Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MPVFH others(1129): Show |
chr10 | 73993116 | 74125169 |
| a0002 | 0/0 | 1134 | 10 | 0 | 2 | 7 | 1 | 0 | 6 | VCL_chr10_73993116_74125169 | VCL | MPVFH others(1129): Show |
chr10 | 73993116 | 74125169 |
| a0003 | 0/0 | 1134 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | VCL_chr10_73993116_74125169 | VCL | MPVFH others(1129): Show |
chr10 | 73993116 | 74125169 |
| a0004 | 0/0 | 1134 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | MPVFH others(1129): Show |
chr10 | 73993116 | 74125169 |
| a0005 | 0/0 | 1134 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | MPVFH others(1129): Show |
chr10 | 73993116 | 74125169 |
| a0006 | 0/0 | 1134 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | MPVFH others(1129): Show |
chr10 | 73993116 | 74125169 |
| a0007 | 0/0 | 1134 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | MPVFH others(1129): Show |
chr10 | 73993116 | 74125169 |
| a0008 | 0/0 | 1134 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | MPVFH others(1129): Show |
chr10 | 73993116 | 74125169 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3402 | 82 | 3 | 24 | 37 | 6 | 11 | VCL_chr10_73993116_74125169 | VCL | ATGCC others(3397): Show |
chr10 | 73993116 | 74125169 | ||
| a0001c0002 | 0/0 | 3402 | 60 | 27 | 13 | 16 | 2 | 2 | VCL_chr10_73993116_74125169 | VCL | ATGCC others(3397): Show |
chr10 | 73993116 | 74125169 | ||
| a0001c0003 | 1/0 | 3402 | 56 | 3 | 13 | 29 | 1 | 9 | VCL_chr10_73993116_74125169 | VCL | ATGCC others(3397): Show |
chr10 | 73993116 | 74125169 | ||
| a0001c0004 | 0/0 | 3402 | 12 | 11 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | ATGCC others(3397): Show |
chr10 | 73993116 | 74125169 | ||
| a0001c0006 | 0/0 | 3402 | 9 | 9 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | ATGCC others(3397): Show |
chr10 | 73993116 | 74125169 | ||
| a0001c0007 | 0/0 | 3402 | 8 | 5 | 3 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | ATGCC others(3397): Show |
chr10 | 73993116 | 74125169 | ||
| a0001c0008 | 0/0 | 3402 | 8 | 6 | 2 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | ATGCC others(3397): Show |
chr10 | 73993116 | 74125169 | ||
| a0001c0009 | 0/0 | 3402 | 5 | 4 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | ATGCC others(3397): Show |
chr10 | 73993116 | 74125169 | ||
| a0001c0011 | 0/0 | 3402 | 2 | 2 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | ATGCC others(3397): Show |
chr10 | 73993116 | 74125169 | ||
| a0001c0012 | 0/0 | 3402 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | ATGCC others(3397): Show |
chr10 | 73993116 | 74125169 | ||
| a0001c0013 | 0/0 | 3402 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | ATGCC others(3397): Show |
chr10 | 73993116 | 74125169 | ||
| a0001c0018 | 0/0 | 3402 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | ATGCC others(3397): Show |
chr10 | 73993116 | 74125169 | ||
| a0002c0005 | 0/0 | 3402 | 9 | 0 | 2 | 6 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | ATGCC others(3397): Show |
chr10 | 73993116 | 74125169 | ||
| a0002c0015 | 0/0 | 3402 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | ATGCC others(3397): Show |
chr10 | 73993116 | 74125169 | ||
| a0003c0010 | 0/0 | 3402 | 4 | 0 | 0 | 4 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | ATGCC others(3397): Show |
chr10 | 73993116 | 74125169 | ||
| a0004c0014 | 0/0 | 3402 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | ATGCC others(3397): Show |
chr10 | 73993116 | 74125169 | ||
| a0005c0016 | 0/0 | 3402 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | ATGCC others(3397): Show |
chr10 | 73993116 | 74125169 | ||
| a0006c0019 | 0/0 | 3402 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | ATGCC others(3397): Show |
chr10 | 73993116 | 74125169 | ||
| a0007c0020 | 0/0 | 3402 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | ATGCC others(3397): Show |
chr10 | 73993116 | 74125169 | ||
| a0008c0017 | 0/0 | 3402 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | ATGCC others(3397): Show |
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 | AGTCG others(5496): Show |
chr10 | 73993116 | 74125169 |
| a0001c0001t0004 | 0/0 | 5500 | 4 | 1 | 2 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5495): Show |
chr10 | 73993116 | 74125169 |
| a0001c0001t0006 | 0/0 | 5499 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5494): Show |
chr10 | 73993116 | 74125169 |
| a0001c0001t0023 | 0/0 | 5501 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5496): Show |
chr10 | 73993116 | 74125169 |
| a0001c0001t0024 | 0/0 | 5501 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5496): Show |
chr10 | 73993116 | 74125169 |
| a0001c0002t0001 | 0/0 | 5501 | 9 | 9 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5496): Show |
chr10 | 73993116 | 74125169 |
| a0001c0002t0003 | 0/0 | 5498 | 26 | 2 | 9 | 12 | 2 | 1 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5493): Show |
chr10 | 73993116 | 74125169 |
| a0001c0002t0004 | 0/0 | 5500 | 4 | 3 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5495): Show |
chr10 | 73993116 | 74125169 |
| a0001c0002t0005 | 0/0 | 5498 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5493): Show |
chr10 | 73993116 | 74125169 |
| a0001c0002t0006 | 0/0 | 5499 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5494): Show |
chr10 | 73993116 | 74125169 |
| a0001c0002t0007 | 0/0 | 5503 | 7 | 1 | 1 | 4 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5498): Show |
chr10 | 73993116 | 74125169 |
| a0001c0002t0011 | 0/0 | 5498 | 4 | 3 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5493): Show |
chr10 | 73993116 | 74125169 |
| a0001c0002t0012 | 0/0 | 5503 | 3 | 3 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5498): Show |
chr10 | 73993116 | 74125169 |
| a0001c0002t0014 | 0/0 | 5501 | 2 | 2 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5496): Show |
chr10 | 73993116 | 74125169 |
| a0001c0002t0015 | 0/0 | 5497 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5492): Show |
chr10 | 73993116 | 74125169 |
| a0001c0002t0019 | 0/0 | 5497 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5492): Show |
chr10 | 73993116 | 74125169 |
| a0001c0002t0020 | 0/0 | 5572 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5567): Show |
chr10 | 73993116 | 74125169 |
| a0001c0003t0001 | 0/0 | 5501 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5496): Show |
chr10 | 73993116 | 74125169 |
| a0001c0003t0002 | 1/0 | 5497 | 47 | 1 | 12 | 25 | 1 | 7 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5492): Show |
chr10 | 73993116 | 74125169 |
| a0001c0003t0008 | 0/0 | 5496 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5491): Show |
chr10 | 73993116 | 74125169 |
| a0001c0003t0009 | 0/0 | 5498 | 5 | 0 | 1 | 2 | 0 | 2 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5493): Show |
chr10 | 73993116 | 74125169 |
| a0001c0003t0021 | 0/0 | 5499 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5494): Show |
chr10 | 73993116 | 74125169 |
| a0001c0003t0022 | 0/0 | 5497 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5492): Show |
chr10 | 73993116 | 74125169 |
| a0001c0004t0002 | 0/0 | 5497 | 11 | 10 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5492): Show |
chr10 | 73993116 | 74125169 |
| a0001c0004t0008 | 0/0 | 5496 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5491): Show |
chr10 | 73993116 | 74125169 |
| a0001c0006t0005 | 0/0 | 5498 | 8 | 8 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5493): Show |
chr10 | 73993116 | 74125169 |
| a0001c0006t0017 | 0/0 | 5498 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5493): Show |
chr10 | 73993116 | 74125169 |
| a0001c0007t0003 | 0/0 | 5498 | 2 | 1 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5493): Show |
chr10 | 73993116 | 74125169 |
| a0001c0007t0004 | 0/0 | 5500 | 3 | 2 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5495): Show |
chr10 | 73993116 | 74125169 |
| a0001c0007t0013 | 0/0 | 5503 | 2 | 2 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5498): Show |
chr10 | 73993116 | 74125169 |
| a0001c0007t0018 | 0/0 | 5502 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5497): Show |
chr10 | 73993116 | 74125169 |
| a0001c0008t0001 | 0/0 | 5501 | 5 | 5 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5496): Show |
chr10 | 73993116 | 74125169 |
| a0001c0008t0006 | 0/0 | 5499 | 3 | 1 | 2 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5494): Show |
chr10 | 73993116 | 74125169 |
| a0001c0009t0002 | 0/0 | 5497 | 5 | 4 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5492): Show |
chr10 | 73993116 | 74125169 |
| a0001c0011t0006 | 0/0 | 5499 | 2 | 2 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5494): Show |
chr10 | 73993116 | 74125169 |
| a0001c0012t0016 | 0/0 | 5501 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5496): Show |
chr10 | 73993116 | 74125169 |
| a0001c0013t0005 | 0/0 | 5498 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5493): Show |
chr10 | 73993116 | 74125169 |
| a0001c0018t0003 | 0/0 | 5498 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5493): Show |
chr10 | 73993116 | 74125169 |
| a0002c0005t0002 | 0/0 | 5497 | 4 | 0 | 0 | 4 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5492): Show |
chr10 | 73993116 | 74125169 |
| a0002c0005t0010 | 0/0 | 5497 | 5 | 0 | 2 | 2 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5492): Show |
chr10 | 73993116 | 74125169 |
| a0002c0015t0002 | 0/0 | 5497 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5492): Show |
chr10 | 73993116 | 74125169 |
| a0003c0010t0008 | 0/0 | 5496 | 4 | 0 | 0 | 4 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5491): Show |
chr10 | 73993116 | 74125169 |
| a0004c0014t0002 | 0/0 | 5497 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5492): Show |
chr10 | 73993116 | 74125169 |
| a0005c0016t0002 | 0/0 | 5497 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5492): Show |
chr10 | 73993116 | 74125169 |
| a0006c0019t0002 | 0/0 | 5497 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5492): Show |
chr10 | 73993116 | 74125169 |
| a0007c0020t0015 | 0/0 | 5497 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5492): Show |
chr10 | 73993116 | 74125169 |
| a0008c0017t0002 | 0/0 | 5497 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | AGTCG others(5492): Show |
chr10 | 73993116 | 74125169 |
| actghapid | grch38/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 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0071 | 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 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0216 | 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 | 0 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0219 | 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 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0234 | 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 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0001g0245 | 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 |
| a0001c0001t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0006g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0001t0023g0238 | 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 |
| a0001c0002t0001g0012 | 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 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0001g0119 | 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 |
| a0001c0002t0001g0232 | 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 |
| a0001c0002t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| 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 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0002t0003g0142 | 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 |
| a0001c0002t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0003g0246 | 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 |
| a0001c0002t0004g0206 | 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 |
| a0001c0002t0006g0067 | 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 |
| a0001c0002t0007g0240 | 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 |
| a0001c0002t0011g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0011g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0011g0005 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0002t0014g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0002t0015g0007 | 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 |
| a0001c0003t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0060 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0002g0085 | 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 |
| a0001c0003t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0003t0002g0134 | 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 |
| 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 |
| a0001c0003t0002g0176 | 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 |
| a0001c0003t0002g0215 | 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 |
| a0001c0003t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0008g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0009g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0009g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0009g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0009g0137 | 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 |
| a0001c0003t0021g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0003t0022g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0004t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0004t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0004t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0004t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0004t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0004t0002g0083 | 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 |
| a0001c0004t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0006t0005g0075 | 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 |
| a0001c0006t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0006t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0006t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0006t0005g0115 | 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 |
| a0001c0007t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0007t0004g0116 | 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 |
| a0001c0007t0013g0079 | 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 |
| a0001c0008t0001g0220 | 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 |
| a0001c0009t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0009t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0009t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0009t0002g0113 | 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 |
| a0001c0011t0006g0112 | 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 |
| a0001c0012t0016g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0001c0013t0005g0110 | 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 |
| a0002c0005t0010g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0002c0005t0010g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0002c0005t0010g0063 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0002c0015t0002g0084 | 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 |
| a0003c0010t0008g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0004c0014t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0005c0016t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0006c0019t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0007c0020t0015g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| a0008c0017t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | g0218 | 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 | g0133 | EUR | FIN | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00423 | hp2 | a0001 | c0002 | t0003 | g0124 | EAS | CHS | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00558 | hp1 | a0001 | c0003 | t0002 | g0058 | EAS | CHS | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00558 | hp2 | a0001 | c0001 | t0023 | g0238 | 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 | g0055 | EAS | CHS | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0236 | 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 | g0210 | 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 | g0005 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0163 | 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 | g0150 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG00741 | hp1 | a0001 | c0003 | t0002 | g0080 | 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 | g0151 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0101 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01074 | hp2 | a0001 | c0007 | t0003 | g0111 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01081 | hp1 | a0001 | c0007 | t0004 | g0116 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01081 | hp2 | a0001 | c0003 | t0002 | g0066 | 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 | g0072 | 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 | g0041 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0149 | 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 | g0229 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01192 | hp2 | a0001 | c0002 | t0003 | g0102 | AMR | PUR | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01243 | hp1 | a0001 | c0002 | t0006 | g0067 | 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 | g0056 | AMR | CLM | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0146 | 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 | g0103 | AMR | CLM | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01258 | hp2 | a0001 | c0003 | t0002 | g0134 | AMR | CLM | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0165 | 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 | g0147 | 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 | g0142 | AMR | CLM | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01433 | hp2 | a0001 | c0009 | t0002 | g0113 | AMR | CLM | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01496 | hp1 | a0001 | c0002 | t0003 | g0246 | AMR | CLM | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01496 | hp2 | a0001 | c0003 | t0002 | g0135 | 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 | g0244 | 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 | g0032 | AMR | PEL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01934 | hp2 | a0001 | c0002 | t0003 | g0033 | 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 | g0219 | AMR | PEL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01978 | hp1 | a0002 | c0005 | t0010 | g0063 | AMR | PEL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01978 | hp2 | a0001 | c0003 | t0009 | g0137 | AMR | PEL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG01981 | hp1 | a0001 | c0003 | t0002 | g0129 | 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 | g0069 | EAS | KHV | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02040 | hp1 | a0001 | c0003 | t0002 | g0215 | 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 | g0040 | 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 | a0004 | c0014 | t0002 | g0096 | EAS | KHV | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02071 | hp1 | a0001 | c0003 | t0002 | g0073 | 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 | g0052 | EAS | KHV | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0061 | 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 | g0212 | EAS | KHV | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02135 | hp1 | a0001 | c0002 | t0003 | g0065 | EAS | KHV | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02135 | hp2 | a0001 | c0001 | t0006 | g0233 | 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 | g0232 | 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 | g0130 | 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 | g0002 | 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 | a0005 | c0016 | t0002 | g0136 | 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 | g0148 | 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 | g0117 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0164 | 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 | g0079 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02615 | hp2 | a0006 | c0019 | t0002 | g0094 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02622 | hp1 | a0001 | c0006 | t0005 | g0077 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0119 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02630 | hp1 | a0001 | c0006 | t0005 | g0075 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02698 | hp1 | a0001 | c0002 | t0003 | g0036 | 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 | g0003 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02717 | hp2 | a0001 | c0006 | t0005 | g0086 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02723 | hp1 | a0001 | c0009 | t0002 | g0011 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02723 | hp2 | a0001 | c0009 | t0002 | g0076 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02809 | hp1 | a0001 | c0006 | t0005 | g0078 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02809 | hp2 | a0001 | c0002 | t0015 | g0007 | 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 | g0015 | 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 | g0115 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02896 | hp2 | a0001 | c0002 | t0004 | g0206 | AFR | GWD | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02897 | hp1 | a0001 | c0006 | t0005 | g0114 | 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 | g0004 | AFR | ESN | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02922 | hp2 | a0001 | c0004 | t0002 | g0057 | AFR | ESN | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02965 | hp1 | a0001 | c0004 | t0002 | g0083 | 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 | g0074 | AFR | ESN | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02976 | hp2 | a0001 | c0004 | t0008 | g0013 | 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 | g0220 | 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 | g0109 | AFR | MSL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03209 | hp2 | a0001 | c0002 | t0014 | g0228 | 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 | a0007 | c0020 | t0015 | g0006 | 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 | g0049 | 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 | g0014 | AFR | ESN | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03540 | hp1 | a0001 | c0013 | t0005 | g0110 | 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 | g0045 | 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 | g0240 | SAS | PJL | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03710 | hp1 | a0001 | c0003 | t0002 | g0064 | 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 | g0144 | SAS | BEB | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03831 | hp2 | a0001 | c0003 | t0002 | g0043 | SAS | BEB | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG03942 | hp2 | a0001 | c0003 | t0002 | g0082 | 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 | g0231 | SAS | STU | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG04199 | hp2 | a0008 | c0017 | t0002 | g0059 | 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 | g0126 | SAS | STU | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18906 | hp1 | a0001 | c0011 | t0006 | g0112 | 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 | g0050 | 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 | g0070 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0237 | 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 | g0048 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0224 | 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 | g0213 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18971 | hp2 | a0001 | c0003 | t0008 | g0042 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18973 | hp1 | a0003 | c0010 | t0008 | g0175 | 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 | g0217 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18983 | hp2 | a0001 | c0003 | t0002 | g0047 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0071 | 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 | g0239 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18998 | hp1 | a0001 | c0003 | t0002 | g0176 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA18998 | hp2 | a0001 | c0003 | t0002 | g0035 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0245 | 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 | g0227 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19004 | hp2 | a0001 | c0003 | t0002 | g0054 | 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 | g0034 | 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 | g0084 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19060 | hp2 | a0001 | c0003 | t0009 | g0037 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19063 | hp1 | a0001 | c0003 | t0009 | g0081 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19070 | hp1 | a0001 | c0003 | t0002 | g0085 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19070 | hp2 | a0001 | c0003 | t0002 | g0242 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0031 | 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 | g0214 | 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 | g0051 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19082 | hp1 | a0001 | c0003 | t0002 | g0053 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0241 | 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 | g0038 | 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 | g0216 | EAS | JPT | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA19091 | hp1 | a0002 | c0005 | t0010 | g0062 | 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 | g0118 | 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 | g0125 | AFR | ASW | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0143 | 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 | g0234 | SAS | GIH | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02486 | hp1 | a0001 | c0009 | t0002 | g0108 | AFR | ACB | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| HG02486 | hp2 | a0001 | c0004 | t0002 | g0044 | 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 | g0039 | 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 | a0001 | c0001 | t0001 | g0155 | REF | REF | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0002 | g0060 | REF | REF | VCL_chr10_73993116_74125169 | VCL | chr10 | 73993116 | 74125169 |
| view | 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 | a0007 | 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 | a0006 | 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 | a0008 | 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 | a0005 | 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 | a0004 | 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 |
| view | 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 | a0001c0007 a0001c0009 a0001c0012 others(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 | a0001c0007 a0001c0009 a0001c0012 others(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 | a0001c0004 a0001c0006 a0001c0009 others(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 | a0001c0004 a0001c0006 a0001c0009 others(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 | a0001c0001 a0001c0012 |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): 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 | a0001c0001 a0001c0002 a0001c0006 others(7): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): 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 |
| view | 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 | a0001c0002t0005 a0001c0006t0005 a0001c0006t0017 others(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 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(15): Show |
122 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(119): 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 | a0001c0007t0013 a0001c0007t0018 |
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 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(28): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(170): 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 | a0001c0002t0003 a0001c0002t0005 a0001c0002t0011 others(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 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0005 others(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 | a0001c0001t0001 a0001c0001t0023 a0001c0001t0024 others(6): Show |
95 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(92): 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 | a0001c0003t0008 a0001c0004t0008 a0001c0007t0018 others(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 | a0001c0002t0003 a0001c0002t0011 a0001c0002t0012 others(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 | a0001c0002t0015 a0007c0020t0015 |
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 | a0001c0002t0011 a0001c0002t0012 a0001c0002t0019 others(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 | a0001c0002t0003 a0001c0007t0003 a0001c0018t0003 |
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 |
| view | 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 | a0001c0001t0004g0004 a0001c0002t0003g0001 a0001c0002t0011g0002 others(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 | a0001c0001t0001g0199 a0001c0001t0001g0204 a0001c0001t0001g0207 others(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 | a0001c0001t0001g0199 a0001c0001t0001g0204 a0001c0001t0001g0207 others(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 | a0001c0002t0001g0012 a0001c0002t0014g0010 a0001c0004t0008g0013 others(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 | a0001c0001t0001g0178 a0001c0001t0001g0199 a0001c0001t0001g0204 others(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 | 64 | a0001c0001t0001g0122 a0001c0001t0001g0131 a0001c0001t0001g0132 others(61): Show |
64 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(61): 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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(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 | a0001c0002t0001g0012 a0001c0002t0001g0200 a0001c0002t0003g0020 others(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 | a0001c0001t0004g0004 a0001c0002t0003g0001 a0001c0002t0011g0002 others(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 | a0001c0001t0001g0178 a0001c0001t0001g0204 a0001c0002t0007g0167 others(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 | 37 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(34): Show |
37 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(34): 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 | a0001c0002t0020g0256 a0001c0011t0006g0255 |
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 | a0001c0002t0020g0256 a0001c0011t0006g0255 |
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 | a0001c0004t0002g0183 a0001c0006t0005g0184 a0001c0006t0005g0192 |
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 | a0001c0002t0003g0020 a0001c0002t0003g0101 a0001c0002t0003g0102 others(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 | a0001c0002t0001g0194 a0001c0002t0004g0195 a0001c0002t0012g0198 others(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 | a0001c0001t0001g0178 a0001c0001t0001g0199 a0001c0001t0001g0204 others(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 | a0001c0001t0004g0004 a0001c0002t0003g0001 a0001c0002t0011g0002 others(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 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
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 | a0001c0001t0001g0178 a0001c0001t0001g0199 a0001c0001t0001g0204 others(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 | a0001c0002t0020g0256 a0001c0011t0006g0255 |
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 | a0001c0001t0004g0004 a0001c0002t0001g0012 a0001c0002t0003g0001 others(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 | a0001c0001t0001g0252 a0001c0002t0003g0097 a0001c0002t0003g0127 others(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 | a0001c0001t0001g0160 a0001c0001t0004g0004 a0001c0002t0003g0001 others(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 | a0001c0001t0004g0004 a0001c0002t0003g0001 a0001c0002t0011g0002 others(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 | a0001c0001t0004g0004 a0001c0002t0003g0001 a0001c0002t0011g0002 others(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 | a0001c0002t0001g0194 a0001c0002t0004g0195 |
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 | a0004c0014t0002g0096 | 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 | a0001c0002t0001g0012 a0001c0002t0014g0010 a0001c0004t0008g0013 others(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 | 166 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(163): 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 | a0001c0002t0004g0188 a0001c0002t0004g0189 |
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 | a0001c0001t0001g0199 a0001c0001t0001g0204 a0001c0001t0001g0207 others(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 | a0001c0002t0020g0256 a0001c0011t0006g0255 |
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 | a0001c0001t0004g0004 a0001c0002t0003g0001 a0001c0002t0011g0002 others(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 | a0001c0007t0004g0120 a0001c0007t0004g0121 |
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 | a0001c0001t0001g0178 a0001c0002t0001g0194 a0001c0002t0004g0195 others(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 | a0001c0004t0002g0183 a0001c0006t0005g0184 a0001c0006t0005g0192 |
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 | a0006c0019t0002g0094 | 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 | a0001c0001t0001g0105 a0001c0002t0003g0028 a0002c0005t0002g0026 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(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 | a0001c0001t0001g0178 a0001c0002t0007g0167 a0001c0002t0007g0177 others(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 | a0001c0002t0020g0256 a0001c0011t0006g0255 |
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 | a0001c0001t0001g0178 a0001c0001t0001g0199 a0001c0001t0001g0204 others(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 | a0001c0001t0001g0178 a0001c0001t0001g0199 a0001c0001t0001g0204 others(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 | a0001c0002t0001g0194 a0001c0002t0004g0195 |
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 | a0001c0001t0001g0031 a0001c0001t0001g0199 a0001c0001t0001g0207 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0138 a0001c0002t0004g0206 others(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 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0002t0001g0012 others(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 | a0001c0004t0002g0183 a0001c0006t0005g0184 a0001c0006t0005g0192 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0051 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0105 a0001c0001t0001g0133 others(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 | a0001c0001t0001g0132 a0001c0002t0005g0187 a0001c0002t0012g0191 others(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 | a0001c0002t0003g0021 a0001c0002t0003g0124 a0001c0002t0006g0067 others(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 | a0001c0003t0009g0197 a0001c0018t0003g0196 |
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 | a0001c0002t0003g0091 a0001c0003t0002g0092 a0003c0010t0008g0088 others(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 | a0001c0001t0001g0178 a0001c0002t0007g0167 a0001c0002t0007g0168 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0002t0003g0087 |
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 | a0001c0001t0004g0004 a0001c0002t0001g0194 a0001c0002t0003g0001 others(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 | a0001c0001t0001g0178 a0001c0001t0001g0199 a0001c0001t0001g0204 others(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 | a0001c0001t0004g0004 a0001c0002t0003g0001 a0001c0002t0011g0002 others(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 | a0001c0002t0001g0012 a0001c0002t0014g0010 a0001c0004t0008g0013 others(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 | a0001c0002t0012g0190 a0001c0002t0012g0191 a0001c0002t0012g0198 others(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 | a0001c0001t0004g0004 a0001c0002t0003g0001 a0001c0002t0011g0002 others(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 | a0001c0003t0002g0085 a0001c0003t0002g0092 a0002c0015t0002g0084 |
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 | a0001c0008t0001g0014 a0001c0008t0001g0015 a0001c0008t0001g0016 others(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 | a0001c0002t0003g0101 | 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 | a0001c0001t0001g0178 a0001c0002t0007g0167 a0001c0002t0007g0168 others(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 | a0001c0002t0001g0119 | 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 | a0001c0001t0001g0207 a0001c0003t0009g0197 a0001c0018t0003g0196 |
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 | a0001c0004t0002g0183 a0001c0006t0005g0184 a0001c0006t0005g0192 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0209 a0001c0001t0001g0229 others(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 | a0001c0001t0001g0122 a0001c0002t0003g0033 a0001c0002t0003g0087 others(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 | 70 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(67): Show |
70 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(67): 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 | a0001c0001t0004g0004 a0001c0002t0003g0001 a0001c0002t0004g0195 others(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 | a0001c0002t0004g0206 a0001c0008t0006g0201 a0001c0008t0006g0202 others(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 | a0001c0008t0001g0014 a0001c0008t0001g0015 a0001c0008t0001g0016 others(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 | a0001c0004t0002g0183 a0001c0006t0005g0184 a0001c0006t0005g0192 |
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 | a0001c0001t0001g0207 a0001c0003t0009g0197 a0001c0018t0003g0196 |
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 | 1 | a0001c0001t0001g0156 | 1 | HG03239.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 | a0001c0002t0012g0190 a0001c0002t0012g0191 a0001c0002t0012g0198 others(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 | a0001c0003t0022g0039 | 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 | a0001c0002t0003g0246 | 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 | 133 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(130): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(130): 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 | 149 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(146): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(146): 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 | a0001c0002t0012g0190 a0001c0002t0012g0191 a0001c0002t0012g0198 others(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 | a0001c0001t0001g0207 a0001c0003t0009g0197 a0001c0018t0003g0196 |
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 | 133 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(130): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(130): 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 | a0001c0002t0001g0012 a0001c0002t0014g0010 a0001c0004t0008g0013 others(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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0153 a0001c0001t0001g0156 a0001c0001t0001g0178 others(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 | a0001c0001t0001g0178 a0001c0002t0007g0167 a0001c0002t0007g0168 others(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 | a0001c0001t0001g0178 a0001c0002t0007g0167 a0001c0002t0007g0168 others(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 | a0001c0004t0002g0183 a0001c0006t0005g0184 a0001c0006t0005g0192 |
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 | a0001c0002t0012g0190 a0001c0002t0012g0191 a0001c0002t0012g0198 |
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 | a0001c0004t0002g0083 | 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 | 163 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(160): Show |
163 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(160): 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 | a0001c0002t0012g0190 a0001c0002t0012g0191 a0001c0002t0012g0198 |
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 | a0001c0008t0001g0014 | 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 | a0001c0001t0001g0207 a0001c0002t0004g0195 a0001c0003t0009g0197 others(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 | 151 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): 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 | a0001c0002t0001g0012 a0001c0002t0014g0010 a0001c0004t0008g0013 others(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 | a0001c0004t0002g0183 a0001c0006t0005g0184 a0001c0006t0005g0192 |
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 | 151 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): 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 | a0001c0003t0009g0137 | 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 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0005g0187 |
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 | a0001c0004t0002g0034 | 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 | a0001c0003t0002g0082 a0001c0006t0005g0078 a0001c0006t0005g0114 others(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 | a0001c0001t0001g0245 a0001c0001t0004g0004 a0001c0002t0003g0001 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0199 a0001c0001t0001g0208 others(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 | a0001c0001t0001g0204 a0001c0001t0001g0221 a0001c0001t0001g0222 others(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 | a0001c0002t0001g0012 a0001c0002t0001g0232 a0001c0002t0004g0188 others(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 | a0001c0002t0004g0189 a0001c0002t0004g0195 a0001c0002t0005g0187 others(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 | a0001c0001t0001g0207 a0001c0002t0012g0198 |
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 | a0001c0001t0001g0178 a0001c0002t0007g0167 a0001c0002t0007g0168 others(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 | 40 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(37): Show |
40 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(37): 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 | a0001c0001t0001g0162 a0001c0001t0001g0199 a0001c0001t0001g0204 others(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 | a0001c0006t0005g0077 | 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 | a0001c0001t0001g0162 a0001c0001t0001g0199 a0001c0001t0001g0204 others(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 | a0001c0007t0018g0100 a0001c0009t0002g0076 |
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 | a0001c0001t0001g0234 | 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 | a0001c0001t0004g0004 a0001c0002t0003g0001 a0001c0002t0011g0002 others(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 | 40 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(37): Show |
40 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(37): 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 | a0004c0014t0002g0096 | 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 | a0001c0001t0001g0221 a0001c0001t0001g0253 a0002c0005t0002g0249 |
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 | a0001c0001t0001g0162 a0001c0001t0001g0199 a0001c0001t0001g0204 others(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 | 40 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(37): Show |
40 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(37): 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 | 40 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(37): Show |
40 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(37): 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 | a0001c0001t0001g0163 a0001c0002t0004g0195 |
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 | a0001c0001t0001g0207 a0001c0001t0004g0004 a0001c0002t0003g0001 others(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 | a0001c0002t0012g0190 a0001c0002t0012g0191 a0001c0002t0012g0198 others(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 | a0001c0002t0003g0001 a0001c0002t0011g0008 |
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 | a0001c0001t0004g0004 | 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 | a0001c0001t0001g0138 a0001c0001t0001g0149 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0204 a0001c0001t0001g0209 a0001c0001t0001g0211 others(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 | a0001c0001t0001g0230 a0001c0002t0001g0118 a0001c0002t0007g0182 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0241 a0001c0003t0002g0085 others(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 | a0001c0001t0001g0213 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0219 others(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 | a0001c0001t0001g0263 a0001c0002t0011g0005 |
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 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0156 a0001c0002t0011g0002 a0001c0006t0017g0185 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0141 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0139 a0001c0001t0001g0145 a0001c0001t0001g0150 others(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 | a0007c0020t0015g0006 | 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 | a0001c0001t0001g0178 a0001c0002t0007g0167 a0001c0002t0007g0168 others(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(17): Show |
2 | a0001c0001t0024g0193 a0001c0002t0003g0166 |
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 | 151 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): 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 | a0001c0006t0005g0075 | 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 | a0001c0002t0012g0190 a0001c0002t0012g0191 a0001c0002t0012g0198 |
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 | a0001c0004t0002g0183 a0001c0006t0005g0184 a0001c0006t0005g0192 |
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 | a0001c0002t0012g0190 a0001c0002t0012g0191 a0001c0002t0012g0198 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0199 a0001c0001t0001g0204 others(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 | 170 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(167): Show |
170 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.168+20955A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74019330 | |||||||
| chr10:74019350 | T | C | 51 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(48): Show |
51 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.168+20975T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74019350 | |||||||
| chr10:74019393 | C | G | 40 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(37): Show |
40 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(37): 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 | a0001c0003t0002g0073 | 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 | a0001c0002t0004g0188 a0001c0002t0004g0189 |
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 | a0001c0003t0002g0073 | 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 | a0001c0002t0012g0190 a0001c0002t0012g0191 a0001c0002t0012g0198 |
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 | a0001c0003t0002g0040 a0001c0003t0002g0041 a0001c0003t0002g0080 |
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 | a0001c0003t0008g0042 | 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 | a0001c0002t0003g0097 a0001c0003t0002g0043 a0001c0003t0002g0080 others(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 | 32 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(29): 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 | a0001c0001t0001g0139 a0001c0001t0001g0164 a0001c0001t0001g0178 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0204 a0001c0001t0001g0207 others(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 | a0001c0001t0001g0199 a0001c0001t0001g0209 a0001c0001t0001g0210 others(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 | a0001c0006t0005g0115 a0001c0007t0003g0107 a0001c0007t0003g0111 others(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 | a0001c0001t0001g0178 a0001c0001t0001g0207 a0001c0002t0003g0001 others(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 | 139 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0131 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(136): 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 | a0001c0004t0002g0183 a0001c0006t0005g0184 a0001c0006t0005g0192 |
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 | 42 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(39): Show |
42 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(39): 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 | a0001c0001t0004g0004 | 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 | a0001c0004t0002g0034 | 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 | a0001c0004t0002g0186 a0001c0007t0003g0107 a0001c0007t0003g0111 others(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 | a0001c0002t0003g0125 | 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 | a0001c0003t0002g0070 | 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 | a0001c0004t0008g0013 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0162 others(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 | a0001c0008t0001g0015 a0001c0008t0001g0016 a0001c0008t0001g0017 |
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 | a0001c0001t0001g0178 a0001c0002t0001g0012 a0001c0002t0003g0001 others(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 | 103 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0131 others(100): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(100): 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 | a0001c0001t0001g0150 a0001c0002t0004g0188 a0001c0002t0004g0189 others(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 | 5 | a0001c0001t0001g0143 a0001c0001t0001g0156 a0001c0001t0001g0165 others(2): Show |
5 | HG01261.hp1 HG01433.hp1 HG02922.hp1 others(2): 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 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0162 others(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 | 164 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0131 others(161): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(161): 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 | a0001c0002t0004g0195 a0001c0004t0002g0186 a0001c0007t0003g0107 others(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 | a0001c0006t0005g0075 | 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 | 42 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(39): Show |
42 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.169-19501T>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 1/21 | chr10 | 74023582 | |||||||
| chr10:74023627 | C | T | 42 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(39): Show |
42 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(39): 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 | a0001c0002t0001g0012 a0001c0002t0014g0010 a0001c0004t0008g0013 |
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 | a0001c0001t0001g0138 a0001c0001t0001g0147 a0001c0001t0001g0149 others(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 | a0002c0015t0002g0084 | 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 | a0002c0015t0002g0084 | 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 | 167 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0131 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(164): 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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0002t0003g0101 a0001c0002t0003g0102 a0001c0002t0003g0103 others(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 | 135 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0131 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(132): 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 | a0001c0002t0020g0256 a0001c0011t0006g0255 |
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 | 164 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0131 others(161): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(161): 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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0004t0002g0183 a0001c0006t0005g0184 a0001c0006t0005g0192 |
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 | a0006c0019t0002g0094 | 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 | 91 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(88): Show |
91 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(88): 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 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0162 others(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 | a0001c0003t0002g0069 | 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 | a0001c0001t0001g0068 | 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 | a0001c0004t0002g0183 a0001c0006t0005g0184 a0001c0006t0005g0192 |
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 | a0001c0004t0002g0183 a0001c0006t0005g0184 a0001c0006t0005g0192 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0162 others(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 | a0001c0008t0006g0201 a0001c0008t0006g0202 a0001c0008t0006g0203 |
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 | 42 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(39): Show |
42 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(39): 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 | a0001c0002t0003g0091 a0001c0003t0008g0042 a0003c0010t0008g0088 others(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 | a0001c0001t0001g0131 a0001c0003t0002g0099 a0001c0006t0005g0184 others(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 | 40 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0138 others(37): Show |
40 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(37): 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 | a0001c0002t0005g0187 a0001c0002t0012g0190 a0001c0002t0012g0191 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0162 a0001c0001t0001g0199 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0204 a0001c0001t0001g0208 others(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 | a0001c0001t0001g0178 a0001c0002t0003g0021 a0001c0002t0003g0127 others(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 | a0001c0001t0001g0140 a0001c0001t0001g0147 a0001c0001t0001g0165 others(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 | 35 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(32): Show |
35 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(32): 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 | a0001c0001t0001g0051 a0001c0003t0002g0035 a0001c0003t0002g0050 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0162 others(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 | a0001c0001t0006g0233 a0001c0002t0003g0001 a0001c0002t0003g0028 others(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 | a0001c0003t0002g0064 a0001c0003t0002g0095 |
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 | a0001c0001t0001g0132 | 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 | a0001c0002t0001g0232 | 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 | a0001c0004t0002g0183 a0001c0006t0005g0184 a0001c0006t0005g0192 |
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 | a0001c0001t0001g0234 | 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 | a0001c0001t0001g0143 | 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 | a0001c0001t0001g0211 | 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 | a0001c0002t0011g0003 | 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 | a0007c0020t0015g0006 | 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 | a0001c0008t0001g0015 a0001c0008t0001g0016 a0001c0008t0001g0017 |
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 | a0001c0007t0013g0079 a0001c0009t0002g0011 |
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 | a0001c0001t0001g0146 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | a0001c0001t0001g0146 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | a0001c0008t0001g0015 a0001c0008t0001g0016 a0001c0008t0001g0017 |
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 | 42 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(39): Show |
42 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(39): 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 | a0001c0003t0002g0066 | 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 | a0001c0001t0001g0160 a0001c0001t0001g0178 a0001c0001t0001g0229 others(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 | 112 | a0001c0001t0001g0068 a0001c0001t0001g0071 a0001c0001t0001g0122 others(109): Show |
112 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(109): 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 | a0001c0001t0001g0031 | 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 | a0001c0003t0002g0066 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0068 others(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 | a0001c0002t0004g0189 a0001c0002t0005g0187 a0001c0002t0011g0002 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0002t0001g0119 | 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 | a0001c0002t0003g0001 a0001c0002t0004g0195 a0001c0002t0011g0002 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0208 a0001c0001t0001g0222 others(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 | a0001c0002t0007g0264 a0001c0002t0020g0256 a0001c0006t0005g0192 others(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 | 121 | a0001c0001t0001g0071 a0001c0001t0001g0131 a0001c0001t0001g0132 others(118): Show |
121 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(118): 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 | a0001c0001t0001g0178 a0001c0002t0003g0020 a0001c0002t0003g0021 others(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 | a0001c0001t0001g0178 a0001c0001t0001g0208 a0001c0002t0003g0023 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0144 a0001c0001t0001g0146 others(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 | a0001c0002t0005g0187 a0001c0003t0002g0173 |
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 | a0001c0002t0004g0195 a0001c0004t0002g0186 a0001c0007t0003g0107 others(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 | a0001c0008t0006g0201 a0001c0008t0006g0202 a0001c0008t0006g0203 |
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 | a0001c0002t0001g0012 a0001c0002t0005g0187 a0001c0002t0012g0190 others(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 | a0001c0004t0002g0057 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0162 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0162 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0162 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0162 others(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 | a0001c0001t0001g0038 a0002c0005t0010g0018 a0002c0005t0010g0062 others(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 | a0001c0001t0001g0239 a0001c0003t0002g0072 a0001c0003t0009g0137 others(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 | a0001c0004t0002g0083 | 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 | a0001c0003t0002g0085 a0001c0003t0002g0092 a0002c0015t0002g0084 |
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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0006t0005g0184 a0001c0006t0005g0192 |
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 | a0002c0005t0002g0026 a0002c0005t0010g0062 |
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 | a0001c0003t0009g0126 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0162 others(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 | a0001c0008t0001g0220 | 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 | a0001c0001t0006g0233 | 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 | a0001c0001t0001g0178 a0001c0002t0007g0167 a0001c0002t0007g0168 others(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 | a0001c0001t0023g0238 | 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 | a0001c0002t0020g0256 a0001c0011t0006g0255 |
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 | a0001c0002t0020g0256 a0001c0011t0006g0255 |
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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | 45 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(42): Show |
45 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(42): 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 | a0001c0004t0002g0044 a0001c0004t0002g0123 a0001c0006t0005g0077 others(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 | 105 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(102): Show |
105 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(102): 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 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0162 others(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 | a0001c0001t0001g0178 a0001c0002t0007g0167 a0001c0002t0007g0168 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0162 others(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 | a0001c0001t0001g0199 a0001c0001t0001g0212 a0001c0001t0001g0250 others(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 | a0001c0002t0003g0001 a0001c0002t0011g0008 |
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 | a0001c0001t0001g0199 a0001c0001t0001g0212 a0001c0001t0001g0250 others(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 | 165 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0131 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(162): 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 | a0001c0004t0002g0183 a0001c0006t0005g0184 a0001c0006t0005g0192 |
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 | a0001c0003t0002g0169 a0002c0005t0010g0171 |
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 | a0001c0002t0004g0188 a0001c0002t0004g0189 |
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 | a0001c0003t0002g0064 | 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 | a0001c0003t0002g0040 | 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 | a0001c0004t0002g0034 a0001c0004t0002g0074 |
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 | a0001c0001t0006g0233 | 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 | a0001c0002t0003g0055 | 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 | a0001c0001t0001g0212 | 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 | a0001c0008t0006g0201 a0001c0008t0006g0202 a0001c0008t0006g0203 |
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 | a0001c0001t0001g0178 a0001c0002t0004g0195 a0001c0002t0007g0167 others(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 | a0001c0007t0018g0100 a0001c0009t0002g0076 |
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 | a0001c0001t0001g0141 a0001c0001t0001g0153 a0001c0001t0001g0211 |
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 | a0001c0001t0001g0229 a0001c0004t0002g0186 a0001c0007t0003g0107 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0162 others(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 | a0001c0004t0002g0186 a0001c0007t0003g0107 a0001c0007t0003g0111 others(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 | 165 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0131 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(162): 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 | a0001c0001t0001g0071 | 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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0002t0020g0256 a0001c0011t0006g0255 |
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 | a0001c0001t0001g0178 a0001c0002t0007g0167 a0001c0002t0007g0168 others(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 | 45 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(42): Show |
45 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(42): 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 | a0001c0002t0005g0187 a0001c0002t0012g0190 a0001c0002t0012g0191 others(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 | 45 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(42): Show |
45 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(42): 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 | a0001c0002t0020g0256 a0001c0011t0006g0255 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0162 others(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 | a0001c0006t0005g0077 a0001c0006t0005g0078 a0001c0006t0005g0086 others(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 | a0001c0002t0020g0256 a0001c0011t0006g0255 |
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 | a0001c0004t0002g0183 a0001c0006t0005g0184 a0001c0006t0005g0192 |
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 | a0001c0001t0001g0229 a0001c0001t0001g0253 a0001c0001t0001g0254 |
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 | 45 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(42): Show |
45 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(42): 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 | a0001c0002t0005g0187 a0001c0002t0012g0190 a0001c0002t0012g0191 others(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 | a0001c0002t0005g0187 a0001c0002t0012g0190 a0001c0002t0012g0191 others(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 | a0001c0001t0001g0150 a0001c0001t0004g0151 |
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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0001t0006g0233 | 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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0002t0005g0187 a0001c0002t0012g0190 a0001c0002t0012g0191 others(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 | a0001c0002t0003g0101 | 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 | a0001c0003t0008g0042 | 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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0031 a0001c0001t0001g0051 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0105 a0001c0001t0001g0138 others(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 | a0001c0002t0001g0119 a0001c0002t0012g0190 a0001c0006t0005g0077 others(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 | a0001c0002t0005g0187 a0001c0002t0012g0191 a0001c0002t0012g0198 |
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 | a0001c0008t0001g0014 | 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 | 45 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(42): Show |
45 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(42): 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 | a0001c0004t0002g0044 a0001c0004t0002g0123 a0001c0006t0005g0077 others(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 | 46 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(43): Show |
46 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(43): 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 | a0001c0001t0001g0218 a0001c0001t0001g0243 a0001c0002t0005g0187 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0144 a0001c0001t0001g0153 others(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 | a0001c0003t0009g0197 a0001c0018t0003g0196 |
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 | a0006c0019t0002g0094 | 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 | a0001c0002t0012g0190 a0001c0002t0012g0191 a0001c0002t0012g0198 |
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 | 124 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0131 others(121): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(121): 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 | a0001c0002t0005g0187 a0001c0002t0012g0190 a0001c0002t0012g0191 others(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 | a0001c0006t0005g0184 a0001c0006t0005g0192 |
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 | 45 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(42): Show |
45 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(42): 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 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0162 others(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 | a0001c0002t0003g0033 a0001c0002t0003g0087 a0001c0002t0003g0097 |
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 | a0001c0006t0005g0114 a0001c0006t0005g0115 |
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 | a0001c0007t0004g0120 a0001c0007t0004g0121 |
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 | a0001c0003t0002g0050 | 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 | 44 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(41): Show |
44 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(41): 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 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0162 others(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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0178 a0001c0002t0007g0167 a0001c0002t0007g0168 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0162 others(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 | a0001c0002t0001g0251 a0001c0006t0005g0075 |
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 | a0001c0001t0001g0163 | 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 | a0001c0008t0001g0015 a0001c0008t0001g0016 a0001c0008t0001g0017 |
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 | a0001c0007t0013g0079 | 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 | a0001c0002t0004g0188 a0001c0002t0004g0189 |
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 | a0001c0001t0001g0213 a0001c0001t0001g0236 a0001c0001t0001g0237 others(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 | a0001c0001t0001g0217 | 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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0162 others(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 | a0001c0008t0001g0015 a0001c0008t0001g0016 a0001c0008t0001g0017 |
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 | a0001c0007t0013g0079 | 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 | a0001c0004t0002g0034 a0001c0004t0002g0074 |
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 | a0001c0002t0020g0256 a0001c0011t0006g0255 |
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 | a0001c0001t0001g0178 a0001c0002t0004g0195 a0001c0002t0007g0167 others(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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0002t0020g0256 a0001c0011t0006g0255 |
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 | a0001c0004t0002g0083 | 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 | a0001c0002t0005g0187 a0001c0002t0012g0190 a0001c0002t0012g0191 others(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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(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 | 101 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0131 others(98): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(98): 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 | a0001c0001t0001g0143 a0001c0001t0001g0150 a0001c0001t0001g0243 others(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 | a0001c0001t0001g0178 a0001c0002t0003g0001 a0001c0002t0004g0189 others(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 | a0001c0002t0004g0188 a0001c0002t0004g0189 |
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 | a0001c0007t0004g0120 a0001c0007t0004g0121 |
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 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0223 others(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 | 164 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0131 others(161): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(161): 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 | 165 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0131 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(162): 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 | a0001c0002t0004g0188 a0001c0002t0004g0189 |
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 | a0001c0001t0001g0218 | 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 | a0001c0002t0003g0061 a0001c0002t0003g0065 |
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 | a0001c0004t0002g0186 a0001c0007t0003g0107 a0001c0007t0003g0111 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0241 a0001c0001t0001g0253 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0138 others(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 | a0001c0001t0001g0210 a0001c0003t0002g0215 |
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 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
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 | a0001c0002t0005g0187 a0001c0002t0012g0190 a0001c0002t0012g0191 others(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 | a0001c0008t0001g0015 a0001c0008t0001g0016 a0001c0008t0001g0017 |
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 | a0001c0001t0004g0148 a0001c0002t0007g0182 a0001c0004t0002g0186 others(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 | 42 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(39): Show |
42 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(39): 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 | a0001c0002t0011g0002 a0001c0002t0011g0003 a0001c0002t0011g0005 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0162 a0001c0001t0001g0199 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0145 a0001c0001t0001g0150 others(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 | a0001c0004t0002g0183 a0001c0007t0003g0107 a0001c0007t0003g0111 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0178 a0001c0001t0001g0210 others(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 | a0001c0002t0012g0190 a0001c0002t0012g0191 a0001c0002t0012g0198 |
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 | a0001c0001t0001g0105 a0001c0002t0003g0036 a0001c0002t0003g0055 others(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 | a0001c0003t0002g0082 a0001c0007t0003g0107 a0001c0007t0003g0111 others(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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0002t0001g0232 | 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 | 108 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0131 others(105): Show |
108 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(105): 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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0001t0001g0217 | 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 | 45 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(42): Show |
45 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(42): 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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0001t0001g0178 a0001c0002t0007g0167 a0001c0002t0007g0168 others(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 | a0001c0008t0001g0015 a0001c0008t0001g0016 a0001c0008t0001g0017 |
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 | a0001c0008t0001g0014 a0001c0008t0001g0220 |
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 | a0001c0002t0020g0256 a0001c0011t0006g0112 a0001c0011t0006g0255 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0162 others(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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0003t0009g0197 a0001c0018t0003g0196 |
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 | a0001c0001t0001g0144 | 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 | 119 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0131 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(116): 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 | a0001c0007t0018g0100 a0001c0009t0002g0076 |
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 | 45 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(42): Show |
45 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(42): 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 | a0001c0002t0005g0187 a0001c0002t0012g0190 a0001c0002t0012g0191 others(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 | 45 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(42): Show |
45 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(42): 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 | a0001c0002t0020g0256 a0001c0011t0006g0255 |
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 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0005g0187 others(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 | a0001c0002t0004g0195 a0001c0002t0007g0167 a0001c0002t0007g0168 others(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 | a0001c0001t0001g0105 a0001c0002t0003g0028 a0001c0003t0002g0085 others(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 | 45 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(42): Show |
45 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(42): 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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0002t0007g0167 a0001c0002t0007g0168 a0001c0002t0007g0177 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(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 | a0001c0002t0003g0021 a0001c0002t0003g0055 |
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 | a0001c0001t0001g0051 a0001c0003t0002g0035 a0001c0003t0002g0053 others(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 | a0001c0002t0020g0256 a0001c0011t0006g0112 a0001c0011t0006g0255 |
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 | a0001c0001t0001g0211 | 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 | a0001c0001t0001g0231 | 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 | 158 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0132 others(155): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(155): 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 | a0001c0001t0001g0199 a0001c0001t0001g0257 a0001c0001t0006g0233 others(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 | a0004c0014t0002g0096 | 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 | a0001c0002t0003g0036 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.240-9718A>C | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74060952 | |||||||
| chr10:74061094 | G | A | 8 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0001t0001g0229 | 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 | 119 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0131 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(116): 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 | a0001c0001t0001g0158 a0001c0001t0004g0004 a0001c0002t0003g0001 others(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 | 109 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0131 others(106): Show |
109 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(106): 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 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0144 others(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 | a0001c0002t0020g0256 a0001c0011t0006g0112 a0001c0011t0006g0255 |
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 | 40 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0138 others(37): Show |
40 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.240-8354C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74062316 | |||||||
| chr10:74062367 | A | AT | 123 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0131 others(120): Show |
123 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(120): 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 | a0001c0001t0001g0164 a0001c0001t0001g0199 a0001c0001t0001g0222 others(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 | a0001c0002t0005g0187 a0001c0002t0012g0190 a0001c0002t0012g0191 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0004t0002g0057 | 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 | a0001c0003t0022g0039 | 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 | a0001c0001t0001g0213 a0001c0001t0001g0237 |
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 | a0001c0002t0006g0067 | 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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0002t0020g0256 a0001c0011t0006g0112 a0001c0011t0006g0255 |
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 | a0001c0002t0003g0001 a0001c0002t0005g0187 a0001c0002t0011g0002 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0002t0007g0167 a0001c0002t0007g0168 a0001c0002t0007g0177 others(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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0006t0005g0086 | 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 | a0001c0004t0008g0013 | 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 | a0001c0002t0020g0256 a0001c0011t0006g0112 a0001c0011t0006g0255 |
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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0002t0001g0012 a0001c0002t0014g0010 a0001c0007t0003g0107 others(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 | a0001c0003t0002g0035 | 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 | a0001c0006t0005g0078 | 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 | a0001c0002t0003g0020 a0001c0002t0003g0103 |
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 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0164 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0004t0002g0183 a0001c0006t0005g0184 a0001c0006t0005g0192 |
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 | a0001c0007t0013g0029 a0001c0007t0013g0079 a0001c0007t0018g0100 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0002t0007g0240 | 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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0002t0003g0033 a0001c0002t0003g0061 a0001c0002t0003g0065 others(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 | 39 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(36): Show |
39 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(36): 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 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0162 others(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 | a0001c0001t0001g0236 a0001c0001t0001g0250 a0001c0002t0001g0117 others(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 | a0001c0001t0001g0247 a0001c0002t0001g0251 |
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 | a0001c0002t0007g0167 a0001c0002t0007g0168 a0001c0002t0007g0177 others(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 | a0001c0007t0003g0111 a0001c0007t0013g0029 a0001c0007t0018g0100 others(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 | a0001c0002t0003g0102 a0001c0004t0002g0183 |
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 | a0001c0007t0003g0107 a0001c0007t0004g0116 a0001c0007t0004g0120 others(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 | a0001c0001t0001g0222 a0001c0002t0003g0125 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0132 others(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 | a0001c0002t0003g0125 a0001c0009t0002g0113 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0204 others(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 | a0001c0001t0001g0213 a0001c0001t0001g0219 a0001c0001t0001g0237 others(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 | a0001c0001t0001g0219 a0001c0001t0001g0245 a0001c0001t0001g0257 others(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 | 41 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(38): Show |
41 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(38): 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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0002t0007g0167 a0001c0002t0007g0168 a0001c0002t0007g0177 others(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 | a0002c0005t0010g0032 a0002c0005t0010g0063 |
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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | 131 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0131 others(128): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): 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 | a0001c0001t0001g0239 a0001c0001t0004g0004 a0001c0002t0001g0232 others(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 | a0001c0003t0002g0025 a0001c0003t0002g0066 |
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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0003t0008g0042 | 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 | a0001c0004t0002g0183 a0001c0006t0005g0184 a0001c0006t0005g0192 |
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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0002t0020g0256 a0001c0011t0006g0112 a0001c0011t0006g0255 |
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 | a0001c0002t0007g0167 a0001c0002t0007g0168 a0001c0002t0007g0177 others(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 | a0001c0002t0003g0020 a0001c0002t0003g0103 |
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 | a0001c0001t0001g0208 a0001c0001t0001g0229 a0001c0001t0001g0248 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0068 |
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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | 41 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(38): Show |
41 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.240-1586G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 2/21 | chr10 | 74069084 | |||||||
| chr10:74069165 | G | A | 107 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0131 others(104): Show |
107 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(104): 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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0164 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0002t0001g0012 a0001c0002t0014g0010 |
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 | a0001c0004t0002g0044 a0001c0004t0002g0049 a0001c0004t0002g0123 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0001t0001g0218 | 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 | a0001c0002t0003g0020 a0001c0002t0003g0103 |
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 | a0008c0017t0002g0059 | 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 | 2 | a0001c0001t0001g0156 a0001c0001t0001g0165 |
2 | HG01261.hp1 HG03239.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 | 152 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0131 others(149): Show |
152 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(149): 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 | a0001c0002t0007g0167 a0001c0002t0007g0168 a0001c0002t0007g0177 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0003t0002g0082 | 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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0001t0001g0257 a0001c0001t0001g0260 a0001c0007t0003g0107 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0002t0003g0061 a0001c0002t0003g0065 |
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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0006t0005g0077 a0001c0006t0005g0078 a0001c0006t0005g0086 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0003t0002g0073 | 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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0001t0001g0204 a0001c0007t0003g0107 a0001c0007t0003g0111 others(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 | a0001c0002t0004g0188 a0001c0002t0004g0189 |
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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0002t0005g0187 a0001c0002t0012g0190 a0001c0002t0012g0191 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0003t0002g0058 | 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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0001t0023g0238 | 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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0144 a0001c0001t0001g0153 others(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 | 41 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(38): Show |
41 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.783+1458G>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 6/21 | chr10 | 74076361 | |||||||
| chr10:74076375 | G | T | 142 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0131 others(139): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): 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 | a0001c0003t0022g0039 | 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 | a0001c0003t0009g0197 a0001c0004t0008g0013 a0001c0018t0003g0196 |
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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0008c0017t0002g0059 | 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 | a0001c0004t0002g0183 a0001c0006t0005g0184 a0001c0006t0005g0192 |
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 | a0001c0002t0003g0021 a0001c0002t0003g0055 |
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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | 157 | a0001c0001t0001g0071 a0001c0001t0001g0122 a0001c0001t0001g0131 others(154): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(154): 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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0002t0001g0012 a0001c0002t0014g0010 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0071 a0001c0001t0001g0122 others(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 | a0001c0003t0009g0197 a0001c0004t0008g0013 a0001c0018t0003g0196 |
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 | a0001c0002t0004g0188 a0001c0002t0004g0189 |
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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0213 a0001c0001t0001g0219 a0001c0001t0001g0236 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0068 |
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 | a0001c0007t0004g0120 a0001c0007t0004g0121 |
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 | a0001c0001t0001g0144 | 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 | a0001c0003t0002g0056 a0001c0003t0002g0072 a0001c0003t0002g0159 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0071 a0001c0001t0001g0122 others(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 | a0001c0002t0003g0001 a0001c0002t0004g0188 a0001c0002t0004g0189 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0009t0002g0011 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0051 others(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 | a0001c0002t0003g0244 | 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 | a0001c0013t0005g0110 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(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 | a0001c0003t0009g0197 a0001c0004t0008g0013 a0001c0018t0003g0196 |
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 | a0001c0002t0007g0167 a0001c0002t0007g0168 a0001c0002t0007g0177 others(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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0009t0002g0113 | 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 | a0001c0002t0003g0028 a0002c0005t0002g0026 a0002c0005t0002g0027 others(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 | a0001c0002t0001g0117 a0001c0002t0003g0246 a0001c0004t0002g0093 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(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 | a0001c0006t0005g0184 a0001c0006t0005g0192 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0071 a0001c0001t0001g0122 others(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 | a0001c0002t0007g0167 a0001c0002t0007g0168 a0001c0002t0007g0177 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0003t0009g0126 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0071 a0001c0001t0001g0122 others(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 | a0001c0004t0002g0057 | 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 | a0001c0003t0002g0066 | 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 | a0002c0005t0010g0018 a0002c0005t0010g0032 a0002c0005t0010g0062 others(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 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0223 others(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 | a0001c0002t0007g0167 a0001c0002t0007g0168 a0001c0002t0007g0177 others(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 | a0001c0001t0001g0208 a0001c0003t0002g0215 a0001c0003t0009g0197 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0071 a0001c0001t0001g0162 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0071 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0071 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0105 a0001c0001t0001g0160 others(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 | a0001c0002t0007g0167 a0001c0002t0007g0168 a0001c0002t0007g0177 others(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 | a0001c0007t0003g0107 a0001c0007t0003g0111 a0001c0007t0004g0116 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0071 a0001c0001t0001g0122 others(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 | a0001c0002t0011g0002 a0001c0002t0011g0003 a0001c0002t0011g0005 others(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 | ||||||
| chr10:74087765 | 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 | a0001c0001t0004g0151 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0071 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0003t0001g0128 |
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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0001t0001g0051 | 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 | a0001c0003t0002g0041 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0071 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(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 | a0001c0002t0005g0187 a0001c0002t0012g0190 a0001c0002t0012g0191 others(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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0001t0004g0151 | 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 | a0001c0002t0003g0001 a0001c0002t0005g0187 a0001c0002t0011g0002 others(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 | a0001c0002t0007g0177 a0001c0002t0007g0264 |
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 | a0001c0002t0007g0177 a0001c0002t0007g0264 |
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 | a0001c0002t0001g0012 a0001c0002t0001g0194 a0001c0002t0001g0200 others(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 | a0001c0006t0005g0075 a0001c0006t0005g0077 a0001c0006t0005g0078 others(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 | a0001c0002t0012g0190 a0001c0002t0012g0191 a0001c0002t0012g0198 |
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 | a0001c0007t0013g0029 a0001c0007t0013g0079 a0001c0007t0018g0100 |
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 | a0001c0006t0005g0075 a0001c0006t0005g0077 a0001c0006t0005g0078 others(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 | a0001c0004t0002g0034 a0001c0004t0002g0044 a0001c0004t0002g0049 others(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 | a0001c0002t0001g0012 a0001c0002t0001g0194 a0001c0002t0001g0200 |
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 | a0001c0009t0002g0076 | 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 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
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 | a0001c0006t0005g0075 a0001c0006t0005g0184 a0001c0006t0005g0192 others(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 | 87 | a0001c0001t0001g0038 a0001c0001t0001g0051 a0001c0001t0001g0071 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(84): 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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0001t0001g0071 a0001c0002t0001g0022 a0001c0002t0001g0119 others(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 | 76 | a0001c0001t0001g0051 a0001c0001t0001g0105 a0001c0001t0001g0122 others(73): Show |
76 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(73): 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 | a0001c0001t0001g0038 a0001c0001t0001g0138 a0001c0001t0001g0140 others(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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0004t0002g0044 a0001c0004t0002g0049 a0001c0004t0002g0057 others(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 | a0001c0006t0005g0075 a0001c0006t0005g0077 a0001c0006t0005g0078 others(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 | a0001c0001t0001g0138 a0001c0002t0005g0187 |
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 | a0001c0007t0013g0029 a0001c0007t0013g0079 a0001c0007t0018g0100 others(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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0004t0002g0034 a0001c0004t0002g0044 a0001c0004t0002g0049 others(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 | a0001c0009t0002g0076 | 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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0007c0020t0015g0006 | 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 | a0001c0002t0003g0061 a0001c0002t0003g0065 |
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 | a0001c0002t0003g0244 | 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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0006t0005g0075 a0001c0006t0005g0184 a0001c0006t0005g0192 others(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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0011t0006g0112 a0001c0011t0006g0255 |
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 | a0001c0002t0004g0188 a0001c0002t0004g0189 |
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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0002t0003g0001 a0001c0002t0005g0187 a0001c0002t0007g0167 others(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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | 159 | a0001c0001t0001g0038 a0001c0001t0001g0051 a0001c0001t0001g0071 others(156): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): 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 | a0001c0007t0013g0029 a0001c0007t0013g0079 a0001c0007t0018g0100 others(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 | a0001c0002t0003g0021 a0001c0002t0003g0028 a0001c0002t0003g0055 |
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 | a0001c0006t0005g0086 | 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 | a0002c0005t0002g0026 a0002c0005t0002g0027 a0002c0005t0002g0249 others(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 | 160 | a0001c0001t0001g0038 a0001c0001t0001g0051 a0001c0001t0001g0071 others(157): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1743+229C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 12/21 | chr10 | 74096084 | |||||||
| chr10:74096149 | A | ACTT | 158 | a0001c0001t0001g0038 a0001c0001t0001g0051 a0001c0001t0001g0071 others(155): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(155): 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 | a0001c0001t0001g0030 a0001c0006t0005g0075 a0001c0006t0005g0115 others(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 | a0001c0006t0005g0077 a0001c0006t0005g0078 a0001c0006t0005g0086 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0165 a0001c0001t0004g0004 |
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 | a0001c0002t0004g0195 a0001c0002t0006g0067 |
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 | a0001c0001t0001g0164 a0001c0001t0001g0226 |
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 | a0001c0001t0001g0146 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | a0001c0007t0013g0029 a0001c0007t0013g0079 a0001c0007t0018g0100 others(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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0002t0001g0117 a0001c0002t0001g0118 a0001c0002t0001g0119 others(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 | a0001c0002t0004g0195 a0001c0002t0005g0187 a0001c0002t0006g0067 others(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 | a0001c0004t0002g0186 a0001c0004t0002g0262 a0001c0009t0002g0181 |
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 | a0001c0002t0004g0195 a0001c0002t0006g0067 a0001c0007t0004g0120 others(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 | a0001c0002t0001g0118 | 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 | a0001c0004t0002g0034 a0001c0004t0002g0044 a0001c0004t0002g0049 others(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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0002t0003g0001 a0001c0002t0007g0167 a0001c0002t0007g0168 others(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 | a0001c0004t0002g0034 a0001c0004t0002g0044 a0001c0004t0002g0049 others(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 | a0001c0001t0001g0144 a0001c0001t0001g0149 a0001c0001t0001g0153 others(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 | 192 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(189): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(189): 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 | a0001c0007t0013g0079 | 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 | a0001c0002t0007g0167 a0001c0002t0007g0168 a0001c0002t0007g0177 others(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 | a0001c0002t0001g0117 a0001c0002t0001g0118 a0001c0002t0001g0119 others(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 | a0001c0001t0001g0178 a0001c0002t0001g0012 a0001c0002t0001g0022 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0138 a0001c0001t0001g0144 others(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 | a0001c0002t0001g0117 a0001c0002t0003g0001 a0001c0002t0003g0028 others(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 | a0001c0002t0007g0168 a0001c0002t0007g0177 a0001c0002t0007g0240 others(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 | a0001c0003t0002g0169 a0001c0003t0002g0170 a0001c0003t0002g0172 others(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 | a0001c0009t0002g0011 a0001c0009t0002g0108 a0001c0009t0002g0113 |
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 | a0001c0003t0002g0215 | 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 | a0001c0002t0003g0001 a0001c0002t0011g0002 a0001c0002t0011g0003 others(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 | a0001c0001t0001g0144 a0001c0001t0001g0230 a0001c0002t0007g0167 others(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 | a0001c0001t0001g0243 a0001c0006t0005g0075 a0001c0006t0005g0077 others(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 | 144 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(141): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.2022+809C>A | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 14/21 | chr10 | 74101906 | |||||||
| chr10:74102040 | AT | A | 172 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(169): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): 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 | a0001c0007t0013g0029 a0001c0007t0013g0079 a0001c0007t0018g0100 others(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 | a0001c0002t0003g0036 | 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 | a0001c0007t0013g0029 a0001c0007t0013g0079 a0001c0007t0018g0100 others(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 | a0001c0007t0004g0120 a0001c0007t0004g0121 |
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 | a0001c0001t0001g0141 a0001c0001t0001g0150 a0001c0001t0004g0151 |
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 | a0001c0001t0001g0237 a0001c0003t0002g0064 a0001c0004t0002g0083 others(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 | a0001c0007t0004g0120 a0001c0007t0004g0121 |
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 | 133 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0051 others(130): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(130): 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 | a0001c0002t0001g0117 | 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 | a0001c0001t0001g0144 | 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 | 161 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(158): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): 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 | a0001c0004t0002g0034 a0001c0004t0002g0044 a0001c0004t0002g0049 others(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 | a0001c0001t0001g0165 | 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 | a0001c0003t0002g0053 | 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 | a0001c0002t0005g0187 a0001c0004t0002g0034 a0001c0004t0002g0044 others(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 | a0001c0003t0002g0072 | 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 | a0001c0002t0003g0055 a0001c0002t0003g0087 a0001c0002t0003g0102 others(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 | a0001c0002t0003g0020 a0001c0002t0007g0180 a0001c0003t0002g0035 others(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 | 120 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(117): 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 | a0001c0002t0005g0187 a0001c0003t0002g0085 a0001c0003t0002g0215 others(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 | a0001c0004t0002g0034 a0001c0004t0002g0044 a0001c0004t0002g0049 others(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 | a0001c0003t0002g0045 | 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 | a0001c0002t0007g0240 | 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 | a0001c0002t0007g0240 | 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 | 109 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(106): Show |
109 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(106): 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 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0023 others(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 | a0001c0007t0013g0029 a0001c0007t0013g0079 a0001c0007t0018g0100 others(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 | 116 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.2559+502C>T | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 17/21 | chr10 | 74107856 | |||||||
| chr10:74107875 | T | C | 151 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): 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 | a0001c0002t0004g0188 a0001c0002t0004g0189 |
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 | a0001c0009t0002g0108 | 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 | a0001c0006t0005g0075 | 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 | 162 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(159): Show |
162 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(159): 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 | a0001c0007t0013g0029 a0001c0007t0013g0079 a0001c0007t0018g0100 others(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 | a0001c0003t0002g0130 | 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 | a0001c0001t0001g0234 | 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 | 93 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(90): Show |
93 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(90): 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 | a0001c0006t0005g0077 a0001c0006t0005g0078 a0001c0006t0005g0086 others(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 | 166 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(163): 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 | a0001c0004t0002g0034 a0001c0004t0002g0044 a0001c0004t0002g0049 others(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 | a0008c0017t0002g0059 | 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 | a0001c0002t0001g0012 a0001c0002t0001g0194 a0001c0002t0001g0200 |
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 | a0001c0002t0005g0187 a0001c0006t0005g0075 a0001c0006t0005g0077 others(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 | a0001c0002t0003g0001 a0001c0002t0003g0020 a0001c0002t0003g0021 others(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 | 117 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(114): Show |
117 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(114): 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 | a0001c0002t0004g0195 a0001c0002t0006g0067 |
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 | a0001c0002t0003g0125 a0001c0007t0003g0107 |
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 | 116 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(113): 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 | a0001c0001t0001g0229 | 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 | a0001c0006t0005g0184 a0001c0006t0005g0192 |
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 | a0001c0007t0013g0029 a0001c0007t0013g0079 a0001c0007t0018g0100 others(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 | a0001c0009t0002g0076 | 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 | a0001c0002t0004g0188 a0001c0002t0004g0189 |
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 | 139 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(136): 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 | a0001c0007t0013g0029 a0001c0007t0013g0079 a0001c0007t0018g0100 others(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 | 96 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(93): Show |
96 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(93): 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 | a0001c0001t0001g0211 a0001c0001t0001g0221 |
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 | a0001c0002t0005g0187 a0001c0006t0005g0075 a0001c0006t0005g0077 others(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 | 90 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(87): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(87): 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 | a0001c0001t0001g0234 | 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 | 109 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(106): Show |
109 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(106): 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 | a0001c0003t0002g0043 a0001c0003t0002g0069 a0001c0009t0002g0011 others(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 | a0001c0003t0002g0082 a0001c0003t0009g0126 a0001c0004t0002g0083 |
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 | a0001c0002t0005g0187 a0001c0006t0005g0075 a0001c0006t0005g0077 others(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 | a0001c0002t0003g0001 a0001c0002t0003g0020 a0001c0002t0003g0021 others(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 | 86 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(83): Show |
86 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(83): 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 | a0001c0001t0001g0146 a0001c0001t0001g0207 a0001c0002t0001g0117 others(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 | a0001c0002t0007g0167 a0001c0002t0007g0168 a0001c0002t0007g0177 others(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 | a0001c0002t0006g0067 | 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 | a0001c0007t0004g0120 a0001c0007t0004g0121 |
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 | a0001c0002t0005g0187 a0001c0004t0008g0013 a0001c0006t0005g0075 others(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 | a0001c0007t0013g0029 a0001c0007t0013g0079 a0001c0007t0018g0100 others(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 | a0001c0002t0003g0033 a0001c0002t0003g0087 a0001c0002t0003g0097 |
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 | a0001c0002t0001g0251 a0001c0002t0007g0167 a0001c0002t0007g0168 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0234 a0001c0002t0005g0187 others(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 | a0001c0001t0001g0243 a0001c0002t0003g0020 a0001c0002t0003g0021 others(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 | a0001c0007t0004g0120 a0001c0007t0004g0121 |
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 | a0001c0003t0002g0058 | 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 | 110 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): 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 | a0001c0001t0001g0160 a0001c0001t0001g0178 a0001c0001t0023g0238 |
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 | a0001c0007t0004g0120 a0001c0007t0004g0121 |
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 | a0001c0002t0003g0246 | 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 | 151 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.3258+1137A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74116036 | |||||||
| chr10:74116251 | C | T | 117 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(114): Show |
117 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(114): 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 | a0001c0001t0001g0224 a0001c0001t0001g0247 a0001c0001t0004g0214 |
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 | a0001c0003t0002g0035 a0001c0003t0002g0054 |
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 | a0001c0004t0002g0034 a0001c0004t0002g0044 a0001c0004t0002g0049 others(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 | a0001c0008t0001g0014 | 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 | 109 | a0001c0001t0001g0038 a0001c0001t0001g0051 a0001c0001t0001g0071 others(106): Show |
109 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(106): 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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0068 others(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 | a0001c0004t0002g0186 a0001c0004t0002g0262 a0001c0009t0002g0181 |
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 | a0001c0001t0001g0239 a0001c0002t0003g0001 a0001c0002t0003g0020 others(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 | a0001c0002t0005g0187 a0001c0006t0005g0075 a0001c0006t0005g0077 others(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 | a0001c0002t0005g0187 a0001c0006t0005g0075 a0001c0006t0005g0077 others(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 | a0001c0002t0005g0187 a0001c0006t0005g0075 a0001c0006t0005g0077 others(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 | a0001c0002t0012g0190 a0001c0002t0012g0191 a0001c0002t0012g0198 |
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 | 109 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(106): Show |
109 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.3259-636C>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74117387 | |||||||
| chr10:74117481 | C | G | 116 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(113): 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 | a0001c0003t0002g0085 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3259-16A>G | VCL | ENSG00000035403.18 | transcript | ENST00000211998.10 | protein_coding | 21/21 | chr10 | 74118007 |