Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 7414 |
|---|---|
| ensemblid | ENSG00000035403.18 |
| hgncid | 12665 |
| symbol | VCL |
| name | vinculin |
| refseq_nuc | NM_014000.3 |
| refseq_prot | NP_054706.1 |
| ensembl_nuc | ENST00000211998.10 |
| ensembl_prot | ENSP00000211998.5 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 73998116 |
| end | 74120169 |
| strand | + |
| ver | v1.2 |
| region | chr10:73998116-74120169 |
| region5000 | chr10:73993116-74125169 |
| regionname0 | VCL_chr10_73998116_74120169 |
| regionname5000 | VCL_chr10_73993116_74125169 |
| 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 | 1134 | 245 | 72 | 57 | 82 | 9 | 23 | 56 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0002 | 0/0 | 1134 | 10 | 0 | 2 | 7 | 1 | 0 | 6 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0003 | 0/0 | 1134 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0004 | 0/0 | 1134 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0005 | 0/0 | 1134 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0006 | 0/0 | 1134 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0007 | 0/0 | 1134 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0008 | 0/0 | 1134 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 3405 | 82 | 3 | 24 | 37 | 6 | 11 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| c0002 | 0/0 | 3405 | 60 | 27 | 13 | 16 | 2 | 2 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| c0003 | 1/0 | 3405 | 56 | 3 | 13 | 29 | 1 | 9 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| c0004 | 0/0 | 3405 | 12 | 11 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| c0005 | 0/0 | 3405 | 9 | 0 | 2 | 6 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| c0006 | 0/0 | 3405 | 9 | 9 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| c0007 | 0/0 | 3405 | 8 | 5 | 3 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| c0008 | 0/0 | 3405 | 8 | 6 | 2 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| c0009 | 0/0 | 3405 | 5 | 4 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| c0010 | 0/0 | 3405 | 4 | 0 | 0 | 4 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| c0011 | 0/0 | 3405 | 2 | 2 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| c0012 | 0/0 | 3405 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| c0013 | 0/0 | 3405 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| c0014 | 0/0 | 3405 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| c0015 | 0/0 | 3405 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| c0016 | 0/0 | 3405 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| c0017 | 0/0 | 3405 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| c0018 | 0/0 | 3405 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| c0019 | 0/0 | 3405 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| c0020 | 0/0 | 3405 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2097 | 90 | 16 | 22 | 34 | 6 | 11 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| t0002 | 1/0 | 2093 | 72 | 16 | 15 | 31 | 1 | 8 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| t0003 | 0/0 | 2094 | 29 | 3 | 10 | 12 | 2 | 2 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| t0004 | 0/0 | 2096 | 11 | 6 | 4 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| t0005 | 0/0 | 2094 | 10 | 10 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| t0006 | 0/0 | 2095 | 7 | 3 | 3 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| t0007 | 0/0 | 2099 | 7 | 1 | 1 | 4 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| t0008 | 0/0 | 2092 | 6 | 1 | 0 | 5 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| t0009 | 0/0 | 2094 | 5 | 0 | 1 | 2 | 0 | 2 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| t0010 | 0/0 | 2093 | 5 | 0 | 2 | 2 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| t0011 | 0/0 | 2094 | 4 | 3 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| t0012 | 0/0 | 2099 | 3 | 3 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| t0013 | 0/0 | 2099 | 2 | 2 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| t0014 | 0/0 | 2097 | 2 | 2 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| t0015 | 0/0 | 2093 | 2 | 2 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| t0016 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| t0017 | 0/0 | 2094 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| t0018 | 0/0 | 2098 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| t0019 | 0/0 | 2093 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| t0020 | 0/0 | 2168 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| t0021 | 0/0 | 2095 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| t0022 | 0/0 | 2093 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| t0023 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| t0024 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0068 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3405 | 82 | 3 | 24 | 37 | 6 | 11 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0002 | 0/0 | 3405 | 60 | 27 | 13 | 16 | 2 | 2 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0003 | 1/0 | 3405 | 56 | 3 | 13 | 29 | 1 | 9 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0004 | 0/0 | 3405 | 12 | 11 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0006 | 0/0 | 3405 | 9 | 9 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0007 | 0/0 | 3405 | 8 | 5 | 3 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0008 | 0/0 | 3405 | 8 | 6 | 2 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0009 | 0/0 | 3405 | 5 | 4 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0011 | 0/0 | 3405 | 2 | 2 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0012 | 0/0 | 3405 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0013 | 0/0 | 3405 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0018 | 0/0 | 3405 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0002c0005 | 0/0 | 3405 | 9 | 0 | 2 | 6 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0002c0015 | 0/0 | 3405 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0003c0010 | 0/0 | 3405 | 4 | 0 | 0 | 4 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0004c0020 | 0/0 | 3405 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0005c0014 | 0/0 | 3405 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0006c0016 | 0/0 | 3405 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0007c0017 | 0/0 | 3405 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0008c0019 | 0/0 | 3405 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5501 | 75 | 1 | 22 | 34 | 6 | 11 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0001t0004 | 0/0 | 5500 | 4 | 1 | 2 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0001t0006 | 0/0 | 5499 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0001t0023 | 0/0 | 5501 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0001t0024 | 0/0 | 5501 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0002t0001 | 0/0 | 5501 | 9 | 9 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0002t0003 | 0/0 | 5498 | 26 | 2 | 9 | 12 | 2 | 1 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0002t0004 | 0/0 | 5500 | 4 | 3 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0002t0005 | 0/0 | 5498 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0002t0006 | 0/0 | 5499 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0002t0007 | 0/0 | 5503 | 7 | 1 | 1 | 4 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0002t0011 | 0/0 | 5498 | 4 | 3 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0002t0012 | 0/0 | 5503 | 3 | 3 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0002t0014 | 0/0 | 5501 | 2 | 2 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0002t0015 | 0/0 | 5497 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0002t0019 | 0/0 | 5497 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0002t0020 | 0/0 | 5572 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0003t0001 | 0/0 | 5501 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0003t0002 | 1/0 | 5497 | 47 | 1 | 12 | 25 | 1 | 7 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0003t0008 | 0/0 | 5496 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0003t0009 | 0/0 | 5498 | 5 | 0 | 1 | 2 | 0 | 2 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0003t0021 | 0/0 | 5499 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0003t0022 | 0/0 | 5497 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0004t0002 | 0/0 | 5497 | 11 | 10 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0004t0008 | 0/0 | 5496 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0006t0005 | 0/0 | 5498 | 8 | 8 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0006t0017 | 0/0 | 5498 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0007t0003 | 0/0 | 5498 | 2 | 1 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0007t0004 | 0/0 | 5500 | 3 | 2 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0007t0013 | 0/0 | 5503 | 2 | 2 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0007t0018 | 0/0 | 5502 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0008t0001 | 0/0 | 5501 | 5 | 5 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0008t0006 | 0/0 | 5499 | 3 | 1 | 2 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0009t0002 | 0/0 | 5497 | 5 | 4 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0011t0006 | 0/0 | 5499 | 2 | 2 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0012t0016 | 0/0 | 5501 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0013t0005 | 0/0 | 5498 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0001c0018t0003 | 0/0 | 5498 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0002c0005t0002 | 0/0 | 5497 | 4 | 0 | 0 | 4 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0002c0005t0010 | 0/0 | 5497 | 5 | 0 | 2 | 2 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0002c0015t0002 | 0/0 | 5497 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0003c0010t0008 | 0/0 | 5496 | 4 | 0 | 0 | 4 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0004c0020t0015 | 0/0 | 5497 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0005c0014t0002 | 0/0 | 5497 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0006c0016t0002 | 0/0 | 5497 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0007c0017t0002 | 0/0 | 5497 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| a0008c0019t0002 | 0/0 | 5497 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | copy fasta | chr10 | 73993116 | 74125169 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0004g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0006g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0023g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0024g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0006g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0007g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0007g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0007g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0007g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0007g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0007g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0007g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0011g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0011g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0011g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0011g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0012g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0012g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0012g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0014g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0014g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0015g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0019g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0020g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0068 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0008g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0009g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0009g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0009g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0009g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0009g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0021g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0022g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0004t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0004t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0004t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0004t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0004t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0004t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0004t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0004t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0004t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0004t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0004t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0004t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0006t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0006t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0006t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0006t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0006t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0006t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0006t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0006t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0006t0017g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0007t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0007t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0007t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0007t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0007t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0007t0013g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0007t0013g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0007t0018g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0008t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0008t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0008t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0008t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0008t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0008t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0008t0006g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0008t0006g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0009t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0009t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0009t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0009t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0009t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0011t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0011t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0012t0016g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0013t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0018t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0002c0005t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0002c0005t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0002c0005t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0002c0005t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0002c0005t0010g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0002c0005t0010g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0002c0005t0010g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0002c0005t0010g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0002c0005t0010g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0002c0015t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0003c0010t0008g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0003c0010t0008g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0003c0010t0008g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0003c0010t0008g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0004c0020t0015g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0005c0014t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0006c0016t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0007c0017t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0008c0019t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | GBR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0213 | EUR | GBR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00280 | hp1 | a0002 | c0005 | t0010 | g0018 | EUR | FIN | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | FIN | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00423 | hp2 | a0001 | c0002 | t0003 | g0126 | EAS | CHS | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00558 | hp1 | a0001 | c0003 | t0002 | g0067 | EAS | CHS | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00558 | hp2 | a0001 | c0001 | t0023 | g0234 | EAS | CHS | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00597 | hp2 | a0001 | c0002 | t0003 | g0065 | EAS | CHS | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00621 | hp2 | a0002 | c0005 | t0002 | g0046 | EAS | CHS | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00639 | hp1 | a0001 | c0003 | t0002 | g0173 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00639 | hp2 | a0001 | c0008 | t0006 | g0202 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00642 | hp1 | a0001 | c0004 | t0002 | g0186 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00642 | hp2 | a0001 | c0002 | t0004 | g0189 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00673 | hp2 | a0001 | c0002 | t0003 | g0021 | EAS | CHS | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00733 | hp2 | a0001 | c0002 | t0007 | g0168 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00735 | hp1 | a0001 | c0002 | t0011 | g0003 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00741 | hp1 | a0001 | c0003 | t0002 | g0078 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01069 | hp1 | a0001 | c0007 | t0018 | g0100 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0149 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0103 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01074 | hp2 | a0001 | c0007 | t0003 | g0115 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01081 | hp1 | a0001 | c0007 | t0004 | g0119 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01081 | hp2 | a0001 | c0003 | t0002 | g0071 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01106 | hp2 | a0001 | c0003 | t0002 | g0075 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01168 | hp2 | a0001 | c0003 | t0002 | g0060 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01192 | hp2 | a0001 | c0002 | t0003 | g0101 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01243 | hp1 | a0001 | c0002 | t0006 | g0084 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01243 | hp2 | a0001 | c0008 | t0006 | g0203 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01255 | hp1 | a0001 | c0003 | t0002 | g0066 | AMR | CLM | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01256 | hp2 | a0001 | c0002 | t0003 | g0020 | AMR | CLM | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01258 | hp1 | a0001 | c0002 | t0003 | g0102 | AMR | CLM | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01258 | hp2 | a0001 | c0003 | t0002 | g0135 | AMR | CLM | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01261 | hp2 | a0001 | c0003 | t0002 | g0025 | AMR | CLM | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01358 | hp1 | a0001 | c0002 | t0003 | g0225 | AMR | CLM | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01433 | hp1 | a0001 | c0002 | t0003 | g0145 | AMR | CLM | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01433 | hp2 | a0001 | c0009 | t0002 | g0118 | AMR | CLM | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01496 | hp1 | a0001 | c0002 | t0003 | g0245 | AMR | CLM | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01496 | hp2 | a0001 | c0003 | t0002 | g0132 | AMR | CLM | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01516 | hp1 | a0001 | c0003 | t0002 | g0098 | EUR | IBS | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | IBS | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01517 | hp2 | a0001 | c0002 | t0003 | g0243 | EUR | IBS | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01884 | hp1 | a0001 | c0002 | t0012 | g0190 | AFR | ACB | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0128 | AFR | ACB | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01934 | hp1 | a0002 | c0005 | t0010 | g0057 | AMR | PEL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01934 | hp2 | a0001 | c0002 | t0003 | g0042 | AMR | PEL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01952 | hp1 | a0001 | c0003 | t0002 | g0170 | AMR | PEL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01978 | hp1 | a0002 | c0005 | t0010 | g0050 | AMR | PEL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01978 | hp2 | a0001 | c0003 | t0009 | g0134 | AMR | PEL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01981 | hp1 | a0001 | c0003 | t0002 | g0130 | AMR | PEL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02015 | hp2 | a0001 | c0003 | t0002 | g0083 | EAS | KHV | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02040 | hp1 | a0001 | c0003 | t0002 | g0212 | EAS | KHV | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02040 | hp2 | a0001 | c0003 | t0002 | g0024 | EAS | KHV | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02055 | hp1 | a0001 | c0002 | t0019 | g0009 | AFR | ACB | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02055 | hp2 | a0001 | c0003 | t0002 | g0051 | AFR | ACB | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02056 | hp2 | a0005 | c0014 | t0002 | g0096 | EAS | KHV | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02071 | hp1 | a0001 | c0003 | t0002 | g0074 | EAS | KHV | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02071 | hp2 | a0001 | c0003 | t0002 | g0161 | EAS | KHV | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02083 | hp1 | a0001 | c0002 | t0003 | g0166 | EAS | KHV | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02083 | hp2 | a0001 | c0003 | t0002 | g0037 | EAS | KHV | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0049 | EAS | KHV | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02132 | hp1 | a0001 | c0003 | t0002 | g0106 | EAS | KHV | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02135 | hp1 | a0001 | c0002 | t0003 | g0070 | EAS | KHV | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02135 | hp2 | a0001 | c0001 | t0006 | g0232 | EAS | KHV | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02165 | hp1 | a0001 | c0002 | t0003 | g0023 | EAS | CDX | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CDX | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02257 | hp1 | a0001 | c0004 | t0002 | g0123 | AFR | ACB | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0231 | AFR | ACB | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | ACB | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02258 | hp2 | a0001 | c0008 | t0001 | g0016 | AFR | ACB | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02273 | hp1 | a0001 | c0003 | t0002 | g0136 | AMR | PEL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02273 | hp2 | a0001 | c0002 | t0003 | g0097 | AMR | PEL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02280 | hp1 | a0001 | c0001 | t0024 | g0193 | AFR | ACB | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02280 | hp2 | a0001 | c0002 | t0011 | g0004 | AFR | ACB | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02293 | hp2 | a0006 | c0016 | t0002 | g0133 | AMR | PEL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0144 | AMR | PEL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02572 | hp1 | a0001 | c0002 | t0004 | g0188 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0109 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02615 | hp1 | a0001 | c0007 | t0013 | g0054 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02615 | hp2 | a0008 | c0019 | t0002 | g0094 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02622 | hp1 | a0001 | c0006 | t0005 | g0076 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0110 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02630 | hp1 | a0001 | c0006 | t0005 | g0085 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02698 | hp1 | a0001 | c0002 | t0003 | g0059 | SAS | PJL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02698 | hp2 | a0001 | c0003 | t0002 | g0095 | SAS | PJL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02717 | hp1 | a0001 | c0002 | t0011 | g0006 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02717 | hp2 | a0001 | c0006 | t0005 | g0080 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02723 | hp1 | a0001 | c0009 | t0002 | g0013 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02723 | hp2 | a0001 | c0009 | t0002 | g0040 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02809 | hp1 | a0001 | c0006 | t0005 | g0077 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02809 | hp2 | a0001 | c0002 | t0015 | g0005 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02818 | hp1 | a0001 | c0007 | t0013 | g0029 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02818 | hp2 | a0001 | c0008 | t0001 | g0014 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02895 | hp1 | a0001 | c0004 | t0002 | g0183 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02895 | hp2 | a0001 | c0007 | t0004 | g0121 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02896 | hp1 | a0001 | c0006 | t0005 | g0111 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02896 | hp2 | a0001 | c0002 | t0004 | g0246 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02897 | hp1 | a0001 | c0006 | t0005 | g0108 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02897 | hp2 | a0001 | c0007 | t0004 | g0120 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | ESN | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02922 | hp2 | a0001 | c0004 | t0002 | g0082 | AFR | ESN | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02965 | hp1 | a0001 | c0004 | t0002 | g0086 | AFR | ESN | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02965 | hp2 | a0001 | c0002 | t0007 | g0182 | AFR | ESN | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02976 | hp1 | a0001 | c0004 | t0002 | g0052 | AFR | ESN | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02976 | hp2 | a0001 | c0004 | t0008 | g0012 | AFR | ESN | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03098 | hp1 | a0001 | c0004 | t0002 | g0262 | AFR | MSL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03098 | hp2 | a0001 | c0006 | t0017 | g0185 | AFR | MSL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03139 | hp1 | a0001 | c0007 | t0003 | g0107 | AFR | ESN | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03139 | hp2 | a0001 | c0008 | t0001 | g0216 | AFR | ESN | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03195 | hp1 | a0001 | c0002 | t0012 | g0191 | AFR | ESN | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03195 | hp2 | a0001 | c0006 | t0005 | g0184 | AFR | ESN | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03209 | hp1 | a0001 | c0012 | t0016 | g0114 | AFR | MSL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03209 | hp2 | a0001 | c0002 | t0014 | g0227 | AFR | MSL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03225 | hp1 | a0001 | c0002 | t0020 | g0256 | AFR | MSL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03225 | hp2 | a0001 | c0006 | t0005 | g0192 | AFR | MSL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03239 | hp2 | a0001 | c0018 | t0003 | g0196 | SAS | PJL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03453 | hp1 | a0001 | c0002 | t0014 | g0010 | AFR | MSL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03453 | hp2 | a0004 | c0020 | t0015 | g0007 | AFR | MSL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03486 | hp1 | a0001 | c0002 | t0011 | g0008 | AFR | MSL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03486 | hp2 | a0001 | c0004 | t0002 | g0081 | AFR | MSL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0194 | AFR | ESN | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03516 | hp2 | a0001 | c0008 | t0001 | g0015 | AFR | ESN | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03540 | hp1 | a0001 | c0013 | t0005 | g0116 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03540 | hp2 | a0001 | c0002 | t0004 | g0195 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03654 | hp1 | a0001 | c0003 | t0009 | g0197 | SAS | PJL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03654 | hp2 | a0001 | c0003 | t0002 | g0047 | SAS | PJL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03669 | hp1 | a0001 | c0003 | t0002 | g0099 | SAS | PJL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03669 | hp2 | a0001 | c0002 | t0007 | g0239 | SAS | PJL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03710 | hp1 | a0001 | c0003 | t0002 | g0053 | SAS | PJL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03831 | hp2 | a0001 | c0003 | t0002 | g0045 | SAS | BEB | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03942 | hp2 | a0001 | c0003 | t0002 | g0055 | SAS | BEB | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | STU | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | STU | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | STU | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG04199 | hp2 | a0007 | c0017 | t0002 | g0039 | SAS | STU | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | STU | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG04228 | hp2 | a0001 | c0003 | t0009 | g0125 | SAS | STU | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18906 | hp1 | a0001 | c0011 | t0006 | g0117 | AFR | YRI | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18906 | hp2 | a0001 | c0008 | t0006 | g0201 | AFR | YRI | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18940 | hp2 | a0001 | c0003 | t0002 | g0092 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18943 | hp2 | a0001 | c0002 | t0007 | g0180 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18946 | hp1 | a0001 | c0003 | t0002 | g0048 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18954 | hp1 | a0001 | c0003 | t0002 | g0019 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18954 | hp2 | a0002 | c0005 | t0002 | g0249 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18957 | hp1 | a0001 | c0002 | t0007 | g0264 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18957 | hp2 | a0001 | c0003 | t0002 | g0072 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18961 | hp2 | a0001 | c0003 | t0002 | g0172 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18964 | hp1 | a0001 | c0002 | t0007 | g0167 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18967 | hp2 | a0001 | c0003 | t0021 | g0036 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18969 | hp2 | a0002 | c0005 | t0002 | g0027 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18971 | hp2 | a0001 | c0003 | t0008 | g0061 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18973 | hp1 | a0003 | c0010 | t0008 | g0176 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18973 | hp2 | a0001 | c0002 | t0003 | g0091 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18975 | hp1 | a0001 | c0003 | t0002 | g0235 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18975 | hp2 | a0001 | c0002 | t0003 | g0028 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18977 | hp2 | a0003 | c0010 | t0008 | g0088 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18978 | hp2 | a0003 | c0010 | t0008 | g0089 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18983 | hp2 | a0001 | c0003 | t0002 | g0063 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18988 | hp2 | a0001 | c0002 | t0003 | g0127 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18994 | hp1 | a0001 | c0002 | t0003 | g0087 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18998 | hp1 | a0001 | c0003 | t0002 | g0175 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18998 | hp2 | a0001 | c0003 | t0002 | g0043 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19002 | hp2 | a0001 | c0003 | t0002 | g0169 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19004 | hp1 | a0001 | c0002 | t0003 | g0206 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19004 | hp2 | a0001 | c0003 | t0002 | g0064 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19009 | hp1 | a0001 | c0002 | t0007 | g0177 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19043 | hp1 | a0001 | c0004 | t0002 | g0058 | AFR | LWK | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19043 | hp2 | a0001 | c0011 | t0006 | g0255 | AFR | LWK | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19055 | hp2 | a0002 | c0015 | t0002 | g0056 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19060 | hp2 | a0001 | c0003 | t0009 | g0034 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19063 | hp1 | a0001 | c0003 | t0009 | g0041 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19070 | hp1 | a0001 | c0003 | t0002 | g0079 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19070 | hp2 | a0001 | c0003 | t0002 | g0241 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19074 | hp2 | a0001 | c0003 | t0002 | g0174 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19077 | hp2 | a0001 | c0003 | t0002 | g0179 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19080 | hp1 | a0001 | c0003 | t0002 | g0205 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19082 | hp1 | a0001 | c0003 | t0002 | g0038 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19087 | hp1 | a0002 | c0005 | t0010 | g0171 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19088 | hp1 | a0003 | c0010 | t0008 | g0090 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19091 | hp1 | a0002 | c0005 | t0010 | g0069 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19091 | hp2 | a0002 | c0005 | t0002 | g0026 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0251 | AFR | YRI | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0112 | AFR | YRI | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA20129 | hp1 | a0001 | c0002 | t0003 | g0001 | AFR | ASW | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA20129 | hp2 | a0001 | c0002 | t0003 | g0124 | AFR | ASW | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | TSI | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA20805 | hp2 | a0001 | c0002 | t0003 | g0104 | EUR | TSI | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA20905 | hp1 | a0001 | c0003 | t0002 | g0159 | SAS | GIH | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | GIH | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02486 | hp1 | a0001 | c0009 | t0002 | g0113 | AFR | ACB | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02486 | hp2 | a0001 | c0004 | t0002 | g0062 | AFR | ACB | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03471 | hp1 | a0001 | c0009 | t0002 | g0181 | AFR | MSL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03471 | hp2 | a0001 | c0002 | t0012 | g0198 | AFR | MSL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0200 | AFR | USA | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG06807 | hp2 | a0001 | c0004 | t0002 | g0093 | AFR | USA | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA20300 | hp1 | a0001 | c0003 | t0022 | g0035 | AFR | USA | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA20300 | hp2 | a0001 | c0002 | t0005 | g0187 | AFR | USA | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA21309 | hp1 | a0001 | c0008 | t0001 | g0017 | AFR | LWK | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | LWK | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0155 | REF | REF | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0002 | g0068 | REF | REF | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:74072795
|
G | T | 1 | a0004 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.565G>T | p.Val189Leu | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/22 | 657/5497 | 565/3405 | 189/1134 | chr10 | 74072795 | ||
| chr10:74094408
|
T | C | 1 | a0008 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.1490T>C | p.Ile497Thr | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 11/22 | 1582/5497 | 1490/3405 | 497/1134 | chr10 | 74094408 | ||
| chr10:74100982
|
A | G | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.1907A>G | p.His636Arg | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/22 | 1999/5497 | 1907/3405 | 636/1134 | chr10 | 74100982 | ||
| chr10:74105351
|
C | G | 1 | a0006 | 1 | HG02293.hp2 | missense_variant&splice_region_variant | MODERATE | c.2432C>G | p.Pro811Arg | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 16/22 | 2524/5497 | 2432/3405 | 811/1134 | chr10 | 74105351 | ||
| chr10:74107267
|
C | G | 1 | a0003 | 4 | NA18973.hp1 NA18977.hp2 NA18978.hp2 others(1): Show |
missense_variant | MODERATE | c.2472C>G | p.Ile824Met | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 17/22 | 2564/5497 | 2472/3405 | 824/1134 | chr10 | 74107267 | ||
| chr10:74107316
|
G | C | 1 | a0005 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.2521G>C | p.Asp841His | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 17/22 | 2613/5497 | 2521/3405 | 841/1134 | chr10 | 74107316 | ||
| chr10:74111964
|
C | T | 1 | a0002 | 10 | HG00280.hp1 HG00621.hp2 HG01934.hp1 others(7): Show |
missense_variant | MODERATE | c.2801C>T | p.Ala934Val | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 19/22 | 2893/5497 | 2801/3405 | 934/1134 | chr10 | 74111964 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:74070769
|
G | A | 4 | a0001c0007a0001c0009a0001c0012others(1): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
synonymous_variant | LOW | c.339G>A | p.Arg113Arg | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 3/22 | 431/5497 | 339/3405 | 113/1134 | chr10 | 74070769 | ||
| chr10:74074888
|
T | C | 4 | a0001c0007a0001c0009a0001c0012others(1): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
synonymous_variant | LOW | c.768T>C | p.Asp256Asp | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/22 | 860/5497 | 768/3405 | 256/1134 | chr10 | 74074888 | ||
| chr10:74083436
|
C | A | 1 | a0001c0008 | 8 | HG00639.hp2 HG01243.hp2 HG02258.hp2 others(5): Show |
synonymous_variant | LOW | c.945C>A | p.Gly315Gly | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/22 | 1037/5497 | 945/3405 | 315/1134 | chr10 | 74083436 | ||
| chr10:74094325
|
C | T | 5 | a0001c0004a0001c0006a0001c0009others(2): Show | 28 | HG00642.hp1 HG01433.hp2 HG02257.hp1 others(25): Show |
synonymous_variant | LOW | c.1407C>T | p.Ala469Ala | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 11/22 | 1499/5497 | 1407/3405 | 469/1134 | chr10 | 74094325 | ||
| chr10:74094424
|
G | A | 5 | a0001c0004a0001c0006a0001c0009others(2): Show | 28 | HG00642.hp1 HG01433.hp2 HG02257.hp1 others(25): Show |
synonymous_variant | LOW | c.1506G>A | p.Arg502Arg | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 11/22 | 1598/5497 | 1506/3405 | 502/1134 | chr10 | 74094424 | ||
| chr10:74094460
|
C | T | 1 | a0001c0011 | 2 | NA18906.hp1 NA19043.hp2 |
splice_region_variant&synonymous_variant | LOW | c.1542C>T | p.Val514Val | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 11/22 | 1634/5497 | 1542/3405 | 514/1134 | chr10 | 74094460 | ||
| chr10:74095783
|
C | T | 1 | a0001c0018 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.1671C>T | p.Asp557Asp | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 12/22 | 1763/5497 | 1671/3405 | 557/1134 | chr10 | 74095783 | ||
| chr10:74105307
|
G | A | 2 | a0001c0001a0001c0012 | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
synonymous_variant | LOW | c.2388G>A | p.Pro796Pro | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 16/22 | 2480/5497 | 2388/3405 | 796/1134 | chr10 | 74105307 | ||
| chr10:74111962
|
G | A | 1 | a0002c0015 | 1 | NA19055.hp2 | synonymous_variant | LOW | c.2799G>A | p.Ala933Ala | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 19/22 | 2891/5497 | 2799/3405 | 933/1134 | chr10 | 74111962 | ||
| chr10:74111977
|
C | G | 10 | a0001c0001a0001c0002a0001c0006others(7): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(170): Show |
synonymous_variant | LOW | c.2814C>G | p.Gly938Gly | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 19/22 | 2906/5497 | 2814/3405 | 938/1134 | chr10 | 74111977 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:74118288
|
T | C | 1 | a0001c0012t0016 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*119T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 22/22 | 119 | chr10 | 74118288 | |||||
| chr10:74118317
|
A | G | 1 | a0001c0001t0024 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*148A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 22/22 | 148 | chr10 | 74118317 | |||||
| chr10:74118461
|
G | C | 4 | a0001c0002t0005a0001c0006t0005a0001c0006t0017others(1): Show | 11 | HG02622.hp1 HG02630.hp1 HG02717.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*292G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 22/22 | 292 | chr10 | 74118461 | |||||
| chr10:74118482
|
A | C | 1 | a0001c0001t0023 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*313A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 22/22 | 313 | chr10 | 74118482 | |||||
| chr10:74119157
|
C | CTA | 18 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(15): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*990_*991dupAT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 22/22 | 992 | INFO_REALIGN_3_PRIME | chr10 | 74119157 | ||||
| chr10:74119372
|
A | C | 1 | a0002c0005t0010 | 5 | HG00280.hp1 HG01934.hp1 HG01978.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1203A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 22/22 | 1203 | chr10 | 74119372 | |||||
| chr10:74119406
|
C | T | 1 | a0001c0003t0022 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1237C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 22/22 | 1237 | chr10 | 74119406 | |||||
| chr10:74119496
|
A | ATATT | 2 | a0001c0007t0013a0001c0007t0018 | 3 | HG01069.hp1 HG02615.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1329_*1332dupATTT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 22/22 | 1333 | INFO_REALIGN_3_PRIME | chr10 | 74119496 | ||||
| chr10:74119576
|
G | A | 1 | a0001c0006t0017 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1407G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 22/22 | 1407 | chr10 | 74119576 | |||||
| chr10:74119753
|
T | A | 31 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(28): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*1584T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 22/22 | 1584 | chr10 | 74119753 | |||||
| chr10:74119805
|
C | T | 1 | a0001c0002t0014 | 2 | HG03209.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1636C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 22/22 | 1636 | chr10 | 74119805 | |||||
| chr10:74119872
|
T | TAAAGA | 1 | a0001c0002t0012 | 3 | HG01884.hp1 HG03195.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1706_*1710dupAGAA others(1): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 22/22 | 1711 | INFO_REALIGN_3_PRIME | chr10 | 74119872 | ||||
| chr10:74119981
|
T | TATC | 1 | a0001c0002t0007 | 7 | HG00733.hp2 HG02965.hp2 HG03669.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1814_*1816dupTCA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 22/22 | 1817 | INFO_REALIGN_3_PRIME | chr10 | 74119981 | ||||
| chr10:74119992
|
G | A | 13 | a0001c0002t0003a0001c0002t0005a0001c0002t0011others(10): Show | 51 | HG00423.hp2 HG00597.hp2 HG00673.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1823G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 22/22 | 1823 | chr10 | 74119992 | |||||
| chr10:74120011
|
T | TA | 9 | a0001c0001t0004a0001c0002t0004a0001c0002t0005others(6): Show | 34 | HG00642.hp2 HG00733.hp2 HG01069.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1862dupA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 22/22 | 1863 | INFO_REALIGN_3_PRIME | chr10 | 74120011 | ||||
| chr10:74120011
|
T | TAA | 9 | a0001c0001t0001a0001c0001t0023a0001c0001t0024others(6): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*1861_*1862dupAA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 22/22 | 1863 | INFO_REALIGN_3_PRIME | chr10 | 74120011 | ||||
| chr10:74120011
|
TA | T | 4 | a0001c0003t0008a0001c0004t0008a0001c0007t0018others(1): Show | 7 | HG01069.hp1 HG02976.hp2 NA18971.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1862delA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 22/22 | 1862 | INFO_REALIGN_3_PRIME | chr10 | 74120011 | ||||
| chr10:74120018
|
A | AC | 6 | a0001c0002t0003a0001c0002t0011a0001c0002t0012others(3): Show | 37 | HG00423.hp2 HG00597.hp2 HG00673.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1849_*1850insC | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 22/22 | 1850 | chr10 | 74120018 | |||||
| chr10:74120021
|
A | C | 2 | a0001c0002t0015a0004c0020t0015 | 2 | HG02809.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1852A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 22/22 | 1852 | chr10 | 74120021 | |||||
| chr10:74120022
|
A | C | 4 | a0001c0002t0011a0001c0002t0012a0001c0002t0019others(1): Show | 9 | HG00735.hp1 HG01884.hp1 HG02055.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1853A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 22/22 | 1853 | chr10 | 74120022 | |||||
| chr10:74120023
|
A | C | 3 | a0001c0002t0003a0001c0007t0003a0001c0018t0003 | 29 | HG00423.hp2 HG00597.hp2 HG00673.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1854A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 22/22 | 1854 | chr10 | 74120023 | |||||
| chr10:74120104
|
A | ATTTTCTG others(67): Show |
1 | a0001c0002t0020 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1958_*1959insTTTT others(70): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 22/22 | 1959 | INFO_REALIGN_3_PRIME | chr10 | 74120104 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:73998681
|
A | G | 1 | a0001c0002t0007g0264 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.168+306A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 73998681 | ||||||
| chr10:73998705
|
T | G | 9 | a0001c0001t0004g0002a0001c0002t0003g0001a0001c0002t0011g0003others(6): Show | 9 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.168+330T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 73998705 | ||||||
| chr10:73998932
|
C | T | 70 | a0001c0001t0001g0199a0001c0001t0001g0204a0001c0001t0001g0207others(67): Show | 70 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.168+557C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 73998932 | ||||||
| chr10:73999290
|
G | T | 1 | a0001c0001t0024g0193 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.168+915G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 73999290 | ||||||
| chr10:73999540
|
C | T | 65 | a0001c0001t0001g0199a0001c0001t0001g0204a0001c0001t0001g0207others(62): Show | 65 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.168+1165C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 73999540 | ||||||
| chr10:73999611
|
G | A | 8 | a0001c0002t0001g0011a0001c0002t0014g0010a0001c0004t0008g0012others(5): Show | 8 | HG02258.hp2 HG02630.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.168+1236G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 73999611 | ||||||
| chr10:74000176
|
TA | T | 113 | a0001c0001t0001g0178a0001c0001t0001g0199a0001c0001t0001g0204others(110): Show | 113 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.168+1803delA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74000176 | |||||
| chr10:74000259
|
C | CT | 65 | a0001c0001t0001g0122a0001c0001t0001g0129a0001c0001t0001g0131others(62): Show | 65 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.168+1904dupT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74000259 | |||||
| chr10:74000259
|
C | CTT | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG00735.hp2 HG01261.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+1903_168+1904d others(4): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74000259 | |||||
| chr10:74000259
|
CT | C | 11 | a0001c0002t0001g0011a0001c0002t0001g0200a0001c0002t0003g0020others(8): Show | 11 | HG00280.hp1 HG00639.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.168+1904delT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74000259 | |||||
| chr10:74000260
|
T | G | 1 | a0001c0001t0001g0199 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.168+1885T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74000260 | ||||||
| chr10:74000331
|
A | G | 9 | a0001c0001t0004g0002a0001c0002t0003g0001a0001c0002t0011g0003others(6): Show | 9 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.168+1956A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74000331 | ||||||
| chr10:74000404
|
C | CTTTG | 18 | a0001c0001t0001g0178a0001c0001t0001g0204a0001c0002t0007g0167others(15): Show | 18 | HG00639.hp1 HG00733.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.168+2053_168+2056d others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74000404 | |||||
| chr10:74000447
|
C | A | 1 | a0001c0002t0003g0021 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.168+2072C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74000447 | ||||||
| chr10:74000598
|
A | G | 1 | a0001c0003t0002g0106 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.168+2223A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74000598 | ||||||
| chr10:74000604
|
G | C | 1 | a0001c0002t0001g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.168+2229G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74000604 | ||||||
| chr10:74000664
|
C | T | 1 | a0001c0008t0001g0017 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.168+2289C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74000664 | ||||||
| chr10:74000935
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.168+2560C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74000935 | ||||||
| chr10:74000944
|
A | G | 38 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(35): Show | 38 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.168+2569A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74000944 | ||||||
| chr10:74001246
|
C | T | 2 | a0001c0002t0020g0256a0001c0011t0006g0255 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.168+2871C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74001246 | ||||||
| chr10:74001302
|
G | A | 2 | a0001c0002t0020g0256a0001c0011t0006g0255 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.168+2927G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74001302 | ||||||
| chr10:74001365
|
A | G | 1 | a0001c0006t0005g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.168+2990A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74001365 | ||||||
| chr10:74001395
|
G | A | 3 | a0001c0004t0002g0183a0001c0006t0005g0184a0001c0006t0005g0192 | 3 | HG02895.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+3020G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74001395 | ||||||
| chr10:74001543
|
C | A | 1 | a0001c0002t0001g0200 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168+3168C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74001543 | ||||||
| chr10:74001713
|
A | G | 5 | a0001c0002t0003g0020a0001c0002t0003g0101a0001c0002t0003g0102others(2): Show | 5 | HG01074.hp1 HG01192.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+3338A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74001713 | ||||||
| chr10:74002052
|
G | A | 5 | a0001c0002t0001g0194a0001c0002t0004g0195a0001c0002t0012g0198others(2): Show | 5 | HG03239.hp2 HG03471.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+3677G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74002052 | ||||||
| chr10:74002102
|
T | G | 97 | a0001c0001t0001g0178a0001c0001t0001g0199a0001c0001t0001g0204others(94): Show | 97 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.168+3727T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74002102 | ||||||
| chr10:74002313
|
C | T | 9 | a0001c0001t0004g0002a0001c0002t0003g0001a0001c0002t0011g0003others(6): Show | 9 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.168+3938C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74002313 | ||||||
| chr10:74002316
|
G | C | 1 | a0001c0003t0001g0128 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.168+3941G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74002316 | ||||||
| chr10:74002570
|
T | C | 1 | a0001c0006t0017g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.168+4195T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74002570 | ||||||
| chr10:74002598
|
A | G | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.168+4223A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74002598 | ||||||
| chr10:74002610
|
A | G | 113 | a0001c0001t0001g0178a0001c0001t0001g0199a0001c0001t0001g0204others(110): Show | 113 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.168+4235A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74002610 | ||||||
| chr10:74002617
|
C | G | 2 | a0001c0002t0020g0256a0001c0011t0006g0255 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.168+4242C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74002617 | ||||||
| chr10:74002691
|
G | C | 1 | a0001c0002t0003g0021 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.168+4316G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74002691 | ||||||
| chr10:74002769
|
C | G | 1 | a0001c0007t0018g0100 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.168+4394C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74002769 | ||||||
| chr10:74002880
|
C | CA | 22 | a0001c0001t0004g0002a0001c0002t0001g0011a0001c0002t0003g0001others(19): Show | 22 | HG00735.hp1 HG02040.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.168+4522dupA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74002880 | |||||
| chr10:74002880
|
CA | C | 7 | a0001c0001t0001g0252a0001c0002t0003g0097a0001c0002t0003g0127others(4): Show | 7 | HG01256.hp1 HG01516.hp1 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+4522delA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74002880 | |||||
| chr10:74002969
|
A | G | 1 | a0001c0004t0002g0186 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.168+4594A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74002969 | ||||||
| chr10:74002985
|
G | GAT | 13 | a0001c0001t0001g0160a0001c0001t0004g0002a0001c0002t0003g0001others(10): Show | 13 | HG00597.hp1 HG00735.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.168+4622_168+4623d others(4): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74002985 | |||||
| chr10:74003272
|
A | G | 1 | a0001c0003t0002g0159 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.168+4897A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74003272 | ||||||
| chr10:74003363
|
G | C | 1 | a0001c0002t0003g0001 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.168+4988G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74003363 | ||||||
| chr10:74003493
|
C | T | 1 | a0001c0002t0001g0251 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.168+5118C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74003493 | ||||||
| chr10:74003804
|
C | T | 9 | a0001c0001t0004g0002a0001c0002t0003g0001a0001c0002t0011g0003others(6): Show | 9 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.168+5429C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74003804 | ||||||
| chr10:74004123
|
CTT | C | 10 | a0001c0001t0004g0002a0001c0002t0003g0001a0001c0002t0011g0003others(7): Show | 10 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.168+5750_168+5751d others(4): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74004123 | |||||
| chr10:74004270
|
C | A | 2 | a0001c0002t0001g0194a0001c0002t0004g0195 | 2 | HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.168+5895C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74004270 | ||||||
| chr10:74004504
|
A | G | 1 | a0005c0014t0002g0096 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.168+6129A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74004504 | ||||||
| chr10:74004591
|
G | T | 1 | a0001c0001t0001g0250 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.168+6216G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74004591 | ||||||
| chr10:74004784
|
A | G | 1 | a0002c0005t0002g0249 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.168+6409A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74004784 | ||||||
| chr10:74004829
|
C | T | 8 | a0001c0002t0001g0011a0001c0002t0014g0010a0001c0004t0008g0012others(5): Show | 8 | HG02258.hp2 HG02630.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.168+6454C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74004829 | ||||||
| chr10:74004865
|
T | C | 167 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.168+6490T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74004865 | ||||||
| chr10:74005050
|
C | T | 1 | a0001c0002t0005g0187 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.168+6675C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74005050 | ||||||
| chr10:74005256
|
T | C | 1 | a0001c0003t0002g0205 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.168+6881T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74005256 | ||||||
| chr10:74005503
|
G | A | 1 | a0001c0002t0007g0168 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.168+7128G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74005503 | ||||||
| chr10:74005646
|
G | A | 2 | a0001c0002t0004g0188a0001c0002t0004g0189 | 2 | HG00642.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.168+7271G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74005646 | ||||||
| chr10:74005664
|
T | C | 65 | a0001c0001t0001g0199a0001c0001t0001g0204a0001c0001t0001g0207others(62): Show | 65 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.168+7289T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74005664 | ||||||
| chr10:74005768
|
A | T | 1 | a0001c0001t0001g0248 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.168+7393A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74005768 | ||||||
| chr10:74005959
|
C | G | 2 | a0001c0002t0020g0256a0001c0011t0006g0255 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.168+7584C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74005959 | ||||||
| chr10:74006032
|
C | T | 10 | a0001c0001t0004g0002a0001c0002t0003g0001a0001c0002t0011g0003others(7): Show | 10 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.168+7657C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74006032 | ||||||
| chr10:74006078
|
G | A | 1 | a0001c0003t0002g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.168+7703G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74006078 | ||||||
| chr10:74006128
|
C | T | 2 | a0001c0007t0004g0120a0001c0007t0004g0121 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.168+7753C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74006128 | ||||||
| chr10:74006622
|
A | G | 1 | a0001c0003t0002g0095 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.168+8247A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74006622 | ||||||
| chr10:74006721
|
G | A | 22 | a0001c0001t0001g0178a0001c0002t0001g0194a0001c0002t0004g0195others(19): Show | 22 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.168+8346G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74006721 | ||||||
| chr10:74006726
|
A | T | 3 | a0001c0004t0002g0183a0001c0006t0005g0184a0001c0006t0005g0192 | 3 | HG02895.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+8351A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74006726 | ||||||
| chr10:74006992
|
A | G | 1 | a0001c0006t0017g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.168+8617A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74006992 | ||||||
| chr10:74007098
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.168+8723G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74007098 | ||||||
| chr10:74007179
|
A | G | 1 | a0008c0019t0002g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.168+8804A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74007179 | ||||||
| chr10:74007512
|
T | A | 4 | a0001c0001t0001g0105a0001c0002t0003g0028a0002c0005t0002g0026others(1): Show | 4 | NA18943.hp1 NA18969.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+9137T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74007512 | ||||||
| chr10:74007642
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.168+9267C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74007642 | ||||||
| chr10:74007773
|
G | A | 9 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(6): Show | 9 | HG00280.hp2 HG00423.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.168+9398G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74007773 | ||||||
| chr10:74007894
|
C | T | 1 | a0001c0001t0024g0193 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.168+9519C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74007894 | ||||||
| chr10:74007895
|
T | A | 1 | a0001c0002t0003g0097 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.168+9520T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74007895 | ||||||
| chr10:74008154
|
A | G | 13 | a0001c0001t0001g0178a0001c0002t0007g0167a0001c0002t0007g0177others(10): Show | 13 | HG00639.hp1 HG01952.hp1 NA18943.hp2 others(10): Show |
intron_variant | MODIFIER | c.168+9779A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74008154 | ||||||
| chr10:74008404
|
A | G | 2 | a0001c0002t0020g0256a0001c0011t0006g0255 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.168+10029A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74008404 | ||||||
| chr10:74008422
|
A | G | 113 | a0001c0001t0001g0178a0001c0001t0001g0199a0001c0001t0001g0204others(110): Show | 113 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.168+10047A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74008422 | ||||||
| chr10:74008814
|
T | C | 1 | a0001c0002t0001g0200 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168+10439T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74008814 | ||||||
| chr10:74008854
|
C | G | 1 | a0001c0004t0002g0093 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.168+10479C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74008854 | ||||||
| chr10:74008890
|
A | G | 113 | a0001c0001t0001g0178a0001c0001t0001g0199a0001c0001t0001g0204others(110): Show | 113 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.168+10515A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74008890 | ||||||
| chr10:74009070
|
G | T | 1 | a0001c0002t0011g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168+10695G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009070 | ||||||
| chr10:74009078
|
G | T | 2 | a0001c0002t0001g0194a0001c0002t0004g0195 | 2 | HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.168+10703G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009078 | ||||||
| chr10:74009213
|
CT | C | 32 | a0001c0001t0001g0033a0001c0001t0001g0199a0001c0001t0001g0207others(29): Show | 32 | HG00099.hp2 HG00639.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.168+10841delT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74009213 | |||||
| chr10:74009215
|
T | TC | 5 | a0001c0001t0001g0030a0001c0001t0001g0138a0001c0002t0004g0246others(2): Show | 5 | HG01358.hp2 HG01516.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+10840_168+1084 others(5): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009215 | ||||||
| chr10:74009215
|
TTC | T | 6 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0002t0001g0011others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+10841_168+1084 others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009215 | ||||||
| chr10:74009215
|
TTCC | T | 3 | a0001c0004t0002g0183a0001c0006t0005g0184a0001c0006t0005g0192 | 3 | HG02895.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+10841_168+1084 others(7): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009215 | ||||||
| chr10:74009216
|
T | C | 39 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(36): Show | 39 | HG00558.hp2 HG00621.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.168+10841T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009216 | ||||||
| chr10:74009216
|
T | TC | 47 | a0001c0001t0001g0044a0001c0001t0001g0105a0001c0001t0001g0131others(44): Show | 47 | HG00280.hp2 HG00597.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.168+10855dupC | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74009216 | |||||
| chr10:74009216
|
T | TCC | 15 | a0001c0001t0001g0129a0001c0002t0005g0187a0001c0002t0012g0191others(12): Show | 15 | HG00423.hp1 HG02056.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.168+10854_168+1085 others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74009216 | |||||
| chr10:74009216
|
TC | T | 15 | a0001c0002t0003g0021a0001c0002t0003g0126a0001c0002t0006g0084others(12): Show | 15 | HG00423.hp2 HG00673.hp2 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.168+10855delC | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74009216 | |||||
| chr10:74009222
|
C | A | 2 | a0001c0003t0009g0197a0001c0018t0003g0196 | 2 | HG03239.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.168+10847C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009222 | ||||||
| chr10:74009223
|
C | A | 1 | a0001c0003t0002g0106 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.168+10848C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009223 | ||||||
| chr10:74009224
|
C | A | 1 | a0001c0001t0001g0139 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.168+10849C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009224 | ||||||
| chr10:74009224
|
C | G | 5 | a0001c0002t0003g0091a0001c0003t0002g0092a0003c0010t0008g0088others(2): Show | 5 | NA18940.hp2 NA18973.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+10849C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009224 | ||||||
| chr10:74009226
|
C | A | 16 | a0001c0001t0001g0178a0001c0002t0007g0167a0001c0002t0007g0168others(13): Show | 16 | HG00639.hp1 HG00733.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.168+10851C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009226 | ||||||
| chr10:74009226
|
C | G | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0002t0003g0087 | 3 | HG01516.hp2 HG01517.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.168+10851C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009226 | ||||||
| chr10:74009230
|
CG | C | 7 | a0001c0001t0004g0002a0001c0002t0001g0194a0001c0002t0003g0001others(4): Show | 7 | HG00735.hp1 HG02922.hp1 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+10856delG | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009230 | ||||||
| chr10:74009231
|
G | C | 102 | a0001c0001t0001g0178a0001c0001t0001g0199a0001c0001t0001g0204others(99): Show | 102 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.168+10856G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009231 | ||||||
| chr10:74009335
|
T | C | 1 | a0001c0004t0002g0186 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.168+10960T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009335 | ||||||
| chr10:74009407
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.168+11032T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009407 | ||||||
| chr10:74009408
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.168+11033G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009408 | ||||||
| chr10:74009419
|
C | T | 9 | a0001c0001t0004g0002a0001c0002t0003g0001a0001c0002t0011g0003others(6): Show | 9 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.168+11044C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009419 | ||||||
| chr10:74009495
|
G | A | 1 | a0001c0001t0024g0193 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.168+11120G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009495 | ||||||
| chr10:74009539
|
A | G | 5 | a0001c0002t0001g0011a0001c0002t0014g0010a0001c0004t0008g0012others(2): Show | 5 | HG02630.hp2 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+11164A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009539 | ||||||
| chr10:74009549
|
G | A | 7 | a0001c0002t0012g0190a0001c0002t0012g0191a0001c0002t0012g0198others(4): Show | 7 | HG01884.hp1 HG01934.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+11174G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009549 | ||||||
| chr10:74009672
|
T | C | 1 | a0001c0001t0024g0193 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.168+11297T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009672 | ||||||
| chr10:74009733
|
C | T | 1 | a0001c0002t0005g0187 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.168+11358C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009733 | ||||||
| chr10:74009764
|
C | T | 1 | a0001c0003t0002g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.168+11389C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009764 | ||||||
| chr10:74009853
|
C | A | 1 | a0001c0004t0002g0186 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.168+11478C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009853 | ||||||
| chr10:74009899
|
C | T | 9 | a0001c0001t0004g0002a0001c0002t0003g0001a0001c0002t0011g0003others(6): Show | 9 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.168+11524C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009899 | ||||||
| chr10:74009925
|
A | G | 3 | a0001c0003t0002g0079a0001c0003t0002g0092a0002c0015t0002g0056 | 3 | NA18940.hp2 NA19055.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.168+11550A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74009925 | ||||||
| chr10:74010074
|
G | A | 4 | a0001c0008t0001g0014a0001c0008t0001g0015a0001c0008t0001g0016others(1): Show | 4 | HG02258.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+11699G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74010074 | ||||||
| chr10:74010169
|
T | G | 1 | a0001c0002t0003g0103 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.168+11794T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74010169 | ||||||
| chr10:74010649
|
A | T | 16 | a0001c0001t0001g0178a0001c0002t0007g0167a0001c0002t0007g0168others(13): Show | 16 | HG00639.hp1 HG00733.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.168+12274A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74010649 | ||||||
| chr10:74010656
|
A | C | 1 | a0001c0001t0001g0226 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.168+12281A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74010656 | ||||||
| chr10:74010690
|
C | T | 1 | a0001c0002t0001g0110 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.168+12315C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74010690 | ||||||
| chr10:74010760
|
T | C | 3 | a0001c0001t0001g0207a0001c0003t0009g0197a0001c0018t0003g0196 | 3 | HG00733.hp1 HG03239.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.168+12385T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74010760 | ||||||
| chr10:74010802
|
C | T | 3 | a0001c0004t0002g0183a0001c0006t0005g0184a0001c0006t0005g0192 | 3 | HG02895.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+12427C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74010802 | ||||||
| chr10:74011090
|
G | C | 1 | a0001c0001t0001g0208 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.168+12715G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74011090 | ||||||
| chr10:74011094
|
C | T | 1 | a0001c0001t0024g0193 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.168+12719C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74011094 | ||||||
| chr10:74011137
|
C | T | 1 | a0001c0002t0001g0200 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168+12762C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74011137 | ||||||
| chr10:74011165
|
C | CA | 31 | a0001c0001t0001g0044a0001c0001t0001g0209a0001c0001t0001g0228others(28): Show | 31 | HG00642.hp1 HG00673.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.168+12816dupA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74011165 | |||||
| chr10:74011165
|
C | CAA | 7 | a0001c0001t0001g0122a0001c0002t0003g0042a0001c0002t0003g0087others(4): Show | 7 | HG01934.hp2 HG02486.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+12815_168+1281 others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74011165 | |||||
| chr10:74011165
|
CA | C | 71 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(68): Show | 71 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.168+12816delA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74011165 | |||||
| chr10:74011165
|
CAA | C | 13 | a0001c0001t0004g0002a0001c0002t0003g0001a0001c0002t0004g0195others(10): Show | 13 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.168+12815_168+1281 others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74011165 | |||||
| chr10:74011299
|
C | T | 4 | a0001c0002t0004g0246a0001c0008t0006g0201a0001c0008t0006g0202others(1): Show | 4 | HG00639.hp2 HG01243.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+12924C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74011299 | ||||||
| chr10:74011430
|
A | G | 4 | a0001c0008t0001g0014a0001c0008t0001g0015a0001c0008t0001g0016others(1): Show | 4 | HG02258.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+13055A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74011430 | ||||||
| chr10:74011441
|
G | A | 1 | a0001c0002t0001g0251 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.168+13066G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74011441 | ||||||
| chr10:74011621
|
T | C | 3 | a0001c0004t0002g0183a0001c0006t0005g0184a0001c0006t0005g0192 | 3 | HG02895.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+13246T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74011621 | ||||||
| chr10:74011737
|
T | G | 3 | a0001c0001t0001g0207a0001c0003t0009g0197a0001c0018t0003g0196 | 3 | HG00733.hp1 HG03239.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.168+13362T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74011737 | ||||||
| chr10:74011996
|
A | C | 1 | a0001c0009t0002g0181 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.168+13621A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74011996 | ||||||
| chr10:74012183
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG03239.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.168+13808C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74012183 | ||||||
| chr10:74012851
|
A | T | 1 | a0001c0002t0007g0264 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.168+14476A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74012851 | ||||||
| chr10:74012968
|
G | A | 5 | a0001c0002t0012g0190a0001c0002t0012g0191a0001c0002t0012g0198others(2): Show | 5 | HG01884.hp1 HG03195.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+14593G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74012968 | ||||||
| chr10:74013161
|
G | T | 1 | a0001c0001t0001g0154 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.168+14786G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74013161 | ||||||
| chr10:74013330
|
G | A | 1 | a0001c0002t0005g0187 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.168+14955G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74013330 | ||||||
| chr10:74013331
|
C | T | 1 | a0001c0002t0005g0187 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.168+14956C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74013331 | ||||||
| chr10:74013454
|
T | C | 1 | a0001c0003t0022g0035 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.168+15079T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74013454 | ||||||
| chr10:74013541
|
A | G | 1 | a0001c0006t0017g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.168+15166A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74013541 | ||||||
| chr10:74013592
|
C | T | 1 | a0001c0002t0003g0245 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.168+15217C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74013592 | ||||||
| chr10:74013604
|
C | G | 134 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.168+15229C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74013604 | ||||||
| chr10:74013792
|
C | T | 1 | a0001c0006t0017g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.168+15417C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74013792 | ||||||
| chr10:74013819
|
G | A | 1 | a0001c0004t0002g0186 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.168+15444G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74013819 | ||||||
| chr10:74013903
|
TA | T | 150 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.168+15538delA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74013903 | |||||
| chr10:74013903
|
TAA | T | 5 | a0001c0002t0012g0190a0001c0002t0012g0191a0001c0002t0012g0198others(2): Show | 5 | HG01884.hp1 HG03195.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+15537_168+1553 others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74013903 | |||||
| chr10:74013975
|
A | C | 3 | a0001c0001t0001g0207a0001c0003t0009g0197a0001c0018t0003g0196 | 3 | HG00733.hp1 HG03239.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.168+15600A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74013975 | ||||||
| chr10:74014124
|
G | A | 1 | a0001c0007t0013g0029 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.168+15749G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74014124 | ||||||
| chr10:74014135
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.168+15760A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74014135 | ||||||
| chr10:74014222
|
C | T | 1 | a0001c0006t0017g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.168+15847C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74014222 | ||||||
| chr10:74014289
|
T | C | 1 | a0001c0002t0003g0021 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.168+15914T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74014289 | ||||||
| chr10:74014381
|
A | G | 134 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.168+16006A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74014381 | ||||||
| chr10:74014401
|
T | G | 8 | a0001c0002t0001g0011a0001c0002t0014g0010a0001c0004t0008g0012others(5): Show | 8 | HG02258.hp2 HG02630.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.168+16026T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74014401 | ||||||
| chr10:74014463
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.168+16088G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74014463 | ||||||
| chr10:74014481
|
C | G | 1 | a0001c0002t0007g0264 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.168+16106C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74014481 | ||||||
| chr10:74014550
|
TA | T | 13 | a0001c0001t0001g0153a0001c0001t0001g0156a0001c0001t0001g0178others(10): Show | 13 | HG01081.hp1 HG01256.hp2 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.168+16190delA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74014550 | |||||
| chr10:74014575
|
C | A | 16 | a0001c0001t0001g0178a0001c0002t0007g0167a0001c0002t0007g0168others(13): Show | 16 | HG00639.hp1 HG00733.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.168+16200C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74014575 | ||||||
| chr10:74014776
|
C | A | 14 | a0001c0001t0001g0178a0001c0002t0007g0167a0001c0002t0007g0168others(11): Show | 14 | HG00639.hp1 HG00733.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.168+16401C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74014776 | ||||||
| chr10:74015059
|
G | T | 3 | a0001c0004t0002g0183a0001c0006t0005g0184a0001c0006t0005g0192 | 3 | HG02895.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+16684G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74015059 | ||||||
| chr10:74015318
|
C | T | 3 | a0001c0002t0012g0190a0001c0002t0012g0191a0001c0002t0012g0198 | 3 | HG01884.hp1 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.168+16943C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74015318 | ||||||
| chr10:74015446
|
C | G | 1 | a0001c0004t0002g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.168+17071C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74015446 | ||||||
| chr10:74015476
|
T | C | 164 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.168+17101T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74015476 | ||||||
| chr10:74015631
|
T | G | 1 | a0001c0001t0001g0030 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.168+17256T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74015631 | ||||||
| chr10:74016022
|
G | T | 3 | a0001c0002t0012g0190a0001c0002t0012g0191a0001c0002t0012g0198 | 3 | HG01884.hp1 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.168+17647G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74016022 | ||||||
| chr10:74016023
|
G | T | 1 | a0001c0001t0001g0152 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.168+17648G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74016023 | ||||||
| chr10:74016264
|
G | A | 1 | a0001c0008t0001g0015 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.168+17889G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74016264 | ||||||
| chr10:74016266
|
A | G | 5 | a0001c0001t0001g0207a0001c0002t0004g0195a0001c0003t0009g0197others(2): Show | 5 | HG00642.hp1 HG00733.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+17891A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74016266 | ||||||
| chr10:74016414
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.168+18039C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74016414 | ||||||
| chr10:74016432
|
A | G | 152 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.168+18057A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74016432 | ||||||
| chr10:74016716
|
G | A | 4 | a0001c0002t0001g0011a0001c0002t0014g0010a0001c0004t0008g0012others(1): Show | 4 | HG02630.hp2 HG02723.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+18341G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74016716 | ||||||
| chr10:74016749
|
T | C | 3 | a0001c0004t0002g0183a0001c0006t0005g0184a0001c0006t0005g0192 | 3 | HG02895.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+18374T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74016749 | ||||||
| chr10:74016813
|
T | C | 152 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.168+18438T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74016813 | ||||||
| chr10:74016939
|
A | G | 1 | a0001c0003t0009g0134 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.168+18564A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74016939 | ||||||
| chr10:74016957
|
A | G | 3 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0005g0187 | 3 | HG00642.hp2 HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.168+18582A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74016957 | ||||||
| chr10:74017008
|
G | A | 1 | a0001c0004t0002g0058 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.168+18633G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74017008 | ||||||
| chr10:74017046
|
C | CT | 5 | a0001c0003t0002g0055a0001c0006t0005g0077a0001c0006t0005g0108others(2): Show | 5 | HG02615.hp1 HG02809.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+18690dupT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74017046 | |||||
| chr10:74017046
|
C | CTTTTTTT others(1): Show |
7 | a0001c0001t0001g0244a0001c0001t0004g0002a0001c0002t0003g0001others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+18683_168+1869 others(12): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74017046 | |||||
| chr10:74017046
|
C | CTTTTTTT others(2): Show |
48 | a0001c0001t0001g0162a0001c0001t0001g0199a0001c0001t0001g0208others(45): Show | 48 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.168+18682_168+1869 others(13): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74017046 | |||||
| chr10:74017046
|
C | CTTTTTTT others(3): Show |
21 | a0001c0001t0001g0204a0001c0001t0001g0221a0001c0001t0001g0222others(18): Show | 21 | HG01981.hp2 HG02165.hp2 HG02602.hp2 others(18): Show |
intron_variant | MODIFIER | c.168+18681_168+1869 others(14): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74017046 | |||||
| chr10:74017046
|
C | CTTTTTTT others(4): Show |
7 | a0001c0002t0001g0011a0001c0002t0001g0231a0001c0002t0004g0188others(4): Show | 7 | HG00642.hp1 HG02257.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+18680_168+1869 others(15): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74017046 | |||||
| chr10:74017046
|
C | CTTTTTTT others(5): Show |
6 | a0001c0002t0004g0189a0001c0002t0004g0195a0001c0002t0005g0187others(3): Show | 6 | HG00642.hp2 HG01884.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+18679_168+1869 others(16): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74017046 | |||||
| chr10:74017046
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0001g0207a0001c0002t0012g0198 | 2 | HG00733.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.168+18678_168+1869 others(17): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74017046 | |||||
| chr10:74017046
|
C | CTTTTTTT others(12): Show |
1 | a0001c0002t0007g0182 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.168+18672_168+1869 others(23): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74017046 | |||||
| chr10:74017046
|
C | CTTTTTTT others(14): Show |
1 | a0001c0009t0002g0181 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.168+18690_168+1869 others(25): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74017046 | |||||
| chr10:74017046
|
CTTT | C | 14 | a0001c0001t0001g0178a0001c0002t0007g0167a0001c0002t0007g0168others(11): Show | 14 | HG00639.hp1 HG00733.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.168+18688_168+1869 others(7): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74017046 | |||||
| chr10:74017046
|
CTTTTT | C | 41 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(38): Show | 41 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.168+18686_168+1869 others(9): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74017046 | |||||
| chr10:74017110
|
G | C | 61 | a0001c0001t0001g0162a0001c0001t0001g0199a0001c0001t0001g0204others(58): Show | 61 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.168+18735G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74017110 | ||||||
| chr10:74017116
|
C | T | 1 | a0001c0006t0005g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.168+18741C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74017116 | ||||||
| chr10:74017118
|
G | A | 61 | a0001c0001t0001g0162a0001c0001t0001g0199a0001c0001t0001g0204others(58): Show | 61 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.168+18743G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74017118 | ||||||
| chr10:74017142
|
G | T | 1 | a0001c0001t0001g0207 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.168+18767G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74017142 | ||||||
| chr10:74017208
|
C | T | 2 | a0001c0007t0018g0100a0001c0009t0002g0040 | 2 | HG01069.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.168+18833C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74017208 | ||||||
| chr10:74017300
|
G | C | 1 | a0001c0001t0001g0233 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.168+18925G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74017300 | ||||||
| chr10:74017337
|
G | A | 9 | a0001c0001t0004g0002a0001c0002t0003g0001a0001c0002t0011g0003others(6): Show | 9 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.168+18962G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74017337 | ||||||
| chr10:74017386
|
G | A | 41 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(38): Show | 41 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.168+19011G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74017386 | ||||||
| chr10:74017422
|
G | A | 1 | a0005c0014t0002g0096 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.168+19047G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74017422 | ||||||
| chr10:74017541
|
TTTTC | T | 3 | a0001c0001t0001g0221a0001c0001t0001g0253a0002c0005t0002g0249 | 3 | HG01169.hp2 HG02165.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.168+19182_168+1918 others(8): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74017541 | |||||
| chr10:74017554
|
TTTC | T | 67 | a0001c0001t0001g0162a0001c0001t0001g0199a0001c0001t0001g0204others(64): Show | 67 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.168+19182_168+1918 others(7): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74017554 | |||||
| chr10:74017732
|
GTATGTGT others(3): Show |
G | 41 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(38): Show | 41 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.168+19361_168+1937 others(14): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74017732 | |||||
| chr10:74017843
|
C | A | 41 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(38): Show | 41 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.168+19468C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74017843 | ||||||
| chr10:74017946
|
C | T | 1 | a0001c0003t0002g0095 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.168+19571C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74017946 | ||||||
| chr10:74018020
|
G | A | 2 | a0001c0001t0001g0165a0001c0002t0004g0195 | 2 | HG00735.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.168+19645G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74018020 | ||||||
| chr10:74018140
|
G | GA | 12 | a0001c0001t0001g0207a0001c0001t0004g0002a0001c0002t0003g0001others(9): Show | 12 | HG00733.hp1 HG00735.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.168+19774dupA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74018140 | |||||
| chr10:74018166
|
GATATATA others(12): Show |
G | 5 | a0001c0002t0012g0190a0001c0002t0012g0191a0001c0002t0012g0198others(2): Show | 5 | HG01884.hp1 HG03195.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+19801_168+1981 others(23): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74018166 | |||||
| chr10:74018177
|
G | GAGATATA others(7): Show |
2 | a0001c0002t0003g0001a0001c0002t0011g0008 | 2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.168+19803_168+1980 others(18): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74018177 | |||||
| chr10:74018177
|
G | GAGATATA others(9): Show |
1 | a0001c0001t0004g0002 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.168+19803_168+1980 others(20): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74018177 | |||||
| chr10:74018177
|
G | GAT | 36 | a0001c0001t0001g0138a0001c0001t0001g0148a0001c0001t0001g0160others(33): Show | 36 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.168+19826_168+1982 others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74018177 | |||||
| chr10:74018177
|
G | GATAT | 19 | a0001c0001t0001g0204a0001c0001t0001g0209a0001c0001t0001g0214others(16): Show | 19 | HG00642.hp1 HG01168.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.168+19824_168+1982 others(8): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74018177 | |||||
| chr10:74018177
|
G | GATATAT | 5 | a0001c0001t0001g0230a0001c0002t0001g0112a0001c0002t0007g0182others(2): Show | 5 | HG02965.hp2 HG03195.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+19822_168+1982 others(10): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74018177 | |||||
| chr10:74018177
|
G | GATATATA others(1): Show |
8 | a0001c0001t0001g0221a0001c0001t0001g0240a0001c0003t0002g0079others(5): Show | 8 | HG02165.hp2 HG02630.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.168+19820_168+1982 others(12): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74018177 | |||||
| chr10:74018177
|
G | GATATATA others(3): Show |
14 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219others(11): Show | 14 | HG01981.hp2 HG02258.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.168+19818_168+1982 others(14): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74018177 | |||||
| chr10:74018177
|
G | GATATATA others(5): Show |
12 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0220others(9): Show | 12 | HG00621.hp1 HG01255.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.168+19816_168+1982 others(16): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74018177 | |||||
| chr10:74018177
|
G | GATATATA others(7): Show |
2 | a0001c0001t0001g0263a0001c0002t0011g0003 | 2 | HG00735.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.168+19814_168+1982 others(18): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74018177 | |||||
| chr10:74018177
|
G | GATATATA others(9): Show |
6 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0165others(3): Show | 6 | HG00735.hp2 HG01258.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+19812_168+1982 others(20): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74018177 | |||||
| chr10:74018177
|
G | GATATATA others(11): Show |
4 | a0001c0001t0001g0156a0001c0002t0011g0004a0001c0006t0017g0185others(1): Show | 4 | HG02280.hp2 HG02723.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+19810_168+1982 others(22): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74018177 | |||||
| chr10:74018177
|
G | GATATATA others(13): Show |
13 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0140others(10): Show | 13 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(10): Show |
intron_variant | MODIFIER | c.168+19808_168+1982 others(24): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74018177 | |||||
| chr10:74018177
|
G | GATATATA others(15): Show |
8 | a0001c0001t0001g0137a0001c0001t0001g0141a0001c0001t0001g0146others(5): Show | 8 | HG00741.hp2 HG01975.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.168+19806_168+1982 others(26): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74018177 | |||||
| chr10:74018177
|
G | GATATATA others(17): Show |
5 | a0001c0001t0001g0139a0001c0001t0001g0147a0001c0001t0001g0151others(2): Show | 5 | HG00738.hp2 HG01106.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+19804_168+1982 others(28): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74018177 | |||||
| chr10:74018177
|
G | GATATATA others(21): Show |
1 | a0001c0003t0001g0128 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.168+19827_168+1982 others(32): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74018177 | |||||
| chr10:74018177
|
G | GATATATA others(33): Show |
1 | a0004c0020t0015g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.168+19827_168+1982 others(44): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74018177 | |||||
| chr10:74018177
|
GAT | G | 14 | a0001c0001t0001g0178a0001c0002t0007g0167a0001c0002t0007g0168others(11): Show | 14 | HG00639.hp1 HG00733.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.168+19826_168+1982 others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74018177 | |||||
| chr10:74018179
|
T | TATATATA others(39): Show |
1 | a0001c0002t0004g0189 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.168+19827_168+1982 others(50): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74018179 | |||||
| chr10:74018181
|
T | TATATATA others(41): Show |
1 | a0001c0002t0004g0188 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.168+19827_168+1982 others(52): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74018181 | |||||
| chr10:74018181
|
TATATATA others(19): Show |
T | 1 | a0001c0001t0001g0122 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.168+19817_168+1984 others(30): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74018181 | |||||
| chr10:74018201
|
T | A | 1 | a0001c0003t0002g0095 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.168+19826T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74018201 | ||||||
| chr10:74018201
|
T | TATATATA others(12): Show |
1 | a0001c0001t0001g0155 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.168+19827_168+1982 others(23): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74018201 | |||||
| chr10:74018201
|
T | TATATATA others(17): Show |
2 | a0001c0001t0024g0193a0001c0002t0003g0166 | 2 | HG02083.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.168+19827_168+1982 others(28): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74018201 | |||||
| chr10:74018202
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0153 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.168+19827_168+1982 others(25): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74018202 | ||||||
| chr10:74018225
|
A | T | 152 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.168+19850A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74018225 | ||||||
| chr10:74018264
|
C | T | 1 | a0001c0006t0005g0085 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.168+19889C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74018264 | ||||||
| chr10:74018633
|
G | A | 3 | a0001c0002t0012g0190a0001c0002t0012g0191a0001c0002t0012g0198 | 3 | HG01884.hp1 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.168+20258G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74018633 | ||||||
| chr10:74018670
|
C | T | 3 | a0001c0004t0002g0183a0001c0006t0005g0184a0001c0006t0005g0192 | 3 | HG02895.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+20295C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74018670 | ||||||
| chr10:74018756
|
G | C | 5 | a0001c0002t0012g0190a0001c0002t0012g0191a0001c0002t0012g0198others(2): Show | 5 | HG01884.hp1 HG03195.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+20381G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74018756 | ||||||
| chr10:74018929
|
C | T | 70 | a0001c0001t0001g0162a0001c0001t0001g0199a0001c0001t0001g0204others(67): Show | 70 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.168+20554C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74018929 | ||||||
| chr10:74019330
|
A | G | 171 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.168+20955A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74019330 | ||||||
| chr10:74019350
|
T | C | 52 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(49): Show | 52 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.168+20975T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74019350 | ||||||
| chr10:74019393
|
C | G | 41 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(38): Show | 41 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.168+21018C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74019393 | ||||||
| chr10:74019411
|
C | T | 1 | a0001c0003t0002g0074 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.168+21036C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74019411 | ||||||
| chr10:74019421
|
C | G | 2 | a0001c0002t0004g0188a0001c0002t0004g0189 | 2 | HG00642.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.168+21046C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74019421 | ||||||
| chr10:74019434
|
G | A | 1 | a0001c0003t0002g0074 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.168+21059G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74019434 | ||||||
| chr10:74019489
|
A | C | 3 | a0001c0002t0012g0190a0001c0002t0012g0191a0001c0002t0012g0198 | 3 | HG01884.hp1 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.168+21114A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74019489 | ||||||
| chr10:74019920
|
G | A | 3 | a0001c0003t0002g0051a0001c0003t0002g0060a0001c0003t0002g0078 | 3 | HG00741.hp1 HG01168.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.168+21545G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74019920 | ||||||
| chr10:74020058
|
C | T | 1 | a0001c0006t0017g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.168+21683C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74020058 | ||||||
| chr10:74020076
|
A | G | 1 | a0001c0002t0003g0166 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.168+21701A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74020076 | ||||||
| chr10:74020200
|
G | A | 1 | a0001c0003t0008g0061 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.168+21825G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74020200 | ||||||
| chr10:74020726
|
A | G | 1 | a0001c0002t0007g0182 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.168+22351A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74020726 | ||||||
| chr10:74020840
|
C | CA | 5 | a0001c0002t0003g0097a0001c0003t0002g0045a0001c0003t0002g0078others(2): Show | 5 | HG00280.hp1 HG00741.hp1 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-22222dupA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74020840 | |||||
| chr10:74020840
|
C | CAAAAA | 33 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.169-22226_169-2222 others(9): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74020840 | |||||
| chr10:74020840
|
C | CAAAAAA | 45 | a0001c0001t0001g0139a0001c0001t0001g0163a0001c0001t0001g0178others(42): Show | 45 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.169-22227_169-2222 others(10): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74020840 | |||||
| chr10:74020840
|
C | CAAAAAAA | 55 | a0001c0001t0001g0162a0001c0001t0001g0204a0001c0001t0001g0207others(52): Show | 55 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.169-22228_169-2222 others(11): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74020840 | |||||
| chr10:74020840
|
C | CAAAAAAA others(1): Show |
14 | a0001c0001t0001g0199a0001c0001t0001g0209a0001c0001t0001g0211others(11): Show | 14 | HG00673.hp1 HG01346.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.169-22229_169-2222 others(12): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74020840 | |||||
| chr10:74020840
|
C | CAAAAAAA others(4): Show |
1 | a0001c0002t0004g0195 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.169-22232_169-2222 others(15): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74020840 | |||||
| chr10:74020840
|
CA | C | 9 | a0001c0006t0005g0111a0001c0007t0003g0107a0001c0007t0003g0115others(6): Show | 9 | HG01074.hp2 HG01081.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.169-22222delA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74020840 | |||||
| chr10:74020984
|
C | G | 27 | a0001c0001t0001g0178a0001c0001t0001g0207a0001c0002t0003g0001others(24): Show | 27 | HG00639.hp1 HG00642.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.169-22099C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74020984 | ||||||
| chr10:74021080
|
C | T | 140 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0129others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.169-22003C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74021080 | ||||||
| chr10:74021090
|
T | C | 3 | a0001c0004t0002g0183a0001c0006t0005g0184a0001c0006t0005g0192 | 3 | HG02895.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.169-21993T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74021090 | ||||||
| chr10:74021178
|
A | C | 43 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(40): Show | 43 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.169-21905A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74021178 | ||||||
| chr10:74021178
|
A | T | 1 | a0001c0001t0004g0002 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.169-21905A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74021178 | ||||||
| chr10:74021418
|
G | T | 1 | a0001c0004t0002g0058 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.169-21665G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74021418 | ||||||
| chr10:74021539
|
A | G | 1 | a0001c0003t0002g0106 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.169-21544A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74021539 | ||||||
| chr10:74021841
|
T | A | 16 | a0001c0004t0002g0186a0001c0007t0003g0107a0001c0007t0003g0115others(13): Show | 16 | HG00642.hp1 HG01069.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.169-21242T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74021841 | ||||||
| chr10:74021954
|
C | T | 1 | a0001c0002t0003g0124 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.169-21129C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74021954 | ||||||
| chr10:74022137
|
C | T | 1 | a0001c0003t0002g0072 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.169-20946C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74022137 | ||||||
| chr10:74022143
|
A | G | 1 | a0001c0004t0008g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.169-20940A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74022143 | ||||||
| chr10:74022202
|
T | G | 101 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0162others(98): Show | 101 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.169-20881T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74022202 | ||||||
| chr10:74022257
|
A | T | 1 | a0001c0001t0001g0260 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.169-20826A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74022257 | ||||||
| chr10:74022260
|
T | A | 1 | a0001c0001t0001g0260 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.169-20823T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74022260 | ||||||
| chr10:74022262
|
C | A | 1 | a0001c0001t0001g0260 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.169-20821C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74022262 | ||||||
| chr10:74022263
|
A | G | 1 | a0001c0001t0001g0260 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.169-20820A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74022263 | ||||||
| chr10:74022264
|
G | T | 1 | a0001c0001t0001g0260 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.169-20819G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74022264 | ||||||
| chr10:74022266
|
C | A | 1 | a0001c0001t0001g0260 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.169-20817C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74022266 | ||||||
| chr10:74022267
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.169-20816C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74022267 | ||||||
| chr10:74022268
|
A | G | 1 | a0001c0001t0001g0260 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.169-20815A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74022268 | ||||||
| chr10:74022269
|
G | T | 1 | a0001c0001t0001g0260 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.169-20814G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74022269 | ||||||
| chr10:74022270
|
G | T | 1 | a0001c0001t0001g0260 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.169-20813G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74022270 | ||||||
| chr10:74022482
|
G | A | 1 | a0001c0002t0004g0195 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.169-20601G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74022482 | ||||||
| chr10:74022541
|
G | A | 1 | a0001c0004t0002g0093 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.169-20542G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74022541 | ||||||
| chr10:74022575
|
GATAA | G | 3 | a0001c0008t0001g0014a0001c0008t0001g0016a0001c0008t0001g0017 | 3 | HG02258.hp2 HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.169-20475_169-2047 others(8): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74022575 | |||||
| chr10:74022596
|
ATAAATAA others(9): Show |
A | 37 | a0001c0001t0001g0178a0001c0002t0001g0011a0001c0002t0003g0001others(34): Show | 37 | HG00639.hp1 HG00733.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.169-20478_169-2046 others(20): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74022596 | |||||
| chr10:74022600
|
ATAAATAA others(5): Show |
A | 104 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0129others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.169-20474_169-2046 others(16): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74022600 | |||||
| chr10:74022604
|
ATAAATAA others(1): Show |
A | 22 | a0001c0001t0001g0147a0001c0002t0004g0188a0001c0002t0004g0189others(19): Show | 22 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.169-20471_169-2046 others(12): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74022604 | |||||
| chr10:74022784
|
G | A | 6 | a0001c0001t0001g0150a0001c0001t0001g0155a0001c0001t0001g0156others(3): Show | 6 | HG01261.hp1 HG01433.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-20299G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74022784 | ||||||
| chr10:74023077
|
A | G | 63 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0162others(60): Show | 63 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.169-20006A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74023077 | ||||||
| chr10:74023265
|
C | T | 165 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0129others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.169-19818C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74023265 | ||||||
| chr10:74023375
|
A | G | 17 | a0001c0002t0004g0195a0001c0004t0002g0186a0001c0007t0003g0107others(14): Show | 17 | HG00642.hp1 HG01069.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.169-19708A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74023375 | ||||||
| chr10:74023476
|
A | G | 1 | a0001c0006t0005g0085 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.169-19607A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74023476 | ||||||
| chr10:74023582
|
T | C | 43 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(40): Show | 43 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.169-19501T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74023582 | ||||||
| chr10:74023627
|
C | T | 43 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(40): Show | 43 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.169-19456C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74023627 | ||||||
| chr10:74023694
|
G | A | 3 | a0001c0002t0001g0011a0001c0002t0014g0010a0001c0004t0008g0012 | 3 | HG02630.hp2 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.169-19389G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74023694 | ||||||
| chr10:74023962
|
A | C | 8 | a0001c0001t0001g0138a0001c0001t0001g0143a0001c0001t0001g0147others(5): Show | 8 | HG00099.hp1 HG00738.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.169-19121A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74023962 | ||||||
| chr10:74024161
|
T | A | 1 | a0002c0015t0002g0056 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.169-18922T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74024161 | ||||||
| chr10:74024175
|
G | C | 1 | a0002c0015t0002g0056 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.169-18908G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74024175 | ||||||
| chr10:74024298
|
C | G | 1 | a0001c0003t0002g0205 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.169-18785C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74024298 | ||||||
| chr10:74024401
|
G | A | 168 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0129others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.169-18682G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74024401 | ||||||
| chr10:74024596
|
C | T | 8 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(5): Show | 8 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.169-18487C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74024596 | ||||||
| chr10:74024611
|
C | CA | 6 | a0001c0002t0003g0101a0001c0002t0003g0102a0001c0002t0003g0103others(3): Show | 6 | HG01074.hp1 HG01192.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-18458dupA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74024611 | |||||
| chr10:74024611
|
CA | C | 136 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0129others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.169-18458delA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74024611 | |||||
| chr10:74024908
|
A | G | 1 | a0001c0006t0017g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.169-18175A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74024908 | ||||||
| chr10:74024916
|
T | G | 2 | a0001c0002t0020g0256a0001c0011t0006g0255 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.169-18167T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74024916 | ||||||
| chr10:74025190
|
G | A | 1 | a0001c0002t0020g0256 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.169-17893G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74025190 | ||||||
| chr10:74025297
|
G | A | 1 | a0001c0001t0001g0250 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.169-17786G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74025297 | ||||||
| chr10:74025311
|
T | C | 165 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0129others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.169-17772T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74025311 | ||||||
| chr10:74025440
|
C | G | 8 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(5): Show | 8 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.169-17643C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74025440 | ||||||
| chr10:74025506
|
C | T | 3 | a0001c0004t0002g0183a0001c0006t0005g0184a0001c0006t0005g0192 | 3 | HG02895.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.169-17577C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74025506 | ||||||
| chr10:74025538
|
C | T | 1 | a0008c0019t0002g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.169-17545C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74025538 | ||||||
| chr10:74025696
|
G | GAGGA | 92 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(89): Show | 92 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.169-17379_169-1737 others(8): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74025696 | |||||
| chr10:74025708
|
G | A | 73 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0162others(70): Show | 73 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.169-17375G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74025708 | ||||||
| chr10:74025759
|
A | T | 1 | a0001c0003t0002g0083 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.169-17324A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74025759 | ||||||
| chr10:74026075
|
A | C | 1 | a0001c0001t0001g0032 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.169-17008A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74026075 | ||||||
| chr10:74026139
|
A | G | 3 | a0001c0004t0002g0183a0001c0006t0005g0184a0001c0006t0005g0192 | 3 | HG02895.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.169-16944A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74026139 | ||||||
| chr10:74026150
|
G | C | 1 | a0002c0005t0002g0026 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.169-16933G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74026150 | ||||||
| chr10:74026573
|
C | T | 3 | a0001c0004t0002g0183a0001c0006t0005g0184a0001c0006t0005g0192 | 3 | HG02895.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.169-16510C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74026573 | ||||||
| chr10:74026637
|
C | A | 62 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0162others(59): Show | 62 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.169-16446C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74026637 | ||||||
| chr10:74026759
|
G | A | 3 | a0001c0008t0006g0201a0001c0008t0006g0202a0001c0008t0006g0203 | 3 | HG00639.hp2 HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.169-16324G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74026759 | ||||||
| chr10:74027104
|
C | T | 43 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(40): Show | 43 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.169-15979C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74027104 | ||||||
| chr10:74027266
|
C | G | 5 | a0001c0002t0003g0091a0001c0003t0008g0061a0003c0010t0008g0088others(2): Show | 5 | NA18971.hp2 NA18973.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-15817C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74027266 | ||||||
| chr10:74027315
|
A | AT | 5 | a0001c0001t0001g0137a0001c0003t0002g0099a0001c0006t0005g0184others(2): Show | 5 | HG01975.hp2 HG02056.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-15755dupT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74027315 | |||||
| chr10:74027315
|
A | ATT | 41 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0138others(38): Show | 41 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.169-15756_169-1575 others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74027315 | |||||
| chr10:74027441
|
A | T | 4 | a0001c0002t0005g0187a0001c0002t0012g0190a0001c0002t0012g0191others(1): Show | 4 | HG01884.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-15642A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74027441 | ||||||
| chr10:74027624
|
T | A | 1 | a0001c0004t0002g0262 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.169-15459T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74027624 | ||||||
| chr10:74027643
|
C | CA | 80 | a0001c0001t0001g0073a0001c0001t0001g0162a0001c0001t0001g0199others(77): Show | 80 | HG00099.hp2 HG00558.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.169-15415dupA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74027643 | |||||
| chr10:74027643
|
C | CAA | 15 | a0001c0001t0001g0122a0001c0001t0001g0204a0001c0001t0001g0208others(12): Show | 15 | HG00621.hp1 HG02015.hp1 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.169-15416_169-1541 others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74027643 | |||||
| chr10:74027643
|
CA | C | 29 | a0001c0001t0001g0178a0001c0002t0003g0021a0001c0002t0003g0127others(26): Show | 29 | HG00280.hp1 HG00639.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.169-15415delA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74027643 | |||||
| chr10:74027643
|
CAA | C | 14 | a0001c0001t0001g0140a0001c0001t0001g0143a0001c0001t0001g0164others(11): Show | 14 | HG00642.hp2 HG01261.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-15416_169-1541 others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74027643 | |||||
| chr10:74027643
|
CAAA | C | 36 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(33): Show | 36 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.169-15417_169-1541 others(7): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74027643 | |||||
| chr10:74027731
|
G | A | 7 | a0001c0001t0001g0031a0001c0003t0002g0037a0001c0003t0002g0038others(4): Show | 7 | HG02083.hp2 NA18946.hp1 NA18998.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-15352G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74027731 | ||||||
| chr10:74027827
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.169-15256A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74027827 | ||||||
| chr10:74028027
|
G | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.169-15056G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74028027 | ||||||
| chr10:74028265
|
G | T | 1 | a0001c0002t0007g0264 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.169-14818G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74028265 | ||||||
| chr10:74028393
|
C | CT | 74 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0162others(71): Show | 74 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.169-14670dupT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74028393 | |||||
| chr10:74028393
|
C | CTT | 10 | a0001c0001t0006g0232a0001c0002t0003g0001a0001c0002t0003g0028others(7): Show | 10 | HG00735.hp1 HG02135.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.169-14671_169-1467 others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74028393 | |||||
| chr10:74028474
|
G | A | 2 | a0001c0003t0002g0053a0001c0003t0002g0095 | 2 | HG02698.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.169-14609G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74028474 | ||||||
| chr10:74028490
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.169-14593G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74028490 | ||||||
| chr10:74028525
|
T | G | 1 | a0001c0002t0001g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.169-14558T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74028525 | ||||||
| chr10:74028571
|
A | ATT | 3 | a0001c0004t0002g0183a0001c0006t0005g0184a0001c0006t0005g0192 | 3 | HG02895.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.169-14508_169-1450 others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74028571 | |||||
| chr10:74029059
|
T | C | 1 | a0001c0001t0001g0233 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.169-14024T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74029059 | ||||||
| chr10:74029150
|
A | G | 1 | a0001c0001t0001g0150 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.169-13933A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74029150 | ||||||
| chr10:74029837
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.169-13246A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74029837 | ||||||
| chr10:74029843
|
T | C | 1 | a0001c0002t0011g0006 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.169-13240T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74029843 | ||||||
| chr10:74029891
|
T | C | 1 | a0004c0020t0015g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169-13192T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74029891 | ||||||
| chr10:74030060
|
T | C | 3 | a0001c0008t0001g0014a0001c0008t0001g0016a0001c0008t0001g0017 | 3 | HG02258.hp2 HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.169-13023T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74030060 | ||||||
| chr10:74030071
|
C | T | 2 | a0001c0007t0013g0054a0001c0009t0002g0013 | 2 | HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.169-13012C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74030071 | ||||||
| chr10:74030325
|
T | C | 1 | a0001c0002t0004g0195 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.169-12758T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74030325 | ||||||
| chr10:74031045
|
T | C | 1 | a0001c0002t0007g0182 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.169-12038T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74031045 | ||||||
| chr10:74031196
|
C | T | 4 | a0001c0001t0001g0142a0001c0001t0001g0157a0001c0001t0001g0158others(1): Show | 4 | HG01255.hp2 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-11887C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74031196 | ||||||
| chr10:74031304
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.169-11779C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74031304 | ||||||
| chr10:74031385
|
T | G | 4 | a0001c0001t0001g0142a0001c0001t0001g0157a0001c0001t0001g0158others(1): Show | 4 | HG01255.hp2 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-11698T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74031385 | ||||||
| chr10:74031439
|
A | G | 3 | a0001c0008t0001g0014a0001c0008t0001g0016a0001c0008t0001g0017 | 3 | HG02258.hp2 HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.169-11644A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74031439 | ||||||
| chr10:74031776
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.169-11307C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74031776 | ||||||
| chr10:74031881
|
G | A | 43 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(40): Show | 43 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.169-11202G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74031881 | ||||||
| chr10:74031933
|
G | A | 1 | a0001c0002t0005g0187 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.169-11150G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74031933 | ||||||
| chr10:74032044
|
A | G | 1 | a0001c0003t0002g0071 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.169-11039A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74032044 | ||||||
| chr10:74032064
|
C | CA | 23 | a0001c0001t0001g0160a0001c0001t0001g0178a0001c0001t0001g0228others(20): Show | 23 | HG00597.hp1 HG00597.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.169-10991dupA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74032064 | |||||
| chr10:74032064
|
CA | C | 113 | a0001c0001t0001g0032a0001c0001t0001g0073a0001c0001t0001g0122others(110): Show | 113 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.169-10991delA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74032064 | |||||
| chr10:74032064
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0033 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.169-11006_169-1099 others(20): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74032064 | |||||
| chr10:74032095
|
C | T | 1 | a0001c0003t0002g0071 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.169-10988C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74032095 | ||||||
| chr10:74032240
|
T | TA | 93 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(90): Show | 93 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.169-10823dupA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74032240 | |||||
| chr10:74032240
|
T | TAA | 9 | a0001c0002t0004g0189a0001c0002t0005g0187a0001c0002t0011g0003others(6): Show | 9 | HG00642.hp2 HG00735.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.169-10824_169-1082 others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74032240 | |||||
| chr10:74032255
|
A | G | 10 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(7): Show | 10 | HG01074.hp2 HG01081.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.169-10828A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74032255 | ||||||
| chr10:74032624
|
C | T | 1 | a0001c0002t0001g0110 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.169-10459C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74032624 | ||||||
| chr10:74032708
|
AAAT | A | 12 | a0001c0002t0003g0001a0001c0002t0004g0195a0001c0002t0011g0003others(9): Show | 12 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.169-10373_169-1037 others(7): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74032708 | |||||
| chr10:74032709
|
AAT | A | 11 | a0001c0001t0001g0122a0001c0001t0001g0208a0001c0001t0001g0222others(8): Show | 11 | HG00642.hp2 HG02015.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.169-10353_169-1035 others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74032709 | |||||
| chr10:74032710
|
AT | A | 4 | a0001c0002t0007g0264a0001c0002t0020g0256a0001c0006t0005g0192others(1): Show | 4 | HG02818.hp1 HG03225.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-10372delT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74032710 | ||||||
| chr10:74032710
|
ATAT | A | 122 | a0001c0001t0001g0073a0001c0001t0001g0129a0001c0001t0001g0131others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.169-10372_169-1037 others(7): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74032710 | ||||||
| chr10:74032711
|
T | A | 56 | a0001c0001t0001g0178a0001c0002t0003g0020a0001c0002t0003g0021others(53): Show | 56 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.169-10372T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74032711 | ||||||
| chr10:74032713
|
T | A | 27 | a0001c0001t0001g0178a0001c0001t0001g0208a0001c0002t0003g0023others(24): Show | 27 | HG00423.hp2 HG00639.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.169-10370T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74032713 | ||||||
| chr10:74032715
|
T | A | 38 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0146others(35): Show | 38 | HG00423.hp2 HG00639.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.169-10368T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74032715 | ||||||
| chr10:74032717
|
T | A | 2 | a0001c0002t0005g0187a0001c0003t0002g0173 | 2 | HG00639.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.169-10366T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74032717 | ||||||
| chr10:74032732
|
T | A | 18 | a0001c0002t0004g0195a0001c0004t0002g0186a0001c0007t0003g0107others(15): Show | 18 | HG00642.hp1 HG01069.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.169-10351T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74032732 | ||||||
| chr10:74032814
|
A | G | 3 | a0001c0008t0006g0201a0001c0008t0006g0202a0001c0008t0006g0203 | 3 | HG00639.hp2 HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.169-10269A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74032814 | ||||||
| chr10:74032835
|
A | G | 11 | a0001c0002t0001g0011a0001c0002t0005g0187a0001c0002t0012g0190others(8): Show | 11 | HG01884.hp1 HG02630.hp2 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.169-10248A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74032835 | ||||||
| chr10:74032894
|
G | A | 1 | a0001c0004t0002g0082 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.169-10189G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74032894 | ||||||
| chr10:74033047
|
A | G | 63 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0162others(60): Show | 63 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.169-10036A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74033047 | ||||||
| chr10:74033076
|
C | T | 1 | a0001c0006t0017g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.169-10007C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74033076 | ||||||
| chr10:74033140
|
A | C | 1 | a0001c0002t0007g0182 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.169-9943A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74033140 | ||||||
| chr10:74033417
|
T | C | 63 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0162others(60): Show | 63 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.169-9666T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74033417 | ||||||
| chr10:74033614
|
C | T | 92 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0162others(89): Show | 92 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.169-9469C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74033614 | ||||||
| chr10:74033643
|
T | C | 1 | a0001c0002t0012g0191 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.169-9440T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74033643 | ||||||
| chr10:74033865
|
C | T | 63 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0162others(60): Show | 63 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.169-9218C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74033865 | ||||||
| chr10:74034022
|
ATG | A | 4 | a0001c0001t0001g0044a0002c0005t0010g0018a0002c0005t0010g0050others(1): Show | 4 | HG00280.hp1 HG01978.hp1 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-9055_169-9054d others(4): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74034022 | |||||
| chr10:74034056
|
G | T | 1 | a0001c0004t0002g0262 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.169-9027G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74034056 | ||||||
| chr10:74034331
|
A | AC | 4 | a0001c0001t0001g0238a0001c0003t0002g0075a0001c0003t0009g0134others(1): Show | 4 | HG01106.hp2 HG01978.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-8748dupC | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74034331 | |||||
| chr10:74034426
|
A | G | 1 | a0001c0002t0004g0195 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.169-8657A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74034426 | ||||||
| chr10:74034682
|
T | C | 1 | a0001c0004t0002g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.169-8401T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74034682 | ||||||
| chr10:74034736
|
A | G | 1 | a0001c0006t0005g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.169-8347A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74034736 | ||||||
| chr10:74034977
|
C | A | 3 | a0001c0003t0002g0079a0001c0003t0002g0092a0002c0015t0002g0056 | 3 | NA18940.hp2 NA19055.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.169-8106C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74034977 | ||||||
| chr10:74035079
|
T | A | 8 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(5): Show | 8 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.169-8004T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74035079 | ||||||
| chr10:74035119
|
A | G | 2 | a0001c0006t0005g0184a0001c0006t0005g0192 | 2 | HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.169-7964A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74035119 | ||||||
| chr10:74035261
|
T | C | 2 | a0002c0005t0002g0026a0002c0005t0010g0069 | 2 | NA19091.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.169-7822T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74035261 | ||||||
| chr10:74035478
|
A | G | 1 | a0001c0003t0009g0125 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.169-7605A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74035478 | ||||||
| chr10:74035803
|
G | A | 71 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0162others(68): Show | 71 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.169-7280G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74035803 | ||||||
| chr10:74036130
|
T | G | 1 | a0001c0004t0002g0093 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.169-6953T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74036130 | ||||||
| chr10:74036184
|
C | A | 1 | a0001c0002t0001g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.169-6899C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74036184 | ||||||
| chr10:74036353
|
C | G | 1 | a0001c0002t0003g0127 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.169-6730C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74036353 | ||||||
| chr10:74036359
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.169-6724C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74036359 | ||||||
| chr10:74036481
|
C | T | 1 | a0001c0008t0001g0216 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.169-6602C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74036481 | ||||||
| chr10:74036531
|
T | A | 1 | a0001c0001t0006g0232 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.169-6552T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74036531 | ||||||
| chr10:74036639
|
G | A | 17 | a0001c0001t0001g0178a0001c0002t0007g0167a0001c0002t0007g0168others(14): Show | 17 | HG00639.hp1 HG00733.hp2 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.169-6444G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74036639 | ||||||
| chr10:74036701
|
T | A | 1 | a0001c0002t0012g0190 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.169-6382T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74036701 | ||||||
| chr10:74036945
|
C | G | 1 | a0001c0001t0023g0234 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.169-6138C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74036945 | ||||||
| chr10:74037035
|
C | T | 2 | a0001c0002t0020g0256a0001c0011t0006g0255 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.169-6048C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74037035 | ||||||
| chr10:74037199
|
A | T | 1 | a0001c0006t0005g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.169-5884A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74037199 | ||||||
| chr10:74037279
|
T | C | 2 | a0001c0002t0020g0256a0001c0011t0006g0255 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.169-5804T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74037279 | ||||||
| chr10:74037288
|
G | C | 1 | a0001c0006t0005g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.169-5795G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74037288 | ||||||
| chr10:74037304
|
G | A | 8 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(5): Show | 8 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.169-5779G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74037304 | ||||||
| chr10:74037914
|
G | A | 46 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(43): Show | 46 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.169-5169G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74037914 | ||||||
| chr10:74037999
|
C | CT | 7 | a0001c0004t0002g0062a0001c0004t0002g0123a0001c0006t0005g0076others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-5068dupT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74037999 | |||||
| chr10:74037999
|
CT | C | 106 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(103): Show | 106 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.169-5068delT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74037999 | |||||
| chr10:74037999
|
CTT | C | 63 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0162others(60): Show | 63 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.169-5069_169-5068d others(4): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74037999 | |||||
| chr10:74038005
|
T | C | 16 | a0001c0001t0001g0178a0001c0002t0007g0167a0001c0002t0007g0168others(13): Show | 16 | HG00639.hp1 HG00733.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.169-5078T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74038005 | ||||||
| chr10:74038006
|
T | C | 63 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0162others(60): Show | 63 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.169-5077T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74038006 | ||||||
| chr10:74038143
|
G | C | 4 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0250others(1): Show | 4 | HG02132.hp2 NA18977.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-4940G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74038143 | ||||||
| chr10:74038186
|
G | A | 2 | a0001c0002t0003g0001a0001c0002t0011g0008 | 2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.169-4897G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74038186 | ||||||
| chr10:74038194
|
G | A | 4 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0250others(1): Show | 4 | HG02132.hp2 NA18977.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-4889G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74038194 | ||||||
| chr10:74038390
|
A | C | 166 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0129others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.169-4693A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74038390 | ||||||
| chr10:74038912
|
T | A | 3 | a0001c0004t0002g0183a0001c0006t0005g0184a0001c0006t0005g0192 | 3 | HG02895.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.169-4171T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74038912 | ||||||
| chr10:74038913
|
A | G | 2 | a0001c0003t0002g0169a0002c0005t0010g0171 | 2 | NA19002.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.169-4170A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74038913 | ||||||
| chr10:74038934
|
G | A | 2 | a0001c0002t0004g0188a0001c0002t0004g0189 | 2 | HG00642.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.169-4149G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74038934 | ||||||
| chr10:74038975
|
G | A | 1 | a0001c0003t0002g0053 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.169-4108G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74038975 | ||||||
| chr10:74039014
|
C | T | 1 | a0001c0003t0002g0051 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.169-4069C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74039014 | ||||||
| chr10:74039061
|
G | A | 2 | a0001c0004t0002g0052a0001c0004t0002g0058 | 2 | HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.169-4022G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74039061 | ||||||
| chr10:74039068
|
C | T | 1 | a0001c0001t0006g0232 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.169-4015C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74039068 | ||||||
| chr10:74039205
|
G | A | 1 | a0001c0002t0003g0065 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.169-3878G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74039205 | ||||||
| chr10:74039285
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.169-3798C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74039285 | ||||||
| chr10:74039509
|
G | A | 3 | a0001c0008t0006g0201a0001c0008t0006g0202a0001c0008t0006g0203 | 3 | HG00639.hp2 HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.169-3574G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74039509 | ||||||
| chr10:74039537
|
G | C | 19 | a0001c0001t0001g0178a0001c0002t0004g0195a0001c0002t0007g0167others(16): Show | 19 | HG00639.hp1 HG00733.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.169-3546G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74039537 | ||||||
| chr10:74039573
|
G | A | 2 | a0001c0007t0018g0100a0001c0009t0002g0040 | 2 | HG01069.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.169-3510G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74039573 | ||||||
| chr10:74039771
|
A | AAAAAG | 3 | a0001c0001t0001g0141a0001c0001t0001g0153a0001c0001t0001g0214 | 3 | HG00741.hp2 HG02129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.169-3287_169-3283d others(7): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74039771 | |||||
| chr10:74039771
|
AAAAAGAA others(3): Show |
A | 19 | a0001c0001t0001g0228a0001c0004t0002g0186a0001c0007t0003g0107others(16): Show | 19 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.169-3292_169-3283d others(12): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74039771 | |||||
| chr10:74039906
|
C | T | 63 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0162others(60): Show | 63 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.169-3177C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74039906 | ||||||
| chr10:74040154
|
A | G | 17 | a0001c0004t0002g0186a0001c0007t0003g0107a0001c0007t0003g0115others(14): Show | 17 | HG00642.hp1 HG01069.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.169-2929A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74040154 | ||||||
| chr10:74040157
|
C | T | 1 | a0001c0003t0002g0159 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.169-2926C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74040157 | ||||||
| chr10:74040406
|
G | C | 166 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0129others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.169-2677G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74040406 | ||||||
| chr10:74040413
|
C | T | 1 | a0001c0006t0005g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.169-2670C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74040413 | ||||||
| chr10:74040433
|
T | A | 1 | a0001c0001t0001g0073 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.169-2650T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74040433 | ||||||
| chr10:74040435
|
C | G | 8 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(5): Show | 8 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.169-2648C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74040435 | ||||||
| chr10:74040444
|
T | A | 2 | a0001c0002t0020g0256a0001c0011t0006g0255 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.169-2639T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74040444 | ||||||
| chr10:74040462
|
C | G | 1 | a0001c0004t0002g0093 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.169-2621C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74040462 | ||||||
| chr10:74040673
|
A | C | 17 | a0001c0001t0001g0178a0001c0002t0007g0167a0001c0002t0007g0168others(14): Show | 17 | HG00639.hp1 HG00733.hp2 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.169-2410A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74040673 | ||||||
| chr10:74041166
|
A | AT | 46 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(43): Show | 46 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.169-1908dupT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74041166 | |||||
| chr10:74041306
|
G | A | 1 | a0001c0001t0024g0193 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.169-1777G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74041306 | ||||||
| chr10:74041423
|
T | C | 4 | a0001c0002t0005g0187a0001c0002t0012g0190a0001c0002t0012g0191others(1): Show | 4 | HG01884.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-1660T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74041423 | ||||||
| chr10:74041737
|
C | CA | 46 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(43): Show | 46 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.169-1332dupA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr10 | 74041737 | |||||
| chr10:74042042
|
A | T | 2 | a0001c0002t0020g0256a0001c0011t0006g0255 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.169-1041A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74042042 | ||||||
| chr10:74042281
|
G | A | 63 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0162others(60): Show | 63 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.169-802G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74042281 | ||||||
| chr10:74042381
|
A | G | 5 | a0001c0006t0005g0076a0001c0006t0005g0077a0001c0006t0005g0080others(2): Show | 5 | HG02622.hp1 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-702A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74042381 | ||||||
| chr10:74042426
|
G | A | 2 | a0001c0002t0020g0256a0001c0011t0006g0255 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.169-657G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74042426 | ||||||
| chr10:74042688
|
G | A | 3 | a0001c0004t0002g0183a0001c0006t0005g0184a0001c0006t0005g0192 | 3 | HG02895.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.169-395G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74042688 | ||||||
| chr10:74042816
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.169-267A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74042816 | ||||||
| chr10:74043301
|
A | T | 3 | a0001c0001t0001g0228a0001c0001t0001g0253a0001c0001t0001g0254 | 3 | HG01168.hp1 HG01169.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.239+148A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74043301 | ||||||
| chr10:74043351
|
A | AT | 46 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(43): Show | 46 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.239+210dupT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74043351 | |||||
| chr10:74043493
|
C | T | 1 | a0001c0002t0003g0166 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.239+340C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74043493 | ||||||
| chr10:74043500
|
C | G | 8 | a0001c0002t0005g0187a0001c0002t0012g0190a0001c0002t0012g0191others(5): Show | 8 | HG01884.hp1 HG03195.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.239+347C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74043500 | ||||||
| chr10:74043581
|
A | G | 8 | a0001c0002t0005g0187a0001c0002t0012g0190a0001c0002t0012g0191others(5): Show | 8 | HG01884.hp1 HG03195.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.239+428A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74043581 | ||||||
| chr10:74043608
|
A | G | 2 | a0001c0001t0001g0147a0001c0001t0004g0149 | 2 | HG00738.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.239+455A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74043608 | ||||||
| chr10:74043627
|
G | A | 8 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(5): Show | 8 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.239+474G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74043627 | ||||||
| chr10:74043660
|
A | G | 8 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(5): Show | 8 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.239+507A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74043660 | ||||||
| chr10:74043980
|
G | A | 8 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(5): Show | 8 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.239+827G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74043980 | ||||||
| chr10:74044039
|
A | T | 1 | a0001c0001t0006g0232 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.239+886A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74044039 | ||||||
| chr10:74044110
|
C | CA | 8 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(5): Show | 8 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.239+969dupA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74044110 | |||||
| chr10:74044110
|
CA | C | 8 | a0001c0002t0005g0187a0001c0002t0012g0190a0001c0002t0012g0191others(5): Show | 8 | HG01884.hp1 HG03195.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.239+969delA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74044110 | |||||
| chr10:74044202
|
A | G | 1 | a0001c0002t0003g0103 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.239+1049A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74044202 | ||||||
| chr10:74044356
|
A | G | 1 | a0001c0003t0008g0061 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.239+1203A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74044356 | ||||||
| chr10:74044609
|
T | G | 1 | a0001c0001t0001g0178 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.239+1456T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74044609 | ||||||
| chr10:74044772
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.239+1619A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74044772 | ||||||
| chr10:74045265
|
G | GGATA | 107 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(104): Show | 107 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(104): Show |
intron_variant | MODIFIER | c.239+2153_239+2156d others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74045265 | |||||
| chr10:74045265
|
G | GGATAGAT others(1): Show |
14 | a0001c0001t0001g0030a0001c0001t0001g0105a0001c0001t0001g0138others(11): Show | 14 | HG00423.hp2 HG00673.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.239+2149_239+2156d others(10): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74045265 | |||||
| chr10:74045265
|
GGATA | G | 8 | a0001c0002t0001g0110a0001c0002t0012g0190a0001c0006t0005g0076others(5): Show | 8 | HG01884.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.239+2153_239+2156d others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74045265 | |||||
| chr10:74045265
|
GGATAGAT others(1): Show |
G | 3 | a0001c0002t0005g0187a0001c0002t0012g0191a0001c0002t0012g0198 | 3 | HG03195.hp1 HG03471.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.239+2149_239+2156d others(10): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74045265 | |||||
| chr10:74045310
|
T | A | 1 | a0001c0008t0001g0015 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.239+2157T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74045310 | ||||||
| chr10:74045354
|
G | A | 46 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(43): Show | 46 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.239+2201G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74045354 | ||||||
| chr10:74045359
|
A | G | 1 | a0001c0001t0024g0193 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.239+2206A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74045359 | ||||||
| chr10:74045555
|
G | A | 1 | a0001c0007t0003g0107 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.239+2402G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74045555 | ||||||
| chr10:74045619
|
T | C | 7 | a0001c0004t0002g0062a0001c0004t0002g0123a0001c0006t0005g0076others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.239+2466T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74045619 | ||||||
| chr10:74045622
|
C | CA | 47 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.239+2487dupA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74045622 | |||||
| chr10:74045622
|
CA | C | 7 | a0001c0001t0001g0213a0001c0001t0001g0242a0001c0002t0005g0187others(4): Show | 7 | HG00099.hp2 HG01884.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.239+2487delA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74045622 | |||||
| chr10:74045756
|
G | A | 1 | a0001c0004t0002g0183 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.239+2603G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74045756 | ||||||
| chr10:74045790
|
C | T | 4 | a0001c0001t0001g0141a0001c0001t0001g0146a0001c0001t0001g0153others(1): Show | 4 | HG00735.hp2 HG00741.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+2637C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74045790 | ||||||
| chr10:74045885
|
A | G | 2 | a0001c0003t0009g0197a0001c0018t0003g0196 | 2 | HG03239.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.239+2732A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74045885 | ||||||
| chr10:74046162
|
C | T | 1 | a0008c0019t0002g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.239+3009C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74046162 | ||||||
| chr10:74046236
|
C | T | 3 | a0001c0002t0012g0190a0001c0002t0012g0191a0001c0002t0012g0198 | 3 | HG01884.hp1 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.239+3083C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74046236 | ||||||
| chr10:74046519
|
C | A | 125 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0129others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.239+3366C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74046519 | ||||||
| chr10:74046709
|
C | A | 8 | a0001c0002t0005g0187a0001c0002t0012g0190a0001c0002t0012g0191others(5): Show | 8 | HG01884.hp1 HG03195.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.239+3556C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74046709 | ||||||
| chr10:74047168
|
A | C | 2 | a0001c0006t0005g0184a0001c0006t0005g0192 | 2 | HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.239+4015A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74047168 | ||||||
| chr10:74047194
|
G | A | 1 | a0001c0002t0005g0187 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.239+4041G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74047194 | ||||||
| chr10:74047282
|
G | A | 46 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(43): Show | 46 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.239+4129G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74047282 | ||||||
| chr10:74047607
|
A | T | 63 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0162others(60): Show | 63 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.239+4454A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74047607 | ||||||
| chr10:74047683
|
T | C | 3 | a0001c0002t0003g0042a0001c0002t0003g0087a0001c0002t0003g0097 | 3 | HG01934.hp2 HG02273.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.239+4530T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74047683 | ||||||
| chr10:74047896
|
G | A | 2 | a0001c0006t0005g0108a0001c0006t0005g0111 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.239+4743G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74047896 | ||||||
| chr10:74048030
|
A | G | 2 | a0001c0007t0004g0120a0001c0007t0004g0121 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.239+4877A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74048030 | ||||||
| chr10:74048379
|
A | G | 1 | a0001c0003t0002g0048 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.239+5226A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74048379 | ||||||
| chr10:74048403
|
G | T | 1 | a0001c0002t0003g0021 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.239+5250G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74048403 | ||||||
| chr10:74048464
|
C | CA | 45 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(42): Show | 45 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.239+5327dupA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74048464 | |||||
| chr10:74048555
|
A | G | 63 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0162others(60): Show | 63 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.239+5402A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74048555 | ||||||
| chr10:74048583
|
G | A | 1 | a0001c0002t0001g0251 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.239+5430G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74048583 | ||||||
| chr10:74048714
|
A | C | 1 | a0001c0001t0001g0240 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.239+5561A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74048714 | ||||||
| chr10:74049106
|
CAAAA | C | 16 | a0001c0001t0001g0178a0001c0002t0007g0167a0001c0002t0007g0168others(13): Show | 16 | HG00639.hp1 HG00733.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.239+5957_239+5960d others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74049106 | |||||
| chr10:74049110
|
A | AAAAC | 61 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0162others(58): Show | 61 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.239+5981_239+5984d others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74049110 | |||||
| chr10:74049110
|
A | C | 2 | a0001c0002t0001g0251a0001c0006t0005g0085 | 2 | HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.239+5957A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74049110 | ||||||
| chr10:74049214
|
C | A | 1 | a0001c0001t0001g0165 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.239+6061C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74049214 | ||||||
| chr10:74049270
|
A | G | 3 | a0001c0008t0001g0014a0001c0008t0001g0016a0001c0008t0001g0017 | 3 | HG02258.hp2 HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.239+6117A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74049270 | ||||||
| chr10:74049448
|
A | G | 1 | a0001c0007t0013g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.239+6295A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74049448 | ||||||
| chr10:74049450
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.239+6297A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74049450 | ||||||
| chr10:74049523
|
G | A | 2 | a0001c0002t0004g0188a0001c0002t0004g0189 | 2 | HG00642.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.239+6370G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74049523 | ||||||
| chr10:74049625
|
G | A | 4 | a0001c0001t0001g0217a0001c0001t0001g0236a0001c0001t0001g0237others(1): Show | 4 | HG00621.hp1 NA18961.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+6472G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74049625 | ||||||
| chr10:74049880
|
G | T | 1 | a0001c0001t0001g0219 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.239+6727G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74049880 | ||||||
| chr10:74050000
|
C | T | 8 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(5): Show | 8 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.239+6847C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74050000 | ||||||
| chr10:74050036
|
G | C | 63 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0162others(60): Show | 63 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.239+6883G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74050036 | ||||||
| chr10:74050066
|
G | A | 3 | a0001c0008t0001g0014a0001c0008t0001g0016a0001c0008t0001g0017 | 3 | HG02258.hp2 HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.239+6913G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74050066 | ||||||
| chr10:74050243
|
C | T | 1 | a0001c0007t0013g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.239+7090C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74050243 | ||||||
| chr10:74050293
|
A | T | 2 | a0001c0004t0002g0052a0001c0004t0002g0058 | 2 | HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.239+7140A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74050293 | ||||||
| chr10:74050339
|
A | T | 2 | a0001c0002t0020g0256a0001c0011t0006g0255 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.239+7186A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74050339 | ||||||
| chr10:74050371
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.239+7218C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74050371 | ||||||
| chr10:74050416
|
A | G | 19 | a0001c0001t0001g0178a0001c0002t0004g0195a0001c0002t0007g0167others(16): Show | 19 | HG00639.hp1 HG00733.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.239+7263A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74050416 | ||||||
| chr10:74050573
|
G | A | 8 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(5): Show | 8 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.239+7420G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74050573 | ||||||
| chr10:74050678
|
C | T | 2 | a0001c0002t0020g0256a0001c0011t0006g0255 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.239+7525C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74050678 | ||||||
| chr10:74050724
|
G | A | 1 | a0001c0004t0002g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.239+7571G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74050724 | ||||||
| chr10:74050761
|
C | T | 8 | a0001c0002t0005g0187a0001c0002t0012g0190a0001c0002t0012g0191others(5): Show | 8 | HG01884.hp1 HG03195.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.239+7608C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74050761 | ||||||
| chr10:74050861
|
AG | A | 8 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(5): Show | 8 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.239+7709delG | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74050861 | ||||||
| chr10:74050932
|
AT | A | 89 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(86): Show | 89 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.239+7804delT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74050932 | |||||
| chr10:74050932
|
ATT | A | 102 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0131others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.239+7803_239+7804d others(4): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74050932 | |||||
| chr10:74050932
|
ATTT | A | 28 | a0001c0001t0001g0147a0001c0001t0001g0150a0001c0001t0001g0242others(25): Show | 28 | HG00642.hp1 HG00738.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.239+7802_239+7804d others(5): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74050932 | |||||
| chr10:74050932
|
ATTTT | A | 22 | a0001c0001t0001g0178a0001c0002t0003g0001a0001c0002t0004g0189others(19): Show | 22 | HG00639.hp1 HG00642.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.239+7801_239+7804d others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74050932 | |||||
| chr10:74051141
|
G | A | 1 | a0001c0006t0017g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.239+7988G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74051141 | ||||||
| chr10:74051259
|
C | T | 2 | a0001c0002t0004g0188a0001c0002t0004g0189 | 2 | HG00642.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.239+8106C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74051259 | ||||||
| chr10:74051301
|
A | C | 2 | a0001c0007t0004g0120a0001c0007t0004g0121 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.239+8148A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74051301 | ||||||
| chr10:74051368
|
C | T | 4 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0224others(1): Show | 4 | NA18940.hp1 NA18983.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+8215C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74051368 | ||||||
| chr10:74051386
|
A | G | 165 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0129others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.239+8233A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74051386 | ||||||
| chr10:74051417
|
A | G | 1 | a0001c0002t0004g0195 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.239+8264A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74051417 | ||||||
| chr10:74051485
|
G | C | 166 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0129others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.239+8332G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74051485 | ||||||
| chr10:74051492
|
C | T | 2 | a0001c0002t0004g0188a0001c0002t0004g0189 | 2 | HG00642.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.239+8339C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74051492 | ||||||
| chr10:74051721
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.239+8568T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74051721 | ||||||
| chr10:74051839
|
A | T | 1 | a0001c0002t0007g0182 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.239+8686A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74051839 | ||||||
| chr10:74051932
|
C | T | 2 | a0001c0002t0003g0049a0001c0002t0003g0070 | 2 | HG02129.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.239+8779C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74051932 | ||||||
| chr10:74052238
|
C | T | 17 | a0001c0004t0002g0186a0001c0007t0003g0107a0001c0007t0003g0115others(14): Show | 17 | HG00642.hp1 HG01069.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.239+9085C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74052238 | ||||||
| chr10:74052268
|
A | G | 1 | a0001c0006t0017g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.239+9115A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74052268 | ||||||
| chr10:74052374
|
G | GT | 20 | a0001c0001t0001g0044a0001c0001t0001g0240a0001c0001t0001g0253others(17): Show | 20 | HG00423.hp2 HG00735.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.239+9241dupT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74052374 | |||||
| chr10:74052374
|
GT | G | 48 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0138others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.239+9241delT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74052374 | |||||
| chr10:74052398
|
A | G | 2 | a0001c0001t0001g0211a0001c0003t0002g0212 | 2 | HG00673.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.239+9245A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74052398 | ||||||
| chr10:74052406
|
T | A | 2 | a0001c0001t0001g0129a0001c0001t0001g0131 | 2 | HG00280.hp2 HG00423.hp1 |
intron_variant | MODIFIER | c.239+9253T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74052406 | ||||||
| chr10:74052578
|
T | G | 1 | a0001c0002t0004g0195 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.239+9425T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74052578 | ||||||
| chr10:74052599
|
A | G | 1 | a0001c0002t0004g0195 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.239+9446A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74052599 | ||||||
| chr10:74052744
|
CT | C | 6 | a0001c0002t0005g0187a0001c0002t0012g0190a0001c0002t0012g0191others(3): Show | 6 | HG00642.hp1 HG01884.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.239+9603delT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74052744 | |||||
| chr10:74052847
|
G | A | 3 | a0001c0008t0001g0014a0001c0008t0001g0016a0001c0008t0001g0017 | 3 | HG02258.hp2 HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.239+9694G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74052847 | ||||||
| chr10:74052936
|
GA | G | 8 | a0001c0001t0004g0144a0001c0002t0007g0182a0001c0004t0002g0186others(5): Show | 8 | HG00642.hp1 HG01069.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.239+9794delA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74052936 | |||||
| chr10:74052936
|
GAA | G | 43 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(40): Show | 43 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.239+9793_239+9794d others(4): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74052936 | |||||
| chr10:74052936
|
GAAA | G | 7 | a0001c0002t0011g0003a0001c0002t0011g0004a0001c0002t0011g0006others(4): Show | 7 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.239+9792_239+9794d others(5): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74052936 | |||||
| chr10:74052944
|
A | T | 1 | a0001c0002t0007g0182 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.239+9791A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74052944 | ||||||
| chr10:74052945
|
AAAT | A | 63 | a0001c0001t0001g0122a0001c0001t0001g0162a0001c0001t0001g0199others(60): Show | 63 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.239+9794_239+9796d others(5): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74052945 | |||||
| chr10:74052946
|
A | T | 11 | a0001c0001t0001g0044a0001c0001t0001g0147a0001c0001t0001g0151others(8): Show | 11 | HG00280.hp1 HG00738.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.239+9793A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74052946 | ||||||
| chr10:74052946
|
AAT | A | 11 | a0001c0004t0002g0183a0001c0007t0003g0107a0001c0007t0003g0115others(8): Show | 11 | HG01074.hp2 HG01081.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.239+9813_239+9814d others(4): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74052946 | |||||
| chr10:74052947
|
ATAT | A | 25 | a0001c0001t0001g0073a0001c0001t0001g0178a0001c0001t0001g0211others(22): Show | 25 | HG00639.hp1 HG00673.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.239+9795_239+9797d others(5): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74052947 | ||||||
| chr10:74052947
|
ATATAT | A | 3 | a0001c0002t0012g0190a0001c0002t0012g0191a0001c0002t0012g0198 | 3 | HG01884.hp1 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.239+9795_239+9799d others(7): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74052947 | ||||||
| chr10:74052948
|
T | A | 14 | a0001c0001t0001g0105a0001c0002t0003g0059a0001c0002t0003g0065others(11): Show | 14 | HG00597.hp2 HG01243.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.239+9795T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74052948 | ||||||
| chr10:74052950
|
T | A | 10 | a0001c0003t0002g0055a0001c0007t0003g0107a0001c0007t0003g0115others(7): Show | 10 | HG01074.hp2 HG01081.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.239+9797T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74052950 | ||||||
| chr10:74052954
|
T | A | 1 | a0001c0002t0012g0191 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.239+9801T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74052954 | ||||||
| chr10:74052978
|
T | A | 1 | a0001c0007t0013g0029 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.239+9825T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74052978 | ||||||
| chr10:74053268
|
A | G | 1 | a0001c0004t0002g0183 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.239+10115A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74053268 | ||||||
| chr10:74053509
|
C | G | 1 | a0001c0001t0001g0230 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.239+10356C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74053509 | ||||||
| chr10:74053573
|
C | T | 8 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(5): Show | 8 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.239+10420C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74053573 | ||||||
| chr10:74053759
|
C | T | 1 | a0001c0002t0001g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.239+10606C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74053759 | ||||||
| chr10:74053776
|
A | G | 109 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0129others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.239+10623A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74053776 | ||||||
| chr10:74054185
|
G | A | 8 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(5): Show | 8 | HG01074.hp2 HG01081.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.239+11032G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74054185 | ||||||
| chr10:74054502
|
C | A | 8 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(5): Show | 8 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.239+11349C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74054502 | ||||||
| chr10:74054647
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.239+11494G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74054647 | ||||||
| chr10:74054659
|
G | A | 1 | a0001c0002t0003g0028 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.239+11506G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74054659 | ||||||
| chr10:74054678
|
C | T | 46 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(43): Show | 46 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.239+11525C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74054678 | ||||||
| chr10:74055126
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.239+11973C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74055126 | ||||||
| chr10:74055199
|
C | T | 8 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(5): Show | 8 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.239+12046C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74055199 | ||||||
| chr10:74056000
|
A | G | 15 | a0001c0001t0001g0178a0001c0002t0007g0167a0001c0002t0007g0168others(12): Show | 15 | HG00639.hp1 HG00733.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.239+12847A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74056000 | ||||||
| chr10:74056196
|
G | GGT | 3 | a0001c0008t0001g0014a0001c0008t0001g0016a0001c0008t0001g0017 | 3 | HG02258.hp2 HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.239+13056_239+1305 others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74056196 | |||||
| chr10:74056207
|
G | A | 2 | a0001c0008t0001g0015a0001c0008t0001g0216 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.239+13054G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74056207 | ||||||
| chr10:74056476
|
A | T | 1 | a0001c0003t0002g0172 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.239+13323A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74056476 | ||||||
| chr10:74057082
|
A | G | 3 | a0001c0002t0020g0256a0001c0011t0006g0117a0001c0011t0006g0255 | 3 | HG03225.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.240-13588A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74057082 | ||||||
| chr10:74057122
|
T | C | 1 | a0001c0003t0002g0095 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.240-13548T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74057122 | ||||||
| chr10:74057252
|
T | G | 1 | a0001c0001t0001g0140 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.240-13418T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74057252 | ||||||
| chr10:74057260
|
A | T | 63 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0162others(60): Show | 63 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.240-13410A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74057260 | ||||||
| chr10:74057266
|
A | C | 1 | a0001c0004t0002g0186 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.240-13404A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74057266 | ||||||
| chr10:74057306
|
C | T | 8 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(5): Show | 8 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.240-13364C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74057306 | ||||||
| chr10:74057412
|
T | A | 1 | a0001c0003t0002g0172 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.240-13258T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74057412 | ||||||
| chr10:74057413
|
A | T | 1 | a0001c0003t0002g0172 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.240-13257A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74057413 | ||||||
| chr10:74057414
|
T | A | 1 | a0001c0003t0002g0172 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.240-13256T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74057414 | ||||||
| chr10:74057523
|
T | A | 2 | a0001c0003t0009g0197a0001c0018t0003g0196 | 2 | HG03239.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.240-13147T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74057523 | ||||||
| chr10:74057819
|
G | T | 1 | a0001c0002t0012g0190 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.240-12851G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74057819 | ||||||
| chr10:74058022
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.240-12648C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74058022 | ||||||
| chr10:74058162
|
G | C | 1 | a0001c0003t0002g0172 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.240-12508G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74058162 | ||||||
| chr10:74058164
|
C | A | 1 | a0001c0003t0002g0172 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.240-12506C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74058164 | ||||||
| chr10:74058165
|
A | G | 1 | a0001c0003t0002g0172 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.240-12505A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74058165 | ||||||
| chr10:74058317
|
T | A | 120 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0129others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.240-12353T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74058317 | ||||||
| chr10:74058362
|
C | T | 2 | a0001c0007t0018g0100a0001c0009t0002g0040 | 2 | HG01069.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.240-12308C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74058362 | ||||||
| chr10:74058370
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.240-12300G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74058370 | ||||||
| chr10:74058388
|
G | A | 46 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(43): Show | 46 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.240-12282G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74058388 | ||||||
| chr10:74058469
|
A | T | 1 | a0001c0003t0002g0172 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.240-12201A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74058469 | ||||||
| chr10:74058734
|
C | T | 4 | a0001c0002t0005g0187a0001c0002t0012g0190a0001c0002t0012g0191others(1): Show | 4 | HG01884.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.240-11936C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74058734 | ||||||
| chr10:74058890
|
G | GGT | 46 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(43): Show | 46 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.240-11764_240-1176 others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74058890 | |||||
| chr10:74058921
|
G | A | 2 | a0001c0002t0020g0256a0001c0011t0006g0255 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.240-11749G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74058921 | ||||||
| chr10:74059099
|
G | C | 11 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0005g0187others(8): Show | 11 | HG00642.hp2 HG01884.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.240-11571G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74059099 | ||||||
| chr10:74059296
|
C | T | 18 | a0001c0002t0004g0195a0001c0002t0007g0167a0001c0002t0007g0168others(15): Show | 18 | HG00639.hp1 HG00733.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.240-11374C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74059296 | ||||||
| chr10:74059409
|
C | CT | 8 | a0001c0001t0001g0105a0001c0002t0003g0028a0001c0003t0002g0079others(5): Show | 8 | HG00621.hp2 NA18940.hp2 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.240-11248dupT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74059409 | |||||
| chr10:74059427
|
C | T | 46 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(43): Show | 46 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.240-11243C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74059427 | ||||||
| chr10:74059651
|
T | C | 8 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(5): Show | 8 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.240-11019T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74059651 | ||||||
| chr10:74059915
|
G | C | 1 | a0001c0002t0004g0195 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.240-10755G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74059915 | ||||||
| chr10:74060033
|
G | T | 15 | a0001c0002t0007g0167a0001c0002t0007g0168a0001c0002t0007g0177others(12): Show | 15 | HG00639.hp1 HG00733.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-10637G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74060033 | ||||||
| chr10:74060157
|
T | TA | 9 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(6): Show | 9 | HG00280.hp2 HG00423.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.240-10512dupA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74060157 | |||||
| chr10:74060266
|
C | T | 2 | a0001c0002t0003g0021a0001c0002t0003g0065 | 2 | HG00597.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.240-10404C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74060266 | ||||||
| chr10:74060356
|
T | C | 4 | a0001c0001t0001g0031a0001c0003t0002g0038a0001c0003t0002g0043others(1): Show | 4 | NA18998.hp2 NA19004.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.240-10314T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74060356 | ||||||
| chr10:74060424
|
G | A | 3 | a0001c0002t0020g0256a0001c0011t0006g0117a0001c0011t0006g0255 | 3 | HG03225.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.240-10246G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74060424 | ||||||
| chr10:74060427
|
T | G | 1 | a0001c0006t0017g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.240-10243T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74060427 | ||||||
| chr10:74060542
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.240-10128G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74060542 | ||||||
| chr10:74060616
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.240-10054A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74060616 | ||||||
| chr10:74060655
|
C | CA | 159 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0129others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.240-9998dupA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74060655 | |||||
| chr10:74060655
|
C | CAA | 11 | a0001c0001t0001g0199a0001c0001t0001g0257a0001c0001t0006g0232others(8): Show | 11 | HG00735.hp1 HG02055.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.240-9999_240-9998d others(4): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74060655 | |||||
| chr10:74060662
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0007t0003g0107 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.240-10002_240-9992 others(14): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74060662 | |||||
| chr10:74060740
|
C | T | 1 | a0005c0014t0002g0096 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.240-9930C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74060740 | ||||||
| chr10:74060952
|
A | C | 1 | a0001c0002t0003g0059 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.240-9718A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74060952 | ||||||
| chr10:74061038
|
T | G | 263 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.240-9632T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74061038 | ||||||
| chr10:74061094
|
G | A | 8 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(5): Show | 8 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.240-9576G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74061094 | ||||||
| chr10:74061137
|
C | T | 8 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(5): Show | 8 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.240-9533C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74061137 | ||||||
| chr10:74061548
|
T | G | 1 | a0001c0001t0001g0228 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.240-9122T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74061548 | ||||||
| chr10:74061855
|
A | G | 120 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0129others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.240-8815A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74061855 | ||||||
| chr10:74061907
|
C | CT | 50 | a0001c0001t0001g0158a0001c0001t0004g0002a0001c0002t0003g0001others(47): Show | 50 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.240-8747dupT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74061907 | |||||
| chr10:74061907
|
C | CTT | 110 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0129others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.240-8748_240-8747d others(4): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74061907 | |||||
| chr10:74061907
|
C | CTTT | 9 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0146others(6): Show | 9 | HG00735.hp2 HG00741.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.240-8749_240-8747d others(5): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74061907 | |||||
| chr10:74062043
|
G | A | 3 | a0001c0002t0020g0256a0001c0011t0006g0117a0001c0011t0006g0255 | 3 | HG03225.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.240-8627G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74062043 | ||||||
| chr10:74062316
|
C | T | 41 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0138others(38): Show | 41 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.240-8354C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74062316 | ||||||
| chr10:74062367
|
A | AT | 124 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0129others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.240-8284dupT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74062367 | |||||
| chr10:74062367
|
A | ATT | 12 | a0001c0001t0001g0163a0001c0001t0001g0199a0001c0001t0001g0222others(9): Show | 12 | HG00558.hp2 HG01256.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.240-8285_240-8284d others(4): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74062367 | |||||
| chr10:74062404
|
C | T | 4 | a0001c0002t0005g0187a0001c0002t0012g0190a0001c0002t0012g0191others(1): Show | 4 | HG01884.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.240-8266C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74062404 | ||||||
| chr10:74062954
|
C | T | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-7716C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74062954 | ||||||
| chr10:74062992
|
C | A | 1 | a0001c0004t0002g0082 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.240-7678C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74062992 | ||||||
| chr10:74063025
|
G | A | 1 | a0001c0003t0022g0035 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.240-7645G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74063025 | ||||||
| chr10:74063026
|
C | T | 2 | a0001c0001t0001g0217a0001c0001t0001g0236 | 2 | NA18961.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.240-7644C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74063026 | ||||||
| chr10:74063090
|
C | T | 1 | a0001c0002t0006g0084 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.240-7580C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74063090 | ||||||
| chr10:74063095
|
A | T | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-7575A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74063095 | ||||||
| chr10:74063111
|
C | T | 3 | a0001c0002t0020g0256a0001c0011t0006g0117a0001c0011t0006g0255 | 3 | HG03225.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.240-7559C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74063111 | ||||||
| chr10:74063240
|
C | T | 18 | a0001c0002t0003g0001a0001c0002t0005g0187a0001c0002t0011g0003others(15): Show | 18 | HG00735.hp1 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.240-7430C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74063240 | ||||||
| chr10:74063339
|
C | G | 1 | a0001c0004t0002g0186 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.240-7331C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74063339 | ||||||
| chr10:74063476
|
T | C | 16 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(13): Show | 16 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.240-7194T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74063476 | ||||||
| chr10:74063523
|
C | T | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-7147C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74063523 | ||||||
| chr10:74064144
|
C | T | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-6526C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74064144 | ||||||
| chr10:74064154
|
A | G | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-6516A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74064154 | ||||||
| chr10:74064201
|
C | G | 8 | a0001c0002t0007g0167a0001c0002t0007g0168a0001c0002t0007g0177others(5): Show | 8 | HG00733.hp2 HG02965.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.240-6469C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74064201 | ||||||
| chr10:74064411
|
CT | C | 11 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(8): Show | 11 | HG00735.hp1 HG02055.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.240-6247delT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74064411 | |||||
| chr10:74064432
|
A | G | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-6238A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74064432 | ||||||
| chr10:74064459
|
G | T | 1 | a0001c0009t0002g0181 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.240-6211G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74064459 | ||||||
| chr10:74064546
|
C | T | 1 | a0001c0006t0005g0080 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.240-6124C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74064546 | ||||||
| chr10:74064554
|
A | G | 1 | a0001c0004t0002g0186 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.240-6116A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74064554 | ||||||
| chr10:74064622
|
C | T | 1 | a0001c0004t0008g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.240-6048C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74064622 | ||||||
| chr10:74064803
|
T | A | 3 | a0001c0002t0020g0256a0001c0011t0006g0117a0001c0011t0006g0255 | 3 | HG03225.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.240-5867T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74064803 | ||||||
| chr10:74064874
|
C | G | 1 | a0001c0002t0007g0168 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.240-5796C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74064874 | ||||||
| chr10:74064959
|
C | T | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-5711C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74064959 | ||||||
| chr10:74065137
|
C | CT | 17 | a0001c0002t0001g0011a0001c0002t0014g0010a0001c0007t0003g0107others(14): Show | 17 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.240-5516dupT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74065137 | |||||
| chr10:74065150
|
T | C | 1 | a0001c0003t0002g0043 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.240-5520T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74065150 | ||||||
| chr10:74065185
|
G | A | 1 | a0001c0006t0005g0077 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.240-5485G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74065185 | ||||||
| chr10:74065223
|
G | A | 2 | a0001c0002t0003g0020a0001c0002t0003g0102 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.240-5447G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74065223 | ||||||
| chr10:74065246
|
C | T | 4 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0163others(1): Show | 4 | HG02056.hp1 HG02602.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.240-5424C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74065246 | ||||||
| chr10:74065371
|
T | A | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-5299T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74065371 | ||||||
| chr10:74065423
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.240-5247C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74065423 | ||||||
| chr10:74065614
|
T | C | 3 | a0001c0004t0002g0183a0001c0006t0005g0184a0001c0006t0005g0192 | 3 | HG02895.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.240-5056T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74065614 | ||||||
| chr10:74065683
|
C | CAA | 6 | a0001c0007t0013g0029a0001c0007t0013g0054a0001c0007t0018g0100others(3): Show | 6 | HG01069.hp1 HG02615.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.240-4976_240-4975d others(4): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74065683 | |||||
| chr10:74065683
|
C | CAAA | 9 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(6): Show | 9 | HG01074.hp2 HG01081.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.240-4977_240-4975d others(5): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74065683 | |||||
| chr10:74065707
|
C | G | 1 | a0001c0002t0007g0239 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.240-4963C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74065707 | ||||||
| chr10:74065771
|
G | C | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-4899G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74065771 | ||||||
| chr10:74065821
|
C | T | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-4849C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74065821 | ||||||
| chr10:74066009
|
T | C | 5 | a0001c0002t0003g0042a0001c0002t0003g0049a0001c0002t0003g0070others(2): Show | 5 | HG01934.hp2 HG02129.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.240-4661T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74066009 | ||||||
| chr10:74066047
|
G | GTA | 40 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(37): Show | 40 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.240-4609_240-4608d others(4): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74066047 | |||||
| chr10:74066047
|
G | GTATATAT others(5): Show |
51 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0162others(48): Show | 51 | HG00099.hp2 HG00558.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.240-4619_240-4608d others(14): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74066047 | |||||
| chr10:74066047
|
G | GTATATAT others(7): Show |
11 | a0001c0001t0001g0237a0001c0001t0001g0250a0001c0002t0001g0109others(8): Show | 11 | HG00621.hp1 HG02040.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.240-4621_240-4608d others(16): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74066047 | |||||
| chr10:74066047
|
G | GTATATAT others(9): Show |
2 | a0001c0001t0001g0247a0001c0002t0001g0251 | 2 | NA19055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.240-4608_240-4607i others(18): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74066047 | |||||
| chr10:74066060
|
TA | T | 7 | a0001c0002t0007g0167a0001c0002t0007g0168a0001c0002t0007g0177others(4): Show | 7 | HG00733.hp2 HG03669.hp2 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.240-4609delA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74066060 | ||||||
| chr10:74066061
|
A | ATATATAT others(2): Show |
5 | a0001c0007t0003g0115a0001c0007t0013g0029a0001c0007t0018g0100others(2): Show | 5 | HG01069.hp1 HG01074.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.240-4608_240-4607i others(11): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74066061 | |||||
| chr10:74066061
|
A | ATATATAT others(4): Show |
1 | a0001c0009t0002g0181 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.240-4608_240-4607i others(13): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74066061 | |||||
| chr10:74066061
|
A | T | 2 | a0001c0002t0003g0101a0001c0004t0002g0183 | 2 | HG01192.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.240-4609A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74066061 | ||||||
| chr10:74066062
|
T | TATATATA others(2): Show |
8 | a0001c0007t0003g0107a0001c0007t0004g0119a0001c0007t0004g0120others(5): Show | 8 | HG01081.hp1 HG01433.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.240-4608_240-4607i others(11): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74066062 | ||||||
| chr10:74066062
|
T | TATATATA others(4): Show |
2 | a0001c0001t0001g0222a0001c0002t0003g0124 | 2 | HG02602.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.240-4608_240-4607i others(13): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74066062 | ||||||
| chr10:74066063
|
T | A | 99 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0129others(96): Show | 99 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.240-4607T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74066063 | ||||||
| chr10:74066064
|
T | A | 2 | a0001c0002t0003g0124a0001c0009t0002g0118 | 2 | HG01433.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.240-4606T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74066064 | ||||||
| chr10:74066065
|
T | A | 50 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0204others(47): Show | 50 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.240-4605T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74066065 | ||||||
| chr10:74066067
|
T | A | 14 | a0001c0001t0001g0217a0001c0001t0001g0220a0001c0001t0001g0236others(11): Show | 14 | HG01952.hp2 HG01975.hp1 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.240-4603T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74066067 | ||||||
| chr10:74066069
|
T | A | 6 | a0001c0001t0001g0220a0001c0001t0001g0244a0001c0001t0001g0257others(3): Show | 6 | HG01952.hp2 HG01975.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.240-4601T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74066069 | ||||||
| chr10:74066122
|
C | T | 1 | a0001c0002t0004g0195 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.240-4548C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74066122 | ||||||
| chr10:74066164
|
A | G | 42 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(39): Show | 42 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.240-4506A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74066164 | ||||||
| chr10:74066166
|
TCTC | T | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-4501_240-4499d others(5): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74066166 | |||||
| chr10:74066224
|
A | T | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-4446A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74066224 | ||||||
| chr10:74066291
|
T | G | 6 | a0001c0002t0007g0167a0001c0002t0007g0168a0001c0002t0007g0177others(3): Show | 6 | HG00733.hp2 HG03669.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.240-4379T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74066291 | ||||||
| chr10:74066305
|
C | T | 2 | a0002c0005t0010g0050a0002c0005t0010g0057 | 2 | HG01934.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.240-4365C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74066305 | ||||||
| chr10:74066471
|
G | A | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-4199G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74066471 | ||||||
| chr10:74066482
|
G | A | 1 | a0001c0002t0004g0189 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.240-4188G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74066482 | ||||||
| chr10:74066673
|
AT | A | 132 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0129others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.240-3981delT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74066673 | |||||
| chr10:74066673
|
ATT | A | 24 | a0001c0001t0001g0238a0001c0001t0004g0002a0001c0002t0001g0231others(21): Show | 24 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.240-3982_240-3981d others(4): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74066673 | |||||
| chr10:74066698
|
A | G | 1 | a0002c0005t0002g0046 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.240-3972A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74066698 | ||||||
| chr10:74066845
|
T | C | 1 | a0001c0003t0002g0205 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.240-3825T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74066845 | ||||||
| chr10:74066999
|
G | A | 2 | a0001c0003t0002g0025a0001c0003t0002g0071 | 2 | HG01081.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.240-3671G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74066999 | ||||||
| chr10:74067375
|
A | AT | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-3292dupT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74067375 | |||||
| chr10:74067389
|
A | G | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-3281A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74067389 | ||||||
| chr10:74067391
|
A | T | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-3279A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74067391 | ||||||
| chr10:74067392
|
G | A | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-3278G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74067392 | ||||||
| chr10:74067394
|
T | C | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-3276T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74067394 | ||||||
| chr10:74067743
|
G | A | 1 | a0001c0003t0008g0061 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.240-2927G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74067743 | ||||||
| chr10:74067813
|
G | A | 3 | a0001c0004t0002g0183a0001c0006t0005g0184a0001c0006t0005g0192 | 3 | HG02895.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.240-2857G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74067813 | ||||||
| chr10:74067872
|
G | A | 11 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(8): Show | 11 | HG00735.hp1 HG02055.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.240-2798G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74067872 | ||||||
| chr10:74067922
|
C | T | 3 | a0001c0002t0020g0256a0001c0011t0006g0117a0001c0011t0006g0255 | 3 | HG03225.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.240-2748C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74067922 | ||||||
| chr10:74068072
|
G | A | 6 | a0001c0002t0007g0167a0001c0002t0007g0168a0001c0002t0007g0177others(3): Show | 6 | HG00733.hp2 HG03669.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.240-2598G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74068072 | ||||||
| chr10:74068349
|
G | T | 2 | a0001c0002t0003g0020a0001c0002t0003g0102 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.240-2321G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74068349 | ||||||
| chr10:74068603
|
G | A | 6 | a0001c0001t0001g0208a0001c0001t0001g0228a0001c0001t0001g0248others(3): Show | 6 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.240-2067G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74068603 | ||||||
| chr10:74068723
|
G | A | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-1947G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74068723 | ||||||
| chr10:74068802
|
T | G | 3 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033 | 3 | NA18984.hp1 NA19009.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.240-1868T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74068802 | ||||||
| chr10:74068941
|
A | ATAAAATT others(13): Show |
15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-1718_240-1717i others(22): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 74068941 | |||||
| chr10:74068956
|
A | G | 1 | a0001c0006t0017g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.240-1714A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74068956 | ||||||
| chr10:74069084
|
G | A | 42 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(39): Show | 42 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.240-1586G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74069084 | ||||||
| chr10:74069165
|
G | A | 108 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0129others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.240-1505G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74069165 | ||||||
| chr10:74069232
|
C | G | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-1438C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74069232 | ||||||
| chr10:74069239
|
T | C | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-1431T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74069239 | ||||||
| chr10:74069453
|
C | G | 4 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0163others(1): Show | 4 | HG02056.hp1 HG02602.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.240-1217C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74069453 | ||||||
| chr10:74069484
|
G | A | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-1186G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74069484 | ||||||
| chr10:74069599
|
C | G | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-1071C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74069599 | ||||||
| chr10:74069607
|
A | G | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-1063A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74069607 | ||||||
| chr10:74069755
|
T | C | 2 | a0001c0002t0001g0011a0001c0002t0014g0010 | 2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.240-915T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74069755 | ||||||
| chr10:74069765
|
AG | A | 8 | a0001c0004t0002g0062a0001c0004t0002g0081a0001c0004t0002g0123others(5): Show | 8 | HG02257.hp1 HG02486.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.240-904delG | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74069765 | ||||||
| chr10:74069766
|
G | A | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-904G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74069766 | ||||||
| chr10:74069927
|
T | G | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-743T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74069927 | ||||||
| chr10:74069991
|
T | C | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-679T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74069991 | ||||||
| chr10:74070314
|
T | C | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-356T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74070314 | ||||||
| chr10:74070315
|
G | A | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-355G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74070315 | ||||||
| chr10:74070524
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.240-146C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74070524 | ||||||
| chr10:74070604
|
T | C | 1 | a0001c0001t0001g0230 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.240-66T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74070604 | ||||||
| chr10:74070923
|
T | C | 2 | a0001c0002t0003g0020a0001c0002t0003g0102 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.391-52T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 3/21 | chr10 | 74070923 | ||||||
| chr10:74071261
|
A | G | 1 | a0007c0017t0002g0039 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.499+178A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 4/21 | chr10 | 74071261 | ||||||
| chr10:74071450
|
T | C | 3 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0164 | 3 | HG01261.hp1 HG03239.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.499+367T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 4/21 | chr10 | 74071450 | ||||||
| chr10:74071480
|
A | G | 1 | a0001c0006t0017g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.499+397A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 4/21 | chr10 | 74071480 | ||||||
| chr10:74071501
|
C | A | 153 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0129others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.499+418C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 4/21 | chr10 | 74071501 | ||||||
| chr10:74071615
|
G | A | 6 | a0001c0002t0007g0167a0001c0002t0007g0168a0001c0002t0007g0177others(3): Show | 6 | HG00733.hp2 HG03669.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.499+532G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 4/21 | chr10 | 74071615 | ||||||
| chr10:74071725
|
G | T | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.499+642G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 4/21 | chr10 | 74071725 | ||||||
| chr10:74072198
|
A | G | 1 | a0001c0003t0002g0055 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.500-532A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 4/21 | chr10 | 74072198 | ||||||
| chr10:74072449
|
T | C | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.500-281T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 4/21 | chr10 | 74072449 | ||||||
| chr10:74072494
|
A | G | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.500-236A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 4/21 | chr10 | 74072494 | ||||||
| chr10:74072856
|
C | T | 1 | a0001c0002t0004g0195 | 1 | HG03540.hp2 | splice_region_variant&intron_variant | LOW | c.622+4C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74072856 | ||||||
| chr10:74072887
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.622+35A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74072887 | ||||||
| chr10:74072897
|
G | C | 1 | a0001c0003t0002g0095 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.622+45G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74072897 | ||||||
| chr10:74072940
|
C | G | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.622+88C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74072940 | ||||||
| chr10:74072941
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.622+89T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74072941 | ||||||
| chr10:74072945
|
C | CT | 17 | a0001c0001t0001g0257a0001c0001t0001g0260a0001c0007t0003g0107others(14): Show | 17 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.622+107dupT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr10 | 74072945 | |||||
| chr10:74073010
|
G | A | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.622+158G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74073010 | ||||||
| chr10:74073021
|
A | ACCTCTGC others(13): Show |
2 | a0001c0002t0003g0049a0001c0002t0003g0070 | 2 | HG02129.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.622+181_622+182ins others(20): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr10 | 74073021 | |||||
| chr10:74073043
|
C | T | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.622+191C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74073043 | ||||||
| chr10:74073047
|
T | C | 1 | a0001c0002t0001g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.622+195T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74073047 | ||||||
| chr10:74073063
|
T | C | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.622+211T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74073063 | ||||||
| chr10:74073219
|
G | A | 5 | a0001c0006t0005g0076a0001c0006t0005g0077a0001c0006t0005g0080others(2): Show | 5 | HG02622.hp1 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.622+367G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74073219 | ||||||
| chr10:74073403
|
G | A | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.622+551G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74073403 | ||||||
| chr10:74073746
|
C | T | 1 | a0001c0003t0002g0106 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.622+894C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74073746 | ||||||
| chr10:74073768
|
C | T | 1 | a0001c0004t0002g0183 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.622+916C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74073768 | ||||||
| chr10:74073836
|
G | A | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.623-907G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74073836 | ||||||
| chr10:74073876
|
A | G | 1 | a0001c0003t0002g0074 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.623-867A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74073876 | ||||||
| chr10:74073898
|
G | A | 1 | a0001c0002t0001g0251 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.623-845G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74073898 | ||||||
| chr10:74074039
|
C | T | 1 | a0001c0003t0002g0205 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.623-704C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74074039 | ||||||
| chr10:74074056
|
C | T | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.623-687C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74074056 | ||||||
| chr10:74074066
|
A | AAAAACAA others(8): Show |
15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.623-672_623-658dup others(15): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr10 | 74074066 | |||||
| chr10:74074110
|
G | C | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.623-633G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74074110 | ||||||
| chr10:74074184
|
C | T | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.623-559C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74074184 | ||||||
| chr10:74074192
|
C | T | 16 | a0001c0001t0001g0204a0001c0007t0003g0107a0001c0007t0003g0115others(13): Show | 16 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.623-551C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74074192 | ||||||
| chr10:74074227
|
A | G | 2 | a0001c0002t0004g0188a0001c0002t0004g0189 | 2 | HG00642.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.623-516A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74074227 | ||||||
| chr10:74074300
|
C | T | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.623-443C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74074300 | ||||||
| chr10:74074312
|
T | G | 1 | a0001c0002t0004g0188 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.623-431T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74074312 | ||||||
| chr10:74074356
|
C | T | 4 | a0001c0002t0005g0187a0001c0002t0012g0190a0001c0002t0012g0191others(1): Show | 4 | HG01884.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.623-387C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74074356 | ||||||
| chr10:74074562
|
A | C | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.623-181A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74074562 | ||||||
| chr10:74074657
|
A | T | 1 | a0001c0003t0002g0067 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.623-86A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74074657 | ||||||
| chr10:74074660
|
T | C | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.623-83T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 5/21 | chr10 | 74074660 | ||||||
| chr10:74075390
|
A | G | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.783+487A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74075390 | ||||||
| chr10:74075457
|
T | G | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.783+554T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74075457 | ||||||
| chr10:74075462
|
G | T | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.783+559G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74075462 | ||||||
| chr10:74075687
|
T | TCTCCAAT others(2): Show |
15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.783+784_783+785ins others(9): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74075687 | ||||||
| chr10:74075689
|
T | A | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.783+786T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74075689 | ||||||
| chr10:74075719
|
G | T | 1 | a0001c0001t0023g0234 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.783+816G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74075719 | ||||||
| chr10:74075750
|
T | A | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.783+847T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74075750 | ||||||
| chr10:74075780
|
C | T | 1 | a0001c0006t0017g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.783+877C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74075780 | ||||||
| chr10:74075800
|
G | A | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.783+897G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74075800 | ||||||
| chr10:74075995
|
C | T | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.783+1092C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74075995 | ||||||
| chr10:74076145
|
C | T | 4 | a0001c0001t0001g0141a0001c0001t0001g0146a0001c0001t0001g0153others(1): Show | 4 | HG00735.hp2 HG00741.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.783+1242C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74076145 | ||||||
| chr10:74076361
|
G | A | 42 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0137others(39): Show | 42 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.783+1458G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74076361 | ||||||
| chr10:74076375
|
G | T | 143 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0129others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.783+1472G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74076375 | ||||||
| chr10:74076439
|
G | A | 1 | a0001c0003t0022g0035 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.783+1536G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74076439 | ||||||
| chr10:74076556
|
G | A | 3 | a0001c0003t0009g0197a0001c0004t0008g0012a0001c0018t0003g0196 | 3 | HG02976.hp2 HG03239.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.783+1653G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74076556 | ||||||
| chr10:74076843
|
C | G | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.783+1940C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74076843 | ||||||
| chr10:74076941
|
C | T | 1 | a0007c0017t0002g0039 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.783+2038C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74076941 | ||||||
| chr10:74076972
|
C | T | 1 | a0001c0002t0007g0182 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.783+2069C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74076972 | ||||||
| chr10:74077136
|
C | T | 3 | a0001c0004t0002g0183a0001c0006t0005g0184a0001c0006t0005g0192 | 3 | HG02895.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.783+2233C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74077136 | ||||||
| chr10:74077189
|
C | T | 2 | a0001c0002t0003g0021a0001c0002t0003g0065 | 2 | HG00597.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.783+2286C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74077189 | ||||||
| chr10:74077401
|
ACTCTACC others(1): Show |
A | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.783+2502_783+2509d others(10): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr10 | 74077401 | |||||
| chr10:74077447
|
T | C | 158 | a0001c0001t0001g0073a0001c0001t0001g0122a0001c0001t0001g0129others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.783+2544T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74077447 | ||||||
| chr10:74077448
|
C | A | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.783+2545C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74077448 | ||||||
| chr10:74077866
|
C | T | 1 | a0003c0010t0008g0088 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.783+2963C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74077866 | ||||||
| chr10:74078063
|
A | G | 1 | a0001c0002t0001g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.783+3160A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74078063 | ||||||
| chr10:74078200
|
G | T | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.783+3297G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74078200 | ||||||
| chr10:74078422
|
T | TA | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.783+3526dupA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr10 | 74078422 | |||||
| chr10:74078654
|
T | C | 10 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(7): Show | 10 | HG01074.hp2 HG01081.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.783+3751T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74078654 | ||||||
| chr10:74078824
|
A | G | 1 | a0002c0005t0002g0027 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.784-3630A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74078824 | ||||||
| chr10:74078830
|
T | A | 1 | a0001c0002t0005g0187 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.784-3624T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74078830 | ||||||
| chr10:74078886
|
A | G | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.784-3568A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74078886 | ||||||
| chr10:74079544
|
C | T | 2 | a0001c0002t0001g0011a0001c0002t0014g0010 | 2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.784-2910C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74079544 | ||||||
| chr10:74079696
|
A | G | 65 | a0001c0001t0001g0044a0001c0001t0001g0073a0001c0001t0001g0122others(62): Show | 65 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.784-2758A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74079696 | ||||||
| chr10:74079892
|
C | T | 1 | a0001c0003t0002g0205 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.784-2562C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74079892 | ||||||
| chr10:74079904
|
A | C | 3 | a0001c0003t0009g0197a0001c0004t0008g0012a0001c0018t0003g0196 | 3 | HG02976.hp2 HG03239.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.784-2550A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74079904 | ||||||
| chr10:74080582
|
G | A | 2 | a0001c0002t0004g0188a0001c0002t0004g0189 | 2 | HG00642.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.784-1872G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74080582 | ||||||
| chr10:74080670
|
T | C | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.784-1784T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74080670 | ||||||
| chr10:74080672
|
GT | G | 56 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(53): Show | 56 | HG00558.hp1 HG00597.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.784-1779delT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr10 | 74080672 | |||||
| chr10:74080814
|
C | A | 15 | a0001c0001t0001g0217a0001c0001t0001g0220a0001c0001t0001g0236others(12): Show | 15 | HG00621.hp1 HG01952.hp2 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.784-1640C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74080814 | ||||||
| chr10:74081122
|
T | G | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.784-1332T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74081122 | ||||||
| chr10:74081149
|
TTC | T | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.784-1303_784-1302d others(4): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr10 | 74081149 | |||||
| chr10:74081512
|
G | A | 1 | a0001c0004t0002g0093 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.784-942G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74081512 | ||||||
| chr10:74081624
|
T | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033 | 3 | NA18984.hp1 NA19009.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.784-830T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74081624 | ||||||
| chr10:74081632
|
T | G | 2 | a0001c0007t0004g0120a0001c0007t0004g0121 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.784-822T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74081632 | ||||||
| chr10:74081660
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.784-794C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74081660 | ||||||
| chr10:74081672
|
T | C | 3 | a0001c0003t0002g0066a0001c0003t0002g0075a0001c0003t0002g0159 | 3 | HG01106.hp2 HG01255.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.784-782T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74081672 | ||||||
| chr10:74081698
|
G | A | 68 | a0001c0001t0001g0044a0001c0001t0001g0073a0001c0001t0001g0122others(65): Show | 68 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.784-756G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74081698 | ||||||
| chr10:74081740
|
G | A | 33 | a0001c0002t0003g0001a0001c0002t0004g0188a0001c0002t0004g0189others(30): Show | 33 | HG00642.hp2 HG00735.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.784-714G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74081740 | ||||||
| chr10:74081810
|
T | C | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.784-644T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74081810 | ||||||
| chr10:74082056
|
T | C | 1 | a0001c0001t0024g0193 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.784-398T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74082056 | ||||||
| chr10:74082229
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.784-225C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74082229 | ||||||
| chr10:74082272
|
T | C | 1 | a0001c0009t0002g0013 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.784-182T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74082272 | ||||||
| chr10:74082394
|
G | A | 135 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(132): Show | 135 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.784-60G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74082394 | ||||||
| chr10:74083041
|
A | AT | 135 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(132): Show | 135 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.875-324dupT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr10 | 74083041 | |||||
| chr10:74083182
|
T | A | 1 | a0001c0002t0003g0243 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.875-184T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 7/21 | chr10 | 74083182 | ||||||
| chr10:74083205
|
T | C | 1 | a0001c0013t0005g0116 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.875-161T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 7/21 | chr10 | 74083205 | ||||||
| chr10:74083342
|
T | A | 221 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(218): Show | 221 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(218): Show |
intron_variant | MODIFIER | c.875-24T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 7/21 | chr10 | 74083342 | ||||||
| chr10:74083684
|
CTTTA | C | 3 | a0001c0003t0009g0197a0001c0004t0008g0012a0001c0018t0003g0196 | 3 | HG02976.hp2 HG03239.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1022+186_1022+189d others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr10 | 74083684 | |||||
| chr10:74083859
|
TTTTG | T | 29 | a0001c0002t0007g0167a0001c0002t0007g0168a0001c0002t0007g0177others(26): Show | 29 | HG00733.hp2 HG01069.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.1022+371_1022+374d others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr10 | 74083859 | |||||
| chr10:74083930
|
C | T | 8 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(5): Show | 8 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1022+417C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74083930 | ||||||
| chr10:74084084
|
C | G | 1 | a0001c0009t0002g0118 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1022+571C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74084084 | ||||||
| chr10:74084169
|
C | T | 6 | a0001c0002t0003g0028a0002c0005t0002g0026a0002c0005t0002g0027others(3): Show | 6 | HG00621.hp2 NA18954.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.1022+656C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74084169 | ||||||
| chr10:74084590
|
TTTTTTC | T | 3 | a0001c0002t0001g0109a0001c0002t0003g0245a0001c0004t0002g0093 | 3 | HG01496.hp1 HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1022+1101_1022+110 others(10): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr10 | 74084590 | |||||
| chr10:74084590
|
TTTTTTCT others(5): Show |
T | 1 | a0001c0003t0002g0099 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1022+1095_1022+110 others(16): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr10 | 74084590 | |||||
| chr10:74084639
|
A | T | 203 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(200): Show | 203 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.1022+1126A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74084639 | ||||||
| chr10:74084740
|
G | A | 2 | a0001c0006t0005g0184a0001c0006t0005g0192 | 2 | HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1022+1227G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74084740 | ||||||
| chr10:74084801
|
G | A | 56 | a0001c0001t0001g0044a0001c0001t0001g0073a0001c0001t0001g0122others(53): Show | 56 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1022+1288G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74084801 | ||||||
| chr10:74084841
|
G | A | 7 | a0001c0002t0007g0167a0001c0002t0007g0168a0001c0002t0007g0177others(4): Show | 7 | HG00733.hp2 HG02965.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.1022+1328G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74084841 | ||||||
| chr10:74084987
|
G | A | 15 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.1022+1474G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74084987 | ||||||
| chr10:74085315
|
G | A | 1 | a0001c0003t0009g0125 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1022+1802G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74085315 | ||||||
| chr10:74085435
|
T | G | 1 | a0001c0001t0001g0261 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1022+1922T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74085435 | ||||||
| chr10:74086127
|
A | T | 70 | a0001c0001t0001g0044a0001c0001t0001g0073a0001c0001t0001g0122others(67): Show | 70 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.1022+2614A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74086127 | ||||||
| chr10:74086316
|
C | T | 1 | a0001c0007t0013g0029 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1022+2803C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74086316 | ||||||
| chr10:74086629
|
G | A | 1 | a0001c0004t0002g0082 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1023-2567G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74086629 | ||||||
| chr10:74087039
|
C | T | 1 | a0001c0003t0002g0071 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1023-2157C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74087039 | ||||||
| chr10:74087153
|
A | G | 5 | a0002c0005t0010g0018a0002c0005t0010g0050a0002c0005t0010g0057others(2): Show | 5 | HG00280.hp1 HG01934.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1023-2043A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74087153 | ||||||
| chr10:74087319
|
A | T | 18 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0224others(15): Show | 18 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1023-1877A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74087319 | ||||||
| chr10:74087319
|
ATTTT | A | 11 | a0001c0002t0007g0167a0001c0002t0007g0168a0001c0002t0007g0177others(8): Show | 11 | HG00733.hp2 HG02895.hp1 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.1023-1869_1023-186 others(8): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr10 | 74087319 | |||||
| chr10:74087323
|
T | A | 5 | a0001c0001t0001g0208a0001c0003t0002g0212a0001c0003t0009g0197others(2): Show | 5 | HG02015.hp1 HG02040.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1023-1873T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74087323 | ||||||
| chr10:74087332
|
G | C | 1 | a0001c0006t0017g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1023-1864G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74087332 | ||||||
| chr10:74087339
|
C | CT | 65 | a0001c0001t0001g0044a0001c0001t0001g0073a0001c0001t0001g0162others(62): Show | 65 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1023-1841dupT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr10 | 74087339 | |||||
| chr10:74087352
|
T | C | 1 | a0001c0003t0002g0161 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1023-1844T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74087352 | ||||||
| chr10:74087358
|
T | A | 69 | a0001c0001t0001g0044a0001c0001t0001g0073a0001c0001t0001g0122others(66): Show | 69 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1023-1838T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74087358 | ||||||
| chr10:74087418
|
T | C | 69 | a0001c0001t0001g0044a0001c0001t0001g0073a0001c0001t0001g0122others(66): Show | 69 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1023-1778T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74087418 | ||||||
| chr10:74087513
|
A | AT | 23 | a0001c0001t0001g0031a0001c0001t0001g0105a0001c0001t0001g0160others(20): Show | 23 | HG00423.hp2 HG00597.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.1023-1663dupT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr10 | 74087513 | |||||
| chr10:74087513
|
A | ATT | 9 | a0001c0002t0007g0167a0001c0002t0007g0168a0001c0002t0007g0177others(6): Show | 9 | HG00733.hp2 HG02895.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.1023-1664_1023-166 others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr10 | 74087513 | |||||
| chr10:74087513
|
AT | A | 12 | a0001c0007t0003g0107a0001c0007t0003g0115a0001c0007t0004g0119others(9): Show | 12 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1023-1663delT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr10 | 74087513 | |||||
| chr10:74087513
|
ATTTT | A | 66 | a0001c0001t0001g0044a0001c0001t0001g0073a0001c0001t0001g0122others(63): Show | 66 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.1023-1666_1023-166 others(8): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr10 | 74087513 | |||||
| chr10:74087513
|
ATTTTTTT | A | 6 | a0001c0002t0011g0003a0001c0002t0011g0004a0001c0002t0011g0006others(3): Show | 6 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1023-1669_1023-166 others(11): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr10 | 74087513 | |||||
| chr10:74087535
|
G | T | 263 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.1023-1661G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74087535 | ||||||
| chr10:74087765
|
C | T | 1 | a0001c0002t0003g0127 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1023-1431C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74087765 | ||||||
| chr10:74087766
|
G | A | 1 | a0001c0009t0002g0181 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1023-1430G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74087766 | ||||||
| chr10:74087821
|
C | T | 1 | a0002c0005t0002g0249 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1023-1375C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74087821 | ||||||
| chr10:74087959
|
C | T | 1 | a0001c0001t0004g0149 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1023-1237C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74087959 | ||||||
| chr10:74088046
|
A | G | 69 | a0001c0001t0001g0044a0001c0001t0001g0073a0001c0001t0001g0122others(66): Show | 69 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1023-1150A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74088046 | ||||||
| chr10:74088098
|
T | C | 110 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(107): Show | 110 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.1023-1098T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74088098 | ||||||
| chr10:74088133
|
C | G | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0003t0001g0128 | 3 | HG01516.hp2 HG01517.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1023-1063C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74088133 | ||||||
| chr10:74088153
|
T | C | 8 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(5): Show | 8 | HG00735.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1023-1043T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74088153 | ||||||
| chr10:74088292
|
C | T | 1 | a0001c0001t0001g0031 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1023-904C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74088292 | ||||||
| chr10:74088379
|
A | G | 1 | a0001c0003t0002g0060 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1023-817A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74088379 | ||||||
| chr10:74088380
|
A | T | 1 | a0001c0001t0001g0222 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1023-816A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74088380 | ||||||
| chr10:74088444
|
G | A | 1 | a0001c0003t0002g0159 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1023-752G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74088444 | ||||||
| chr10:74088579
|
A | T | 1 | a0003c0010t0008g0090 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1023-617A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74088579 | ||||||
| chr10:74088706
|
T | A | 69 | a0001c0001t0001g0044a0001c0001t0001g0073a0001c0001t0001g0122others(66): Show | 69 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1023-490T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74088706 | ||||||
| chr10:74088742
|
T | C | 1 | a0001c0006t0017g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1023-454T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74088742 | ||||||
| chr10:74088759
|
G | A | 217 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(214): Show | 217 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.1023-437G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74088759 | ||||||
| chr10:74088759
|
G | C | 4 | a0001c0002t0005g0187a0001c0002t0012g0190a0001c0002t0012g0191others(1): Show | 4 | HG01884.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1023-437G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74088759 | ||||||
| chr10:74088986
|
G | A | 1 | a0001c0002t0012g0198 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1023-210G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 8/21 | chr10 | 74088986 | ||||||
| chr10:74089745
|
T | C | 20 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(17): Show | 20 | HG00735.hp1 HG01074.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1177-278T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 9/21 | chr10 | 74089745 | ||||||
| chr10:74089777
|
G | A | 1 | a0001c0001t0004g0149 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1177-246G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 9/21 | chr10 | 74089777 | ||||||
| chr10:74089865
|
T | TCA | 20 | a0001c0002t0003g0001a0001c0002t0005g0187a0001c0002t0011g0003others(17): Show | 20 | HG00735.hp1 HG01069.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1177-158_1177-157i others(4): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 9/21 | chr10 | 74089865 | ||||||
| chr10:74089964
|
T | A | 2 | a0001c0002t0007g0177a0001c0002t0007g0264 | 2 | NA18957.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1177-59T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 9/21 | chr10 | 74089964 | ||||||
| chr10:74089965
|
A | T | 2 | a0001c0002t0007g0177a0001c0002t0007g0264 | 2 | NA18957.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1177-58A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 9/21 | chr10 | 74089965 | ||||||
| chr10:74090008
|
C | T | 1 | a0001c0007t0018g0100 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1177-15C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 9/21 | chr10 | 74090008 | ||||||
| chr10:74090233
|
C | A | 7 | a0001c0002t0001g0011a0001c0002t0001g0194a0001c0002t0001g0200others(4): Show | 7 | HG02257.hp2 HG02630.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1352+35C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74090233 | ||||||
| chr10:74090562
|
G | A | 10 | a0001c0006t0005g0076a0001c0006t0005g0077a0001c0006t0005g0080others(7): Show | 10 | HG02622.hp1 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1352+364G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74090562 | ||||||
| chr10:74090722
|
C | T | 3 | a0001c0002t0012g0190a0001c0002t0012g0191a0001c0002t0012g0198 | 3 | HG01884.hp1 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1352+524C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74090722 | ||||||
| chr10:74090798
|
A | T | 3 | a0001c0007t0013g0029a0001c0007t0013g0054a0001c0007t0018g0100 | 3 | HG01069.hp1 HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1352+600A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74090798 | ||||||
| chr10:74090920
|
C | A | 10 | a0001c0006t0005g0076a0001c0006t0005g0077a0001c0006t0005g0080others(7): Show | 10 | HG02622.hp1 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1352+722C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74090920 | ||||||
| chr10:74090947
|
C | T | 18 | a0001c0004t0002g0052a0001c0004t0002g0058a0001c0004t0002g0062others(15): Show | 18 | HG00642.hp1 HG01433.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1352+749C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74090947 | ||||||
| chr10:74090990
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1352+792G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74090990 | ||||||
| chr10:74091076
|
C | T | 3 | a0001c0002t0001g0011a0001c0002t0001g0194a0001c0002t0001g0200 | 3 | HG02630.hp2 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1352+878C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74091076 | ||||||
| chr10:74091144
|
C | T | 1 | a0001c0009t0002g0040 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1352+946C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74091144 | ||||||
| chr10:74091315
|
A | G | 2 | a0001c0001t0001g0129a0001c0001t0001g0131 | 2 | HG00280.hp2 HG00423.hp1 |
intron_variant | MODIFIER | c.1352+1117A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74091315 | ||||||
| chr10:74091317
|
G | T | 5 | a0001c0006t0005g0085a0001c0006t0005g0184a0001c0006t0005g0192others(2): Show | 5 | HG02630.hp1 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1352+1119G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74091317 | ||||||
| chr10:74091491
|
G | A | 88 | a0001c0001t0001g0031a0001c0001t0001g0044a0001c0001t0001g0073others(85): Show | 88 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.1352+1293G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74091491 | ||||||
| chr10:74091546
|
G | A | 1 | a0001c0003t0002g0099 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1352+1348G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74091546 | ||||||
| chr10:74091626
|
TA | T | 18 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(15): Show | 18 | HG00735.hp1 HG01069.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1352+1436delA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 74091626 | |||||
| chr10:74091791
|
C | CA | 30 | a0001c0001t0001g0073a0001c0002t0001g0022a0001c0002t0001g0110others(27): Show | 30 | HG00423.hp2 HG01106.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.1352+1616dupA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 74091791 | |||||
| chr10:74091791
|
C | CAA | 77 | a0001c0001t0001g0031a0001c0001t0001g0105a0001c0001t0001g0122others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.1352+1615_1352+161 others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 74091791 | |||||
| chr10:74091791
|
C | CAAA | 18 | a0001c0001t0001g0044a0001c0001t0001g0138a0001c0001t0001g0140others(15): Show | 18 | HG00621.hp1 HG00673.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.1352+1614_1352+161 others(7): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 74091791 | |||||
| chr10:74091791
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0002t0007g0168 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1352+1606_1352+161 others(15): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 74091791 | |||||
| chr10:74091791
|
CAAAAAAA others(7): Show |
C | 13 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(10): Show | 13 | HG00735.hp1 HG01074.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1352+1603_1352+161 others(18): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 74091791 | |||||
| chr10:74091810
|
AAAAAG | A | 15 | a0001c0004t0002g0062a0001c0004t0002g0081a0001c0004t0002g0082others(12): Show | 15 | HG00642.hp1 HG01433.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.1352+1627_1352+163 others(9): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 74091810 | |||||
| chr10:74091815
|
G | A | 10 | a0001c0006t0005g0076a0001c0006t0005g0077a0001c0006t0005g0080others(7): Show | 10 | HG02622.hp1 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1352+1617G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74091815 | ||||||
| chr10:74091871
|
G | A | 2 | a0001c0001t0001g0138a0001c0002t0005g0187 | 2 | HG01358.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1352+1673G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74091871 | ||||||
| chr10:74091887
|
T | C | 5 | a0001c0007t0013g0029a0001c0007t0013g0054a0001c0007t0018g0100others(2): Show | 5 | HG01069.hp1 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1352+1689T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74091887 | ||||||
| chr10:74091958
|
G | C | 1 | a0001c0001t0001g0122 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1352+1760G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74091958 | ||||||
| chr10:74091971
|
T | C | 46 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(43): Show | 46 | HG00642.hp1 HG00735.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.1352+1773T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74091971 | ||||||
| chr10:74092057
|
C | T | 28 | a0001c0004t0002g0052a0001c0004t0002g0058a0001c0004t0002g0062others(25): Show | 28 | HG00642.hp1 HG01433.hp2 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.1352+1859C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74092057 | ||||||
| chr10:74092157
|
C | T | 1 | a0001c0009t0002g0040 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1352+1959C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74092157 | ||||||
| chr10:74092264
|
A | G | 13 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(10): Show | 13 | HG00735.hp1 HG01074.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1353-2007A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74092264 | ||||||
| chr10:74092489
|
A | C | 1 | a0004c0020t0015g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1353-1782A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74092489 | ||||||
| chr10:74092605
|
T | C | 1 | a0001c0002t0005g0187 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1353-1666T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74092605 | ||||||
| chr10:74092643
|
G | A | 1 | a0001c0002t0007g0182 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1353-1628G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74092643 | ||||||
| chr10:74092673
|
A | G | 2 | a0001c0002t0003g0049a0001c0002t0003g0070 | 2 | HG02129.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1353-1598A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74092673 | ||||||
| chr10:74093077
|
A | T | 1 | a0001c0002t0003g0243 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1353-1194A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74093077 | ||||||
| chr10:74093236
|
G | A | 13 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(10): Show | 13 | HG00735.hp1 HG01074.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1353-1035G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74093236 | ||||||
| chr10:74093245
|
C | T | 4 | a0001c0006t0005g0085a0001c0006t0005g0184a0001c0006t0005g0192others(1): Show | 4 | HG02630.hp1 HG03195.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1353-1026C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74093245 | ||||||
| chr10:74093251
|
C | T | 13 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(10): Show | 13 | HG00735.hp1 HG01074.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1353-1020C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74093251 | ||||||
| chr10:74093310
|
C | A | 2 | a0001c0011t0006g0117a0001c0011t0006g0255 | 2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1353-961C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74093310 | ||||||
| chr10:74093326
|
G | A | 2 | a0001c0002t0004g0188a0001c0002t0004g0189 | 2 | HG00642.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1353-945G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74093326 | ||||||
| chr10:74093636
|
AT | A | 18 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(15): Show | 18 | HG00735.hp1 HG01069.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1353-624delT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 74093636 | |||||
| chr10:74093657
|
G | T | 1 | a0001c0007t0018g0100 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1353-614G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74093657 | ||||||
| chr10:74093693
|
A | G | 54 | a0001c0002t0003g0001a0001c0002t0005g0187a0001c0002t0007g0167others(51): Show | 54 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.1353-578A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74093693 | ||||||
| chr10:74093698
|
C | A | 1 | a0001c0001t0001g0162 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1353-573C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74093698 | ||||||
| chr10:74093876
|
T | C | 18 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(15): Show | 18 | HG00735.hp1 HG01069.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1353-395T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74093876 | ||||||
| chr10:74093959
|
G | A | 46 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(43): Show | 46 | HG00642.hp1 HG00735.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.1353-312G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74093959 | ||||||
| chr10:74094038
|
C | T | 160 | a0001c0001t0001g0031a0001c0001t0001g0044a0001c0001t0001g0073others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1353-233C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74094038 | ||||||
| chr10:74094068
|
A | G | 5 | a0001c0007t0013g0029a0001c0007t0013g0054a0001c0007t0018g0100others(2): Show | 5 | HG01069.hp1 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1353-203A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 10/21 | chr10 | 74094068 | ||||||
| chr10:74094530
|
G | A | 3 | a0001c0002t0003g0021a0001c0002t0003g0028a0001c0002t0003g0065 | 3 | HG00597.hp2 HG00673.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1543+69G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 11/21 | chr10 | 74094530 | ||||||
| chr10:74094837
|
G | T | 1 | a0001c0006t0005g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1543+376G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 11/21 | chr10 | 74094837 | ||||||
| chr10:74094942
|
C | T | 1 | a0001c0002t0007g0182 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1543+481C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 11/21 | chr10 | 74094942 | ||||||
| chr10:74095063
|
T | C | 1 | a0001c0003t0002g0099 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1544-593T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 11/21 | chr10 | 74095063 | ||||||
| chr10:74095636
|
T | C | 1 | a0001c0006t0005g0080 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1544-20T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 11/21 | chr10 | 74095636 | ||||||
| chr10:74095912
|
G | A | 4 | a0002c0005t0002g0026a0002c0005t0002g0027a0002c0005t0002g0249others(1): Show | 4 | NA18954.hp2 NA18969.hp2 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1743+57G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 12/21 | chr10 | 74095912 | ||||||
| chr10:74096084
|
C | T | 161 | a0001c0001t0001g0031a0001c0001t0001g0044a0001c0001t0001g0073others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.1743+229C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 12/21 | chr10 | 74096084 | ||||||
| chr10:74096149
|
A | ACTT | 159 | a0001c0001t0001g0031a0001c0001t0001g0044a0001c0001t0001g0073others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.1743+295_1743+297d others(5): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr10 | 74096149 | |||||
| chr10:74096150
|
C | CT | 6 | a0001c0001t0001g0030a0001c0006t0005g0085a0001c0006t0005g0111others(3): Show | 6 | HG02630.hp1 HG02896.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1743+310dupT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr10 | 74096150 | |||||
| chr10:74096150
|
C | CTT | 5 | a0001c0006t0005g0076a0001c0006t0005g0077a0001c0006t0005g0080others(2): Show | 5 | HG02622.hp1 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1743+309_1743+310d others(4): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr10 | 74096150 | |||||
| chr10:74096222
|
C | T | 3 | a0001c0001t0001g0150a0001c0001t0001g0164a0001c0001t0004g0002 | 3 | HG01261.hp1 HG02922.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1743+367C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 12/21 | chr10 | 74096222 | ||||||
| chr10:74096328
|
G | C | 2 | a0001c0002t0004g0195a0001c0002t0006g0084 | 2 | HG01243.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1743+473G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 12/21 | chr10 | 74096328 | ||||||
| chr10:74096440
|
C | A | 2 | a0001c0001t0001g0163a0001c0001t0001g0226 | 2 | HG02602.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1743+585C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 12/21 | chr10 | 74096440 | ||||||
| chr10:74096576
|
A | G | 4 | a0001c0001t0001g0142a0001c0001t0001g0157a0001c0001t0001g0158others(1): Show | 4 | HG01255.hp2 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1744-628A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 12/21 | chr10 | 74096576 | ||||||
| chr10:74097010
|
AC | A | 5 | a0001c0007t0013g0029a0001c0007t0013g0054a0001c0007t0018g0100others(2): Show | 5 | HG01069.hp1 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1744-192delC | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr10 | 74097010 | |||||
| chr10:74097529
|
G | C | 13 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(10): Show | 13 | HG00735.hp1 HG01074.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1872+197G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 13/21 | chr10 | 74097529 | ||||||
| chr10:74097531
|
A | C | 13 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0112others(10): Show | 13 | HG00639.hp2 HG01081.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1872+199A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 13/21 | chr10 | 74097531 | ||||||
| chr10:74097539
|
A | G | 1 | a0001c0007t0003g0107 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1872+207A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 13/21 | chr10 | 74097539 | ||||||
| chr10:74097705
|
T | C | 1 | a0003c0010t0008g0090 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1872+373T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 13/21 | chr10 | 74097705 | ||||||
| chr10:74097824
|
T | G | 5 | a0001c0002t0004g0195a0001c0002t0005g0187a0001c0002t0006g0084others(2): Show | 5 | HG01243.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1872+492T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 13/21 | chr10 | 74097824 | ||||||
| chr10:74097888
|
A | G | 3 | a0001c0004t0002g0186a0001c0004t0002g0262a0001c0009t0002g0181 | 3 | HG00642.hp1 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1872+556A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 13/21 | chr10 | 74097888 | ||||||
| chr10:74097902
|
C | T | 1 | a0001c0002t0001g0200 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1872+570C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 13/21 | chr10 | 74097902 | ||||||
| chr10:74098022
|
T | G | 1 | a0001c0002t0005g0187 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1872+690T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 13/21 | chr10 | 74098022 | ||||||
| chr10:74098047
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1872+715G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 13/21 | chr10 | 74098047 | ||||||
| chr10:74098196
|
C | T | 1 | a0001c0002t0005g0187 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1872+864C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 13/21 | chr10 | 74098196 | ||||||
| chr10:74098197
|
G | A | 4 | a0001c0002t0004g0195a0001c0002t0006g0084a0001c0007t0004g0120others(1): Show | 4 | HG01243.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1872+865G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 13/21 | chr10 | 74098197 | ||||||
| chr10:74098754
|
C | T | 1 | a0001c0002t0001g0112 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1872+1422C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 13/21 | chr10 | 74098754 | ||||||
| chr10:74099267
|
C | G | 28 | a0001c0004t0002g0052a0001c0004t0002g0058a0001c0004t0002g0062others(25): Show | 28 | HG00642.hp1 HG01433.hp2 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.1873-1681C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 13/21 | chr10 | 74099267 | ||||||
| chr10:74099444
|
TCCTA | T | 41 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(38): Show | 41 | HG00642.hp1 HG00735.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.1873-1499_1873-149 others(8): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr10 | 74099444 | |||||
| chr10:74099455
|
G | A | 53 | a0001c0002t0003g0001a0001c0002t0007g0167a0001c0002t0007g0168others(50): Show | 53 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1873-1493G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 13/21 | chr10 | 74099455 | ||||||
| chr10:74099642
|
C | T | 1 | a0001c0009t0002g0181 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1873-1306C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 13/21 | chr10 | 74099642 | ||||||
| chr10:74099791
|
G | T | 17 | a0001c0004t0002g0052a0001c0004t0002g0058a0001c0004t0002g0062others(14): Show | 17 | HG00642.hp1 HG01433.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1873-1157G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 13/21 | chr10 | 74099791 | ||||||
| chr10:74099944
|
T | A | 4 | a0001c0001t0001g0146a0001c0001t0001g0148a0001c0001t0001g0153others(1): Show | 4 | HG00735.hp2 HG01169.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1873-1004T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 13/21 | chr10 | 74099944 | ||||||
| chr10:74100265
|
C | T | 1 | a0001c0004t0002g0183 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1873-683C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 13/21 | chr10 | 74100265 | ||||||
| chr10:74100340
|
A | G | 193 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1873-608A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 13/21 | chr10 | 74100340 | ||||||
| chr10:74100705
|
T | C | 1 | a0002c0005t0002g0026 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1873-243T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 13/21 | chr10 | 74100705 | ||||||
| chr10:74100765
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1873-183C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 13/21 | chr10 | 74100765 | ||||||
| chr10:74100766
|
G | A | 1 | a0002c0005t0002g0046 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1873-182G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 13/21 | chr10 | 74100766 | ||||||
| chr10:74101230
|
A | G | 1 | a0001c0007t0013g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2022+133A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | chr10 | 74101230 | ||||||
| chr10:74101251
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2022+154T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | chr10 | 74101251 | ||||||
| chr10:74101264
|
C | T | 6 | a0001c0002t0007g0167a0001c0002t0007g0168a0001c0002t0007g0177others(3): Show | 6 | HG00733.hp2 HG03669.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.2022+167C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | chr10 | 74101264 | ||||||
| chr10:74101280
|
G | GT | 13 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0112others(10): Show | 13 | HG00639.hp2 HG01081.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.2022+186dupT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr10 | 74101280 | |||||
| chr10:74101323
|
C | CA | 10 | a0001c0001t0001g0178a0001c0002t0001g0011a0001c0002t0001g0022others(7): Show | 10 | HG02257.hp2 HG02258.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2022+239dupA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr10 | 74101323 | |||||
| chr10:74101542
|
G | GT | 74 | a0001c0001t0001g0105a0001c0001t0001g0138a0001c0001t0001g0146others(71): Show | 74 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.2022+469dupT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr10 | 74101542 | |||||
| chr10:74101542
|
G | GTT | 28 | a0001c0002t0001g0109a0001c0002t0003g0001a0001c0002t0003g0028others(25): Show | 28 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.2022+468_2022+469d others(4): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr10 | 74101542 | |||||
| chr10:74101542
|
G | GTTT | 6 | a0001c0002t0007g0168a0001c0002t0007g0177a0001c0002t0007g0239others(3): Show | 6 | HG00733.hp2 HG00735.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.2022+467_2022+469d others(5): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr10 | 74101542 | |||||
| chr10:74101542
|
GT | G | 6 | a0001c0003t0002g0169a0001c0003t0002g0170a0001c0003t0002g0172others(3): Show | 6 | HG00639.hp1 HG01952.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.2022+469delT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr10 | 74101542 | |||||
| chr10:74101557
|
T | A | 3 | a0001c0009t0002g0013a0001c0009t0002g0113a0001c0009t0002g0118 | 3 | HG01433.hp2 HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2022+460T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | chr10 | 74101557 | ||||||
| chr10:74101670
|
C | T | 1 | a0001c0003t0002g0212 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2022+573C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | chr10 | 74101670 | ||||||
| chr10:74101717
|
G | A | 13 | a0001c0002t0003g0001a0001c0002t0011g0003a0001c0002t0011g0004others(10): Show | 13 | HG00735.hp1 HG01074.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2022+620G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | chr10 | 74101717 | ||||||
| chr10:74101862
|
C | CT | 9 | a0001c0001t0001g0146a0001c0001t0001g0230a0001c0002t0007g0167others(6): Show | 9 | HG00733.hp2 HG03669.hp2 HG03831.hp1 others(6): Show |
intron_variant | MODIFIER | c.2022+783dupT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr10 | 74101862 | |||||
| chr10:74101862
|
CT | C | 12 | a0001c0001t0001g0242a0001c0006t0005g0076a0001c0006t0005g0077others(9): Show | 12 | HG02622.hp1 HG02630.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.2022+783delT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr10 | 74101862 | |||||
| chr10:74101906
|
C | A | 145 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.2022+809C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | chr10 | 74101906 | ||||||
| chr10:74102040
|
AT | A | 173 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.2022+949delT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr10 | 74102040 | |||||
| chr10:74102108
|
G | A | 5 | a0001c0007t0013g0029a0001c0007t0013g0054a0001c0007t0018g0100others(2): Show | 5 | HG01069.hp1 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2022+1011G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | chr10 | 74102108 | ||||||
| chr10:74102111
|
C | T | 1 | a0001c0002t0003g0059 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2022+1014C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | chr10 | 74102111 | ||||||
| chr10:74102234
|
G | GT | 6 | a0001c0007t0013g0029a0001c0007t0013g0054a0001c0007t0018g0100others(3): Show | 6 | HG01069.hp1 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2022+1153dupT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr10 | 74102234 | |||||
| chr10:74102250
|
T | A | 2 | a0001c0007t0004g0120a0001c0007t0004g0121 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2022+1153T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | chr10 | 74102250 | ||||||
| chr10:74102311
|
T | A | 1 | a0001c0002t0007g0182 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2022+1214T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | chr10 | 74102311 | ||||||
| chr10:74102352
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2022+1255T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | chr10 | 74102352 | ||||||
| chr10:74102492
|
T | C | 1 | a0001c0001t0024g0193 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2023-1328T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | chr10 | 74102492 | ||||||
| chr10:74102519
|
A | T | 3 | a0001c0001t0001g0141a0001c0001t0001g0147a0001c0001t0004g0149 | 3 | HG00738.hp2 HG00741.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.2023-1301A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | chr10 | 74102519 | ||||||
| chr10:74102743
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2023-1077C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | chr10 | 74102743 | ||||||
| chr10:74102869
|
G | GT | 8 | a0001c0001t0001g0236a0001c0003t0002g0053a0001c0004t0002g0086others(5): Show | 8 | HG02622.hp1 HG02717.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2023-938dupT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr10 | 74102869 | |||||
| chr10:74103278
|
A | G | 1 | a0001c0007t0018g0100 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2023-542A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | chr10 | 74103278 | ||||||
| chr10:74103554
|
T | C | 1 | a0001c0002t0003g0104 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2023-266T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | chr10 | 74103554 | ||||||
| chr10:74103705
|
G | C | 2 | a0001c0007t0004g0120a0001c0007t0004g0121 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2023-115G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | chr10 | 74103705 | ||||||
| chr10:74103992
|
C | T | 134 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.2131+64C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 15/21 | chr10 | 74103992 | ||||||
| chr10:74104033
|
C | T | 1 | a0001c0002t0001g0109 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2131+105C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 15/21 | chr10 | 74104033 | ||||||
| chr10:74104205
|
A | T | 1 | a0001c0001t0001g0146 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2131+277A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 15/21 | chr10 | 74104205 | ||||||
| chr10:74104446
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2131+518C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 15/21 | chr10 | 74104446 | ||||||
| chr10:74104614
|
G | C | 162 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.2132-437G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 15/21 | chr10 | 74104614 | ||||||
| chr10:74104693
|
G | A | 18 | a0001c0004t0002g0052a0001c0004t0002g0058a0001c0004t0002g0062others(15): Show | 18 | HG00642.hp1 HG01433.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2132-358G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 15/21 | chr10 | 74104693 | ||||||
| chr10:74104703
|
A | G | 1 | a0001c0002t0003g0091 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2132-348A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 15/21 | chr10 | 74104703 | ||||||
| chr10:74105401
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2434+48C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 16/21 | chr10 | 74105401 | ||||||
| chr10:74105478
|
T | A | 1 | a0001c0003t0002g0038 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2434+125T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 16/21 | chr10 | 74105478 | ||||||
| chr10:74105512
|
G | A | 29 | a0001c0002t0005g0187a0001c0004t0002g0052a0001c0004t0002g0058others(26): Show | 29 | HG00642.hp1 HG01433.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.2434+159G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 16/21 | chr10 | 74105512 | ||||||
| chr10:74105567
|
C | G | 1 | a0001c0001t0001g0222 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2434+214C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 16/21 | chr10 | 74105567 | ||||||
| chr10:74105797
|
C | T | 1 | a0001c0003t0002g0075 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2434+444C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 16/21 | chr10 | 74105797 | ||||||
| chr10:74105912
|
C | CT | 12 | a0001c0002t0003g0065a0001c0002t0003g0087a0001c0002t0003g0101others(9): Show | 12 | HG00597.hp2 HG01192.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.2434+581dupT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr10 | 74105912 | |||||
| chr10:74105912
|
C | T | 1 | a0001c0007t0003g0107 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2434+559C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 16/21 | chr10 | 74105912 | ||||||
| chr10:74105912
|
CT | C | 5 | a0001c0002t0003g0020a0001c0002t0007g0180a0001c0003t0002g0043others(2): Show | 5 | HG01243.hp2 HG01256.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.2434+581delT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr10 | 74105912 | |||||
| chr10:74105912
|
CTT | C | 121 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.2434+580_2434+581d others(4): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr10 | 74105912 | |||||
| chr10:74105912
|
CTTT | C | 13 | a0001c0002t0005g0187a0001c0003t0002g0079a0001c0003t0002g0212others(10): Show | 13 | HG02040.hp1 HG02622.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2434+579_2434+581d others(5): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr10 | 74105912 | |||||
| chr10:74105914
|
T | TTTTTAGT others(42): Show |
18 | a0001c0004t0002g0052a0001c0004t0002g0058a0001c0004t0002g0062others(15): Show | 18 | HG00642.hp1 HG01433.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2434+565_2434+566i others(51): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr10 | 74105914 | |||||
| chr10:74106061
|
C | T | 1 | a0001c0003t0002g0047 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2434+708C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 16/21 | chr10 | 74106061 | ||||||
| chr10:74106247
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2434+894G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 16/21 | chr10 | 74106247 | ||||||
| chr10:74106471
|
AATTTTGA others(4): Show |
A | 1 | a0001c0002t0007g0239 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2435-753_2435-743d others(13): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr10 | 74106471 | |||||
| chr10:74106559
|
G | A | 1 | a0001c0003t0002g0161 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2435-671G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 16/21 | chr10 | 74106559 | ||||||
| chr10:74107090
|
C | G | 1 | a0001c0002t0007g0239 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2435-140C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 16/21 | chr10 | 74107090 | ||||||
| chr10:74107091
|
C | G | 1 | a0001c0001t0024g0193 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2435-139C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 16/21 | chr10 | 74107091 | ||||||
| chr10:74107171
|
C | A | 110 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.2435-59C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 16/21 | chr10 | 74107171 | ||||||
| chr10:74107435
|
G | T | 30 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0023others(27): Show | 30 | HG00423.hp2 HG00597.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.2559+81G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 17/21 | chr10 | 74107435 | ||||||
| chr10:74107710
|
G | C | 5 | a0001c0007t0013g0029a0001c0007t0013g0054a0001c0007t0018g0100others(2): Show | 5 | HG01069.hp1 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2559+356G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 17/21 | chr10 | 74107710 | ||||||
| chr10:74107786
|
T | A | 1 | a0001c0002t0007g0182 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2559+432T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 17/21 | chr10 | 74107786 | ||||||
| chr10:74107856
|
C | T | 117 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.2559+502C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 17/21 | chr10 | 74107856 | ||||||
| chr10:74107875
|
T | C | 152 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.2559+521T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 17/21 | chr10 | 74107875 | ||||||
| chr10:74107882
|
A | G | 2 | a0001c0002t0004g0188a0001c0002t0004g0189 | 2 | HG00642.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2559+528A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 17/21 | chr10 | 74107882 | ||||||
| chr10:74108129
|
C | A | 1 | a0001c0002t0011g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2559+775C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 17/21 | chr10 | 74108129 | ||||||
| chr10:74108226
|
T | A | 1 | a0001c0009t0002g0113 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2560-745T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 17/21 | chr10 | 74108226 | ||||||
| chr10:74108329
|
G | A | 1 | a0001c0006t0005g0085 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2560-642G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 17/21 | chr10 | 74108329 | ||||||
| chr10:74108356
|
C | T | 163 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.2560-615C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 17/21 | chr10 | 74108356 | ||||||
| chr10:74108531
|
G | T | 1 | a0001c0002t0003g0023 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2560-440G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 17/21 | chr10 | 74108531 | ||||||
| chr10:74108532
|
C | T | 5 | a0001c0007t0013g0029a0001c0007t0013g0054a0001c0007t0018g0100others(2): Show | 5 | HG01069.hp1 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2560-439C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 17/21 | chr10 | 74108532 | ||||||
| chr10:74108865
|
A | T | 1 | a0001c0003t0002g0136 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2560-106A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 17/21 | chr10 | 74108865 | ||||||
| chr10:74108949
|
C | A | 1 | a0001c0001t0001g0233 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2560-22C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 17/21 | chr10 | 74108949 | ||||||
| chr10:74109307
|
T | C | 94 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.2745+151T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 18/21 | chr10 | 74109307 | ||||||
| chr10:74109576
|
C | CTTTTCTT | 5 | a0001c0006t0005g0076a0001c0006t0005g0077a0001c0006t0005g0080others(2): Show | 5 | HG02622.hp1 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2745+424_2745+425i others(9): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr10 | 74109576 | |||||
| chr10:74109576
|
C | CTTTTTTT | 167 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.2745+423_2745+429d others(9): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr10 | 74109576 | |||||
| chr10:74109601
|
G | A | 18 | a0001c0004t0002g0052a0001c0004t0002g0058a0001c0004t0002g0062others(15): Show | 18 | HG00642.hp1 HG01433.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2745+445G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 18/21 | chr10 | 74109601 | ||||||
| chr10:74109779
|
C | T | 1 | a0007c0017t0002g0039 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2745+623C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 18/21 | chr10 | 74109779 | ||||||
| chr10:74109901
|
T | A | 3 | a0001c0002t0001g0011a0001c0002t0001g0194a0001c0002t0001g0200 | 3 | HG02630.hp2 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2745+745T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 18/21 | chr10 | 74109901 | ||||||
| chr10:74109964
|
C | T | 11 | a0001c0002t0005g0187a0001c0006t0005g0076a0001c0006t0005g0077others(8): Show | 11 | HG02622.hp1 HG02630.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.2745+808C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 18/21 | chr10 | 74109964 | ||||||
| chr10:74109996
|
T | C | 51 | a0001c0002t0003g0001a0001c0002t0003g0020a0001c0002t0003g0021others(48): Show | 51 | HG00423.hp2 HG00597.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.2745+840T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 18/21 | chr10 | 74109996 | ||||||
| chr10:74110180
|
A | G | 118 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.2745+1024A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 18/21 | chr10 | 74110180 | ||||||
| chr10:74110217
|
G | C | 2 | a0001c0002t0004g0195a0001c0002t0006g0084 | 2 | HG01243.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2745+1061G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 18/21 | chr10 | 74110217 | ||||||
| chr10:74110303
|
T | C | 1 | a0001c0018t0003g0196 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2745+1147T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 18/21 | chr10 | 74110303 | ||||||
| chr10:74110665
|
A | G | 2 | a0001c0002t0003g0124a0001c0007t0003g0107 | 2 | HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2746-1244A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 18/21 | chr10 | 74110665 | ||||||
| chr10:74111132
|
C | G | 117 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.2746-777C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 18/21 | chr10 | 74111132 | ||||||
| chr10:74111539
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2746-370C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 18/21 | chr10 | 74111539 | ||||||
| chr10:74111556
|
C | A | 1 | a0001c0002t0003g0001 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2746-353C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 18/21 | chr10 | 74111556 | ||||||
| chr10:74111577
|
A | T | 1 | a0001c0001t0001g0228 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2746-332A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 18/21 | chr10 | 74111577 | ||||||
| chr10:74111610
|
A | T | 2 | a0001c0006t0005g0184a0001c0006t0005g0192 | 2 | HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2746-299A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 18/21 | chr10 | 74111610 | ||||||
| chr10:74112337
|
G | C | 1 | a0001c0003t0002g0099 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2949+225G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 19/21 | chr10 | 74112337 | ||||||
| chr10:74112993
|
C | T | 5 | a0001c0007t0013g0029a0001c0007t0013g0054a0001c0007t0018g0100others(2): Show | 5 | HG01069.hp1 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2949+881C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 19/21 | chr10 | 74112993 | ||||||
| chr10:74113002
|
C | T | 1 | a0001c0003t0009g0197 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2949+890C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 19/21 | chr10 | 74113002 | ||||||
| chr10:74113090
|
C | A | 1 | a0001c0009t0002g0040 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2949+978C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 19/21 | chr10 | 74113090 | ||||||
| chr10:74113130
|
A | G | 1 | a0001c0002t0001g0200 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2949+1018A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 19/21 | chr10 | 74113130 | ||||||
| chr10:74113256
|
A | G | 2 | a0001c0002t0004g0188a0001c0002t0004g0189 | 2 | HG00642.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2950-928A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 19/21 | chr10 | 74113256 | ||||||
| chr10:74113407
|
C | T | 140 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.2950-777C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 19/21 | chr10 | 74113407 | ||||||
| chr10:74113506
|
T | C | 5 | a0001c0007t0013g0029a0001c0007t0013g0054a0001c0007t0018g0100others(2): Show | 5 | HG01069.hp1 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2950-678T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 19/21 | chr10 | 74113506 | ||||||
| chr10:74113578
|
CT | C | 97 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.2950-592delT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr10 | 74113578 | |||||
| chr10:74113586
|
T | C | 2 | a0001c0001t0001g0214a0001c0001t0001g0221 | 2 | HG02129.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2950-598T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 19/21 | chr10 | 74113586 | ||||||
| chr10:74113651
|
G | C | 11 | a0001c0002t0005g0187a0001c0006t0005g0076a0001c0006t0005g0077others(8): Show | 11 | HG02622.hp1 HG02630.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.2950-533G>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 19/21 | chr10 | 74113651 | ||||||
| chr10:74113881
|
C | T | 91 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.2950-303C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 19/21 | chr10 | 74113881 | ||||||
| chr10:74114031
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2950-153G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 19/21 | chr10 | 74114031 | ||||||
| chr10:74114134
|
C | T | 110 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.2950-50C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 19/21 | chr10 | 74114134 | ||||||
| chr10:74114408
|
C | CGT | 6 | a0001c0003t0002g0045a0001c0003t0002g0083a0001c0009t0002g0013others(3): Show | 6 | HG01433.hp2 HG02015.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3153+49_3153+50dup others(2): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr10 | 74114408 | |||||
| chr10:74114408
|
C | CGTGTGTG others(3): Show |
1 | a0001c0007t0018g0100 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.3153+41_3153+50dup others(10): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr10 | 74114408 | |||||
| chr10:74114408
|
CGT | C | 3 | a0001c0003t0002g0055a0001c0003t0009g0125a0001c0004t0002g0086 | 3 | HG02965.hp1 HG03942.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.3153+49_3153+50del others(2): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr10 | 74114408 | |||||
| chr10:74114408
|
CGTGTGT | C | 11 | a0001c0002t0005g0187a0001c0006t0005g0076a0001c0006t0005g0077others(8): Show | 11 | HG02622.hp1 HG02630.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.3153+45_3153+50del others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr10 | 74114408 | |||||
| chr10:74114408
|
CGTGTGTG others(1): Show |
C | 40 | a0001c0002t0003g0001a0001c0002t0003g0020a0001c0002t0003g0021others(37): Show | 40 | HG00423.hp2 HG00597.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.3153+43_3153+50del others(8): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr10 | 74114408 | |||||
| chr10:74114434
|
T | C | 87 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(84): Show | 87 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.3153+47T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 20/21 | chr10 | 74114434 | ||||||
| chr10:74114434
|
T | TGC | 20 | a0001c0001t0001g0142a0001c0001t0001g0207a0001c0002t0001g0109others(17): Show | 20 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.3153+48_3153+49ins others(2): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr10 | 74114434 | |||||
| chr10:74114434
|
T | TGTGC | 6 | a0001c0002t0007g0167a0001c0002t0007g0168a0001c0002t0007g0177others(3): Show | 6 | HG00733.hp2 HG03209.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.3153+51_3153+54dup others(4): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr10 | 74114434 | |||||
| chr10:74114434
|
T | TGTGTGTG others(3): Show |
1 | a0001c0002t0006g0084 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3153+50_3153+51ins others(10): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr10 | 74114434 | |||||
| chr10:74114434
|
T | TGTGTGTG others(7): Show |
2 | a0001c0007t0004g0120a0001c0007t0004g0121 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3153+50_3153+51ins others(14): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr10 | 74114434 | |||||
| chr10:74114436
|
T | C | 12 | a0001c0002t0005g0187a0001c0004t0008g0012a0001c0006t0005g0076others(9): Show | 12 | HG02622.hp1 HG02630.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.3153+49T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 20/21 | chr10 | 74114436 | ||||||
| chr10:74114642
|
C | A | 1 | a0001c0002t0003g0097 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.3154-153C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 20/21 | chr10 | 74114642 | ||||||
| chr10:74114657
|
A | G | 5 | a0001c0007t0013g0029a0001c0007t0013g0054a0001c0007t0018g0100others(2): Show | 5 | HG01069.hp1 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.3154-138A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 20/21 | chr10 | 74114657 | ||||||
| chr10:74114682
|
G | A | 3 | a0001c0002t0003g0042a0001c0002t0003g0087a0001c0002t0003g0097 | 3 | HG01934.hp2 HG02273.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.3154-113G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 20/21 | chr10 | 74114682 | ||||||
| chr10:74115000
|
G | A | 1 | a0001c0002t0005g0187 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3258+101G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74115000 | ||||||
| chr10:74115145
|
T | C | 1 | a0001c0001t0001g0250 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.3258+246T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74115145 | ||||||
| chr10:74115242
|
CAAAACAC others(67): Show |
C | 1 | a0001c0002t0020g0256 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3258+345_3258+418d others(76): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr10 | 74115242 | |||||
| chr10:74115387
|
G | GATAA | 13 | a0001c0002t0001g0251a0001c0002t0007g0167a0001c0002t0007g0168others(10): Show | 13 | HG00733.hp2 HG00735.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.3258+517_3258+520d others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr10 | 74115387 | |||||
| chr10:74115387
|
GATAA | G | 14 | a0001c0001t0001g0044a0001c0001t0001g0233a0001c0002t0005g0187others(11): Show | 14 | HG00741.hp1 HG02622.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.3258+517_3258+520d others(6): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr10 | 74115387 | |||||
| chr10:74115387
|
GATAAATA others(1): Show |
G | 32 | a0001c0001t0001g0242a0001c0002t0003g0020a0001c0002t0003g0021others(29): Show | 32 | HG00423.hp2 HG00597.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.3258+513_3258+520d others(10): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr10 | 74115387 | |||||
| chr10:74115395
|
A | G | 2 | a0001c0007t0004g0120a0001c0007t0004g0121 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3258+496A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74115395 | ||||||
| chr10:74115416
|
A | G | 1 | a0001c0003t0002g0067 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3258+517A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74115416 | ||||||
| chr10:74115420
|
G | A | 1 | a0001c0002t0007g0182 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3258+521G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74115420 | ||||||
| chr10:74115458
|
T | G | 111 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.3258+559T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74115458 | ||||||
| chr10:74115502
|
G | A | 3 | a0001c0001t0001g0160a0001c0001t0001g0178a0001c0001t0023g0234 | 3 | HG00558.hp2 HG00597.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.3258+603G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74115502 | ||||||
| chr10:74115704
|
T | G | 2 | a0001c0007t0004g0120a0001c0007t0004g0121 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3258+805T>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74115704 | ||||||
| chr10:74115751
|
G | A | 1 | a0001c0003t0002g0019 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.3258+852G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74115751 | ||||||
| chr10:74116025
|
C | A | 1 | a0001c0002t0003g0245 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3258+1126C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74116025 | ||||||
| chr10:74116036
|
A | G | 152 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.3258+1137A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74116036 | ||||||
| chr10:74116251
|
C | T | 118 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.3258+1352C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74116251 | ||||||
| chr10:74116362
|
C | T | 1 | a0001c0002t0014g0010 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3258+1463C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74116362 | ||||||
| chr10:74116587
|
G | T | 3 | a0001c0001t0001g0223a0001c0001t0001g0247a0001c0001t0004g0215 | 3 | NA18969.hp1 NA19055.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.3259-1436G>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74116587 | ||||||
| chr10:74116594
|
G | A | 2 | a0001c0003t0002g0043a0001c0003t0002g0064 | 2 | NA18998.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.3259-1429G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74116594 | ||||||
| chr10:74116617
|
C | T | 18 | a0001c0004t0002g0052a0001c0004t0002g0058a0001c0004t0002g0062others(15): Show | 18 | HG00642.hp1 HG01433.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.3259-1406C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74116617 | ||||||
| chr10:74116683
|
T | C | 1 | a0001c0008t0001g0015 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3259-1340T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74116683 | ||||||
| chr10:74116686
|
C | CA | 110 | a0001c0001t0001g0031a0001c0001t0001g0044a0001c0001t0001g0073others(107): Show | 110 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.3259-1325dupA | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr10 | 74116686 | |||||
| chr10:74116696
|
A | AT | 4 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(1): Show | 4 | HG00099.hp1 NA18984.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.3259-1327_3259-132 others(5): Show |
VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74116696 | ||||||
| chr10:74116698
|
AT | A | 3 | a0001c0004t0002g0186a0001c0004t0002g0262a0001c0009t0002g0181 | 3 | HG00642.hp1 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3259-1324delT | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74116698 | ||||||
| chr10:74116699
|
T | A | 52 | a0001c0001t0001g0238a0001c0002t0003g0001a0001c0002t0003g0020others(49): Show | 52 | HG00423.hp2 HG00597.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.3259-1324T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74116699 | ||||||
| chr10:74116700
|
A | T | 10 | a0001c0002t0005g0187a0001c0006t0005g0076a0001c0006t0005g0077others(7): Show | 10 | HG02622.hp1 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.3259-1323A>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74116700 | ||||||
| chr10:74116702
|
T | A | 11 | a0001c0002t0005g0187a0001c0006t0005g0076a0001c0006t0005g0077others(8): Show | 11 | HG02622.hp1 HG02630.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.3259-1321T>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74116702 | ||||||
| chr10:74116730
|
C | A | 11 | a0001c0002t0005g0187a0001c0006t0005g0076a0001c0006t0005g0077others(8): Show | 11 | HG02622.hp1 HG02630.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.3259-1293C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74116730 | ||||||
| chr10:74116939
|
G | A | 1 | a0001c0006t0005g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3259-1084G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74116939 | ||||||
| chr10:74117011
|
A | G | 3 | a0001c0002t0012g0190a0001c0002t0012g0191a0001c0002t0012g0198 | 3 | HG01884.hp1 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3259-1012A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74117011 | ||||||
| chr10:74117387
|
C | G | 110 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.3259-636C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74117387 | ||||||
| chr10:74117481
|
C | G | 117 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.3259-542C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74117481 | ||||||
| chr10:74118007
|
A | G | 1 | a0001c0003t0002g0079 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3259-16A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74118007 |