|
C | T | 13 | a0001c0001t0003g0024a0001c0001t0005g0006a0001c0001t0005g0007others(10): Show | 16 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.724+2180G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117150911 | ||||||
| chr1:117150984
|
T | C | 13 | a0001c0001t0003g0024a0001c0001t0005g0006a0001c0001t0005g0007others(10): Show | 16 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.724+2107A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117150984 | ||||||
| chr1:117151034
|
G | A | 3 | a0001c0001t0001g0049a0001c0001t0001g0144a0001c0001t0001g0167 | 3 | HG01192.hp1 HG03831.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.724+2057C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151034 | ||||||
| chr1:117151046
|
T | G | 1 | a0001c0001t0003g0186 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.724+2045A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151046 | ||||||
| chr1:117151100
|
C | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0112 | 2 | HG02735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.724+1991G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151100 | ||||||
| chr1:117151103
|
A | C | 1 | a0001c0001t0005g0182 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.724+1988T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151103 | ||||||
| chr1:117151200
|
C | CT | 87 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0002g0002others(84): Show | 93 | HG00408.hp1 HG01099.hp1 HG01106.hp2 others(90): Show |
intron_variant | MODIFIER | c.724+1890dupA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151200 | ||||||
| chr1:117151249
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.724+1842G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151249 | ||||||
| chr1:117151271
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.724+1820A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151271 | ||||||
| chr1:117151281
|
T | C | 100 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0002g0002others(97): Show | 106 | HG00408.hp1 HG01099.hp1 HG01106.hp2 others(103): Show |
intron_variant | MODIFIER | c.724+1810A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151281 | ||||||
| chr1:117151354
|
C | T | 1 | a0001c0001t0002g0005 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.724+1737G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151354 | ||||||
| chr1:117151408
|
G | C | 1 | a0002c0002t0002g0204 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.724+1683C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151408 | ||||||
| chr1:117151418
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.724+1673A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151418 | ||||||
| chr1:117151507
|
C | T | 15 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0037others(12): Show | 16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.724+1584G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151507 | ||||||
| chr1:117151516
|
G | A | 15 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0037others(12): Show | 16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.724+1575C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151516 | ||||||
| chr1:117151523
|
C | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG01257.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.724+1568G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151523 | ||||||
| chr1:117151535
|
T | TATTGGTC others(17): Show |
19 | a0001c0001t0002g0011a0001c0001t0002g0021a0001c0001t0002g0145others(16): Show | 22 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.724+1532_724+1555d others(26): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151535 | ||||||
| chr1:117151535
|
T | TATTGGTC others(17): Show |
1 | a0001c0001t0002g0146 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.724+1555_724+1556i others(26): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151535 | ||||||
| chr1:117151716
|
C | T | 4 | a0001c0001t0003g0143a0001c0001t0007g0013a0001c0001t0007g0127others(1): Show | 4 | HG02818.hp1 HG03098.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.724+1375G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151716 | ||||||
| chr1:117151767
|
T | C | 5 | a0001c0001t0001g0040a0001c0001t0001g0216a0001c0001t0001g0217others(2): Show | 5 | HG01175.hp1 HG03491.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.724+1324A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151767 | ||||||
| chr1:117151922
|
T | C | 1 | a0001c0001t0003g0185 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.724+1169A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151922 | ||||||
| chr1:117152072
|
G | A | 19 | a0001c0001t0003g0010a0001c0001t0003g0018a0001c0001t0003g0038others(16): Show | 19 | HG01099.hp1 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.724+1019C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117152072 | ||||||
| chr1:117152200
|
T | C | 96 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0002g0002others(93): Show | 102 | HG00408.hp1 HG01099.hp1 HG01106.hp2 others(99): Show |
intron_variant | MODIFIER | c.724+891A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117152200 | ||||||
| chr1:117152201
|
G | A | 15 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0037others(12): Show | 16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.724+890C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117152201 | ||||||
| chr1:117152474
|
G | A | 15 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0037others(12): Show | 16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.724+617C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117152474 | ||||||
| chr1:117152647
|
T | A | 15 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0037others(12): Show | 16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.724+444A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117152647 | ||||||
| chr1:117152688
|
GC | G | 15 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0037others(12): Show | 16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.724+402delG | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117152688 | ||||||
| chr1:117153016
|
A | G | 1 | a0001c0001t0001g0180 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.724+75T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117153016 | ||||||
| chr1:117153415
|
G | A | 98 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0002g0002others(95): Show | 104 | HG01099.hp1 HG01106.hp2 HG01243.hp2 others(101): Show |
intron_variant | MODIFIER | c.446-46C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117153415 | ||||||
| chr1:117153461
|
A | AT | 25 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0210others(22): Show | 28 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.446-93dupA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117153461 | ||||||
| chr1:117153461
|
AT | A | 22 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0067others(19): Show | 22 | HG00408.hp2 HG01099.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.446-93delA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117153461 | ||||||
| chr1:117153526
|
A | G | 100 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0002g0002others(97): Show | 106 | HG00408.hp1 HG01099.hp1 HG01106.hp2 others(103): Show |
intron_variant | MODIFIER | c.446-157T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117153526 | ||||||
| chr1:117153577
|
C | A | 36 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0011others(33): Show | 41 | HG02083.hp1 HG02109.hp2 HG02257.hp2 others(38): Show |
intron_variant | MODIFIER | c.446-208G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117153577 | ||||||
| chr1:117153825
|
C | T | 3 | a0001c0001t0001g0051a0001c0001t0001g0057a0001c0001t0001g0070 | 3 | HG02145.hp2 HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.446-456G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117153825 | ||||||
| chr1:117153967
|
G | T | 1 | a0001c0001t0003g0215 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.446-598C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117153967 | ||||||
| chr1:117153968
|
C | T | 1 | a0001c0001t0003g0215 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.446-599G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117153968 | ||||||
| chr1:117154302
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.446-933G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117154302 | ||||||
| chr1:117154484
|
C | A | 1 | a0001c0001t0006g0228 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.446-1115G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117154484 | ||||||
| chr1:117154570
|
G | T | 3 | a0001c0001t0001g0210a0001c0001t0010g0211a0001c0001t0010g0212 | 3 | HG02895.hp1 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.446-1201C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117154570 | ||||||
| chr1:117154708
|
G | T | 1 | a0001c0001t0001g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.446-1339C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117154708 | ||||||
| chr1:117154746
|
G | T | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044 | 3 | HG00642.hp2 HG01943.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.446-1377C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117154746 | ||||||
| chr1:117154783
|
C | CA | 4 | a0001c0001t0001g0157a0001c0001t0002g0002a0001c0001t0002g0166others(1): Show | 5 | HG02615.hp1 HG03017.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.446-1415dupT | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117154783 | ||||||
| chr1:117154783
|
CA | C | 18 | a0001c0001t0001g0017a0001c0001t0001g0071a0001c0001t0001g0076others(15): Show | 18 | HG01243.hp1 HG01515.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.446-1415delT | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117154783 | ||||||
| chr1:117154800
|
A | G | 12 | a0001c0001t0003g0024a0001c0001t0005g0006a0001c0001t0005g0007others(9): Show | 15 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.446-1431T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117154800 | ||||||
| chr1:117154843
|
A | G | 23 | a0001c0001t0003g0010a0001c0001t0003g0018a0001c0001t0003g0038others(20): Show | 23 | HG01099.hp1 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.446-1474T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117154843 | ||||||
| chr1:117155442
|
A | C | 2 | a0001c0001t0001g0138a0001c0001t0001g0200 | 2 | HG01243.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.445+1132T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117155442 | ||||||
| chr1:117155838
|
C | A | 1 | a0001c0001t0001g0163 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.445+736G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117155838 | ||||||
| chr1:117155910
|
A | G | 23 | a0001c0001t0003g0010a0001c0001t0003g0018a0001c0001t0003g0038others(20): Show | 23 | HG01099.hp1 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.445+664T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117155910 | ||||||
| chr1:117155945
|
T | C | 80 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0002g0002others(77): Show | 85 | HG00408.hp1 HG01099.hp1 HG01106.hp2 others(82): Show |
intron_variant | MODIFIER | c.445+629A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117155945 | ||||||
| chr1:117155992
|
G | T | 5 | a0001c0001t0003g0143a0001c0001t0007g0013a0001c0001t0007g0127others(2): Show | 5 | HG02818.hp1 HG03098.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+582C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117155992 | ||||||
| chr1:117156184
|
T | C | 2 | a0001c0001t0003g0197a0001c0001t0003g0198 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.445+390A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117156184 | ||||||
| chr1:117156198
|
T | C | 1 | a0001c0001t0004g0116 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.445+376A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117156198 | ||||||
| chr1:117157003
|
C | T | 13 | a0001c0001t0003g0024a0001c0001t0005g0006a0001c0001t0005g0007others(10): Show | 16 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.98-82G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157003 | ||||||
| chr1:117157092
|
G | GAT | 61 | a0001c0001t0001g0026a0001c0001t0001g0093a0001c0001t0001g0104others(58): Show | 67 | HG00408.hp1 HG00741.hp1 HG01255.hp1 others(64): Show |
intron_variant | MODIFIER | c.98-173_98-172dupAT | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | ||||||
| chr1:117157092
|
G | GATAT | 5 | a0001c0001t0002g0145a0001c0001t0005g0016a0001c0001t0007g0136others(2): Show | 5 | HG01361.hp1 HG02976.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.98-175_98-172dupAT others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | ||||||
| chr1:117157092
|
G | GATATAT | 5 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0002g0146others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.98-177_98-172dupAT others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | ||||||
| chr1:117157092
|
G | GATATATA others(1): Show |
4 | a0001c0001t0002g0063a0001c0001t0007g0175a0001c0001t0011g0015others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-179_98-172dupAT others(6): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | ||||||
| chr1:117157092
|
G | GATATATA others(3): Show |
2 | a0002c0002t0003g0172a0002c0002t0003g0214 | 2 | HG01433.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.98-181_98-172dupAT others(8): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | ||||||
| chr1:117157092
|
G | GATATATA others(9): Show |
1 | a0001c0001t0002g0050 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.98-187_98-172dupAT others(14): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | ||||||
| chr1:117157092
|
G | GATATATA others(11): Show |
2 | a0001c0001t0007g0189a0001c0001t0007g0203 | 2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.98-189_98-172dupAT others(16): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | ||||||
| chr1:117157092
|
G | GATATATA others(13): Show |
3 | a0001c0001t0002g0019a0001c0001t0002g0168a0001c0001t0003g0151 | 3 | HG02486.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.98-191_98-172dupAT others(18): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | ||||||
| chr1:117157092
|
G | GATATATA others(15): Show |
11 | a0001c0001t0002g0004a0001c0001t0002g0105a0001c0001t0002g0131others(8): Show | 12 | HG01099.hp1 HG01243.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.98-193_98-172dupAT others(20): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | ||||||
| chr1:117157092
|
G | GATATATA others(17): Show |
2 | a0001c0001t0003g0010a0001c0001t0003g0174 | 2 | HG02109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.98-172_98-171insAT others(22): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | ||||||
| chr1:117157092
|
G | GATATATA others(19): Show |
8 | a0001c0001t0002g0037a0001c0001t0002g0074a0001c0001t0002g0075others(5): Show | 8 | HG01515.hp1 HG01517.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.98-172_98-171insAT others(24): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | ||||||
| chr1:117157092
|
G | GATATATA others(21): Show |
4 | a0001c0001t0002g0041a0001c0001t0003g0038a0001c0001t0003g0117others(1): Show | 4 | HG01106.hp2 HG02965.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-172_98-171insAT others(26): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | ||||||
| chr1:117157092
|
G | GATATATA others(23): Show |
3 | a0001c0001t0003g0018a0001c0001t0003g0195a0001c0001t0003g0215 | 3 | HG02647.hp1 NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.98-172_98-171insAT others(28): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | ||||||
| chr1:117157092
|
G | GATATATA others(25): Show |
2 | a0001c0001t0002g0191a0001c0001t0003g0185 | 2 | NA18906.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.98-172_98-171insAT others(30): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | ||||||
| chr1:117157092
|
G | GATATATA others(27): Show |
1 | a0001c0001t0002g0170 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.98-172_98-171insAT others(32): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | ||||||
| chr1:117157092
|
G | GATATATA others(29): Show |
1 | a0001c0001t0002g0110 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.98-172_98-171insAT others(34): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | ||||||
| chr1:117157430
|
G | T | 3 | a0001c0001t0001g0009a0001c0001t0001g0059a0001c0001t0001g0078 | 3 | HG00280.hp1 HG00323.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.98-509C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157430 | ||||||
| chr1:117157526
|
C | A | 4 | a0001c0001t0003g0010a0001c0001t0003g0174a0001c0001t0003g0192others(1): Show | 4 | HG02109.hp1 HG02965.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-605G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157526 | ||||||
| chr1:117157576
|
C | T | 1 | a0001c0001t0003g0185 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.98-655G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157576 | ||||||
| chr1:117157595
|
C | T | 13 | a0001c0001t0003g0024a0001c0001t0005g0006a0001c0001t0005g0007others(10): Show | 16 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.98-674G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157595 | ||||||
| chr1:117157674
|
C | T | 2 | a0001c0001t0002g0170a0001c0001t0002g0191 | 2 | NA18964.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.98-753G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157674 | ||||||
| chr1:117157899
|
G | C | 1 | a0001c0001t0002g0145 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-978C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157899 | ||||||
| chr1:117158083
|
T | C | 19 | a0001c0001t0003g0010a0001c0001t0003g0018a0001c0001t0003g0038others(16): Show | 19 | HG01099.hp1 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.98-1162A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117158083 | ||||||
| chr1:117158189
|
C | T | 1 | a0001c0001t0003g0152 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.98-1268G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117158189 | ||||||
| chr1:117158214
|
A | C | 30 | a0001c0001t0001g0124a0001c0001t0002g0002a0001c0001t0002g0005others(27): Show | 32 | HG00408.hp1 HG02083.hp1 HG02523.hp2 others(29): Show |
intron_variant | MODIFIER | c.98-1293T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117158214 | ||||||
| chr1:117158232
|
G | A | 12 | a0001c0001t0003g0024a0001c0001t0005g0006a0001c0001t0005g0007others(9): Show | 15 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.98-1311C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117158232 | ||||||
| chr1:117158285
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.98-1364G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117158285 | ||||||
| chr1:117158479
|
G | T | 1 | a0001c0001t0001g0096 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.98-1558C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117158479 | ||||||
| chr1:117158546
|
A | T | 13 | a0001c0001t0001g0200a0001c0001t0003g0186a0001c0001t0003g0188others(10): Show | 13 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.98-1625T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117158546 | ||||||
| chr1:117158720
|
C | T | 1 | a0001c0001t0002g0037 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.98-1799G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117158720 | ||||||
| chr1:117158799
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.98-1878G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117158799 | ||||||
| chr1:117158856
|
A | G | 2 | a0001c0001t0003g0024a0001c0001t0011g0015 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.98-1935T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117158856 | ||||||
| chr1:117158934
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.98-2013T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117158934 | ||||||
| chr1:117158958
|
C | G | 1 | a0001c0001t0003g0215 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.98-2037G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117158958 | ||||||
| chr1:117159023
|
A | T | 84 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0124others(81): Show | 87 | HG00408.hp1 HG01099.hp1 HG01106.hp2 others(84): Show |
intron_variant | MODIFIER | c.98-2102T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117159023 | ||||||
| chr1:117159384
|
C | G | 13 | a0001c0001t0001g0200a0001c0001t0003g0186a0001c0001t0003g0188others(10): Show | 13 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.98-2463G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117159384 | ||||||
| chr1:117159494
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.98-2573G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117159494 | ||||||
| chr1:117159738
|
T | G | 2 | a0001c0001t0002g0171a0002c0002t0002g0221 | 2 | HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.98-2817A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117159738 | ||||||
| chr1:117159766
|
T | A | 86 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0124others(83): Show | 89 | HG01099.hp1 HG01106.hp2 HG01243.hp2 others(86): Show |
intron_variant | MODIFIER | c.98-2845A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117159766 | ||||||
| chr1:117159966
|
C | G | 15 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0037others(12): Show | 16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.98-3045G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117159966 | ||||||
| chr1:117160040
|
G | A | 7 | a0001c0001t0001g0124a0001c0001t0002g0063a0001c0001t0002g0090others(4): Show | 7 | NA18747.hp2 NA18939.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-3119C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117160040 | ||||||
| chr1:117160162
|
G | C | 1 | a0001c0001t0001g0088 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.98-3241C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117160162 | ||||||
| chr1:117160395
|
A | C | 1 | a0001c0001t0007g0175 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.98-3474T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117160395 | ||||||
| chr1:117160540
|
G | A | 8 | a0001c0001t0001g0062a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG01255.hp2 HG01258.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.98-3619C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117160540 | ||||||
| chr1:117160560
|
G | T | 1 | a0001c0001t0001g0058 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.98-3639C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117160560 | ||||||
| chr1:117160622
|
T | G | 15 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0037others(12): Show | 16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.98-3701A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117160622 | ||||||
| chr1:117160701
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.98-3780A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117160701 | ||||||
| chr1:117160954
|
G | C | 1 | a0001c0001t0001g0158 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.98-4033C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117160954 | ||||||
| chr1:117161394
|
C | T | 52 | a0001c0001t0001g0200a0001c0001t0002g0004a0001c0001t0002g0019others(49): Show | 53 | HG01099.hp1 HG01106.hp2 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.98-4473G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117161394 | ||||||
| chr1:117161686
|
A | C | 1 | a0001c0001t0003g0208 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.98-4765T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117161686 | ||||||
| chr1:117161734
|
C | T | 19 | a0001c0001t0003g0010a0001c0001t0003g0018a0001c0001t0003g0038others(16): Show | 19 | HG01099.hp1 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.98-4813G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117161734 | ||||||
| chr1:117161794
|
A | G | 2 | a0001c0001t0004g0119a0001c0001t0004g0181 | 2 | HG02056.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.98-4873T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117161794 | ||||||
| chr1:117161878
|
G | A | 48 | a0001c0001t0001g0200a0001c0001t0002g0004a0001c0001t0002g0019others(45): Show | 49 | HG01099.hp1 HG01106.hp2 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.98-4957C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117161878 | ||||||
| chr1:117162190
|
C | G | 1 | a0001c0001t0004g0036 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.98-5269G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117162190 | ||||||
| chr1:117162341
|
C | T | 13 | a0001c0001t0001g0200a0001c0001t0003g0186a0001c0001t0003g0188others(10): Show | 13 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.98-5420G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117162341 | ||||||
| chr1:117162398
|
A | G | 239 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(236): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.98-5477T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117162398 | ||||||
| chr1:117162635
|
T | G | 13 | a0001c0001t0001g0200a0001c0001t0003g0186a0001c0001t0003g0188others(10): Show | 13 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.98-5714A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117162635 | ||||||
| chr1:117162747
|
C | T | 28 | a0001c0001t0001g0200a0001c0001t0002g0004a0001c0001t0002g0019others(25): Show | 29 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.98-5826G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117162747 | ||||||
| chr1:117162798
|
G | A | 1 | a0001c0001t0007g0175 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.98-5877C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117162798 | ||||||
| chr1:117163008
|
A | G | 30 | a0001c0001t0001g0124a0001c0001t0002g0002a0001c0001t0002g0005others(27): Show | 32 | HG00408.hp1 HG02083.hp1 HG02523.hp2 others(29): Show |
intron_variant | MODIFIER | c.98-6087T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117163008 | ||||||
| chr1:117163101
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.98-6180C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117163101 | ||||||
| chr1:117163306
|
T | A | 1 | a0001c0001t0012g0048 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.98-6385A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117163306 | ||||||
| chr1:117163413
|
T | A | 77 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0124others(74): Show | 83 | HG00408.hp1 HG01106.hp2 HG01243.hp2 others(80): Show |
intron_variant | MODIFIER | c.98-6492A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117163413 | ||||||
| chr1:117163872
|
G | A | 1 | a0001c0001t0004g0045 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.97+6235C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117163872 | ||||||
| chr1:117164012
|
G | T | 1 | a0001c0001t0002g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.97+6095C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117164012 | ||||||
| chr1:117164118
|
C | T | 3 | a0001c0001t0004g0036a0001c0001t0004g0101a0001c0001t0014g0149 | 3 | HG01361.hp1 HG03669.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.97+5989G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117164118 | ||||||
| chr1:117164342
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.97+5765G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117164342 | ||||||
| chr1:117164356
|
G | C | 3 | a0001c0001t0003g0197a0001c0001t0003g0198a0001c0001t0003g0199 | 3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.97+5751C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117164356 | ||||||
| chr1:117164369
|
C | T | 3 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0003g0209 | 3 | HG03130.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.97+5738G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117164369 | ||||||
| chr1:117164510
|
G | A | 1 | a0001c0001t0004g0154 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.97+5597C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117164510 | ||||||
| chr1:117164515
|
TA | T | 16 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0222others(13): Show | 19 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.97+5591delT | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117164515 | ||||||
| chr1:117164537
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.97+5570C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117164537 | ||||||
| chr1:117164722
|
T | G | 26 | a0001c0001t0001g0124a0001c0001t0002g0002a0001c0001t0002g0005others(23): Show | 28 | HG00408.hp1 HG02083.hp1 HG02523.hp2 others(25): Show |
intron_variant | MODIFIER | c.97+5385A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117164722 | ||||||
| chr1:117164728
|
A | T | 3 | a0001c0001t0001g0222a0001c0001t0003g0024a0001c0001t0011g0015 | 3 | HG02109.hp2 HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.97+5379T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117164728 | ||||||
| chr1:117164767
|
C | G | 1 | a0001c0001t0001g0088 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.97+5340G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117164767 | ||||||
| chr1:117165040
|
T | C | 4 | a0001c0001t0007g0175a0002c0002t0001g0056a0002c0002t0002g0204others(1): Show | 4 | HG03225.hp2 HG03486.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+5067A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117165040 | ||||||
| chr1:117165202
|
T | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0034 | 2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.97+4905A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117165202 | ||||||
| chr1:117165309
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.97+4798A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117165309 | ||||||
| chr1:117165454
|
C | T | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044 | 3 | HG00642.hp2 HG01943.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.97+4653G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117165454 | ||||||
| chr1:117165542
|
G | A | 3 | a0001c0001t0002g0032a0001c0001t0004g0147a0001c0001t0004g0148 | 3 | HG01255.hp1 HG01361.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.97+4565C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117165542 | ||||||
| chr1:117165579
|
C | A | 1 | a0001c0001t0001g0223 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.97+4528G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117165579 | ||||||
| chr1:117165611
|
A | C | 108 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0026others(105): Show | 114 | HG00408.hp1 HG01099.hp1 HG01106.hp2 others(111): Show |
intron_variant | MODIFIER | c.97+4496T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117165611 | ||||||
| chr1:117165712
|
G | A | 3 | a0001c0001t0001g0124a0001c0001t0002g0159a0001c0001t0002g0165 | 3 | NA18747.hp2 NA18969.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.97+4395C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117165712 | ||||||
| chr1:117165812
|
G | A | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 13 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.97+4295C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117165812 | ||||||
| chr1:117165855
|
T | C | 108 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0026others(105): Show | 114 | HG00408.hp1 HG01099.hp1 HG01106.hp2 others(111): Show |
intron_variant | MODIFIER | c.97+4252A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117165855 | ||||||
| chr1:117166042
|
T | C | 15 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0037others(12): Show | 16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.97+4065A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166042 | ||||||
| chr1:117166083
|
G | A | 3 | a0001c0001t0003g0129a0001c0001t0003g0135a0001c0001t0003g0151 | 3 | HG02486.hp1 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.97+4024C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166083 | ||||||
| chr1:117166102
|
T | A | 15 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0037others(12): Show | 16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.97+4005A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166102 | ||||||
| chr1:117166133
|
T | C | 4 | a0001c0001t0001g0051a0001c0001t0001g0057a0001c0001t0001g0070others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+3974A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166133 | ||||||
| chr1:117166149
|
G | A | 6 | a0001c0001t0001g0040a0001c0001t0001g0216a0001c0001t0001g0217others(3): Show | 6 | HG01175.hp1 HG02976.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.97+3958C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166149 | ||||||
| chr1:117166199
|
C | T | 25 | a0001c0001t0001g0124a0001c0001t0001g0213a0001c0001t0002g0002others(22): Show | 27 | HG02083.hp1 HG02523.hp2 HG02572.hp1 others(24): Show |
intron_variant | MODIFIER | c.97+3908G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166199 | ||||||
| chr1:117166200
|
G | T | 1 | a0001c0001t0001g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.97+3907C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166200 | ||||||
| chr1:117166247
|
A | G | 26 | a0001c0001t0001g0124a0001c0001t0002g0002a0001c0001t0002g0005others(23): Show | 28 | HG00408.hp1 HG02083.hp1 HG02523.hp2 others(25): Show |
intron_variant | MODIFIER | c.97+3860T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166247 | ||||||
| chr1:117166291
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.97+3816T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166291 | ||||||
| chr1:117166375
|
T | C | 1 | a0001c0001t0003g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.97+3732A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166375 | ||||||
| chr1:117166466
|
C | G | 8 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0134others(5): Show | 8 | HG01099.hp1 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+3641G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166466 | ||||||
| chr1:117166539
|
G | C | 2 | a0002c0002t0002g0204a0002c0002t0002g0221 | 2 | HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.97+3568C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166539 | ||||||
| chr1:117166654
|
C | CA | 12 | a0001c0001t0001g0081a0001c0001t0001g0089a0001c0001t0002g0224others(9): Show | 12 | HG00408.hp1 HG01099.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+3452dupT | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166654 | ||||||
| chr1:117166816
|
G | C | 1 | a0001c0001t0001g0098 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.97+3291C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166816 | ||||||
| chr1:117166842
|
AG | A | 4 | a0001c0001t0001g0222a0001c0001t0003g0010a0001c0001t0003g0024others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+3264delC | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166842 | ||||||
| chr1:117167071
|
C | T | 12 | a0001c0001t0001g0200a0001c0001t0003g0188a0001c0001t0003g0196others(9): Show | 12 | HG02055.hp1 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+3036G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117167071 | ||||||
| chr1:117167090
|
C | CA | 108 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0026others(105): Show | 114 | HG00408.hp1 HG01099.hp1 HG01106.hp2 others(111): Show |
intron_variant | MODIFIER | c.97+3016dupT | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117167090 | ||||||
| chr1:117167304
|
T | C | 1 | a0001c0001t0007g0175 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.97+2803A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117167304 | ||||||
| chr1:117167445
|
T | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG01257.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.97+2662A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117167445 | ||||||
| chr1:117167466
|
C | G | 15 | a0001c0001t0001g0222a0001c0001t0002g0220a0001c0001t0003g0010others(12): Show | 18 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.97+2641G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117167466 | ||||||
| chr1:117167470
|
T | G | 3 | a0001c0001t0002g0002a0001c0001t0002g0083a0001c0001t0002g0166 | 4 | NA18953.hp2 NA18999.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+2637A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117167470 | ||||||
| chr1:117167507
|
G | A | 4 | a0001c0001t0001g0222a0001c0001t0003g0010a0001c0001t0003g0024others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+2600C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117167507 | ||||||
| chr1:117167591
|
G | A | 1 | a0001c0001t0002g0005 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.97+2516C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117167591 | ||||||
| chr1:117167649
|
T | C | 2 | a0001c0001t0003g0038a0001c0001t0003g0039 | 2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.97+2458A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117167649 | ||||||
| chr1:117167843
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0034 | 2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.97+2264T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117167843 | ||||||
| chr1:117168012
|
A | C | 1 | a0001c0001t0001g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.97+2095T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117168012 | ||||||
| chr1:117168013
|
C | A | 12 | a0001c0001t0001g0200a0001c0001t0003g0188a0001c0001t0003g0196others(9): Show | 12 | HG02055.hp1 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+2094G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117168013 | ||||||
| chr1:117168061
|
T | C | 3 | a0001c0001t0003g0174a0001c0001t0003g0192a0001c0001t0003g0195 | 3 | HG02109.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97+2046A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117168061 | ||||||
| chr1:117168093
|
A | C | 6 | a0002c0002t0001g0056a0002c0002t0002g0204a0002c0002t0002g0221others(3): Show | 6 | HG01433.hp1 HG01884.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+2014T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117168093 | ||||||
| chr1:117168183
|
T | C | 1 | a0001c0001t0016g0240 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.97+1924A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117168183 | ||||||
| chr1:117168208
|
A | G | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 13 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.97+1899T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117168208 | ||||||
| chr1:117168349
|
T | C | 3 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0006g0226 | 3 | NA18955.hp1 NA18964.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.97+1758A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117168349 | ||||||
| chr1:117168433
|
T | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0153a0001c0001t0003g0152 | 3 | HG03195.hp2 HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.97+1674A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117168433 | ||||||
| chr1:117168539
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.97+1568T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117168539 | ||||||
| chr1:117168725
|
A | G | 55 | a0001c0001t0001g0200a0001c0001t0001g0222a0001c0001t0002g0220others(52): Show | 58 | HG01099.hp1 HG01433.hp1 HG01884.hp2 others(55): Show |
intron_variant | MODIFIER | c.97+1382T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117168725 | ||||||
| chr1:117168730
|
G | A | 5 | a0001c0001t0002g0004a0001c0001t0002g0041a0001c0001t0002g0074others(2): Show | 6 | HG01106.hp2 HG01358.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+1377C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117168730 | ||||||
| chr1:117168980
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.97+1127G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117168980 | ||||||
| chr1:117169073
|
C | A | 1 | a0001c0001t0013g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.97+1034G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117169073 | ||||||
| chr1:117169183
|
T | G | 13 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0003g0188others(10): Show | 13 | HG02055.hp1 HG02451.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.97+924A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117169183 | ||||||
| chr1:117169289
|
G | A | 15 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0037others(12): Show | 16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.97+818C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117169289 | ||||||
| chr1:117169313
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.97+794T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117169313 | ||||||
| chr1:117169415
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.97+692C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117169415 | ||||||
| chr1:117169423
|
G | A | 24 | a0001c0001t0001g0222a0001c0001t0003g0010a0001c0001t0003g0018others(21): Show | 24 | HG01099.hp1 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.97+684C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117169423 | ||||||
| chr1:117169436
|
C | G | 1 | a0001c0001t0001g0098 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.97+671G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117169436 | ||||||
| chr1:117169453
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.97+654G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117169453 | ||||||
| chr1:117169483
|
C | T | 78 | a0001c0001t0001g0124a0001c0001t0001g0200a0001c0001t0001g0213others(75): Show | 83 | HG01099.hp1 HG01433.hp1 HG01884.hp2 others(80): Show |
intron_variant | MODIFIER | c.97+624G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117169483 | ||||||
| chr1:117169758
|
T | G | 2 | a0002c0002t0002g0204a0002c0002t0002g0221 | 2 | HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.97+349A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117169758 | ||||||
| chr1:117169808
|
T | C | 1 | a0002c0002t0002g0204 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.97+299A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117169808 | ||||||
| chr1:117170007
|
T | A | 72 | a0001c0001t0001g0124a0001c0001t0001g0200a0001c0001t0001g0213others(69): Show | 77 | HG01099.hp1 HG01891.hp1 HG02055.hp1 others(74): Show |
intron_variant | MODIFIER | c.97+100A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117170007 | ||||||
| chr1:117170482
|
T | C | 6 | a0002c0002t0001g0056a0002c0002t0002g0204a0002c0002t0002g0221others(3): Show | 6 | HG01433.hp1 HG01884.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-311A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117170482 | ||||||
| chr1:117170512
|
G | A | 4 | a0001c0001t0001g0222a0001c0001t0003g0010a0001c0001t0003g0024others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-341C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117170512 | ||||||
| chr1:117170736
|
A | C | 1 | a0001c0001t0001g0061 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.33-565T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117170736 | ||||||
| chr1:117170886
|
C | T | 5 | a0001c0001t0003g0196a0001c0001t0003g0207a0001c0001t0008g0126others(2): Show | 5 | HG02055.hp1 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-715G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117170886 | ||||||
| chr1:117170887
|
G | A | 1 | a0001c0001t0003g0039 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.33-716C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117170887 | ||||||
| chr1:117171016
|
C | G | 6 | a0001c0001t0001g0100a0001c0001t0001g0120a0001c0001t0001g0121others(3): Show | 6 | HG00621.hp1 HG02074.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-845G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171016 | ||||||
| chr1:117171080
|
A | G | 17 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(14): Show | 20 | HG01433.hp1 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.33-909T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171080 | ||||||
| chr1:117171081
|
C | T | 238 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(235): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.33-910G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171081 | ||||||
| chr1:117171152
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.33-981G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171152 | ||||||
| chr1:117171173
|
G | A | 18 | a0001c0001t0001g0222a0001c0001t0003g0010a0001c0001t0003g0018others(15): Show | 18 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.33-1002C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171173 | ||||||
| chr1:117171212
|
T | C | 1 | a0001c0001t0006g0230 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.33-1041A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171212 | ||||||
| chr1:117171333
|
T | C | 45 | a0001c0001t0001g0112a0001c0001t0001g0124a0001c0001t0001g0222others(42): Show | 47 | HG02083.hp1 HG02109.hp2 HG02258.hp1 others(44): Show |
intron_variant | MODIFIER | c.33-1162A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171333 | ||||||
| chr1:117171474
|
C | G | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.33-1303G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171474 | ||||||
| chr1:117171568
|
T | A | 11 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0026others(8): Show | 11 | HG02055.hp2 HG02280.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-1397A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171568 | ||||||
| chr1:117171598
|
C | T | 13 | a0001c0001t0002g0004a0001c0001t0002g0037a0001c0001t0002g0041others(10): Show | 14 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.33-1427G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171598 | ||||||
| chr1:117171662
|
C | T | 8 | a0001c0001t0001g0213a0001c0001t0002g0021a0001c0001t0003g0038others(5): Show | 8 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.33-1491G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171662 | ||||||
| chr1:117171879
|
A | G | 1 | a0001c0001t0012g0048 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.33-1708T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171879 | ||||||
| chr1:117171903
|
C | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0153a0001c0001t0003g0152 | 3 | HG03195.hp2 HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.33-1732G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171903 | ||||||
| chr1:117171945
|
G | A | 19 | a0001c0001t0001g0112a0001c0001t0002g0002a0001c0001t0002g0005others(16): Show | 21 | HG02083.hp1 HG02523.hp2 HG02818.hp1 others(18): Show |
intron_variant | MODIFIER | c.33-1774C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171945 | ||||||
| chr1:117172127
|
T | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(201): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.33-1956A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117172127 | ||||||
| chr1:117172331
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.33-2160C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117172331 | ||||||
| chr1:117172345
|
T | C | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 13 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.33-2174A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117172345 | ||||||
| chr1:117172404
|
C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(136): Show | 143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.33-2233G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117172404 | ||||||
| chr1:117172547
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.33-2376A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117172547 | ||||||
| chr1:117172578
|
ATTT | A | 32 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0026others(29): Show | 35 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.33-2410_33-2408del others(3): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117172578 | ||||||
| chr1:117172640
|
T | C | 1 | a0001c0001t0003g0152 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.33-2469A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117172640 | ||||||
| chr1:117172640
|
TC | T | 9 | a0001c0001t0001g0213a0001c0001t0002g0021a0001c0001t0003g0038others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.33-2470delG | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117172640 | ||||||
| chr1:117172666
|
T | C | 13 | a0001c0001t0002g0004a0001c0001t0002g0037a0001c0001t0002g0041others(10): Show | 14 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.33-2495A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117172666 | ||||||
| chr1:117172789
|
TAAATGCA others(18): Show |
T | 123 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(120): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.33-2643_33-2619del others(25): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117172789 | ||||||
| chr1:117172859
|
C | T | 38 | a0001c0001t0001g0112a0001c0001t0001g0124a0001c0001t0002g0002others(35): Show | 40 | HG02083.hp1 HG02486.hp1 HG02523.hp2 others(37): Show |
intron_variant | MODIFIER | c.33-2688G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117172859 | ||||||
| chr1:117172864
|
G | A | 38 | a0001c0001t0001g0112a0001c0001t0001g0124a0001c0001t0002g0002others(35): Show | 40 | HG02083.hp1 HG02486.hp1 HG02523.hp2 others(37): Show |
intron_variant | MODIFIER | c.33-2693C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117172864 | ||||||
| chr1:117173081
|
G | A | 6 | a0001c0001t0001g0026a0001c0001t0001g0210a0001c0001t0002g0029others(3): Show | 6 | HG02055.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-2910C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173081 | ||||||
| chr1:117173104
|
G | C | 2 | a0002c0002t0003g0172a0002c0002t0003g0214 | 2 | HG01433.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.33-2933C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173104 | ||||||
| chr1:117173154
|
G | A | 1 | a0001c0001t0003g0134 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.33-2983C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173154 | ||||||
| chr1:117173159
|
C | T | 1 | a0001c0001t0007g0175 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.33-2988G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173159 | ||||||
| chr1:117173195
|
C | A | 11 | a0001c0001t0002g0004a0001c0001t0002g0037a0001c0001t0002g0041others(8): Show | 12 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.33-3024G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173195 | ||||||
| chr1:117173365
|
A | AAC | 116 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(113): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.33-3196_33-3195dup others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173365 | ||||||
| chr1:117173365
|
A | AACAC | 48 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0054others(45): Show | 52 | HG01099.hp1 HG01106.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.33-3198_33-3195dup others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173365 | ||||||
| chr1:117173365
|
A | AACACAC | 21 | a0001c0001t0001g0210a0001c0001t0001g0213a0001c0001t0001g0222others(18): Show | 22 | HG02109.hp2 HG02257.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.33-3200_33-3195dup others(6): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173365 | ||||||
| chr1:117173365
|
A | AACACACA others(1): Show |
6 | a0001c0001t0001g0017a0001c0001t0002g0171a0001c0001t0003g0010others(3): Show | 7 | HG02895.hp2 HG02970.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-3202_33-3195dup others(8): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173365 | ||||||
| chr1:117173365
|
A | AACACACA others(3): Show |
8 | a0001c0001t0001g0020a0001c0001t0001g0153a0001c0001t0001g0223others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-3204_33-3195dup others(10): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173365 | ||||||
| chr1:117173365
|
A | AACACACA others(7): Show |
1 | a0001c0001t0001g0034 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.33-3208_33-3195dup others(14): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173365 | ||||||
| chr1:117173365
|
AAC | A | 14 | a0001c0001t0001g0163a0001c0001t0002g0019a0001c0001t0002g0220others(11): Show | 14 | HG02486.hp1 HG02615.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.33-3196_33-3195del others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173365 | ||||||
| chr1:117173365
|
AACAC | A | 4 | a0001c0001t0002g0021a0001c0001t0003g0174a0001c0001t0003g0192others(1): Show | 4 | HG02109.hp1 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-3198_33-3195del others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173365 | ||||||
| chr1:117173484
|
T | A | 20 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(17): Show | 21 | HG00642.hp2 HG00741.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.33-3313A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173484 | ||||||
| chr1:117173491
|
T | G | 2 | a0001c0001t0002g0019a0001c0001t0003g0151 | 2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.33-3320A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173491 | ||||||
| chr1:117173492
|
C | A | 10 | a0001c0001t0002g0004a0001c0001t0002g0037a0001c0001t0002g0041others(7): Show | 11 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-3321G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173492 | ||||||
| chr1:117173531
|
T | C | 28 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0026others(25): Show | 30 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.33-3360A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173531 | ||||||
| chr1:117173654
|
T | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(129): Show | 133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.33-3483A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173654 | ||||||
| chr1:117173771
|
G | A | 2 | a0001c0001t0002g0029a0001c0001t0003g0186 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.33-3600C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173771 | ||||||
| chr1:117173914
|
C | T | 1 | a0001c0001t0004g0035 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.33-3743G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173914 | ||||||
| chr1:117174057
|
TGC | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(125): Show | 129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.33-3888_33-3887del others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117174057 | ||||||
| chr1:117174094
|
A | G | 2 | a0001c0001t0001g0111a0001c0001t0001g0133 | 2 | HG01975.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.33-3923T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117174094 | ||||||
| chr1:117174111
|
G | C | 1 | a0001c0001t0001g0109 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.33-3940C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117174111 | ||||||
| chr1:117174142
|
C | T | 1 | a0001c0001t0007g0175 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.33-3971G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117174142 | ||||||
| chr1:117174323
|
T | C | 1 | a0001c0001t0003g0137 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.33-4152A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117174323 | ||||||
| chr1:117174413
|
C | T | 21 | a0001c0001t0001g0069a0001c0001t0001g0084a0001c0001t0001g0089others(18): Show | 21 | HG00408.hp2 HG00621.hp1 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.33-4242G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117174413 | ||||||
| chr1:117174577
|
G | A | 10 | a0001c0001t0002g0004a0001c0001t0002g0037a0001c0001t0002g0041others(7): Show | 11 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-4406C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117174577 | ||||||
| chr1:117174638
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.33-4467C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117174638 | ||||||
| chr1:117174680
|
T | C | 10 | a0001c0001t0002g0004a0001c0001t0002g0037a0001c0001t0002g0041others(7): Show | 11 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-4509A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117174680 | ||||||
| chr1:117174691
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.33-4520G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117174691 | ||||||
| chr1:117174867
|
G | A | 25 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0153others(22): Show | 27 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.33-4696C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117174867 | ||||||
| chr1:117174947
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.33-4776G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117174947 | ||||||
| chr1:117175086
|
A | AGCT | 13 | a0001c0001t0002g0019a0001c0001t0002g0220a0001c0001t0003g0129others(10): Show | 13 | HG02486.hp1 HG02615.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.33-4918_33-4916dup others(3): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175086 | ||||||
| chr1:117175229
|
A | G | 1 | a0001c0001t0002g0170 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.33-5058T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175229 | ||||||
| chr1:117175374
|
C | T | 1 | a0001c0001t0004g0064 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.33-5203G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175374 | ||||||
| chr1:117175406
|
T | C | 10 | a0001c0001t0002g0004a0001c0001t0002g0037a0001c0001t0002g0041others(7): Show | 11 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-5235A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175406 | ||||||
| chr1:117175427
|
A | G | 9 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0153others(6): Show | 9 | HG02055.hp2 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.33-5256T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175427 | ||||||
| chr1:117175433
|
C | T | 10 | a0001c0001t0002g0004a0001c0001t0002g0037a0001c0001t0002g0041others(7): Show | 11 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-5262G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175433 | ||||||
| chr1:117175621
|
G | A | 15 | a0001c0001t0002g0021a0001c0001t0003g0010a0001c0001t0003g0038others(12): Show | 17 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.33-5450C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175621 | ||||||
| chr1:117175755
|
ATC | A | 13 | a0001c0001t0001g0082a0001c0001t0001g0099a0001c0001t0001g0180others(10): Show | 14 | HG00323.hp1 HG01106.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.33-5586_33-5585del others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175755 | ||||||
| chr1:117175765
|
C | A | 10 | a0001c0001t0002g0004a0001c0001t0002g0037a0001c0001t0002g0041others(7): Show | 11 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-5594G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175765 | ||||||
| chr1:117175769
|
C | CT | 13 | a0001c0001t0001g0026a0001c0001t0002g0019a0001c0001t0002g0220others(10): Show | 13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.33-5599dupA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175769 | ||||||
| chr1:117175771
|
C | CT | 10 | a0001c0001t0001g0213a0001c0001t0001g0222a0001c0001t0002g0011others(7): Show | 10 | HG02258.hp1 HG02572.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.33-5601dupA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175771 | ||||||
| chr1:117175771
|
C | T | 14 | a0001c0001t0001g0026a0001c0001t0002g0019a0001c0001t0002g0220others(11): Show | 14 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.33-5600G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175771 | ||||||
| chr1:117175772
|
TC | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(130): Show | 134 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.33-5602delG | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175772 | ||||||
| chr1:117175773
|
C | T | 71 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0026others(68): Show | 76 | HG01099.hp1 HG01884.hp2 HG01891.hp1 others(73): Show |
intron_variant | MODIFIER | c.33-5602G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175773 | ||||||
| chr1:117175874
|
G | A | 14 | a0001c0001t0001g0026a0001c0001t0002g0019a0001c0001t0002g0220others(11): Show | 14 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.33-5703C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175874 | ||||||
| chr1:117175928
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.33-5757C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175928 | ||||||
| chr1:117175931
|
C | T | 28 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0034others(25): Show | 30 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.33-5760G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175931 | ||||||
| chr1:117175942
|
T | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0034a0002c0002t0003g0173 | 3 | HG01884.hp2 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.33-5771A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175942 | ||||||
| chr1:117176000
|
C | T | 9 | a0001c0001t0003g0010a0001c0001t0005g0006a0001c0001t0005g0007others(6): Show | 11 | HG01891.hp1 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.33-5829G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176000 | ||||||
| chr1:117176114
|
A | G | 7 | a0001c0001t0002g0021a0001c0001t0003g0038a0001c0001t0003g0039others(4): Show | 7 | HG01099.hp1 HG02109.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-5943T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176114 | ||||||
| chr1:117176157
|
C | T | 217 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(214): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.33-5986G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176157 | ||||||
| chr1:117176175
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(214): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.33-6004T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176175 | ||||||
| chr1:117176312
|
G | T | 1 | a0001c0001t0007g0175 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.33-6141C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176312 | ||||||
| chr1:117176426
|
CAAG | C | 27 | a0001c0001t0001g0112a0001c0001t0001g0124a0001c0001t0002g0002others(24): Show | 30 | HG02083.hp1 HG02257.hp2 HG02523.hp2 others(27): Show |
intron_variant | MODIFIER | c.33-6258_33-6256del others(3): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176426 | ||||||
| chr1:117176509
|
A | G | 10 | a0001c0001t0002g0004a0001c0001t0002g0037a0001c0001t0002g0041others(7): Show | 11 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-6338T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176509 | ||||||
| chr1:117176513
|
A | G | 24 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0061others(21): Show | 24 | HG00323.hp1 HG00408.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.33-6342T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176513 | ||||||
| chr1:117176557
|
A | C | 1 | a0001c0001t0001g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.33-6386T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176557 | ||||||
| chr1:117176641
|
A | G | 2 | a0001c0001t0001g0092a0001c0001t0001g0115 | 2 | HG01099.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.33-6470T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176641 | ||||||
| chr1:117176680
|
T | A | 1 | a0001c0001t0001g0223 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.33-6509A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176680 | ||||||
| chr1:117176822
|
A | G | 10 | a0001c0001t0002g0004a0001c0001t0002g0037a0001c0001t0002g0041others(7): Show | 11 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-6651T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176822 | ||||||
| chr1:117176853
|
C | CT | 4 | a0002c0002t0002g0204a0002c0002t0002g0221a0002c0002t0003g0172others(1): Show | 4 | HG01433.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-6683dupA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176853 | ||||||
| chr1:117176955
|
C | T | 15 | a0001c0001t0001g0026a0001c0001t0002g0019a0001c0001t0002g0220others(12): Show | 15 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.33-6784G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176955 | ||||||
| chr1:117176992
|
G | A | 26 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0034others(23): Show | 28 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.33-6821C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176992 | ||||||
| chr1:117177040
|
T | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(215): Show | 225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.33-6869A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117177040 | ||||||
| chr1:117177115
|
C | G | 1 | a0001c0001t0003g0024 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.33-6944G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117177115 | ||||||
| chr1:117177116
|
A | G | 1 | a0001c0001t0003g0024 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.33-6945T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117177116 | ||||||
| chr1:117177677
|
C | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0034others(6): Show | 9 | HG01884.hp2 HG02280.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.33-7506G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117177677 | ||||||
| chr1:117177697
|
G | C | 10 | a0001c0001t0002g0004a0001c0001t0002g0037a0001c0001t0002g0041others(7): Show | 11 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-7526C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117177697 | ||||||
| chr1:117177724
|
A | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(204): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.33-7553T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117177724 | ||||||
| chr1:117177921
|
C | CT | 27 | a0001c0001t0001g0026a0001c0001t0001g0053a0001c0001t0002g0004others(24): Show | 28 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.33-7751dupA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117177921 | ||||||
| chr1:117178113
|
A | T | 6 | a0001c0001t0001g0210a0001c0001t0001g0213a0001c0001t0001g0222others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-7942T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178113 | ||||||
| chr1:117178202
|
G | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0034a0002c0002t0003g0173 | 3 | HG01884.hp2 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.33-8031C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178202 | ||||||
| chr1:117178238
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.33-8067A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178238 | ||||||
| chr1:117178250
|
C | CT | 204 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(201): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.33-8080dupA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178250 | ||||||
| chr1:117178258
|
T | TTC | 14 | a0001c0001t0001g0026a0001c0001t0002g0019a0001c0001t0002g0220others(11): Show | 14 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.33-8088_33-8087ins others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178258 | ||||||
| chr1:117178259
|
C | T | 14 | a0001c0001t0001g0026a0001c0001t0002g0019a0001c0001t0002g0220others(11): Show | 14 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.33-8088G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178259 | ||||||
| chr1:117178300
|
A | C | 1 | a0001c0001t0001g0053 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.33-8129T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178300 | ||||||
| chr1:117178352
|
G | A | 8 | a0001c0001t0001g0062a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG01255.hp2 HG01258.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-8181C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178352 | ||||||
| chr1:117178370
|
C | A | 1 | a0002c0002t0002g0204 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.33-8199G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178370 | ||||||
| chr1:117178388
|
C | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(180): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.33-8217G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178388 | ||||||
| chr1:117178547
|
T | C | 217 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(214): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.33-8376A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178547 | ||||||
| chr1:117178588
|
G | GT | 8 | a0001c0001t0001g0042a0001c0001t0002g0027a0001c0001t0002g0029others(5): Show | 8 | HG00642.hp2 HG01175.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-8418dupA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178588 | ||||||
| chr1:117178588
|
G | GTT | 32 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0026others(29): Show | 32 | HG01884.hp2 HG01975.hp1 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.33-8419_33-8418dup others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178588 | ||||||
| chr1:117178588
|
G | GTTT | 148 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(145): Show | 154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.33-8420_33-8418dup others(3): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178588 | ||||||
| chr1:117178588
|
G | GTTTT | 21 | a0001c0001t0001g0030a0001c0001t0001g0084a0001c0001t0001g0093others(18): Show | 21 | HG00408.hp1 HG00642.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.33-8421_33-8418dup others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178588 | ||||||
| chr1:117178729
|
G | A | 163 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(160): Show | 167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.33-8558C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178729 | ||||||
| chr1:117178736
|
T | G | 207 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(204): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.33-8565A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178736 | ||||||
| chr1:117178750
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.33-8579G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178750 | ||||||
| chr1:117178751
|
G | A | 100 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0022others(97): Show | 101 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.33-8580C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178751 | ||||||
| chr1:117178816
|
C | T | 6 | a0001c0001t0001g0210a0001c0001t0001g0213a0001c0001t0001g0222others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-8645G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178816 | ||||||
| chr1:117178923
|
T | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(204): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.33-8752A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178923 | ||||||
| chr1:117179135
|
T | G | 6 | a0001c0001t0001g0020a0001c0001t0001g0153a0001c0001t0001g0223others(3): Show | 6 | HG03041.hp1 HG03195.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-8964A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117179135 | ||||||
| chr1:117179144
|
C | G | 1 | a0001c0001t0001g0138 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.33-8973G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117179144 | ||||||
| chr1:117179184
|
A | G | 1 | a0001c0001t0005g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.33-9013T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117179184 | ||||||
| chr1:117179209
|
C | T | 20 | a0001c0001t0001g0020a0001c0001t0001g0153a0001c0001t0002g0021others(17): Show | 22 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.33-9038G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117179209 | ||||||
| chr1:117179245
|
T | C | 26 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0034others(23): Show | 28 | HG01099.hp1 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.33-9074A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117179245 | ||||||
| chr1:117179246
|
G | A | 1 | a0002c0002t0002g0221 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.33-9075C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117179246 | ||||||
| chr1:117179265
|
C | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(119): Show | 123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.33-9094G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117179265 | ||||||
| chr1:117179338
|
G | T | 1 | a0001c0001t0002g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.33-9167C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117179338 | ||||||
| chr1:117179376
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(218): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.33-9205C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117179376 | ||||||
| chr1:117179558
|
G | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(218): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.33-9387C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117179558 | ||||||
| chr1:117179948
|
C | T | 6 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0182others(3): Show | 8 | HG02280.hp2 HG02647.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-9777G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117179948 | ||||||
| chr1:117179960
|
G | C | 2 | a0001c0001t0013g0025a0002c0002t0001g0056 | 2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.33-9789C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117179960 | ||||||
| chr1:117180070
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.33-9899T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117180070 | ||||||
| chr1:117180124
|
C | G | 1 | a0002c0002t0003g0173 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.33-9953G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117180124 | ||||||
| chr1:117180214
|
C | CA | 22 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0034others(19): Show | 24 | HG01099.hp1 HG01884.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.33-10044dupT | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117180214 | ||||||
| chr1:117180313
|
T | C | 22 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0034others(19): Show | 24 | HG01099.hp1 HG01884.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.33-10142A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117180313 | ||||||
| chr1:117180350
|
T | G | 22 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0034others(19): Show | 24 | HG01099.hp1 HG01884.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.33-10179A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117180350 | ||||||
| chr1:117180418
|
A | G | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.33-10247T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117180418 | ||||||
| chr1:117180625
|
C | G | 23 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0034others(20): Show | 25 | HG01099.hp1 HG01884.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.33-10454G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117180625 | ||||||
| chr1:117180685
|
T | A | 13 | a0001c0001t0002g0004a0001c0001t0002g0037a0001c0001t0002g0041others(10): Show | 14 | HG00741.hp1 HG01106.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.33-10514A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117180685 | ||||||
| chr1:117180776
|
C | G | 28 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(25): Show | 31 | HG00621.hp2 HG00642.hp2 HG01943.hp2 others(28): Show |
intron_variant | MODIFIER | c.33-10605G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117180776 | ||||||
| chr1:117180790
|
G | A | 1 | a0001c0001t0004g0154 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.33-10619C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117180790 | ||||||
| chr1:117180941
|
C | T | 9 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0026others(6): Show | 9 | HG01433.hp1 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.33-10770G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117180941 | ||||||
| chr1:117180967
|
G | C | 3 | a0001c0001t0001g0014a0001c0001t0002g0029a0001c0001t0003g0186 | 3 | HG03041.hp1 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-10796C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117180967 | ||||||
| chr1:117181009
|
C | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0022others(176): Show | 185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.33-10838G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117181009 | ||||||
| chr1:117181146
|
G | T | 173 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0023others(170): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.33-10975C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117181146 | ||||||
| chr1:117181156
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG01257.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.33-10985G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117181156 | ||||||
| chr1:117181165
|
C | T | 1 | a0001c0001t0002g0220 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.33-10994G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117181165 | ||||||
| chr1:117181253
|
C | CA | 103 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0030others(100): Show | 106 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.33-11083dupT | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117181253 | ||||||
| chr1:117181253
|
CA | C | 21 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0026others(18): Show | 22 | HG00741.hp1 HG01106.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-11083delT | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117181253 | ||||||
| chr1:117181419
|
C | T | 27 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(24): Show | 29 | HG00621.hp2 HG00642.hp2 HG01943.hp2 others(26): Show |
intron_variant | MODIFIER | c.33-11248G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117181419 | ||||||
| chr1:117181736
|
G | T | 4 | a0001c0001t0003g0143a0001c0001t0003g0174a0001c0001t0007g0127others(1): Show | 4 | HG02109.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-11565C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117181736 | ||||||
| chr1:117181777
|
C | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0153a0001c0001t0003g0152others(2): Show | 5 | HG01891.hp1 HG03195.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-11606G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117181777 | ||||||
| chr1:117181796
|
G | A | 2 | a0001c0001t0003g0192a0001c0001t0003g0195 | 2 | HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.33-11625C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117181796 | ||||||
| chr1:117181872
|
G | A | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.33-11701C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117181872 | ||||||
| chr1:117182339
|
A | G | 1 | a0001c0001t0002g0220 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.33-12168T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117182339 | ||||||
| chr1:117182450
|
C | T | 9 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0026others(6): Show | 9 | HG01433.hp1 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.33-12279G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117182450 | ||||||
| chr1:117182549
|
A | T | 9 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0026others(6): Show | 9 | HG01433.hp1 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.33-12378T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117182549 | ||||||
| chr1:117182584
|
C | T | 2 | a0001c0001t0005g0006a0001c0001t0005g0184 | 3 | HG02280.hp2 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.33-12413G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117182584 | ||||||
| chr1:117182669
|
C | T | 4 | a0001c0001t0001g0051a0001c0001t0001g0057a0001c0001t0001g0070others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-12498G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117182669 | ||||||
| chr1:117182880
|
C | G | 25 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(22): Show | 27 | HG00621.hp2 HG00642.hp2 HG01943.hp2 others(24): Show |
intron_variant | MODIFIER | c.33-12709G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117182880 | ||||||
| chr1:117182949
|
C | A | 1 | a0001c0001t0005g0182 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.33-12778G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117182949 | ||||||
| chr1:117183067
|
G | T | 11 | a0001c0001t0001g0062a0001c0001t0001g0076a0001c0001t0001g0077others(8): Show | 11 | HG00323.hp1 HG01255.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-12896C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117183067 | ||||||
| chr1:117183720
|
C | T | 6 | a0001c0001t0002g0019a0001c0001t0003g0129a0001c0001t0003g0135others(3): Show | 6 | HG02486.hp1 HG02622.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-13549G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117183720 | ||||||
| chr1:117183916
|
T | C | 1 | a0001c0001t0002g0021 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.33-13745A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117183916 | ||||||
| chr1:117184163
|
C | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0156 | 2 | HG02523.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.33-13992G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117184163 | ||||||
| chr1:117184394
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.33-14223G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117184394 | ||||||
| chr1:117184535
|
T | A | 1 | a0001c0001t0001g0109 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.33-14364A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117184535 | ||||||
| chr1:117184580
|
C | T | 1 | a0001c0001t0003g0039 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.33-14409G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117184580 | ||||||
| chr1:117184745
|
C | T | 28 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(25): Show | 30 | HG00621.hp2 HG00642.hp2 HG01943.hp2 others(27): Show |
intron_variant | MODIFIER | c.33-14574G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117184745 | ||||||
| chr1:117185085
|
G | A | 6 | a0001c0001t0002g0019a0001c0001t0003g0129a0001c0001t0003g0135others(3): Show | 6 | HG02486.hp1 HG02622.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-14914C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117185085 | ||||||
| chr1:117185103
|
A | C | 5 | a0001c0001t0001g0040a0001c0001t0001g0216a0001c0001t0001g0217others(2): Show | 5 | HG01175.hp1 HG03491.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-14932T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117185103 | ||||||
| chr1:117185315
|
C | T | 1 | a0002c0002t0002g0204 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.33-15144G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117185315 | ||||||
| chr1:117185579
|
A | C | 3 | a0001c0001t0001g0210a0001c0001t0010g0211a0001c0001t0010g0212 | 3 | HG02895.hp1 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.33-15408T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117185579 | ||||||
| chr1:117186016
|
T | A | 2 | a0001c0001t0001g0153a0001c0001t0003g0152 | 2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.33-15845A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186016 | ||||||
| chr1:117186030
|
A | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0031others(124): Show | 130 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.33-15859T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186030 | ||||||
| chr1:117186036
|
T | C | 1 | a0001c0001t0005g0182 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.33-15865A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186036 | ||||||
| chr1:117186103
|
T | C | 1 | a0002c0002t0001g0056 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.33-15932A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186103 | ||||||
| chr1:117186219
|
C | T | 2 | a0001c0001t0005g0006a0001c0001t0005g0184 | 3 | HG02280.hp2 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.33-16048G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186219 | ||||||
| chr1:117186283
|
C | A | 8 | a0001c0001t0001g0138a0001c0001t0003g0137a0001c0001t0003g0139others(5): Show | 8 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-16112G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186283 | ||||||
| chr1:117186283
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.33-16112G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186283 | ||||||
| chr1:117186619
|
A | T | 1 | a0001c0001t0003g0143 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.33-16448T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186619 | ||||||
| chr1:117186734
|
C | T | 5 | a0001c0001t0001g0040a0001c0001t0001g0216a0001c0001t0001g0217others(2): Show | 5 | HG01175.hp1 HG03491.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-16563G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186734 | ||||||
| chr1:117186747
|
C | T | 8 | a0001c0001t0002g0171a0001c0001t0005g0006a0001c0001t0005g0007others(5): Show | 10 | HG02280.hp2 HG02647.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.33-16576G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186747 | ||||||
| chr1:117186799
|
G | A | 2 | a0001c0001t0003g0010a0002c0002t0003g0172 | 2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.33-16628C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186799 | ||||||
| chr1:117186840
|
C | A | 1 | a0001c0001t0003g0142 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.33-16669G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186840 | ||||||
| chr1:117186894
|
T | C | 12 | a0001c0001t0002g0004a0001c0001t0002g0032a0001c0001t0002g0037others(9): Show | 13 | HG00741.hp1 HG01106.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.33-16723A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186894 | ||||||
| chr1:117187061
|
T | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0031others(118): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.33-16890A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187061 | ||||||
| chr1:117187074
|
T | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(203): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.33-16903A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187074 | ||||||
| chr1:117187301
|
C | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0030others(128): Show | 134 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.33-17130G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187301 | ||||||
| chr1:117187309
|
C | CA | 135 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0020others(132): Show | 141 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.33-17139dupT | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187309 | ||||||
| chr1:117187309
|
C | CAA | 23 | a0001c0001t0001g0014a0001c0001t0001g0049a0001c0001t0001g0053others(20): Show | 23 | HG00408.hp1 HG00741.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.33-17140_33-17139d others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187309 | ||||||
| chr1:117187309
|
C | CAAA | 9 | a0001c0001t0002g0019a0001c0001t0003g0129a0001c0001t0003g0135others(6): Show | 9 | HG02486.hp1 HG02622.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.33-17141_33-17139d others(5): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187309 | ||||||
| chr1:117187309
|
CAA | C | 28 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0042others(25): Show | 30 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.33-17140_33-17139d others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187309 | ||||||
| chr1:117187353
|
T | C | 2 | a0001c0001t0002g0029a0001c0001t0003g0186 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.33-17182A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187353 | ||||||
| chr1:117187426
|
G | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0030others(128): Show | 134 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.33-17255C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187426 | ||||||
| chr1:117187452
|
A | G | 33 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0042others(30): Show | 35 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.33-17281T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187452 | ||||||
| chr1:117187601
|
G | C | 33 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0042others(30): Show | 35 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.33-17430C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187601 | ||||||
| chr1:117187668
|
C | T | 1 | a0001c0001t0002g0011 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.33-17497G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187668 | ||||||
| chr1:117187814
|
G | A | 3 | a0001c0001t0003g0024a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG02109.hp2 HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.33-17643C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187814 | ||||||
| chr1:117187918
|
T | A | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044 | 3 | HG00642.hp2 HG01943.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.33-17747A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187918 | ||||||
| chr1:117188001
|
G | A | 34 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0210others(31): Show | 35 | HG00741.hp1 HG01099.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.33-17830C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117188001 | ||||||
| chr1:117188058
|
T | C | 8 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(5): Show | 8 | HG01433.hp1 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.33-17887A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117188058 | ||||||
| chr1:117188084
|
C | T | 34 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0210others(31): Show | 35 | HG00741.hp1 HG01099.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.33-17913G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117188084 | ||||||
| chr1:117188157
|
A | G | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.33-17986T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117188157 | ||||||
| chr1:117188221
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.33-18050C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117188221 | ||||||
| chr1:117188441
|
G | A | 33 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0042others(30): Show | 35 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.33-18270C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117188441 | ||||||
| chr1:117188515
|
G | A | 1 | a0001c0001t0005g0183 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.33-18344C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117188515 | ||||||
| chr1:117188598
|
A | G | 1 | a0002c0002t0003g0172 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.33-18427T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117188598 | ||||||
| chr1:117188617
|
A | C | 2 | a0001c0001t0001g0153a0001c0001t0003g0152 | 2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.33-18446T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117188617 | ||||||
| chr1:117188879
|
C | G | 1 | a0002c0002t0002g0204 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.33-18708G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117188879 | ||||||
| chr1:117188935
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.33-18764T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117188935 | ||||||
| chr1:117189019
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.33-18848C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117189019 | ||||||
| chr1:117189350
|
G | A | 115 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0017others(112): Show | 120 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(117): Show |
intron_variant | MODIFIER | c.33-19179C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117189350 | ||||||
| chr1:117189351
|
T | A | 2 | a0001c0001t0003g0038a0001c0001t0003g0039 | 2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.33-19180A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117189351 | ||||||
| chr1:117189509
|
C | G | 1 | a0001c0001t0001g0086 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.33-19338G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117189509 | ||||||
| chr1:117189549
|
G | A | 29 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0210others(26): Show | 30 | HG00741.hp1 HG01106.hp2 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.33-19378C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117189549 | ||||||
| chr1:117189671
|
A | G | 1 | a0001c0001t0003g0139 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.33-19500T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117189671 | ||||||
| chr1:117189790
|
T | A | 4 | a0001c0001t0001g0051a0001c0001t0001g0057a0001c0001t0001g0070others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-19619A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117189790 | ||||||
| chr1:117189811
|
C | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(203): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.33-19640G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117189811 | ||||||
| chr1:117189894
|
C | A | 35 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0042others(32): Show | 37 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.33-19723G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117189894 | ||||||
| chr1:117189910
|
C | CAAG | 215 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(212): Show | 223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.33-19742_33-19740d others(5): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117189910 | ||||||
| chr1:117190236
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.33-20065G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117190236 | ||||||
| chr1:117190252
|
A | G | 4 | a0001c0001t0003g0188a0001c0001t0008g0126a0001c0001t0008g0193others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-20081T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117190252 | ||||||
| chr1:117190278
|
T | G | 12 | a0001c0001t0002g0029a0001c0001t0002g0171a0001c0001t0003g0018others(9): Show | 14 | HG02280.hp2 HG02647.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.33-20107A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117190278 | ||||||
| chr1:117190544
|
A | C | 1 | a0001c0001t0001g0157 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.32+20280T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117190544 | ||||||
| chr1:117190594
|
C | A | 5 | a0001c0001t0001g0210a0001c0001t0001g0213a0001c0001t0001g0222others(2): Show | 5 | HG02572.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+20230G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117190594 | ||||||
| chr1:117190664
|
C | G | 2 | a0001c0001t0005g0007a0001c0001t0015g0239 | 3 | HG02895.hp2 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.32+20160G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117190664 | ||||||
| chr1:117190853
|
T | C | 14 | a0001c0001t0002g0029a0001c0001t0002g0171a0001c0001t0003g0018others(11): Show | 16 | HG02257.hp1 HG02280.hp2 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.32+19971A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117190853 | ||||||
| chr1:117190879
|
G | A | 1 | a0001c0001t0003g0024 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.32+19945C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117190879 | ||||||
| chr1:117191068
|
C | T | 2 | a0001c0001t0002g0029a0001c0001t0003g0186 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.32+19756G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117191068 | ||||||
| chr1:117191144
|
G | A | 2 | a0001c0001t0004g0119a0001c0001t0004g0181 | 2 | HG02056.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.32+19680C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117191144 | ||||||
| chr1:117191406
|
C | A | 1 | a0001c0001t0002g0041 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.32+19418G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117191406 | ||||||
| chr1:117191638
|
C | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | NA18939.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.32+19186G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117191638 | ||||||
| chr1:117191639
|
G | A | 5 | a0001c0001t0001g0210a0001c0001t0001g0213a0001c0001t0001g0222others(2): Show | 5 | HG02572.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+19185C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117191639 | ||||||
| chr1:117191675
|
G | A | 12 | a0001c0001t0002g0004a0001c0001t0002g0032a0001c0001t0002g0037others(9): Show | 13 | HG00741.hp1 HG01106.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.32+19149C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117191675 | ||||||
| chr1:117191868
|
G | C | 1 | a0001c0001t0001g0138 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.32+18956C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117191868 | ||||||
| chr1:117191879
|
C | T | 1 | a0001c0001t0004g0181 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.32+18945G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117191879 | ||||||
| chr1:117191929
|
T | A | 2 | a0001c0001t0003g0038a0001c0001t0003g0039 | 2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.32+18895A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117191929 | ||||||
| chr1:117191971
|
G | A | 2 | a0001c0001t0003g0038a0001c0001t0003g0039 | 2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.32+18853C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117191971 | ||||||
| chr1:117191978
|
T | C | 1 | a0001c0001t0004g0154 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.32+18846A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117191978 | ||||||
| chr1:117191991
|
T | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(212): Show | 223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.32+18833A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117191991 | ||||||
| chr1:117192008
|
G | GAT | 10 | a0001c0001t0001g0065a0001c0001t0001g0068a0001c0001t0001g0085others(7): Show | 10 | HG00140.hp1 HG00741.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.32+18814_32+18815d others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117192008 | ||||||
| chr1:117192008
|
G | GATAT | 39 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0042others(36): Show | 42 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.32+18812_32+18815d others(6): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117192008 | ||||||
| chr1:117192008
|
G | GATATAT | 6 | a0001c0001t0001g0044a0001c0001t0002g0005a0001c0001t0002g0029others(3): Show | 7 | HG01943.hp2 HG03041.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+18810_32+18815d others(8): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117192008 | ||||||
| chr1:117192008
|
G | GATATATA others(3): Show |
1 | a0001c0001t0002g0145 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.32+18815_32+18816i others(12): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117192008 | ||||||
| chr1:117192008
|
G | GATATATA others(5): Show |
1 | a0001c0001t0002g0146 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.32+18815_32+18816i others(14): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117192008 | ||||||
| chr1:117192010
|
T | G | 1 | a0001c0001t0001g0104 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.32+18814A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117192010 | ||||||
| chr1:117192016
|
G | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(201): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.32+18808C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117192016 | ||||||
| chr1:117192028
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.32+18796A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117192028 | ||||||
| chr1:117192057
|
A | G | 9 | a0001c0001t0002g0019a0001c0001t0003g0129a0001c0001t0003g0135others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.32+18767T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117192057 | ||||||
| chr1:117192069
|
G | A | 1 | a0002c0002t0002g0204 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.32+18755C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117192069 | ||||||
| chr1:117192659
|
G | A | 1 | a0001c0001t0004g0101 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.32+18165C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117192659 | ||||||
| chr1:117192925
|
G | T | 12 | a0001c0001t0002g0029a0001c0001t0002g0171a0001c0001t0003g0018others(9): Show | 14 | HG02280.hp2 HG02647.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.32+17899C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117192925 | ||||||
| chr1:117193124
|
T | C | 1 | a0001c0001t0002g0224 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.32+17700A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117193124 | ||||||
| chr1:117193244
|
T | C | 35 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0042others(32): Show | 37 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.32+17580A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117193244 | ||||||
| chr1:117193257
|
C | A | 1 | a0001c0001t0007g0175 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.32+17567G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117193257 | ||||||
| chr1:117193261
|
A | T | 21 | a0001c0001t0001g0122a0001c0001t0001g0138a0001c0001t0002g0050others(18): Show | 21 | HG00741.hp2 HG01243.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.32+17563T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117193261 | ||||||
| chr1:117193349
|
T | C | 30 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0042others(27): Show | 32 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.32+17475A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117193349 | ||||||
| chr1:117193415
|
G | A | 1 | a0001c0001t0016g0240 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.32+17409C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117193415 | ||||||
| chr1:117193577
|
A | AC | 206 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(203): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.32+17246dupG | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117193577 | ||||||
| chr1:117193632
|
A | G | 9 | a0001c0001t0002g0019a0001c0001t0003g0129a0001c0001t0003g0135others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.32+17192T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117193632 | ||||||
| chr1:117193673
|
T | G | 15 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0002g0004others(12): Show | 16 | HG00741.hp1 HG01099.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.32+17151A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117193673 | ||||||
| chr1:117193895
|
T | C | 9 | a0001c0001t0002g0063a0001c0001t0002g0090a0001c0001t0002g0095others(6): Show | 9 | HG01515.hp2 HG02056.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.32+16929A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117193895 | ||||||
| chr1:117193928
|
A | G | 9 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(6): Show | 9 | HG01433.hp1 HG01891.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.32+16896T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117193928 | ||||||
| chr1:117193963
|
A | G | 2 | a0001c0001t0003g0038a0001c0001t0003g0039 | 2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.32+16861T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117193963 | ||||||
| chr1:117194073
|
G | A | 1 | a0001c0001t0004g0154 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.32+16751C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117194073 | ||||||
| chr1:117194114
|
A | G | 5 | a0001c0001t0001g0210a0001c0001t0001g0213a0001c0001t0001g0222others(2): Show | 5 | HG02572.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+16710T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117194114 | ||||||
| chr1:117194192
|
T | C | 1 | a0001c0001t0005g0183 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.32+16632A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117194192 | ||||||
| chr1:117194770
|
A | G | 2 | a0001c0001t0001g0223a0001c0001t0011g0015 | 2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.32+16054T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117194770 | ||||||
| chr1:117194864
|
A | G | 207 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(204): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.32+15960T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117194864 | ||||||
| chr1:117195072
|
C | CCTGA | 81 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0026others(78): Show | 85 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.32+15751_32+15752i others(6): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195072 | ||||||
| chr1:117195114
|
C | T | 81 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0026others(78): Show | 85 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.32+15710G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195114 | ||||||
| chr1:117195170
|
G | A | 1 | a0001c0001t0012g0048 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.32+15654C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195170 | ||||||
| chr1:117195262
|
A | AAAT | 25 | a0001c0001t0001g0084a0001c0001t0001g0112a0001c0001t0001g0157others(22): Show | 25 | HG00642.hp1 HG02056.hp2 HG02083.hp1 others(22): Show |
intron_variant | MODIFIER | c.32+15559_32+15561d others(5): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195262 | ||||||
| chr1:117195262
|
A | AAATAAT | 31 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0042others(28): Show | 34 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.32+15556_32+15561d others(8): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195262 | ||||||
| chr1:117195262
|
A | AAATAATA others(2): Show |
9 | a0001c0001t0001g0156a0001c0001t0001g0167a0001c0001t0001g0176others(6): Show | 10 | HG00621.hp2 HG01192.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.32+15553_32+15561d others(11): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195262 | ||||||
| chr1:117195262
|
AAAT | A | 15 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0049others(12): Show | 15 | HG01099.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.32+15559_32+15561d others(5): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195262 | ||||||
| chr1:117195262
|
AAATAAT | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0031others(104): Show | 111 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.32+15556_32+15561d others(8): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195262 | ||||||
| chr1:117195262
|
AAATAATA others(2): Show |
A | 7 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0201others(4): Show | 7 | HG01433.hp1 HG01891.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+15553_32+15561d others(11): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195262 | ||||||
| chr1:117195312
|
A | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0034a0002c0002t0003g0173 | 3 | HG01884.hp2 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.32+15512T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195312 | ||||||
| chr1:117195357
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.32+15467G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195357 | ||||||
| chr1:117195417
|
G | A | 1 | a0001c0001t0001g0014 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32+15407C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195417 | ||||||
| chr1:117195533
|
C | T | 3 | a0001c0001t0005g0047a0001c0001t0007g0175a0002c0002t0003g0172 | 3 | HG02622.hp1 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.32+15291G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195533 | ||||||
| chr1:117195570
|
T | C | 2 | a0001c0001t0001g0223a0001c0001t0011g0015 | 2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.32+15254A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195570 | ||||||
| chr1:117195670
|
T | A | 1 | a0001c0001t0003g0010 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.32+15154A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195670 | ||||||
| chr1:117195680
|
G | A | 2 | a0001c0001t0004g0119a0001c0001t0004g0181 | 2 | HG02056.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.32+15144C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195680 | ||||||
| chr1:117195890
|
C | T | 1 | a0001c0001t0004g0132 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.32+14934G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195890 | ||||||
| chr1:117195954
|
C | T | 4 | a0001c0001t0001g0051a0001c0001t0001g0057a0001c0001t0001g0070others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+14870G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195954 | ||||||
| chr1:117196015
|
A | G | 113 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0017others(110): Show | 118 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(115): Show |
intron_variant | MODIFIER | c.32+14809T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196015 | ||||||
| chr1:117196091
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0003g0152 | 2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.32+14733C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196091 | ||||||
| chr1:117196118
|
C | T | 14 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0002g0004others(11): Show | 15 | HG00741.hp1 HG01106.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.32+14706G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196118 | ||||||
| chr1:117196193
|
A | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0049others(86): Show | 92 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.32+14631T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196193 | ||||||
| chr1:117196389
|
CAT | C | 12 | a0001c0001t0003g0024a0001c0001t0003g0134a0001c0001t0003g0207others(9): Show | 12 | HG01099.hp1 HG02056.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.32+14433_32+14434d others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196389 | ||||||
| chr1:117196401
|
T | G | 6 | a0001c0001t0001g0097a0001c0001t0001g0158a0001c0001t0001g0167others(3): Show | 7 | HG01192.hp1 HG02257.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+14423A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196401 | ||||||
| chr1:117196401
|
T | TAG | 5 | a0001c0001t0002g0019a0001c0001t0003g0129a0001c0001t0003g0135others(2): Show | 5 | HG02486.hp1 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+14422_32+14423i others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196401 | ||||||
| chr1:117196403
|
T | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(73): Show | 82 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.32+14421A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196403 | ||||||
| chr1:117196403
|
T | TAG | 3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0002g0206 | 3 | HG02083.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.32+14419_32+14420d others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196403 | ||||||
| chr1:117196403
|
TAG | T | 30 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0060others(27): Show | 30 | HG00642.hp1 HG01884.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.32+14419_32+14420d others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196403 | ||||||
| chr1:117196405
|
G | T | 69 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(66): Show | 70 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.32+14419C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196405 | ||||||
| chr1:117196407
|
G | T | 27 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0052others(24): Show | 28 | HG00642.hp1 HG01258.hp1 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.32+14417C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196407 | ||||||
| chr1:117196409
|
G | T | 6 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0080others(3): Show | 6 | HG01258.hp1 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.32+14415C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196409 | ||||||
| chr1:117196425
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0007g0012 | 2 | HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.32+14399G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196425 | ||||||
| chr1:117196480
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.32+14344C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196480 | ||||||
| chr1:117196482
|
T | C | 2 | a0001c0001t0001g0223a0001c0001t0011g0015 | 2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.32+14342A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196482 | ||||||
| chr1:117196580
|
A | T | 1 | a0001c0001t0001g0030 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.32+14244T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196580 | ||||||
| chr1:117196631
|
T | C | 1 | a0001c0001t0003g0135 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.32+14193A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196631 | ||||||
| chr1:117196824
|
A | C | 2 | a0001c0001t0003g0038a0001c0001t0003g0039 | 2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.32+14000T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196824 | ||||||
| chr1:117196919
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.32+13905C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196919 | ||||||
| chr1:117197176
|
G | A | 113 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0026others(110): Show | 116 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.32+13648C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117197176 | ||||||
| chr1:117197190
|
G | A | 1 | a0001c0001t0002g0171 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.32+13634C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117197190 | ||||||
| chr1:117197210
|
G | A | 1 | a0001c0001t0001g0014 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32+13614C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117197210 | ||||||
| chr1:117197224
|
C | T | 113 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0026others(110): Show | 116 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.32+13600G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117197224 | ||||||
| chr1:117197291
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0011g0015 | 2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.32+13533C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117197291 | ||||||
| chr1:117197311
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.32+13513G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117197311 | ||||||
| chr1:117197315
|
T | A | 1 | a0001c0001t0013g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.32+13509A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117197315 | ||||||
| chr1:117197598
|
G | A | 50 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0026others(47): Show | 52 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.32+13226C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117197598 | ||||||
| chr1:117197734
|
C | T | 1 | a0001c0001t0004g0130 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.32+13090G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117197734 | ||||||
| chr1:117197735
|
A | G | 77 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0026others(74): Show | 80 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.32+13089T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117197735 | ||||||
| chr1:117197820
|
T | C | 1 | a0001c0001t0007g0175 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.32+13004A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117197820 | ||||||
| chr1:117198061
|
C | A | 2 | a0001c0001t0004g0147a0001c0001t0004g0148 | 2 | HG01255.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.32+12763G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117198061 | ||||||
| chr1:117198181
|
G | T | 1 | a0001c0001t0003g0024 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.32+12643C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117198181 | ||||||
| chr1:117198418
|
C | A | 31 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(28): Show | 33 | HG00741.hp1 HG01106.hp2 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.32+12406G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117198418 | ||||||
| chr1:117198500
|
G | A | 1 | a0001c0001t0003g0185 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.32+12324C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117198500 | ||||||
| chr1:117198508
|
C | T | 8 | a0001c0001t0002g0171a0001c0001t0005g0006a0001c0001t0005g0007others(5): Show | 10 | HG02145.hp1 HG02280.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.32+12316G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117198508 | ||||||
| chr1:117198517
|
C | G | 1 | a0001c0001t0001g0164 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.32+12307G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117198517 | ||||||
| chr1:117198633
|
C | T | 199 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(196): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.32+12191G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117198633 | ||||||
| chr1:117198841
|
C | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(196): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.32+11983G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117198841 | ||||||
| chr1:117198913
|
G | A | 19 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0002g0011others(16): Show | 19 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.32+11911C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117198913 | ||||||
| chr1:117199098
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.32+11726C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117199098 | ||||||
| chr1:117199177
|
T | A | 1 | a0001c0001t0003g0134 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.32+11647A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117199177 | ||||||
| chr1:117199225
|
C | CTTCT | 199 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(196): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.32+11598_32+11599i others(6): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117199225 | ||||||
| chr1:117199314
|
A | G | 7 | a0001c0001t0002g0171a0001c0001t0005g0006a0001c0001t0005g0007others(4): Show | 9 | HG02280.hp2 HG02647.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.32+11510T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117199314 | ||||||
| chr1:117199421
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.32+11403C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117199421 | ||||||
| chr1:117199446
|
C | T | 157 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(154): Show | 163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.32+11378G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117199446 | ||||||
| chr1:117199605
|
C | T | 16 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0163others(13): Show | 16 | HG00642.hp1 HG01433.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.32+11219G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117199605 | ||||||
| chr1:117199611
|
C | T | 1 | a0001c0001t0001g0014 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32+11213G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117199611 | ||||||
| chr1:117199633
|
A | AT | 12 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0026others(9): Show | 12 | HG02055.hp2 HG02109.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.32+11190dupA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117199633 | ||||||
| chr1:117199633
|
AT | A | 8 | a0001c0001t0001g0044a0001c0001t0001g0099a0001c0001t0001g0100others(5): Show | 8 | HG00323.hp1 HG01943.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.32+11190delA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117199633 | ||||||
| chr1:117199776
|
C | T | 12 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0002g0032others(9): Show | 12 | HG00741.hp1 HG01106.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.32+11048G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117199776 | ||||||
| chr1:117199895
|
A | C | 1 | a0001c0001t0007g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.32+10929T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117199895 | ||||||
| chr1:117200130
|
A | T | 1 | a0001c0001t0002g0005 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.32+10694T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117200130 | ||||||
| chr1:117200240
|
T | C | 3 | a0001c0001t0001g0069a0001c0001t0001g0113a0001c0001t0001g0114 | 3 | NA18939.hp1 NA18999.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.32+10584A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117200240 | ||||||
| chr1:117200449
|
A | T | 1 | a0002c0002t0002g0221 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.32+10375T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117200449 | ||||||
| chr1:117200494
|
C | T | 1 | a0001c0001t0003g0134 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.32+10330G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117200494 | ||||||
| chr1:117200569
|
C | G | 2 | a0001c0001t0011g0015a0002c0002t0002g0204 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.32+10255G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117200569 | ||||||
| chr1:117200581
|
T | A | 2 | a0001c0001t0011g0015a0002c0002t0002g0204 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.32+10243A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117200581 | ||||||
| chr1:117200586
|
C | T | 1 | a0001c0001t0003g0024 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.32+10238G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117200586 | ||||||
| chr1:117200704
|
C | T | 2 | a0001c0001t0001g0213a0001c0001t0001g0222 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.32+10120G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117200704 | ||||||
| chr1:117200824
|
C | T | 1 | a0002c0002t0002g0221 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.32+10000G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117200824 | ||||||
| chr1:117200858
|
C | A | 1 | a0001c0001t0012g0048 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.32+9966G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117200858 | ||||||
| chr1:117200979
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.32+9845C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117200979 | ||||||
| chr1:117201086
|
T | G | 2 | a0001c0001t0011g0015a0002c0002t0002g0204 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.32+9738A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117201086 | ||||||
| chr1:117201346
|
G | A | 3 | a0001c0001t0003g0174a0002c0002t0003g0172a0002c0002t0003g0173 | 3 | HG01884.hp2 HG02109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.32+9478C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117201346 | ||||||
| chr1:117201360
|
T | C | 3 | a0001c0001t0001g0153a0001c0001t0003g0151a0001c0001t0003g0152 | 3 | HG02486.hp1 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.32+9464A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117201360 | ||||||
| chr1:117201531
|
T | C | 1 | a0001c0001t0002g0146 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.32+9293A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117201531 | ||||||
| chr1:117201534
|
G | A | 1 | a0001c0001t0003g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.32+9290C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117201534 | ||||||
| chr1:117201641
|
A | T | 4 | a0001c0001t0003g0024a0001c0001t0003g0174a0002c0002t0003g0172others(1): Show | 4 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+9183T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117201641 | ||||||
| chr1:117201642
|
C | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(2): Show | 5 | HG02451.hp1 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+9182G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117201642 | ||||||
| chr1:117201682
|
A | G | 8 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0003g0024others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.32+9142T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117201682 | ||||||
| chr1:117201791
|
C | G | 1 | a0001c0001t0004g0130 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.32+9033G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117201791 | ||||||
| chr1:117201823
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.32+9001A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117201823 | ||||||
| chr1:117201855
|
T | C | 1 | a0001c0001t0003g0024 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.32+8969A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117201855 | ||||||
| chr1:117202027
|
C | G | 1 | a0001c0001t0001g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.32+8797G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117202027 | ||||||
| chr1:117202188
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.32+8636T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117202188 | ||||||
| chr1:117202316
|
C | T | 7 | a0001c0001t0002g0171a0001c0001t0003g0185a0001c0001t0005g0006others(4): Show | 9 | HG02280.hp2 HG02647.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.32+8508G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117202316 | ||||||
| chr1:117202330
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.32+8494G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117202330 | ||||||
| chr1:117202396
|
G | C | 1 | a0002c0002t0002g0221 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.32+8428C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117202396 | ||||||
| chr1:117202538
|
A | G | 4 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0005g0016others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+8286T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117202538 | ||||||
| chr1:117202861
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0005g0016 | 3 | HG02647.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.32+7963C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117202861 | ||||||
| chr1:117203088
|
C | G | 1 | a0001c0001t0001g0216 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.32+7736G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203088 | ||||||
| chr1:117203203
|
T | A | 8 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(5): Show | 8 | HG00642.hp1 HG01943.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.32+7621A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203203 | ||||||
| chr1:117203325
|
T | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(235): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.32+7499A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203325 | ||||||
| chr1:117203390
|
C | T | 2 | a0001c0001t0002g0074a0001c0001t0002g0075 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.32+7434G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203390 | ||||||
| chr1:117203428
|
T | C | 3 | a0001c0001t0003g0174a0002c0002t0003g0172a0002c0002t0003g0173 | 3 | HG01884.hp2 HG02109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.32+7396A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203428 | ||||||
| chr1:117203460
|
AAG | A | 4 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0005g0016others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+7362_32+7363del others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203460 | ||||||
| chr1:117203534
|
G | C | 19 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0034others(16): Show | 19 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.32+7290C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203534 | ||||||
| chr1:117203583
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.32+7241G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203583 | ||||||
| chr1:117203589
|
C | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0049others(111): Show | 118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.32+7235G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203589 | ||||||
| chr1:117203660
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.32+7164G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203660 | ||||||
| chr1:117203781
|
A | C | 1 | a0001c0001t0001g0051 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.32+7043T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203781 | ||||||
| chr1:117203783
|
C | A | 4 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0005g0016others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+7041G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203783 | ||||||
| chr1:117203951
|
C | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0017others(156): Show | 163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.32+6873G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203951 | ||||||
| chr1:117204017
|
G | A | 68 | a0001c0001t0001g0017a0001c0001t0001g0030a0001c0001t0001g0031others(65): Show | 69 | HG00642.hp2 HG00741.hp1 HG01099.hp1 others(66): Show |
intron_variant | MODIFIER | c.32+6807C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204017 | ||||||
| chr1:117204019
|
A | G | 2 | a0001c0001t0005g0047a0001c0001t0012g0048 | 2 | HG02145.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.32+6805T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204019 | ||||||
| chr1:117204046
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0005g0016others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+6778C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204046 | ||||||
| chr1:117204048
|
T | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0072others(3): Show | 7 | HG00280.hp2 HG01106.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+6776A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204048 | ||||||
| chr1:117204049
|
G | A | 238 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(235): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.32+6775C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204049 | ||||||
| chr1:117204169
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0005g0016others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+6655G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204169 | ||||||
| chr1:117204472
|
T | A | 23 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0034others(20): Show | 23 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.32+6352A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204472 | ||||||
| chr1:117204489
|
T | C | 8 | a0001c0001t0002g0011a0001c0001t0002g0220a0001c0001t0003g0010others(5): Show | 8 | HG02055.hp1 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.32+6335A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204489 | ||||||
| chr1:117204531
|
T | C | 4 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0005g0016others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+6293A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204531 | ||||||
| chr1:117204594
|
C | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(2): Show | 5 | HG02451.hp1 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+6230G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204594 | ||||||
| chr1:117204598
|
G | T | 7 | a0001c0001t0002g0171a0001c0001t0003g0185a0001c0001t0005g0006others(4): Show | 9 | HG02280.hp2 HG02647.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.32+6226C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204598 | ||||||
| chr1:117204642
|
G | A | 3 | a0001c0001t0003g0174a0002c0002t0003g0172a0002c0002t0003g0173 | 3 | HG01884.hp2 HG02109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.32+6182C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204642 | ||||||
| chr1:117204662
|
G | T | 4 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0005g0016others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+6162C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204662 | ||||||
| chr1:117204726
|
T | C | 4 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0005g0016others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+6098A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204726 | ||||||
| chr1:117204814
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0072others(3): Show | 7 | HG00280.hp2 HG01106.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+6010G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204814 | ||||||
| chr1:117204840
|
TGGGCAAC others(5): Show |
T | 186 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0030others(183): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.32+5972_32+5983del others(12): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204840 | ||||||
| chr1:117204971
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.32+5853G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204971 | ||||||
| chr1:117205009
|
T | TACGCATA others(29): Show |
4 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0005g0016others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+5814_32+5815ins others(36): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205009 | ||||||
| chr1:117205021
|
TAC | T | 4 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0005g0016others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+5801_32+5802del others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205021 | ||||||
| chr1:117205025
|
C | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0030others(183): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.32+5799G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205025 | ||||||
| chr1:117205028
|
A | G | 4 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0005g0016others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+5796T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205028 | ||||||
| chr1:117205063
|
A | G | 4 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0005g0016others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+5761T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205063 | ||||||
| chr1:117205078
|
CATGTATA others(7): Show |
C | 186 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0030others(183): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.32+5732_32+5745del others(14): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205078 | ||||||
| chr1:117205081
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0005g0016others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+5743C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205081 | ||||||
| chr1:117205087
|
GTATGTAT others(3): Show |
G | 3 | a0001c0001t0003g0174a0002c0002t0003g0172a0002c0002t0003g0173 | 3 | HG01884.hp2 HG02109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.32+5727_32+5736del others(10): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205087 | ||||||
| chr1:117205127
|
A | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(209): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.32+5697T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205127 | ||||||
| chr1:117205136
|
A | G | 2 | a0001c0001t0001g0223a0002c0002t0002g0221 | 2 | HG06807.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.32+5688T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205136 | ||||||
| chr1:117205142
|
T | TTATA | 4 | a0001c0001t0001g0051a0001c0001t0001g0057a0001c0001t0001g0070others(1): Show | 4 | HG02145.hp2 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+5681_32+5682ins others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205142 | ||||||
| chr1:117205144
|
T | A | 13 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0051others(10): Show | 13 | HG01261.hp1 HG02004.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.32+5680A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205144 | ||||||
| chr1:117205144
|
T | TTA | 39 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(36): Show | 41 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.32+5678_32+5679dup others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205144 | ||||||
| chr1:117205144
|
T | TTATA | 56 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0034others(53): Show | 56 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.32+5676_32+5679dup others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205144 | ||||||
| chr1:117205149
|
TATATATA others(18): Show |
T | 4 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0005g0016others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+5650_32+5674del others(25): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205149 | ||||||
| chr1:117205155
|
T | G | 1 | a0001c0001t0004g0101 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.32+5669A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205155 | ||||||
| chr1:117205155
|
T | TAG | 10 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0141others(7): Show | 11 | HG02257.hp2 HG02572.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+5668_32+5669ins others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205155 | ||||||
| chr1:117205157
|
T | G | 16 | a0001c0001t0001g0071a0001c0001t0001g0180a0001c0001t0002g0206others(13): Show | 17 | HG01261.hp1 HG02083.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.32+5667A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205157 | ||||||
| chr1:117205157
|
T | TAG | 13 | a0001c0001t0001g0138a0001c0001t0001g0144a0001c0001t0001g0153others(10): Show | 13 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.32+5665_32+5666dup others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205157 | ||||||
| chr1:117205157
|
T | TAGAG | 14 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0106others(11): Show | 14 | HG00140.hp2 HG01192.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.32+5663_32+5666dup others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205157 | ||||||
| chr1:117205157
|
T | TATAG | 48 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0049others(45): Show | 51 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.32+5666_32+5667ins others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205157 | ||||||
| chr1:117205157
|
T | TATATAG | 3 | a0001c0001t0005g0047a0001c0001t0006g0235a0001c0001t0012g0048 | 3 | HG01515.hp2 HG02145.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.32+5666_32+5667ins others(6): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205157 | ||||||
| chr1:117205159
|
G | T | 96 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0022others(93): Show | 98 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.32+5665C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205159 | ||||||
| chr1:117205161
|
G | T | 35 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0022others(32): Show | 35 | HG00621.hp1 HG00741.hp1 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.32+5663C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205161 | ||||||
| chr1:117205163
|
G | T | 8 | a0001c0001t0001g0034a0001c0001t0001g0213a0001c0001t0002g0032others(5): Show | 8 | HG01255.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.32+5661C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205163 | ||||||
| chr1:117205176
|
A | G | 7 | a0001c0001t0001g0017a0001c0001t0001g0150a0001c0001t0002g0050others(4): Show | 7 | HG02004.hp1 HG02056.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+5648T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205176 | ||||||
| chr1:117205181
|
G | C | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | NA18939.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.32+5643C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205181 | ||||||
| chr1:117205190
|
C | T | 163 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0049others(160): Show | 169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.32+5634G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205190 | ||||||
| chr1:117205218
|
C | G | 4 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0005g0016others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+5606G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205218 | ||||||
| chr1:117205244
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0005g0016others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+5580G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205244 | ||||||
| chr1:117205251
|
G | C | 4 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0005g0016others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+5573C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205251 | ||||||
| chr1:117205360
|
A | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0017others(187): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.32+5464T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205360 | ||||||
| chr1:117205405
|
C | T | 23 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0034others(20): Show | 23 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.32+5419G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205405 | ||||||
| chr1:117205467
|
T | C | 3 | a0001c0001t0003g0207a0001c0001t0003g0208a0001c0001t0003g0209 | 3 | HG02630.hp2 HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.32+5357A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205467 | ||||||
| chr1:117205550
|
A | G | 1 | a0001c0001t0009g0225 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.32+5274T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205550 | ||||||
| chr1:117205884
|
A | T | 4 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0005g0016others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+4940T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205884 | ||||||
| chr1:117205886
|
C | T | 1 | a0001c0001t0013g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.32+4938G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205886 | ||||||
| chr1:117205949
|
C | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0030others(183): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.32+4875G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205949 | ||||||
| chr1:117206148
|
AT | A | 22 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0022others(19): Show | 24 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.32+4675delA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206148 | ||||||
| chr1:117206148
|
ATT | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0030others(167): Show | 175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.32+4674_32+4675del others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206148 | ||||||
| chr1:117206148
|
ATTT | A | 16 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(13): Show | 17 | HG00408.hp2 HG00621.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.32+4673_32+4675del others(3): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206148 | ||||||
| chr1:117206176
|
C | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(2): Show | 5 | HG02451.hp1 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+4648G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206176 | ||||||
| chr1:117206203
|
A | C | 1 | a0001c0001t0014g0149 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.32+4621T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206203 | ||||||
| chr1:117206308
|
T | A | 2 | a0001c0001t0003g0215a0002c0002t0003g0214 | 2 | HG01433.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.32+4516A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206308 | ||||||
| chr1:117206408
|
A | G | 1 | a0001c0001t0014g0149 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.32+4416T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206408 | ||||||
| chr1:117206497
|
T | C | 3 | a0001c0001t0001g0014a0001c0001t0007g0012a0001c0001t0007g0013 | 3 | HG02723.hp1 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.32+4327A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206497 | ||||||
| chr1:117206576
|
C | T | 3 | a0001c0001t0007g0127a0001c0001t0007g0136a0001c0001t0008g0126 | 3 | HG02055.hp1 HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.32+4248G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206576 | ||||||
| chr1:117206585
|
C | G | 3 | a0001c0001t0001g0223a0001c0001t0003g0024a0002c0002t0002g0221 | 3 | HG02109.hp2 HG06807.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.32+4239G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206585 | ||||||
| chr1:117206608
|
G | A | 1 | a0001c0001t0007g0136 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.32+4216C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206608 | ||||||
| chr1:117206645
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0005g0016 | 3 | HG02647.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.32+4179G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206645 | ||||||
| chr1:117206669
|
T | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0017others(204): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.32+4155A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206669 | ||||||
| chr1:117206670
|
C | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0017others(204): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.32+4154G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206670 | ||||||
| chr1:117206671
|
T | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0017others(204): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.32+4153A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206671 | ||||||
| chr1:117206672
|
G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0017others(204): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.32+4152C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206672 | ||||||
| chr1:117206673
|
TTGA | T | 207 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0017others(204): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.32+4148_32+4150del others(3): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206673 | ||||||
| chr1:117206677
|
T | G | 207 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0017others(204): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.32+4147A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206677 | ||||||
| chr1:117206845
|
A | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(209): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.32+3979T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206845 | ||||||
| chr1:117206959
|
T | C | 1 | a0001c0001t0015g0239 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.32+3865A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206959 | ||||||
| chr1:117207069
|
G | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0115 | 3 | HG01257.hp2 HG03704.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.32+3755C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207069 | ||||||
| chr1:117207135
|
T | C | 1 | a0001c0001t0006g0238 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.32+3689A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207135 | ||||||
| chr1:117207147
|
G | A | 3 | a0001c0001t0001g0210a0001c0001t0010g0211a0001c0001t0010g0212 | 3 | HG02895.hp1 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.32+3677C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207147 | ||||||
| chr1:117207149
|
A | G | 3 | a0001c0001t0001g0223a0001c0001t0003g0024a0002c0002t0002g0221 | 3 | HG02109.hp2 HG06807.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.32+3675T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207149 | ||||||
| chr1:117207187
|
C | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0017others(187): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.32+3637G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207187 | ||||||
| chr1:117207224
|
A | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0030others(183): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.32+3600T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207224 | ||||||
| chr1:117207323
|
G | A | 1 | a0001c0001t0001g0014 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32+3501C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207323 | ||||||
| chr1:117207334
|
T | C | 1 | a0001c0001t0007g0175 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.32+3490A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207334 | ||||||
| chr1:117207393
|
A | G | 4 | a0001c0001t0001g0014a0001c0001t0007g0012a0001c0001t0007g0013others(1): Show | 4 | HG02723.hp1 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+3431T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207393 | ||||||
| chr1:117207532
|
C | T | 1 | a0001c0001t0015g0239 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.32+3292G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207532 | ||||||
| chr1:117207565
|
C | T | 10 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(7): Show | 10 | HG00621.hp1 HG00741.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.32+3259G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207565 | ||||||
| chr1:117207773
|
T | C | 6 | a0001c0001t0001g0144a0001c0001t0001g0153a0001c0001t0002g0145others(3): Show | 6 | HG02486.hp1 HG03130.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.32+3051A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207773 | ||||||
| chr1:117207989
|
C | T | 237 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(234): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.32+2835G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207989 | ||||||
| chr1:117207990
|
G | T | 1 | a0001c0001t0004g0118 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.32+2834C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207990 | ||||||
| chr1:117208064
|
C | T | 45 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(42): Show | 47 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.32+2760G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208064 | ||||||
| chr1:117208097
|
A | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0017others(116): Show | 123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.32+2727T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208097 | ||||||
| chr1:117208170
|
C | T | 2 | a0001c0001t0003g0117a0001c0001t0004g0116 | 2 | HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.32+2654G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208170 | ||||||
| chr1:117208177
|
T | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0017others(185): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.32+2647A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208177 | ||||||
| chr1:117208195
|
G | C | 1 | a0001c0001t0001g0222 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.32+2629C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208195 | ||||||
| chr1:117208245
|
A | G | 7 | a0001c0001t0002g0171a0001c0001t0003g0185a0001c0001t0005g0006others(4): Show | 9 | HG02280.hp2 HG02647.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.32+2579T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208245 | ||||||
| chr1:117208249
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.32+2575T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208249 | ||||||
| chr1:117208326
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.32+2498T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208326 | ||||||
| chr1:117208342
|
A | G | 1 | a0001c0001t0002g0005 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.32+2482T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208342 | ||||||
| chr1:117208383
|
A | G | 4 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0005g0016others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+2441T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208383 | ||||||
| chr1:117208409
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0005g0016others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+2415G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208409 | ||||||
| chr1:117208442
|
A | C | 2 | a0001c0001t0005g0047a0001c0001t0012g0048 | 2 | HG02145.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.32+2382T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208442 | ||||||
| chr1:117208743
|
C | T | 45 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(42): Show | 47 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.32+2081G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208743 | ||||||
| chr1:117208824
|
A | C | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(6): Show | 9 | HG02258.hp1 HG02451.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.32+2000T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208824 | ||||||
| chr1:117208894
|
A | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0017others(185): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.32+1930T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208894 | ||||||
| chr1:117209089
|
G | A | 2 | a0001c0001t0002g0168a0001c0001t0003g0169 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.32+1735C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209089 | ||||||
| chr1:117209103
|
C | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0049others(93): Show | 99 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.32+1721G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209103 | ||||||
| chr1:117209114
|
G | A | 18 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0034others(15): Show | 18 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.32+1710C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209114 | ||||||
| chr1:117209129
|
G | A | 1 | a0001c0001t0003g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.32+1695C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209129 | ||||||
| chr1:117209145
|
C | T | 238 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(235): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.32+1679G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209145 | ||||||
| chr1:117209241
|
T | G | 1 | a0001c0001t0002g0170 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.32+1583A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209241 | ||||||
| chr1:117209278
|
C | T | 2 | a0001c0001t0005g0047a0001c0001t0012g0048 | 2 | HG02145.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.32+1546G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209278 | ||||||
| chr1:117209380
|
T | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(234): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.32+1444A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209380 | ||||||
| chr1:117209389
|
A | G | 4 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0005g0016others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+1435T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209389 | ||||||
| chr1:117209430
|
G | T | 26 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(23): Show | 26 | HG00642.hp1 HG01891.hp2 HG01943.hp1 others(23): Show |
intron_variant | MODIFIER | c.32+1394C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209430 | ||||||
| chr1:117209483
|
T | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(188): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.32+1341A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209483 | ||||||
| chr1:117209488
|
C | A | 1 | a0001c0001t0014g0149 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.32+1336G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209488 | ||||||
| chr1:117209604
|
A | G | 1 | a0001c0001t0011g0015 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.32+1220T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209604 | ||||||
| chr1:117209723
|
C | T | 2 | a0001c0001t0004g0045a0001c0001t0004g0046 | 2 | HG01928.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.32+1101G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209723 | ||||||
| chr1:117209849
|
C | A | 1 | a0001c0001t0001g0150 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.32+975G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209849 | ||||||
| chr1:117209859
|
G | A | 233 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(230): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.32+965C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209859 | ||||||
| chr1:117209876
|
G | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0049others(157): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.32+948C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209876 | ||||||
| chr1:117209975
|
G | T | 1 | a0001c0001t0013g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.32+849C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209975 | ||||||
| chr1:117210091
|
T | A | 1 | a0001c0001t0002g0224 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.32+733A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210091 | ||||||
| chr1:117210137
|
G | A | 3 | a0001c0001t0001g0153a0001c0001t0003g0151a0001c0001t0003g0152 | 3 | HG02486.hp1 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.32+687C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210137 | ||||||
| chr1:117210212
|
T | TCAG | 20 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(17): Show | 21 | HG00408.hp2 HG01175.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.32+609_32+611dupCT others(1): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210212 | ||||||
| chr1:117210212
|
T | TCAGCAG | 9 | a0001c0001t0001g0014a0001c0001t0001g0176a0001c0001t0002g0171others(6): Show | 9 | HG00621.hp2 HG01884.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.32+606_32+611dupCT others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210212 | ||||||
| chr1:117210212
|
T | TCAGCAGC others(2): Show |
18 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(15): Show | 21 | HG00642.hp1 HG01943.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.32+603_32+611dupCT others(7): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210212 | ||||||
| chr1:117210212
|
T | TCAGCAGC others(5): Show |
21 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(18): Show | 21 | HG01891.hp2 HG02083.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.32+600_32+611dupCT others(10): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210212 | ||||||
| chr1:117210212
|
T | TCAGCAGC others(8): Show |
3 | a0001c0001t0001g0213a0001c0001t0001g0222a0002c0002t0002g0221 | 3 | HG02572.hp1 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.32+597_32+611dupCT others(13): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210212 | ||||||
| chr1:117210212
|
T | TCAGCAGC others(11): Show |
1 | a0001c0001t0001g0223 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.32+594_32+611dupCT others(16): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210212 | ||||||
| chr1:117210212
|
TCAGCAG | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.32+606_32+611delCT others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210212 | ||||||
| chr1:117210212
|
TCAGCAGC others(2): Show |
T | 4 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0005g0016others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+603_32+611delCT others(7): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210212 | ||||||
| chr1:117210315
|
G | A | 2 | a0001c0001t0003g0215a0002c0002t0003g0214 | 2 | HG01433.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.32+509C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210315 | ||||||
| chr1:117210354
|
A | G | 3 | a0001c0001t0001g0014a0001c0001t0007g0012a0001c0001t0007g0013 | 3 | HG02723.hp1 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.32+470T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210354 | ||||||
| chr1:117210435
|
C | T | 2 | a0001c0001t0002g0011a0001c0001t0003g0010 | 2 | HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.32+389G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210435 | ||||||
| chr1:117210468
|
C | A | 4 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(1): Show | 4 | HG01175.hp1 HG03491.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+356G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210468 | ||||||
| chr1:117210493
|
C | A | 1 | a0001c0001t0002g0220 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.32+331G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210493 | ||||||
| chr1:117210540
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.32+284G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210540 | ||||||
| chr1:117210546
|
C | A | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0002c0002t0002g0221 | 3 | HG03139.hp2 HG06807.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.32+278G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210546 | ||||||
| chr1:117210573
|
G | A | 1 | a0001c0001t0002g0224 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.32+251C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210573 |