Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 7447 |
|---|---|
| ensemblid | ENSG00000163032.12 |
| hgncid | 12722 |
| symbol | VSNL1 |
| name | visinin like 1 |
| refseq_nuc | NM_003385.5 |
| refseq_prot | NP_003376.2 |
| ensembl_nuc | ENST00000295156.9 |
| ensembl_prot | ENSP00000295156.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 17540696 |
| end | 17657018 |
| strand | + |
| ver | v1.2 |
| region | chr2:17540696-17657018 |
| region5000 | chr2:17535696-17662018 |
| regionname0 | VSNL1_chr2_17540696_17657018 |
| regionname5000 | VSNL1_chr2_17535696_17662018 |
| 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 | 191 | 232 | 82 | 54 | 54 | 16 | 24 | 36 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| 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 | 576 | 232 | 82 | 54 | 54 | 16 | 24 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| 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 | 1849 | 40 | 3 | 8 | 26 | 0 | 3 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0002 | 0/0 | 1857 | 19 | 1 | 6 | 2 | 6 | 4 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0003 | 0/0 | 1857 | 13 | 6 | 5 | 1 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0004 | 0/0 | 1855 | 12 | 8 | 1 | 0 | 2 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0005 | 0/0 | 1853 | 11 | 8 | 3 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0006 | 1/0 | 1853 | 10 | 0 | 4 | 2 | 2 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0007 | 0/0 | 1852 | 9 | 6 | 3 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0008 | 0/0 | 1849 | 8 | 7 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0009 | 0/0 | 1855 | 8 | 0 | 2 | 4 | 1 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0010 | 0/0 | 1845 | 7 | 6 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0011 | 0/0 | 1848 | 7 | 1 | 4 | 0 | 0 | 2 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0012 | 0/0 | 1859 | 7 | 0 | 0 | 3 | 0 | 4 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0013 | 0/1 | 1861 | 7 | 0 | 5 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0014 | 0/0 | 1859 | 6 | 1 | 2 | 2 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0015 | 0/0 | 1851 | 5 | 0 | 2 | 1 | 1 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0016 | 0/0 | 1853 | 5 | 1 | 1 | 3 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0017 | 0/0 | 1857 | 5 | 5 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0018 | 0/0 | 1861 | 5 | 0 | 0 | 5 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0019 | 0/0 | 1847 | 4 | 1 | 1 | 1 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0020 | 0/0 | 1847 | 4 | 4 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0021 | 0/0 | 1850 | 4 | 3 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0022 | 0/0 | 1847 | 3 | 3 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0023 | 0/0 | 1851 | 3 | 3 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0024 | 0/0 | 1855 | 3 | 2 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0025 | 0/0 | 1857 | 3 | 2 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0026 | 0/0 | 1849 | 2 | 1 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0027 | 0/0 | 1851 | 2 | 0 | 1 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0028 | 0/0 | 1850 | 2 | 0 | 1 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0029 | 0/0 | 1860 | 2 | 2 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0030 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0031 | 0/0 | 1841 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0032 | 0/0 | 1838 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0033 | 0/0 | 1846 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0034 | 0/0 | 1846 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0035 | 0/0 | 1853 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0036 | 0/0 | 1853 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0037 | 0/0 | 1855 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0038 | 0/0 | 1850 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0039 | 0/0 | 1857 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0040 | 0/0 | 1859 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0041 | 0/0 | 1864 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0042 | 0/0 | 1862 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0043 | 0/0 | 1864 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0044 | 0/0 | 1857 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| t0045 | 0/0 | 1853 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| 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 | 2 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0069 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0225 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| 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 | 576 | 232 | 82 | 54 | 54 | 16 | 24 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2424 | 40 | 3 | 8 | 26 | 0 | 3 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0002 | 0/0 | 2432 | 19 | 1 | 6 | 2 | 6 | 4 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0003 | 0/0 | 2432 | 13 | 6 | 5 | 1 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0004 | 0/0 | 2430 | 12 | 8 | 1 | 0 | 2 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0005 | 0/0 | 2428 | 11 | 8 | 3 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0006 | 1/0 | 2428 | 10 | 0 | 4 | 2 | 2 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0007 | 0/0 | 2427 | 9 | 6 | 3 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0008 | 0/0 | 2424 | 8 | 7 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0009 | 0/0 | 2430 | 8 | 0 | 2 | 4 | 1 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0010 | 0/0 | 2420 | 7 | 6 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0011 | 0/0 | 2423 | 7 | 1 | 4 | 0 | 0 | 2 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0012 | 0/0 | 2434 | 7 | 0 | 0 | 3 | 0 | 4 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0013 | 0/1 | 2436 | 7 | 0 | 5 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0014 | 0/0 | 2434 | 6 | 1 | 2 | 2 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0015 | 0/0 | 2426 | 5 | 0 | 2 | 1 | 1 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0016 | 0/0 | 2428 | 5 | 1 | 1 | 3 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0017 | 0/0 | 2432 | 5 | 5 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0018 | 0/0 | 2436 | 5 | 0 | 0 | 5 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0019 | 0/0 | 2422 | 4 | 1 | 1 | 1 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0020 | 0/0 | 2422 | 4 | 4 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0021 | 0/0 | 2425 | 4 | 3 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0022 | 0/0 | 2422 | 3 | 3 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0023 | 0/0 | 2426 | 3 | 3 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0024 | 0/0 | 2430 | 3 | 2 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0025 | 0/0 | 2432 | 3 | 2 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0026 | 0/0 | 2424 | 2 | 1 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0027 | 0/0 | 2426 | 2 | 0 | 1 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0028 | 0/0 | 2425 | 2 | 0 | 1 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0029 | 0/0 | 2435 | 2 | 2 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0030 | 0/0 | 2414 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0031 | 0/0 | 2416 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0032 | 0/0 | 2413 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0033 | 0/0 | 2421 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0034 | 0/0 | 2421 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0035 | 0/0 | 2428 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0036 | 0/0 | 2428 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0037 | 0/0 | 2430 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0038 | 0/0 | 2425 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0039 | 0/0 | 2432 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0040 | 0/0 | 2434 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0041 | 0/0 | 2439 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0042 | 0/0 | 2437 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0043 | 0/0 | 2439 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0044 | 0/0 | 2432 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| a0001c0001t0045 | 0/0 | 2428 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | copy fasta | chr2 | 17535696 | 17662018 |
| 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 | 2 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0004g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0004g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0005g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0005g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0005g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0006g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0006g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0006g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0006g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0006g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0006g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0006g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0006g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0006g0225 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0007g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0007g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0007g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0007g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0007g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0008g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0008g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0008g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0008g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0008g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0008g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0008g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0008g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0009g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0009g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0009g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0009g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0009g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0009g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0009g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0009g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0010g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0010g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0010g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0010g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0010g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0010g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0010g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0011g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0011g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0011g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0011g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0011g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0011g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0011g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0012g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0012g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0012g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0012g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0012g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0012g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0012g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0013g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0013g0069 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0013g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0013g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0013g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0013g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0013g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0014g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0014g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0014g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0014g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0014g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0014g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0015g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0015g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0015g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0015g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0015g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0016g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0016g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0016g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0016g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0016g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0017g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0017g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0017g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0017g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0017g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0018g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0018g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0018g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0018g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0019g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0019g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0019g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0019g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0020g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0020g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0020g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0020g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0021g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0021g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0021g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0021g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0022g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0022g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0022g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0023g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0023g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0023g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0024g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0024g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0024g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0025g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0025g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0025g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0026g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0026g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0027g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0027g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0028g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0028g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0029g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0029g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0030g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0031g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0032g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0033g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0034g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0035g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0036g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0037g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0038g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0039g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0040g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0041g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0042g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0043g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0044g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| a0001c0001t0045g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0006 | g0056 | EUR | GBR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0161 | EUR | GBR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG00140 | hp1 | a0001 | c0001 | t0027 | g0026 | EUR | GBR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG00140 | hp2 | a0001 | c0001 | t0015 | g0109 | EUR | GBR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0157 | EUR | FIN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0019 | EUR | FIN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG00323 | hp1 | a0001 | c0001 | t0009 | g0044 | EUR | FIN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG00323 | hp2 | a0001 | c0001 | t0013 | g0070 | EUR | FIN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG00408 | hp1 | a0001 | c0001 | t0006 | g0191 | EAS | CHS | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG00438 | hp2 | a0001 | c0001 | t0009 | g0176 | EAS | CHS | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG00639 | hp1 | a0001 | c0001 | t0011 | g0200 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG00639 | hp2 | a0001 | c0001 | t0016 | g0168 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG00642 | hp1 | a0001 | c0001 | t0009 | g0028 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG00642 | hp2 | a0001 | c0001 | t0006 | g0185 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0088 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0071 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG00738 | hp2 | a0001 | c0001 | t0006 | g0016 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG00741 | hp1 | a0001 | c0001 | t0015 | g0014 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01069 | hp1 | a0001 | c0001 | t0007 | g0111 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01069 | hp2 | a0001 | c0001 | t0006 | g0197 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01070 | hp2 | a0001 | c0001 | t0011 | g0101 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0112 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01074 | hp2 | a0001 | c0001 | t0011 | g0199 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01099 | hp1 | a0001 | c0001 | t0014 | g0224 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0104 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01109 | hp2 | a0001 | c0001 | t0008 | g0120 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0017 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01175 | hp1 | a0001 | c0001 | t0009 | g0083 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01175 | hp2 | a0001 | c0001 | t0027 | g0013 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01192 | hp1 | a0001 | c0001 | t0013 | g0074 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0020 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01243 | hp1 | a0001 | c0001 | t0043 | g0220 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01243 | hp2 | a0001 | c0001 | t0015 | g0041 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01256 | hp1 | a0001 | c0001 | t0013 | g0072 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01256 | hp2 | a0001 | c0001 | t0019 | g0182 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01257 | hp1 | a0001 | c0001 | t0013 | g0095 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0025 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01258 | hp1 | a0001 | c0001 | t0013 | g0073 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0024 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0206 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01358 | hp2 | a0001 | c0001 | t0013 | g0068 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01433 | hp1 | a0001 | c0001 | t0014 | g0089 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01433 | hp2 | a0001 | c0001 | t0011 | g0110 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01496 | hp1 | a0001 | c0001 | t0034 | g0108 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01496 | hp2 | a0001 | c0001 | t0041 | g0096 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0147 | EUR | IBS | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0085 | EUR | IBS | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0146 | EUR | IBS | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0015 | EUR | IBS | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0213 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01891 | hp2 | a0001 | c0001 | t0017 | g0081 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01934 | hp2 | a0001 | c0001 | t0021 | g0201 | AMR | PEL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01981 | hp1 | a0001 | c0001 | t0028 | g0032 | AMR | PEL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0086 | AMR | PEL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0087 | AMR | PEL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02015 | hp2 | a0001 | c0001 | t0006 | g0173 | EAS | KHV | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02040 | hp1 | a0001 | c0001 | t0009 | g0175 | EAS | KHV | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0129 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02145 | hp1 | a0001 | c0001 | t0010 | g0187 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02145 | hp2 | a0001 | c0001 | t0038 | g0207 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02155 | hp1 | a0001 | c0001 | t0019 | g0042 | EAS | CDX | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | CDX | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02257 | hp1 | a0001 | c0001 | t0020 | g0210 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0107 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02258 | hp1 | a0001 | c0001 | t0017 | g0223 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0211 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02280 | hp2 | a0001 | c0001 | t0020 | g0122 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0090 | AMR | PEL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02451 | hp1 | a0001 | c0001 | t0025 | g0160 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02451 | hp2 | a0001 | c0001 | t0042 | g0218 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02572 | hp1 | a0001 | c0001 | t0010 | g0136 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02602 | hp1 | a0001 | c0001 | t0015 | g0021 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02602 | hp2 | a0001 | c0001 | t0028 | g0010 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02615 | hp1 | a0001 | c0001 | t0030 | g0141 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02615 | hp2 | a0001 | c0001 | t0023 | g0084 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0105 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02622 | hp2 | a0001 | c0001 | t0008 | g0138 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02630 | hp1 | a0001 | c0001 | t0020 | g0123 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0143 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0117 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02717 | hp2 | a0001 | c0001 | t0010 | g0080 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02723 | hp2 | a0001 | c0001 | t0037 | g0137 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0179 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0215 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02809 | hp2 | a0001 | c0001 | t0008 | g0139 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0006 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02886 | hp2 | a0001 | c0001 | t0040 | g0135 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0098 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02896 | hp2 | a0001 | c0001 | t0024 | g0169 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0097 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02897 | hp2 | a0001 | c0001 | t0024 | g0170 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02922 | hp1 | a0001 | c0001 | t0017 | g0008 | AFR | ESN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02922 | hp2 | a0001 | c0001 | t0029 | g0221 | AFR | ESN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02965 | hp1 | a0001 | c0001 | t0036 | g0005 | AFR | ESN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02965 | hp2 | a0001 | c0001 | t0022 | g0126 | AFR | ESN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0128 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03041 | hp2 | a0001 | c0001 | t0035 | g0228 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03098 | hp1 | a0001 | c0001 | t0016 | g0172 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03098 | hp2 | a0001 | c0001 | t0014 | g0106 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03130 | hp1 | a0001 | c0001 | t0017 | g0066 | AFR | ESN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03130 | hp2 | a0001 | c0001 | t0029 | g0219 | AFR | ESN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0002 | AFR | ESN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0208 | AFR | ESN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03195 | hp1 | a0001 | c0001 | t0020 | g0124 | AFR | ESN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0214 | AFR | ESN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0130 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03225 | hp1 | a0001 | c0001 | t0010 | g0121 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0078 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0029 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03239 | hp2 | a0001 | c0001 | t0011 | g0100 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03453 | hp1 | a0001 | c0001 | t0010 | g0079 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0227 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0119 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03486 | hp2 | a0001 | c0001 | t0023 | g0004 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03516 | hp1 | a0001 | c0001 | t0021 | g0092 | AFR | ESN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | ESN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0113 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03540 | hp2 | a0001 | c0001 | t0017 | g0067 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03579 | hp2 | a0001 | c0001 | t0019 | g0205 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03654 | hp1 | a0001 | c0001 | t0039 | g0102 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03654 | hp2 | a0001 | c0001 | t0019 | g0063 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03669 | hp1 | a0001 | c0001 | t0010 | g0164 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03669 | hp2 | a0001 | c0001 | t0012 | g0152 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03688 | hp1 | a0001 | c0001 | t0012 | g0144 | SAS | STU | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | STU | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03710 | hp2 | a0001 | c0001 | t0011 | g0093 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | BEB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0155 | SAS | BEB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG04204 | hp1 | a0001 | c0001 | t0009 | g0165 | SAS | STU | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG04204 | hp2 | a0001 | c0001 | t0031 | g0178 | SAS | STU | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG04228 | hp1 | a0001 | c0001 | t0012 | g0198 | SAS | STU | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG04228 | hp2 | a0001 | c0001 | t0014 | g0094 | SAS | STU | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0229 | AFR | YRI | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0007 | AFR | YRI | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18612 | hp2 | a0001 | c0001 | t0012 | g0192 | EAS | CHB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18906 | hp1 | a0001 | c0001 | t0022 | g0127 | AFR | YRI | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0216 | AFR | YRI | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18942 | hp2 | a0001 | c0001 | t0018 | g0003 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18945 | hp2 | a0001 | c0001 | t0024 | g0167 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18948 | hp1 | a0001 | c0001 | t0045 | g0196 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18977 | hp1 | a0001 | c0001 | t0018 | g0189 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18977 | hp2 | a0001 | c0001 | t0016 | g0038 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18980 | hp2 | a0001 | c0001 | t0009 | g0188 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18983 | hp1 | a0001 | c0001 | t0044 | g0030 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18983 | hp2 | a0001 | c0001 | t0018 | g0003 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18993 | hp1 | a0001 | c0001 | t0016 | g0163 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18998 | hp1 | a0001 | c0001 | t0009 | g0195 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA19011 | hp2 | a0001 | c0001 | t0012 | g0190 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | LWK | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA19030 | hp2 | a0001 | c0001 | t0022 | g0125 | AFR | LWK | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA19043 | hp1 | a0001 | c0001 | t0025 | g0171 | AFR | LWK | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA19043 | hp2 | a0001 | c0001 | t0026 | g0203 | AFR | LWK | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA19055 | hp1 | a0001 | c0001 | t0018 | g0058 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA19055 | hp2 | a0001 | c0001 | t0018 | g0194 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA19064 | hp1 | a0001 | c0001 | t0025 | g0037 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA19064 | hp2 | a0001 | c0001 | t0012 | g0193 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA19067 | hp2 | a0001 | c0001 | t0014 | g0082 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA19070 | hp2 | a0001 | c0001 | t0016 | g0166 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA19077 | hp2 | a0001 | c0001 | t0015 | g0162 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0226 | AFR | YRI | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0115 | AFR | YRI | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA20129 | hp1 | a0001 | c0001 | t0011 | g0116 | AFR | ASW | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0140 | AFR | ASW | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA20752 | hp1 | a0001 | c0001 | t0026 | g0204 | EUR | TSI | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0156 | EUR | TSI | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0132 | EUR | TSI | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA20805 | hp2 | a0001 | c0001 | t0006 | g0039 | EUR | TSI | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA20905 | hp1 | a0001 | c0001 | t0032 | g0217 | SAS | GIH | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA20905 | hp2 | a0001 | c0001 | t0012 | g0154 | SAS | GIH | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0212 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02109 | hp2 | a0001 | c0001 | t0021 | g0091 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02486 | hp1 | a0001 | c0001 | t0021 | g0202 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0183 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02559 | hp1 | a0001 | c0001 | t0023 | g0142 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0075 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03471 | hp1 | a0001 | c0001 | t0033 | g0209 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0118 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18955 | hp1 | a0001 | c0001 | t0014 | g0103 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0013 | g0069 | REF | REF | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0006 | g0225 | REF | REF | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:17540852
|
T | C | 1 | a0001c0001t0026 | 2 | NA19043.hp2 NA20752.hp1 |
5_prime_UTR_variant | MODIFIER | c.-72T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/4 | 51223 | chr2 | 17540852 | |||||
| chr2:17655455
|
T | TCA | 6 | a0001c0001t0004a0001c0001t0009a0001c0001t0021others(3): Show | 29 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*106_*107dupCA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 108 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | ||||
| chr2:17655455
|
T | TCACA | 7 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(4): Show | 51 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*104_*107dupCACA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 108 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | ||||
| chr2:17655455
|
T | TCACACA | 3 | a0001c0001t0012a0001c0001t0014a0001c0001t0040 | 14 | HG01099.hp1 HG01433.hp1 HG02886.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*102_*107dupCACACA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 108 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | ||||
| chr2:17655455
|
T | TCACACAC others(1): Show |
2 | a0001c0001t0013a0001c0001t0018 | 12 | HG00323.hp2 HG01192.hp1 HG01256.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*100_*107dupCACACA others(2): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 108 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | ||||
| chr2:17655455
|
T | TCACACAC others(5): Show |
1 | a0001c0001t0029 | 2 | HG02922.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*96_*107dupCACACAC others(5): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 108 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | ||||
| chr2:17655455
|
T | TCACACAC others(7): Show |
1 | a0001c0001t0042 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*94_*107dupCACACAC others(7): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 108 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | ||||
| chr2:17655455
|
T | TCACACAC others(9): Show |
1 | a0001c0001t0043 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*92_*107dupCACACAC others(9): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 108 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | ||||
| chr2:17655455
|
TCA | T | 5 | a0001c0001t0015a0001c0001t0023a0001c0001t0027others(2): Show | 12 | HG00140.hp1 HG00140.hp2 HG00741.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*106_*107delCA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 106 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | ||||
| chr2:17655455
|
TCACA | T | 3 | a0001c0001t0001a0001c0001t0008a0001c0001t0026 | 50 | HG00408.hp2 HG00438.hp1 HG00735.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*104_*107delCACA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 104 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | ||||
| chr2:17655455
|
TCACACA | T | 3 | a0001c0001t0019a0001c0001t0020a0001c0001t0022 | 11 | HG01256.hp2 HG02155.hp1 HG02257.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*102_*107delCACACA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 102 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | ||||
| chr2:17655455
|
TCACACAC others(1): Show |
T | 1 | a0001c0001t0010 | 7 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*100_*107delCACACA others(2): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 100 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | ||||
| chr2:17655455
|
TCACACAC others(3): Show |
T | 1 | a0001c0001t0032 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*98_*107delCACACAC others(3): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 98 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | ||||
| chr2:17655455
|
TCACACAC others(5): Show |
T | 1 | a0001c0001t0031 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*96_*107delCACACAC others(5): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 96 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | ||||
| chr2:17655455
|
TCACACAC others(7): Show |
T | 1 | a0001c0001t0030 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*94_*107delCACACAC others(7): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 94 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | ||||
| chr2:17655498
|
CACA | C | 1 | a0001c0001t0028 | 2 | HG01981.hp1 HG02602.hp2 |
3_prime_UTR_variant | MODIFIER | c.*106_*108delCAA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 106 | INFO_REALIGN_3_PRIME | chr2 | 17655498 | ||||
| chr2:17655501
|
A | ACACACAC others(4): Show |
1 | a0001c0001t0041 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*107_*108insCACACA others(5): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 108 | chr2 | 17655501 | |||||
| chr2:17655502
|
A | C | 2 | a0001c0001t0044a0001c0001t0045 | 2 | NA18948.hp1 NA18983.hp1 |
3_prime_UTR_variant | MODIFIER | c.*108A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 108 | chr2 | 17655502 | |||||
| chr2:17655570
|
T | G | 1 | a0001c0001t0035 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*176T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 176 | chr2 | 17655570 | |||||
| chr2:17655815
|
T | A | 1 | a0001c0001t0039 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*421T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 421 | chr2 | 17655815 | |||||
| chr2:17656392
|
C | T | 1 | a0001c0001t0034 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*998C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 998 | chr2 | 17656392 | |||||
| chr2:17656474
|
C | T | 8 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(5): Show | 53 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1080C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 1080 | chr2 | 17656474 | |||||
| chr2:17656598
|
TAACAG | T | 10 | a0001c0001t0007a0001c0001t0011a0001c0001t0021others(7): Show | 28 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1213_*1217delAGAA others(1): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 1213 | INFO_REALIGN_3_PRIME | chr2 | 17656598 | ||||
| chr2:17656725
|
A | G | 20 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(17): Show | 91 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*1331A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 1331 | chr2 | 17656725 | |||||
| chr2:17656755
|
G | A | 3 | a0001c0001t0016a0001c0001t0024a0001c0001t0025 | 11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1361G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 1361 | chr2 | 17656755 | |||||
| chr2:17656869
|
C | A | 1 | a0001c0001t0020 | 4 | HG02257.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1475C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 1475 | chr2 | 17656869 | |||||
| chr2:17656906
|
G | C | 1 | a0001c0001t0038 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1512G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 1512 | chr2 | 17656906 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:17541155
|
G | GTC | 4 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0023g0004others(1): Show | 4 | HG02886.hp1 HG02965.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6+239_-6+240dupCT | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17541155 | |||||
| chr2:17541330
|
T | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(202): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.-6+412T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17541330 | ||||||
| chr2:17541367
|
G | A | 1 | a0001c0001t0017g0008 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-6+449G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17541367 | ||||||
| chr2:17541387
|
G | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(55): Show | 59 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.-6+469G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17541387 | ||||||
| chr2:17541430
|
C | A | 2 | a0001c0001t0017g0066a0001c0001t0017g0067 | 2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-6+512C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17541430 | ||||||
| chr2:17541461
|
C | A | 11 | a0001c0001t0004g0211a0001c0001t0007g0206a0001c0001t0007g0208others(8): Show | 11 | HG01261.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-6+543C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17541461 | ||||||
| chr2:17541530
|
GA | G | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+616delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17541530 | |||||
| chr2:17541917
|
G | A | 7 | a0001c0001t0005g0071a0001c0001t0013g0068a0001c0001t0013g0069others(4): Show | 7 | HG00323.hp2 HG00738.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6+999G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17541917 | ||||||
| chr2:17542068
|
A | G | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+1150A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17542068 | ||||||
| chr2:17542094
|
A | G | 2 | a0001c0001t0021g0201a0001c0001t0021g0202 | 2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-6+1176A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17542094 | ||||||
| chr2:17542205
|
TTG | T | 47 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(44): Show | 47 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.-6+1298_-6+1299del others(2): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17542205 | |||||
| chr2:17542292
|
A | G | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+1374A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17542292 | ||||||
| chr2:17542297
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-6+1379A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17542297 | ||||||
| chr2:17542418
|
G | T | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-6+1500G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17542418 | ||||||
| chr2:17542663
|
T | C | 1 | a0001c0001t0004g0115 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-6+1745T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17542663 | ||||||
| chr2:17542679
|
G | T | 2 | a0001c0001t0011g0199a0001c0001t0011g0200 | 2 | HG00639.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.-6+1761G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17542679 | ||||||
| chr2:17542726
|
A | G | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+1808A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17542726 | ||||||
| chr2:17542791
|
T | C | 3 | a0001c0001t0011g0116a0001c0001t0011g0199a0001c0001t0011g0200 | 3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-6+1873T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17542791 | ||||||
| chr2:17542831
|
G | T | 1 | a0001c0001t0012g0198 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-6+1913G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17542831 | ||||||
| chr2:17543196
|
G | C | 2 | a0001c0001t0013g0068a0001c0001t0013g0069 | 2 | HG01358.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-6+2278G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17543196 | ||||||
| chr2:17543633
|
G | T | 1 | a0001c0001t0007g0216 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-6+2715G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17543633 | ||||||
| chr2:17543930
|
T | C | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+3012T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17543930 | ||||||
| chr2:17544008
|
A | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(56): Show | 60 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.-6+3090A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17544008 | ||||||
| chr2:17544419
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-6+3501G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17544419 | ||||||
| chr2:17544668
|
A | G | 10 | a0001c0001t0006g0191a0001c0001t0009g0188a0001c0001t0009g0195others(7): Show | 11 | HG00408.hp1 NA18612.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.-6+3750A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17544668 | ||||||
| chr2:17544800
|
G | A | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+3882G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17544800 | ||||||
| chr2:17544835
|
T | C | 8 | a0001c0001t0003g0117a0001c0001t0003g0118a0001c0001t0008g0006others(5): Show | 8 | HG01109.hp2 HG02717.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-6+3917T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17544835 | ||||||
| chr2:17544960
|
C | T | 1 | a0001c0001t0010g0187 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-6+4042C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17544960 | ||||||
| chr2:17545032
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-6+4114C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17545032 | ||||||
| chr2:17545243
|
C | G | 2 | a0001c0001t0026g0203a0001c0001t0026g0204 | 2 | NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+4325C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17545243 | ||||||
| chr2:17545343
|
T | G | 1 | a0001c0001t0010g0121 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-6+4425T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17545343 | ||||||
| chr2:17545851
|
T | C | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+4933T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17545851 | ||||||
| chr2:17545942
|
G | T | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+5024G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17545942 | ||||||
| chr2:17546242
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-6+5324C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17546242 | ||||||
| chr2:17546412
|
G | GT | 58 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(55): Show | 59 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.-6+5502dupT | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17546412 | |||||
| chr2:17546817
|
G | A | 1 | a0001c0001t0011g0116 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-6+5899G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17546817 | ||||||
| chr2:17546933
|
AT | A | 11 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(8): Show | 12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-6+6016delT | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17546933 | ||||||
| chr2:17547187
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-6+6269G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17547187 | ||||||
| chr2:17547435
|
A | G | 1 | a0001c0001t0007g0215 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-6+6517A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17547435 | ||||||
| chr2:17547704
|
T | C | 1 | a0001c0001t0028g0010 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-6+6786T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17547704 | ||||||
| chr2:17547929
|
G | A | 1 | a0001c0001t0002g0132 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-6+7011G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17547929 | ||||||
| chr2:17548019
|
T | G | 3 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077 | 3 | HG02559.hp2 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-6+7101T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17548019 | ||||||
| chr2:17548048
|
C | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(56): Show | 60 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.-6+7130C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17548048 | ||||||
| chr2:17548056
|
C | T | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+7138C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17548056 | ||||||
| chr2:17548562
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-6+7644T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17548562 | ||||||
| chr2:17548948
|
T | C | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+8030T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17548948 | ||||||
| chr2:17548952
|
T | C | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18967.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.-6+8034T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17548952 | ||||||
| chr2:17549130
|
T | C | 3 | a0001c0001t0010g0121a0001c0001t0010g0136a0001c0001t0040g0135 | 3 | HG02572.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-6+8212T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17549130 | ||||||
| chr2:17549162
|
T | C | 17 | a0001c0001t0008g0138a0001c0001t0008g0139a0001c0001t0008g0140others(14): Show | 17 | HG00639.hp1 HG01074.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.-6+8244T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17549162 | ||||||
| chr2:17549172
|
C | A | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+8254C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17549172 | ||||||
| chr2:17549490
|
C | T | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+8572C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17549490 | ||||||
| chr2:17549631
|
C | T | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+8713C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17549631 | ||||||
| chr2:17549686
|
A | C | 2 | a0001c0001t0010g0121a0001c0001t0010g0136 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-6+8768A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17549686 | ||||||
| chr2:17549897
|
G | A | 1 | a0001c0001t0012g0144 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-6+8979G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17549897 | ||||||
| chr2:17550067
|
C | T | 1 | a0001c0001t0003g0114 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-6+9149C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17550067 | ||||||
| chr2:17550383
|
A | G | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-6+9465A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17550383 | ||||||
| chr2:17550392
|
G | A | 3 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147 | 3 | HG00741.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-6+9474G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17550392 | ||||||
| chr2:17550501
|
G | C | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+9583G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17550501 | ||||||
| chr2:17550843
|
T | A | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-6+9925T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17550843 | ||||||
| chr2:17550910
|
T | C | 3 | a0001c0001t0010g0078a0001c0001t0010g0079a0001c0001t0010g0080 | 3 | HG02717.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-6+9992T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17550910 | ||||||
| chr2:17551156
|
G | C | 7 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(4): Show | 7 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6+10238G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17551156 | ||||||
| chr2:17551236
|
A | G | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+10318A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17551236 | ||||||
| chr2:17551763
|
A | G | 1 | a0001c0001t0006g0185 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-6+10845A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17551763 | ||||||
| chr2:17551896
|
T | TA | 59 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0018others(56): Show | 60 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.-6+10998dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17551896 | |||||
| chr2:17551896
|
T | TAA | 5 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(2): Show | 5 | HG00741.hp2 HG01261.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+10997_-6+10998d others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17551896 | |||||
| chr2:17551896
|
TA | T | 15 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(12): Show | 16 | HG00639.hp1 HG01074.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-6+10998delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17551896 | |||||
| chr2:17551918
|
C | G | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+11000C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17551918 | ||||||
| chr2:17551926
|
T | C | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+11008T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17551926 | ||||||
| chr2:17551970
|
G | A | 1 | a0001c0001t0040g0135 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-6+11052G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17551970 | ||||||
| chr2:17552043
|
C | CA | 80 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(77): Show | 81 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.-6+11132dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17552043 | |||||
| chr2:17552092
|
C | G | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+11174C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17552092 | ||||||
| chr2:17552199
|
C | CA | 86 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(83): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-6+11294dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17552199 | |||||
| chr2:17552199
|
C | CAA | 6 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0004g0015others(3): Show | 6 | HG00741.hp1 HG01123.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6+11293_-6+11294d others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17552199 | |||||
| chr2:17552213
|
C | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(55): Show | 59 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.-6+11295C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17552213 | ||||||
| chr2:17552243
|
G | T | 1 | a0001c0001t0005g0229 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-6+11325G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17552243 | ||||||
| chr2:17552307
|
T | A | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+11389T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17552307 | ||||||
| chr2:17552523
|
C | T | 5 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(2): Show | 6 | HG02055.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+11605C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17552523 | ||||||
| chr2:17552588
|
C | G | 2 | a0001c0001t0004g0015a0001c0001t0004g0029 | 2 | HG01517.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-6+11670C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17552588 | ||||||
| chr2:17552661
|
T | C | 11 | a0001c0001t0008g0138a0001c0001t0008g0139a0001c0001t0008g0140others(8): Show | 11 | HG01934.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-6+11743T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17552661 | ||||||
| chr2:17552661
|
T | G | 1 | a0001c0001t0009g0083 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-6+11743T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17552661 | ||||||
| chr2:17552831
|
A | G | 1 | a0001c0001t0004g0113 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-6+11913A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17552831 | ||||||
| chr2:17552950
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-6+12032C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17552950 | ||||||
| chr2:17552969
|
A | C | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+12051A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17552969 | ||||||
| chr2:17553033
|
G | A | 1 | a0001c0001t0023g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-6+12115G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17553033 | ||||||
| chr2:17553040
|
C | T | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+12122C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17553040 | ||||||
| chr2:17553054
|
G | C | 1 | a0001c0001t0028g0032 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-6+12136G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17553054 | ||||||
| chr2:17553333
|
T | C | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+12415T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17553333 | ||||||
| chr2:17553465
|
A | T | 48 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(45): Show | 49 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.-6+12547A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17553465 | ||||||
| chr2:17553531
|
T | C | 2 | a0001c0001t0011g0199a0001c0001t0011g0200 | 2 | HG00639.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.-6+12613T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17553531 | ||||||
| chr2:17553769
|
G | A | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+12851G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17553769 | ||||||
| chr2:17553775
|
CACGA | C | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+12859_-6+12862d others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17553775 | |||||
| chr2:17553777
|
C | T | 1 | a0001c0001t0008g0143 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-6+12859C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17553777 | ||||||
| chr2:17553815
|
T | A | 7 | a0001c0001t0008g0138a0001c0001t0008g0139a0001c0001t0008g0140others(4): Show | 7 | HG02559.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6+12897T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17553815 | ||||||
| chr2:17553916
|
C | T | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+12998C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17553916 | ||||||
| chr2:17554054
|
G | A | 47 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(44): Show | 47 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.-6+13136G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17554054 | ||||||
| chr2:17554148
|
G | A | 1 | a0001c0001t0003g0085 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-6+13230G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17554148 | ||||||
| chr2:17554166
|
A | C | 1 | a0001c0001t0012g0144 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-6+13248A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17554166 | ||||||
| chr2:17554263
|
A | C | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+13345A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17554263 | ||||||
| chr2:17554493
|
C | T | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+13575C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17554493 | ||||||
| chr2:17554561
|
T | A | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+13643T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17554561 | ||||||
| chr2:17554575
|
C | T | 1 | a0001c0001t0012g0144 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-6+13657C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17554575 | ||||||
| chr2:17554583
|
T | G | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-6+13665T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17554583 | ||||||
| chr2:17554594
|
A | T | 58 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(55): Show | 59 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.-6+13676A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17554594 | ||||||
| chr2:17554687
|
A | C | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+13769A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17554687 | ||||||
| chr2:17554737
|
C | T | 11 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(8): Show | 12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-6+13819C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17554737 | ||||||
| chr2:17554827
|
A | G | 1 | a0001c0001t0014g0224 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-6+13909A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17554827 | ||||||
| chr2:17555019
|
T | TTTTAAAA others(10): Show |
3 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158 | 3 | HG00280.hp1 HG02055.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-6+14109_-6+14110i others(19): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17555019 | |||||
| chr2:17555186
|
A | G | 2 | a0001c0001t0021g0201a0001c0001t0021g0202 | 2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-6+14268A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17555186 | ||||||
| chr2:17555416
|
C | T | 3 | a0001c0001t0010g0121a0001c0001t0010g0136a0001c0001t0040g0135 | 3 | HG02572.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-6+14498C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17555416 | ||||||
| chr2:17555454
|
A | G | 1 | a0001c0001t0009g0028 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-6+14536A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17555454 | ||||||
| chr2:17555682
|
A | G | 11 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(8): Show | 12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-6+14764A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17555682 | ||||||
| chr2:17555689
|
C | T | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+14771C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17555689 | ||||||
| chr2:17555763
|
T | G | 1 | a0001c0001t0011g0116 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-6+14845T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17555763 | ||||||
| chr2:17555873
|
G | A | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+14955G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17555873 | ||||||
| chr2:17555895
|
T | A | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+14977T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17555895 | ||||||
| chr2:17555946
|
A | G | 2 | a0001c0001t0007g0111a0001c0001t0007g0112 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-6+15028A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17555946 | ||||||
| chr2:17555997
|
C | T | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+15079C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17555997 | ||||||
| chr2:17556246
|
T | C | 1 | a0001c0001t0010g0164 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-6+15328T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556246 | ||||||
| chr2:17556304
|
A | G | 11 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(8): Show | 12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-6+15386A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556304 | ||||||
| chr2:17556495
|
T | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(56): Show | 60 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.-6+15577T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556495 | ||||||
| chr2:17556630
|
A | C | 2 | a0001c0001t0026g0203a0001c0001t0026g0204 | 2 | NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+15712A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556630 | ||||||
| chr2:17556649
|
G | A | 1 | a0001c0001t0044g0030 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-6+15731G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556649 | ||||||
| chr2:17556684
|
T | C | 1 | a0001c0001t0005g0128 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-6+15766T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556684 | ||||||
| chr2:17556697
|
G | A | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+15779G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556697 | ||||||
| chr2:17556724
|
G | C | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+15806G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556724 | ||||||
| chr2:17556766
|
T | C | 1 | a0001c0001t0001g0033 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-6+15848T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556766 | ||||||
| chr2:17556767
|
A | T | 1 | a0001c0001t0001g0033 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-6+15849A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556767 | ||||||
| chr2:17556768
|
C | G | 1 | a0001c0001t0001g0033 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-6+15850C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556768 | ||||||
| chr2:17556769
|
C | A | 1 | a0001c0001t0001g0033 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-6+15851C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556769 | ||||||
| chr2:17556932
|
C | T | 58 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(55): Show | 59 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.-6+16014C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556932 | ||||||
| chr2:17556952
|
A | G | 1 | a0001c0001t0004g0183 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-6+16034A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556952 | ||||||
| chr2:17557096
|
C | T | 2 | a0001c0001t0021g0201a0001c0001t0021g0202 | 2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-6+16178C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17557096 | ||||||
| chr2:17557275
|
A | G | 2 | a0001c0001t0026g0203a0001c0001t0026g0204 | 2 | NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+16357A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17557275 | ||||||
| chr2:17557399
|
T | C | 6 | a0001c0001t0003g0085a0001c0001t0003g0086a0001c0001t0003g0087others(3): Show | 6 | HG00735.hp1 HG01433.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6+16481T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17557399 | ||||||
| chr2:17557487
|
A | G | 48 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.-6+16569A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17557487 | ||||||
| chr2:17557507
|
T | C | 1 | a0001c0001t0009g0165 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-6+16589T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17557507 | ||||||
| chr2:17557524
|
A | G | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+16606A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17557524 | ||||||
| chr2:17557654
|
C | T | 2 | a0001c0001t0026g0203a0001c0001t0026g0204 | 2 | NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+16736C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17557654 | ||||||
| chr2:17557841
|
A | C | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+16923A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17557841 | ||||||
| chr2:17557864
|
C | T | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+16946C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17557864 | ||||||
| chr2:17558071
|
G | A | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+17153G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17558071 | ||||||
| chr2:17558091
|
C | T | 1 | a0001c0001t0011g0110 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-6+17173C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17558091 | ||||||
| chr2:17558160
|
C | T | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+17242C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17558160 | ||||||
| chr2:17558326
|
G | A | 11 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(8): Show | 12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-6+17408G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17558326 | ||||||
| chr2:17558571
|
G | A | 1 | a0001c0001t0026g0203 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-6+17653G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17558571 | ||||||
| chr2:17558576
|
T | C | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+17658T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17558576 | ||||||
| chr2:17558596
|
A | C | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+17678A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17558596 | ||||||
| chr2:17558627
|
C | T | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+17709C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17558627 | ||||||
| chr2:17559109
|
G | T | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+18191G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17559109 | ||||||
| chr2:17559213
|
C | A | 2 | a0001c0001t0003g0086a0001c0001t0003g0087 | 2 | HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.-6+18295C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17559213 | ||||||
| chr2:17559323
|
G | A | 1 | a0001c0001t0002g0159 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-6+18405G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17559323 | ||||||
| chr2:17559408
|
C | CA | 23 | a0001c0001t0001g0034a0001c0001t0005g0002a0001c0001t0005g0129others(20): Show | 24 | HG01069.hp2 HG01256.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.-6+18501dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17559408 | |||||
| chr2:17559419
|
AC | A | 13 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0002g0161others(10): Show | 13 | HG00099.hp2 HG01123.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.-6+18502delC | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17559419 | ||||||
| chr2:17559420
|
C | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(172): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.-6+18502C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17559420 | ||||||
| chr2:17559683
|
C | T | 1 | a0001c0001t0015g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-6+18765C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17559683 | ||||||
| chr2:17559789
|
A | G | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+18871A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17559789 | ||||||
| chr2:17559820
|
C | T | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+18902C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17559820 | ||||||
| chr2:17560061
|
T | A | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+19143T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560061 | ||||||
| chr2:17560126
|
T | G | 1 | a0001c0001t0003g0088 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-6+19208T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560126 | ||||||
| chr2:17560197
|
C | CAT | 210 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(207): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.-6+19289_-6+19290d others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17560197 | |||||
| chr2:17560197
|
C | CATAT | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+19287_-6+19290d others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17560197 | |||||
| chr2:17560214
|
A | G | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+19296A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560214 | ||||||
| chr2:17560233
|
A | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(202): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.-6+19315A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560233 | ||||||
| chr2:17560258
|
G | C | 58 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(55): Show | 59 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.-6+19340G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560258 | ||||||
| chr2:17560378
|
G | A | 1 | a0001c0001t0014g0094 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-6+19460G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560378 | ||||||
| chr2:17560580
|
T | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.-6+19662T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560580 | ||||||
| chr2:17560626
|
T | C | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+19708T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560626 | ||||||
| chr2:17560679
|
G | T | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+19761G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560679 | ||||||
| chr2:17560719
|
A | G | 2 | a0001c0001t0014g0224a0001c0001t0017g0223 | 2 | HG01099.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-6+19801A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560719 | ||||||
| chr2:17560730
|
G | A | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+19812G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560730 | ||||||
| chr2:17560843
|
G | A | 4 | a0001c0001t0029g0219a0001c0001t0029g0221a0001c0001t0042g0218others(1): Show | 4 | HG01243.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6+19925G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560843 | ||||||
| chr2:17560937
|
G | A | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+20019G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560937 | ||||||
| chr2:17560975
|
T | C | 2 | a0001c0001t0021g0091a0001c0001t0021g0092 | 2 | HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-6+20057T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560975 | ||||||
| chr2:17561232
|
G | T | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+20314G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17561232 | ||||||
| chr2:17561287
|
T | C | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+20369T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17561287 | ||||||
| chr2:17561360
|
G | A | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+20442G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17561360 | ||||||
| chr2:17561836
|
T | C | 3 | a0001c0001t0002g0153a0001c0001t0006g0185a0001c0001t0012g0152 | 3 | HG00642.hp2 HG01168.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-6+20918T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17561836 | ||||||
| chr2:17562043
|
T | G | 2 | a0001c0001t0016g0166a0001c0001t0024g0167 | 2 | NA18945.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-6+21125T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17562043 | ||||||
| chr2:17562068
|
T | G | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+21150T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17562068 | ||||||
| chr2:17562179
|
T | C | 3 | a0001c0001t0019g0205a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+21261T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17562179 | ||||||
| chr2:17562268
|
A | G | 1 | a0001c0001t0003g0077 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-6+21350A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17562268 | ||||||
| chr2:17562395
|
A | C | 1 | a0001c0001t0029g0221 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-6+21477A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17562395 | ||||||
| chr2:17562545
|
A | G | 1 | a0001c0001t0003g0085 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-6+21627A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17562545 | ||||||
| chr2:17562547
|
A | C | 1 | a0001c0001t0034g0108 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-6+21629A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17562547 | ||||||
| chr2:17562595
|
A | G | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-6+21677A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17562595 | ||||||
| chr2:17562648
|
A | G | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+21730A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17562648 | ||||||
| chr2:17562870
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0015g0014 | 2 | HG00741.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-6+21952C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17562870 | ||||||
| chr2:17563224
|
C | T | 1 | a0001c0001t0014g0224 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-6+22306C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17563224 | ||||||
| chr2:17563231
|
G | A | 1 | a0001c0001t0011g0110 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-6+22313G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17563231 | ||||||
| chr2:17563320
|
G | A | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+22402G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17563320 | ||||||
| chr2:17563394
|
T | C | 3 | a0001c0001t0010g0121a0001c0001t0010g0136a0001c0001t0040g0135 | 3 | HG02572.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-6+22476T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17563394 | ||||||
| chr2:17563581
|
T | G | 2 | a0001c0001t0006g0016a0001c0001t0028g0010 | 2 | HG00738.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-6+22663T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17563581 | ||||||
| chr2:17563585
|
C | T | 1 | a0001c0001t0017g0008 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-6+22667C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17563585 | ||||||
| chr2:17563679
|
G | A | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-6+22761G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17563679 | ||||||
| chr2:17563685
|
G | A | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+22767G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17563685 | ||||||
| chr2:17563707
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-6+22789C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17563707 | ||||||
| chr2:17563751
|
T | C | 2 | a0001c0001t0002g0035a0001c0001t0002g0036 | 2 | HG02129.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.-6+22833T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17563751 | ||||||
| chr2:17563789
|
GA | G | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+22878delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17563789 | |||||
| chr2:17563910
|
T | C | 1 | a0001c0001t0015g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-6+22992T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17563910 | ||||||
| chr2:17564162
|
T | G | 2 | a0001c0001t0016g0038a0001c0001t0025g0037 | 2 | NA18977.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-6+23244T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17564162 | ||||||
| chr2:17564388
|
T | A | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+23470T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17564388 | ||||||
| chr2:17564478
|
A | G | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+23560A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17564478 | ||||||
| chr2:17564574
|
G | GT | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+23665dupT | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17564574 | |||||
| chr2:17564643
|
C | T | 3 | a0001c0001t0010g0121a0001c0001t0010g0136a0001c0001t0040g0135 | 3 | HG02572.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-6+23725C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17564643 | ||||||
| chr2:17565032
|
T | C | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+24114T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17565032 | ||||||
| chr2:17565071
|
A | G | 3 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158 | 3 | HG00280.hp1 HG02055.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-6+24153A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17565071 | ||||||
| chr2:17565169
|
A | G | 6 | a0001c0001t0016g0168a0001c0001t0016g0172a0001c0001t0024g0169others(3): Show | 6 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6+24251A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17565169 | ||||||
| chr2:17565402
|
C | CA | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+24487dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17565402 | |||||
| chr2:17565617
|
A | G | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+24699A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17565617 | ||||||
| chr2:17565810
|
C | T | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-6+24892C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17565810 | ||||||
| chr2:17565840
|
T | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.-6+24922T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17565840 | ||||||
| chr2:17565919
|
C | T | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+25001C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17565919 | ||||||
| chr2:17566075
|
A | G | 1 | a0001c0001t0026g0203 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-6+25157A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17566075 | ||||||
| chr2:17566163
|
T | A | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+25245T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17566163 | ||||||
| chr2:17566201
|
T | C | 1 | a0001c0001t0004g0183 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-6+25283T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17566201 | ||||||
| chr2:17566222
|
C | G | 1 | a0001c0001t0035g0228 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-6+25304C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17566222 | ||||||
| chr2:17566284
|
A | G | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-6+25366A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17566284 | ||||||
| chr2:17566301
|
T | A | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+25383T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17566301 | ||||||
| chr2:17566324
|
A | G | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+25406A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17566324 | ||||||
| chr2:17566599
|
A | T | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-25471A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17566599 | ||||||
| chr2:17566731
|
A | G | 6 | a0001c0001t0010g0078a0001c0001t0010g0079a0001c0001t0010g0080others(3): Show | 6 | HG01496.hp1 HG02109.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5-25339A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17566731 | ||||||
| chr2:17566732
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(76): Show | 80 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.-5-25338C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17566732 | ||||||
| chr2:17566787
|
C | T | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-25283C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17566787 | ||||||
| chr2:17566969
|
C | A | 1 | a0001c0001t0017g0081 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-5-25101C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17566969 | ||||||
| chr2:17567141
|
T | C | 1 | a0001c0001t0001g0064 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-5-24929T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567141 | ||||||
| chr2:17567156
|
G | A | 1 | a0001c0001t0004g0183 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-5-24914G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567156 | ||||||
| chr2:17567275
|
C | G | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-24795C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567275 | ||||||
| chr2:17567331
|
A | G | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-24739A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567331 | ||||||
| chr2:17567343
|
T | G | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-24727T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567343 | ||||||
| chr2:17567353
|
C | CT | 48 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0222others(45): Show | 48 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-5-24693dupT | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17567353 | |||||
| chr2:17567353
|
C | CTT | 73 | a0001c0001t0002g0131a0001c0001t0002g0145a0001c0001t0002g0146others(70): Show | 74 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.-5-24694_-5-24693d others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17567353 | |||||
| chr2:17567353
|
C | CTTT | 21 | a0001c0001t0001g0040a0001c0001t0002g0132a0001c0001t0002g0153others(18): Show | 21 | HG01069.hp2 HG01168.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-5-24695_-5-24693d others(5): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17567353 | |||||
| chr2:17567353
|
C | CTTTT | 47 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(44): Show | 48 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.-5-24696_-5-24693d others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17567353 | |||||
| chr2:17567353
|
C | CTTTTT | 7 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0062others(4): Show | 7 | HG01175.hp2 HG01934.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.-5-24697_-5-24693d others(7): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17567353 | |||||
| chr2:17567353
|
CTT | C | 26 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(23): Show | 27 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.-5-24694_-5-24693d others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17567353 | |||||
| chr2:17567377
|
T | A | 26 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(23): Show | 27 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.-5-24693T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567377 | ||||||
| chr2:17567377
|
T | TTTTTTTT others(7): Show |
1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-5-24693_-5-24692i others(16): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567377 | ||||||
| chr2:17567397
|
C | T | 2 | a0001c0001t0027g0013a0001c0001t0027g0026 | 2 | HG00140.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-5-24673C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567397 | ||||||
| chr2:17567410
|
G | A | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-5-24660G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567410 | ||||||
| chr2:17567469
|
C | G | 38 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(35): Show | 38 | HG00323.hp2 HG00735.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.-5-24601C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567469 | ||||||
| chr2:17567535
|
T | G | 2 | a0001c0001t0014g0224a0001c0001t0017g0223 | 2 | HG01099.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-5-24535T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567535 | ||||||
| chr2:17567561
|
T | C | 2 | a0001c0001t0021g0201a0001c0001t0021g0202 | 2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-5-24509T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567561 | ||||||
| chr2:17567678
|
C | T | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-24392C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567678 | ||||||
| chr2:17567682
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-5-24388A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567682 | ||||||
| chr2:17567830
|
T | C | 1 | a0001c0001t0025g0037 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-5-24240T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567830 | ||||||
| chr2:17568158
|
T | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.-5-23912T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17568158 | ||||||
| chr2:17568215
|
T | C | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-23855T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17568215 | ||||||
| chr2:17568382
|
C | T | 26 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(23): Show | 27 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.-5-23688C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17568382 | ||||||
| chr2:17568573
|
C | T | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-23497C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17568573 | ||||||
| chr2:17568592
|
C | T | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-23478C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17568592 | ||||||
| chr2:17568627
|
C | A | 3 | a0001c0001t0010g0121a0001c0001t0010g0136a0001c0001t0040g0135 | 3 | HG02572.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-5-23443C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17568627 | ||||||
| chr2:17569014
|
A | C | 58 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(55): Show | 59 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.-5-23056A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17569014 | ||||||
| chr2:17569223
|
C | T | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-22847C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17569223 | ||||||
| chr2:17569239
|
T | G | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-22831T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17569239 | ||||||
| chr2:17569289
|
A | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18967.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.-5-22781A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17569289 | ||||||
| chr2:17569294
|
G | A | 1 | a0001c0001t0028g0032 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-5-22776G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17569294 | ||||||
| chr2:17569306
|
C | CAA | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-22755_-5-22754d others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17569306 | |||||
| chr2:17569317
|
T | A | 1 | a0001c0001t0004g0107 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-5-22753T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17569317 | ||||||
| chr2:17569606
|
T | G | 7 | a0001c0001t0008g0138a0001c0001t0008g0139a0001c0001t0008g0140others(4): Show | 7 | HG02559.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-5-22464T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17569606 | ||||||
| chr2:17569633
|
A | G | 3 | a0001c0001t0011g0116a0001c0001t0011g0199a0001c0001t0011g0200 | 3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-5-22437A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17569633 | ||||||
| chr2:17569650
|
A | G | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-5-22420A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17569650 | ||||||
| chr2:17569692
|
A | ACTCT | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-22377_-5-22374d others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17569692 | |||||
| chr2:17569714
|
G | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.-5-22356G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17569714 | ||||||
| chr2:17569880
|
C | T | 1 | a0001c0001t0014g0106 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-5-22190C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17569880 | ||||||
| chr2:17570011
|
G | C | 1 | a0001c0001t0006g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-5-22059G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17570011 | ||||||
| chr2:17570184
|
G | T | 1 | a0001c0001t0026g0204 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-5-21886G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17570184 | ||||||
| chr2:17570336
|
C | T | 1 | a0001c0001t0015g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-5-21734C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17570336 | ||||||
| chr2:17570366
|
G | A | 3 | a0001c0001t0011g0116a0001c0001t0011g0199a0001c0001t0011g0200 | 3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-5-21704G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17570366 | ||||||
| chr2:17570389
|
C | G | 1 | a0001c0001t0006g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-5-21681C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17570389 | ||||||
| chr2:17570861
|
A | T | 1 | a0001c0001t0006g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-5-21209A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17570861 | ||||||
| chr2:17570866
|
G | A | 1 | a0001c0001t0004g0183 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-5-21204G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17570866 | ||||||
| chr2:17570923
|
A | T | 1 | a0001c0001t0010g0080 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-5-21147A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17570923 | ||||||
| chr2:17570951
|
A | T | 11 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(8): Show | 12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5-21119A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17570951 | ||||||
| chr2:17570957
|
C | T | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-21113C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17570957 | ||||||
| chr2:17571271
|
G | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(56): Show | 60 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.-5-20799G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571271 | ||||||
| chr2:17571314
|
G | T | 1 | a0001c0001t0017g0008 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-5-20756G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571314 | ||||||
| chr2:17571354
|
T | C | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-20716T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571354 | ||||||
| chr2:17571546
|
C | T | 5 | a0001c0001t0008g0138a0001c0001t0008g0139a0001c0001t0008g0140others(2): Show | 5 | HG02615.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-20524C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571546 | ||||||
| chr2:17571585
|
A | T | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20485A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571585 | ||||||
| chr2:17571588
|
A | T | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20482A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571588 | ||||||
| chr2:17571589
|
A | T | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20481A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571589 | ||||||
| chr2:17571590
|
A | T | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20480A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571590 | ||||||
| chr2:17571592
|
A | T | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20478A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571592 | ||||||
| chr2:17571596
|
A | T | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20474A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571596 | ||||||
| chr2:17571601
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20469G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571601 | ||||||
| chr2:17571602
|
C | A | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20468C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571602 | ||||||
| chr2:17571604
|
C | A | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20466C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571604 | ||||||
| chr2:17571605
|
C | A | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20465C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571605 | ||||||
| chr2:17571606
|
T | A | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20464T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571606 | ||||||
| chr2:17571608
|
C | G | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20462C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571608 | ||||||
| chr2:17571609
|
T | A | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20461T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571609 | ||||||
| chr2:17571613
|
C | A | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20457C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571613 | ||||||
| chr2:17571615
|
C | A | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20455C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571615 | ||||||
| chr2:17571616
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20454C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571616 | ||||||
| chr2:17571617
|
A | T | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20453A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571617 | ||||||
| chr2:17571619
|
G | C | 1 | a0001c0001t0002g0036 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-5-20451G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571619 | ||||||
| chr2:17571620
|
G | C | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20450G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571620 | ||||||
| chr2:17571622
|
C | A | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20448C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571622 | ||||||
| chr2:17571624
|
A | T | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20446A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571624 | ||||||
| chr2:17571625
|
T | C | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20445T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571625 | ||||||
| chr2:17571627
|
C | T | 3 | a0001c0001t0002g0035a0001c0001t0009g0195a0001c0001t0045g0196 | 3 | HG02129.hp2 NA18948.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.-5-20443C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571627 | ||||||
| chr2:17571629
|
A | G | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20441A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571629 | ||||||
| chr2:17571631
|
G | C | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20439G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571631 | ||||||
| chr2:17571634
|
C | G | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20436C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571634 | ||||||
| chr2:17571637
|
A | T | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20433A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571637 | ||||||
| chr2:17571638
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20432G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571638 | ||||||
| chr2:17571647
|
C | A | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20423C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571647 | ||||||
| chr2:17571652
|
C | G | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20418C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571652 | ||||||
| chr2:17571654
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20416G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571654 | ||||||
| chr2:17571655
|
ACCAGGTT others(4): Show |
A | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20412_-5-20402d others(13): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17571655 | |||||
| chr2:17571667
|
C | A | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20403C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571667 | ||||||
| chr2:17571668
|
C | A | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20402C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571668 | ||||||
| chr2:17571672
|
T | A | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20398T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571672 | ||||||
| chr2:17571673
|
T | A | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20397T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571673 | ||||||
| chr2:17571674
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20396G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571674 | ||||||
| chr2:17571682
|
C | A | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20388C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571682 | ||||||
| chr2:17571686
|
C | A | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20384C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571686 | ||||||
| chr2:17571687
|
T | G | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20383T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571687 | ||||||
| chr2:17571689
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20381G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571689 | ||||||
| chr2:17571695
|
G | GAACTGCT others(4): Show |
1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20375_-5-20374i others(13): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571695 | ||||||
| chr2:17571699
|
A | G | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20371A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571699 | ||||||
| chr2:17571704
|
C | A | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20366C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571704 | ||||||
| chr2:17571706
|
A | G | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20364A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571706 | ||||||
| chr2:17571710
|
A | G | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20360A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571710 | ||||||
| chr2:17571740
|
T | A | 1 | a0001c0001t0015g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-5-20330T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571740 | ||||||
| chr2:17572035
|
A | G | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-20035A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17572035 | ||||||
| chr2:17572045
|
C | T | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-20025C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17572045 | ||||||
| chr2:17572063
|
C | T | 2 | a0001c0001t0001g0181a0001c0001t0019g0182 | 2 | HG01123.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.-5-20007C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17572063 | ||||||
| chr2:17572064
|
G | T | 2 | a0001c0001t0014g0224a0001c0001t0017g0223 | 2 | HG01099.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-5-20006G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17572064 | ||||||
| chr2:17572099
|
T | C | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-19971T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17572099 | ||||||
| chr2:17572383
|
G | A | 1 | a0001c0001t0003g0088 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-5-19687G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17572383 | ||||||
| chr2:17572404
|
A | G | 1 | a0001c0001t0002g0158 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-5-19666A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17572404 | ||||||
| chr2:17572569
|
C | T | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-19501C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17572569 | ||||||
| chr2:17572886
|
TTTGA | T | 32 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(29): Show | 34 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(31): Show |
intron_variant | MODIFIER | c.-5-19180_-5-19177d others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17572886 | |||||
| chr2:17573040
|
T | C | 23 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0002g0161others(20): Show | 23 | HG00099.hp2 HG00639.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-5-19030T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17573040 | ||||||
| chr2:17573049
|
A | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(103): Show | 108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.-5-19021A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17573049 | ||||||
| chr2:17573128
|
T | C | 2 | a0001c0001t0014g0224a0001c0001t0017g0223 | 2 | HG01099.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-5-18942T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17573128 | ||||||
| chr2:17573131
|
G | A | 1 | a0001c0001t0007g0208 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-5-18939G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17573131 | ||||||
| chr2:17573339
|
G | T | 1 | a0001c0001t0001g0065 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-5-18731G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17573339 | ||||||
| chr2:17573453
|
C | CA | 33 | a0001c0001t0001g0133a0001c0001t0001g0174a0001c0001t0001g0177others(30): Show | 34 | HG00408.hp1 HG00438.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-5-18604dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17573453 | |||||
| chr2:17573502
|
A | G | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-18568A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17573502 | ||||||
| chr2:17573510
|
G | A | 23 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0002g0161others(20): Show | 23 | HG00099.hp2 HG00639.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-5-18560G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17573510 | ||||||
| chr2:17573599
|
G | T | 228 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(225): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.-5-18471G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17573599 | ||||||
| chr2:17573965
|
T | A | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-18105T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17573965 | ||||||
| chr2:17573990
|
C | G | 1 | a0001c0001t0017g0008 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-5-18080C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17573990 | ||||||
| chr2:17574162
|
C | T | 1 | a0001c0001t0044g0030 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-5-17908C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574162 | ||||||
| chr2:17574172
|
G | T | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-17898G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574172 | ||||||
| chr2:17574202
|
T | TC | 25 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(22): Show | 26 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.-5-17860dupC | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17574202 | |||||
| chr2:17574332
|
A | G | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-17738A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574332 | ||||||
| chr2:17574445
|
G | A | 11 | a0001c0001t0008g0138a0001c0001t0008g0139a0001c0001t0008g0140others(8): Show | 11 | HG01934.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5-17625G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574445 | ||||||
| chr2:17574451
|
C | A | 18 | a0001c0001t0004g0183a0001c0001t0008g0138a0001c0001t0008g0139others(15): Show | 18 | HG00639.hp1 HG01074.hp2 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.-5-17619C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574451 | ||||||
| chr2:17574471
|
ATCTT | A | 8 | a0001c0001t0003g0117a0001c0001t0003g0118a0001c0001t0008g0006others(5): Show | 8 | HG01109.hp2 HG02717.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5-17594_-5-17591d others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17574471 | |||||
| chr2:17574492
|
G | A | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-17578G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574492 | ||||||
| chr2:17574494
|
TA | T | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-17574delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17574494 | |||||
| chr2:17574699
|
C | A | 1 | a0001c0001t0001g0057 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-5-17371C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574699 | ||||||
| chr2:17574769
|
T | G | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-17301T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574769 | ||||||
| chr2:17574803
|
G | A | 11 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(8): Show | 12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5-17267G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574803 | ||||||
| chr2:17574832
|
T | A | 26 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(23): Show | 27 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.-5-17238T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574832 | ||||||
| chr2:17574911
|
C | T | 1 | a0001c0001t0002g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-5-17159C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574911 | ||||||
| chr2:17574917
|
C | A | 2 | a0001c0001t0017g0066a0001c0001t0017g0067 | 2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-5-17153C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574917 | ||||||
| chr2:17574999
|
A | T | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-17071A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574999 | ||||||
| chr2:17575044
|
G | C | 11 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(8): Show | 12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5-17026G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575044 | ||||||
| chr2:17575116
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(76): Show | 80 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.-5-16954C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575116 | ||||||
| chr2:17575127
|
C | A | 23 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0002g0161others(20): Show | 23 | HG00099.hp2 HG00639.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-5-16943C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575127 | ||||||
| chr2:17575129
|
A | G | 20 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0145others(17): Show | 20 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.-5-16941A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575129 | ||||||
| chr2:17575132
|
A | G | 3 | a0001c0001t0011g0116a0001c0001t0011g0199a0001c0001t0011g0200 | 3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-5-16938A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575132 | ||||||
| chr2:17575174
|
C | A | 2 | a0001c0001t0021g0201a0001c0001t0021g0202 | 2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-5-16896C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575174 | ||||||
| chr2:17575309
|
T | G | 1 | a0001c0001t0001g0018 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-5-16761T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575309 | ||||||
| chr2:17575339
|
T | A | 3 | a0001c0001t0010g0121a0001c0001t0010g0136a0001c0001t0040g0135 | 3 | HG02572.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-5-16731T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575339 | ||||||
| chr2:17575534
|
T | A | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-16536T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575534 | ||||||
| chr2:17575564
|
C | T | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-16506C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575564 | ||||||
| chr2:17575629
|
A | G | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-16441A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575629 | ||||||
| chr2:17575659
|
C | T | 1 | a0001c0001t0010g0079 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-5-16411C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575659 | ||||||
| chr2:17575696
|
C | T | 1 | a0001c0001t0004g0105 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-5-16374C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575696 | ||||||
| chr2:17575697
|
G | A | 11 | a0001c0001t0008g0138a0001c0001t0008g0139a0001c0001t0008g0140others(8): Show | 11 | HG01934.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5-16373G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575697 | ||||||
| chr2:17575771
|
G | A | 2 | a0001c0001t0021g0201a0001c0001t0021g0202 | 2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-5-16299G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575771 | ||||||
| chr2:17575824
|
T | C | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-16246T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575824 | ||||||
| chr2:17575955
|
A | G | 8 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0002g0161others(5): Show | 8 | HG00099.hp2 HG01123.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-16115A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575955 | ||||||
| chr2:17575969
|
AT | A | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-16099delT | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17575969 | |||||
| chr2:17576126
|
C | G | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-15944C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17576126 | ||||||
| chr2:17576171
|
T | C | 2 | a0001c0001t0018g0058a0001c0001t0019g0042 | 2 | HG02155.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.-5-15899T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17576171 | ||||||
| chr2:17576257
|
T | G | 5 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0008g0119others(2): Show | 5 | HG02886.hp1 HG02965.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-15813T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17576257 | ||||||
| chr2:17576531
|
G | T | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-15539G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17576531 | ||||||
| chr2:17576621
|
T | C | 1 | a0001c0001t0033g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-5-15449T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17576621 | ||||||
| chr2:17576840
|
C | CTGGTATG others(2): Show |
27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-15229_-5-15228i others(11): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17576840 | |||||
| chr2:17576992
|
A | T | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-15078A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17576992 | ||||||
| chr2:17577079
|
T | C | 3 | a0001c0001t0010g0121a0001c0001t0010g0136a0001c0001t0040g0135 | 3 | HG02572.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-5-14991T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17577079 | ||||||
| chr2:17577177
|
C | T | 2 | a0001c0001t0017g0066a0001c0001t0017g0067 | 2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-5-14893C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17577177 | ||||||
| chr2:17577205
|
C | T | 1 | a0001c0001t0009g0165 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-5-14865C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17577205 | ||||||
| chr2:17577476
|
A | G | 2 | a0001c0001t0027g0013a0001c0001t0027g0026 | 2 | HG00140.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-5-14594A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17577476 | ||||||
| chr2:17577736
|
A | G | 1 | a0001c0001t0014g0106 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-5-14334A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17577736 | ||||||
| chr2:17577792
|
T | C | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-14278T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17577792 | ||||||
| chr2:17578002
|
T | C | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-14068T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17578002 | ||||||
| chr2:17578244
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-5-13826C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17578244 | ||||||
| chr2:17578432
|
G | C | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-13638G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17578432 | ||||||
| chr2:17578440
|
T | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(202): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.-5-13630T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17578440 | ||||||
| chr2:17578498
|
C | G | 11 | a0001c0001t0008g0138a0001c0001t0008g0139a0001c0001t0008g0140others(8): Show | 11 | HG01934.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5-13572C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17578498 | ||||||
| chr2:17578542
|
G | A | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-13528G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17578542 | ||||||
| chr2:17578854
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-5-13216G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17578854 | ||||||
| chr2:17578901
|
A | G | 47 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(44): Show | 47 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.-5-13169A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17578901 | ||||||
| chr2:17578922
|
T | C | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-13148T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17578922 | ||||||
| chr2:17579122
|
A | T | 1 | a0001c0001t0002g0060 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-5-12948A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17579122 | ||||||
| chr2:17579210
|
G | C | 1 | a0001c0001t0015g0014 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-5-12860G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17579210 | ||||||
| chr2:17579361
|
C | T | 1 | a0001c0001t0001g0222 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-5-12709C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17579361 | ||||||
| chr2:17579652
|
C | A | 11 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(8): Show | 12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5-12418C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17579652 | ||||||
| chr2:17579679
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-5-12391T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17579679 | ||||||
| chr2:17579734
|
A | G | 1 | a0001c0001t0006g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-5-12336A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17579734 | ||||||
| chr2:17580108
|
G | A | 11 | a0001c0001t0004g0211a0001c0001t0007g0206a0001c0001t0007g0208others(8): Show | 11 | HG01261.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5-11962G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17580108 | ||||||
| chr2:17580225
|
G | A | 1 | a0001c0001t0013g0068 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-5-11845G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17580225 | ||||||
| chr2:17580387
|
C | G | 1 | a0001c0001t0012g0198 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-5-11683C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17580387 | ||||||
| chr2:17580612
|
T | G | 1 | a0001c0001t0019g0063 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-5-11458T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17580612 | ||||||
| chr2:17580618
|
A | T | 1 | a0001c0001t0017g0067 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-5-11452A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17580618 | ||||||
| chr2:17580640
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-5-11430C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17580640 | ||||||
| chr2:17580674
|
C | A | 1 | a0001c0001t0001g0009 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-5-11396C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17580674 | ||||||
| chr2:17580736
|
C | T | 1 | a0001c0001t0005g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-5-11334C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17580736 | ||||||
| chr2:17580825
|
G | A | 2 | a0001c0001t0013g0068a0001c0001t0013g0069 | 2 | HG01358.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-5-11245G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17580825 | ||||||
| chr2:17580997
|
C | A | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-11073C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17580997 | ||||||
| chr2:17581185
|
A | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(54): Show | 58 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.-5-10885A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17581185 | ||||||
| chr2:17581518
|
T | G | 1 | a0001c0001t0006g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-5-10552T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17581518 | ||||||
| chr2:17581526
|
G | T | 22 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(19): Show | 22 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-5-10544G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17581526 | ||||||
| chr2:17581572
|
A | G | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-10498A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17581572 | ||||||
| chr2:17581765
|
TTC | T | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-10299_-5-10298d others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17581765 | |||||
| chr2:17581994
|
T | G | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-10076T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17581994 | ||||||
| chr2:17582015
|
T | G | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-10055T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17582015 | ||||||
| chr2:17582084
|
AC | A | 3 | a0001c0001t0004g0107a0001c0001t0004g0113a0001c0001t0017g0081 | 3 | HG01891.hp2 HG02257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-5-9984delC | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17582084 | |||||
| chr2:17582117
|
G | A | 11 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(8): Show | 12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5-9953G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17582117 | ||||||
| chr2:17582256
|
G | A | 1 | a0001c0001t0002g0159 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-5-9814G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17582256 | ||||||
| chr2:17582431
|
T | C | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-9639T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17582431 | ||||||
| chr2:17582435
|
A | C | 5 | a0001c0001t0016g0172a0001c0001t0024g0169a0001c0001t0024g0170others(2): Show | 5 | HG02451.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-9635A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17582435 | ||||||
| chr2:17582456
|
T | G | 1 | a0001c0001t0004g0019 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-5-9614T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17582456 | ||||||
| chr2:17582459
|
G | A | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-9611G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17582459 | ||||||
| chr2:17582555
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(76): Show | 80 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.-5-9515T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17582555 | ||||||
| chr2:17582560
|
C | G | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-9510C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17582560 | ||||||
| chr2:17582608
|
G | C | 1 | a0001c0001t0032g0217 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-5-9462G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17582608 | ||||||
| chr2:17582880
|
A | G | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-9190A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17582880 | ||||||
| chr2:17582971
|
C | T | 1 | a0001c0001t0006g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-5-9099C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17582971 | ||||||
| chr2:17583084
|
T | C | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-8986T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17583084 | ||||||
| chr2:17583169
|
T | G | 1 | a0001c0001t0011g0199 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-5-8901T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17583169 | ||||||
| chr2:17583213
|
G | A | 1 | a0001c0001t0020g0210 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-5-8857G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17583213 | ||||||
| chr2:17583330
|
T | C | 1 | a0001c0001t0013g0068 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-5-8740T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17583330 | ||||||
| chr2:17583561
|
T | C | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-8509T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17583561 | ||||||
| chr2:17583652
|
A | G | 26 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(23): Show | 27 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.-5-8418A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17583652 | ||||||
| chr2:17583666
|
C | G | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0016g0163 | 3 | NA18967.hp2 NA18989.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.-5-8404C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17583666 | ||||||
| chr2:17583819
|
T | C | 2 | a0001c0001t0001g0222a0001c0001t0032g0217 | 2 | NA19030.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-5-8251T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17583819 | ||||||
| chr2:17584052
|
T | C | 1 | a0001c0001t0002g0149 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-5-8018T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584052 | ||||||
| chr2:17584076
|
T | C | 1 | a0001c0001t0018g0058 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-5-7994T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584076 | ||||||
| chr2:17584149
|
T | C | 26 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(23): Show | 27 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.-5-7921T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584149 | ||||||
| chr2:17584198
|
A | T | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-7872A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584198 | ||||||
| chr2:17584214
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-5-7856C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584214 | ||||||
| chr2:17584250
|
AG | A | 22 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(19): Show | 22 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-5-7817delG | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17584250 | |||||
| chr2:17584278
|
A | G | 2 | a0001c0001t0021g0201a0001c0001t0021g0202 | 2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-5-7792A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584278 | ||||||
| chr2:17584312
|
G | A | 1 | a0001c0001t0002g0132 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-5-7758G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584312 | ||||||
| chr2:17584370
|
G | A | 11 | a0001c0001t0004g0211a0001c0001t0007g0206a0001c0001t0007g0208others(8): Show | 11 | HG01261.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5-7700G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584370 | ||||||
| chr2:17584794
|
C | G | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-7276C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584794 | ||||||
| chr2:17584827
|
T | C | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-7243T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584827 | ||||||
| chr2:17584836
|
C | T | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-7234C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584836 | ||||||
| chr2:17584838
|
TAA | T | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-7231_-5-7230del others(2): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584838 | ||||||
| chr2:17584841
|
C | G | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-7229C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584841 | ||||||
| chr2:17584842
|
A | T | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-7228A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584842 | ||||||
| chr2:17584851
|
C | T | 1 | a0001c0001t0010g0164 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-5-7219C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584851 | ||||||
| chr2:17584875
|
C | T | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-7195C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584875 | ||||||
| chr2:17584936
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0003g0086 | 2 | HG01981.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.-5-7134G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584936 | ||||||
| chr2:17585331
|
A | G | 41 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(38): Show | 42 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.-5-6739A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17585331 | ||||||
| chr2:17585382
|
T | TA | 47 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(44): Show | 47 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.-5-6674dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17585382 | |||||
| chr2:17585382
|
TA | T | 10 | a0001c0001t0001g0011a0001c0001t0001g0055a0001c0001t0001g0057others(7): Show | 10 | HG00099.hp1 HG00639.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.-5-6674delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17585382 | |||||
| chr2:17585382
|
TAA | T | 39 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(36): Show | 40 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-5-6675_-5-6674del others(2): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17585382 | |||||
| chr2:17585393
|
A | AC | 3 | a0001c0001t0003g0117a0001c0001t0003g0118a0001c0001t0014g0106 | 3 | HG02717.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-5-6677_-5-6676ins others(1): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17585393 | ||||||
| chr2:17585470
|
C | T | 1 | a0001c0001t0009g0165 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-5-6600C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17585470 | ||||||
| chr2:17585639
|
T | C | 45 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(42): Show | 46 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-5-6431T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17585639 | ||||||
| chr2:17585749
|
T | C | 56 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(53): Show | 57 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.-5-6321T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17585749 | ||||||
| chr2:17585807
|
TC | T | 3 | a0001c0001t0006g0173a0001c0001t0015g0162a0001c0001t0017g0067 | 3 | HG02015.hp2 HG03540.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-5-6262delC | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17585807 | ||||||
| chr2:17585808
|
C | T | 52 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(49): Show | 53 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.-5-6262C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17585808 | ||||||
| chr2:17585826
|
G | A | 11 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(8): Show | 12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5-6244G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17585826 | ||||||
| chr2:17586074
|
G | T | 1 | a0001c0001t0006g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-5-5996G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586074 | ||||||
| chr2:17586078
|
G | A | 1 | a0001c0001t0034g0108 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-5-5992G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586078 | ||||||
| chr2:17586089
|
A | T | 1 | a0001c0001t0006g0173 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-5-5981A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586089 | ||||||
| chr2:17586341
|
G | A | 45 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(42): Show | 46 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-5-5729G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586341 | ||||||
| chr2:17586405
|
C | A | 1 | a0001c0001t0001g0222 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-5-5665C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586405 | ||||||
| chr2:17586447
|
G | A | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-5-5623G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586447 | ||||||
| chr2:17586493
|
C | T | 45 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(42): Show | 46 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-5-5577C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586493 | ||||||
| chr2:17586610
|
C | T | 45 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(42): Show | 46 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-5-5460C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586610 | ||||||
| chr2:17586666
|
AC | A | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.-5-5403delC | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586666 | ||||||
| chr2:17586679
|
A | T | 1 | a0001c0001t0007g0215 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-5-5391A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586679 | ||||||
| chr2:17586714
|
C | T | 1 | a0001c0001t0002g0151 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-5-5356C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586714 | ||||||
| chr2:17586715
|
G | A | 45 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(42): Show | 46 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-5-5355G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586715 | ||||||
| chr2:17586740
|
T | A | 6 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0008g0119others(3): Show | 6 | HG01109.hp2 HG02886.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-5330T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586740 | ||||||
| chr2:17586748
|
C | T | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.-5-5322C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586748 | ||||||
| chr2:17586917
|
C | T | 1 | a0001c0001t0017g0223 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-5-5153C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586917 | ||||||
| chr2:17586943
|
A | G | 1 | a0001c0001t0021g0202 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-5-5127A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586943 | ||||||
| chr2:17586995
|
G | A | 3 | a0001c0001t0010g0078a0001c0001t0010g0079a0001c0001t0010g0080 | 3 | HG02717.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-5-5075G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586995 | ||||||
| chr2:17587095
|
A | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(188): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.-5-4975A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587095 | ||||||
| chr2:17587109
|
G | T | 1 | a0001c0001t0001g0054 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-5-4961G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587109 | ||||||
| chr2:17587151
|
A | T | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.-5-4919A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587151 | ||||||
| chr2:17587179
|
C | T | 1 | a0001c0001t0044g0030 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-5-4891C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587179 | ||||||
| chr2:17587296
|
A | G | 1 | a0001c0001t0026g0203 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-5-4774A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587296 | ||||||
| chr2:17587345
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(53): Show | 57 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.-5-4725G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587345 | ||||||
| chr2:17587348
|
A | AAC | 44 | a0001c0001t0001g0027a0001c0001t0001g0043a0001c0001t0001g0181others(41): Show | 44 | HG00140.hp2 HG00642.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.-5-4676_-5-4675dup others(2): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587348 | |||||
| chr2:17587348
|
A | AACAC | 13 | a0001c0001t0004g0017a0001c0001t0004g0097a0001c0001t0004g0098others(10): Show | 13 | HG01109.hp2 HG01168.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.-5-4678_-5-4675dup others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587348 | |||||
| chr2:17587348
|
A | AACACAC | 8 | a0001c0001t0001g0012a0001c0001t0004g0115a0001c0001t0005g0229others(5): Show | 8 | HG00738.hp2 HG01123.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-4680_-5-4675dup others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587348 | |||||
| chr2:17587348
|
A | AACACACA others(3): Show |
1 | a0001c0001t0032g0217 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-5-4684_-5-4675dup others(10): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587348 | |||||
| chr2:17587348
|
A | AACACACA others(5): Show |
1 | a0001c0001t0004g0211 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-5-4686_-5-4675dup others(12): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587348 | |||||
| chr2:17587348
|
AAC | A | 62 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(59): Show | 63 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.-5-4676_-5-4675del others(2): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587348 | |||||
| chr2:17587348
|
AACAC | A | 13 | a0001c0001t0001g0009a0001c0001t0001g0062a0001c0001t0004g0015others(10): Show | 13 | HG00438.hp1 HG01243.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.-5-4678_-5-4675del others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587348 | |||||
| chr2:17587348
|
AACACAC | A | 5 | a0001c0001t0010g0121a0001c0001t0010g0136a0001c0001t0012g0144others(2): Show | 5 | HG01981.hp1 HG02572.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-4680_-5-4675del others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587348 | |||||
| chr2:17587348
|
AACACACA others(7): Show |
A | 1 | a0001c0001t0004g0019 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-5-4688_-5-4675del others(14): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587348 | |||||
| chr2:17587394
|
C | CACACACA others(5): Show |
1 | a0001c0001t0016g0166 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-5-4675_-5-4674ins others(12): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587394 | |||||
| chr2:17587394
|
C | CACACAT | 5 | a0001c0001t0016g0172a0001c0001t0024g0169a0001c0001t0024g0170others(2): Show | 5 | HG02451.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-4675_-5-4674ins others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587394 | |||||
| chr2:17587394
|
C | CACAT | 4 | a0001c0001t0016g0163a0001c0001t0016g0168a0001c0001t0024g0167others(1): Show | 4 | HG00639.hp2 NA18945.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5-4675_-5-4674ins others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587394 | |||||
| chr2:17587394
|
C | CAT | 6 | a0001c0001t0006g0197a0001c0001t0008g0138a0001c0001t0009g0188others(3): Show | 6 | HG01069.hp2 HG01934.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-4671_-5-4670dup others(2): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587394 | |||||
| chr2:17587394
|
C | T | 28 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(25): Show | 29 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(26): Show |
intron_variant | MODIFIER | c.-5-4676C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587394 | ||||||
| chr2:17587488
|
C | T | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.-5-4582C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587488 | ||||||
| chr2:17587526
|
C | G | 45 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(42): Show | 46 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-5-4544C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587526 | ||||||
| chr2:17587540
|
C | T | 1 | a0001c0001t0015g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-5-4530C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587540 | ||||||
| chr2:17587556
|
C | A | 1 | a0001c0001t0034g0108 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-5-4514C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587556 | ||||||
| chr2:17587588
|
G | C | 10 | a0001c0001t0016g0163a0001c0001t0016g0166a0001c0001t0016g0168others(7): Show | 10 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.-5-4482G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587588 | ||||||
| chr2:17587652
|
C | G | 45 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(42): Show | 46 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-5-4418C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587652 | ||||||
| chr2:17587670
|
T | C | 45 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(42): Show | 46 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-5-4400T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587670 | ||||||
| chr2:17587701
|
C | T | 45 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(42): Show | 46 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-5-4369C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587701 | ||||||
| chr2:17587784
|
G | A | 6 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0008g0119others(3): Show | 6 | HG01109.hp2 HG02886.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-4286G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587784 | ||||||
| chr2:17587811
|
A | G | 45 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(42): Show | 46 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-5-4259A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587811 | ||||||
| chr2:17587889
|
G | A | 48 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.-5-4181G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587889 | ||||||
| chr2:17587917
|
A | G | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-5-4153A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587917 | ||||||
| chr2:17588183
|
G | A | 3 | a0001c0001t0011g0116a0001c0001t0011g0199a0001c0001t0011g0200 | 3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-5-3887G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17588183 | ||||||
| chr2:17588408
|
A | G | 216 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.-5-3662A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17588408 | ||||||
| chr2:17588717
|
A | T | 52 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(49): Show | 53 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.-5-3353A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17588717 | ||||||
| chr2:17588828
|
T | C | 47 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(44): Show | 48 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.-5-3242T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17588828 | ||||||
| chr2:17588968
|
C | T | 1 | a0001c0001t0034g0108 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-5-3102C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17588968 | ||||||
| chr2:17588971
|
T | A | 1 | a0001c0001t0012g0144 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-5-3099T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17588971 | ||||||
| chr2:17589009
|
A | T | 49 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(46): Show | 50 | HG00408.hp1 HG00438.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.-5-3061A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17589009 | ||||||
| chr2:17589030
|
A | G | 1 | a0001c0001t0016g0163 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-5-3040A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17589030 | ||||||
| chr2:17589176
|
T | C | 46 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(43): Show | 47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-5-2894T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17589176 | ||||||
| chr2:17589305
|
G | C | 1 | a0001c0001t0043g0220 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-5-2765G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17589305 | ||||||
| chr2:17589315
|
A | C | 1 | a0001c0001t0003g0104 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-5-2755A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17589315 | ||||||
| chr2:17589385
|
C | T | 1 | a0001c0001t0001g0018 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-5-2685C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17589385 | ||||||
| chr2:17589479
|
C | T | 1 | a0001c0001t0003g0104 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-5-2591C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17589479 | ||||||
| chr2:17589485
|
A | G | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-5-2585A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17589485 | ||||||
| chr2:17589626
|
G | A | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.-5-2444G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17589626 | ||||||
| chr2:17589670
|
T | C | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.-5-2400T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17589670 | ||||||
| chr2:17589861
|
C | T | 2 | a0001c0001t0027g0013a0001c0001t0027g0026 | 2 | HG00140.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-5-2209C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17589861 | ||||||
| chr2:17589940
|
G | A | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.-5-2130G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17589940 | ||||||
| chr2:17589950
|
TTCCTGTT others(5): Show |
T | 48 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.-5-2114_-5-2103del others(12): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17589950 | |||||
| chr2:17590009
|
C | T | 18 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0145others(15): Show | 18 | HG00099.hp2 HG00280.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.-5-2061C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17590009 | ||||||
| chr2:17590140
|
T | C | 1 | a0001c0001t0023g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-5-1930T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17590140 | ||||||
| chr2:17590146
|
T | C | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-5-1924T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17590146 | ||||||
| chr2:17590179
|
G | A | 3 | a0001c0001t0011g0116a0001c0001t0011g0199a0001c0001t0011g0200 | 3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-5-1891G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17590179 | ||||||
| chr2:17590387
|
C | A | 1 | a0001c0001t0002g0035 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-1683C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17590387 | ||||||
| chr2:17590829
|
G | C | 1 | a0001c0001t0002g0132 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-5-1241G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17590829 | ||||||
| chr2:17591039
|
A | T | 6 | a0001c0001t0007g0208a0001c0001t0007g0213a0001c0001t0007g0214others(3): Show | 6 | HG01891.hp1 HG02257.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-1031A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17591039 | ||||||
| chr2:17591150
|
A | C | 1 | a0001c0001t0006g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-5-920A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17591150 | ||||||
| chr2:17591238
|
G | T | 3 | a0001c0001t0010g0121a0001c0001t0010g0136a0001c0001t0040g0135 | 3 | HG02572.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-5-832G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17591238 | ||||||
| chr2:17591317
|
A | T | 2 | a0001c0001t0005g0002a0001c0001t0005g0129 | 3 | HG02055.hp2 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-5-753A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17591317 | ||||||
| chr2:17591804
|
T | C | 2 | a0001c0001t0017g0066a0001c0001t0017g0067 | 2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-5-266T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17591804 | ||||||
| chr2:17591978
|
C | T | 2 | a0001c0001t0001g0222a0001c0001t0032g0217 | 2 | NA19030.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-5-92C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17591978 | ||||||
| chr2:17592257
|
G | A | 128 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(125): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.162+21G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592257 | ||||||
| chr2:17592361
|
T | C | 3 | a0001c0001t0011g0116a0001c0001t0011g0199a0001c0001t0011g0200 | 3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.162+125T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592361 | ||||||
| chr2:17592489
|
T | C | 5 | a0001c0001t0016g0172a0001c0001t0024g0169a0001c0001t0024g0170others(2): Show | 5 | HG02451.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+253T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592489 | ||||||
| chr2:17592605
|
A | AAAAGTAC | 46 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(43): Show | 47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+371_162+377dup others(7): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592605 | |||||
| chr2:17592636
|
CTCTCTTT others(10): Show |
C | 1 | a0001c0001t0010g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.162+402_162+418del others(17): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592636 | |||||
| chr2:17592636
|
CTCTCTTT others(11): Show |
C | 1 | a0001c0001t0010g0121 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.162+402_162+419del others(18): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592636 | |||||
| chr2:17592640
|
C | CTTTTTTT others(3): Show |
4 | a0001c0001t0004g0211a0001c0001t0007g0206a0001c0001t0020g0210others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+434_162+443dup others(10): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | |||||
| chr2:17592640
|
CTTTTTTT others(1): Show |
C | 38 | a0001c0001t0002g0131a0001c0001t0003g0075a0001c0001t0003g0076others(35): Show | 38 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.162+436_162+443del others(8): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | |||||
| chr2:17592640
|
CTTTTTTT others(2): Show |
C | 32 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0132others(29): Show | 32 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.162+435_162+443del others(9): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | |||||
| chr2:17592640
|
CTTTTTTT others(3): Show |
C | 6 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0064others(3): Show | 6 | HG00438.hp1 HG01175.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+434_162+443del others(10): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | |||||
| chr2:17592640
|
CTTTTTTT others(4): Show |
C | 49 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0018others(46): Show | 50 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.162+433_162+443del others(11): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | |||||
| chr2:17592640
|
CTTTTTTT others(5): Show |
C | 28 | a0001c0001t0001g0011a0001c0001t0001g0065a0001c0001t0006g0039others(25): Show | 28 | HG00323.hp1 HG00639.hp2 HG01934.hp2 others(25): Show |
intron_variant | MODIFIER | c.162+432_162+443del others(12): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | |||||
| chr2:17592640
|
CTTTTTTT others(6): Show |
C | 5 | a0001c0001t0016g0166a0001c0001t0017g0008a0001c0001t0017g0066others(2): Show | 5 | HG02922.hp1 HG03130.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+431_162+443del others(13): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | |||||
| chr2:17592640
|
CTTTTTTT others(7): Show |
C | 10 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(7): Show | 11 | HG02055.hp2 HG02630.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+430_162+443del others(14): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | |||||
| chr2:17592640
|
CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0020g0122a0001c0001t0022g0126 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.162+429_162+443del others(15): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | |||||
| chr2:17592640
|
CTTTTTTT others(9): Show |
C | 4 | a0001c0001t0029g0219a0001c0001t0029g0221a0001c0001t0042g0218others(1): Show | 4 | HG01243.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+428_162+443del others(16): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | |||||
| chr2:17592640
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.162+427_162+443del others(17): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | |||||
| chr2:17592640
|
CTTTTTTT others(12): Show |
C | 9 | a0001c0001t0006g0191a0001c0001t0009g0188a0001c0001t0009g0195others(6): Show | 10 | HG00408.hp1 NA18612.hp2 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.162+425_162+443del others(19): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | |||||
| chr2:17592640
|
CTTTTTTT others(13): Show |
C | 13 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(10): Show | 13 | HG00438.hp2 HG02015.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.162+424_162+443del others(20): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | |||||
| chr2:17592642
|
T | C | 1 | a0001c0001t0005g0229 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.162+406T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592642 | ||||||
| chr2:17592648
|
T | C | 1 | a0001c0001t0021g0092 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.162+412T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592648 | ||||||
| chr2:17592649
|
T | C | 4 | a0001c0001t0003g0086a0001c0001t0003g0087a0001c0001t0014g0106others(1): Show | 4 | HG01981.hp2 HG02004.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+413T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592649 | ||||||
| chr2:17592650
|
T | C | 32 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(29): Show | 32 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.162+414T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592650 | ||||||
| chr2:17592651
|
T | C | 10 | a0001c0001t0003g0099a0001c0001t0004g0098a0001c0001t0004g0105others(7): Show | 10 | HG01069.hp1 HG01070.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.162+415T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592651 | ||||||
| chr2:17592652
|
T | C | 1 | a0001c0001t0004g0097 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.162+416T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592652 | ||||||
| chr2:17592653
|
T | C | 2 | a0001c0001t0006g0197a0001c0001t0016g0038 | 2 | HG01069.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.162+417T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592653 | ||||||
| chr2:17592654
|
T | C | 18 | a0001c0001t0008g0138a0001c0001t0008g0139a0001c0001t0008g0140others(15): Show | 18 | HG00639.hp2 HG01934.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.162+418T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592654 | ||||||
| chr2:17592655
|
T | C | 4 | a0001c0001t0016g0166a0001c0001t0017g0066a0001c0001t0017g0067others(1): Show | 4 | HG03130.hp1 HG03540.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+419T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592655 | ||||||
| chr2:17592659
|
T | C | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.162+423T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592659 | ||||||
| chr2:17592661
|
T | C | 9 | a0001c0001t0006g0191a0001c0001t0009g0188a0001c0001t0009g0195others(6): Show | 10 | HG00408.hp1 NA18612.hp2 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.162+425T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592661 | ||||||
| chr2:17592662
|
T | C | 12 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(9): Show | 12 | HG00438.hp2 HG02015.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.162+426T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592662 | ||||||
| chr2:17592731
|
A | C | 46 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(43): Show | 47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+495A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592731 | ||||||
| chr2:17592879
|
C | T | 46 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(43): Show | 47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+643C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592879 | ||||||
| chr2:17592886
|
G | A | 46 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(43): Show | 47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+650G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592886 | ||||||
| chr2:17592967
|
C | A | 3 | a0001c0001t0011g0116a0001c0001t0011g0199a0001c0001t0011g0200 | 3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.162+731C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592967 | ||||||
| chr2:17593154
|
G | A | 1 | a0001c0001t0004g0183 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.162+918G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593154 | ||||||
| chr2:17593239
|
T | C | 11 | a0001c0001t0008g0138a0001c0001t0008g0139a0001c0001t0008g0140others(8): Show | 11 | HG01934.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.162+1003T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593239 | ||||||
| chr2:17593367
|
A | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(125): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.162+1131A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593367 | ||||||
| chr2:17593379
|
T | C | 46 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(43): Show | 47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+1143T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593379 | ||||||
| chr2:17593418
|
G | C | 46 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(43): Show | 47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+1182G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593418 | ||||||
| chr2:17593434
|
T | C | 46 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(43): Show | 47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+1198T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593434 | ||||||
| chr2:17593479
|
A | G | 46 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(43): Show | 47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+1243A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593479 | ||||||
| chr2:17593551
|
T | C | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.162+1315T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593551 | ||||||
| chr2:17593566
|
T | C | 1 | a0001c0001t0003g0085 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.162+1330T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593566 | ||||||
| chr2:17593645
|
G | A | 46 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(43): Show | 47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+1409G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593645 | ||||||
| chr2:17593765
|
A | G | 47 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(44): Show | 48 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.162+1529A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593765 | ||||||
| chr2:17593894
|
C | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(202): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.162+1658C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593894 | ||||||
| chr2:17593938
|
T | C | 46 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(43): Show | 47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+1702T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593938 | ||||||
| chr2:17593995
|
G | C | 2 | a0001c0001t0012g0154a0001c0001t0012g0198 | 2 | HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.162+1759G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593995 | ||||||
| chr2:17594122
|
C | T | 11 | a0001c0001t0008g0138a0001c0001t0008g0139a0001c0001t0008g0140others(8): Show | 11 | HG01934.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.162+1886C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594122 | ||||||
| chr2:17594192
|
T | C | 2 | a0001c0001t0010g0121a0001c0001t0010g0136 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.162+1956T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594192 | ||||||
| chr2:17594440
|
A | C | 1 | a0001c0001t0004g0211 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.162+2204A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594440 | ||||||
| chr2:17594457
|
C | G | 1 | a0001c0001t0026g0204 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.162+2221C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594457 | ||||||
| chr2:17594521
|
T | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(225): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.162+2285T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594521 | ||||||
| chr2:17594526
|
T | C | 46 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(43): Show | 47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+2290T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594526 | ||||||
| chr2:17594561
|
G | A | 46 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(43): Show | 47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+2325G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594561 | ||||||
| chr2:17594573
|
G | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(55): Show | 59 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.162+2337G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594573 | ||||||
| chr2:17594578
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.162+2342A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594578 | ||||||
| chr2:17594663
|
G | C | 58 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(55): Show | 59 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.162+2427G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594663 | ||||||
| chr2:17594701
|
C | G | 3 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147 | 3 | HG00741.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.162+2465C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594701 | ||||||
| chr2:17594736
|
A | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(196): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.162+2500A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594736 | ||||||
| chr2:17594786
|
G | A | 45 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(42): Show | 46 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.162+2550G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594786 | ||||||
| chr2:17594811
|
G | A | 47 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(44): Show | 48 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.162+2575G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594811 | ||||||
| chr2:17595159
|
C | T | 58 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(55): Show | 59 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.162+2923C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17595159 | ||||||
| chr2:17595397
|
C | G | 1 | a0001c0001t0001g0222 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.162+3161C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17595397 | ||||||
| chr2:17595482
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.162+3246A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17595482 | ||||||
| chr2:17595539
|
A | G | 1 | a0001c0001t0012g0152 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.162+3303A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17595539 | ||||||
| chr2:17595721
|
TG | T | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+3486delG | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17595721 | ||||||
| chr2:17595730
|
G | A | 46 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(43): Show | 47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+3494G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17595730 | ||||||
| chr2:17595851
|
A | G | 1 | a0001c0001t0040g0135 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.162+3615A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17595851 | ||||||
| chr2:17595947
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.162+3711C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17595947 | ||||||
| chr2:17596101
|
A | G | 5 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0181others(2): Show | 5 | HG00099.hp1 HG01123.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+3865A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596101 | ||||||
| chr2:17596122
|
T | C | 4 | a0001c0001t0004g0183a0001c0001t0011g0116a0001c0001t0011g0199others(1): Show | 4 | HG00639.hp1 HG01074.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+3886T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596122 | ||||||
| chr2:17596151
|
A | G | 1 | a0001c0001t0021g0201 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.162+3915A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596151 | ||||||
| chr2:17596169
|
C | T | 1 | a0001c0001t0007g0216 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.162+3933C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596169 | ||||||
| chr2:17596223
|
C | T | 2 | a0001c0001t0002g0060a0001c0001t0006g0197 | 2 | HG01069.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.162+3987C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596223 | ||||||
| chr2:17596224
|
G | A | 2 | a0001c0001t0017g0066a0001c0001t0017g0067 | 2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.162+3988G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596224 | ||||||
| chr2:17596457
|
C | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(79): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.162+4221C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596457 | ||||||
| chr2:17596458
|
A | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(125): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.162+4222A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596458 | ||||||
| chr2:17596459
|
C | T | 1 | a0001c0001t0006g0173 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.162+4223C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596459 | ||||||
| chr2:17596679
|
A | T | 1 | a0001c0001t0006g0185 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.162+4443A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596679 | ||||||
| chr2:17596760
|
G | A | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+4524G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596760 | ||||||
| chr2:17596774
|
TGA | T | 14 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(11): Show | 15 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.162+4542_162+4543d others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17596774 | |||||
| chr2:17596817
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(202): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.162+4581A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596817 | ||||||
| chr2:17596862
|
C | T | 46 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(43): Show | 47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+4626C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596862 | ||||||
| chr2:17596959
|
A | C | 11 | a0001c0001t0016g0038a0001c0001t0016g0163a0001c0001t0016g0166others(8): Show | 11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+4723A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596959 | ||||||
| chr2:17597013
|
C | T | 1 | a0001c0001t0015g0162 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.162+4777C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17597013 | ||||||
| chr2:17597021
|
G | A | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+4785G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17597021 | ||||||
| chr2:17597022
|
A | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(79): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.162+4786A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17597022 | ||||||
| chr2:17597062
|
C | G | 37 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(34): Show | 38 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.162+4826C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17597062 | ||||||
| chr2:17597062
|
C | T | 1 | a0001c0001t0003g0076 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.162+4826C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17597062 | ||||||
| chr2:17597237
|
C | A | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.162+5001C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17597237 | ||||||
| chr2:17597441
|
C | T | 37 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(34): Show | 38 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.162+5205C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17597441 | ||||||
| chr2:17597511
|
C | G | 37 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(34): Show | 38 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.162+5275C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17597511 | ||||||
| chr2:17597515
|
T | A | 25 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(22): Show | 26 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.162+5279T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17597515 | ||||||
| chr2:17597676
|
C | T | 2 | a0001c0001t0017g0066a0001c0001t0017g0067 | 2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.162+5440C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17597676 | ||||||
| chr2:17597677
|
A | G | 46 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(43): Show | 47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+5441A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17597677 | ||||||
| chr2:17597755
|
TC | T | 25 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(22): Show | 26 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.162+5520delC | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17597755 | ||||||
| chr2:17598021
|
A | T | 1 | a0001c0001t0017g0008 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.162+5785A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17598021 | ||||||
| chr2:17598064
|
G | A | 5 | a0001c0001t0016g0172a0001c0001t0024g0169a0001c0001t0024g0170others(2): Show | 5 | HG02451.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+5828G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17598064 | ||||||
| chr2:17598374
|
A | T | 37 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(34): Show | 38 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.162+6138A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17598374 | ||||||
| chr2:17598486
|
C | G | 1 | a0001c0001t0045g0196 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.162+6250C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17598486 | ||||||
| chr2:17598534
|
G | A | 1 | a0001c0001t0017g0066 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.162+6298G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17598534 | ||||||
| chr2:17598552
|
A | C | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+6316A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17598552 | ||||||
| chr2:17598575
|
A | G | 1 | a0001c0001t0006g0185 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.162+6339A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17598575 | ||||||
| chr2:17598738
|
A | C | 1 | a0001c0001t0017g0066 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.162+6502A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17598738 | ||||||
| chr2:17598739
|
G | T | 1 | a0001c0001t0002g0155 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.162+6503G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17598739 | ||||||
| chr2:17598814
|
C | G | 43 | a0001c0001t0001g0222a0001c0001t0004g0211a0001c0001t0005g0226others(40): Show | 43 | HG01099.hp1 HG01109.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.162+6578C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17598814 | ||||||
| chr2:17599022
|
C | T | 1 | a0001c0001t0035g0228 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.162+6786C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17599022 | ||||||
| chr2:17599156
|
G | C | 170 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(167): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.162+6920G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17599156 | ||||||
| chr2:17599193
|
C | T | 1 | a0001c0001t0015g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.162+6957C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17599193 | ||||||
| chr2:17599216
|
G | A | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.162+6980G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17599216 | ||||||
| chr2:17599413
|
A | G | 6 | a0001c0001t0010g0078a0001c0001t0010g0079a0001c0001t0010g0080others(3): Show | 6 | HG01496.hp1 HG02109.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+7177A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17599413 | ||||||
| chr2:17599417
|
T | C | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+7181T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17599417 | ||||||
| chr2:17599424
|
T | A | 170 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(167): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.162+7188T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17599424 | ||||||
| chr2:17599446
|
T | C | 14 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(11): Show | 15 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.162+7210T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17599446 | ||||||
| chr2:17599466
|
T | A | 37 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(34): Show | 39 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.162+7230T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17599466 | ||||||
| chr2:17599594
|
C | G | 86 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(83): Show | 87 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.162+7358C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17599594 | ||||||
| chr2:17600064
|
A | T | 1 | a0001c0001t0005g0229 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.162+7828A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17600064 | ||||||
| chr2:17600112
|
A | G | 1 | a0001c0001t0019g0042 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.162+7876A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17600112 | ||||||
| chr2:17600124
|
T | C | 1 | a0001c0001t0006g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.162+7888T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17600124 | ||||||
| chr2:17600295
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.162+8059G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17600295 | ||||||
| chr2:17600537
|
T | G | 3 | a0001c0001t0003g0117a0001c0001t0003g0118a0001c0001t0014g0106 | 3 | HG02717.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.162+8301T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17600537 | ||||||
| chr2:17600619
|
T | C | 1 | a0001c0001t0009g0083 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.162+8383T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17600619 | ||||||
| chr2:17601052
|
A | T | 11 | a0001c0001t0016g0038a0001c0001t0016g0163a0001c0001t0016g0166others(8): Show | 11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+8816A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17601052 | ||||||
| chr2:17601289
|
A | T | 169 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(166): Show | 171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.162+9053A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17601289 | ||||||
| chr2:17601596
|
A | G | 1 | a0001c0001t0006g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.162+9360A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17601596 | ||||||
| chr2:17601627
|
C | T | 4 | a0001c0001t0007g0208a0001c0001t0007g0213a0001c0001t0007g0214others(1): Show | 4 | HG01891.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+9391C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17601627 | ||||||
| chr2:17601657
|
A | G | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+9421A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17601657 | ||||||
| chr2:17601923
|
G | A | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+9687G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17601923 | ||||||
| chr2:17602186
|
C | T | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+9950C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17602186 | ||||||
| chr2:17602211
|
G | A | 2 | a0001c0001t0012g0154a0001c0001t0012g0198 | 2 | HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.162+9975G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17602211 | ||||||
| chr2:17602574
|
C | T | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+10338C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17602574 | ||||||
| chr2:17602614
|
C | G | 2 | a0001c0001t0017g0066a0001c0001t0017g0067 | 2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.162+10378C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17602614 | ||||||
| chr2:17602697
|
G | A | 5 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(2): Show | 6 | HG02055.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+10461G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17602697 | ||||||
| chr2:17602763
|
TAAAATAA others(1): Show |
T | 23 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.162+10537_162+1054 others(12): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17602763 | |||||
| chr2:17602890
|
T | C | 47 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(44): Show | 48 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.162+10654T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17602890 | ||||||
| chr2:17602891
|
G | A | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.162+10655G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17602891 | ||||||
| chr2:17602927
|
A | G | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+10691A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17602927 | ||||||
| chr2:17602936
|
C | T | 4 | a0001c0001t0004g0183a0001c0001t0011g0116a0001c0001t0011g0199others(1): Show | 4 | HG00639.hp1 HG01074.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+10700C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17602936 | ||||||
| chr2:17602968
|
A | G | 11 | a0001c0001t0016g0038a0001c0001t0016g0163a0001c0001t0016g0166others(8): Show | 11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+10732A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17602968 | ||||||
| chr2:17603052
|
G | A | 47 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(44): Show | 48 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.162+10816G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17603052 | ||||||
| chr2:17603336
|
G | T | 34 | a0001c0001t0001g0222a0001c0001t0004g0211a0001c0001t0005g0226others(31): Show | 34 | HG01099.hp1 HG01109.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.162+11100G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17603336 | ||||||
| chr2:17603514
|
C | G | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+11278C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17603514 | ||||||
| chr2:17603719
|
C | T | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+11483C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17603719 | ||||||
| chr2:17603856
|
C | T | 21 | a0001c0001t0004g0211a0001c0001t0005g0226a0001c0001t0005g0227others(18): Show | 21 | HG01099.hp1 HG01243.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.162+11620C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17603856 | ||||||
| chr2:17604113
|
G | A | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+11877G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17604113 | ||||||
| chr2:17604190
|
A | T | 1 | a0001c0001t0015g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.162+11954A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17604190 | ||||||
| chr2:17604249
|
T | G | 10 | a0001c0001t0003g0104a0001c0001t0005g0071a0001c0001t0013g0068others(7): Show | 10 | HG00323.hp2 HG00738.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.162+12013T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17604249 | ||||||
| chr2:17604263
|
G | C | 2 | a0001c0001t0008g0119a0001c0001t0008g0120 | 2 | HG01109.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.162+12027G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17604263 | ||||||
| chr2:17604320
|
T | A | 1 | a0001c0001t0021g0201 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.162+12084T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17604320 | ||||||
| chr2:17604599
|
C | T | 1 | a0001c0001t0026g0204 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.162+12363C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17604599 | ||||||
| chr2:17604686
|
G | A | 47 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(44): Show | 48 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.162+12450G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17604686 | ||||||
| chr2:17604720
|
G | T | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+12484G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17604720 | ||||||
| chr2:17604990
|
T | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.162+12754T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17604990 | ||||||
| chr2:17605038
|
C | T | 4 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0005g0024others(1): Show | 4 | HG00280.hp2 HG01168.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+12802C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605038 | ||||||
| chr2:17605195
|
G | A | 3 | a0001c0001t0011g0116a0001c0001t0011g0199a0001c0001t0011g0200 | 3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.162+12959G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605195 | ||||||
| chr2:17605261
|
A | T | 1 | a0001c0001t0001g0009 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.162+13025A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605261 | ||||||
| chr2:17605291
|
G | A | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+13055G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605291 | ||||||
| chr2:17605292
|
C | A | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.162+13056C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605292 | ||||||
| chr2:17605337
|
A | G | 1 | a0001c0001t0015g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.162+13101A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605337 | ||||||
| chr2:17605364
|
C | G | 11 | a0001c0001t0016g0038a0001c0001t0016g0163a0001c0001t0016g0166others(8): Show | 11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+13128C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605364 | ||||||
| chr2:17605392
|
CT | C | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+13158delT | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17605392 | |||||
| chr2:17605464
|
A | T | 1 | a0001c0001t0001g0177 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.162+13228A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605464 | ||||||
| chr2:17605466
|
C | T | 11 | a0001c0001t0008g0138a0001c0001t0008g0139a0001c0001t0008g0140others(8): Show | 11 | HG01934.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.162+13230C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605466 | ||||||
| chr2:17605491
|
G | A | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+13255G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605491 | ||||||
| chr2:17605517
|
C | T | 1 | a0001c0001t0023g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.162+13281C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605517 | ||||||
| chr2:17605569
|
G | A | 1 | a0001c0001t0017g0008 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.162+13333G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605569 | ||||||
| chr2:17605829
|
T | A | 4 | a0001c0001t0006g0179a0001c0001t0010g0164a0001c0001t0010g0187others(1): Show | 4 | HG02145.hp1 HG02735.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+13593T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605829 | ||||||
| chr2:17605933
|
G | A | 1 | a0001c0001t0003g0088 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.162+13697G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605933 | ||||||
| chr2:17605999
|
C | T | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+13763C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605999 | ||||||
| chr2:17606186
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.162+13950C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17606186 | ||||||
| chr2:17606289
|
A | G | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+14053A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17606289 | ||||||
| chr2:17606308
|
C | CA | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+14072_162+1407 others(5): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17606308 | ||||||
| chr2:17606314
|
C | G | 11 | a0001c0001t0016g0038a0001c0001t0016g0163a0001c0001t0016g0166others(8): Show | 11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+14078C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17606314 | ||||||
| chr2:17606632
|
A | G | 170 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(167): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.162+14396A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17606632 | ||||||
| chr2:17606936
|
G | A | 1 | a0001c0001t0003g0075 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.162+14700G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17606936 | ||||||
| chr2:17607023
|
A | G | 4 | a0001c0001t0005g0226a0001c0001t0005g0227a0001c0001t0005g0229others(1): Show | 4 | HG03041.hp2 HG03453.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+14787A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17607023 | ||||||
| chr2:17607161
|
C | T | 34 | a0001c0001t0001g0222a0001c0001t0004g0211a0001c0001t0005g0226others(31): Show | 34 | HG01099.hp1 HG01109.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.162+14925C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17607161 | ||||||
| chr2:17607202
|
A | G | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+14966A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17607202 | ||||||
| chr2:17607225
|
G | A | 6 | a0001c0001t0010g0078a0001c0001t0010g0079a0001c0001t0010g0080others(3): Show | 6 | HG01496.hp1 HG02109.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+14989G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17607225 | ||||||
| chr2:17607476
|
G | T | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+15240G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17607476 | ||||||
| chr2:17607487
|
A | G | 1 | a0001c0001t0006g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.162+15251A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17607487 | ||||||
| chr2:17607523
|
G | C | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+15287G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17607523 | ||||||
| chr2:17607836
|
A | T | 47 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(44): Show | 48 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.162+15600A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17607836 | ||||||
| chr2:17607846
|
A | C | 1 | a0001c0001t0006g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.162+15610A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17607846 | ||||||
| chr2:17607853
|
T | A | 11 | a0001c0001t0008g0138a0001c0001t0008g0139a0001c0001t0008g0140others(8): Show | 11 | HG01934.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.162+15617T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17607853 | ||||||
| chr2:17607887
|
A | T | 4 | a0001c0001t0029g0219a0001c0001t0029g0221a0001c0001t0042g0218others(1): Show | 4 | HG01243.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+15651A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17607887 | ||||||
| chr2:17607986
|
C | T | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+15750C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17607986 | ||||||
| chr2:17608087
|
C | T | 1 | a0001c0001t0010g0078 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.162+15851C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17608087 | ||||||
| chr2:17608321
|
G | T | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.162+16085G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17608321 | ||||||
| chr2:17608337
|
G | A | 7 | a0001c0001t0005g0071a0001c0001t0013g0068a0001c0001t0013g0069others(4): Show | 7 | HG00323.hp2 HG00738.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.162+16101G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17608337 | ||||||
| chr2:17608461
|
G | A | 5 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0181others(2): Show | 5 | HG00099.hp1 HG01123.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+16225G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17608461 | ||||||
| chr2:17608866
|
T | C | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+16630T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17608866 | ||||||
| chr2:17609024
|
T | A | 1 | a0001c0001t0004g0183 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.162+16788T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609024 | ||||||
| chr2:17609045
|
G | A | 2 | a0001c0001t0010g0121a0001c0001t0010g0136 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.162+16809G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609045 | ||||||
| chr2:17609175
|
C | G | 6 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0153others(3): Show | 6 | HG00642.hp2 HG01168.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+16939C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609175 | ||||||
| chr2:17609246
|
C | T | 78 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(75): Show | 79 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.162+17010C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609246 | ||||||
| chr2:17609368
|
C | T | 1 | a0001c0001t0007g0216 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.162+17132C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609368 | ||||||
| chr2:17609504
|
G | C | 6 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0008g0119others(3): Show | 6 | HG01109.hp2 HG02886.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+17268G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609504 | ||||||
| chr2:17609515
|
T | C | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+17279T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609515 | ||||||
| chr2:17609609
|
T | C | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+17373T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609609 | ||||||
| chr2:17609642
|
A | C | 2 | a0001c0001t0005g0024a0001c0001t0005g0025 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.162+17406A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609642 | ||||||
| chr2:17609781
|
C | G | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+17545C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609781 | ||||||
| chr2:17609914
|
C | T | 3 | a0001c0001t0011g0116a0001c0001t0011g0199a0001c0001t0011g0200 | 3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.162+17678C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609914 | ||||||
| chr2:17609940
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0017g0066 | 2 | HG02015.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.162+17704C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609940 | ||||||
| chr2:17609964
|
T | G | 1 | a0001c0001t0004g0183 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.162+17728T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609964 | ||||||
| chr2:17609973
|
A | G | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+17737A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609973 | ||||||
| chr2:17610208
|
A | G | 3 | a0001c0001t0011g0116a0001c0001t0011g0199a0001c0001t0011g0200 | 3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.162+17972A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17610208 | ||||||
| chr2:17610215
|
T | C | 5 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(2): Show | 6 | HG02055.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+17979T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17610215 | ||||||
| chr2:17610771
|
G | T | 7 | a0001c0001t0003g0099a0001c0001t0004g0097a0001c0001t0004g0098others(4): Show | 7 | HG01891.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.162+18535G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17610771 | ||||||
| chr2:17610948
|
C | G | 47 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(44): Show | 48 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.162+18712C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17610948 | ||||||
| chr2:17611092
|
G | A | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+18856G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17611092 | ||||||
| chr2:17611312
|
C | T | 1 | a0001c0001t0008g0140 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.162+19076C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17611312 | ||||||
| chr2:17611431
|
G | A | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+19195G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17611431 | ||||||
| chr2:17611563
|
C | T | 34 | a0001c0001t0001g0222a0001c0001t0004g0211a0001c0001t0005g0226others(31): Show | 34 | HG01099.hp1 HG01109.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.162+19327C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17611563 | ||||||
| chr2:17611642
|
ACT | A | 4 | a0001c0001t0029g0219a0001c0001t0029g0221a0001c0001t0042g0218others(1): Show | 4 | HG01243.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+19411_162+1941 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17611642 | |||||
| chr2:17611826
|
A | G | 47 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(44): Show | 48 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.162+19590A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17611826 | ||||||
| chr2:17611828
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.162+19592T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17611828 | ||||||
| chr2:17611861
|
C | T | 170 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(167): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.162+19625C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17611861 | ||||||
| chr2:17612062
|
C | CTG | 18 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(15): Show | 18 | HG00642.hp2 HG00741.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.162+19837_162+1983 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17612062 | |||||
| chr2:17612062
|
CTG | C | 29 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(26): Show | 30 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(27): Show |
intron_variant | MODIFIER | c.162+19837_162+1983 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17612062 | |||||
| chr2:17612091
|
T | C | 47 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(44): Show | 48 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.162+19855T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17612091 | ||||||
| chr2:17612113
|
G | A | 4 | a0001c0001t0005g0226a0001c0001t0005g0227a0001c0001t0005g0229others(1): Show | 4 | HG03041.hp2 HG03453.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+19877G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17612113 | ||||||
| chr2:17612115
|
G | A | 11 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(8): Show | 12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.162+19879G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17612115 | ||||||
| chr2:17612298
|
G | A | 6 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0008g0119others(3): Show | 6 | HG01109.hp2 HG02886.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+20062G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17612298 | ||||||
| chr2:17612430
|
T | C | 169 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(166): Show | 171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.162+20194T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17612430 | ||||||
| chr2:17612627
|
C | T | 1 | a0001c0001t0010g0080 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.162+20391C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17612627 | ||||||
| chr2:17612967
|
G | A | 2 | a0001c0001t0010g0121a0001c0001t0010g0136 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.162+20731G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17612967 | ||||||
| chr2:17613064
|
A | G | 1 | a0001c0001t0038g0207 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.162+20828A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17613064 | ||||||
| chr2:17613087
|
G | A | 10 | a0001c0001t0003g0104a0001c0001t0005g0071a0001c0001t0013g0068others(7): Show | 10 | HG00323.hp2 HG00738.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.162+20851G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17613087 | ||||||
| chr2:17613137
|
C | G | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+20901C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17613137 | ||||||
| chr2:17613205
|
T | G | 170 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(167): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.162+20969T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17613205 | ||||||
| chr2:17613383
|
A | G | 1 | a0001c0001t0004g0105 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.162+21147A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17613383 | ||||||
| chr2:17613462
|
G | A | 3 | a0001c0001t0011g0116a0001c0001t0011g0199a0001c0001t0011g0200 | 3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.162+21226G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17613462 | ||||||
| chr2:17613530
|
C | T | 4 | a0001c0001t0004g0183a0001c0001t0011g0116a0001c0001t0011g0199others(1): Show | 4 | HG00639.hp1 HG01074.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+21294C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17613530 | ||||||
| chr2:17613635
|
A | G | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+21399A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17613635 | ||||||
| chr2:17613640
|
T | A | 2 | a0001c0001t0011g0093a0001c0001t0011g0100 | 2 | HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.162+21404T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17613640 | ||||||
| chr2:17613741
|
T | A | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+21505T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17613741 | ||||||
| chr2:17613757
|
C | T | 19 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(16): Show | 20 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.162+21521C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17613757 | ||||||
| chr2:17614018
|
C | T | 4 | a0001c0001t0006g0179a0001c0001t0010g0164a0001c0001t0010g0187others(1): Show | 4 | HG02145.hp1 HG02735.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+21782C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17614018 | ||||||
| chr2:17614030
|
T | C | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+21794T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17614030 | ||||||
| chr2:17614342
|
C | T | 10 | a0001c0001t0003g0104a0001c0001t0005g0071a0001c0001t0013g0068others(7): Show | 10 | HG00323.hp2 HG00738.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.162+22106C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17614342 | ||||||
| chr2:17614715
|
A | T | 2 | a0001c0001t0014g0224a0001c0001t0017g0223 | 2 | HG01099.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.162+22479A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17614715 | ||||||
| chr2:17614740
|
C | A | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+22504C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17614740 | ||||||
| chr2:17614851
|
G | A | 1 | a0001c0001t0032g0217 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.162+22615G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17614851 | ||||||
| chr2:17614898
|
C | T | 136 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(133): Show | 138 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.162+22662C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17614898 | ||||||
| chr2:17614906
|
A | C | 1 | a0001c0001t0006g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.162+22670A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17614906 | ||||||
| chr2:17614934
|
T | C | 1 | a0001c0001t0006g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.162+22698T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17614934 | ||||||
| chr2:17615038
|
T | C | 1 | a0001c0001t0010g0187 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.162+22802T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17615038 | ||||||
| chr2:17615120
|
A | T | 1 | a0001c0001t0002g0159 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.162+22884A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17615120 | ||||||
| chr2:17615248
|
T | A | 1 | a0001c0001t0016g0163 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.162+23012T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17615248 | ||||||
| chr2:17615250
|
G | T | 1 | a0001c0001t0016g0163 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.162+23014G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17615250 | ||||||
| chr2:17615557
|
T | C | 11 | a0001c0001t0016g0038a0001c0001t0016g0163a0001c0001t0016g0166others(8): Show | 11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+23321T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17615557 | ||||||
| chr2:17616016
|
T | C | 1 | a0001c0001t0009g0083 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.162+23780T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17616016 | ||||||
| chr2:17616193
|
T | G | 1 | a0001c0001t0017g0066 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.162+23957T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17616193 | ||||||
| chr2:17616210
|
C | T | 1 | a0001c0001t0011g0101 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.162+23974C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17616210 | ||||||
| chr2:17616241
|
G | A | 1 | a0001c0001t0004g0183 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.162+24005G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17616241 | ||||||
| chr2:17616330
|
G | A | 1 | a0001c0001t0012g0152 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.162+24094G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17616330 | ||||||
| chr2:17616391
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.162+24155C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17616391 | ||||||
| chr2:17616790
|
C | T | 11 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(8): Show | 12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.162+24554C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17616790 | ||||||
| chr2:17616978
|
G | GT | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+24742_162+2474 others(5): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17616978 | ||||||
| chr2:17617054
|
C | G | 1 | a0001c0001t0040g0135 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.162+24818C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17617054 | ||||||
| chr2:17617179
|
G | A | 4 | a0001c0001t0029g0219a0001c0001t0029g0221a0001c0001t0042g0218others(1): Show | 4 | HG01243.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+24943G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17617179 | ||||||
| chr2:17617235
|
C | T | 1 | a0001c0001t0031g0178 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.162+24999C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17617235 | ||||||
| chr2:17617257
|
G | T | 1 | a0001c0001t0002g0159 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.162+25021G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17617257 | ||||||
| chr2:17617262
|
A | G | 1 | a0001c0001t0002g0159 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.162+25026A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17617262 | ||||||
| chr2:17617495
|
TA | T | 29 | a0001c0001t0001g0047a0001c0001t0001g0053a0001c0001t0001g0222others(26): Show | 29 | HG00639.hp1 HG01074.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.162+25271delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17617495 | |||||
| chr2:17617510
|
G | A | 21 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(18): Show | 22 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.162+25274G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17617510 | ||||||
| chr2:17617627
|
G | A | 1 | a0001c0001t0008g0007 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.162+25391G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17617627 | ||||||
| chr2:17617705
|
G | A | 11 | a0001c0001t0008g0138a0001c0001t0008g0139a0001c0001t0008g0140others(8): Show | 11 | HG01934.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.162+25469G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17617705 | ||||||
| chr2:17617737
|
G | A | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+25501G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17617737 | ||||||
| chr2:17617885
|
A | ACACATGC others(15): Show |
24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+25650_162+2565 others(26): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17617885 | |||||
| chr2:17617889
|
G | A | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+25653G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17617889 | ||||||
| chr2:17617889
|
G | GCA | 20 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(17): Show | 21 | HG01069.hp2 HG01934.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.162+25673_162+2567 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17617889 | |||||
| chr2:17617889
|
G | GCACA | 5 | a0001c0001t0020g0122a0001c0001t0020g0123a0001c0001t0020g0124others(2): Show | 5 | HG02280.hp2 HG02630.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+25671_162+2567 others(8): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17617889 | |||||
| chr2:17618021
|
C | T | 46 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(43): Show | 47 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.162+25785C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17618021 | ||||||
| chr2:17618034
|
T | C | 1 | a0001c0001t0002g0153 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.162+25798T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17618034 | ||||||
| chr2:17618087
|
C | G | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.162+25851C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17618087 | ||||||
| chr2:17618232
|
T | G | 14 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(11): Show | 15 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.162+25996T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17618232 | ||||||
| chr2:17618294
|
A | G | 1 | a0001c0001t0004g0019 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.162+26058A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17618294 | ||||||
| chr2:17618308
|
T | C | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.162+26072T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17618308 | ||||||
| chr2:17618929
|
T | A | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.162+26693T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17618929 | ||||||
| chr2:17619011
|
G | T | 2 | a0001c0001t0017g0066a0001c0001t0017g0067 | 2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.162+26775G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17619011 | ||||||
| chr2:17619115
|
C | T | 9 | a0001c0001t0003g0104a0001c0001t0005g0071a0001c0001t0013g0068others(6): Show | 9 | HG00323.hp2 HG00738.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.162+26879C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17619115 | ||||||
| chr2:17619290
|
C | G | 26 | a0001c0001t0001g0222a0001c0001t0004g0211a0001c0001t0005g0226others(23): Show | 26 | HG00639.hp1 HG01074.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.162+27054C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17619290 | ||||||
| chr2:17619322
|
C | T | 27 | a0001c0001t0004g0115a0001c0001t0004g0183a0001c0001t0005g0002others(24): Show | 28 | HG00639.hp2 HG02055.hp2 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.162+27086C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17619322 | ||||||
| chr2:17619834
|
G | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0033others(2): Show | 5 | HG00408.hp2 NA18612.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+27598G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17619834 | ||||||
| chr2:17619862
|
TA | T | 6 | a0001c0001t0001g0047a0001c0001t0002g0159a0001c0001t0002g0161others(3): Show | 6 | HG00099.hp2 HG01099.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+27639delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17619862 | |||||
| chr2:17619862
|
TAA | T | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.162+27638_162+2763 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17619862 | |||||
| chr2:17619881
|
TC | T | 37 | a0001c0001t0001g0222a0001c0001t0004g0211a0001c0001t0005g0226others(34): Show | 37 | HG00639.hp1 HG01074.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.162+27653delC | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17619881 | |||||
| chr2:17619888
|
C | G | 2 | a0001c0001t0019g0205a0001c0001t0044g0030 | 2 | HG03579.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.162+27652C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17619888 | ||||||
| chr2:17619888
|
C | T | 47 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(44): Show | 48 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.162+27652C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17619888 | ||||||
| chr2:17620130
|
T | A | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.162+27894T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17620130 | ||||||
| chr2:17620221
|
A | G | 46 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(43): Show | 47 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.162+27985A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17620221 | ||||||
| chr2:17620566
|
G | A | 1 | a0001c0001t0001g0018 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.162+28330G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17620566 | ||||||
| chr2:17620768
|
CA | C | 5 | a0001c0001t0008g0139a0001c0001t0008g0143a0001c0001t0010g0121others(2): Show | 5 | HG02572.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+28541delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17620768 | |||||
| chr2:17620917
|
G | A | 48 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.163-28493G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17620917 | ||||||
| chr2:17621004
|
C | A | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-28406C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17621004 | ||||||
| chr2:17621184
|
C | T | 1 | a0001c0001t0007g0206 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.163-28226C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17621184 | ||||||
| chr2:17621189
|
A | G | 1 | a0001c0001t0004g0183 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.163-28221A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17621189 | ||||||
| chr2:17621306
|
C | T | 1 | a0001c0001t0006g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.163-28104C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17621306 | ||||||
| chr2:17621312
|
C | CCTTTTCT others(5): Show |
22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-28085_163-2807 others(16): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17621312 | |||||
| chr2:17621549
|
C | G | 4 | a0001c0001t0029g0219a0001c0001t0029g0221a0001c0001t0042g0218others(1): Show | 4 | HG01243.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-27861C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17621549 | ||||||
| chr2:17621651
|
G | T | 1 | a0001c0001t0007g0215 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.163-27759G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17621651 | ||||||
| chr2:17621728
|
A | G | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-27682A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17621728 | ||||||
| chr2:17621834
|
C | T | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-27576C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17621834 | ||||||
| chr2:17622208
|
A | G | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-27202A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622208 | ||||||
| chr2:17622212
|
C | CA | 31 | a0001c0001t0001g0057a0001c0001t0001g0222a0001c0001t0003g0114others(28): Show | 31 | HG00639.hp1 HG01074.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.163-27182dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622212 | |||||
| chr2:17622212
|
C | CAA | 11 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(8): Show | 12 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-27183_163-2718 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622212 | |||||
| chr2:17622212
|
CAA | C | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-27183_163-2718 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622212 | |||||
| chr2:17622334
|
C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0027others(1): Show | 5 | HG00735.hp2 HG00741.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-27076C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622334 | ||||||
| chr2:17622424
|
G | A | 6 | a0001c0001t0003g0085a0001c0001t0003g0086a0001c0001t0003g0087others(3): Show | 6 | HG00735.hp1 HG01433.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-26986G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622424 | ||||||
| chr2:17622430
|
G | A | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-26980G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622430 | ||||||
| chr2:17622440
|
G | T | 22 | a0001c0001t0004g0211a0001c0001t0005g0226a0001c0001t0005g0227others(19): Show | 22 | HG00639.hp1 HG01074.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.163-26970G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622440 | ||||||
| chr2:17622441
|
T | C | 1 | a0001c0001t0044g0030 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.163-26969T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622441 | ||||||
| chr2:17622453
|
G | A | 1 | a0001c0001t0003g0099 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.163-26957G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622453 | ||||||
| chr2:17622481
|
G | A | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-26929G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622481 | ||||||
| chr2:17622497
|
C | CA | 27 | a0001c0001t0003g0085a0001c0001t0003g0099a0001c0001t0003g0114others(24): Show | 27 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.163-26901dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622497 | |||||
| chr2:17622504
|
AAAAAAGA others(7): Show |
A | 3 | a0001c0001t0006g0179a0001c0001t0017g0008a0001c0001t0031g0178 | 3 | HG02735.hp2 HG02922.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.163-26901_163-2688 others(18): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622504 | |||||
| chr2:17622506
|
AAAAGAAA others(5): Show |
A | 20 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(17): Show | 20 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.163-26900_163-2688 others(16): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622506 | |||||
| chr2:17622507
|
AAAGAAAG others(4): Show |
A | 1 | a0001c0001t0004g0113 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.163-26900_163-2689 others(15): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622507 | |||||
| chr2:17622519
|
AAAAGAAA others(54): Show |
A | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-26875_163-2681 others(65): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622519 | |||||
| chr2:17622528
|
AAAGAAAA others(21): Show |
A | 1 | a0001c0001t0006g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.163-26879_163-2685 others(32): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622528 | |||||
| chr2:17622528
|
AAAGAAAA others(29): Show |
A | 1 | a0001c0001t0004g0183 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.163-26879_163-2684 others(40): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622528 | |||||
| chr2:17622531
|
GAAAAGAA others(20): Show |
G | 1 | a0001c0001t0010g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.163-26877_163-2685 others(31): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622531 | |||||
| chr2:17622532
|
A | AAAAG | 7 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0051others(4): Show | 7 | HG00099.hp2 HG02015.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-26810_163-2680 others(8): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622532 | |||||
| chr2:17622532
|
A | AAAGAAAG others(4): Show |
2 | a0001c0001t0001g0052a0001c0001t0028g0032 | 2 | HG01981.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.163-26876_163-2687 others(15): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622532 | |||||
| chr2:17622532
|
AAAAG | A | 30 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0040others(27): Show | 30 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.163-26810_163-2680 others(8): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622532 | |||||
| chr2:17622532
|
AAAAGAAA others(1): Show |
A | 42 | a0001c0001t0001g0027a0001c0001t0001g0043a0001c0001t0001g0049others(39): Show | 42 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.163-26814_163-2680 others(12): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622532 | |||||
| chr2:17622532
|
AAAAGAAA others(5): Show |
A | 29 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0048others(26): Show | 29 | HG00280.hp1 HG00438.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.163-26818_163-2680 others(16): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622532 | |||||
| chr2:17622532
|
AAAAGAAA others(9): Show |
A | 16 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0045others(13): Show | 18 | HG00735.hp2 HG01074.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.163-26822_163-2680 others(20): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622532 | |||||
| chr2:17622532
|
AAAAGAAA others(13): Show |
A | 10 | a0001c0001t0002g0131a0001c0001t0005g0229a0001c0001t0007g0208others(7): Show | 10 | HG00639.hp2 HG02896.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.163-26826_163-2680 others(24): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622532 | |||||
| chr2:17622532
|
AAAAGAAA others(17): Show |
A | 7 | a0001c0001t0007g0213a0001c0001t0007g0216a0001c0001t0010g0121others(4): Show | 7 | HG01099.hp1 HG01891.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-26830_163-2680 others(28): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622532 | |||||
| chr2:17622532
|
AAAAGAAA others(21): Show |
A | 7 | a0001c0001t0005g0071a0001c0001t0007g0215a0001c0001t0011g0110others(4): Show | 7 | HG00323.hp2 HG00738.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-26834_163-2680 others(32): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622532 | |||||
| chr2:17622532
|
AAAAGAAA others(25): Show |
A | 4 | a0001c0001t0003g0085a0001c0001t0011g0093a0001c0001t0011g0100others(1): Show | 4 | HG01516.hp2 HG02886.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-26838_163-2680 others(36): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622532 | |||||
| chr2:17622542
|
A | AAGAAAGA others(3): Show |
1 | a0001c0001t0019g0042 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.163-26866_163-2685 others(14): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622542 | |||||
| chr2:17622545
|
AAAG | A | 4 | a0001c0001t0003g0076a0001c0001t0003g0077a0001c0001t0006g0179others(1): Show | 4 | HG01192.hp1 HG02723.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-26862_163-2686 others(7): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622545 | |||||
| chr2:17622545
|
AAAGAAAG | A | 7 | a0001c0001t0003g0075a0001c0001t0003g0086a0001c0001t0003g0087others(4): Show | 7 | HG01175.hp1 HG01981.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-26862_163-2685 others(11): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622545 | |||||
| chr2:17622545
|
AAAGAAAG others(4): Show |
A | 12 | a0001c0001t0003g0088a0001c0001t0003g0090a0001c0001t0003g0104others(9): Show | 12 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-26862_163-2685 others(15): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622545 | |||||
| chr2:17622576
|
GAAAGAAA others(18): Show |
G | 1 | a0001c0001t0014g0103 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.163-26820_163-2679 others(29): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622576 | |||||
| chr2:17622600
|
GA | G | 23 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(20): Show | 24 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-26806delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622600 | |||||
| chr2:17622604
|
A | G | 1 | a0001c0001t0006g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.163-26806A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622604 | ||||||
| chr2:17622613
|
G | A | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-26797G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622613 | ||||||
| chr2:17622826
|
G | C | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-26584G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622826 | ||||||
| chr2:17622842
|
C | T | 4 | a0001c0001t0029g0219a0001c0001t0029g0221a0001c0001t0042g0218others(1): Show | 4 | HG01243.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-26568C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622842 | ||||||
| chr2:17622877
|
G | A | 9 | a0001c0001t0008g0138a0001c0001t0008g0139a0001c0001t0008g0140others(6): Show | 9 | HG01934.hp2 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.163-26533G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622877 | ||||||
| chr2:17623169
|
T | TA | 11 | a0001c0001t0016g0038a0001c0001t0016g0163a0001c0001t0016g0166others(8): Show | 11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-26233dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17623169 | |||||
| chr2:17623170
|
A | T | 1 | a0001c0001t0002g0060 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.163-26240A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623170 | ||||||
| chr2:17623273
|
A | G | 46 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(43): Show | 47 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.163-26137A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623273 | ||||||
| chr2:17623318
|
G | T | 1 | a0001c0001t0002g0159 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.163-26092G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623318 | ||||||
| chr2:17623397
|
C | T | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-26013C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623397 | ||||||
| chr2:17623399
|
G | A | 1 | a0001c0001t0023g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.163-26011G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623399 | ||||||
| chr2:17623432
|
G | C | 1 | a0001c0001t0002g0159 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.163-25978G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623432 | ||||||
| chr2:17623458
|
A | G | 2 | a0001c0001t0012g0154a0001c0001t0012g0198 | 2 | HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.163-25952A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623458 | ||||||
| chr2:17623486
|
G | A | 10 | a0001c0001t0003g0104a0001c0001t0005g0071a0001c0001t0013g0068others(7): Show | 10 | HG00323.hp2 HG00738.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.163-25924G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623486 | ||||||
| chr2:17623493
|
C | G | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-25917C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623493 | ||||||
| chr2:17623562
|
C | T | 2 | a0001c0001t0007g0111a0001c0001t0007g0112 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.163-25848C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623562 | ||||||
| chr2:17623602
|
G | A | 1 | a0001c0001t0002g0153 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.163-25808G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623602 | ||||||
| chr2:17623604
|
A | C | 11 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(8): Show | 12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.163-25806A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623604 | ||||||
| chr2:17623638
|
G | C | 159 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(156): Show | 161 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.163-25772G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623638 | ||||||
| chr2:17623648
|
C | T | 1 | a0001c0001t0016g0038 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.163-25762C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623648 | ||||||
| chr2:17623669
|
C | CA | 25 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0043others(22): Show | 25 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.163-25718dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17623669 | |||||
| chr2:17623669
|
CA | C | 81 | a0001c0001t0001g0031a0001c0001t0002g0035a0001c0001t0002g0036others(78): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.163-25718delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17623669 | |||||
| chr2:17623669
|
CAA | C | 36 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(33): Show | 37 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.163-25719_163-2571 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17623669 | |||||
| chr2:17623959
|
T | G | 3 | a0001c0001t0003g0117a0001c0001t0003g0118a0001c0001t0014g0106 | 3 | HG02717.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.163-25451T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623959 | ||||||
| chr2:17624387
|
A | G | 1 | a0001c0001t0006g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.163-25023A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17624387 | ||||||
| chr2:17624401
|
A | C | 1 | a0001c0001t0001g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.163-25009A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17624401 | ||||||
| chr2:17624512
|
T | G | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-24898T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17624512 | ||||||
| chr2:17624519
|
T | G | 1 | a0001c0001t0006g0016 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.163-24891T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17624519 | ||||||
| chr2:17624592
|
G | A | 1 | a0001c0001t0003g0114 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.163-24818G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17624592 | ||||||
| chr2:17624611
|
G | A | 11 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(8): Show | 12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.163-24799G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17624611 | ||||||
| chr2:17624677
|
A | G | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-24733A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17624677 | ||||||
| chr2:17624732
|
A | G | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-24678A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17624732 | ||||||
| chr2:17624896
|
A | T | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-24514A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17624896 | ||||||
| chr2:17625054
|
G | A | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-24356G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17625054 | ||||||
| chr2:17625087
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.163-24323T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17625087 | ||||||
| chr2:17625145
|
G | T | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-24265G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17625145 | ||||||
| chr2:17625162
|
G | C | 1 | a0001c0001t0001g0180 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.163-24248G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17625162 | ||||||
| chr2:17625312
|
A | G | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-24098A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17625312 | ||||||
| chr2:17625387
|
C | T | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-24023C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17625387 | ||||||
| chr2:17625493
|
T | C | 2 | a0001c0001t0029g0219a0001c0001t0043g0220 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.163-23917T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17625493 | ||||||
| chr2:17625840
|
A | AT | 35 | a0001c0001t0001g0018a0001c0001t0001g0027a0001c0001t0001g0053others(32): Show | 36 | HG00639.hp2 HG00735.hp1 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.163-23547dupT | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17625840 | |||||
| chr2:17625840
|
A | ATT | 7 | a0001c0001t0004g0115a0001c0001t0006g0197a0001c0001t0010g0136others(4): Show | 7 | HG01069.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-23548_163-2354 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17625840 | |||||
| chr2:17625840
|
AT | A | 71 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.163-23547delT | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17625840 | |||||
| chr2:17625840
|
ATT | A | 10 | a0001c0001t0002g0149a0001c0001t0005g0226a0001c0001t0006g0191others(7): Show | 11 | HG00408.hp1 HG02698.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-23548_163-2354 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17625840 | |||||
| chr2:17625888
|
C | T | 1 | a0001c0001t0040g0135 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.163-23522C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17625888 | ||||||
| chr2:17626021
|
G | T | 1 | a0001c0001t0006g0039 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.163-23389G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17626021 | ||||||
| chr2:17626170
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.163-23240G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17626170 | ||||||
| chr2:17626202
|
C | T | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-23208C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17626202 | ||||||
| chr2:17626312
|
T | C | 46 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(43): Show | 47 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.163-23098T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17626312 | ||||||
| chr2:17626359
|
A | G | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-23051A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17626359 | ||||||
| chr2:17626499
|
T | C | 2 | a0001c0001t0024g0169a0001c0001t0024g0170 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.163-22911T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17626499 | ||||||
| chr2:17626603
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.163-22807A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17626603 | ||||||
| chr2:17626764
|
T | C | 2 | a0001c0001t0006g0197a0001c0001t0023g0084 | 2 | HG01069.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.163-22646T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17626764 | ||||||
| chr2:17626849
|
AATG | A | 11 | a0001c0001t0004g0211a0001c0001t0007g0206a0001c0001t0007g0208others(8): Show | 11 | HG01261.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.163-22556_163-2255 others(7): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17626849 | |||||
| chr2:17626866
|
G | C | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-22544G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17626866 | ||||||
| chr2:17626917
|
G | C | 26 | a0001c0001t0001g0222a0001c0001t0004g0211a0001c0001t0005g0226others(23): Show | 26 | HG00639.hp1 HG01074.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.163-22493G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17626917 | ||||||
| chr2:17627174
|
T | A | 1 | a0001c0001t0001g0065 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.163-22236T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17627174 | ||||||
| chr2:17627284
|
C | T | 48 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.163-22126C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17627284 | ||||||
| chr2:17627330
|
A | G | 1 | a0001c0001t0006g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.163-22080A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17627330 | ||||||
| chr2:17627904
|
C | T | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-21506C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17627904 | ||||||
| chr2:17628218
|
C | T | 1 | a0001c0001t0011g0101 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.163-21192C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17628218 | ||||||
| chr2:17628226
|
C | G | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0186 | 3 | NA18967.hp2 NA18978.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.163-21184C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17628226 | ||||||
| chr2:17628274
|
T | G | 2 | a0001c0001t0014g0082a0001c0001t0014g0103 | 2 | NA18955.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.163-21136T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17628274 | ||||||
| chr2:17628361
|
G | A | 1 | a0001c0001t0040g0135 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.163-21049G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17628361 | ||||||
| chr2:17628396
|
A | G | 1 | a0001c0001t0007g0208 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.163-21014A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17628396 | ||||||
| chr2:17628480
|
A | G | 4 | a0001c0001t0029g0219a0001c0001t0029g0221a0001c0001t0042g0218others(1): Show | 4 | HG01243.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-20930A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17628480 | ||||||
| chr2:17628509
|
C | CA | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-20900dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17628509 | |||||
| chr2:17628629
|
C | T | 1 | a0001c0001t0031g0178 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.163-20781C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17628629 | ||||||
| chr2:17629035
|
G | T | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-20375G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17629035 | ||||||
| chr2:17629261
|
A | C | 60 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(57): Show | 60 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.163-20149A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17629261 | ||||||
| chr2:17629378
|
T | C | 2 | a0001c0001t0021g0091a0001c0001t0021g0092 | 2 | HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.163-20032T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17629378 | ||||||
| chr2:17629555
|
T | C | 48 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.163-19855T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17629555 | ||||||
| chr2:17629575
|
C | T | 2 | a0001c0001t0023g0142a0001c0001t0037g0137 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.163-19835C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17629575 | ||||||
| chr2:17629727
|
C | T | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-19683C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17629727 | ||||||
| chr2:17629835
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.163-19575C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17629835 | ||||||
| chr2:17629859
|
G | A | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-19551G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17629859 | ||||||
| chr2:17629971
|
T | C | 1 | a0001c0001t0003g0104 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.163-19439T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17629971 | ||||||
| chr2:17630015
|
G | A | 2 | a0001c0001t0001g0222a0001c0001t0032g0217 | 2 | NA19030.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.163-19395G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17630015 | ||||||
| chr2:17630087
|
C | A | 122 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(119): Show | 124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.163-19323C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17630087 | ||||||
| chr2:17630111
|
A | C | 170 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(167): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.163-19299A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17630111 | ||||||
| chr2:17630209
|
T | C | 6 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0008g0119others(3): Show | 6 | HG01109.hp2 HG02886.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-19201T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17630209 | ||||||
| chr2:17630463
|
A | G | 1 | a0001c0001t0004g0183 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.163-18947A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17630463 | ||||||
| chr2:17630679
|
G | A | 11 | a0001c0001t0004g0211a0001c0001t0007g0206a0001c0001t0007g0208others(8): Show | 11 | HG01261.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.163-18731G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17630679 | ||||||
| chr2:17630749
|
C | T | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-18661C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17630749 | ||||||
| chr2:17630961
|
T | C | 3 | a0001c0001t0003g0117a0001c0001t0003g0118a0001c0001t0014g0106 | 3 | HG02717.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.163-18449T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17630961 | ||||||
| chr2:17631026
|
C | T | 1 | a0001c0001t0017g0081 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.163-18384C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17631026 | ||||||
| chr2:17631074
|
G | A | 1 | a0001c0001t0017g0066 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.163-18336G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17631074 | ||||||
| chr2:17631275
|
C | T | 3 | a0001c0001t0011g0116a0001c0001t0011g0199a0001c0001t0011g0200 | 3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.163-18135C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17631275 | ||||||
| chr2:17631361
|
A | G | 5 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(2): Show | 6 | HG02055.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-18049A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17631361 | ||||||
| chr2:17631614
|
T | A | 1 | a0001c0001t0006g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.163-17796T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17631614 | ||||||
| chr2:17631623
|
C | T | 2 | a0001c0001t0009g0175a0001c0001t0009g0176 | 2 | HG00438.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.163-17787C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17631623 | ||||||
| chr2:17631675
|
T | C | 7 | a0001c0001t0005g0226a0001c0001t0005g0227a0001c0001t0005g0229others(4): Show | 7 | HG00639.hp1 HG01074.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-17735T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17631675 | ||||||
| chr2:17631764
|
G | A | 46 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(43): Show | 47 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.163-17646G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17631764 | ||||||
| chr2:17631805
|
C | T | 1 | a0001c0001t0007g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.163-17605C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17631805 | ||||||
| chr2:17631806
|
G | A | 24 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0131others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-17604G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17631806 | ||||||
| chr2:17631823
|
A | C | 170 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(167): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.163-17587A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17631823 | ||||||
| chr2:17631973
|
G | A | 1 | a0001c0001t0006g0039 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.163-17437G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17631973 | ||||||
| chr2:17632003
|
C | T | 4 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0023g0004others(1): Show | 4 | HG02886.hp1 HG02965.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-17407C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17632003 | ||||||
| chr2:17632011
|
C | T | 18 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0145others(15): Show | 18 | HG00099.hp2 HG00280.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.163-17399C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17632011 | ||||||
| chr2:17632012
|
A | G | 151 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(148): Show | 152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.163-17398A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17632012 | ||||||
| chr2:17632252
|
T | A | 5 | a0001c0001t0010g0121a0001c0001t0010g0136a0001c0001t0017g0066others(2): Show | 5 | HG02572.hp1 HG02886.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-17158T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17632252 | ||||||
| chr2:17632280
|
T | G | 1 | a0001c0001t0006g0039 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.163-17130T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17632280 | ||||||
| chr2:17632403
|
T | C | 176 | a0001c0001t0001g0012a0001c0001t0001g0134a0001c0001t0001g0174others(173): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.163-17007T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17632403 | ||||||
| chr2:17632466
|
A | G | 17 | a0001c0001t0005g0229a0001c0001t0008g0006a0001c0001t0008g0007others(14): Show | 17 | HG01109.hp2 HG02559.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.163-16944A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17632466 | ||||||
| chr2:17632483
|
T | C | 6 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0008g0119others(3): Show | 6 | HG01109.hp2 HG02886.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-16927T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17632483 | ||||||
| chr2:17632607
|
A | G | 1 | a0001c0001t0040g0135 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.163-16803A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17632607 | ||||||
| chr2:17632763
|
T | C | 176 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(173): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.163-16647T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17632763 | ||||||
| chr2:17633109
|
C | T | 13 | a0001c0001t0008g0138a0001c0001t0008g0139a0001c0001t0008g0140others(10): Show | 13 | HG01934.hp2 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.163-16301C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17633109 | ||||||
| chr2:17633321
|
C | T | 3 | a0001c0001t0010g0164a0001c0001t0010g0187a0001c0001t0031g0178 | 3 | HG02145.hp1 HG03669.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.163-16089C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17633321 | ||||||
| chr2:17633347
|
A | G | 1 | a0001c0001t0006g0056 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.163-16063A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17633347 | ||||||
| chr2:17633348
|
CA | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.163-16038delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17633348 | |||||
| chr2:17633348
|
CAA | C | 41 | a0001c0001t0001g0181a0001c0001t0002g0147a0001c0001t0002g0153others(38): Show | 41 | HG00140.hp1 HG00639.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.163-16039_163-1603 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17633348 | |||||
| chr2:17633428
|
A | C | 6 | a0001c0001t0016g0038a0001c0001t0016g0163a0001c0001t0016g0166others(3): Show | 6 | HG00639.hp2 NA18945.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-15982A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17633428 | ||||||
| chr2:17633882
|
C | G | 1 | a0001c0001t0002g0060 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.163-15528C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17633882 | ||||||
| chr2:17633921
|
A | G | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-15489A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17633921 | ||||||
| chr2:17634462
|
C | T | 1 | a0001c0001t0006g0173 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.163-14948C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17634462 | ||||||
| chr2:17634506
|
G | C | 1 | a0001c0001t0040g0135 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.163-14904G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17634506 | ||||||
| chr2:17634567
|
G | A | 1 | a0001c0001t0015g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.163-14843G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17634567 | ||||||
| chr2:17634588
|
T | C | 11 | a0001c0001t0016g0038a0001c0001t0016g0163a0001c0001t0016g0166others(8): Show | 11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-14822T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17634588 | ||||||
| chr2:17634790
|
C | T | 1 | a0001c0001t0003g0099 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.163-14620C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17634790 | ||||||
| chr2:17634866
|
G | A | 1 | a0001c0001t0040g0135 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.163-14544G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17634866 | ||||||
| chr2:17634874
|
G | C | 1 | a0001c0001t0001g0040 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.163-14536G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17634874 | ||||||
| chr2:17634898
|
G | A | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-14512G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17634898 | ||||||
| chr2:17634927
|
C | T | 1 | a0001c0001t0004g0183 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.163-14483C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17634927 | ||||||
| chr2:17634991
|
T | C | 2 | a0001c0001t0033g0209a0001c0001t0034g0108 | 2 | HG01496.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.163-14419T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17634991 | ||||||
| chr2:17635059
|
A | G | 95 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(92): Show | 97 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.163-14351A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17635059 | ||||||
| chr2:17635209
|
C | A | 11 | a0001c0001t0016g0038a0001c0001t0016g0163a0001c0001t0016g0166others(8): Show | 11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-14201C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17635209 | ||||||
| chr2:17635220
|
A | G | 19 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0008g0119others(16): Show | 19 | HG01109.hp2 HG01934.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.163-14190A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17635220 | ||||||
| chr2:17635515
|
C | A | 1 | a0001c0001t0009g0188 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.163-13895C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17635515 | ||||||
| chr2:17635567
|
A | G | 1 | a0001c0001t0016g0168 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.163-13843A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17635567 | ||||||
| chr2:17635645
|
T | C | 1 | a0001c0001t0006g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.163-13765T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17635645 | ||||||
| chr2:17636045
|
A | C | 19 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0008g0119others(16): Show | 19 | HG01109.hp2 HG01934.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.163-13365A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17636045 | ||||||
| chr2:17636065
|
C | G | 11 | a0001c0001t0016g0038a0001c0001t0016g0163a0001c0001t0016g0166others(8): Show | 11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-13345C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17636065 | ||||||
| chr2:17636106
|
T | C | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-13304T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17636106 | ||||||
| chr2:17636108
|
T | A | 9 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(6): Show | 10 | HG01069.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.163-13302T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17636108 | ||||||
| chr2:17636263
|
A | G | 1 | a0001c0001t0011g0101 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.163-13147A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17636263 | ||||||
| chr2:17636571
|
G | A | 44 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(41): Show | 44 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.163-12839G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17636571 | ||||||
| chr2:17636722
|
ATT | A | 167 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0060others(164): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.163-12677_163-1267 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17636722 | |||||
| chr2:17636722
|
ATTT | A | 11 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(8): Show | 11 | HG02015.hp2 HG02056.hp1 HG03579.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-12678_163-1267 others(7): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17636722 | |||||
| chr2:17636817
|
G | A | 1 | a0001c0001t0006g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.163-12593G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17636817 | ||||||
| chr2:17636832
|
G | T | 5 | a0001c0001t0016g0172a0001c0001t0024g0169a0001c0001t0024g0170others(2): Show | 5 | HG02451.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-12578G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17636832 | ||||||
| chr2:17636895
|
T | C | 10 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(7): Show | 10 | HG02015.hp2 HG02056.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.163-12515T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17636895 | ||||||
| chr2:17637205
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.163-12205G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17637205 | ||||||
| chr2:17637271
|
C | T | 11 | a0001c0001t0016g0038a0001c0001t0016g0163a0001c0001t0016g0166others(8): Show | 11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-12139C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17637271 | ||||||
| chr2:17637272
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.163-12138G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17637272 | ||||||
| chr2:17637365
|
CAG | C | 11 | a0001c0001t0016g0038a0001c0001t0016g0163a0001c0001t0016g0166others(8): Show | 11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-12042_163-1204 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17637365 | |||||
| chr2:17637586
|
T | C | 2 | a0001c0001t0022g0126a0001c0001t0022g0127 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.163-11824T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17637586 | ||||||
| chr2:17637616
|
G | A | 1 | a0001c0001t0002g0161 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.163-11794G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17637616 | ||||||
| chr2:17637752
|
C | T | 1 | a0001c0001t0001g0222 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.163-11658C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17637752 | ||||||
| chr2:17638057
|
A | T | 1 | a0001c0001t0001g0027 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.163-11353A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17638057 | ||||||
| chr2:17638142
|
A | G | 11 | a0001c0001t0016g0038a0001c0001t0016g0163a0001c0001t0016g0166others(8): Show | 11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-11268A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17638142 | ||||||
| chr2:17638182
|
CACTA | C | 2 | a0001c0001t0010g0121a0001c0001t0010g0136 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.163-11222_163-1121 others(8): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17638182 | |||||
| chr2:17638562
|
G | A | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-10848G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17638562 | ||||||
| chr2:17638703
|
C | A | 1 | a0001c0001t0010g0080 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163-10707C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17638703 | ||||||
| chr2:17638909
|
A | G | 2 | a0001c0001t0011g0101a0001c0001t0011g0110 | 2 | HG01070.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.163-10501A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17638909 | ||||||
| chr2:17639050
|
T | C | 11 | a0001c0001t0016g0038a0001c0001t0016g0163a0001c0001t0016g0166others(8): Show | 11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-10360T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17639050 | ||||||
| chr2:17639178
|
T | C | 1 | a0001c0001t0009g0188 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.163-10232T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17639178 | ||||||
| chr2:17639471
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.163-9939A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17639471 | ||||||
| chr2:17639789
|
A | T | 47 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(44): Show | 47 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.163-9621A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17639789 | ||||||
| chr2:17639890
|
C | A | 1 | a0001c0001t0003g0104 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.163-9520C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17639890 | ||||||
| chr2:17639916
|
CA | C | 2 | a0001c0001t0017g0008a0001c0001t0017g0223 | 2 | HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.163-9493delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17639916 | ||||||
| chr2:17640067
|
C | T | 1 | a0001c0001t0015g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.163-9343C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17640067 | ||||||
| chr2:17640110
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.163-9300C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17640110 | ||||||
| chr2:17640207
|
C | T | 2 | a0001c0001t0014g0082a0001c0001t0014g0103 | 2 | NA18955.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.163-9203C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17640207 | ||||||
| chr2:17640252
|
C | CA | 70 | a0001c0001t0001g0047a0001c0001t0003g0075a0001c0001t0003g0076others(67): Show | 70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.163-9141dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17640252 | |||||
| chr2:17640270
|
G | A | 12 | a0001c0001t0004g0183a0001c0001t0016g0038a0001c0001t0016g0163others(9): Show | 12 | HG00639.hp2 HG02451.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-9140G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17640270 | ||||||
| chr2:17640554
|
C | T | 1 | a0001c0001t0015g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.163-8856C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17640554 | ||||||
| chr2:17640699
|
T | C | 19 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(16): Show | 19 | HG00140.hp1 HG00735.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.163-8711T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17640699 | ||||||
| chr2:17641322
|
G | C | 1 | a0001c0001t0044g0030 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.163-8088G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17641322 | ||||||
| chr2:17641385
|
A | G | 1 | a0001c0001t0013g0070 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.163-8025A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17641385 | ||||||
| chr2:17641408
|
A | G | 38 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0060others(35): Show | 39 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.163-8002A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17641408 | ||||||
| chr2:17642042
|
T | C | 1 | a0001c0001t0001g0053 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.163-7368T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17642042 | ||||||
| chr2:17642080
|
A | G | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-7330A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17642080 | ||||||
| chr2:17642225
|
G | A | 33 | a0001c0001t0007g0111a0001c0001t0007g0112a0001c0001t0007g0206others(30): Show | 33 | HG00140.hp2 HG00639.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.163-7185G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17642225 | ||||||
| chr2:17642309
|
C | CT | 10 | a0001c0001t0001g0034a0001c0001t0001g0133a0001c0001t0001g0134others(7): Show | 10 | HG02015.hp2 HG04204.hp1 NA18747.hp1 others(7): Show |
intron_variant | MODIFIER | c.163-7084dupT | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | |||||
| chr2:17642309
|
C | CTTT | 9 | a0001c0001t0003g0075a0001c0001t0020g0122a0001c0001t0020g0123others(6): Show | 9 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.163-7086_163-7084d others(5): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | |||||
| chr2:17642309
|
C | CTTTTTT | 15 | a0001c0001t0003g0076a0001c0001t0003g0077a0001c0001t0003g0085others(12): Show | 15 | HG00140.hp1 HG00735.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.163-7089_163-7084d others(8): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | |||||
| chr2:17642309
|
C | CTTTTTTT others(4): Show |
9 | a0001c0001t0016g0038a0001c0001t0016g0166a0001c0001t0016g0168others(6): Show | 9 | HG00639.hp2 HG02896.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.163-7094_163-7084d others(13): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | |||||
| chr2:17642309
|
C | CTTTTTTT others(5): Show |
4 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0016g0163others(1): Show | 4 | HG00280.hp2 HG01168.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-7095_163-7084d others(14): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | |||||
| chr2:17642309
|
C | CTTTTTTT others(6): Show |
3 | a0001c0001t0004g0015a0001c0001t0004g0029a0001c0001t0005g0024 | 3 | HG01258.hp2 HG01517.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.163-7096_163-7084d others(15): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | |||||
| chr2:17642309
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0013g0073 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.163-7097_163-7084d others(16): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | |||||
| chr2:17642309
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0040g0135 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.163-7100_163-7084d others(19): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | |||||
| chr2:17642309
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0002g0153 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.163-7084_163-7083i others(20): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | |||||
| chr2:17642309
|
C | CTTTTTTT others(12): Show |
10 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0132others(7): Show | 10 | HG02129.hp2 HG02155.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.163-7084_163-7083i others(21): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | |||||
| chr2:17642309
|
C | CTTTTTTT others(13): Show |
21 | a0001c0001t0002g0060a0001c0001t0002g0131a0001c0001t0002g0146others(18): Show | 22 | HG00408.hp1 HG00642.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.163-7084_163-7083i others(22): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | |||||
| chr2:17642309
|
C | CTTTTTTT others(14): Show |
11 | a0001c0001t0002g0145a0001c0001t0002g0150a0001c0001t0002g0151others(8): Show | 11 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-7084_163-7083i others(23): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | |||||
| chr2:17642309
|
C | CTTTTTTT others(15): Show |
1 | a0001c0001t0002g0159 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.163-7084_163-7083i others(24): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | |||||
| chr2:17642309
|
C | CTTTTTTT others(16): Show |
3 | a0001c0001t0005g0025a0001c0001t0013g0095a0001c0001t0041g0096 | 3 | HG01257.hp1 HG01257.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.163-7084_163-7083i others(25): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | |||||
| chr2:17642309
|
C | CTTTTTTT others(17): Show |
1 | a0001c0001t0013g0072 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.163-7084_163-7083i others(26): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | |||||
| chr2:17642309
|
C | CTTTTTTT others(18): Show |
6 | a0001c0001t0004g0098a0001c0001t0005g0071a0001c0001t0013g0068others(3): Show | 6 | HG00738.hp1 HG01192.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-7084_163-7083i others(27): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | |||||
| chr2:17642309
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0004g0097 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.163-7084_163-7083i others(28): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | |||||
| chr2:17642309
|
C | CTTTTTTT others(20): Show |
1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-7084_163-7083i others(29): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | |||||
| chr2:17642309
|
C | CTTTTTTT others(21): Show |
6 | a0001c0001t0004g0105a0001c0001t0004g0107a0001c0001t0004g0211others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-7084_163-7083i others(30): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | |||||
| chr2:17642309
|
C | CTTTTTTT others(22): Show |
3 | a0001c0001t0003g0099a0001c0001t0004g0113a0001c0001t0005g0229 | 3 | HG03209.hp1 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.163-7084_163-7083i others(31): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | |||||
| chr2:17642309
|
C | CTTTTTTT others(26): Show |
1 | a0001c0001t0005g0226 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.163-7084_163-7083i others(35): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | |||||
| chr2:17642309
|
CTT | C | 36 | a0001c0001t0007g0111a0001c0001t0007g0112a0001c0001t0007g0206others(33): Show | 36 | HG00140.hp2 HG00639.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.163-7085_163-7084d others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | |||||
| chr2:17642324
|
T | C | 5 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(2): Show | 6 | HG02055.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-7086T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17642324 | ||||||
| chr2:17642509
|
C | T | 1 | a0001c0001t0016g0163 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.163-6901C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17642509 | ||||||
| chr2:17642523
|
T | C | 8 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0008g0119others(5): Show | 8 | HG01109.hp2 HG02258.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.163-6887T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17642523 | ||||||
| chr2:17642530
|
G | A | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-6880G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17642530 | ||||||
| chr2:17642554
|
C | T | 2 | a0001c0001t0018g0058a0001c0001t0019g0042 | 2 | HG02155.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.163-6856C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17642554 | ||||||
| chr2:17642600
|
G | A | 104 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(101): Show | 105 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.163-6810G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17642600 | ||||||
| chr2:17642702
|
G | A | 1 | a0001c0001t0021g0202 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.163-6708G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17642702 | ||||||
| chr2:17642714
|
C | G | 11 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(8): Show | 11 | HG02015.hp2 HG02056.hp1 HG03579.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-6696C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17642714 | ||||||
| chr2:17642848
|
T | C | 8 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(5): Show | 8 | HG02015.hp2 HG02056.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.163-6562T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17642848 | ||||||
| chr2:17643069
|
ATG | A | 3 | a0001c0001t0010g0078a0001c0001t0010g0079a0001c0001t0010g0080 | 3 | HG02717.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.163-6337_163-6336d others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17643069 | |||||
| chr2:17643102
|
C | A | 1 | a0001c0001t0006g0179 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.163-6308C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17643102 | ||||||
| chr2:17643113
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.163-6297G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17643113 | ||||||
| chr2:17643219
|
T | A | 2 | a0001c0001t0009g0195a0001c0001t0045g0196 | 2 | NA18948.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.163-6191T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17643219 | ||||||
| chr2:17643353
|
C | T | 1 | a0001c0001t0018g0189 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.163-6057C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17643353 | ||||||
| chr2:17643416
|
A | G | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-5994A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17643416 | ||||||
| chr2:17643628
|
C | T | 4 | a0001c0001t0005g0226a0001c0001t0005g0227a0001c0001t0005g0229others(1): Show | 4 | HG03041.hp2 HG03453.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-5782C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17643628 | ||||||
| chr2:17643643
|
C | T | 1 | a0001c0001t0039g0102 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.163-5767C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17643643 | ||||||
| chr2:17643836
|
A | G | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-5574A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17643836 | ||||||
| chr2:17643913
|
C | T | 51 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(48): Show | 52 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.163-5497C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17643913 | ||||||
| chr2:17644036
|
CTT | C | 2 | a0001c0001t0017g0008a0001c0001t0017g0223 | 2 | HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.163-5373_163-5372d others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17644036 | ||||||
| chr2:17644079
|
G | A | 32 | a0001c0001t0007g0111a0001c0001t0007g0112a0001c0001t0007g0206others(29): Show | 32 | HG00140.hp2 HG00639.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.163-5331G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17644079 | ||||||
| chr2:17644725
|
T | G | 14 | a0001c0001t0007g0111a0001c0001t0007g0112a0001c0001t0010g0078others(11): Show | 14 | HG01069.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.163-4685T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17644725 | ||||||
| chr2:17644751
|
C | T | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-4659C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17644751 | ||||||
| chr2:17644764
|
A | G | 3 | a0001c0001t0003g0086a0001c0001t0003g0087a0001c0001t0003g0104 | 3 | HG01109.hp1 HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.163-4646A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17644764 | ||||||
| chr2:17645111
|
T | A | 1 | a0001c0001t0001g0052 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.163-4299T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17645111 | ||||||
| chr2:17645184
|
T | C | 2 | a0001c0001t0009g0195a0001c0001t0045g0196 | 2 | NA18948.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.163-4226T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17645184 | ||||||
| chr2:17645310
|
C | T | 8 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0008g0119others(5): Show | 8 | HG01109.hp2 HG02258.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.163-4100C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17645310 | ||||||
| chr2:17645577
|
C | T | 7 | a0001c0001t0008g0138a0001c0001t0008g0139a0001c0001t0008g0140others(4): Show | 7 | HG02559.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-3833C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17645577 | ||||||
| chr2:17645850
|
CA | C | 59 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(56): Show | 60 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.163-3559delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17645850 | ||||||
| chr2:17646158
|
AC | A | 5 | a0001c0001t0004g0115a0001c0001t0005g0002a0001c0001t0005g0128others(2): Show | 6 | HG02055.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-3251delC | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17646158 | ||||||
| chr2:17646568
|
A | G | 10 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(7): Show | 10 | HG02015.hp2 HG02056.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.163-2842A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17646568 | ||||||
| chr2:17646753
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.163-2657T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17646753 | ||||||
| chr2:17646758
|
C | T | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-2652C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17646758 | ||||||
| chr2:17646865
|
G | A | 11 | a0001c0001t0016g0038a0001c0001t0016g0163a0001c0001t0016g0166others(8): Show | 11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-2545G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17646865 | ||||||
| chr2:17647020
|
T | C | 2 | a0001c0001t0010g0121a0001c0001t0010g0136 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.163-2390T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17647020 | ||||||
| chr2:17647072
|
T | C | 1 | a0001c0001t0006g0185 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.163-2338T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17647072 | ||||||
| chr2:17647177
|
G | A | 3 | a0001c0001t0003g0086a0001c0001t0003g0087a0001c0001t0003g0104 | 3 | HG01109.hp1 HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.163-2233G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17647177 | ||||||
| chr2:17647344
|
G | A | 1 | a0001c0001t0013g0070 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.163-2066G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17647344 | ||||||
| chr2:17647379
|
G | C | 1 | a0001c0001t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-2031G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17647379 | ||||||
| chr2:17647416
|
C | T | 137 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(134): Show | 138 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.163-1994C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17647416 | ||||||
| chr2:17647610
|
T | C | 1 | a0001c0001t0021g0201 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.163-1800T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17647610 | ||||||
| chr2:17647769
|
T | C | 1 | a0001c0001t0002g0153 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.163-1641T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17647769 | ||||||
| chr2:17647847
|
T | C | 13 | a0001c0001t0010g0121a0001c0001t0010g0136a0001c0001t0016g0038others(10): Show | 13 | HG00639.hp2 HG02451.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.163-1563T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17647847 | ||||||
| chr2:17648182
|
T | C | 1 | a0001c0001t0014g0224 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.163-1228T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17648182 | ||||||
| chr2:17648214
|
C | T | 2 | a0001c0001t0010g0121a0001c0001t0010g0136 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.163-1196C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17648214 | ||||||
| chr2:17648332
|
A | C | 1 | a0001c0001t0004g0019 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.163-1078A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17648332 | ||||||
| chr2:17648761
|
C | A | 3 | a0001c0001t0003g0086a0001c0001t0003g0087a0001c0001t0003g0104 | 3 | HG01109.hp1 HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.163-649C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17648761 | ||||||
| chr2:17648864
|
A | G | 3 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077 | 3 | HG02559.hp2 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.163-546A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17648864 | ||||||
| chr2:17648890
|
T | C | 1 | a0001c0001t0009g0165 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.163-520T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17648890 | ||||||
| chr2:17648993
|
G | C | 3 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0023 | 3 | HG00408.hp2 HG00438.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.163-417G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17648993 | ||||||
| chr2:17649070
|
G | A | 1 | a0001c0001t0021g0092 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.163-340G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17649070 | ||||||
| chr2:17649142
|
T | C | 2 | a0001c0001t0002g0035a0001c0001t0002g0036 | 2 | HG02129.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.163-268T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17649142 | ||||||
| chr2:17649332
|
T | G | 12 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(9): Show | 12 | HG02056.hp1 HG02129.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.163-78T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17649332 | ||||||
| chr2:17649644
|
T | C | 1 | a0001c0001t0007g0214 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.378+19T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17649644 | ||||||
| chr2:17649724
|
G | A | 1 | a0001c0001t0003g0077 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.378+99G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17649724 | ||||||
| chr2:17649746
|
C | T | 2 | a0001c0001t0021g0201a0001c0001t0021g0202 | 2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.378+121C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17649746 | ||||||
| chr2:17649920
|
T | G | 2 | a0001c0001t0021g0091a0001c0001t0021g0092 | 2 | HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.378+295T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17649920 | ||||||
| chr2:17649933
|
G | A | 1 | a0001c0001t0030g0141 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.378+308G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17649933 | ||||||
| chr2:17649962
|
G | A | 1 | a0001c0001t0012g0144 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.378+337G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17649962 | ||||||
| chr2:17650050
|
G | A | 1 | a0001c0001t0031g0178 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.378+425G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17650050 | ||||||
| chr2:17650351
|
C | T | 176 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(173): Show | 178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.378+726C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17650351 | ||||||
| chr2:17650427
|
C | T | 2 | a0001c0001t0010g0121a0001c0001t0010g0136 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.378+802C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17650427 | ||||||
| chr2:17650791
|
T | G | 11 | a0001c0001t0016g0038a0001c0001t0016g0163a0001c0001t0016g0166others(8): Show | 11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.378+1166T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17650791 | ||||||
| chr2:17651261
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.378+1636G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17651261 | ||||||
| chr2:17651659
|
C | T | 1 | a0001c0001t0015g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.378+2034C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17651659 | ||||||
| chr2:17651706
|
TTC | T | 3 | a0001c0001t0010g0121a0001c0001t0010g0136a0001c0001t0019g0205 | 3 | HG02572.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.378+2085_378+2086d others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 17651706 | |||||
| chr2:17652120
|
A | G | 88 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(85): Show | 89 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.378+2495A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17652120 | ||||||
| chr2:17652207
|
TC | T | 88 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(85): Show | 89 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.378+2584delC | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 17652207 | |||||
| chr2:17652209
|
C | G | 88 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(85): Show | 89 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.378+2584C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17652209 | ||||||
| chr2:17652316
|
G | T | 1 | a0001c0001t0003g0088 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.378+2691G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17652316 | ||||||
| chr2:17652372
|
T | C | 110 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(107): Show | 111 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.378+2747T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17652372 | ||||||
| chr2:17652688
|
A | G | 1 | a0001c0001t0015g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.379-2509A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17652688 | ||||||
| chr2:17653185
|
C | T | 104 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(101): Show | 104 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.379-2012C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17653185 | ||||||
| chr2:17653348
|
T | A | 8 | a0001c0001t0007g0206a0001c0001t0007g0208a0001c0001t0007g0212others(5): Show | 8 | HG01261.hp1 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-1849T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17653348 | ||||||
| chr2:17653391
|
C | T | 1 | a0001c0001t0002g0060 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.379-1806C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17653391 | ||||||
| chr2:17653434
|
C | T | 2 | a0001c0001t0008g0119a0001c0001t0008g0120 | 2 | HG01109.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.379-1763C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17653434 | ||||||
| chr2:17653487
|
T | C | 88 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(85): Show | 89 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.379-1710T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17653487 | ||||||
| chr2:17653603
|
T | C | 1 | a0001c0001t0003g0114 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.379-1594T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17653603 | ||||||
| chr2:17653636
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.379-1561C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17653636 | ||||||
| chr2:17653782
|
A | C | 90 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(87): Show | 91 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.379-1415A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17653782 | ||||||
| chr2:17653797
|
C | G | 88 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(85): Show | 89 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.379-1400C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17653797 | ||||||
| chr2:17653828
|
T | A | 88 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(85): Show | 89 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.379-1369T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17653828 | ||||||
| chr2:17653991
|
C | T | 8 | a0001c0001t0020g0122a0001c0001t0020g0123a0001c0001t0020g0124others(5): Show | 8 | HG02257.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.379-1206C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17653991 | ||||||
| chr2:17653992
|
A | G | 88 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0077others(85): Show | 89 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.379-1205A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17653992 | ||||||
| chr2:17654022
|
A | G | 1 | a0001c0001t0015g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.379-1175A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17654022 | ||||||
| chr2:17654115
|
G | A | 1 | a0001c0001t0006g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.379-1082G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17654115 | ||||||
| chr2:17654368
|
A | G | 9 | a0001c0001t0010g0078a0001c0001t0010g0079a0001c0001t0010g0080others(6): Show | 9 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.379-829A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17654368 | ||||||
| chr2:17654456
|
A | G | 1 | a0001c0001t0009g0044 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.379-741A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17654456 | ||||||
| chr2:17654507
|
T | C | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(19): Show | 22 | HG00140.hp2 HG01069.hp2 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.379-690T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17654507 | ||||||
| chr2:17654626
|
C | T | 1 | a0001c0001t0010g0187 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.379-571C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17654626 | ||||||
| chr2:17654788
|
A | G | 3 | a0001c0001t0013g0072a0001c0001t0013g0073a0001c0001t0013g0074 | 3 | HG01192.hp1 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.379-409A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17654788 | ||||||
| chr2:17654794
|
C | G | 2 | a0001c0001t0001g0011a0001c0001t0007g0206 | 2 | HG01261.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.379-403C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17654794 | ||||||
| chr2:17654953
|
T | C | 2 | a0001c0001t0021g0201a0001c0001t0021g0202 | 2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.379-244T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17654953 | ||||||
| chr2:17655183
|
C | CT | 25 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0174others(22): Show | 25 | HG00140.hp2 HG00639.hp1 HG01069.hp2 others(22): Show |
splice_region_variant&intron_variant | LOW | c.379-8dupT | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 17655183 |