Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 200403 |
|---|---|
| ensemblid | ENSG00000168658.20 |
| hgncid | 28385 |
| symbol | VWA3B |
| name | von Willebrand factor A domain containing 3B |
| refseq_nuc | NM_144992.5 |
| refseq_prot | NP_659429.4 |
| ensembl_nuc | ENST00000477737.6 |
| ensembl_prot | ENSP00000417955.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 98087167 |
| end | 98313299 |
| strand | + |
| ver | v1.2 |
| region | chr2:98087167-98313299 |
| region5000 | chr2:98082167-98318299 |
| regionname0 | VWA3B_chr2_98087167_98313299 |
| regionname5000 | VWA3B_chr2_98082167_98318299 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1294 | 96 | 19 | 19 | 44 | 3 | 10 | 30 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0002 | 0/0 | 1294 | 63 | 13 | 20 | 22 | 7 | 1 | 18 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0003 | 0/0 | 1294 | 30 | 10 | 4 | 14 | 1 | 1 | 10 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0004 | 0/0 | 1294 | 10 | 0 | 1 | 9 | 0 | 0 | 8 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0005 | 0/0 | 1294 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0006 | 0/0 | 1294 | 6 | 5 | 0 | 1 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0007 | 0/0 | 1294 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0008 | 0/0 | 1294 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0009 | 0/0 | 1294 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0010 | 0/0 | 1294 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0011 | 0/0 | 1294 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0012 | 0/0 | 218 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0013 | 0/0 | 1294 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0014 | 0/0 | 371 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0015 | 0/0 | 1294 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0016 | 0/0 | 1294 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0017 | 0/0 | 1294 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0018 | 1/0 | 1294 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0019 | 0/0 | 1294 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0020 | 0/0 | 742 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0021 | 0/0 | 1294 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0022 | 0/0 | 1294 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0023 | 0/0 | 1294 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0024 | 0/0 | 1294 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0025 | 0/0 | 1294 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0026 | 0/0 | 571 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 3885 | 85 | 16 | 15 | 41 | 3 | 9 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0002 | 0/0 | 3885 | 53 | 10 | 16 | 20 | 6 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0003 | 0/0 | 3885 | 28 | 9 | 4 | 14 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0004 | 0/0 | 3885 | 11 | 3 | 4 | 3 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0005 | 0/0 | 3885 | 10 | 0 | 1 | 9 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0006 | 0/0 | 3885 | 6 | 0 | 3 | 2 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0007 | 0/0 | 3885 | 6 | 5 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0008 | 0/0 | 3885 | 5 | 5 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0009 | 0/0 | 3885 | 4 | 0 | 4 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0010 | 0/0 | 3885 | 3 | 3 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0011 | 0/0 | 3885 | 2 | 0 | 2 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0012 | 0/0 | 3885 | 2 | 2 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0013 | 0/0 | 3885 | 2 | 0 | 0 | 0 | 1 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0014 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0015 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0016 | 0/0 | 3885 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0017 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0018 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0019 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0020 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0021 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0022 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0023 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0024 | 0/0 | 3885 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0025 | 1/0 | 3885 | 1 | 0 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0026 | 0/0 | 3885 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0027 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0028 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0029 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0030 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0031 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0032 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0033 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0034 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0035 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| c0036 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1180 | 79 | 6 | 19 | 39 | 4 | 9 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| t0002 | 0/0 | 1180 | 50 | 0 | 15 | 28 | 5 | 2 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| t0003 | 0/0 | 1180 | 43 | 17 | 8 | 13 | 3 | 2 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| t0004 | 0/0 | 1180 | 29 | 12 | 9 | 3 | 4 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| t0005 | 0/0 | 1180 | 7 | 7 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| t0006 | 0/0 | 1180 | 4 | 0 | 0 | 4 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| t0007 | 0/0 | 1180 | 3 | 0 | 0 | 3 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| t0008 | 0/0 | 1180 | 3 | 0 | 0 | 3 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| t0009 | 0/0 | 1181 | 3 | 3 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| t0010 | 0/0 | 1180 | 2 | 2 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| t0011 | 0/0 | 1182 | 2 | 2 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| t0012 | 0/0 | 1180 | 2 | 2 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| t0013 | 0/0 | 1180 | 2 | 2 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| t0014 | 0/0 | 1180 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| t0015 | 0/0 | 1180 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| t0016 | 0/0 | 1181 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| t0017 | 0/0 | 1181 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| t0018 | 0/0 | 1180 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| t0019 | 0/0 | 1145 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| t0020 | 0/0 | 1182 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| t0021 | 0/0 | 1180 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| t0022 | 0/0 | 1180 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| t0023 | 0/0 | 1180 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| t0024 | 0/0 | 1180 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0175 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0176 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3885 | 85 | 16 | 15 | 41 | 3 | 9 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0001c0004 | 0/0 | 3885 | 11 | 3 | 4 | 3 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0002c0002 | 0/0 | 3885 | 53 | 10 | 16 | 20 | 6 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0002c0006 | 0/0 | 3885 | 6 | 0 | 3 | 2 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0002c0012 | 0/0 | 3885 | 2 | 2 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0002c0016 | 0/0 | 3885 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0002c0019 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0003c0003 | 0/0 | 3885 | 28 | 9 | 4 | 14 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0003c0017 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0003c0032 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0004c0005 | 0/0 | 3885 | 10 | 0 | 1 | 9 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0005c0008 | 0/0 | 3885 | 5 | 5 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0005c0020 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0006c0007 | 0/0 | 3885 | 6 | 5 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0007c0009 | 0/0 | 3885 | 4 | 0 | 4 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0008c0010 | 0/0 | 3885 | 3 | 3 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0009c0011 | 0/0 | 3885 | 2 | 0 | 2 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0010c0013 | 0/0 | 3885 | 2 | 0 | 0 | 0 | 1 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0011c0015 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0011c0022 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0012c0035 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0012c0036 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0013c0014 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0014c0030 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0015c0029 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0016c0028 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0017c0027 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0018c0025 | 1/0 | 3885 | 1 | 0 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0019c0024 | 0/0 | 3885 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0020c0026 | 0/0 | 3885 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0021c0021 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0022c0023 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0023c0031 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0024c0034 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0025c0033 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0026c0018 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5064 | 67 | 6 | 13 | 35 | 3 | 9 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0001c0001t0002 | 0/0 | 5064 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0001c0001t0003 | 0/0 | 5064 | 6 | 5 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0001c0001t0005 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0001c0001t0006 | 0/0 | 5064 | 2 | 0 | 0 | 2 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0001c0001t0007 | 0/0 | 5064 | 3 | 0 | 0 | 3 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0001c0001t0010 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0001c0001t0013 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0001c0001t0015 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0001c0001t0016 | 0/0 | 5065 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0001c0001t0023 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0001c0004t0001 | 0/0 | 5064 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0001c0004t0003 | 0/0 | 5064 | 7 | 1 | 2 | 3 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0001c0004t0004 | 0/0 | 5064 | 2 | 1 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0001c0004t0013 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0002c0002t0001 | 0/0 | 5064 | 3 | 0 | 2 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0002c0002t0002 | 0/0 | 5064 | 26 | 0 | 8 | 16 | 2 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0002c0002t0003 | 0/0 | 5064 | 2 | 1 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0002c0002t0004 | 0/0 | 5064 | 17 | 7 | 5 | 0 | 4 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0002c0002t0008 | 0/0 | 5064 | 3 | 0 | 0 | 3 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0002c0002t0021 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0002c0002t0024 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0002c0006t0002 | 0/0 | 5064 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0002c0006t0004 | 0/0 | 5064 | 5 | 0 | 3 | 2 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0002c0012t0004 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0002c0012t0011 | 0/0 | 5066 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0002c0016t0020 | 0/0 | 5066 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0002c0019t0011 | 0/0 | 5066 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0003c0003t0001 | 0/0 | 5064 | 3 | 0 | 0 | 3 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0003c0003t0003 | 0/0 | 5064 | 18 | 4 | 4 | 9 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0003c0003t0005 | 0/0 | 5064 | 5 | 5 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0003c0003t0006 | 0/0 | 5064 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0003c0003t0018 | 0/0 | 5064 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0003c0017t0005 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0003c0032t0003 | 0/0 | 5064 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0004c0005t0002 | 0/0 | 5064 | 10 | 0 | 1 | 9 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0005c0008t0003 | 0/0 | 5064 | 5 | 5 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0005c0020t0003 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0006c0007t0002 | 0/0 | 5064 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0006c0007t0004 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0006c0007t0009 | 0/0 | 5065 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0006c0007t0012 | 0/0 | 5064 | 2 | 2 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0006c0007t0019 | 0/0 | 5029 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0007c0009t0002 | 0/0 | 5064 | 4 | 0 | 4 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0008c0010t0004 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0008c0010t0009 | 0/0 | 5065 | 2 | 2 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0009c0011t0001 | 0/0 | 5064 | 2 | 0 | 2 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0010c0013t0002 | 0/0 | 5064 | 2 | 0 | 0 | 0 | 1 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0011c0015t0001 | 0/0 | 5064 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0011c0022t0003 | 0/0 | 5064 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0012c0035t0004 | 0/0 | 5064 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0012c0036t0003 | 0/0 | 5064 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0013c0014t0017 | 0/0 | 5065 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0014c0030t0002 | 0/0 | 5064 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0015c0029t0004 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0016c0028t0002 | 0/0 | 5064 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0017c0027t0002 | 0/0 | 5064 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0018c0025t0001 | 1/0 | 5064 | 1 | 0 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0019c0024t0001 | 0/0 | 5064 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0020c0026t0002 | 0/0 | 5064 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0021c0021t0003 | 0/0 | 5064 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0022c0023t0002 | 0/0 | 5064 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0023c0031t0014 | 0/0 | 5064 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0024c0034t0022 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0025c0033t0006 | 0/0 | 5064 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| a0026c0018t0010 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | copy fasta | chr2 | 98082167 | 98318299 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0176 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0006g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0007g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0007g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0007g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0010g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0013g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0015g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0016g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0001t0023g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0004t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0004t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0004t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0004t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0004t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0004t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0004t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0004t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0004t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0004t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0001c0004t0013g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0004g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0004g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0004g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0004g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0004g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0004g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0004g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0008g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0008g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0008g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0021g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0002t0024g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0006t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0006t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0006t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0006t0004g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0006t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0006t0004g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0012t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0012t0011g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0016t0020g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0002c0019t0011g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0003t0018g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0017t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0003c0032t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0004c0005t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0004c0005t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0004c0005t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0004c0005t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0004c0005t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0004c0005t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0004c0005t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0004c0005t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0004c0005t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0004c0005t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0005c0008t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0005c0008t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0005c0008t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0005c0008t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0005c0008t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0005c0020t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0006c0007t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0006c0007t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0006c0007t0009g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0006c0007t0012g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0006c0007t0012g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0006c0007t0019g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0007c0009t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0007c0009t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0007c0009t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0007c0009t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0008c0010t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0008c0010t0009g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0008c0010t0009g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0009c0011t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0009c0011t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0010c0013t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0010c0013t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0011c0015t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0011c0022t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0012c0035t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0012c0036t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0013c0014t0017g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0014c0030t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0015c0029t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0016c0028t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0017c0027t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0018c0025t0001g0175 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0019c0024t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0020c0026t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0021c0021t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0022c0023t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0023c0031t0014g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0024c0034t0022g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0025c0033t0006g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| a0026c0018t0010g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0014 | c0030 | t0002 | g0120 | EUR | GBR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00140 | hp2 | a0002 | c0002 | t0004 | g0033 | EUR | GBR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00280 | hp1 | a0011 | c0015 | t0001 | g0112 | EUR | FIN | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0219 | EUR | FIN | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00323 | hp1 | a0011 | c0022 | t0003 | g0038 | EUR | FIN | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00323 | hp2 | a0002 | c0006 | t0002 | g0113 | EUR | FIN | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00408 | hp1 | a0004 | c0005 | t0002 | g0185 | EAS | CHS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00423 | hp1 | a0003 | c0003 | t0018 | g0081 | EAS | CHS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | CHS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00609 | hp1 | a0002 | c0002 | t0008 | g0177 | EAS | CHS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00609 | hp2 | a0012 | c0035 | t0004 | g0064 | EAS | CHS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0169 | EAS | CHS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0094 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00673 | hp1 | a0003 | c0003 | t0003 | g0066 | EAS | CHS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00733 | hp1 | a0002 | c0002 | t0004 | g0035 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00733 | hp2 | a0002 | c0006 | t0004 | g0021 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0174 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0223 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0173 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01070 | hp1 | a0002 | c0002 | t0004 | g0037 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0222 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01071 | hp1 | a0007 | c0009 | t0002 | g0091 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01071 | hp2 | a0002 | c0002 | t0004 | g0036 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01081 | hp1 | a0007 | c0009 | t0002 | g0092 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01081 | hp2 | a0001 | c0004 | t0003 | g0010 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0180 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01167 | hp1 | a0019 | c0024 | t0001 | g0103 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0116 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01175 | hp2 | a0003 | c0003 | t0003 | g0068 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0224 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01243 | hp2 | a0020 | c0026 | t0002 | g0210 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01255 | hp1 | a0002 | c0002 | t0004 | g0032 | AMR | CLM | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01255 | hp2 | a0009 | c0011 | t0001 | g0213 | AMR | CLM | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01257 | hp1 | a0007 | c0009 | t0002 | g0140 | AMR | CLM | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01257 | hp2 | a0001 | c0004 | t0004 | g0023 | AMR | CLM | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01258 | hp1 | a0007 | c0009 | t0002 | g0139 | AMR | CLM | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01258 | hp2 | a0009 | c0011 | t0001 | g0171 | AMR | CLM | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01261 | hp1 | a0003 | c0003 | t0003 | g0072 | AMR | CLM | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01261 | hp2 | a0002 | c0002 | t0003 | g0024 | AMR | CLM | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01346 | hp1 | a0004 | c0005 | t0002 | g0107 | AMR | CLM | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01346 | hp2 | a0003 | c0003 | t0003 | g0073 | AMR | CLM | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01358 | hp1 | a0002 | c0016 | t0020 | g0031 | AMR | CLM | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01358 | hp2 | a0002 | c0002 | t0004 | g0043 | AMR | CLM | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01361 | hp1 | a0003 | c0003 | t0003 | g0053 | AMR | CLM | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | CLM | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0102 | AMR | CLM | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01515 | hp1 | a0010 | c0013 | t0002 | g0141 | EUR | IBS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | IBS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01516 | hp1 | a0002 | c0002 | t0004 | g0041 | EUR | IBS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | IBS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01517 | hp1 | a0002 | c0002 | t0004 | g0039 | EUR | IBS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0178 | EUR | IBS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01891 | hp1 | a0006 | c0007 | t0009 | g0080 | AFR | ACB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01891 | hp2 | a0006 | c0007 | t0004 | g0067 | AFR | ACB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01952 | hp1 | a0001 | c0004 | t0001 | g0220 | AMR | PEL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02056 | hp1 | a0017 | c0027 | t0002 | g0084 | EAS | KHV | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02056 | hp2 | a0001 | c0004 | t0003 | g0013 | EAS | KHV | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02080 | hp1 | a0003 | c0003 | t0003 | g0052 | EAS | KHV | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0108 | EAS | KHV | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CDX | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CDX | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CDX | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02165 | hp2 | a0016 | c0028 | t0002 | g0085 | EAS | CDX | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02280 | hp2 | a0002 | c0019 | t0011 | g0228 | AFR | ACB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0221 | AMR | PEL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02293 | hp2 | a0001 | c0004 | t0003 | g0017 | AMR | PEL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02300 | hp2 | a0002 | c0006 | t0004 | g0019 | AMR | PEL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02572 | hp1 | a0003 | c0017 | t0005 | g0056 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02572 | hp2 | a0013 | c0014 | t0017 | g0126 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02615 | hp1 | a0005 | c0008 | t0003 | g0235 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02615 | hp2 | a0003 | c0003 | t0005 | g0058 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0045 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02647 | hp2 | a0002 | c0002 | t0004 | g0005 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02717 | hp1 | a0003 | c0003 | t0005 | g0079 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02717 | hp2 | a0003 | c0003 | t0003 | g0060 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02723 | hp1 | a0015 | c0029 | t0004 | g0046 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02723 | hp2 | a0003 | c0003 | t0003 | g0055 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02735 | hp1 | a0002 | c0002 | t0004 | g0030 | SAS | PJL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02886 | hp1 | a0003 | c0003 | t0005 | g0069 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02886 | hp2 | a0003 | c0003 | t0003 | g0048 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02895 | hp1 | a0001 | c0004 | t0003 | g0044 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02895 | hp2 | a0005 | c0020 | t0003 | g0230 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02896 | hp1 | a0002 | c0002 | t0004 | g0011 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02897 | hp2 | a0005 | c0008 | t0003 | g0231 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02922 | hp1 | a0006 | c0007 | t0012 | g0050 | AFR | ESN | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0238 | AFR | ESN | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02976 | hp1 | a0003 | c0003 | t0003 | g0054 | AFR | ESN | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02976 | hp2 | a0008 | c0010 | t0004 | g0227 | AFR | ESN | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03041 | hp1 | a0002 | c0002 | t0004 | g0022 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03041 | hp2 | a0002 | c0002 | t0003 | g0027 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03098 | hp1 | a0006 | c0007 | t0012 | g0051 | AFR | MSL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | MSL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03130 | hp1 | a0005 | c0008 | t0003 | g0233 | AFR | ESN | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03130 | hp2 | a0003 | c0003 | t0005 | g0057 | AFR | ESN | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03139 | hp1 | a0001 | c0001 | t0015 | g0134 | AFR | ESN | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03139 | hp2 | a0006 | c0007 | t0019 | g0059 | AFR | ESN | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ESN | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03195 | hp2 | a0008 | c0010 | t0009 | g0240 | AFR | ESN | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03209 | hp1 | a0001 | c0001 | t0013 | g0028 | AFR | MSL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | MSL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03225 | hp1 | a0002 | c0012 | t0011 | g0226 | AFR | MSL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03225 | hp2 | a0001 | c0001 | t0023 | g0009 | AFR | MSL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03486 | hp1 | a0002 | c0002 | t0024 | g0008 | AFR | MSL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03486 | hp2 | a0002 | c0002 | t0004 | g0003 | AFR | MSL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03540 | hp1 | a0005 | c0008 | t0003 | g0229 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03540 | hp2 | a0026 | c0018 | t0010 | g0129 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03579 | hp2 | a0002 | c0002 | t0004 | g0004 | AFR | MSL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03927 | hp2 | a0022 | c0023 | t0002 | g0154 | SAS | BEB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03942 | hp1 | a0003 | c0032 | t0003 | g0062 | SAS | BEB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | STU | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG04228 | hp2 | a0010 | c0013 | t0002 | g0104 | SAS | STU | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0128 | AFR | YRI | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18522 | hp2 | a0002 | c0002 | t0021 | g0006 | AFR | YRI | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18612 | hp2 | a0003 | c0003 | t0003 | g0070 | EAS | CHB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18906 | hp1 | a0024 | c0034 | t0022 | g0078 | AFR | YRI | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18906 | hp2 | a0005 | c0008 | t0003 | g0234 | AFR | YRI | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0194 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18941 | hp2 | a0001 | c0001 | t0016 | g0152 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18942 | hp1 | a0003 | c0003 | t0003 | g0049 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18942 | hp2 | a0004 | c0005 | t0002 | g0100 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18945 | hp1 | a0001 | c0001 | t0006 | g0181 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18945 | hp2 | a0001 | c0001 | t0007 | g0148 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18946 | hp1 | a0002 | c0006 | t0004 | g0016 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18948 | hp1 | a0004 | c0005 | t0002 | g0101 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18951 | hp1 | a0023 | c0031 | t0014 | g0097 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18951 | hp2 | a0001 | c0004 | t0003 | g0026 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18954 | hp1 | a0002 | c0006 | t0004 | g0015 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18959 | hp2 | a0003 | c0003 | t0001 | g0199 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18963 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18963 | hp2 | a0001 | c0001 | t0007 | g0146 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18977 | hp2 | a0003 | c0003 | t0003 | g0074 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18983 | hp1 | a0001 | c0001 | t0006 | g0198 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18983 | hp2 | a0002 | c0002 | t0008 | g0196 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18985 | hp1 | a0004 | c0005 | t0002 | g0124 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18985 | hp2 | a0003 | c0003 | t0003 | g0076 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0162 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18992 | hp2 | a0003 | c0003 | t0003 | g0071 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18995 | hp2 | a0002 | c0002 | t0008 | g0086 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18998 | hp2 | a0004 | c0005 | t0002 | g0093 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18999 | hp1 | a0004 | c0005 | t0002 | g0125 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0217 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19009 | hp2 | a0003 | c0003 | t0001 | g0202 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19064 | hp2 | a0012 | c0036 | t0003 | g0063 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19065 | hp1 | a0003 | c0003 | t0006 | g0200 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19065 | hp2 | a0004 | c0005 | t0002 | g0225 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19066 | hp2 | a0003 | c0003 | t0003 | g0075 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19074 | hp1 | a0001 | c0004 | t0003 | g0025 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19080 | hp1 | a0001 | c0001 | t0007 | g0147 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19080 | hp2 | a0004 | c0005 | t0002 | g0099 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0189 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19087 | hp1 | a0003 | c0003 | t0003 | g0065 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19087 | hp2 | a0006 | c0007 | t0002 | g0182 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19088 | hp1 | a0003 | c0003 | t0001 | g0201 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19088 | hp2 | a0004 | c0005 | t0002 | g0098 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19090 | hp1 | a0025 | c0033 | t0006 | g0214 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0197 | EUR | TSI | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA20752 | hp2 | a0021 | c0021 | t0003 | g0042 | EUR | TSI | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA20805 | hp1 | a0003 | c0003 | t0003 | g0077 | EUR | TSI | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA20805 | hp2 | a0002 | c0002 | t0004 | g0040 | EUR | TSI | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | GIH | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA20905 | hp2 | a0001 | c0004 | t0003 | g0020 | SAS | GIH | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01123 | hp1 | a0002 | c0006 | t0004 | g0237 | AMR | CLM | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02109 | hp1 | a0003 | c0003 | t0005 | g0061 | AFR | ACB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02109 | hp2 | a0002 | c0012 | t0004 | g0007 | AFR | ACB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02486 | hp1 | a0001 | c0004 | t0004 | g0018 | AFR | ACB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0047 | AFR | ACB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03471 | hp1 | a0008 | c0010 | t0009 | g0239 | AFR | MSL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG03471 | hp2 | a0001 | c0004 | t0013 | g0029 | AFR | MSL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG06807 | hp1 | a0002 | c0002 | t0004 | g0002 | AFR | USA | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | USA | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA20300 | hp1 | a0002 | c0002 | t0004 | g0014 | AFR | USA | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | USA | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0176 | REF | REF | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| homoSapiens_grch38 | hp1 | a0018 | c0025 | t0001 | g0175 | REF | REF | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:98093183
|
C | A | 1 | a0013 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.91C>A | p.Gln31Lys | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/28 | 320/5064 | 91/3885 | 31/1294 | chr2 | 98093183 | ||
| chr2:98119693
|
C | A | 1 | a0026 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.472C>A | p.Leu158Met | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 4/28 | 701/5064 | 472/3885 | 158/1294 | chr2 | 98119693 | ||
| chr2:98119762
|
C | T | 5 | a0003a0006a0012others(2): Show | 40 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(37): Show |
missense_variant&splice_region_variant | MODERATE | c.541C>T | p.Arg181Trp | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 4/28 | 770/5064 | 541/3885 | 181/1294 | chr2 | 98119762 | ||
| chr2:98121411
|
G | T | 1 | a0012 | 2 | HG00609.hp2 NA19064.hp2 |
stop_gained | HIGH | c.655G>T | p.Glu219* | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/28 | 884/5064 | 655/3885 | 219/1294 | chr2 | 98121411 | ||
| chr2:98121421
|
G | A | 1 | a0009 | 2 | HG01255.hp2 HG01258.hp2 |
missense_variant | MODERATE | c.665G>A | p.Arg222His | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/28 | 894/5064 | 665/3885 | 222/1294 | chr2 | 98121421 | ||
| chr2:98128239
|
A | G | 1 | a0023 | 1 | NA18951.hp1 | missense_variant&splice_region_variant | MODERATE | c.703A>G | p.Ile235Val | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/28 | 932/5064 | 703/3885 | 235/1294 | chr2 | 98128239 | ||
| chr2:98162934
|
G | A | 1 | a0012 | 2 | HG00609.hp2 NA19064.hp2 |
missense_variant | MODERATE | c.1072G>A | p.Val358Met | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/28 | 1301/5064 | 1072/3885 | 358/1294 | chr2 | 98162934 | ||
| chr2:98162955
|
G | A | 2 | a0005a0008 | 9 | HG02615.hp1 HG02895.hp2 HG02897.hp2 others(6): Show |
missense_variant | MODERATE | c.1093G>A | p.Asp365Asn | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/28 | 1322/5064 | 1093/3885 | 365/1294 | chr2 | 98162955 | ||
| chr2:98162976
|
G | T | 1 | a0014 | 1 | HG00140.hp1 | stop_gained&splice_region_variant | HIGH | c.1114G>T | p.Glu372* | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/28 | 1343/5064 | 1114/3885 | 372/1294 | chr2 | 98162976 | ||
| chr2:98181046
|
C | T | 1 | a0024 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.1145C>T | p.Ser382Leu | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/28 | 1374/5064 | 1145/3885 | 382/1294 | chr2 | 98181046 | ||
| chr2:98181196
|
C | G | 1 | a0015 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.1295C>G | p.Ser432Cys | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/28 | 1524/5064 | 1295/3885 | 432/1294 | chr2 | 98181196 | ||
| chr2:98188030
|
C | T | 2 | a0016a0017 | 2 | HG02056.hp1 HG02165.hp2 |
missense_variant | MODERATE | c.1367C>T | p.Pro456Leu | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/28 | 1596/5064 | 1367/3885 | 456/1294 | chr2 | 98188030 | ||
| chr2:98192969
|
T | C | 3 | a0011a0021a0022 | 4 | HG00280.hp1 HG00323.hp1 HG03927.hp2 others(1): Show |
missense_variant | MODERATE | c.1538T>C | p.Ile513Thr | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 11/28 | 1767/5064 | 1538/3885 | 513/1294 | chr2 | 98192969 | ||
| chr2:98194469
|
C | T | 1 | a0026 | 1 | HG03540.hp2 | stop_gained | HIGH | c.1714C>T | p.Gln572* | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/28 | 1943/5064 | 1714/3885 | 572/1294 | chr2 | 98194469 | ||
| chr2:98228211
|
C | G | 15 | a0001a0003a0005others(12): Show | 150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
missense_variant | MODERATE | c.2029C>G | p.Leu677Val | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 15/28 | 2258/5064 | 2029/3885 | 677/1294 | chr2 | 98228211 | ||
| chr2:98230126
|
C | T | 1 | a0020 | 1 | HG01243.hp2 | stop_gained | HIGH | c.2227C>T | p.Gln743* | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/28 | 2456/5064 | 2227/3885 | 743/1294 | chr2 | 98230126 | ||
| chr2:98234687
|
C | G | 1 | a0016 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.2348C>G | p.Ser783Cys | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 17/28 | 2577/5064 | 2348/3885 | 783/1294 | chr2 | 98234687 | ||
| chr2:98234701
|
G | A | 1 | a0019 | 1 | HG01167.hp1 | missense_variant | MODERATE | c.2362G>A | p.Ala788Thr | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 17/28 | 2591/5064 | 2362/3885 | 788/1294 | chr2 | 98234701 | ||
| chr2:98234743
|
C | T | 1 | a0024 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.2404C>T | p.Arg802Trp | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 17/28 | 2633/5064 | 2404/3885 | 802/1294 | chr2 | 98234743 | ||
| chr2:98236669
|
C | T | 1 | a0025 | 1 | NA19090.hp1 | missense_variant | MODERATE | c.2612C>T | p.Pro871Leu | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/28 | 2841/5064 | 2612/3885 | 871/1294 | chr2 | 98236669 | ||
| chr2:98236710
|
G | A | 11 | a0001a0003a0005others(8): Show | 142 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(139): Show |
missense_variant | MODERATE | c.2653G>A | p.Val885Met | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/28 | 2882/5064 | 2653/3885 | 885/1294 | chr2 | 98236710 | ||
| chr2:98311966
|
C | G | 2 | a0010a0014 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
missense_variant | MODERATE | c.3669C>G | p.Asp1223Glu | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 27/28 | 3898/5064 | 3669/3885 | 1223/1294 | chr2 | 98311966 | ||
| chr2:98312031
|
G | A | 24 | a0001a0002a0003others(21): Show | 237 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(234): Show |
missense_variant&splice_region_variant | MODERATE | c.3734G>A | p.Arg1245Lys | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 27/28 | 3963/5064 | 3734/3885 | 1245/1294 | chr2 | 98312031 | ||
| chr2:98312294
|
C | T | 3 | a0004a0012a0023 | 12 | HG00408.hp1 HG00609.hp2 HG01346.hp1 others(9): Show |
missense_variant | MODERATE | c.3830C>T | p.Thr1277Ile | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 28/28 | 4059/5064 | 3830/3885 | 1277/1294 | chr2 | 98312294 | ||
| chr2:98313284
|
G | GA | 5 | a0001a0002a0006others(2): Show | 8 | HG01358.hp1 HG01891.hp1 HG02280.hp2 others(5): Show |
splice_region_variant | LOW | c.*947dupA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr2 | 98313284 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:98093221
|
T | C | 4 | a0001c0004a0002c0006a0002c0016others(1): Show | 19 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(16): Show |
synonymous_variant | LOW | c.129T>C | p.His43His | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/28 | 358/5064 | 129/3885 | 43/1294 | chr2 | 98093221 | ||
| chr2:98115692
|
T | C | 1 | a0003c0017 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.237T>C | p.Tyr79Tyr | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/28 | 466/5064 | 237/3885 | 79/1294 | chr2 | 98115692 | ||
| chr2:98128277
|
T | C | 1 | a0002c0019 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.741T>C | p.Pro247Pro | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/28 | 970/5064 | 741/3885 | 247/1294 | chr2 | 98128277 | ||
| chr2:98236475
|
C | T | 1 | a0026c0018 | 1 | HG03540.hp2 | splice_region_variant&synonymous_variant | LOW | c.2514C>T | p.His838His | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 18/28 | 2743/5064 | 2514/3885 | 838/1294 | chr2 | 98236475 | ||
| chr2:98290534
|
A | C | 3 | a0002c0012a0002c0016a0002c0019 | 4 | HG01358.hp1 HG02109.hp2 HG02280.hp2 others(1): Show |
synonymous_variant | LOW | c.3069A>C | p.Pro1023Pro | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/28 | 3298/5064 | 3069/3885 | 1023/1294 | chr2 | 98290534 | ||
| chr2:98300087
|
T | C | 1 | a0003c0032 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.3291T>C | p.Asp1097Asp | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/28 | 3520/5064 | 3291/3885 | 1097/1294 | chr2 | 98300087 | ||
| chr2:98300135
|
C | G | 1 | a0005c0020 | 1 | HG02895.hp2 | synonymous_variant | LOW | c.3339C>G | p.Val1113Val | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/28 | 3568/5064 | 3339/3885 | 1113/1294 | chr2 | 98300135 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:98087167
|
A | G | 2 | a0001c0001t0023a0002c0002t0024 | 2 | HG03225.hp2 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-229A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/28 | 5926 | chr2 | 98087167 | |||||
| chr2:98087196
|
G | T | 33 | a0001c0001t0003a0001c0001t0005a0001c0001t0013others(30): Show | 93 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(90): Show |
5_prime_UTR_variant | MODIFIER | c.-200G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/28 | 5897 | chr2 | 98087196 | |||||
| chr2:98087197
|
C | T | 2 | a0001c0001t0023a0002c0002t0024 | 2 | HG03225.hp2 HG03486.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-199C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/28 | chr2 | 98087197 | ||||||
| chr2:98312398
|
G | A | 1 | a0023c0031t0014 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*49G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 28/28 | 49 | chr2 | 98312398 | |||||
| chr2:98312434
|
C | T | 1 | a0024c0034t0022 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*85C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 28/28 | 85 | chr2 | 98312434 | |||||
| chr2:98312466
|
A | G | 35 | a0001c0001t0002a0001c0001t0010a0001c0001t0013others(32): Show | 97 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*117A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 28/28 | 117 | chr2 | 98312466 | |||||
| chr2:98312668
|
A | G | 1 | a0002c0002t0021 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*319A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 28/28 | 319 | chr2 | 98312668 | |||||
| chr2:98312745
|
A | AT | 3 | a0002c0012t0011a0002c0016t0020a0002c0019t0011 | 3 | HG01358.hp1 HG02280.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*396_*397insT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 28/28 | 397 | chr2 | 98312745 | |||||
| chr2:98312746
|
A | T | 31 | a0001c0001t0002a0001c0004t0004a0002c0002t0002others(28): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*397A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 28/28 | 397 | chr2 | 98312746 | |||||
| chr2:98312965
|
T | A | 4 | a0001c0001t0005a0001c0001t0015a0003c0003t0005others(1): Show | 8 | HG02109.hp1 HG02572.hp1 HG02615.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*616T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 28/28 | 616 | chr2 | 98312965 | |||||
| chr2:98313027
|
A | T | 4 | a0001c0001t0006a0003c0003t0006a0003c0003t0018others(1): Show | 5 | HG00423.hp1 NA18945.hp1 NA18983.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*678A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 28/28 | 678 | chr2 | 98313027 | |||||
| chr2:98313075
|
G | A | 1 | a0001c0001t0007 | 3 | NA18945.hp2 NA18963.hp2 NA19080.hp1 |
3_prime_UTR_variant | MODIFIER | c.*726G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 28/28 | 726 | chr2 | 98313075 | |||||
| chr2:98313108
|
ACAGGTCA others(28): Show |
A | 1 | a0006c0007t0019 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*760_*794delCAGGTC others(29): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 28/28 | 760 | chr2 | 98313108 | |||||
| chr2:98313149
|
C | T | 31 | a0001c0001t0002a0001c0004t0004a0002c0002t0002others(28): Show | 92 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*800C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 28/28 | 800 | chr2 | 98313149 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:98087409
|
C | T | 4 | a0001c0001t0003g0238a0002c0006t0004g0237a0008c0010t0009g0239others(1): Show | 4 | HG01123.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+46C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98087409 | ||||||
| chr2:98087436
|
G | C | 1 | a0002c0002t0002g0001 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-33+73G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98087436 | ||||||
| chr2:98087575
|
A | G | 13 | a0001c0001t0003g0232a0001c0001t0003g0236a0001c0001t0003g0238others(10): Show | 13 | HG02280.hp2 HG02615.hp1 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.-33+212A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98087575 | ||||||
| chr2:98087877
|
G | C | 81 | a0001c0001t0003g0012a0001c0001t0003g0034a0001c0001t0003g0047others(78): Show | 81 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.-33+514G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98087877 | ||||||
| chr2:98087915
|
C | T | 33 | a0003c0003t0003g0049a0003c0003t0003g0052a0003c0003t0003g0053others(30): Show | 33 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.-33+552C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98087915 | ||||||
| chr2:98087978
|
A | G | 1 | a0002c0012t0011g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-33+615A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98087978 | ||||||
| chr2:98088434
|
G | C | 1 | a0001c0001t0001g0082 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-33+1071G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98088434 | ||||||
| chr2:98088669
|
A | G | 4 | a0001c0001t0003g0047a0001c0001t0005g0045a0003c0003t0003g0048others(1): Show | 4 | HG02486.hp2 HG02647.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+1306A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98088669 | ||||||
| chr2:98088763
|
T | C | 1 | a0008c0010t0004g0227 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-33+1400T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98088763 | ||||||
| chr2:98088840
|
G | A | 1 | a0002c0019t0011g0228 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-33+1477G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98088840 | ||||||
| chr2:98089197
|
T | C | 1 | a0003c0003t0003g0049 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-33+1834T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98089197 | ||||||
| chr2:98089491
|
G | A | 1 | a0008c0010t0004g0227 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-33+2128G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98089491 | ||||||
| chr2:98089539
|
G | C | 1 | a0002c0012t0011g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-33+2176G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98089539 | ||||||
| chr2:98089541
|
C | T | 81 | a0001c0001t0003g0012a0001c0001t0003g0034a0001c0001t0003g0047others(78): Show | 81 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.-33+2178C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98089541 | ||||||
| chr2:98089658
|
TTTTCCAG others(23): Show |
T | 1 | a0001c0001t0001g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-33+2300_-33+2329d others(32): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 98089658 | |||||
| chr2:98089662
|
C | CCAGACAA others(22): Show |
7 | a0001c0001t0001g0088a0002c0002t0002g0087a0002c0002t0008g0086others(4): Show | 7 | HG00597.hp1 HG02056.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33+2347_-33+2375d others(31): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 98089662 | |||||
| chr2:98089662
|
C | CCAGACAA others(51): Show |
1 | a0006c0007t0012g0050 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-33+2318_-33+2375d others(60): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 98089662 | |||||
| chr2:98089662
|
CCAGACAA others(22): Show |
C | 2 | a0003c0003t0018g0081a0004c0005t0002g0225 | 2 | HG00423.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-33+2347_-33+2375d others(31): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 98089662 | |||||
| chr2:98089691
|
T | C | 1 | a0001c0001t0001g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-33+2328T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98089691 | ||||||
| chr2:98089752
|
C | A | 1 | a0001c0001t0001g0089 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-33+2389C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98089752 | ||||||
| chr2:98089769
|
G | A | 8 | a0001c0001t0023g0009a0002c0002t0004g0002a0002c0002t0004g0003others(5): Show | 8 | HG02109.hp2 HG02647.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33+2406G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98089769 | ||||||
| chr2:98089812
|
A | G | 2 | a0001c0001t0023g0009a0002c0002t0024g0008 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-33+2449A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98089812 | ||||||
| chr2:98089858
|
A | G | 81 | a0001c0001t0003g0012a0001c0001t0003g0034a0001c0001t0003g0047others(78): Show | 81 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.-33+2495A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98089858 | ||||||
| chr2:98089864
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-33+2501G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98089864 | ||||||
| chr2:98090213
|
C | G | 5 | a0001c0004t0001g0220a0002c0002t0002g0221a0002c0002t0002g0222others(2): Show | 5 | HG00741.hp1 HG01070.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-2848C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98090213 | ||||||
| chr2:98090404
|
C | T | 1 | a0002c0002t0002g0219 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-32-2657C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98090404 | ||||||
| chr2:98090589
|
G | A | 81 | a0001c0001t0003g0012a0001c0001t0003g0034a0001c0001t0003g0047others(78): Show | 81 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.-32-2472G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98090589 | ||||||
| chr2:98090699
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-32-2362T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98090699 | ||||||
| chr2:98090775
|
A | C | 5 | a0001c0001t0001g0088a0002c0002t0002g0087a0002c0002t0008g0086others(2): Show | 5 | HG00597.hp1 HG02056.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32-2286A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98090775 | ||||||
| chr2:98091009
|
C | T | 1 | a0001c0004t0003g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-32-2052C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98091009 | ||||||
| chr2:98091044
|
G | A | 1 | a0001c0004t0003g0010 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-32-2017G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98091044 | ||||||
| chr2:98091124
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-32-1937C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98091124 | ||||||
| chr2:98091346
|
G | C | 38 | a0001c0001t0001g0090a0001c0001t0001g0105a0001c0001t0001g0106others(35): Show | 38 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.-32-1715G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98091346 | ||||||
| chr2:98091766
|
T | G | 30 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(27): Show | 30 | HG00423.hp2 HG01099.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.-32-1295T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98091766 | ||||||
| chr2:98091811
|
C | T | 3 | a0003c0003t0005g0079a0006c0007t0009g0080a0024c0034t0022g0078 | 3 | HG01891.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-32-1250C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98091811 | ||||||
| chr2:98091812
|
A | G | 1 | a0002c0002t0002g0217 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-32-1249A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98091812 | ||||||
| chr2:98091912
|
T | C | 5 | a0001c0001t0001g0088a0002c0002t0002g0087a0002c0002t0008g0086others(2): Show | 5 | HG00597.hp1 HG02056.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32-1149T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98091912 | ||||||
| chr2:98091947
|
T | A | 36 | a0001c0001t0003g0012a0001c0001t0003g0034a0001c0001t0013g0028others(33): Show | 36 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.-32-1114T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98091947 | ||||||
| chr2:98092228
|
C | T | 1 | a0003c0003t0018g0081 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-32-833C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98092228 | ||||||
| chr2:98092381
|
A | G | 1 | a0002c0002t0004g0043 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-32-680A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98092381 | ||||||
| chr2:98092441
|
G | A | 23 | a0001c0001t0003g0012a0001c0001t0013g0028a0001c0001t0023g0009others(20): Show | 23 | HG00733.hp2 HG01081.hp2 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.-32-620G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98092441 | ||||||
| chr2:98092448
|
G | T | 1 | a0004c0005t0002g0125 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-32-613G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98092448 | ||||||
| chr2:98092814
|
T | TTG | 3 | a0002c0002t0021g0006a0002c0012t0004g0007a0006c0007t0009g0080 | 3 | HG01891.hp1 HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-32-245_-32-244dup others(2): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 98092814 | |||||
| chr2:98092814
|
T | TTGTA | 3 | a0001c0001t0001g0153a0001c0001t0001g0155a0022c0023t0002g0154 | 3 | HG02698.hp2 HG03927.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.-32-245_-32-242dup others(4): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 98092814 | |||||
| chr2:98092816
|
G | GTA | 52 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0133others(49): Show | 52 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.-32-202_-32-201dup others(2): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 98092816 | |||||
| chr2:98092816
|
G | GTATATA | 9 | a0001c0001t0001g0082a0001c0001t0001g0206a0001c0001t0001g0207others(6): Show | 9 | HG00621.hp1 HG00673.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.-32-206_-32-201dup others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 98092816 | |||||
| chr2:98092816
|
G | GTATATAT others(1): Show |
7 | a0001c0001t0001g0211a0001c0001t0002g0212a0002c0002t0002g0223others(4): Show | 7 | HG00741.hp1 HG01243.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.-32-208_-32-201dup others(8): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 98092816 | |||||
| chr2:98092816
|
G | GTATATAT others(3): Show |
4 | a0001c0001t0001g0215a0001c0001t0013g0028a0009c0011t0001g0213others(1): Show | 4 | HG01255.hp2 HG02155.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-210_-32-201dup others(10): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 98092816 | |||||
| chr2:98092816
|
G | GTATATAT others(5): Show |
1 | a0002c0002t0002g0224 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-32-212_-32-201dup others(12): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 98092816 | |||||
| chr2:98092816
|
GTA | G | 37 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0109others(34): Show | 37 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.-32-202_-32-201del others(2): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 98092816 | |||||
| chr2:98092816
|
GTATA | G | 22 | a0001c0001t0001g0144a0001c0001t0001g0161a0001c0004t0003g0020others(19): Show | 22 | HG00280.hp2 HG00639.hp2 HG02155.hp1 others(19): Show |
intron_variant | MODIFIER | c.-32-204_-32-201del others(4): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 98092816 | |||||
| chr2:98092816
|
GTATATA | G | 13 | a0001c0001t0003g0047a0001c0001t0005g0045a0001c0004t0003g0013others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.-32-206_-32-201del others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 98092816 | |||||
| chr2:98092816
|
GTATATAT others(1): Show |
G | 3 | a0001c0001t0003g0012a0002c0002t0004g0030a0002c0016t0020g0031 | 3 | HG01358.hp1 HG02735.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-32-208_-32-201del others(8): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 98092816 | |||||
| chr2:98092816
|
GTATATAT others(3): Show |
G | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0002c0002t0004g0011 | 3 | HG02896.hp1 NA19056.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-32-210_-32-201del others(10): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 98092816 | |||||
| chr2:98092816
|
GTATATAT others(5): Show |
G | 8 | a0001c0001t0001g0088a0001c0001t0001g0157a0001c0001t0001g0158others(5): Show | 8 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.-32-212_-32-201del others(12): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 98092816 | |||||
| chr2:98092816
|
GTATATAT others(7): Show |
G | 4 | a0001c0001t0001g0083a0001c0001t0001g0156a0016c0028t0002g0085others(1): Show | 4 | HG02056.hp1 HG02165.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-214_-32-201del others(14): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 98092816 | |||||
| chr2:98092816
|
GTATATAT others(17): Show |
G | 13 | a0001c0001t0003g0232a0001c0001t0003g0238a0002c0019t0011g0228others(10): Show | 13 | HG01361.hp1 HG02280.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-32-224_-32-201del others(24): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 98092816 | |||||
| chr2:98092818
|
A | ATG | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG01099.hp2 HG04184.hp2 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-242_-32-241ins others(2): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 98092818 | |||||
| chr2:98092818
|
A | G | 1 | a0003c0003t0005g0079 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-32-243A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98092818 | ||||||
| chr2:98092820
|
A | G | 6 | a0001c0001t0001g0145a0001c0001t0007g0146a0001c0001t0007g0147others(3): Show | 6 | HG03471.hp2 HG03579.hp1 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32-241A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98092820 | ||||||
| chr2:98092822
|
A | G | 1 | a0002c0002t0004g0005 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-32-239A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98092822 | ||||||
| chr2:98092824
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-32-237A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98092824 | ||||||
| chr2:98092830
|
A | G | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | NA19056.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-32-231A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98092830 | ||||||
| chr2:98092860
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0216 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-32-201_-32-200ins others(10): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98092860 | ||||||
| chr2:98092899
|
A | G | 11 | a0001c0001t0001g0082a0001c0001t0001g0165a0001c0001t0001g0183others(8): Show | 11 | HG00621.hp1 HG01361.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.-32-162A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98092899 | ||||||
| chr2:98093780
|
C | T | 78 | a0001c0001t0003g0012a0001c0001t0003g0047a0001c0001t0003g0236others(75): Show | 78 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.196+492C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98093780 | ||||||
| chr2:98093797
|
C | T | 24 | a0003c0003t0001g0199a0003c0003t0001g0201a0003c0003t0001g0202others(21): Show | 24 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.196+509C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98093797 | ||||||
| chr2:98093946
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.196+658G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98093946 | ||||||
| chr2:98093952
|
G | A | 1 | a0020c0026t0002g0210 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.196+664G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98093952 | ||||||
| chr2:98094014
|
C | G | 11 | a0003c0003t0003g0048a0003c0003t0003g0053a0003c0003t0003g0054others(8): Show | 11 | HG01361.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.196+726C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98094014 | ||||||
| chr2:98094076
|
A | G | 78 | a0001c0001t0003g0012a0001c0001t0003g0047a0001c0001t0003g0236others(75): Show | 78 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.196+788A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98094076 | ||||||
| chr2:98094217
|
A | G | 1 | a0002c0012t0011g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.196+929A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98094217 | ||||||
| chr2:98094875
|
C | T | 144 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0127others(141): Show | 144 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.196+1587C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98094875 | ||||||
| chr2:98095089
|
G | A | 1 | a0002c0006t0004g0019 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.196+1801G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98095089 | ||||||
| chr2:98095686
|
G | A | 1 | a0003c0017t0005g0056 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.196+2398G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98095686 | ||||||
| chr2:98095797
|
A | G | 2 | a0001c0001t0006g0181a0001c0001t0006g0198 | 2 | NA18945.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.196+2509A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98095797 | ||||||
| chr2:98096285
|
T | A | 1 | a0011c0022t0003g0038 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.196+2997T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98096285 | ||||||
| chr2:98096347
|
C | T | 1 | a0002c0002t0004g0022 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.196+3059C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98096347 | ||||||
| chr2:98096592
|
C | A | 4 | a0002c0002t0002g0221a0002c0002t0002g0222a0002c0002t0002g0223others(1): Show | 4 | HG00741.hp1 HG01070.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+3304C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98096592 | ||||||
| chr2:98096670
|
T | G | 9 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0136others(6): Show | 9 | HG01123.hp2 HG01167.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.196+3382T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98096670 | ||||||
| chr2:98096777
|
T | C | 3 | a0001c0001t0003g0238a0008c0010t0009g0239a0008c0010t0009g0240 | 3 | HG02922.hp2 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.196+3489T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98096777 | ||||||
| chr2:98097578
|
A | G | 2 | a0001c0004t0003g0025a0001c0004t0003g0026 | 2 | NA18951.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.196+4290A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98097578 | ||||||
| chr2:98097691
|
A | G | 1 | a0002c0002t0002g0001 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.196+4403A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98097691 | ||||||
| chr2:98097982
|
G | A | 29 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(26): Show | 29 | HG01099.hp2 HG01123.hp2 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.196+4694G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98097982 | ||||||
| chr2:98097982
|
G | T | 1 | a0003c0017t0005g0056 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.196+4694G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98097982 | ||||||
| chr2:98098447
|
CT | C | 5 | a0003c0003t0003g0068a0003c0003t0003g0072a0003c0003t0003g0073others(2): Show | 5 | HG01175.hp2 HG01261.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+5164delT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 98098447 | |||||
| chr2:98098454
|
A | G | 5 | a0003c0003t0003g0068a0003c0003t0003g0072a0003c0003t0003g0073others(2): Show | 5 | HG01175.hp2 HG01261.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+5166A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98098454 | ||||||
| chr2:98098517
|
A | G | 2 | a0001c0001t0023g0009a0002c0002t0024g0008 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.196+5229A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98098517 | ||||||
| chr2:98098637
|
A | G | 1 | a0020c0026t0002g0210 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.196+5349A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98098637 | ||||||
| chr2:98098778
|
C | A | 51 | a0001c0001t0001g0082a0001c0001t0001g0089a0001c0001t0001g0114others(48): Show | 51 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.196+5490C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98098778 | ||||||
| chr2:98099109
|
A | G | 1 | a0001c0004t0004g0018 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.196+5821A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98099109 | ||||||
| chr2:98099233
|
T | G | 10 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.196+5945T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98099233 | ||||||
| chr2:98099274
|
A | G | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.196+5986A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98099274 | ||||||
| chr2:98099282
|
G | A | 1 | a0001c0004t0003g0020 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.196+5994G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98099282 | ||||||
| chr2:98099401
|
A | G | 40 | a0003c0003t0001g0199a0003c0003t0001g0201a0003c0003t0001g0202others(37): Show | 40 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.196+6113A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98099401 | ||||||
| chr2:98099930
|
G | T | 144 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0127others(141): Show | 144 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.196+6642G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98099930 | ||||||
| chr2:98100247
|
G | A | 10 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.196+6959G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98100247 | ||||||
| chr2:98100405
|
G | T | 2 | a0001c0001t0001g0155a0001c0001t0016g0152 | 2 | NA18941.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.196+7117G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98100405 | ||||||
| chr2:98100480
|
A | G | 144 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0127others(141): Show | 144 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.196+7192A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98100480 | ||||||
| chr2:98100495
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.196+7207C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98100495 | ||||||
| chr2:98100631
|
A | G | 224 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(221): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.196+7343A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98100631 | ||||||
| chr2:98100829
|
A | G | 3 | a0002c0002t0002g0162a0002c0002t0002g0164a0002c0002t0002g0194 | 3 | NA18941.hp1 NA18946.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.196+7541A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98100829 | ||||||
| chr2:98100943
|
G | C | 1 | a0001c0001t0015g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.196+7655G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98100943 | ||||||
| chr2:98101171
|
C | T | 2 | a0001c0004t0003g0017a0002c0006t0004g0021 | 2 | HG00733.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.196+7883C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98101171 | ||||||
| chr2:98101283
|
T | C | 7 | a0003c0003t0001g0199a0003c0003t0001g0201a0003c0003t0001g0202others(4): Show | 7 | NA18959.hp2 NA18977.hp2 NA18985.hp2 others(4): Show |
intron_variant | MODIFIER | c.196+7995T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98101283 | ||||||
| chr2:98101308
|
T | C | 10 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.196+8020T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98101308 | ||||||
| chr2:98101315
|
T | G | 1 | a0005c0008t0003g0229 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.196+8027T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98101315 | ||||||
| chr2:98101570
|
A | G | 1 | a0002c0002t0002g0163 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.196+8282A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98101570 | ||||||
| chr2:98101622
|
G | A | 10 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.196+8334G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98101622 | ||||||
| chr2:98101724
|
G | T | 38 | a0001c0001t0003g0012a0001c0001t0003g0047a0001c0001t0003g0236others(35): Show | 38 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.196+8436G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98101724 | ||||||
| chr2:98102019
|
G | A | 1 | a0009c0011t0001g0171 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.196+8731G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98102019 | ||||||
| chr2:98102027
|
G | C | 1 | a0001c0001t0001g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.196+8739G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98102027 | ||||||
| chr2:98102053
|
A | C | 1 | a0002c0012t0011g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.196+8765A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98102053 | ||||||
| chr2:98102124
|
C | CACCGCCC others(2): Show |
27 | a0001c0001t0003g0012a0001c0001t0003g0236a0001c0001t0013g0028others(24): Show | 27 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.196+8838_196+8839i others(11): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 98102124 | |||||
| chr2:98102127
|
T | C | 145 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0127others(142): Show | 145 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.196+8839T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98102127 | ||||||
| chr2:98102338
|
C | T | 14 | a0001c0001t0001g0130a0001c0001t0001g0142a0001c0001t0001g0143others(11): Show | 14 | HG00408.hp1 HG01099.hp2 HG02698.hp2 others(11): Show |
intron_variant | MODIFIER | c.196+9050C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98102338 | ||||||
| chr2:98102348
|
G | A | 2 | a0001c0004t0003g0010a0001c0004t0004g0018 | 2 | HG01081.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.196+9060G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98102348 | ||||||
| chr2:98102486
|
C | T | 2 | a0001c0001t0001g0083a0002c0012t0011g0226 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.196+9198C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98102486 | ||||||
| chr2:98102518
|
C | CG | 5 | a0001c0001t0001g0186a0001c0001t0003g0034a0001c0001t0003g0236others(2): Show | 5 | HG01175.hp2 HG01496.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+9234dupG | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 98102518 | |||||
| chr2:98102521
|
G | A | 1 | a0001c0001t0003g0238 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.196+9233G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98102521 | ||||||
| chr2:98102540
|
C | A | 1 | a0002c0002t0004g0032 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.196+9252C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98102540 | ||||||
| chr2:98102611
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.196+9323G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98102611 | ||||||
| chr2:98102660
|
G | A | 12 | a0001c0001t0003g0232a0001c0001t0003g0238a0002c0019t0011g0228others(9): Show | 12 | HG02280.hp2 HG02615.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.196+9372G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98102660 | ||||||
| chr2:98102677
|
G | A | 10 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.196+9389G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98102677 | ||||||
| chr2:98102767
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.196+9479A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98102767 | ||||||
| chr2:98103432
|
T | C | 1 | a0001c0004t0003g0013 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.196+10144T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98103432 | ||||||
| chr2:98103490
|
A | G | 2 | a0001c0001t0001g0083a0002c0012t0011g0226 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.196+10202A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98103490 | ||||||
| chr2:98103776
|
T | C | 3 | a0002c0002t0002g0162a0002c0002t0002g0164a0002c0002t0002g0194 | 3 | NA18941.hp1 NA18946.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.196+10488T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98103776 | ||||||
| chr2:98103830
|
G | T | 3 | a0001c0001t0001g0193a0001c0001t0001g0208a0002c0002t0002g0217 | 3 | NA18939.hp2 NA18948.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.196+10542G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98103830 | ||||||
| chr2:98103834
|
A | G | 1 | a0002c0012t0011g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.196+10546A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98103834 | ||||||
| chr2:98104124
|
A | G | 8 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(5): Show | 8 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.196+10836A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98104124 | ||||||
| chr2:98104156
|
A | G | 1 | a0003c0003t0003g0071 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.196+10868A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98104156 | ||||||
| chr2:98104523
|
C | A | 24 | a0001c0001t0003g0232a0001c0001t0003g0238a0002c0002t0004g0030others(21): Show | 24 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.197-11129C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98104523 | ||||||
| chr2:98104605
|
A | G | 1 | a0003c0003t0018g0081 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.197-11047A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98104605 | ||||||
| chr2:98104683
|
A | G | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.197-10969A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98104683 | ||||||
| chr2:98104876
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.197-10776A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98104876 | ||||||
| chr2:98104877
|
T | A | 1 | a0001c0001t0001g0187 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.197-10775T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98104877 | ||||||
| chr2:98104901
|
T | A | 1 | a0001c0001t0001g0188 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.197-10751T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98104901 | ||||||
| chr2:98104903
|
A | T | 1 | a0001c0001t0001g0188 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.197-10749A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98104903 | ||||||
| chr2:98105625
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.197-10027G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98105625 | ||||||
| chr2:98105761
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.197-9891T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98105761 | ||||||
| chr2:98105764
|
A | AT | 38 | a0003c0003t0001g0199a0003c0003t0001g0201a0003c0003t0001g0202others(35): Show | 38 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.197-9878dupT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 98105764 | |||||
| chr2:98105964
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.197-9688G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98105964 | ||||||
| chr2:98106077
|
G | A | 12 | a0002c0002t0004g0030a0002c0002t0004g0032a0002c0002t0004g0033others(9): Show | 12 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.197-9575G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98106077 | ||||||
| chr2:98106136
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.197-9516C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98106136 | ||||||
| chr2:98106194
|
T | C | 50 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0156others(47): Show | 50 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.197-9458T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98106194 | ||||||
| chr2:98106635
|
AT | A | 10 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.197-9009delT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 98106635 | |||||
| chr2:98106792
|
C | T | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.197-8860C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98106792 | ||||||
| chr2:98106863
|
GCT | G | 12 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0170others(9): Show | 12 | HG00597.hp2 HG00639.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.197-8786_197-8785d others(4): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 98106863 | |||||
| chr2:98106909
|
C | T | 4 | a0002c0002t0002g0221a0002c0002t0002g0222a0002c0002t0002g0223others(1): Show | 4 | HG00741.hp1 HG01070.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-8743C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98106909 | ||||||
| chr2:98107039
|
G | C | 1 | a0001c0001t0010g0128 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.197-8613G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98107039 | ||||||
| chr2:98107062
|
T | C | 1 | a0002c0002t0002g0189 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.197-8590T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98107062 | ||||||
| chr2:98107644
|
T | G | 1 | a0002c0019t0011g0228 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.197-8008T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98107644 | ||||||
| chr2:98107800
|
C | A | 10 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.197-7852C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98107800 | ||||||
| chr2:98107938
|
C | A | 29 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(26): Show | 29 | HG01099.hp2 HG01123.hp2 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.197-7714C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98107938 | ||||||
| chr2:98108076
|
A | G | 3 | a0001c0001t0003g0047a0001c0001t0005g0045a0015c0029t0004g0046 | 3 | HG02486.hp2 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.197-7576A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98108076 | ||||||
| chr2:98108613
|
C | A | 2 | a0002c0006t0002g0113a0011c0015t0001g0112 | 2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.197-7039C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98108613 | ||||||
| chr2:98108994
|
C | CT | 41 | a0001c0001t0001g0083a0001c0001t0003g0047a0001c0001t0003g0236others(38): Show | 41 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.197-6643dupT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 98108994 | |||||
| chr2:98109192
|
A | G | 4 | a0002c0002t0004g0002a0002c0002t0004g0005a0002c0002t0021g0006others(1): Show | 4 | HG02109.hp2 HG02647.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-6460A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98109192 | ||||||
| chr2:98109283
|
C | T | 9 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0136others(6): Show | 9 | HG01123.hp2 HG01167.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.197-6369C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98109283 | ||||||
| chr2:98109305
|
T | C | 1 | a0002c0012t0011g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.197-6347T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98109305 | ||||||
| chr2:98109355
|
T | C | 10 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.197-6297T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98109355 | ||||||
| chr2:98109419
|
A | G | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.197-6233A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98109419 | ||||||
| chr2:98109734
|
T | C | 1 | a0002c0002t0004g0005 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.197-5918T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98109734 | ||||||
| chr2:98109792
|
C | CT | 11 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(8): Show | 11 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.197-5845dupT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 98109792 | |||||
| chr2:98110080
|
C | CT | 38 | a0001c0001t0003g0012a0001c0001t0003g0047a0001c0001t0003g0236others(35): Show | 38 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.197-5561dupT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 98110080 | |||||
| chr2:98110283
|
T | C | 1 | a0002c0002t0004g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.197-5369T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98110283 | ||||||
| chr2:98110374
|
A | G | 12 | a0002c0002t0004g0030a0002c0002t0004g0032a0002c0002t0004g0033others(9): Show | 12 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.197-5278A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98110374 | ||||||
| chr2:98110440
|
G | T | 50 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0156others(47): Show | 50 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.197-5212G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98110440 | ||||||
| chr2:98111007
|
C | T | 1 | a0002c0002t0002g0189 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.197-4645C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98111007 | ||||||
| chr2:98111315
|
A | G | 1 | a0002c0002t0002g0197 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.197-4337A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98111315 | ||||||
| chr2:98111356
|
C | T | 4 | a0002c0002t0002g0221a0002c0002t0002g0222a0002c0002t0002g0223others(1): Show | 4 | HG00741.hp1 HG01070.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-4296C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98111356 | ||||||
| chr2:98111475
|
C | T | 1 | a0014c0030t0002g0120 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.197-4177C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98111475 | ||||||
| chr2:98111707
|
T | C | 1 | a0001c0004t0003g0017 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.197-3945T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98111707 | ||||||
| chr2:98111745
|
A | T | 50 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0156others(47): Show | 50 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.197-3907A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98111745 | ||||||
| chr2:98111851
|
C | A | 10 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.197-3801C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98111851 | ||||||
| chr2:98112281
|
GGT | G | 130 | a0001c0001t0001g0083a0001c0001t0001g0127a0001c0001t0001g0130others(127): Show | 130 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.197-3351_197-3350d others(4): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 98112281 | |||||
| chr2:98112301
|
T | G | 13 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(10): Show | 13 | HG00544.hp1 HG00597.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.197-3351T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98112301 | ||||||
| chr2:98112303
|
G | T | 14 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(11): Show | 14 | HG00544.hp1 HG00597.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.197-3349G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98112303 | ||||||
| chr2:98112305
|
T | G | 1 | a0023c0031t0014g0097 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.197-3347T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98112305 | ||||||
| chr2:98112444
|
T | C | 1 | a0001c0001t0010g0128 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.197-3208T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98112444 | ||||||
| chr2:98112973
|
C | T | 40 | a0003c0003t0001g0199a0003c0003t0001g0201a0003c0003t0001g0202others(37): Show | 40 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.197-2679C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98112973 | ||||||
| chr2:98112984
|
A | G | 2 | a0001c0001t0001g0170a0001c0001t0001g0192 | 2 | HG00735.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.197-2668A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98112984 | ||||||
| chr2:98113286
|
C | T | 38 | a0001c0001t0003g0012a0001c0001t0003g0047a0001c0001t0003g0236others(35): Show | 38 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.197-2366C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98113286 | ||||||
| chr2:98113472
|
C | T | 38 | a0003c0003t0001g0199a0003c0003t0001g0201a0003c0003t0001g0202others(35): Show | 38 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.197-2180C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98113472 | ||||||
| chr2:98113583
|
T | A | 40 | a0003c0003t0001g0199a0003c0003t0001g0201a0003c0003t0001g0202others(37): Show | 40 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.197-2069T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98113583 | ||||||
| chr2:98113764
|
G | T | 38 | a0001c0001t0003g0012a0001c0001t0003g0047a0001c0001t0003g0236others(35): Show | 38 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.197-1888G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98113764 | ||||||
| chr2:98113855
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.197-1797C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98113855 | ||||||
| chr2:98113983
|
T | C | 2 | a0008c0010t0009g0239a0008c0010t0009g0240 | 2 | HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.197-1669T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98113983 | ||||||
| chr2:98113987
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.197-1665C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98113987 | ||||||
| chr2:98114157
|
T | C | 1 | a0020c0026t0002g0210 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.197-1495T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98114157 | ||||||
| chr2:98114352
|
A | C | 144 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0127others(141): Show | 144 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.197-1300A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98114352 | ||||||
| chr2:98114473
|
C | T | 1 | a0003c0003t0005g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.197-1179C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98114473 | ||||||
| chr2:98114673
|
C | T | 4 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0144others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-979C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98114673 | ||||||
| chr2:98114707
|
C | T | 1 | a0001c0001t0023g0009 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.197-945C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98114707 | ||||||
| chr2:98114980
|
G | A | 2 | a0002c0002t0004g0003a0002c0002t0004g0004 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.197-672G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98114980 | ||||||
| chr2:98114996
|
G | C | 1 | a0013c0014t0017g0126 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.197-656G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98114996 | ||||||
| chr2:98115060
|
C | T | 1 | a0020c0026t0002g0210 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.197-592C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98115060 | ||||||
| chr2:98115082
|
C | T | 4 | a0001c0001t0003g0236a0001c0001t0013g0028a0002c0002t0003g0024others(1): Show | 4 | HG01261.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-570C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98115082 | ||||||
| chr2:98115101
|
CT | C | 37 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0117others(34): Show | 37 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.197-534delT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 98115101 | |||||
| chr2:98115167
|
C | A | 1 | a0002c0002t0002g0197 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.197-485C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98115167 | ||||||
| chr2:98115472
|
G | C | 30 | a0001c0001t0003g0012a0001c0001t0003g0047a0001c0001t0003g0236others(27): Show | 30 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.197-180G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 2/27 | chr2 | 98115472 | ||||||
| chr2:98115863
|
T | A | 2 | a0001c0001t0023g0009a0002c0002t0024g0008 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.291+117T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98115863 | ||||||
| chr2:98116120
|
A | G | 1 | a0001c0001t0006g0198 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.291+374A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98116120 | ||||||
| chr2:98116156
|
A | G | 2 | a0001c0004t0003g0017a0002c0006t0004g0021 | 2 | HG00733.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.291+410A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98116156 | ||||||
| chr2:98116452
|
G | T | 2 | a0001c0001t0023g0009a0002c0002t0024g0008 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.291+706G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98116452 | ||||||
| chr2:98116469
|
G | A | 50 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0156others(47): Show | 50 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.291+723G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98116469 | ||||||
| chr2:98116560
|
G | T | 1 | a0001c0001t0001g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.291+814G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98116560 | ||||||
| chr2:98116605
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.291+859C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98116605 | ||||||
| chr2:98116609
|
C | A | 29 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(26): Show | 29 | HG01099.hp2 HG01123.hp2 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.291+863C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98116609 | ||||||
| chr2:98116740
|
A | G | 3 | a0002c0006t0002g0113a0002c0006t0004g0237a0011c0015t0001g0112 | 3 | HG00280.hp1 HG00323.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.291+994A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98116740 | ||||||
| chr2:98117059
|
G | C | 1 | a0002c0002t0004g0035 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.291+1313G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98117059 | ||||||
| chr2:98117408
|
G | A | 1 | a0003c0003t0003g0075 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.291+1662G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98117408 | ||||||
| chr2:98117748
|
CT | C | 93 | a0001c0001t0001g0083a0001c0001t0001g0127a0001c0001t0001g0130others(90): Show | 93 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.292-1744delT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 98117748 | |||||
| chr2:98117784
|
C | G | 1 | a0002c0002t0002g0169 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.292-1729C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98117784 | ||||||
| chr2:98117929
|
G | C | 10 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.292-1584G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98117929 | ||||||
| chr2:98118281
|
G | A | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.292-1232G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98118281 | ||||||
| chr2:98118419
|
C | G | 1 | a0002c0006t0004g0237 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.292-1094C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98118419 | ||||||
| chr2:98118496
|
C | T | 1 | a0005c0008t0003g0235 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.292-1017C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98118496 | ||||||
| chr2:98118644
|
G | A | 12 | a0002c0002t0004g0030a0002c0002t0004g0032a0002c0002t0004g0033others(9): Show | 12 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.292-869G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98118644 | ||||||
| chr2:98118722
|
C | T | 1 | a0002c0002t0002g0180 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.292-791C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98118722 | ||||||
| chr2:98118745
|
C | CTAAAA | 28 | a0001c0001t0001g0083a0001c0001t0001g0170a0002c0002t0001g0190others(25): Show | 28 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.292-741_292-737dup others(5): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 98118745 | |||||
| chr2:98118745
|
C | CTAAAATA others(3): Show |
8 | a0001c0001t0001g0088a0001c0001t0001g0157a0001c0001t0001g0158others(5): Show | 8 | HG00544.hp1 HG00597.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.292-746_292-737dup others(10): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 98118745 | |||||
| chr2:98118745
|
C | CTAAAATA others(8): Show |
2 | a0001c0001t0001g0156a0002c0012t0011g0226 | 2 | HG03225.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.292-751_292-737dup others(15): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 98118745 | |||||
| chr2:98118782
|
T | G | 1 | a0001c0001t0001g0142 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.292-731T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98118782 | ||||||
| chr2:98118863
|
C | T | 1 | a0002c0012t0011g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.292-650C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98118863 | ||||||
| chr2:98118974
|
T | A | 12 | a0002c0002t0004g0030a0002c0002t0004g0032a0002c0002t0004g0033others(9): Show | 12 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.292-539T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98118974 | ||||||
| chr2:98119083
|
C | T | 1 | a0002c0016t0020g0031 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.292-430C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98119083 | ||||||
| chr2:98119158
|
G | T | 9 | a0004c0005t0002g0093a0004c0005t0002g0098a0004c0005t0002g0099others(6): Show | 9 | NA18942.hp2 NA18948.hp1 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.292-355G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98119158 | ||||||
| chr2:98119174
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.292-339C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98119174 | ||||||
| chr2:98119207
|
T | G | 1 | a0002c0012t0011g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.292-306T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98119207 | ||||||
| chr2:98119233
|
C | T | 10 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.292-280C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98119233 | ||||||
| chr2:98119895
|
A | G | 1 | a0001c0004t0013g0029 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.542+132A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 4/27 | chr2 | 98119895 | ||||||
| chr2:98120220
|
A | G | 1 | a0019c0024t0001g0103 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.542+457A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 4/27 | chr2 | 98120220 | ||||||
| chr2:98120480
|
A | G | 10 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.542+717A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 4/27 | chr2 | 98120480 | ||||||
| chr2:98120598
|
T | C | 1 | a0020c0026t0002g0210 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.543-701T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 4/27 | chr2 | 98120598 | ||||||
| chr2:98120730
|
T | A | 50 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0156others(47): Show | 50 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.543-569T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 4/27 | chr2 | 98120730 | ||||||
| chr2:98120806
|
A | G | 1 | a0002c0002t0002g0180 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.543-493A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 4/27 | chr2 | 98120806 | ||||||
| chr2:98121729
|
C | T | 2 | a0001c0001t0001g0083a0002c0012t0011g0226 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.702+271C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98121729 | ||||||
| chr2:98121730
|
G | A | 4 | a0002c0002t0004g0002a0002c0002t0004g0005a0002c0002t0021g0006others(1): Show | 4 | HG02109.hp2 HG02647.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+272G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98121730 | ||||||
| chr2:98121749
|
C | G | 30 | a0001c0001t0003g0012a0001c0001t0003g0047a0001c0001t0003g0236others(27): Show | 30 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.702+291C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98121749 | ||||||
| chr2:98121855
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0167 | 2 | NA18982.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.702+397G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98121855 | ||||||
| chr2:98121962
|
T | C | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.702+504T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98121962 | ||||||
| chr2:98121988
|
C | T | 1 | a0013c0014t0017g0126 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.702+530C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98121988 | ||||||
| chr2:98122003
|
C | T | 2 | a0001c0001t0001g0105a0001c0001t0001g0167 | 2 | NA18982.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.702+545C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98122003 | ||||||
| chr2:98122194
|
G | C | 1 | a0003c0003t0003g0070 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.702+736G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98122194 | ||||||
| chr2:98122390
|
A | G | 1 | a0010c0013t0002g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.702+932A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98122390 | ||||||
| chr2:98122550
|
T | C | 1 | a0003c0003t0003g0071 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.702+1092T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98122550 | ||||||
| chr2:98122650
|
G | A | 12 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0156others(9): Show | 12 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.702+1192G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98122650 | ||||||
| chr2:98122793
|
C | T | 1 | a0002c0002t0002g0169 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.702+1335C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98122793 | ||||||
| chr2:98122852
|
A | G | 1 | a0002c0002t0004g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.702+1394A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98122852 | ||||||
| chr2:98123265
|
A | T | 10 | a0001c0001t0001g0205a0004c0005t0002g0093a0004c0005t0002g0098others(7): Show | 10 | HG04184.hp1 NA18942.hp2 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.702+1807A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98123265 | ||||||
| chr2:98123368
|
G | A | 9 | a0001c0001t0003g0232a0001c0001t0003g0238a0005c0008t0003g0229others(6): Show | 9 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.702+1910G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98123368 | ||||||
| chr2:98123391
|
G | A | 1 | a0003c0032t0003g0062 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.702+1933G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98123391 | ||||||
| chr2:98123482
|
G | A | 41 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0003g0012others(38): Show | 41 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.702+2024G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98123482 | ||||||
| chr2:98123617
|
A | G | 1 | a0013c0014t0017g0126 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.702+2159A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98123617 | ||||||
| chr2:98123622
|
T | C | 41 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0003g0012others(38): Show | 41 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.702+2164T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98123622 | ||||||
| chr2:98123809
|
G | A | 1 | a0004c0005t0002g0185 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.702+2351G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98123809 | ||||||
| chr2:98124124
|
C | G | 1 | a0014c0030t0002g0120 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.702+2666C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98124124 | ||||||
| chr2:98124135
|
A | G | 1 | a0002c0016t0020g0031 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.702+2677A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98124135 | ||||||
| chr2:98124145
|
T | C | 1 | a0003c0032t0003g0062 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.702+2687T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98124145 | ||||||
| chr2:98124442
|
G | A | 1 | a0002c0002t0024g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.702+2984G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98124442 | ||||||
| chr2:98124551
|
G | A | 1 | a0003c0003t0003g0053 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.702+3093G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98124551 | ||||||
| chr2:98124579
|
A | G | 2 | a0002c0002t0004g0036a0002c0002t0004g0037 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.702+3121A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98124579 | ||||||
| chr2:98124591
|
G | A | 53 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0135others(50): Show | 53 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.702+3133G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98124591 | ||||||
| chr2:98124618
|
AGTGTTCA others(3): Show |
A | 1 | a0003c0003t0001g0199 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.702+3165_702+3174d others(12): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr2 | 98124618 | |||||
| chr2:98124716
|
T | G | 40 | a0003c0003t0001g0199a0003c0003t0001g0201a0003c0003t0001g0202others(37): Show | 40 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.702+3258T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98124716 | ||||||
| chr2:98124925
|
T | G | 13 | a0001c0001t0001g0130a0001c0001t0001g0142a0001c0001t0001g0143others(10): Show | 13 | HG01099.hp2 HG02698.hp2 HG03927.hp2 others(10): Show |
intron_variant | MODIFIER | c.703-3314T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98124925 | ||||||
| chr2:98124984
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0192 | 2 | HG00735.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.703-3255C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98124984 | ||||||
| chr2:98125380
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.703-2859C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98125380 | ||||||
| chr2:98125812
|
T | C | 16 | a0001c0004t0001g0220a0001c0004t0003g0010a0001c0004t0003g0013others(13): Show | 16 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.703-2427T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98125812 | ||||||
| chr2:98125932
|
G | A | 1 | a0002c0006t0004g0015 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.703-2307G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98125932 | ||||||
| chr2:98125959
|
C | T | 5 | a0003c0003t0003g0068a0003c0003t0003g0072a0003c0003t0003g0073others(2): Show | 5 | HG01175.hp2 HG01261.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-2280C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98125959 | ||||||
| chr2:98126034
|
G | A | 2 | a0002c0002t0004g0032a0021c0021t0003g0042 | 2 | HG01255.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.703-2205G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98126034 | ||||||
| chr2:98126034
|
G | C | 11 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0003g0012others(8): Show | 11 | HG01167.hp2 HG01261.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.703-2205G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98126034 | ||||||
| chr2:98126039
|
G | T | 1 | a0002c0006t0004g0019 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.703-2200G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98126039 | ||||||
| chr2:98126271
|
G | A | 2 | a0001c0001t0001g0205a0004c0005t0002g0124 | 2 | HG04184.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.703-1968G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98126271 | ||||||
| chr2:98126324
|
G | A | 10 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.703-1915G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98126324 | ||||||
| chr2:98126515
|
C | G | 10 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.703-1724C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98126515 | ||||||
| chr2:98126667
|
G | A | 61 | a0001c0001t0001g0082a0001c0001t0001g0089a0001c0001t0001g0105others(58): Show | 61 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.703-1572G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98126667 | ||||||
| chr2:98126872
|
C | T | 1 | a0002c0012t0011g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.703-1367C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98126872 | ||||||
| chr2:98127265
|
T | C | 1 | a0002c0012t0011g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.703-974T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98127265 | ||||||
| chr2:98127296
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.703-943A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98127296 | ||||||
| chr2:98127411
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0192 | 2 | HG00735.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.703-828C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98127411 | ||||||
| chr2:98127494
|
A | G | 1 | a0002c0002t0002g0169 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.703-745A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98127494 | ||||||
| chr2:98127568
|
A | G | 2 | a0003c0003t0003g0075a0025c0033t0006g0214 | 2 | NA19066.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.703-671A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98127568 | ||||||
| chr2:98127591
|
G | T | 3 | a0001c0001t0003g0047a0001c0001t0005g0045a0015c0029t0004g0046 | 3 | HG02486.hp2 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.703-648G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98127591 | ||||||
| chr2:98127592
|
G | T | 1 | a0002c0012t0011g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.703-647G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98127592 | ||||||
| chr2:98127593
|
C | CG | 25 | a0001c0001t0001g0083a0001c0001t0001g0106a0001c0001t0001g0117others(22): Show | 25 | HG00544.hp2 HG00621.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.703-632dupG | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr2 | 98127593 | |||||
| chr2:98127593
|
C | CGG | 34 | a0001c0001t0001g0082a0001c0001t0001g0137a0001c0001t0001g0165others(31): Show | 34 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.703-633_703-632dup others(2): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr2 | 98127593 | |||||
| chr2:98127593
|
C | G | 3 | a0001c0001t0003g0047a0002c0012t0011g0226a0003c0003t0001g0199 | 3 | HG02486.hp2 HG03225.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.703-646C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98127593 | ||||||
| chr2:98127593
|
CG | C | 42 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0130others(39): Show | 42 | HG00609.hp1 HG00639.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.703-632delG | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr2 | 98127593 | |||||
| chr2:98127593
|
CGG | C | 19 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0138others(16): Show | 19 | HG01099.hp2 HG01517.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.703-633_703-632del others(2): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr2 | 98127593 | |||||
| chr2:98127593
|
CGGG | C | 38 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0136others(35): Show | 38 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.703-634_703-632del others(3): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr2 | 98127593 | |||||
| chr2:98127595
|
G | C | 1 | a0001c0001t0003g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.703-644G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98127595 | ||||||
| chr2:98127596
|
G | C | 3 | a0001c0001t0005g0045a0002c0012t0011g0226a0015c0029t0004g0046 | 3 | HG02647.hp1 HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.703-643G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98127596 | ||||||
| chr2:98127608
|
T | G | 1 | a0003c0003t0005g0079 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.703-631T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98127608 | ||||||
| chr2:98127946
|
G | A | 41 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0003g0012others(38): Show | 41 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.703-293G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98127946 | ||||||
| chr2:98128452
|
T | A | 3 | a0007c0009t0002g0091a0007c0009t0002g0092a0010c0013t0002g0104 | 3 | HG01071.hp1 HG01081.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.872+44T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98128452 | ||||||
| chr2:98128522
|
C | A | 1 | a0002c0002t0004g0005 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.872+114C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98128522 | ||||||
| chr2:98128533
|
A | G | 10 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.872+125A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98128533 | ||||||
| chr2:98128536
|
A | T | 1 | a0002c0002t0004g0005 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.872+128A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98128536 | ||||||
| chr2:98128560
|
T | A | 10 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.872+152T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98128560 | ||||||
| chr2:98128761
|
G | A | 119 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0109others(116): Show | 119 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.872+353G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98128761 | ||||||
| chr2:98128939
|
G | A | 2 | a0001c0001t0010g0128a0026c0018t0010g0129 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.872+531G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98128939 | ||||||
| chr2:98129096
|
AC | A | 118 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0109others(115): Show | 118 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.872+689delC | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98129096 | ||||||
| chr2:98129206
|
G | GGA | 7 | a0001c0001t0001g0144a0002c0002t0002g0221a0002c0002t0002g0222others(4): Show | 7 | HG00741.hp1 HG01070.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.872+816_872+817dup others(2): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 98129206 | |||||
| chr2:98129206
|
G | GGAGA | 14 | a0001c0001t0001g0088a0001c0001t0001g0131a0001c0001t0001g0132others(11): Show | 14 | HG00544.hp1 HG00597.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.872+814_872+817dup others(4): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 98129206 | |||||
| chr2:98129206
|
G | GGAGAGA | 4 | a0001c0001t0001g0145a0001c0001t0010g0128a0006c0007t0012g0050others(1): Show | 4 | HG02922.hp1 HG03098.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.872+812_872+817dup others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 98129206 | |||||
| chr2:98129206
|
G | GGGGA | 10 | a0003c0003t0003g0048a0003c0003t0003g0054a0003c0003t0003g0055others(7): Show | 10 | HG01891.hp1 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.872+799_872+800ins others(4): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 98129206 | |||||
| chr2:98129206
|
G | GGGGAGA | 16 | a0001c0001t0003g0047a0001c0001t0003g0236a0001c0001t0013g0028others(13): Show | 16 | HG01081.hp2 HG01358.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.872+799_872+800ins others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 98129206 | |||||
| chr2:98129208
|
A | G | 4 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0021g0006others(1): Show | 4 | HG02109.hp2 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.872+800A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98129208 | ||||||
| chr2:98129224
|
A | AGAGAGAG others(3): Show |
1 | a0002c0002t0004g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.872+817_872+818ins others(10): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 98129224 | |||||
| chr2:98129224
|
A | AGAGAGAG others(1): Show |
7 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0003g0012others(4): Show | 7 | HG01167.hp2 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.872+817_872+818ins others(8): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 98129224 | |||||
| chr2:98129224
|
A | AGAGAGAG others(3): Show |
1 | a0002c0012t0011g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.872+817_872+818ins others(10): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 98129224 | |||||
| chr2:98129224
|
A | AGAGAGAG others(9): Show |
1 | a0003c0003t0001g0199 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.872+817_872+818ins others(16): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 98129224 | |||||
| chr2:98129224
|
A | AGAGAGT | 9 | a0002c0002t0004g0030a0002c0002t0004g0032a0002c0002t0004g0033others(6): Show | 9 | HG00140.hp2 HG00323.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.872+817_872+818ins others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 98129224 | |||||
| chr2:98129224
|
A | AGAGAGTG others(1): Show |
8 | a0001c0001t0001g0127a0001c0001t0001g0149a0001c0001t0001g0151others(5): Show | 8 | HG01099.hp2 HG01123.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.872+817_872+818ins others(8): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 98129224 | |||||
| chr2:98129224
|
A | AGAGAGTG others(3): Show |
9 | a0001c0001t0001g0130a0001c0001t0001g0142a0001c0001t0001g0143others(6): Show | 9 | HG00423.hp1 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.872+817_872+818ins others(10): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 98129224 | |||||
| chr2:98129224
|
A | AGAGAGTG others(5): Show |
14 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0138others(11): Show | 14 | HG00639.hp1 HG01168.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.872+817_872+818ins others(12): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 98129224 | |||||
| chr2:98129224
|
A | AGAGAGTG others(7): Show |
21 | a0001c0001t0001g0083a0003c0003t0001g0201a0003c0003t0001g0202others(18): Show | 21 | HG00140.hp1 HG01071.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.872+817_872+818ins others(14): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 98129224 | |||||
| chr2:98129224
|
A | AGAGAGTG others(9): Show |
8 | a0001c0001t0001g0090a0002c0019t0011g0228a0003c0003t0003g0052others(5): Show | 8 | HG02080.hp1 HG02165.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.872+817_872+818ins others(16): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 98129224 | |||||
| chr2:98129224
|
A | AGAGAGTG others(11): Show |
7 | a0003c0003t0003g0049a0003c0003t0003g0060a0003c0003t0003g0066others(4): Show | 7 | HG00609.hp2 HG00673.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.872+817_872+818ins others(18): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 98129224 | |||||
| chr2:98129224
|
A | AGAGAGTG others(13): Show |
7 | a0001c0001t0001g0137a0001c0001t0001g0205a0003c0003t0003g0076others(4): Show | 7 | HG01168.hp1 HG04184.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.872+817_872+818ins others(20): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 98129224 | |||||
| chr2:98129224
|
A | AGAGAGTG others(15): Show |
2 | a0004c0005t0002g0093a0004c0005t0002g0124 | 2 | NA18985.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.872+817_872+818ins others(22): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 98129224 | |||||
| chr2:98129224
|
A | AGT | 7 | a0001c0001t0001g0186a0001c0004t0003g0017a0001c0004t0004g0023others(4): Show | 7 | HG00323.hp2 HG00733.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.872+850_872+851dup others(2): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 98129224 | |||||
| chr2:98129224
|
A | AGTGTGTG others(3): Show |
2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | NA18612.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.872+842_872+851dup others(10): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 98129224 | |||||
| chr2:98129224
|
A | AGTGTGTG others(5): Show |
6 | a0001c0001t0001g0119a0001c0001t0001g0216a0002c0002t0002g0110others(3): Show | 6 | NA18939.hp1 NA18962.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.872+840_872+851dup others(12): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 98129224 | |||||
| chr2:98129224
|
A | AGTGTGTG others(7): Show |
2 | a0001c0001t0001g0106a0002c0002t0002g0001 | 2 | HG00544.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.872+838_872+851dup others(14): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 98129224 | |||||
| chr2:98129224
|
A | T | 5 | a0001c0001t0023g0009a0001c0004t0013g0029a0002c0002t0002g0096others(2): Show | 5 | HG01261.hp2 HG03225.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.872+816A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98129224 | ||||||
| chr2:98129224
|
AGT | A | 5 | a0001c0001t0001g0105a0001c0001t0001g0167a0001c0004t0003g0025others(2): Show | 5 | NA18951.hp2 NA18959.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.872+850_872+851del others(2): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 98129224 | |||||
| chr2:98129226
|
T | A | 19 | a0001c0001t0003g0047a0002c0002t0004g0002a0002c0002t0004g0003others(16): Show | 19 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.872+818T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98129226 | ||||||
| chr2:98129228
|
T | A | 5 | a0002c0002t0004g0002a0002c0002t0004g0003a0002c0002t0004g0004others(2): Show | 5 | HG02109.hp2 HG03486.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.872+820T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98129228 | ||||||
| chr2:98129230
|
T | A | 2 | a0002c0002t0004g0002a0002c0002t0021g0006 | 2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.872+822T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98129230 | ||||||
| chr2:98129260
|
G | T | 11 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(8): Show | 11 | HG00544.hp1 HG00597.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.872+852G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98129260 | ||||||
| chr2:98129261
|
A | G | 1 | a0001c0004t0001g0220 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.872+853A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98129261 | ||||||
| chr2:98129278
|
A | G | 1 | a0001c0004t0001g0220 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.872+870A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98129278 | ||||||
| chr2:98129346
|
C | T | 12 | a0002c0002t0004g0030a0002c0002t0004g0032a0002c0002t0004g0033others(9): Show | 12 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.872+938C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98129346 | ||||||
| chr2:98129347
|
G | A | 3 | a0003c0003t0003g0060a0006c0007t0004g0067a0024c0034t0022g0078 | 3 | HG01891.hp2 HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.872+939G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98129347 | ||||||
| chr2:98129419
|
G | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0206 | 2 | HG00673.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.872+1011G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98129419 | ||||||
| chr2:98129431
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.872+1023A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98129431 | ||||||
| chr2:98129486
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.872+1078A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98129486 | ||||||
| chr2:98129747
|
T | C | 161 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0106others(158): Show | 161 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.872+1339T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98129747 | ||||||
| chr2:98129918
|
A | G | 163 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0090others(160): Show | 163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.872+1510A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98129918 | ||||||
| chr2:98129927
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.872+1519C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98129927 | ||||||
| chr2:98130030
|
G | A | 32 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0109others(29): Show | 32 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.872+1622G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98130030 | ||||||
| chr2:98130073
|
G | T | 1 | a0001c0001t0001g0118 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.872+1665G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98130073 | ||||||
| chr2:98130191
|
T | C | 1 | a0001c0004t0003g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.872+1783T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98130191 | ||||||
| chr2:98130305
|
C | T | 2 | a0002c0002t0004g0032a0021c0021t0003g0042 | 2 | HG01255.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.872+1897C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98130305 | ||||||
| chr2:98130327
|
G | A | 2 | a0002c0006t0002g0113a0011c0015t0001g0112 | 2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.872+1919G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98130327 | ||||||
| chr2:98130418
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.872+2010C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98130418 | ||||||
| chr2:98130483
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.872+2075A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98130483 | ||||||
| chr2:98130542
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.872+2134G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98130542 | ||||||
| chr2:98130588
|
C | T | 2 | a0001c0004t0003g0017a0002c0006t0004g0021 | 2 | HG00733.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.872+2180C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98130588 | ||||||
| chr2:98130814
|
A | G | 1 | a0003c0003t0003g0070 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.872+2406A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98130814 | ||||||
| chr2:98130971
|
A | G | 10 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.872+2563A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98130971 | ||||||
| chr2:98130998
|
C | T | 32 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0109others(29): Show | 32 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.872+2590C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98130998 | ||||||
| chr2:98131244
|
T | G | 37 | a0001c0001t0003g0047a0001c0001t0003g0236a0001c0001t0005g0045others(34): Show | 37 | HG01081.hp2 HG01261.hp2 HG01358.hp1 others(34): Show |
intron_variant | MODIFIER | c.873-2580T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98131244 | ||||||
| chr2:98131632
|
C | T | 10 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.873-2192C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98131632 | ||||||
| chr2:98131736
|
C | T | 1 | a0002c0002t0008g0177 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.873-2088C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98131736 | ||||||
| chr2:98131765
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.873-2059G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98131765 | ||||||
| chr2:98131878
|
G | A | 1 | a0010c0013t0002g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.873-1946G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98131878 | ||||||
| chr2:98131905
|
T | C | 1 | a0003c0003t0003g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.873-1919T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98131905 | ||||||
| chr2:98131972
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.873-1852T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98131972 | ||||||
| chr2:98132660
|
C | G | 29 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0109others(26): Show | 29 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.873-1164C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98132660 | ||||||
| chr2:98132898
|
G | A | 2 | a0002c0002t0008g0177a0002c0002t0008g0196 | 2 | HG00609.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.873-926G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98132898 | ||||||
| chr2:98133007
|
T | A | 164 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0106others(161): Show | 164 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.873-817T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98133007 | ||||||
| chr2:98133057
|
A | G | 10 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.873-767A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98133057 | ||||||
| chr2:98133123
|
A | G | 1 | a0002c0002t0002g0219 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.873-701A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98133123 | ||||||
| chr2:98133195
|
T | C | 1 | a0001c0004t0003g0020 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.873-629T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98133195 | ||||||
| chr2:98133427
|
C | T | 32 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(29): Show | 32 | HG01099.hp2 HG01123.hp2 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.873-397C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98133427 | ||||||
| chr2:98133466
|
C | A | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.873-358C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98133466 | ||||||
| chr2:98133493
|
A | G | 1 | a0004c0005t0002g0124 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.873-331A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | chr2 | 98133493 | ||||||
| chr2:98134067
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.988+128C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98134067 | ||||||
| chr2:98134177
|
C | T | 2 | a0003c0003t0003g0075a0025c0033t0006g0214 | 2 | NA19066.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.988+238C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98134177 | ||||||
| chr2:98134284
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.988+345C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98134284 | ||||||
| chr2:98134537
|
A | T | 1 | a0001c0004t0003g0010 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.988+598A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98134537 | ||||||
| chr2:98134590
|
C | T | 117 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0109others(114): Show | 117 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.988+651C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98134590 | ||||||
| chr2:98134827
|
T | C | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.988+888T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98134827 | ||||||
| chr2:98134929
|
T | C | 164 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0106others(161): Show | 164 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.988+990T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98134929 | ||||||
| chr2:98134966
|
A | G | 1 | a0002c0002t0002g0221 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.988+1027A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98134966 | ||||||
| chr2:98135083
|
G | T | 10 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.988+1144G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98135083 | ||||||
| chr2:98135325
|
C | CT | 11 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0206others(8): Show | 11 | HG00609.hp1 HG00673.hp2 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.988+1414dupT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 98135325 | |||||
| chr2:98135325
|
CT | C | 38 | a0001c0001t0001g0118a0001c0001t0001g0142a0001c0001t0001g0150others(35): Show | 38 | HG01081.hp2 HG01175.hp1 HG01261.hp2 others(35): Show |
intron_variant | MODIFIER | c.988+1414delT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 98135325 | |||||
| chr2:98135325
|
CTT | C | 66 | a0001c0001t0001g0083a0001c0001t0001g0090a0001c0001t0001g0106others(63): Show | 66 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.988+1413_988+1414d others(4): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 98135325 | |||||
| chr2:98135325
|
CTTT | C | 52 | a0001c0001t0001g0088a0001c0001t0001g0131a0001c0001t0001g0137others(49): Show | 52 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.988+1412_988+1414d others(5): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 98135325 | |||||
| chr2:98135325
|
CTTTTTTT others(2): Show |
C | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0003g0012others(3): Show | 6 | HG01167.hp2 HG02280.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.988+1406_988+1414d others(11): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 98135325 | |||||
| chr2:98135332
|
T | C | 1 | a0003c0003t0003g0076 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.988+1393T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98135332 | ||||||
| chr2:98135333
|
T | C | 10 | a0001c0001t0003g0232a0003c0003t0003g0074a0003c0003t0018g0081others(7): Show | 10 | HG00423.hp1 HG02615.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.988+1394T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98135333 | ||||||
| chr2:98135334
|
T | C | 39 | a0001c0001t0001g0137a0001c0001t0003g0238a0002c0002t0004g0030others(36): Show | 39 | HG00140.hp2 HG00323.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.988+1395T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98135334 | ||||||
| chr2:98135341
|
T | C | 1 | a0002c0012t0011g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.988+1402T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98135341 | ||||||
| chr2:98135359
|
A | G | 165 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0090others(162): Show | 165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.988+1420A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98135359 | ||||||
| chr2:98135461
|
G | A | 32 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0109others(29): Show | 32 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.988+1522G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98135461 | ||||||
| chr2:98135490
|
T | C | 1 | a0002c0012t0011g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.988+1551T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98135490 | ||||||
| chr2:98135492
|
C | T | 11 | a0003c0003t0003g0048a0003c0003t0003g0053a0003c0003t0003g0054others(8): Show | 11 | HG01361.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.988+1553C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98135492 | ||||||
| chr2:98135496
|
C | T | 7 | a0003c0003t0003g0048a0003c0003t0003g0054a0003c0003t0003g0055others(4): Show | 7 | HG02109.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.988+1557C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98135496 | ||||||
| chr2:98135546
|
G | A | 1 | a0004c0005t0002g0124 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.988+1607G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98135546 | ||||||
| chr2:98135582
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.988+1643G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98135582 | ||||||
| chr2:98135587
|
G | A | 1 | a0002c0002t0002g0001 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.988+1648G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98135587 | ||||||
| chr2:98135615
|
G | A | 1 | a0002c0002t0002g0123 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.988+1676G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98135615 | ||||||
| chr2:98136576
|
C | T | 2 | a0001c0001t0003g0236a0001c0001t0013g0028 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.988+2637C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98136576 | ||||||
| chr2:98136602
|
C | CA | 35 | a0001c0001t0003g0236a0001c0001t0013g0028a0001c0001t0023g0009others(32): Show | 35 | HG01081.hp2 HG01261.hp2 HG01358.hp1 others(32): Show |
intron_variant | MODIFIER | c.988+2677dupA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 98136602 | |||||
| chr2:98136748
|
A | C | 36 | a0001c0001t0003g0047a0001c0001t0003g0236a0001c0001t0005g0045others(33): Show | 36 | HG01081.hp2 HG01261.hp2 HG01358.hp1 others(33): Show |
intron_variant | MODIFIER | c.988+2809A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98136748 | ||||||
| chr2:98136822
|
C | T | 1 | a0001c0004t0001g0220 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.988+2883C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98136822 | ||||||
| chr2:98136855
|
A | T | 1 | a0001c0001t0001g0208 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.988+2916A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98136855 | ||||||
| chr2:98137009
|
C | T | 1 | a0002c0002t0001g0102 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.988+3070C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98137009 | ||||||
| chr2:98137065
|
G | C | 2 | a0003c0003t0003g0065a0003c0003t0003g0066 | 2 | HG00673.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.988+3126G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98137065 | ||||||
| chr2:98137113
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.988+3174T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98137113 | ||||||
| chr2:98137262
|
C | T | 1 | a0013c0014t0017g0126 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.988+3323C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98137262 | ||||||
| chr2:98137434
|
A | T | 1 | a0002c0012t0011g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.988+3495A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98137434 | ||||||
| chr2:98137559
|
G | A | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.988+3620G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98137559 | ||||||
| chr2:98137578
|
A | C | 38 | a0001c0001t0003g0047a0001c0001t0003g0236a0001c0001t0005g0045others(35): Show | 38 | HG01081.hp2 HG01261.hp2 HG01358.hp1 others(35): Show |
intron_variant | MODIFIER | c.988+3639A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98137578 | ||||||
| chr2:98137859
|
TAAC | T | 36 | a0001c0001t0003g0047a0001c0001t0003g0236a0001c0001t0005g0045others(33): Show | 36 | HG01081.hp2 HG01261.hp2 HG01358.hp1 others(33): Show |
intron_variant | MODIFIER | c.988+3923_988+3925d others(5): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 98137859 | |||||
| chr2:98137863
|
A | C | 32 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0109others(29): Show | 32 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.988+3924A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98137863 | ||||||
| chr2:98138257
|
G | A | 1 | a0002c0012t0011g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.988+4318G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98138257 | ||||||
| chr2:98138782
|
A | G | 1 | a0001c0004t0003g0020 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.988+4843A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98138782 | ||||||
| chr2:98138789
|
G | T | 117 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0109others(114): Show | 117 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.988+4850G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98138789 | ||||||
| chr2:98138856
|
C | T | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.988+4917C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98138856 | ||||||
| chr2:98138946
|
A | C | 165 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0090others(162): Show | 165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.988+5007A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98138946 | ||||||
| chr2:98139196
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.988+5257C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98139196 | ||||||
| chr2:98139201
|
C | T | 32 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(29): Show | 32 | HG01099.hp2 HG01123.hp2 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.988+5262C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98139201 | ||||||
| chr2:98139216
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.988+5277C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98139216 | ||||||
| chr2:98139273
|
C | T | 1 | a0002c0002t0004g0033 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.988+5334C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98139273 | ||||||
| chr2:98139284
|
C | G | 1 | a0003c0003t0005g0069 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.988+5345C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98139284 | ||||||
| chr2:98139292
|
C | T | 12 | a0002c0002t0004g0030a0002c0002t0004g0032a0002c0002t0004g0033others(9): Show | 12 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.988+5353C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98139292 | ||||||
| chr2:98139322
|
G | A | 36 | a0001c0001t0003g0047a0001c0001t0003g0236a0001c0001t0005g0045others(33): Show | 36 | HG01081.hp2 HG01261.hp2 HG01358.hp1 others(33): Show |
intron_variant | MODIFIER | c.988+5383G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98139322 | ||||||
| chr2:98139373
|
C | T | 4 | a0002c0002t0004g0002a0002c0002t0004g0005a0002c0002t0021g0006others(1): Show | 4 | HG02109.hp2 HG02647.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.988+5434C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98139373 | ||||||
| chr2:98139385
|
C | T | 32 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0109others(29): Show | 32 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.988+5446C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98139385 | ||||||
| chr2:98139393
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0016g0152 | 2 | NA18941.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.988+5454C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98139393 | ||||||
| chr2:98139394
|
G | A | 1 | a0002c0012t0011g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.988+5455G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98139394 | ||||||
| chr2:98139609
|
T | C | 164 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0106others(161): Show | 164 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.988+5670T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98139609 | ||||||
| chr2:98139741
|
G | A | 7 | a0003c0003t0001g0199a0003c0003t0001g0201a0003c0003t0001g0202others(4): Show | 7 | NA18959.hp2 NA18977.hp2 NA18985.hp2 others(4): Show |
intron_variant | MODIFIER | c.988+5802G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98139741 | ||||||
| chr2:98139951
|
C | T | 1 | a0012c0036t0003g0063 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.988+6012C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98139951 | ||||||
| chr2:98140044
|
A | G | 1 | a0001c0004t0003g0017 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.988+6105A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98140044 | ||||||
| chr2:98140053
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.988+6114C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98140053 | ||||||
| chr2:98140180
|
G | T | 1 | a0003c0003t0003g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.988+6241G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98140180 | ||||||
| chr2:98140439
|
T | A | 36 | a0001c0001t0003g0047a0001c0001t0003g0236a0001c0001t0005g0045others(33): Show | 36 | HG01081.hp2 HG01261.hp2 HG01358.hp1 others(33): Show |
intron_variant | MODIFIER | c.988+6500T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98140439 | ||||||
| chr2:98140524
|
A | C | 2 | a0001c0004t0003g0025a0001c0004t0003g0026 | 2 | NA18951.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.988+6585A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98140524 | ||||||
| chr2:98140547
|
C | T | 2 | a0001c0004t0003g0025a0001c0004t0003g0026 | 2 | NA18951.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.988+6608C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98140547 | ||||||
| chr2:98141004
|
G | A | 32 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(29): Show | 32 | HG01099.hp2 HG01123.hp2 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.988+7065G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98141004 | ||||||
| chr2:98141024
|
C | A | 1 | a0001c0004t0004g0018 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.988+7085C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98141024 | ||||||
| chr2:98141044
|
T | C | 1 | a0001c0001t0001g0203 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.988+7105T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98141044 | ||||||
| chr2:98141072
|
G | A | 2 | a0001c0004t0003g0017a0002c0006t0004g0021 | 2 | HG00733.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.988+7133G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98141072 | ||||||
| chr2:98141147
|
T | C | 1 | a0003c0003t0003g0077 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.988+7208T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98141147 | ||||||
| chr2:98141239
|
C | T | 2 | a0001c0001t0023g0009a0002c0002t0024g0008 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.988+7300C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98141239 | ||||||
| chr2:98141298
|
G | T | 32 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(29): Show | 32 | HG01099.hp2 HG01123.hp2 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.988+7359G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98141298 | ||||||
| chr2:98141860
|
C | T | 117 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0109others(114): Show | 117 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.988+7921C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98141860 | ||||||
| chr2:98141921
|
C | G | 1 | a0001c0001t0001g0188 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.988+7982C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98141921 | ||||||
| chr2:98142042
|
G | A | 117 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0109others(114): Show | 117 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.988+8103G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98142042 | ||||||
| chr2:98142182
|
T | A | 1 | a0002c0002t0004g0022 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.988+8243T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98142182 | ||||||
| chr2:98142277
|
C | G | 1 | a0020c0026t0002g0210 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.988+8338C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98142277 | ||||||
| chr2:98142327
|
G | T | 1 | a0002c0016t0020g0031 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.988+8388G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98142327 | ||||||
| chr2:98142351
|
G | T | 26 | a0001c0001t0001g0137a0003c0003t0001g0199a0003c0003t0001g0201others(23): Show | 26 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.988+8412G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98142351 | ||||||
| chr2:98142384
|
G | A | 165 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0090others(162): Show | 165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.988+8445G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98142384 | ||||||
| chr2:98142892
|
C | G | 1 | a0002c0012t0011g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.988+8953C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98142892 | ||||||
| chr2:98142908
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.988+8969C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98142908 | ||||||
| chr2:98143417
|
A | C | 1 | a0020c0026t0002g0210 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.988+9478A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98143417 | ||||||
| chr2:98143440
|
C | T | 1 | a0002c0002t0024g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.988+9501C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98143440 | ||||||
| chr2:98143539
|
G | T | 1 | a0001c0001t0001g0195 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.988+9600G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98143539 | ||||||
| chr2:98143637
|
A | T | 2 | a0007c0009t0002g0139a0007c0009t0002g0140 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.988+9698A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98143637 | ||||||
| chr2:98143703
|
G | A | 1 | a0001c0004t0001g0220 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.988+9764G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98143703 | ||||||
| chr2:98143752
|
C | CT | 33 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0156others(30): Show | 33 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.988+9830dupT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 98143752 | |||||
| chr2:98144092
|
G | C | 28 | a0001c0001t0003g0047a0001c0001t0003g0236a0001c0001t0005g0045others(25): Show | 28 | HG01081.hp2 HG01261.hp2 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.988+10153G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98144092 | ||||||
| chr2:98144152
|
G | T | 38 | a0001c0001t0001g0137a0001c0001t0003g0232a0001c0001t0003g0238others(35): Show | 38 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.988+10213G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98144152 | ||||||
| chr2:98144435
|
C | T | 10 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.988+10496C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98144435 | ||||||
| chr2:98144566
|
CT | C | 118 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0109others(115): Show | 118 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.988+10641delT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 98144566 | |||||
| chr2:98144614
|
T | G | 32 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0109others(29): Show | 32 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.988+10675T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98144614 | ||||||
| chr2:98144766
|
C | G | 1 | a0002c0019t0011g0228 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.988+10827C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98144766 | ||||||
| chr2:98144800
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.988+10861C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98144800 | ||||||
| chr2:98144826
|
C | CA | 165 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0090others(162): Show | 165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.988+10889dupA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 98144826 | |||||
| chr2:98144928
|
A | G | 165 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0090others(162): Show | 165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.988+10989A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98144928 | ||||||
| chr2:98144947
|
T | C | 10 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.988+11008T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98144947 | ||||||
| chr2:98145080
|
T | C | 1 | a0009c0011t0001g0213 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.988+11141T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98145080 | ||||||
| chr2:98145126
|
A | G | 36 | a0001c0001t0003g0047a0001c0001t0003g0236a0001c0001t0005g0045others(33): Show | 36 | HG01081.hp2 HG01261.hp2 HG01358.hp1 others(33): Show |
intron_variant | MODIFIER | c.988+11187A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98145126 | ||||||
| chr2:98145727
|
G | GT | 14 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0135others(11): Show | 14 | HG00408.hp2 HG01167.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.988+11798dupT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 98145727 | |||||
| chr2:98145765
|
G | A | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.988+11826G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98145765 | ||||||
| chr2:98145905
|
A | G | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.988+11966A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98145905 | ||||||
| chr2:98146031
|
A | G | 164 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0106others(161): Show | 164 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.988+12092A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98146031 | ||||||
| chr2:98146053
|
A | G | 12 | a0002c0002t0004g0030a0002c0002t0004g0032a0002c0002t0004g0033others(9): Show | 12 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.988+12114A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98146053 | ||||||
| chr2:98146548
|
T | G | 10 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.988+12609T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98146548 | ||||||
| chr2:98146645
|
A | G | 1 | a0002c0002t0024g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.988+12706A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98146645 | ||||||
| chr2:98146696
|
C | T | 32 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0109others(29): Show | 32 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.988+12757C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98146696 | ||||||
| chr2:98146828
|
C | T | 7 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0003g0012others(4): Show | 7 | HG01167.hp2 HG02280.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.988+12889C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98146828 | ||||||
| chr2:98146906
|
C | T | 1 | a0013c0014t0017g0126 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.988+12967C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98146906 | ||||||
| chr2:98147114
|
T | C | 2 | a0001c0004t0003g0017a0002c0006t0004g0021 | 2 | HG00733.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.988+13175T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98147114 | ||||||
| chr2:98147403
|
G | A | 1 | a0002c0002t0002g0111 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.988+13464G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98147403 | ||||||
| chr2:98147701
|
T | G | 5 | a0001c0001t0003g0012a0001c0001t0003g0236a0001c0001t0013g0028others(2): Show | 5 | HG01261.hp2 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.988+13762T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98147701 | ||||||
| chr2:98147748
|
C | T | 83 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(80): Show | 83 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.988+13809C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98147748 | ||||||
| chr2:98147792
|
C | G | 1 | a0002c0012t0011g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.988+13853C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98147792 | ||||||
| chr2:98148177
|
T | C | 73 | a0001c0001t0001g0137a0001c0001t0003g0047a0001c0001t0003g0232others(70): Show | 73 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.988+14238T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98148177 | ||||||
| chr2:98148203
|
A | G | 3 | a0001c0001t0007g0146a0001c0001t0007g0147a0001c0001t0007g0148 | 3 | NA18945.hp2 NA18963.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.988+14264A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98148203 | ||||||
| chr2:98148240
|
C | T | 1 | a0002c0002t0004g0030 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.988+14301C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98148240 | ||||||
| chr2:98148310
|
G | A | 10 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.988+14371G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98148310 | ||||||
| chr2:98148439
|
C | T | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.989-14412C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98148439 | ||||||
| chr2:98148460
|
T | C | 84 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0105others(81): Show | 84 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.989-14391T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98148460 | ||||||
| chr2:98148510
|
A | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.989-14341A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98148510 | ||||||
| chr2:98148988
|
A | T | 4 | a0001c0001t0001g0083a0001c0001t0023g0009a0002c0002t0024g0008others(1): Show | 4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.989-13863A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98148988 | ||||||
| chr2:98149452
|
C | T | 1 | a0004c0005t0002g0185 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.989-13399C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98149452 | ||||||
| chr2:98149628
|
G | A | 1 | a0003c0003t0003g0048 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.989-13223G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98149628 | ||||||
| chr2:98149851
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.989-13000A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98149851 | ||||||
| chr2:98150087
|
A | G | 72 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(69): Show | 72 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.989-12764A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98150087 | ||||||
| chr2:98150354
|
G | A | 1 | a0008c0010t0004g0227 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.989-12497G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98150354 | ||||||
| chr2:98150505
|
C | A | 2 | a0001c0004t0003g0044a0003c0003t0003g0053 | 2 | HG01361.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.989-12346C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98150505 | ||||||
| chr2:98150603
|
G | A | 4 | a0001c0001t0001g0083a0001c0001t0023g0009a0002c0002t0024g0008others(1): Show | 4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.989-12248G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98150603 | ||||||
| chr2:98150769
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.989-12082C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98150769 | ||||||
| chr2:98150781
|
G | A | 66 | a0001c0001t0001g0082a0001c0001t0001g0089a0001c0001t0001g0105others(63): Show | 66 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.989-12070G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98150781 | ||||||
| chr2:98150884
|
A | G | 7 | a0003c0003t0003g0048a0003c0003t0003g0055a0003c0003t0005g0058others(4): Show | 7 | HG02109.hp1 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.989-11967A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98150884 | ||||||
| chr2:98151102
|
T | C | 24 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0003g0232others(21): Show | 24 | HG01071.hp1 HG01081.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.989-11749T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98151102 | ||||||
| chr2:98151119
|
A | AT | 12 | a0001c0001t0001g0083a0001c0001t0001g0144a0001c0001t0001g0145others(9): Show | 12 | HG01123.hp1 HG01243.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.989-11717dupT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 98151119 | |||||
| chr2:98151176
|
G | A | 1 | a0002c0002t0002g0116 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.989-11675G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98151176 | ||||||
| chr2:98151215
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.989-11636C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98151215 | ||||||
| chr2:98151461
|
G | A | 4 | a0001c0001t0001g0083a0001c0001t0023g0009a0002c0002t0024g0008others(1): Show | 4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.989-11390G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98151461 | ||||||
| chr2:98151499
|
TGGCCAGA others(2497): Show |
T | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.989-11348_989-8845 others(3): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 98151499 | |||||
| chr2:98151519
|
T | A | 82 | a0001c0001t0001g0083a0001c0001t0001g0127a0001c0001t0001g0130others(79): Show | 82 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.989-11332T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98151519 | ||||||
| chr2:98151872
|
C | T | 1 | a0009c0011t0001g0171 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.989-10979C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98151872 | ||||||
| chr2:98152137
|
A | AG | 3 | a0001c0001t0001g0144a0001c0001t0001g0145a0013c0014t0017g0126 | 3 | HG02572.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.989-10712dupG | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 98152137 | |||||
| chr2:98152322
|
C | T | 1 | a0014c0030t0002g0120 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.989-10529C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98152322 | ||||||
| chr2:98152907
|
C | T | 3 | a0001c0001t0001g0144a0001c0001t0001g0145a0013c0014t0017g0126 | 3 | HG02572.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.989-9944C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98152907 | ||||||
| chr2:98153059
|
C | T | 4 | a0001c0001t0003g0236a0001c0001t0013g0028a0002c0002t0003g0024others(1): Show | 4 | HG01261.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.989-9792C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98153059 | ||||||
| chr2:98153098
|
C | G | 2 | a0007c0009t0002g0091a0007c0009t0002g0092 | 2 | HG01071.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.989-9753C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98153098 | ||||||
| chr2:98153195
|
ACTAT | A | 9 | a0005c0008t0003g0229a0005c0008t0003g0231a0005c0008t0003g0233others(6): Show | 9 | HG02615.hp1 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.989-9654_989-9651d others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 98153195 | |||||
| chr2:98153201
|
A | G | 9 | a0005c0008t0003g0229a0005c0008t0003g0231a0005c0008t0003g0233others(6): Show | 9 | HG02615.hp1 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.989-9650A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98153201 | ||||||
| chr2:98153300
|
G | T | 2 | a0002c0002t0004g0036a0002c0002t0004g0037 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.989-9551G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98153300 | ||||||
| chr2:98153423
|
C | T | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.989-9428C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98153423 | ||||||
| chr2:98153478
|
A | T | 2 | a0001c0001t0001g0105a0001c0001t0001g0167 | 2 | NA18982.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.989-9373A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98153478 | ||||||
| chr2:98153523
|
G | A | 2 | a0001c0001t0023g0009a0002c0002t0024g0008 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.989-9328G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98153523 | ||||||
| chr2:98153762
|
C | T | 1 | a0002c0002t0004g0032 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.989-9089C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98153762 | ||||||
| chr2:98153872
|
T | A | 1 | a0002c0002t0004g0003 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.989-8979T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98153872 | ||||||
| chr2:98154115
|
G | A | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.989-8736G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98154115 | ||||||
| chr2:98154158
|
A | G | 3 | a0001c0001t0023g0009a0002c0002t0024g0008a0020c0026t0002g0210 | 3 | HG01243.hp2 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.989-8693A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98154158 | ||||||
| chr2:98154359
|
G | A | 2 | a0002c0002t0002g0095a0002c0002t0002g0096 | 2 | NA18993.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.989-8492G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98154359 | ||||||
| chr2:98154389
|
A | G | 1 | a0001c0004t0003g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.989-8462A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98154389 | ||||||
| chr2:98154527
|
G | A | 1 | a0006c0007t0009g0080 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.989-8324G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98154527 | ||||||
| chr2:98154676
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | NA19056.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.989-8175T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98154676 | ||||||
| chr2:98155081
|
G | A | 9 | a0005c0008t0003g0229a0005c0008t0003g0231a0005c0008t0003g0233others(6): Show | 9 | HG02615.hp1 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.989-7770G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98155081 | ||||||
| chr2:98155130
|
G | A | 6 | a0001c0001t0001g0178a0001c0001t0001g0179a0002c0002t0002g0173others(3): Show | 6 | HG00280.hp2 HG00735.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.989-7721G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98155130 | ||||||
| chr2:98155293
|
G | A | 1 | a0024c0034t0022g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.989-7558G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98155293 | ||||||
| chr2:98155402
|
A | G | 1 | a0002c0012t0004g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.989-7449A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98155402 | ||||||
| chr2:98155699
|
A | G | 3 | a0001c0001t0001g0144a0001c0001t0001g0145a0013c0014t0017g0126 | 3 | HG02572.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.989-7152A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98155699 | ||||||
| chr2:98156091
|
A | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0203 | 2 | HG00621.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.989-6760A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98156091 | ||||||
| chr2:98156164
|
G | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0187 | 2 | HG00423.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.989-6687G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98156164 | ||||||
| chr2:98156188
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.989-6663G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98156188 | ||||||
| chr2:98156486
|
G | A | 3 | a0001c0001t0003g0047a0001c0001t0005g0045a0015c0029t0004g0046 | 3 | HG02486.hp2 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.989-6365G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98156486 | ||||||
| chr2:98156666
|
GT | G | 68 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0135others(65): Show | 68 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.989-6166delT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 98156666 | |||||
| chr2:98156668
|
T | TG | 74 | a0001c0001t0001g0082a0001c0001t0001g0089a0001c0001t0001g0105others(71): Show | 74 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.989-6183_989-6182i others(3): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98156668 | ||||||
| chr2:98156669
|
T | G | 83 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0090others(80): Show | 83 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.989-6182T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98156669 | ||||||
| chr2:98156670
|
T | G | 68 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0135others(65): Show | 68 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.989-6181T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98156670 | ||||||
| chr2:98156898
|
A | G | 87 | a0001c0001t0001g0083a0001c0001t0001g0127a0001c0001t0001g0130others(84): Show | 87 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(84): Show |
intron_variant | MODIFIER | c.989-5953A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98156898 | ||||||
| chr2:98156917
|
G | A | 1 | a0003c0003t0018g0081 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.989-5934G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98156917 | ||||||
| chr2:98156918
|
G | T | 1 | a0015c0029t0004g0046 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.989-5933G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98156918 | ||||||
| chr2:98157041
|
C | T | 192 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(189): Show | 192 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.989-5810C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98157041 | ||||||
| chr2:98157833
|
T | TC | 239 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(236): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.989-5015dupC | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 98157833 | |||||
| chr2:98157959
|
T | A | 4 | a0005c0008t0003g0229a0005c0008t0003g0231a0005c0008t0003g0233others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.989-4892T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98157959 | ||||||
| chr2:98157962
|
A | G | 1 | a0004c0005t0002g0107 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.989-4889A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98157962 | ||||||
| chr2:98158295
|
A | G | 4 | a0001c0001t0001g0083a0001c0001t0023g0009a0002c0002t0024g0008others(1): Show | 4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.989-4556A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98158295 | ||||||
| chr2:98158317
|
A | G | 80 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0089others(77): Show | 80 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.989-4534A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98158317 | ||||||
| chr2:98158510
|
C | T | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.989-4341C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98158510 | ||||||
| chr2:98158530
|
T | C | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.989-4321T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98158530 | ||||||
| chr2:98158609
|
C | T | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.989-4242C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98158609 | ||||||
| chr2:98158655
|
C | T | 80 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0089others(77): Show | 80 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.989-4196C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98158655 | ||||||
| chr2:98158710
|
TG | T | 192 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(189): Show | 192 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.989-4136delG | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 98158710 | |||||
| chr2:98158835
|
G | A | 80 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0089others(77): Show | 80 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.989-4016G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98158835 | ||||||
| chr2:98158847
|
A | G | 1 | a0003c0003t0003g0068 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.989-4004A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98158847 | ||||||
| chr2:98158966
|
A | G | 1 | a0002c0002t0004g0032 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.989-3885A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98158966 | ||||||
| chr2:98159134
|
C | T | 1 | a0002c0002t0004g0005 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.989-3717C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98159134 | ||||||
| chr2:98159222
|
C | T | 1 | a0020c0026t0002g0210 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.989-3629C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98159222 | ||||||
| chr2:98159409
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.989-3442C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98159409 | ||||||
| chr2:98159457
|
C | T | 31 | a0001c0001t0001g0137a0001c0001t0001g0215a0002c0002t0004g0036others(28): Show | 31 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.989-3394C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98159457 | ||||||
| chr2:98159553
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.989-3298A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98159553 | ||||||
| chr2:98159787
|
C | T | 71 | a0001c0001t0001g0083a0001c0001t0001g0127a0001c0001t0001g0130others(68): Show | 71 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.989-3064C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98159787 | ||||||
| chr2:98160007
|
T | TA | 82 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0089others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.989-2828dupA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 98160007 | |||||
| chr2:98160007
|
TA | T | 9 | a0001c0001t0001g0083a0001c0001t0001g0122a0001c0001t0001g0178others(6): Show | 9 | HG01517.hp2 HG02056.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.989-2828delA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 98160007 | |||||
| chr2:98160030
|
T | G | 2 | a0012c0035t0004g0064a0012c0036t0003g0063 | 2 | HG00609.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.989-2821T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98160030 | ||||||
| chr2:98160082
|
A | T | 1 | a0001c0001t0001g0130 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.989-2769A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98160082 | ||||||
| chr2:98160393
|
C | T | 31 | a0001c0001t0001g0137a0001c0001t0001g0215a0002c0002t0004g0036others(28): Show | 31 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.989-2458C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98160393 | ||||||
| chr2:98160398
|
T | C | 1 | a0003c0003t0005g0069 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.989-2453T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98160398 | ||||||
| chr2:98161049
|
G | A | 1 | a0021c0021t0003g0042 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.989-1802G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98161049 | ||||||
| chr2:98161175
|
G | T | 1 | a0009c0011t0001g0213 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.989-1676G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98161175 | ||||||
| chr2:98161210
|
G | A | 80 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0089others(77): Show | 80 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.989-1641G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98161210 | ||||||
| chr2:98161361
|
C | T | 2 | a0001c0001t0001g0117a0002c0002t0002g0116 | 2 | HG01168.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.989-1490C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98161361 | ||||||
| chr2:98161365
|
G | A | 1 | a0001c0004t0003g0013 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.989-1486G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98161365 | ||||||
| chr2:98161529
|
G | A | 71 | a0001c0001t0001g0083a0001c0001t0001g0127a0001c0001t0001g0130others(68): Show | 71 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.989-1322G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98161529 | ||||||
| chr2:98161542
|
C | T | 4 | a0001c0001t0001g0115a0001c0001t0001g0144a0001c0001t0001g0145others(1): Show | 4 | HG00597.hp2 HG02572.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.989-1309C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98161542 | ||||||
| chr2:98161568
|
A | C | 73 | a0001c0001t0001g0083a0001c0001t0001g0127a0001c0001t0001g0130others(70): Show | 73 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.989-1283A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98161568 | ||||||
| chr2:98161616
|
A | G | 167 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(164): Show | 167 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.989-1235A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98161616 | ||||||
| chr2:98161907
|
A | G | 3 | a0001c0001t0001g0144a0001c0001t0001g0145a0013c0014t0017g0126 | 3 | HG02572.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.989-944A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98161907 | ||||||
| chr2:98161926
|
C | T | 1 | a0003c0003t0005g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.989-925C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98161926 | ||||||
| chr2:98161959
|
G | A | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.989-892G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98161959 | ||||||
| chr2:98162035
|
C | G | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.989-816C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98162035 | ||||||
| chr2:98162107
|
C | A | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.989-744C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98162107 | ||||||
| chr2:98163161
|
ATG | A | 7 | a0005c0008t0003g0229a0005c0008t0003g0233a0005c0008t0003g0234others(4): Show | 7 | HG02615.hp1 HG02976.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1114+200_1114+201d others(4): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98163161 | |||||
| chr2:98163162
|
T | C | 11 | a0001c0001t0001g0083a0001c0001t0023g0009a0002c0002t0004g0002others(8): Show | 11 | HG01243.hp2 HG02056.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.1114+186T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98163162 | ||||||
| chr2:98163291
|
G | C | 9 | a0005c0008t0003g0229a0005c0008t0003g0231a0005c0008t0003g0233others(6): Show | 9 | HG02615.hp1 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114+315G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98163291 | ||||||
| chr2:98163371
|
C | T | 31 | a0001c0001t0001g0137a0001c0001t0001g0155a0001c0001t0001g0215others(28): Show | 31 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.1114+395C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98163371 | ||||||
| chr2:98163477
|
A | G | 169 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(166): Show | 169 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.1114+501A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98163477 | ||||||
| chr2:98163538
|
A | G | 37 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(34): Show | 37 | HG01099.hp2 HG01123.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.1114+562A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98163538 | ||||||
| chr2:98163539
|
A | C | 4 | a0001c0001t0001g0083a0001c0001t0023g0009a0002c0002t0024g0008others(1): Show | 4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114+563A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98163539 | ||||||
| chr2:98163598
|
A | C | 1 | a0002c0002t0001g0190 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1114+622A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98163598 | ||||||
| chr2:98163840
|
C | T | 1 | a0020c0026t0002g0210 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1114+864C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98163840 | ||||||
| chr2:98163939
|
G | A | 1 | a0002c0002t0002g0116 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1114+963G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98163939 | ||||||
| chr2:98164054
|
G | A | 1 | a0024c0034t0022g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1114+1078G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98164054 | ||||||
| chr2:98164281
|
G | T | 2 | a0001c0004t0003g0017a0002c0006t0004g0021 | 2 | HG00733.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1114+1305G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98164281 | ||||||
| chr2:98164727
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1114+1751T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98164727 | ||||||
| chr2:98164765
|
C | T | 1 | a0024c0034t0022g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1114+1789C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98164765 | ||||||
| chr2:98164825
|
C | G | 27 | a0001c0001t0001g0137a0001c0001t0001g0215a0002c0002t0004g0036others(24): Show | 27 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.1114+1849C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98164825 | ||||||
| chr2:98164839
|
C | T | 1 | a0002c0002t0004g0003 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1114+1863C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98164839 | ||||||
| chr2:98164905
|
C | G | 1 | a0003c0003t0003g0052 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1114+1929C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98164905 | ||||||
| chr2:98164945
|
T | C | 1 | a0024c0034t0022g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1114+1969T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98164945 | ||||||
| chr2:98164980
|
C | T | 3 | a0002c0002t0004g0002a0002c0002t0004g0005a0002c0002t0021g0006 | 3 | HG02647.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1114+2004C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98164980 | ||||||
| chr2:98165168
|
C | T | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0003g0012others(3): Show | 6 | HG01167.hp2 HG02280.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1114+2192C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98165168 | ||||||
| chr2:98165222
|
A | T | 1 | a0024c0034t0022g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1114+2246A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98165222 | ||||||
| chr2:98165297
|
C | T | 1 | a0020c0026t0002g0210 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1114+2321C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98165297 | ||||||
| chr2:98165360
|
T | C | 1 | a0001c0001t0003g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1114+2384T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98165360 | ||||||
| chr2:98165384
|
C | T | 73 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0089others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.1114+2408C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98165384 | ||||||
| chr2:98165385
|
G | A | 1 | a0003c0003t0003g0065 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1114+2409G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98165385 | ||||||
| chr2:98165402
|
G | A | 1 | a0002c0002t0002g0163 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1114+2426G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98165402 | ||||||
| chr2:98165437
|
A | T | 1 | a0002c0002t0004g0040 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1114+2461A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98165437 | ||||||
| chr2:98165473
|
C | T | 9 | a0005c0008t0003g0229a0005c0008t0003g0231a0005c0008t0003g0233others(6): Show | 9 | HG02615.hp1 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114+2497C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98165473 | ||||||
| chr2:98165922
|
G | C | 1 | a0003c0003t0018g0081 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1114+2946G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98165922 | ||||||
| chr2:98165986
|
A | G | 1 | a0001c0001t0001g0114 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1114+3010A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98165986 | ||||||
| chr2:98166065
|
G | A | 1 | a0001c0001t0023g0009 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1114+3089G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98166065 | ||||||
| chr2:98166174
|
C | G | 29 | a0001c0001t0001g0137a0001c0001t0001g0215a0002c0002t0004g0036others(26): Show | 29 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.1114+3198C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98166174 | ||||||
| chr2:98166231
|
G | A | 1 | a0024c0034t0022g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1114+3255G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98166231 | ||||||
| chr2:98166513
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1114+3537G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98166513 | ||||||
| chr2:98166799
|
T | TACACAC | 3 | a0001c0001t0001g0144a0001c0001t0001g0145a0013c0014t0017g0126 | 3 | HG02572.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1114+3844_1114+384 others(10): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98166799 | |||||
| chr2:98166799
|
T | TACACACA others(3): Show |
12 | a0001c0001t0001g0204a0003c0032t0003g0062a0005c0008t0003g0229others(9): Show | 12 | HG01243.hp2 HG02615.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.1114+3840_1114+384 others(14): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98166799 | |||||
| chr2:98166799
|
T | TACACACA others(5): Show |
65 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0089others(62): Show | 65 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.1114+3838_1114+384 others(16): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98166799 | |||||
| chr2:98166799
|
T | TACACACA others(7): Show |
36 | a0001c0001t0001g0133a0001c0001t0001g0167a0001c0001t0001g0184others(33): Show | 36 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.1114+3836_1114+384 others(18): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98166799 | |||||
| chr2:98166799
|
T | TACACACA others(9): Show |
25 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0136others(22): Show | 25 | HG01123.hp2 HG01167.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.1114+3834_1114+384 others(20): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98166799 | |||||
| chr2:98166799
|
T | TACACACA others(11): Show |
32 | a0001c0001t0001g0083a0001c0001t0001g0137a0001c0001t0001g0138others(29): Show | 32 | HG01081.hp2 HG01099.hp2 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.1114+3832_1114+384 others(22): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98166799 | |||||
| chr2:98166799
|
T | TACACACA others(13): Show |
7 | a0001c0001t0001g0132a0001c0001t0003g0236a0001c0001t0013g0028others(4): Show | 7 | HG01346.hp2 HG02056.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.1114+3830_1114+384 others(24): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98166799 | |||||
| chr2:98166799
|
T | TACACACA others(15): Show |
3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0003g0232 | 3 | HG02896.hp2 HG03209.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1114+3828_1114+384 others(26): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98166799 | |||||
| chr2:98166799
|
T | TACACACA others(17): Show |
2 | a0007c0009t0002g0091a0007c0009t0002g0092 | 2 | HG01071.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1114+3826_1114+384 others(28): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98166799 | |||||
| chr2:98166799
|
TAC | T | 39 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0109others(36): Show | 39 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.1114+3848_1114+384 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98166799 | |||||
| chr2:98166980
|
G | A | 1 | a0001c0001t0003g0238 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1114+4004G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98166980 | ||||||
| chr2:98166984
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1114+4008G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98166984 | ||||||
| chr2:98167075
|
C | A | 7 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0158others(4): Show | 7 | HG00544.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.1114+4099C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98167075 | ||||||
| chr2:98167327
|
T | C | 1 | a0024c0034t0022g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1114+4351T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98167327 | ||||||
| chr2:98167581
|
G | A | 1 | a0002c0002t0004g0011 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1114+4605G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98167581 | ||||||
| chr2:98167812
|
T | C | 166 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(163): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1114+4836T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98167812 | ||||||
| chr2:98168000
|
C | A | 2 | a0007c0009t0002g0091a0007c0009t0002g0092 | 2 | HG01071.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1114+5024C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98168000 | ||||||
| chr2:98168351
|
T | G | 9 | a0004c0005t0002g0093a0004c0005t0002g0098a0004c0005t0002g0099others(6): Show | 9 | NA18942.hp2 NA18948.hp1 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.1114+5375T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98168351 | ||||||
| chr2:98168370
|
C | CACAT | 8 | a0001c0004t0003g0013a0001c0004t0003g0020a0001c0004t0003g0025others(5): Show | 8 | HG01358.hp1 HG02056.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.1114+5397_1114+539 others(8): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98168370 | |||||
| chr2:98168372
|
C | CAT | 15 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0003g0232others(12): Show | 15 | HG01071.hp1 HG01081.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1114+5397_1114+539 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98168372 | |||||
| chr2:98168376
|
T | C | 24 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0003g0232others(21): Show | 24 | HG01071.hp1 HG01081.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1114+5400T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98168376 | ||||||
| chr2:98168376
|
T | TAC | 40 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0137others(37): Show | 40 | HG00423.hp1 HG00673.hp1 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.1114+5432_1114+543 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98168376 | |||||
| chr2:98168376
|
T | TACAC | 63 | a0001c0001t0001g0082a0001c0001t0001g0089a0001c0001t0001g0105others(60): Show | 63 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.1114+5430_1114+543 others(8): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98168376 | |||||
| chr2:98168376
|
T | TACACAC | 6 | a0001c0001t0001g0133a0001c0001t0001g0193a0001c0001t0001g0207others(3): Show | 6 | HG00423.hp2 HG00609.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.1114+5428_1114+543 others(10): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98168376 | |||||
| chr2:98168376
|
T | TACACACA others(3): Show |
2 | a0002c0002t0004g0032a0021c0021t0003g0042 | 2 | HG01255.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1114+5424_1114+543 others(14): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98168376 | |||||
| chr2:98168376
|
TAC | T | 47 | a0001c0001t0001g0083a0001c0001t0001g0090a0001c0001t0001g0106others(44): Show | 47 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.1114+5432_1114+543 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98168376 | |||||
| chr2:98168376
|
TACAC | T | 6 | a0001c0001t0003g0047a0001c0001t0005g0045a0001c0001t0023g0009others(3): Show | 6 | HG01243.hp2 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1114+5430_1114+543 others(8): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98168376 | |||||
| chr2:98168409
|
A | ACAC | 3 | a0001c0001t0001g0172a0001c0001t0001g0183a0001c0004t0001g0220 | 3 | HG01952.hp1 HG01952.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1114+5433_1114+543 others(7): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98168409 | ||||||
| chr2:98168539
|
A | G | 1 | a0002c0002t0024g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1114+5563A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98168539 | ||||||
| chr2:98168559
|
GCATACTG others(35): Show |
G | 1 | a0001c0001t0001g0114 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1114+5645_1114+568 others(46): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98168559 | |||||
| chr2:98168887
|
C | T | 1 | a0024c0034t0022g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1114+5911C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98168887 | ||||||
| chr2:98168905
|
G | C | 1 | a0001c0001t0001g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1114+5929G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98168905 | ||||||
| chr2:98169310
|
A | G | 1 | a0002c0002t0008g0177 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1114+6334A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98169310 | ||||||
| chr2:98169460
|
GA | G | 6 | a0005c0008t0003g0229a0005c0008t0003g0231a0005c0008t0003g0233others(3): Show | 6 | HG02615.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1114+6494delA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98169460 | |||||
| chr2:98169547
|
A | C | 1 | a0001c0001t0001g0133 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1114+6571A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98169547 | ||||||
| chr2:98169570
|
T | C | 82 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0089others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1114+6594T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98169570 | ||||||
| chr2:98169620
|
G | A | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1114+6644G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98169620 | ||||||
| chr2:98169659
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1114+6683G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98169659 | ||||||
| chr2:98169715
|
C | CTG | 18 | a0001c0001t0001g0082a0001c0001t0001g0133a0001c0001t0001g0137others(15): Show | 18 | HG00423.hp2 HG00621.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1114+6785_1114+678 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98169715 | |||||
| chr2:98169715
|
C | CTGTG | 9 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0191others(6): Show | 9 | HG00621.hp2 HG00735.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114+6783_1114+678 others(8): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98169715 | |||||
| chr2:98169715
|
C | CTGTGTG | 6 | a0001c0001t0001g0106a0002c0002t0004g0032a0002c0006t0004g0016others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(3): Show |
intron_variant | MODIFIER | c.1114+6781_1114+678 others(10): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98169715 | |||||
| chr2:98169715
|
CTG | C | 21 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0117others(18): Show | 21 | HG00408.hp1 HG00423.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.1114+6785_1114+678 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98169715 | |||||
| chr2:98169715
|
CTGTG | C | 49 | a0001c0001t0001g0083a0001c0001t0001g0131a0001c0001t0001g0132others(46): Show | 49 | HG00544.hp1 HG00597.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1114+6783_1114+678 others(8): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98169715 | |||||
| chr2:98169715
|
CTGTGTG | C | 24 | a0001c0001t0001g0127a0001c0001t0001g0138a0001c0001t0001g0176others(21): Show | 24 | HG00639.hp2 HG01070.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.1114+6781_1114+678 others(10): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98169715 | |||||
| chr2:98169715
|
CTGTGTGT others(1): Show |
C | 6 | a0001c0001t0001g0144a0001c0001t0001g0159a0001c0001t0003g0232others(3): Show | 6 | HG02280.hp2 HG03209.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1114+6779_1114+678 others(12): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98169715 | |||||
| chr2:98169715
|
CTGTGTGT others(3): Show |
C | 36 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0136others(33): Show | 36 | HG01099.hp2 HG01167.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1114+6777_1114+678 others(14): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98169715 | |||||
| chr2:98169715
|
CTGTGTGT others(5): Show |
C | 10 | a0001c0001t0001g0089a0005c0008t0003g0229a0005c0008t0003g0231others(7): Show | 10 | HG02615.hp1 HG02895.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.1114+6775_1114+678 others(16): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98169715 | |||||
| chr2:98169766
|
T | C | 1 | a0013c0014t0017g0126 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1114+6790T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98169766 | ||||||
| chr2:98169947
|
C | T | 1 | a0016c0028t0002g0085 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1114+6971C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98169947 | ||||||
| chr2:98170152
|
C | G | 9 | a0005c0008t0003g0229a0005c0008t0003g0231a0005c0008t0003g0233others(6): Show | 9 | HG02615.hp1 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114+7176C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98170152 | ||||||
| chr2:98170352
|
C | A | 1 | a0002c0002t0004g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1114+7376C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98170352 | ||||||
| chr2:98170377
|
T | G | 3 | a0002c0002t0004g0002a0002c0002t0004g0005a0002c0002t0021g0006 | 3 | HG02647.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1114+7401T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98170377 | ||||||
| chr2:98170430
|
A | G | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1114+7454A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98170430 | ||||||
| chr2:98170598
|
G | C | 1 | a0002c0019t0011g0228 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1114+7622G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98170598 | ||||||
| chr2:98170609
|
A | AT | 76 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0089others(73): Show | 76 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.1114+7647dupT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98170609 | |||||
| chr2:98170751
|
T | C | 1 | a0024c0034t0022g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1114+7775T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98170751 | ||||||
| chr2:98171147
|
A | G | 1 | a0020c0026t0002g0210 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1114+8171A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98171147 | ||||||
| chr2:98171470
|
C | T | 1 | a0005c0008t0003g0234 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1114+8494C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98171470 | ||||||
| chr2:98171488
|
A | G | 162 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(159): Show | 162 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1114+8512A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98171488 | ||||||
| chr2:98171552
|
G | C | 1 | a0006c0007t0004g0067 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1114+8576G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98171552 | ||||||
| chr2:98171590
|
C | T | 2 | a0003c0003t0003g0074a0003c0003t0003g0076 | 2 | NA18977.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1114+8614C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98171590 | ||||||
| chr2:98171841
|
G | A | 1 | a0024c0034t0022g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1114+8865G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98171841 | ||||||
| chr2:98171993
|
C | T | 3 | a0001c0001t0001g0144a0001c0001t0001g0145a0013c0014t0017g0126 | 3 | HG02572.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1114+9017C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98171993 | ||||||
| chr2:98172074
|
A | G | 29 | a0001c0001t0001g0137a0001c0001t0001g0215a0002c0002t0004g0036others(26): Show | 29 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.1115-8942A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98172074 | ||||||
| chr2:98172294
|
A | G | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1115-8722A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98172294 | ||||||
| chr2:98172346
|
TCAGGGGC others(8): Show |
T | 239 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(236): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1115-8654_1115-864 others(19): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98172346 | |||||
| chr2:98172377
|
A | G | 1 | a0002c0002t0004g0033 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1115-8639A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98172377 | ||||||
| chr2:98172382
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1115-8634G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98172382 | ||||||
| chr2:98172684
|
G | A | 4 | a0001c0004t0003g0017a0002c0006t0004g0015a0002c0006t0004g0016others(1): Show | 4 | HG00733.hp2 HG02293.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.1115-8332G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98172684 | ||||||
| chr2:98172889
|
G | A | 22 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0136others(19): Show | 22 | HG01123.hp2 HG01167.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.1115-8127G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98172889 | ||||||
| chr2:98173221
|
C | T | 39 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0109others(36): Show | 39 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.1115-7795C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98173221 | ||||||
| chr2:98173665
|
G | T | 33 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0135others(30): Show | 33 | HG01099.hp2 HG01123.hp2 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.1115-7351G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98173665 | ||||||
| chr2:98173761
|
A | G | 3 | a0001c0001t0003g0047a0001c0001t0005g0045a0015c0029t0004g0046 | 3 | HG02486.hp2 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1115-7255A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98173761 | ||||||
| chr2:98173891
|
C | T | 83 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0089others(80): Show | 83 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1115-7125C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98173891 | ||||||
| chr2:98173971
|
G | GA | 83 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0089others(80): Show | 83 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1115-7035dupA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98173971 | |||||
| chr2:98174075
|
A | T | 5 | a0001c0001t0001g0083a0001c0001t0023g0009a0002c0002t0004g0005others(2): Show | 5 | HG01243.hp2 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1115-6941A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98174075 | ||||||
| chr2:98174171
|
G | A | 2 | a0002c0002t0002g0095a0002c0002t0002g0096 | 2 | NA18993.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1115-6845G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98174171 | ||||||
| chr2:98174300
|
C | T | 29 | a0001c0001t0001g0137a0001c0001t0001g0215a0002c0002t0004g0036others(26): Show | 29 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.1115-6716C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98174300 | ||||||
| chr2:98174434
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1115-6582C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98174434 | ||||||
| chr2:98174576
|
G | A | 2 | a0002c0012t0011g0226a0002c0019t0011g0228 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1115-6440G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98174576 | ||||||
| chr2:98174624
|
G | C | 1 | a0002c0002t0002g0173 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1115-6392G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98174624 | ||||||
| chr2:98174692
|
G | T | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1115-6324G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98174692 | ||||||
| chr2:98174916
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1115-6100A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98174916 | ||||||
| chr2:98174970
|
T | C | 164 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(161): Show | 164 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.1115-6046T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98174970 | ||||||
| chr2:98175100
|
C | A | 2 | a0002c0002t0004g0002a0002c0002t0021g0006 | 2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1115-5916C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98175100 | ||||||
| chr2:98175110
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1115-5906A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98175110 | ||||||
| chr2:98175148
|
C | T | 4 | a0001c0001t0003g0236a0001c0001t0013g0028a0002c0002t0003g0024others(1): Show | 4 | HG01261.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1115-5868C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98175148 | ||||||
| chr2:98175266
|
G | A | 9 | a0001c0001t0001g0130a0001c0001t0001g0142a0001c0001t0001g0143others(6): Show | 9 | HG01099.hp2 HG02698.hp2 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.1115-5750G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98175266 | ||||||
| chr2:98175287
|
C | T | 2 | a0003c0003t0003g0070a0003c0003t0003g0071 | 2 | NA18612.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1115-5729C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98175287 | ||||||
| chr2:98175293
|
G | A | 1 | a0002c0002t0004g0005 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1115-5723G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98175293 | ||||||
| chr2:98175456
|
A | G | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1115-5560A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98175456 | ||||||
| chr2:98175598
|
C | T | 1 | a0002c0002t0004g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1115-5418C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98175598 | ||||||
| chr2:98176137
|
C | T | 1 | a0003c0003t0018g0081 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1115-4879C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98176137 | ||||||
| chr2:98176221
|
A | G | 5 | a0002c0002t0004g0005a0002c0012t0011g0226a0002c0019t0011g0228others(2): Show | 5 | HG02280.hp2 HG02647.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1115-4795A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98176221 | ||||||
| chr2:98176284
|
C | G | 1 | a0001c0001t0006g0198 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1115-4732C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98176284 | ||||||
| chr2:98176340
|
A | G | 1 | a0020c0026t0002g0210 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1115-4676A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98176340 | ||||||
| chr2:98176604
|
G | A | 1 | a0001c0001t0006g0198 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1115-4412G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98176604 | ||||||
| chr2:98176651
|
C | T | 1 | a0001c0004t0013g0029 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1115-4365C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98176651 | ||||||
| chr2:98176967
|
G | A | 1 | a0002c0002t0004g0011 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1115-4049G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98176967 | ||||||
| chr2:98177110
|
G | A | 1 | a0002c0002t0002g0222 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1115-3906G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98177110 | ||||||
| chr2:98177171
|
G | A | 1 | a0024c0034t0022g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1115-3845G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98177171 | ||||||
| chr2:98177645
|
A | G | 1 | a0002c0002t0002g0189 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1115-3371A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98177645 | ||||||
| chr2:98177723
|
G | C | 9 | a0003c0003t0003g0048a0003c0003t0003g0055a0003c0003t0005g0057others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1115-3293G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98177723 | ||||||
| chr2:98177733
|
G | A | 1 | a0003c0003t0005g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1115-3283G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98177733 | ||||||
| chr2:98177916
|
G | C | 1 | a0006c0007t0004g0067 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1115-3100G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98177916 | ||||||
| chr2:98178405
|
T | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0218 | 2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1115-2611T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98178405 | ||||||
| chr2:98178640
|
T | C | 1 | a0024c0034t0022g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1115-2376T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98178640 | ||||||
| chr2:98178942
|
G | A | 1 | a0002c0002t0004g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1115-2074G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98178942 | ||||||
| chr2:98179032
|
C | T | 7 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0159others(4): Show | 7 | HG00544.hp1 HG01358.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1115-1984C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98179032 | ||||||
| chr2:98179217
|
A | C | 1 | a0001c0001t0001g0157 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1115-1799A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98179217 | ||||||
| chr2:98179329
|
C | G | 87 | a0001c0001t0001g0089a0001c0001t0001g0117a0001c0001t0001g0118others(84): Show | 87 | HG00423.hp1 HG00639.hp1 HG00733.hp2 others(84): Show |
intron_variant | MODIFIER | c.1115-1687C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98179329 | ||||||
| chr2:98179410
|
T | TG | 216 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(213): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1115-1604dupG | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98179410 | |||||
| chr2:98179527
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1115-1489A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98179527 | ||||||
| chr2:98179562
|
G | A | 2 | a0002c0002t0004g0004a0006c0007t0019g0059 | 2 | HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1115-1454G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98179562 | ||||||
| chr2:98179565
|
T | A | 198 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0090others(195): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1115-1451T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98179565 | ||||||
| chr2:98179777
|
TTC | T | 4 | a0001c0001t0001g0144a0003c0003t0003g0072a0003c0003t0003g0077others(1): Show | 4 | HG01261.hp1 HG06807.hp2 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.1115-1235_1115-123 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98179777 | |||||
| chr2:98179781
|
C | T | 1 | a0003c0003t0001g0199 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1115-1235C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98179781 | ||||||
| chr2:98179783
|
T | C | 1 | a0003c0003t0001g0199 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1115-1233T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98179783 | ||||||
| chr2:98179784
|
T | C | 4 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0004g0005others(1): Show | 4 | HG01261.hp2 HG02647.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1115-1232T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98179784 | ||||||
| chr2:98179786
|
T | TTTTC | 9 | a0001c0001t0001g0155a0001c0001t0001g0178a0001c0001t0001g0179others(6): Show | 9 | HG00733.hp2 HG00735.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.1115-1190_1115-118 others(8): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98179786 | |||||
| chr2:98179786
|
T | TTTTCTTT others(5): Show |
1 | a0002c0002t0002g0173 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1115-1198_1115-118 others(16): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98179786 | |||||
| chr2:98179786
|
T | TTTTCTTT others(9): Show |
1 | a0002c0002t0002g0180 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1115-1202_1115-118 others(20): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98179786 | |||||
| chr2:98179786
|
TTTTC | T | 38 | a0001c0001t0001g0117a0001c0001t0001g0127a0001c0001t0001g0130others(35): Show | 38 | HG00609.hp1 HG01099.hp2 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.1115-1190_1115-118 others(8): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98179786 | |||||
| chr2:98179786
|
TTTTCTTT others(1): Show |
T | 43 | a0001c0001t0001g0083a0001c0001t0001g0089a0001c0001t0001g0118others(40): Show | 43 | HG00140.hp1 HG00423.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.1115-1194_1115-118 others(12): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98179786 | |||||
| chr2:98179786
|
TTTTCTTT others(5): Show |
T | 41 | a0001c0001t0001g0106a0001c0001t0001g0114a0001c0001t0001g0119others(38): Show | 41 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.1115-1198_1115-118 others(16): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98179786 | |||||
| chr2:98179786
|
TTTTCTTT others(9): Show |
T | 8 | a0001c0001t0001g0090a0001c0001t0001g0195a0002c0002t0003g0024others(5): Show | 8 | HG01261.hp2 HG02040.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.1115-1202_1115-118 others(20): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98179786 | |||||
| chr2:98179786
|
TTTTCTTT others(13): Show |
T | 1 | a0002c0002t0004g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1115-1206_1115-118 others(24): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98179786 | |||||
| chr2:98179789
|
T | C | 1 | a0003c0003t0001g0199 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1115-1227T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98179789 | ||||||
| chr2:98179790
|
C | T | 1 | a0003c0003t0001g0199 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1115-1226C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98179790 | ||||||
| chr2:98179798
|
C | CTT | 66 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0105others(63): Show | 66 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.1115-1216_1115-121 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98179798 | |||||
| chr2:98179800
|
TTC | T | 3 | a0002c0006t0002g0113a0002c0012t0004g0007a0002c0016t0020g0031 | 3 | HG00323.hp2 HG01358.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1115-1214_1115-121 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98179800 | |||||
| chr2:98179824
|
T | C | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1115-1192T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98179824 | ||||||
| chr2:98179830
|
T | C | 1 | a0002c0006t0002g0113 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1115-1186T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98179830 | ||||||
| chr2:98179832
|
C | T | 1 | a0002c0006t0002g0113 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1115-1184C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98179832 | ||||||
| chr2:98179832
|
CTTTCTTT others(11): Show |
C | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1115-1170_1115-115 others(22): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98179832 | |||||
| chr2:98179883
|
CCT | C | 79 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0127others(76): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.1115-1124_1115-112 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98179883 | |||||
| chr2:98179887
|
T | TCTCTCTT others(49): Show |
1 | a0002c0002t0024g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1115-1128_1115-107 others(60): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98179887 | |||||
| chr2:98179916
|
T | C | 1 | a0004c0005t0002g0100 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1115-1100T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98179916 | ||||||
| chr2:98179918
|
TCCTTCCT others(1): Show |
T | 42 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0114others(39): Show | 42 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.1115-1086_1115-107 others(12): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98179918 | |||||
| chr2:98179970
|
A | ATCTC | 8 | a0001c0001t0001g0083a0002c0002t0003g0024a0002c0002t0003g0027others(5): Show | 8 | HG01261.hp2 HG02056.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1115-1043_1115-104 others(8): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98179970 | |||||
| chr2:98180042
|
T | C | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1115-974T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98180042 | ||||||
| chr2:98180086
|
CTCTT | C | 9 | a0001c0001t0005g0045a0003c0003t0003g0048a0003c0003t0003g0055others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1115-916_1115-913d others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 98180086 | |||||
| chr2:98180280
|
C | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | NA19056.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1115-736C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98180280 | ||||||
| chr2:98180288
|
A | G | 13 | a0001c0001t0003g0238a0002c0002t0004g0002a0005c0008t0003g0231others(10): Show | 13 | HG01891.hp2 HG02056.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.1115-728A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98180288 | ||||||
| chr2:98180382
|
C | T | 5 | a0001c0001t0001g0083a0002c0002t0003g0024a0002c0002t0003g0027others(2): Show | 5 | HG01261.hp2 HG01358.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1115-634C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98180382 | ||||||
| chr2:98180389
|
G | A | 21 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0136others(18): Show | 21 | HG01123.hp2 HG01167.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1115-627G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98180389 | ||||||
| chr2:98180409
|
G | T | 18 | a0001c0001t0001g0083a0001c0001t0003g0238a0002c0002t0003g0024others(15): Show | 18 | HG01261.hp2 HG01358.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1115-607G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98180409 | ||||||
| chr2:98180435
|
A | C | 2 | a0001c0001t0003g0232a0001c0004t0013g0029 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1115-581A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98180435 | ||||||
| chr2:98180456
|
T | C | 8 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0004g0005others(5): Show | 8 | HG01261.hp2 HG01358.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1115-560T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98180456 | ||||||
| chr2:98180550
|
G | A | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1115-466G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98180550 | ||||||
| chr2:98180672
|
C | T | 1 | a0012c0036t0003g0063 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1115-344C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98180672 | ||||||
| chr2:98180743
|
G | A | 1 | a0002c0012t0011g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1115-273G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98180743 | ||||||
| chr2:98180983
|
A | T | 13 | a0001c0001t0001g0130a0001c0001t0001g0142a0001c0001t0001g0143others(10): Show | 13 | HG01099.hp2 HG02698.hp2 HG02735.hp2 others(10): Show |
intron_variant | MODIFIER | c.1115-33A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98180983 | ||||||
| chr2:98181281
|
C | T | 147 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0089others(144): Show | 147 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.1311+69C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98181281 | ||||||
| chr2:98181613
|
T | C | 1 | a0002c0006t0002g0113 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1311+401T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98181613 | ||||||
| chr2:98181656
|
A | G | 1 | a0001c0004t0003g0010 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1311+444A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98181656 | ||||||
| chr2:98181842
|
T | C | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1311+630T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98181842 | ||||||
| chr2:98182114
|
A | G | 65 | a0001c0001t0001g0083a0001c0001t0001g0106a0001c0001t0001g0114others(62): Show | 65 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1311+902A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98182114 | ||||||
| chr2:98182180
|
A | T | 1 | a0002c0002t0024g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1311+968A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98182180 | ||||||
| chr2:98182183
|
C | T | 1 | a0006c0007t0019g0059 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1311+971C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98182183 | ||||||
| chr2:98182211
|
T | G | 1 | a0001c0001t0005g0045 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1311+999T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98182211 | ||||||
| chr2:98182212
|
G | T | 1 | a0001c0001t0005g0045 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1311+1000G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98182212 | ||||||
| chr2:98182320
|
A | C | 1 | a0001c0001t0001g0127 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1311+1108A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98182320 | ||||||
| chr2:98182592
|
T | C | 13 | a0001c0001t0001g0083a0001c0001t0003g0238a0002c0012t0004g0007others(10): Show | 13 | HG01358.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1311+1380T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98182592 | ||||||
| chr2:98182691
|
G | A | 1 | a0004c0005t0002g0099 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1311+1479G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98182691 | ||||||
| chr2:98182729
|
G | A | 1 | a0002c0002t0003g0024 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1311+1517G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98182729 | ||||||
| chr2:98182913
|
A | G | 3 | a0001c0004t0003g0013a0001c0004t0003g0025a0001c0004t0003g0026 | 3 | HG02056.hp2 NA18951.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1311+1701A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98182913 | ||||||
| chr2:98182968
|
C | T | 1 | a0002c0002t0024g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1311+1756C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98182968 | ||||||
| chr2:98183189
|
C | CT | 6 | a0001c0001t0001g0133a0001c0004t0013g0029a0002c0002t0004g0002others(3): Show | 6 | HG00423.hp2 HG01123.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1311+1998dupT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 98183189 | |||||
| chr2:98183189
|
C | CTTTTTTT others(1): Show |
10 | a0001c0001t0001g0083a0001c0001t0003g0238a0002c0016t0020g0031others(7): Show | 10 | HG01358.hp1 HG01891.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1311+1991_1311+199 others(12): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 98183189 | |||||
| chr2:98183189
|
C | CTTTTTTT others(6): Show |
1 | a0016c0028t0002g0085 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1311+1986_1311+199 others(17): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 98183189 | |||||
| chr2:98183189
|
C | CTTTTTTT others(7): Show |
1 | a0017c0027t0002g0084 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1311+1985_1311+199 others(18): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 98183189 | |||||
| chr2:98183189
|
C | T | 5 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0158others(2): Show | 5 | HG00544.hp1 HG02040.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.1311+1977C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98183189 | ||||||
| chr2:98183189
|
CTT | C | 42 | a0001c0001t0001g0106a0001c0001t0001g0114a0001c0001t0001g0119others(39): Show | 42 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.1311+1997_1311+199 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 98183189 | |||||
| chr2:98183428
|
G | A | 6 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0121others(3): Show | 6 | HG00544.hp2 HG04184.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.1311+2216G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98183428 | ||||||
| chr2:98183456
|
G | T | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1311+2244G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98183456 | ||||||
| chr2:98183522
|
T | A | 11 | a0001c0001t0001g0083a0001c0001t0003g0238a0005c0008t0003g0231others(8): Show | 11 | HG01891.hp2 HG02572.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1311+2310T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98183522 | ||||||
| chr2:98184097
|
G | T | 9 | a0001c0001t0001g0088a0001c0001t0001g0156a0001c0001t0001g0158others(6): Show | 9 | HG00544.hp1 HG02040.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1311+2885G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98184097 | ||||||
| chr2:98184160
|
G | A | 13 | a0001c0001t0001g0083a0001c0001t0003g0238a0002c0012t0004g0007others(10): Show | 13 | HG01358.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1311+2948G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98184160 | ||||||
| chr2:98184260
|
A | G | 223 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(220): Show | 223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1311+3048A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98184260 | ||||||
| chr2:98184373
|
C | T | 13 | a0002c0002t0002g0162a0002c0002t0002g0164a0002c0002t0002g0168others(10): Show | 13 | HG00621.hp2 HG00741.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.1311+3161C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98184373 | ||||||
| chr2:98184374
|
G | A | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1311+3162G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98184374 | ||||||
| chr2:98184478
|
G | C | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1311+3266G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98184478 | ||||||
| chr2:98184658
|
C | G | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1312-3317C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98184658 | ||||||
| chr2:98184684
|
G | A | 3 | a0001c0001t0007g0146a0001c0001t0007g0147a0001c0001t0007g0148 | 3 | NA18945.hp2 NA18963.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1312-3291G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98184684 | ||||||
| chr2:98184860
|
G | A | 32 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(29): Show | 32 | HG00423.hp1 HG00735.hp2 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.1312-3115G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98184860 | ||||||
| chr2:98185047
|
T | C | 2 | a0002c0002t0004g0003a0002c0002t0004g0004 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1312-2928T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98185047 | ||||||
| chr2:98185097
|
T | A | 1 | a0002c0002t0021g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1312-2878T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98185097 | ||||||
| chr2:98185158
|
C | G | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1312-2817C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98185158 | ||||||
| chr2:98185213
|
G | GCGCTATT others(1): Show |
4 | a0001c0001t0001g0144a0001c0001t0001g0145a0003c0003t0003g0054others(1): Show | 4 | HG02717.hp2 HG02976.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312-2760_1312-275 others(12): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 98185213 | |||||
| chr2:98185215
|
G | GCTATTCC others(11): Show |
2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1312-2757_1312-274 others(22): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 98185215 | |||||
| chr2:98185540
|
G | A | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1312-2435G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98185540 | ||||||
| chr2:98185622
|
G | A | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1312-2353G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98185622 | ||||||
| chr2:98185635
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1312-2340C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98185635 | ||||||
| chr2:98185712
|
G | A | 1 | a0001c0004t0003g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1312-2263G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98185712 | ||||||
| chr2:98185948
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1312-2027C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98185948 | ||||||
| chr2:98185960
|
G | A | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1312-2015G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98185960 | ||||||
| chr2:98186046
|
C | G | 1 | a0001c0004t0003g0026 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1312-1929C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98186046 | ||||||
| chr2:98186094
|
G | A | 205 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0089others(202): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1312-1881G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98186094 | ||||||
| chr2:98186158
|
A | AT | 183 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0089others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1312-1799dupT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 98186158 | |||||
| chr2:98186158
|
A | ATT | 21 | a0001c0001t0001g0118a0001c0001t0001g0135a0001c0001t0001g0136others(18): Show | 21 | HG00639.hp1 HG00639.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.1312-1800_1312-179 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 98186158 | |||||
| chr2:98186184
|
A | G | 2 | a0002c0002t0003g0024a0002c0002t0003g0027 | 2 | HG01261.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1312-1791A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98186184 | ||||||
| chr2:98186372
|
G | A | 2 | a0002c0002t0004g0003a0002c0002t0004g0004 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1312-1603G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98186372 | ||||||
| chr2:98186405
|
C | G | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1312-1570C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98186405 | ||||||
| chr2:98186408
|
G | A | 1 | a0013c0014t0017g0126 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1312-1567G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98186408 | ||||||
| chr2:98186562
|
C | A | 223 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(220): Show | 223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1312-1413C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98186562 | ||||||
| chr2:98186663
|
C | T | 68 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0105others(65): Show | 68 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1312-1312C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98186663 | ||||||
| chr2:98186685
|
G | A | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1312-1290G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98186685 | ||||||
| chr2:98186713
|
C | T | 1 | a0024c0034t0022g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1312-1262C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98186713 | ||||||
| chr2:98186730
|
A | G | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1312-1245A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98186730 | ||||||
| chr2:98186830
|
T | C | 13 | a0001c0001t0001g0083a0001c0001t0003g0238a0002c0012t0004g0007others(10): Show | 13 | HG01358.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1312-1145T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98186830 | ||||||
| chr2:98187079
|
A | G | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1312-896A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98187079 | ||||||
| chr2:98187153
|
G | A | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1312-822G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98187153 | ||||||
| chr2:98187170
|
G | C | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1312-805G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98187170 | ||||||
| chr2:98187237
|
C | T | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1312-738C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98187237 | ||||||
| chr2:98187314
|
G | C | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1312-661G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98187314 | ||||||
| chr2:98187419
|
C | T | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1312-556C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98187419 | ||||||
| chr2:98187420
|
G | A | 1 | a0001c0004t0004g0023 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1312-555G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98187420 | ||||||
| chr2:98187429
|
A | G | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1312-546A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98187429 | ||||||
| chr2:98187465
|
G | A | 4 | a0001c0001t0001g0117a0002c0002t0002g0116a0003c0003t0003g0054others(1): Show | 4 | HG01168.hp2 HG01516.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1312-510G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98187465 | ||||||
| chr2:98187635
|
T | TCTCTCC | 5 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0003g0012others(2): Show | 5 | HG01167.hp2 HG02280.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312-327_1312-322d others(8): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 98187635 | |||||
| chr2:98187658
|
C | CTGTGTGT others(3): Show |
1 | a0002c0002t0021g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1312-312_1312-311i others(12): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 98187658 | |||||
| chr2:98187658
|
C | CTGTGTGT others(5): Show |
1 | a0002c0002t0004g0003 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1312-312_1312-311i others(14): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 98187658 | |||||
| chr2:98187658
|
C | CTGTGTGT others(9): Show |
1 | a0002c0002t0004g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1312-312_1312-311i others(18): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 98187658 | |||||
| chr2:98187664
|
C | CTG | 54 | a0001c0001t0001g0117a0001c0001t0001g0127a0001c0001t0001g0135others(51): Show | 54 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.1312-273_1312-272d others(4): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 98187664 | |||||
| chr2:98187664
|
C | CTGTG | 10 | a0001c0001t0001g0172a0001c0001t0001g0183a0001c0001t0001g0192others(7): Show | 10 | HG00280.hp2 HG00735.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.1312-275_1312-272d others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 98187664 | |||||
| chr2:98187664
|
C | CTGTGTG | 4 | a0002c0012t0011g0226a0003c0003t0003g0048a0007c0009t0002g0091others(1): Show | 4 | HG01071.hp1 HG01081.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1312-277_1312-272d others(8): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 98187664 | |||||
| chr2:98187664
|
C | CTGTGTGT others(1): Show |
3 | a0002c0002t0003g0027a0002c0002t0004g0005a0008c0010t0004g0227 | 3 | HG02647.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1312-279_1312-272d others(10): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 98187664 | |||||
| chr2:98187664
|
C | CTGTGTGT others(3): Show |
1 | a0003c0003t0006g0200 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1312-281_1312-272d others(12): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 98187664 | |||||
| chr2:98187664
|
C | CTGTGTGT others(5): Show |
1 | a0002c0019t0011g0228 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1312-283_1312-272d others(14): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 98187664 | |||||
| chr2:98187664
|
C | G | 3 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0021g0006 | 3 | HG03486.hp2 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1312-311C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98187664 | ||||||
| chr2:98187664
|
CTG | C | 23 | a0001c0001t0001g0083a0001c0001t0001g0138a0001c0001t0001g0170others(20): Show | 23 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1312-273_1312-272d others(4): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 98187664 | |||||
| chr2:98187664
|
CTGTG | C | 93 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0090others(90): Show | 93 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1312-275_1312-272d others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 98187664 | |||||
| chr2:98187664
|
CTGTGTG | C | 32 | a0001c0001t0001g0114a0001c0001t0001g0131a0001c0001t0001g0132others(29): Show | 32 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.1312-277_1312-272d others(8): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 98187664 | |||||
| chr2:98187664
|
CTGTGTGT others(5): Show |
C | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1312-283_1312-272d others(14): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 98187664 | |||||
| chr2:98187664
|
CTGTGTGT others(17): Show |
C | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1312-295_1312-272d others(26): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 98187664 | |||||
| chr2:98187705
|
G | T | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1312-270G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98187705 | ||||||
| chr2:98187791
|
A | C | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1312-184A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98187791 | ||||||
| chr2:98187851
|
G | A | 229 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(226): Show | 229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1312-124G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98187851 | ||||||
| chr2:98187879
|
G | A | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1312-96G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98187879 | ||||||
| chr2:98187922
|
C | A | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1312-53C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98187922 | ||||||
| chr2:98188298
|
C | T | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1466+169C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98188298 | ||||||
| chr2:98188336
|
G | A | 13 | a0001c0001t0001g0083a0001c0001t0003g0238a0002c0012t0004g0007others(10): Show | 13 | HG01358.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1466+207G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98188336 | ||||||
| chr2:98188339
|
T | C | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1466+210T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98188339 | ||||||
| chr2:98188638
|
G | A | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1466+509G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98188638 | ||||||
| chr2:98188812
|
T | G | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1466+683T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98188812 | ||||||
| chr2:98188869
|
A | G | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1466+740A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98188869 | ||||||
| chr2:98188963
|
C | T | 1 | a0001c0001t0003g0238 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1466+834C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98188963 | ||||||
| chr2:98189021
|
C | T | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1466+892C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98189021 | ||||||
| chr2:98189049
|
C | A | 1 | a0002c0002t0004g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1466+920C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98189049 | ||||||
| chr2:98189119
|
G | A | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1466+990G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98189119 | ||||||
| chr2:98189125
|
T | C | 1 | a0001c0001t0005g0045 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1466+996T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98189125 | ||||||
| chr2:98189135
|
G | T | 13 | a0001c0001t0001g0083a0001c0001t0003g0238a0002c0012t0004g0007others(10): Show | 13 | HG01358.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1466+1006G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98189135 | ||||||
| chr2:98189146
|
C | T | 1 | a0020c0026t0002g0210 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1466+1017C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98189146 | ||||||
| chr2:98189252
|
A | T | 1 | a0004c0005t0002g0093 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1466+1123A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98189252 | ||||||
| chr2:98189264
|
A | G | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1466+1135A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98189264 | ||||||
| chr2:98189321
|
C | T | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1466+1192C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98189321 | ||||||
| chr2:98189517
|
T | C | 1 | a0010c0013t0002g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1466+1388T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98189517 | ||||||
| chr2:98189580
|
A | G | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1466+1451A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98189580 | ||||||
| chr2:98189725
|
T | C | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1466+1596T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98189725 | ||||||
| chr2:98189842
|
G | A | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1466+1713G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98189842 | ||||||
| chr2:98189843
|
C | T | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1466+1714C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98189843 | ||||||
| chr2:98190166
|
A | G | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1466+2037A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98190166 | ||||||
| chr2:98190203
|
G | A | 1 | a0002c0002t0024g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1466+2074G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98190203 | ||||||
| chr2:98190394
|
G | A | 1 | a0002c0002t0004g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1466+2265G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98190394 | ||||||
| chr2:98190428
|
A | G | 32 | a0001c0001t0001g0114a0001c0001t0001g0151a0002c0002t0001g0094others(29): Show | 32 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.1466+2299A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98190428 | ||||||
| chr2:98190483
|
A | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1466+2354A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98190483 | ||||||
| chr2:98190567
|
A | G | 88 | a0001c0001t0001g0106a0001c0001t0001g0117a0001c0001t0001g0118others(85): Show | 88 | HG00423.hp1 HG00544.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.1467-2331A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98190567 | ||||||
| chr2:98190698
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1467-2200G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98190698 | ||||||
| chr2:98190753
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1467-2145A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98190753 | ||||||
| chr2:98190757
|
A | T | 239 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(236): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1467-2141A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98190757 | ||||||
| chr2:98190821
|
G | A | 1 | a0020c0026t0002g0210 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1467-2077G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98190821 | ||||||
| chr2:98191110
|
C | T | 1 | a0002c0006t0004g0019 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1467-1788C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98191110 | ||||||
| chr2:98191289
|
C | T | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1467-1609C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98191289 | ||||||
| chr2:98191290
|
A | G | 229 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(226): Show | 229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1467-1608A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98191290 | ||||||
| chr2:98191529
|
A | G | 1 | a0002c0002t0021g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1467-1369A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98191529 | ||||||
| chr2:98191997
|
A | G | 3 | a0001c0001t0003g0047a0005c0008t0003g0229a0015c0029t0004g0046 | 3 | HG02486.hp2 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1467-901A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98191997 | ||||||
| chr2:98192088
|
T | A | 1 | a0003c0003t0003g0071 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1467-810T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98192088 | ||||||
| chr2:98192162
|
A | G | 223 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(220): Show | 223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1467-736A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98192162 | ||||||
| chr2:98192322
|
G | A | 1 | a0002c0002t0024g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1467-576G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98192322 | ||||||
| chr2:98192427
|
A | G | 1 | a0001c0004t0003g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1467-471A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98192427 | ||||||
| chr2:98192438
|
A | G | 3 | a0001c0001t0003g0047a0005c0008t0003g0229a0015c0029t0004g0046 | 3 | HG02486.hp2 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1467-460A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98192438 | ||||||
| chr2:98192825
|
G | A | 13 | a0001c0001t0001g0083a0001c0001t0003g0238a0002c0012t0004g0007others(10): Show | 13 | HG01358.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1467-73G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98192825 | ||||||
| chr2:98193053
|
G | T | 1 | a0001c0001t0001g0167 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1605+17G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 11/27 | chr2 | 98193053 | ||||||
| chr2:98193664
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1605+628C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 11/27 | chr2 | 98193664 | ||||||
| chr2:98193665
|
G | T | 1 | a0020c0026t0002g0210 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1605+629G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 11/27 | chr2 | 98193665 | ||||||
| chr2:98193751
|
G | A | 13 | a0001c0001t0001g0083a0001c0001t0003g0238a0002c0012t0004g0007others(10): Show | 13 | HG01358.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1606-610G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 11/27 | chr2 | 98193751 | ||||||
| chr2:98193835
|
G | A | 1 | a0003c0003t0003g0053 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1606-526G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 11/27 | chr2 | 98193835 | ||||||
| chr2:98194026
|
G | A | 1 | a0002c0002t0002g0168 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1606-335G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 11/27 | chr2 | 98194026 | ||||||
| chr2:98194309
|
C | A | 13 | a0001c0001t0001g0083a0001c0001t0003g0238a0002c0012t0004g0007others(10): Show | 13 | HG01358.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1606-52C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 11/27 | chr2 | 98194309 | ||||||
| chr2:98194612
|
A | G | 223 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(220): Show | 223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1737+120A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98194612 | ||||||
| chr2:98194646
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1737+154G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98194646 | ||||||
| chr2:98195050
|
T | C | 3 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0021g0006 | 3 | HG03486.hp2 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1737+558T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98195050 | ||||||
| chr2:98195169
|
T | C | 6 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0121others(3): Show | 6 | HG00544.hp2 HG04184.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.1737+677T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98195169 | ||||||
| chr2:98195437
|
C | T | 1 | a0001c0004t0003g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1737+945C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98195437 | ||||||
| chr2:98195743
|
G | A | 1 | a0003c0003t0003g0053 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1737+1251G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98195743 | ||||||
| chr2:98196079
|
C | G | 1 | a0010c0013t0002g0141 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1737+1587C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98196079 | ||||||
| chr2:98196171
|
A | T | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1737+1679A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98196171 | ||||||
| chr2:98196755
|
G | T | 1 | a0003c0003t0005g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1737+2263G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98196755 | ||||||
| chr2:98196986
|
T | G | 1 | a0002c0002t0004g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1737+2494T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98196986 | ||||||
| chr2:98197048
|
C | T | 142 | a0001c0001t0001g0089a0001c0001t0001g0106a0001c0001t0001g0114others(139): Show | 142 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.1737+2556C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98197048 | ||||||
| chr2:98197063
|
G | A | 1 | a0003c0003t0003g0068 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1737+2571G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98197063 | ||||||
| chr2:98197127
|
A | G | 2 | a0001c0001t0003g0236a0001c0001t0013g0028 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1737+2635A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98197127 | ||||||
| chr2:98197191
|
G | A | 3 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0021g0006 | 3 | HG03486.hp2 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1737+2699G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98197191 | ||||||
| chr2:98197319
|
G | A | 2 | a0002c0002t0008g0177a0002c0002t0008g0196 | 2 | HG00609.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1737+2827G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98197319 | ||||||
| chr2:98197470
|
T | C | 8 | a0004c0005t0002g0093a0004c0005t0002g0100a0004c0005t0002g0101others(5): Show | 8 | HG00408.hp1 HG00609.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.1737+2978T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98197470 | ||||||
| chr2:98197559
|
T | C | 2 | a0001c0001t0001g0145a0002c0002t0004g0002 | 2 | HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1737+3067T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98197559 | ||||||
| chr2:98197591
|
T | C | 54 | a0001c0001t0001g0082a0001c0001t0001g0090a0001c0001t0001g0105others(51): Show | 54 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.1737+3099T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98197591 | ||||||
| chr2:98197768
|
T | A | 1 | a0002c0002t0002g0111 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1737+3276T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98197768 | ||||||
| chr2:98198113
|
T | C | 2 | a0005c0008t0003g0231a0005c0020t0003g0230 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1737+3621T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98198113 | ||||||
| chr2:98198137
|
C | T | 3 | a0008c0010t0009g0239a0008c0010t0009g0240a0013c0014t0017g0126 | 3 | HG02572.hp2 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1737+3645C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98198137 | ||||||
| chr2:98198155
|
T | G | 1 | a0001c0001t0001g0130 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1737+3663T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98198155 | ||||||
| chr2:98198356
|
C | G | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1737+3864C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98198356 | ||||||
| chr2:98198548
|
TA | T | 203 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(200): Show | 203 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.1737+4067delA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | 98198548 | |||||
| chr2:98198639
|
T | C | 1 | a0012c0036t0003g0063 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1737+4147T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98198639 | ||||||
| chr2:98198856
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1737+4364G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98198856 | ||||||
| chr2:98198962
|
C | T | 1 | a0001c0004t0003g0013 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1737+4470C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98198962 | ||||||
| chr2:98198964
|
G | A | 1 | a0002c0002t0004g0032 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1737+4472G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98198964 | ||||||
| chr2:98199063
|
G | A | 4 | a0001c0001t0001g0130a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG00673.hp1 NA18993.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.1737+4571G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98199063 | ||||||
| chr2:98199071
|
C | A | 1 | a0003c0003t0003g0054 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1737+4579C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98199071 | ||||||
| chr2:98199072
|
G | A | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1737+4580G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98199072 | ||||||
| chr2:98199086
|
C | CA | 163 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(160): Show | 163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1737+4609dupA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | 98199086 | |||||
| chr2:98199086
|
C | CAA | 9 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0236others(6): Show | 9 | HG02056.hp1 HG03098.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.1737+4608_1737+460 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | 98199086 | |||||
| chr2:98199518
|
G | A | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1737+5026G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98199518 | ||||||
| chr2:98199547
|
T | A | 210 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(207): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1737+5055T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98199547 | ||||||
| chr2:98199738
|
T | C | 1 | a0001c0001t0001g0167 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1737+5246T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98199738 | ||||||
| chr2:98199977
|
A | G | 2 | a0001c0001t0001g0150a0001c0001t0001g0211 | 2 | HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1737+5485A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98199977 | ||||||
| chr2:98199988
|
C | A | 5 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(2): Show | 5 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+5496C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98199988 | ||||||
| chr2:98200193
|
G | C | 5 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(2): Show | 5 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+5701G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98200193 | ||||||
| chr2:98200277
|
T | A | 4 | a0001c0001t0001g0127a0001c0004t0004g0023a0007c0009t0002g0091others(1): Show | 4 | HG01071.hp1 HG01081.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+5785T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98200277 | ||||||
| chr2:98200322
|
C | G | 5 | a0002c0012t0004g0007a0002c0016t0020g0031a0008c0010t0009g0239others(2): Show | 5 | HG01358.hp1 HG02109.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1737+5830C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98200322 | ||||||
| chr2:98200410
|
C | T | 100 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0106others(97): Show | 100 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.1737+5918C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98200410 | ||||||
| chr2:98200449
|
A | G | 5 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(2): Show | 5 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+5957A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98200449 | ||||||
| chr2:98200539
|
T | A | 5 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(2): Show | 5 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+6047T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98200539 | ||||||
| chr2:98200540
|
CT | C | 5 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(2): Show | 5 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+6049delT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98200540 | ||||||
| chr2:98200542
|
CA | C | 11 | a0001c0001t0001g0082a0001c0001t0001g0144a0001c0001t0001g0209others(8): Show | 11 | HG00621.hp1 HG01358.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.1737+6069delA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | 98200542 | |||||
| chr2:98200542
|
CAA | C | 53 | a0001c0001t0001g0090a0001c0001t0001g0105a0001c0001t0001g0109others(50): Show | 53 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.1737+6068_1737+606 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | 98200542 | |||||
| chr2:98200543
|
A | C | 5 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(2): Show | 5 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+6051A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98200543 | ||||||
| chr2:98200544
|
A | C | 5 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(2): Show | 5 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+6052A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98200544 | ||||||
| chr2:98200545
|
A | C | 1 | a0010c0013t0002g0141 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1737+6053A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98200545 | ||||||
| chr2:98200708
|
A | G | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1737+6216A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98200708 | ||||||
| chr2:98200841
|
T | C | 1 | a0002c0002t0004g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1737+6349T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98200841 | ||||||
| chr2:98200876
|
T | A | 1 | a0002c0002t0004g0005 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1737+6384T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98200876 | ||||||
| chr2:98201019
|
A | T | 1 | a0001c0001t0001g0137 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1737+6527A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98201019 | ||||||
| chr2:98201023
|
T | A | 1 | a0001c0001t0001g0186 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1737+6531T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98201023 | ||||||
| chr2:98201106
|
A | G | 1 | a0002c0002t0021g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1737+6614A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98201106 | ||||||
| chr2:98201120
|
C | G | 1 | a0002c0002t0024g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1737+6628C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98201120 | ||||||
| chr2:98201419
|
C | T | 5 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(2): Show | 5 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+6927C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98201419 | ||||||
| chr2:98201596
|
T | C | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1737+7104T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98201596 | ||||||
| chr2:98201625
|
G | GT | 5 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(2): Show | 5 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+7141dupT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | 98201625 | |||||
| chr2:98201942
|
T | C | 1 | a0003c0003t0003g0071 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1737+7450T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98201942 | ||||||
| chr2:98202208
|
T | G | 5 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(2): Show | 5 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+7716T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98202208 | ||||||
| chr2:98202222
|
T | A | 53 | a0001c0001t0001g0082a0001c0001t0001g0090a0001c0001t0001g0105others(50): Show | 53 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.1737+7730T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98202222 | ||||||
| chr2:98202447
|
G | GAAATTTG others(11): Show |
2 | a0002c0012t0004g0007a0002c0016t0020g0031 | 2 | HG01358.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1737+7958_1737+795 others(22): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | 98202447 | |||||
| chr2:98202451
|
C | A | 2 | a0002c0012t0004g0007a0002c0016t0020g0031 | 2 | HG01358.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1737+7959C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98202451 | ||||||
| chr2:98202455
|
C | A | 2 | a0002c0012t0004g0007a0002c0016t0020g0031 | 2 | HG01358.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1737+7963C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98202455 | ||||||
| chr2:98202456
|
T | C | 2 | a0002c0012t0004g0007a0002c0016t0020g0031 | 2 | HG01358.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1737+7964T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98202456 | ||||||
| chr2:98202533
|
C | T | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1737+8041C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98202533 | ||||||
| chr2:98202821
|
G | GTTTA | 5 | a0003c0003t0006g0200a0007c0009t0002g0139a0007c0009t0002g0140others(2): Show | 5 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+8353_1737+835 others(8): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | 98202821 | |||||
| chr2:98202862
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1737+8370C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98202862 | ||||||
| chr2:98202895
|
T | C | 1 | a0020c0026t0002g0210 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1737+8403T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98202895 | ||||||
| chr2:98203014
|
G | A | 1 | a0016c0028t0002g0085 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1737+8522G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98203014 | ||||||
| chr2:98203021
|
C | T | 1 | a0002c0002t0003g0027 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1737+8529C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98203021 | ||||||
| chr2:98203043
|
G | A | 57 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0089others(54): Show | 57 | HG00140.hp1 HG00423.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1737+8551G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98203043 | ||||||
| chr2:98203121
|
A | G | 13 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0030others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.1737+8629A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98203121 | ||||||
| chr2:98203122
|
C | T | 12 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0030others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.1737+8630C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98203122 | ||||||
| chr2:98203123
|
A | G | 13 | a0001c0001t0001g0218a0002c0002t0004g0003a0002c0002t0004g0004others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.1737+8631A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98203123 | ||||||
| chr2:98203130
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1737+8638C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98203130 | ||||||
| chr2:98203147
|
G | A | 2 | a0001c0001t0001g0176a0003c0032t0003g0062 | 2 | HG03942.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1737+8655G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98203147 | ||||||
| chr2:98203149
|
C | T | 5 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(2): Show | 5 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+8657C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98203149 | ||||||
| chr2:98203335
|
G | A | 1 | a0002c0006t0004g0237 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1738-8595G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98203335 | ||||||
| chr2:98203496
|
A | T | 1 | a0002c0002t0024g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1738-8434A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98203496 | ||||||
| chr2:98203567
|
G | A | 146 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(143): Show | 146 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.1738-8363G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98203567 | ||||||
| chr2:98203680
|
C | G | 6 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0004g0002others(3): Show | 6 | HG01261.hp2 HG02723.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1738-8250C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98203680 | ||||||
| chr2:98203972
|
T | C | 2 | a0002c0002t0004g0005a0008c0010t0004g0227 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1738-7958T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98203972 | ||||||
| chr2:98203983
|
C | T | 26 | a0002c0002t0002g0173a0002c0002t0003g0024a0002c0002t0003g0027others(23): Show | 26 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.1738-7947C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98203983 | ||||||
| chr2:98204058
|
A | G | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-7872A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98204058 | ||||||
| chr2:98204217
|
A | G | 1 | a0026c0018t0010g0129 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1738-7713A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98204217 | ||||||
| chr2:98204391
|
A | C | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1738-7539A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98204391 | ||||||
| chr2:98204489
|
T | G | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-7441T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98204489 | ||||||
| chr2:98204594
|
T | A | 183 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1738-7336T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98204594 | ||||||
| chr2:98204639
|
C | T | 183 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1738-7291C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98204639 | ||||||
| chr2:98204988
|
G | A | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-6942G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98204988 | ||||||
| chr2:98204993
|
C | G | 9 | a0001c0001t0005g0045a0001c0001t0015g0134a0003c0003t0003g0048others(6): Show | 9 | HG02109.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1738-6937C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98204993 | ||||||
| chr2:98205057
|
C | G | 1 | a0006c0007t0012g0050 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1738-6873C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98205057 | ||||||
| chr2:98205286
|
T | A | 183 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1738-6644T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98205286 | ||||||
| chr2:98205298
|
C | T | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-6632C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98205298 | ||||||
| chr2:98205667
|
T | C | 2 | a0001c0001t0001g0176a0001c0001t0001g0207 | 2 | HG02735.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1738-6263T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98205667 | ||||||
| chr2:98205770
|
A | C | 183 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1738-6160A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98205770 | ||||||
| chr2:98206028
|
A | G | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-5902A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98206028 | ||||||
| chr2:98206068
|
C | T | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-5862C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98206068 | ||||||
| chr2:98206378
|
G | C | 145 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(142): Show | 145 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1738-5552G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98206378 | ||||||
| chr2:98206526
|
A | G | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-5404A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98206526 | ||||||
| chr2:98206719
|
T | A | 1 | a0003c0003t0005g0069 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1738-5211T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98206719 | ||||||
| chr2:98206798
|
A | T | 12 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.1738-5132A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98206798 | ||||||
| chr2:98206841
|
G | A | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-5089G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98206841 | ||||||
| chr2:98206972
|
A | G | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-4958A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98206972 | ||||||
| chr2:98207262
|
T | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0122 | 2 | HG00408.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1738-4668T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98207262 | ||||||
| chr2:98207308
|
C | G | 2 | a0007c0009t0002g0091a0007c0009t0002g0092 | 2 | HG01071.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1738-4622C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98207308 | ||||||
| chr2:98207347
|
C | T | 3 | a0001c0001t0001g0118a0001c0001t0001g0218a0003c0003t0003g0053 | 3 | HG00639.hp1 HG01175.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1738-4583C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98207347 | ||||||
| chr2:98207515
|
T | G | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-4415T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98207515 | ||||||
| chr2:98207528
|
A | G | 2 | a0002c0012t0004g0007a0002c0016t0020g0031 | 2 | HG01358.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1738-4402A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98207528 | ||||||
| chr2:98207547
|
T | C | 1 | a0002c0006t0004g0016 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1738-4383T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98207547 | ||||||
| chr2:98207580
|
G | T | 1 | a0001c0004t0003g0020 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1738-4350G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98207580 | ||||||
| chr2:98207709
|
G | A | 46 | a0001c0001t0001g0082a0001c0001t0001g0090a0001c0001t0001g0105others(43): Show | 46 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.1738-4221G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98207709 | ||||||
| chr2:98207730
|
G | A | 38 | a0002c0002t0001g0094a0002c0002t0001g0102a0002c0002t0002g0001others(35): Show | 38 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.1738-4200G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98207730 | ||||||
| chr2:98207756
|
C | T | 1 | a0003c0003t0003g0068 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1738-4174C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98207756 | ||||||
| chr2:98207959
|
A | T | 1 | a0003c0003t0003g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1738-3971A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98207959 | ||||||
| chr2:98207994
|
A | G | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-3936A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98207994 | ||||||
| chr2:98208027
|
A | G | 1 | a0022c0023t0002g0154 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1738-3903A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98208027 | ||||||
| chr2:98208194
|
T | A | 182 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(179): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1738-3736T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98208194 | ||||||
| chr2:98208246
|
C | T | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1738-3684C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98208246 | ||||||
| chr2:98208270
|
C | T | 1 | a0002c0016t0020g0031 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1738-3660C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98208270 | ||||||
| chr2:98208324
|
T | C | 1 | a0002c0002t0002g0163 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1738-3606T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98208324 | ||||||
| chr2:98208377
|
G | A | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-3553G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98208377 | ||||||
| chr2:98208421
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1738-3509C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98208421 | ||||||
| chr2:98208503
|
C | T | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-3427C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98208503 | ||||||
| chr2:98208551
|
G | A | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-3379G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98208551 | ||||||
| chr2:98208581
|
A | T | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1738-3349A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98208581 | ||||||
| chr2:98208753
|
T | C | 144 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.1738-3177T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98208753 | ||||||
| chr2:98209320
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1738-2610G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98209320 | ||||||
| chr2:98209571
|
C | T | 2 | a0002c0002t0004g0002a0015c0029t0004g0046 | 2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1738-2359C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98209571 | ||||||
| chr2:98209731
|
C | T | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-2199C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98209731 | ||||||
| chr2:98209740
|
G | T | 144 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.1738-2190G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98209740 | ||||||
| chr2:98209848
|
T | C | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-2082T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98209848 | ||||||
| chr2:98209902
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1738-2028T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98209902 | ||||||
| chr2:98210031
|
G | T | 1 | a0002c0002t0004g0022 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1738-1899G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98210031 | ||||||
| chr2:98210147
|
G | A | 1 | a0002c0012t0004g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1738-1783G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98210147 | ||||||
| chr2:98210186
|
T | C | 1 | a0002c0002t0002g0111 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1738-1744T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98210186 | ||||||
| chr2:98210204
|
C | G | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-1726C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98210204 | ||||||
| chr2:98210347
|
G | A | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-1583G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98210347 | ||||||
| chr2:98210388
|
C | T | 1 | a0002c0002t0004g0033 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1738-1542C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98210388 | ||||||
| chr2:98210412
|
C | T | 4 | a0002c0002t0002g0173a0002c0002t0004g0035a0002c0002t0004g0039others(1): Show | 4 | HG00733.hp1 HG00741.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738-1518C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98210412 | ||||||
| chr2:98210555
|
C | A | 1 | a0020c0026t0002g0210 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1738-1375C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98210555 | ||||||
| chr2:98210654
|
G | C | 1 | a0003c0003t0001g0202 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1738-1276G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98210654 | ||||||
| chr2:98210693
|
T | G | 227 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(224): Show | 227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.1738-1237T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98210693 | ||||||
| chr2:98210803
|
C | CT | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-1124dupT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | 98210803 | |||||
| chr2:98211023
|
T | C | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-907T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98211023 | ||||||
| chr2:98211028
|
C | T | 3 | a0001c0004t0004g0023a0007c0009t0002g0091a0007c0009t0002g0092 | 3 | HG01071.hp1 HG01081.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.1738-902C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98211028 | ||||||
| chr2:98211098
|
G | C | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1738-832G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98211098 | ||||||
| chr2:98211239
|
G | C | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-691G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98211239 | ||||||
| chr2:98211348
|
T | C | 1 | a0001c0001t0023g0009 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1738-582T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98211348 | ||||||
| chr2:98211404
|
C | T | 182 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(179): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1738-526C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98211404 | ||||||
| chr2:98211685
|
T | TGTC | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-244_1738-242d others(5): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | 98211685 | |||||
| chr2:98211926
|
G | A | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1738-4G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98211926 | ||||||
| chr2:98212235
|
A | G | 1 | a0026c0018t0010g0129 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1836+207A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98212235 | ||||||
| chr2:98212344
|
T | C | 38 | a0002c0002t0002g0173a0002c0002t0003g0024a0002c0002t0003g0027others(35): Show | 38 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.1836+316T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98212344 | ||||||
| chr2:98212455
|
T | C | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1836+427T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98212455 | ||||||
| chr2:98212590
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1836+562G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98212590 | ||||||
| chr2:98212774
|
A | G | 182 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(179): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1836+746A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98212774 | ||||||
| chr2:98212830
|
T | TC | 239 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(236): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1836+802_1836+803i others(3): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98212830 | ||||||
| chr2:98212978
|
T | C | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1836+950T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98212978 | ||||||
| chr2:98213045
|
C | T | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1836+1017C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98213045 | ||||||
| chr2:98213110
|
C | G | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1836+1082C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98213110 | ||||||
| chr2:98213279
|
C | T | 2 | a0007c0009t0002g0139a0007c0009t0002g0140 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1836+1251C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98213279 | ||||||
| chr2:98213324
|
C | T | 2 | a0002c0002t0004g0005a0008c0010t0004g0227 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1836+1296C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98213324 | ||||||
| chr2:98213383
|
G | A | 30 | a0002c0002t0002g0173a0002c0002t0003g0024a0002c0002t0003g0027others(27): Show | 30 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1836+1355G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98213383 | ||||||
| chr2:98213490
|
C | T | 1 | a0002c0019t0011g0228 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1836+1462C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98213490 | ||||||
| chr2:98213629
|
G | A | 5 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0003g0012others(2): Show | 5 | HG01167.hp2 HG02280.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1836+1601G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98213629 | ||||||
| chr2:98213699
|
G | A | 2 | a0002c0002t0004g0003a0002c0002t0004g0004 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1836+1671G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98213699 | ||||||
| chr2:98213919
|
G | A | 1 | a0003c0003t0003g0049 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1836+1891G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98213919 | ||||||
| chr2:98214178
|
G | A | 12 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.1836+2150G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98214178 | ||||||
| chr2:98214221
|
C | CAA | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1836+2200_1836+220 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr2 | 98214221 | |||||
| chr2:98214269
|
A | T | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1836+2241A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98214269 | ||||||
| chr2:98214279
|
T | G | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1836+2251T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98214279 | ||||||
| chr2:98214497
|
C | G | 2 | a0002c0012t0011g0226a0002c0019t0011g0228 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1836+2469C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98214497 | ||||||
| chr2:98214703
|
G | A | 2 | a0002c0012t0011g0226a0002c0019t0011g0228 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1836+2675G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98214703 | ||||||
| chr2:98214783
|
T | A | 4 | a0001c0001t0003g0232a0001c0001t0010g0128a0001c0004t0013g0029others(1): Show | 4 | HG03209.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1836+2755T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98214783 | ||||||
| chr2:98214915
|
T | C | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1836+2887T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98214915 | ||||||
| chr2:98214971
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1837-2875C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98214971 | ||||||
| chr2:98214980
|
G | C | 1 | a0002c0002t0001g0102 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1837-2866G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98214980 | ||||||
| chr2:98215202
|
A | G | 229 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(226): Show | 229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1837-2644A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98215202 | ||||||
| chr2:98215229
|
T | G | 3 | a0001c0001t0001g0191a0001c0001t0001g0195a0001c0001t0001g0216 | 3 | HG02040.hp2 NA18954.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.1837-2617T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98215229 | ||||||
| chr2:98215306
|
T | G | 1 | a0001c0001t0001g0138 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1837-2540T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98215306 | ||||||
| chr2:98215390
|
G | A | 18 | a0002c0002t0002g0173a0002c0002t0004g0005a0002c0002t0004g0030others(15): Show | 18 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.1837-2456G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98215390 | ||||||
| chr2:98215513
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1837-2333G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98215513 | ||||||
| chr2:98215581
|
A | G | 7 | a0007c0009t0002g0139a0007c0009t0002g0140a0009c0011t0001g0213others(4): Show | 7 | HG00140.hp1 HG01255.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1837-2265A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98215581 | ||||||
| chr2:98215640
|
C | A | 2 | a0002c0012t0004g0007a0002c0016t0020g0031 | 2 | HG01358.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1837-2206C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98215640 | ||||||
| chr2:98215887
|
A | AT | 28 | a0002c0002t0002g0173a0002c0002t0003g0024a0002c0002t0003g0027others(25): Show | 28 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.1837-1950dupT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr2 | 98215887 | |||||
| chr2:98215887
|
AT | A | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1837-1950delT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr2 | 98215887 | |||||
| chr2:98216098
|
C | T | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1837-1748C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98216098 | ||||||
| chr2:98216391
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1837-1455A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98216391 | ||||||
| chr2:98216397
|
A | G | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1837-1449A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98216397 | ||||||
| chr2:98216703
|
A | C | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1837-1143A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98216703 | ||||||
| chr2:98216982
|
A | ACC | 7 | a0002c0002t0004g0005a0006c0007t0009g0080a0008c0010t0004g0227others(4): Show | 7 | HG01891.hp1 HG02056.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.1837-862_1837-861d others(4): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr2 | 98216982 | |||||
| chr2:98216982
|
A | ACCC | 24 | a0001c0001t0001g0122a0001c0001t0001g0144a0001c0001t0001g0145others(21): Show | 24 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.1837-863_1837-861d others(5): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr2 | 98216982 | |||||
| chr2:98216982
|
A | ACCCC | 83 | a0001c0001t0001g0082a0001c0001t0001g0090a0001c0001t0001g0105others(80): Show | 83 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1837-861_1837-860i others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr2 | 98216982 | |||||
| chr2:98216982
|
A | ACCCCC | 34 | a0001c0001t0001g0106a0001c0001t0001g0114a0001c0001t0001g0115others(31): Show | 34 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.1837-861_1837-860i others(7): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr2 | 98216982 | |||||
| chr2:98216983
|
C | CCA | 9 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0033others(6): Show | 9 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.1837-862_1837-861i others(4): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr2 | 98216983 | |||||
| chr2:98216985
|
C | CCCCG | 14 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0089others(11): Show | 14 | HG02486.hp2 HG02615.hp1 HG02895.hp2 others(11): Show |
intron_variant | MODIFIER | c.1837-861_1837-860i others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98216985 | ||||||
| chr2:98216985
|
C | CCCG | 4 | a0001c0001t0001g0137a0001c0001t0003g0034a0009c0011t0001g0171others(1): Show | 4 | HG01168.hp1 HG01255.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1837-861_1837-860i others(5): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98216985 | ||||||
| chr2:98216986
|
G | A | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1837-860G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98216986 | ||||||
| chr2:98216986
|
G | C | 176 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(173): Show | 176 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1837-860G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98216986 | ||||||
| chr2:98216991
|
G | A | 1 | a0005c0008t0003g0233 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1837-855G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98216991 | ||||||
| chr2:98217056
|
C | T | 5 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0003g0012others(2): Show | 5 | HG01167.hp2 HG02280.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1837-790C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98217056 | ||||||
| chr2:98217131
|
C | T | 182 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(179): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1837-715C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98217131 | ||||||
| chr2:98217196
|
A | T | 10 | a0001c0001t0001g0118a0001c0001t0001g0218a0001c0004t0003g0013others(7): Show | 10 | HG00423.hp1 HG00639.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.1837-650A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98217196 | ||||||
| chr2:98217253
|
A | G | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1837-593A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98217253 | ||||||
| chr2:98217581
|
C | T | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1837-265C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98217581 | ||||||
| chr2:98217595
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1837-251A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98217595 | ||||||
| chr2:98217665
|
A | C | 3 | a0001c0004t0004g0023a0007c0009t0002g0091a0007c0009t0002g0092 | 3 | HG01071.hp1 HG01081.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.1837-181A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98217665 | ||||||
| chr2:98218087
|
G | A | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2019+59G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98218087 | ||||||
| chr2:98218188
|
T | C | 4 | a0001c0001t0001g0155a0001c0001t0001g0204a0001c0001t0016g0152others(1): Show | 4 | NA18941.hp2 NA18986.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.2019+160T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98218188 | ||||||
| chr2:98218366
|
T | C | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2019+338T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98218366 | ||||||
| chr2:98218419
|
A | C | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2019+391A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98218419 | ||||||
| chr2:98218702
|
T | C | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2019+674T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98218702 | ||||||
| chr2:98218826
|
A | G | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2019+798A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98218826 | ||||||
| chr2:98218829
|
T | C | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2019+801T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98218829 | ||||||
| chr2:98218892
|
G | A | 1 | a0002c0002t0004g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2019+864G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98218892 | ||||||
| chr2:98218946
|
C | T | 144 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.2019+918C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98218946 | ||||||
| chr2:98219115
|
C | T | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2019+1087C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98219115 | ||||||
| chr2:98219152
|
A | T | 2 | a0008c0010t0009g0239a0008c0010t0009g0240 | 2 | HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2019+1124A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98219152 | ||||||
| chr2:98219426
|
A | T | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2019+1398A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98219426 | ||||||
| chr2:98219488
|
G | A | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2019+1460G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98219488 | ||||||
| chr2:98219499
|
C | T | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2019+1471C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98219499 | ||||||
| chr2:98219609
|
G | A | 1 | a0003c0003t0003g0076 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2019+1581G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98219609 | ||||||
| chr2:98219800
|
A | G | 143 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(140): Show | 143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.2019+1772A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98219800 | ||||||
| chr2:98219880
|
C | T | 2 | a0011c0015t0001g0112a0011c0022t0003g0038 | 2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.2019+1852C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98219880 | ||||||
| chr2:98220009
|
A | T | 1 | a0003c0003t0003g0049 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2019+1981A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98220009 | ||||||
| chr2:98220014
|
G | T | 1 | a0001c0004t0003g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2019+1986G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98220014 | ||||||
| chr2:98220055
|
T | C | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2019+2027T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98220055 | ||||||
| chr2:98220069
|
C | T | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2019+2041C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98220069 | ||||||
| chr2:98220088
|
C | T | 1 | a0002c0002t0004g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2019+2060C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98220088 | ||||||
| chr2:98220144
|
A | G | 2 | a0002c0002t0002g0164a0006c0007t0002g0182 | 2 | NA18946.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.2019+2116A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98220144 | ||||||
| chr2:98220165
|
T | TA | 5 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0004g0040others(2): Show | 5 | HG01261.hp2 HG03041.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2019+2159dupA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr2 | 98220165 | |||||
| chr2:98220165
|
TA | T | 189 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(186): Show | 189 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.2019+2159delA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr2 | 98220165 | |||||
| chr2:98220165
|
TAA | T | 5 | a0001c0001t0001g0206a0002c0002t0002g0194a0002c0002t0004g0002others(2): Show | 5 | HG00323.hp1 HG00673.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.2019+2158_2019+215 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr2 | 98220165 | |||||
| chr2:98220165
|
TAAA | T | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2019+2157_2019+215 others(7): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr2 | 98220165 | |||||
| chr2:98220315
|
G | A | 144 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.2019+2287G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98220315 | ||||||
| chr2:98220544
|
C | T | 3 | a0001c0001t0007g0146a0001c0001t0007g0147a0001c0001t0007g0148 | 3 | NA18945.hp2 NA18963.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.2019+2516C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98220544 | ||||||
| chr2:98220550
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0153 | 2 | HG01099.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.2019+2522C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98220550 | ||||||
| chr2:98220957
|
C | T | 1 | a0004c0005t0002g0093 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2019+2929C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98220957 | ||||||
| chr2:98221070
|
G | A | 1 | a0001c0001t0023g0009 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2019+3042G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98221070 | ||||||
| chr2:98221130
|
T | TA | 10 | a0001c0001t0001g0144a0001c0001t0001g0145a0006c0007t0012g0050others(7): Show | 10 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2019+3115dupA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr2 | 98221130 | |||||
| chr2:98221158
|
G | A | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2019+3130G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98221158 | ||||||
| chr2:98221245
|
A | G | 1 | a0022c0023t0002g0154 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2019+3217A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98221245 | ||||||
| chr2:98221313
|
C | G | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2019+3285C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98221313 | ||||||
| chr2:98221347
|
C | T | 4 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0021g0006others(1): Show | 4 | HG01261.hp2 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2019+3319C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98221347 | ||||||
| chr2:98221407
|
A | G | 1 | a0002c0002t0004g0040 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2019+3379A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98221407 | ||||||
| chr2:98221925
|
C | T | 4 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0211others(1): Show | 4 | HG03942.hp2 NA19066.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.2019+3897C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98221925 | ||||||
| chr2:98221949
|
A | C | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2019+3921A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98221949 | ||||||
| chr2:98222038
|
G | T | 1 | a0020c0026t0002g0210 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2019+4010G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98222038 | ||||||
| chr2:98222042
|
C | T | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2019+4014C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98222042 | ||||||
| chr2:98222097
|
TC | T | 6 | a0002c0002t0004g0003a0002c0002t0004g0004a0006c0007t0009g0080others(3): Show | 6 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.2019+4070delC | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98222097 | ||||||
| chr2:98222363
|
C | T | 11 | a0001c0001t0001g0082a0001c0001t0001g0109a0001c0001t0001g0122others(8): Show | 11 | HG00408.hp2 HG00621.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.2019+4335C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98222363 | ||||||
| chr2:98222513
|
G | A | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2019+4485G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98222513 | ||||||
| chr2:98222579
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2019+4551T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98222579 | ||||||
| chr2:98222601
|
C | A | 144 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.2019+4573C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98222601 | ||||||
| chr2:98222644
|
G | T | 9 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0033others(6): Show | 9 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.2019+4616G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98222644 | ||||||
| chr2:98222646
|
G | C | 1 | a0001c0001t0001g0089 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2019+4618G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98222646 | ||||||
| chr2:98222651
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2019+4623C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98222651 | ||||||
| chr2:98222674
|
G | A | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2019+4646G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98222674 | ||||||
| chr2:98222684
|
G | A | 1 | a0002c0019t0011g0228 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2019+4656G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98222684 | ||||||
| chr2:98222706
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2019+4678A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98222706 | ||||||
| chr2:98222726
|
T | G | 1 | a0001c0001t0003g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2019+4698T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98222726 | ||||||
| chr2:98222746
|
G | A | 144 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.2019+4718G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98222746 | ||||||
| chr2:98222794
|
G | A | 2 | a0002c0002t0004g0011a0006c0007t0009g0080 | 2 | HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.2019+4766G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98222794 | ||||||
| chr2:98222830
|
A | C | 9 | a0001c0001t0005g0045a0001c0001t0015g0134a0003c0003t0003g0048others(6): Show | 9 | HG02109.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2019+4802A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98222830 | ||||||
| chr2:98222868
|
A | T | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2019+4840A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98222868 | ||||||
| chr2:98222904
|
A | G | 26 | a0002c0002t0002g0173a0002c0002t0003g0024a0002c0002t0003g0027others(23): Show | 26 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.2019+4876A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98222904 | ||||||
| chr2:98223016
|
A | G | 144 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.2019+4988A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98223016 | ||||||
| chr2:98223033
|
G | T | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2019+5005G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98223033 | ||||||
| chr2:98223061
|
A | G | 144 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.2019+5033A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98223061 | ||||||
| chr2:98223076
|
T | A | 239 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(236): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.2019+5048T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98223076 | ||||||
| chr2:98223145
|
A | T | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2020-5057A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98223145 | ||||||
| chr2:98223266
|
C | A | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2020-4936C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98223266 | ||||||
| chr2:98223308
|
C | CA | 141 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(138): Show | 141 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.2020-4879dupA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr2 | 98223308 | |||||
| chr2:98223308
|
C | CAA | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2020-4880_2020-487 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr2 | 98223308 | |||||
| chr2:98223666
|
G | A | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2020-4536G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98223666 | ||||||
| chr2:98223875
|
C | T | 1 | a0012c0036t0003g0063 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2020-4327C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98223875 | ||||||
| chr2:98223876
|
G | A | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2020-4326G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98223876 | ||||||
| chr2:98223913
|
A | G | 1 | a0002c0002t0024g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2020-4289A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98223913 | ||||||
| chr2:98224003
|
C | T | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2020-4199C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98224003 | ||||||
| chr2:98224035
|
C | T | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2020-4167C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98224035 | ||||||
| chr2:98224123
|
C | T | 182 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(179): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.2020-4079C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98224123 | ||||||
| chr2:98224166
|
A | G | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2020-4036A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98224166 | ||||||
| chr2:98224299
|
T | C | 2 | a0002c0012t0011g0226a0002c0019t0011g0228 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2020-3903T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98224299 | ||||||
| chr2:98224599
|
GT | G | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2020-3600delT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr2 | 98224599 | |||||
| chr2:98224620
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2020-3582G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98224620 | ||||||
| chr2:98224722
|
C | G | 1 | a0001c0001t0001g0157 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2020-3480C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98224722 | ||||||
| chr2:98224753
|
T | TA | 221 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(218): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.2020-3436dupA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr2 | 98224753 | |||||
| chr2:98224913
|
A | G | 2 | a0008c0010t0009g0239a0008c0010t0009g0240 | 2 | HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2020-3289A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98224913 | ||||||
| chr2:98224963
|
C | CT | 26 | a0002c0002t0002g0173a0002c0002t0003g0024a0002c0002t0003g0027others(23): Show | 26 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.2020-3230dupT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr2 | 98224963 | |||||
| chr2:98225014
|
A | G | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2020-3188A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98225014 | ||||||
| chr2:98225048
|
C | T | 8 | a0001c0001t0005g0045a0001c0001t0015g0134a0003c0003t0003g0048others(5): Show | 8 | HG02109.hp1 HG02572.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2020-3154C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98225048 | ||||||
| chr2:98225123
|
G | A | 1 | a0003c0003t0005g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2020-3079G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98225123 | ||||||
| chr2:98225165
|
T | C | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2020-3037T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98225165 | ||||||
| chr2:98225189
|
T | A | 2 | a0001c0004t0003g0025a0001c0004t0003g0026 | 2 | NA18951.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.2020-3013T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98225189 | ||||||
| chr2:98225376
|
G | A | 144 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.2020-2826G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98225376 | ||||||
| chr2:98225458
|
T | C | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2020-2744T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98225458 | ||||||
| chr2:98225624
|
G | A | 4 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0021g0006others(1): Show | 4 | HG01261.hp2 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2020-2578G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98225624 | ||||||
| chr2:98225664
|
C | T | 182 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(179): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.2020-2538C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98225664 | ||||||
| chr2:98225685
|
A | C | 38 | a0002c0002t0001g0094a0002c0002t0001g0102a0002c0002t0002g0001others(35): Show | 38 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.2020-2517A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98225685 | ||||||
| chr2:98225705
|
C | CA | 20 | a0001c0001t0001g0156a0001c0001t0001g0158a0001c0001t0001g0159others(17): Show | 20 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.2020-2483dupA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr2 | 98225705 | |||||
| chr2:98225705
|
C | CAA | 6 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(3): Show | 6 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2020-2484_2020-248 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr2 | 98225705 | |||||
| chr2:98225817
|
T | G | 1 | a0001c0001t0001g0188 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2020-2385T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98225817 | ||||||
| chr2:98225856
|
A | G | 3 | a0001c0001t0007g0146a0001c0001t0007g0147a0001c0001t0007g0148 | 3 | NA18945.hp2 NA18963.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.2020-2346A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98225856 | ||||||
| chr2:98225908
|
T | C | 1 | a0002c0002t0004g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2020-2294T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98225908 | ||||||
| chr2:98226603
|
T | TGGGAGAC others(69): Show |
12 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0151others(9): Show | 12 | HG00544.hp1 HG00597.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.2020-1596_2020-152 others(80): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr2 | 98226603 | |||||
| chr2:98226910
|
C | T | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2020-1292C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98226910 | ||||||
| chr2:98226983
|
C | T | 47 | a0001c0001t0001g0082a0001c0001t0001g0090a0001c0001t0001g0105others(44): Show | 47 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.2020-1219C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98226983 | ||||||
| chr2:98227052
|
G | A | 1 | a0003c0003t0006g0200 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2020-1150G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98227052 | ||||||
| chr2:98227178
|
A | G | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2020-1024A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98227178 | ||||||
| chr2:98227213
|
C | G | 144 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.2020-989C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98227213 | ||||||
| chr2:98227265
|
A | G | 1 | a0004c0005t0002g0098 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2020-937A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98227265 | ||||||
| chr2:98227393
|
G | T | 4 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0021g0006others(1): Show | 4 | HG01261.hp2 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2020-809G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98227393 | ||||||
| chr2:98227781
|
C | T | 2 | a0002c0002t0004g0005a0008c0010t0004g0227 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2020-421C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98227781 | ||||||
| chr2:98227871
|
G | A | 229 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(226): Show | 229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.2020-331G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98227871 | ||||||
| chr2:98228112
|
A | G | 150 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(147): Show | 150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.2020-90A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98228112 | ||||||
| chr2:98228455
|
G | A | 44 | a0002c0002t0001g0094a0002c0002t0001g0102a0002c0002t0002g0001others(41): Show | 44 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.2150+123G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 15/27 | chr2 | 98228455 | ||||||
| chr2:98228562
|
C | T | 1 | a0002c0006t0004g0019 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2150+230C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 15/27 | chr2 | 98228562 | ||||||
| chr2:98228575
|
G | A | 12 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.2150+243G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 15/27 | chr2 | 98228575 | ||||||
| chr2:98228602
|
C | T | 17 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(14): Show | 17 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.2150+270C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 15/27 | chr2 | 98228602 | ||||||
| chr2:98228606
|
G | C | 1 | a0001c0004t0003g0010 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2150+274G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 15/27 | chr2 | 98228606 | ||||||
| chr2:98228663
|
A | G | 6 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0021g0006others(3): Show | 6 | HG01261.hp2 HG02922.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2150+331A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 15/27 | chr2 | 98228663 | ||||||
| chr2:98228885
|
A | G | 149 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(146): Show | 149 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.2150+553A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 15/27 | chr2 | 98228885 | ||||||
| chr2:98228990
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2150+658A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 15/27 | chr2 | 98228990 | ||||||
| chr2:98229009
|
G | A | 2 | a0002c0002t0004g0005a0008c0010t0004g0227 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2150+677G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 15/27 | chr2 | 98229009 | ||||||
| chr2:98229166
|
G | A | 2 | a0002c0002t0003g0024a0002c0002t0003g0027 | 2 | HG01261.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2150+834G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 15/27 | chr2 | 98229166 | ||||||
| chr2:98229296
|
T | C | 3 | a0002c0002t0001g0094a0002c0002t0001g0102a0019c0024t0001g0103 | 3 | HG00639.hp2 HG01167.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.2151-754T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 15/27 | chr2 | 98229296 | ||||||
| chr2:98229417
|
C | T | 1 | a0005c0008t0003g0234 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2151-633C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 15/27 | chr2 | 98229417 | ||||||
| chr2:98229606
|
A | G | 5 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(2): Show | 5 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2151-444A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 15/27 | chr2 | 98229606 | ||||||
| chr2:98229630
|
A | G | 229 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(226): Show | 229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.2151-420A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 15/27 | chr2 | 98229630 | ||||||
| chr2:98229670
|
C | T | 17 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(14): Show | 17 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.2151-380C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 15/27 | chr2 | 98229670 | ||||||
| chr2:98229728
|
A | C | 4 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0021g0006others(1): Show | 4 | HG01261.hp2 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2151-322A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 15/27 | chr2 | 98229728 | ||||||
| chr2:98229770
|
G | T | 144 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.2151-280G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 15/27 | chr2 | 98229770 | ||||||
| chr2:98229838
|
T | C | 144 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.2151-212T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 15/27 | chr2 | 98229838 | ||||||
| chr2:98229942
|
A | T | 226 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(223): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.2151-108A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 15/27 | chr2 | 98229942 | ||||||
| chr2:98229951
|
A | G | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2151-99A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 15/27 | chr2 | 98229951 | ||||||
| chr2:98230008
|
C | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0207 | 2 | HG02735.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2151-42C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 15/27 | chr2 | 98230008 | ||||||
| chr2:98230400
|
G | A | 2 | a0002c0002t0004g0036a0002c0002t0004g0037 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2308+193G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98230400 | ||||||
| chr2:98230499
|
G | A | 4 | a0001c0001t0003g0232a0001c0001t0010g0128a0001c0004t0013g0029others(1): Show | 4 | HG03209.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2308+292G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98230499 | ||||||
| chr2:98230831
|
G | A | 44 | a0002c0002t0001g0094a0002c0002t0001g0102a0002c0002t0002g0001others(41): Show | 44 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.2308+624G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98230831 | ||||||
| chr2:98231065
|
G | A | 2 | a0002c0002t0004g0003a0002c0002t0004g0004 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2308+858G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98231065 | ||||||
| chr2:98231092
|
C | A | 4 | a0002c0002t0004g0011a0002c0006t0004g0016a0002c0006t0004g0021others(1): Show | 4 | HG00733.hp2 HG02896.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2308+885C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98231092 | ||||||
| chr2:98231107
|
T | C | 40 | a0002c0002t0001g0094a0002c0002t0001g0102a0002c0002t0002g0001others(37): Show | 40 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.2308+900T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98231107 | ||||||
| chr2:98231169
|
G | C | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2308+962G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98231169 | ||||||
| chr2:98231751
|
T | C | 4 | a0001c0001t0001g0161a0001c0001t0001g0206a0003c0003t0003g0070others(1): Show | 4 | HG00673.hp2 HG02155.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.2308+1544T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98231751 | ||||||
| chr2:98231872
|
T | C | 149 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(146): Show | 149 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.2308+1665T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98231872 | ||||||
| chr2:98231943
|
C | T | 5 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(2): Show | 5 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2308+1736C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98231943 | ||||||
| chr2:98231951
|
C | T | 182 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(179): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.2308+1744C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98231951 | ||||||
| chr2:98231966
|
T | C | 1 | a0002c0002t0021g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2308+1759T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98231966 | ||||||
| chr2:98232091
|
T | C | 1 | a0003c0003t0003g0054 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2308+1884T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98232091 | ||||||
| chr2:98232185
|
A | C | 2 | a0002c0002t0004g0003a0002c0002t0004g0004 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2308+1978A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98232185 | ||||||
| chr2:98232253
|
A | G | 1 | a0002c0002t0002g0217 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2308+2046A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98232253 | ||||||
| chr2:98232390
|
G | A | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2308+2183G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98232390 | ||||||
| chr2:98232567
|
T | C | 2 | a0002c0012t0011g0226a0002c0019t0011g0228 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2309-2081T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98232567 | ||||||
| chr2:98232642
|
A | C | 2 | a0002c0012t0004g0007a0002c0016t0020g0031 | 2 | HG01358.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2309-2006A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98232642 | ||||||
| chr2:98232881
|
G | A | 1 | a0002c0006t0004g0015 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2309-1767G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98232881 | ||||||
| chr2:98232991
|
A | C | 5 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(2): Show | 5 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2309-1657A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98232991 | ||||||
| chr2:98233228
|
A | G | 1 | a0002c0002t0008g0196 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2309-1420A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98233228 | ||||||
| chr2:98233330
|
T | C | 182 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(179): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.2309-1318T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98233330 | ||||||
| chr2:98233364
|
G | A | 4 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0021g0006others(1): Show | 4 | HG01261.hp2 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2309-1284G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98233364 | ||||||
| chr2:98233824
|
T | G | 149 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(146): Show | 149 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.2309-824T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98233824 | ||||||
| chr2:98234101
|
C | G | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2309-547C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98234101 | ||||||
| chr2:98234146
|
T | G | 2 | a0002c0002t0004g0005a0008c0010t0004g0227 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2309-502T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98234146 | ||||||
| chr2:98234164
|
A | G | 227 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(224): Show | 227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.2309-484A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98234164 | ||||||
| chr2:98234430
|
T | A | 5 | a0001c0001t0001g0127a0001c0001t0001g0144a0001c0001t0001g0145others(2): Show | 5 | HG01123.hp2 HG02717.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.2309-218T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98234430 | ||||||
| chr2:98234478
|
A | G | 2 | a0002c0002t0004g0002a0015c0029t0004g0046 | 2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2309-170A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98234478 | ||||||
| chr2:98234839
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2428+72G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 17/27 | chr2 | 98234839 | ||||||
| chr2:98235110
|
C | A | 144 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.2428+343C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 17/27 | chr2 | 98235110 | ||||||
| chr2:98235168
|
C | T | 182 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(179): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.2428+401C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 17/27 | chr2 | 98235168 | ||||||
| chr2:98235394
|
C | T | 5 | a0007c0009t0002g0139a0007c0009t0002g0140a0010c0013t0002g0104others(2): Show | 5 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2428+627C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 17/27 | chr2 | 98235394 | ||||||
| chr2:98235477
|
G | C | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2428+710G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 17/27 | chr2 | 98235477 | ||||||
| chr2:98235495
|
G | A | 2 | a0002c0002t0004g0003a0002c0002t0004g0004 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2428+728G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 17/27 | chr2 | 98235495 | ||||||
| chr2:98235518
|
A | G | 148 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(145): Show | 148 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.2428+751A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 17/27 | chr2 | 98235518 | ||||||
| chr2:98235577
|
C | T | 27 | a0002c0002t0002g0173a0002c0002t0003g0024a0002c0002t0003g0027others(24): Show | 27 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.2428+810C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 17/27 | chr2 | 98235577 | ||||||
| chr2:98235838
|
G | A | 1 | a0002c0016t0020g0031 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2429-552G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 17/27 | chr2 | 98235838 | ||||||
| chr2:98235912
|
G | T | 182 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(179): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.2429-478G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 17/27 | chr2 | 98235912 | ||||||
| chr2:98236036
|
C | G | 1 | a0001c0001t0001g0109 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2429-354C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 17/27 | chr2 | 98236036 | ||||||
| chr2:98236097
|
G | A | 2 | a0002c0012t0011g0226a0002c0019t0011g0228 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2429-293G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 17/27 | chr2 | 98236097 | ||||||
| chr2:98236176
|
T | A | 1 | a0002c0002t0004g0040 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2429-214T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 17/27 | chr2 | 98236176 | ||||||
| chr2:98236258
|
A | T | 1 | a0001c0001t0006g0181 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2429-132A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 17/27 | chr2 | 98236258 | ||||||
| chr2:98236901
|
C | A | 149 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(146): Show | 149 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.2673+171C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98236901 | ||||||
| chr2:98236910
|
G | T | 155 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(152): Show | 155 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.2673+180G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98236910 | ||||||
| chr2:98236918
|
G | A | 4 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0021g0006others(1): Show | 4 | HG01261.hp2 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2673+188G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98236918 | ||||||
| chr2:98237070
|
A | G | 149 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(146): Show | 149 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.2673+340A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98237070 | ||||||
| chr2:98237498
|
G | A | 2 | a0001c0001t0003g0236a0001c0001t0013g0028 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2673+768G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98237498 | ||||||
| chr2:98237769
|
A | AACAATAT others(2757): Show |
1 | a0002c0002t0002g0096 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2673+1050_2673+105 others(2768): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr2 | 98237769 | |||||
| chr2:98237860
|
A | G | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2673+1130A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98237860 | ||||||
| chr2:98237883
|
G | A | 14 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0004g0003others(11): Show | 14 | HG01261.hp2 HG01358.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2673+1153G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98237883 | ||||||
| chr2:98237927
|
A | T | 155 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(152): Show | 155 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.2673+1197A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98237927 | ||||||
| chr2:98238480
|
A | G | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2673+1750A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98238480 | ||||||
| chr2:98238489
|
A | C | 1 | a0001c0001t0001g0184 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2673+1759A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98238489 | ||||||
| chr2:98238503
|
T | C | 1 | a0002c0002t0002g0169 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2673+1773T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98238503 | ||||||
| chr2:98238544
|
C | T | 14 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0089others(11): Show | 14 | HG02486.hp2 HG02615.hp1 HG02895.hp1 others(11): Show |
intron_variant | MODIFIER | c.2673+1814C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98238544 | ||||||
| chr2:98238555
|
G | A | 1 | a0002c0002t0004g0011 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2673+1825G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98238555 | ||||||
| chr2:98238820
|
A | G | 1 | a0003c0003t0003g0068 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2673+2090A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98238820 | ||||||
| chr2:98239034
|
G | A | 149 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(146): Show | 149 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.2673+2304G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98239034 | ||||||
| chr2:98239055
|
C | T | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2673+2325C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98239055 | ||||||
| chr2:98239339
|
CTCGTGCT others(10): Show |
C | 149 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(146): Show | 149 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.2673+2629_2673+264 others(21): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr2 | 98239339 | |||||
| chr2:98239342
|
G | A | 2 | a0002c0012t0011g0226a0002c0019t0011g0228 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2673+2612G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98239342 | ||||||
| chr2:98239541
|
A | T | 6 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(3): Show | 6 | HG01891.hp1 HG02056.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.2673+2811A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98239541 | ||||||
| chr2:98239545
|
T | G | 38 | a0002c0002t0001g0094a0002c0002t0001g0102a0002c0002t0002g0001others(35): Show | 38 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.2673+2815T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98239545 | ||||||
| chr2:98239781
|
G | A | 1 | a0026c0018t0010g0129 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2673+3051G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98239781 | ||||||
| chr2:98239871
|
G | A | 1 | a0020c0026t0002g0210 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2673+3141G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98239871 | ||||||
| chr2:98240406
|
G | T | 2 | a0002c0012t0004g0007a0002c0016t0020g0031 | 2 | HG01358.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2673+3676G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98240406 | ||||||
| chr2:98240418
|
G | A | 226 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(223): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.2673+3688G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98240418 | ||||||
| chr2:98240478
|
C | T | 1 | a0001c0004t0013g0029 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2673+3748C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98240478 | ||||||
| chr2:98240497
|
G | A | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.2673+3767G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98240497 | ||||||
| chr2:98240538
|
C | T | 182 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(179): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.2673+3808C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98240538 | ||||||
| chr2:98240597
|
A | G | 4 | a0002c0002t0004g0011a0002c0006t0004g0016a0002c0006t0004g0021others(1): Show | 4 | HG00733.hp2 HG02896.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2673+3867A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98240597 | ||||||
| chr2:98240722
|
T | C | 1 | a0003c0003t0003g0068 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2673+3992T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98240722 | ||||||
| chr2:98240922
|
T | G | 2 | a0001c0001t0003g0236a0001c0001t0013g0028 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2673+4192T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98240922 | ||||||
| chr2:98241138
|
G | C | 143 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(140): Show | 143 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.2673+4408G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98241138 | ||||||
| chr2:98241160
|
G | A | 2 | a0002c0002t0003g0024a0002c0002t0003g0027 | 2 | HG01261.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2673+4430G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98241160 | ||||||
| chr2:98241307
|
G | T | 40 | a0001c0001t0002g0212a0002c0002t0002g0001a0002c0002t0002g0087others(37): Show | 40 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.2673+4577G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98241307 | ||||||
| chr2:98241423
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2673+4693G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98241423 | ||||||
| chr2:98241430
|
C | T | 136 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(133): Show | 136 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.2673+4700C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98241430 | ||||||
| chr2:98241513
|
G | A | 43 | a0001c0001t0001g0082a0001c0001t0001g0090a0001c0001t0001g0105others(40): Show | 43 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(40): Show |
intron_variant | MODIFIER | c.2673+4783G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98241513 | ||||||
| chr2:98241673
|
C | T | 12 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0131others(9): Show | 12 | HG02486.hp2 HG02615.hp1 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.2673+4943C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98241673 | ||||||
| chr2:98241725
|
A | G | 183 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.2673+4995A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98241725 | ||||||
| chr2:98241763
|
A | G | 150 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(147): Show | 150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.2673+5033A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98241763 | ||||||
| chr2:98241845
|
C | G | 125 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(122): Show | 125 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.2673+5115C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98241845 | ||||||
| chr2:98242009
|
C | A | 1 | a0001c0001t0010g0128 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2673+5279C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98242009 | ||||||
| chr2:98242323
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2673+5593G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98242323 | ||||||
| chr2:98242531
|
C | G | 1 | a0002c0006t0004g0021 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2673+5801C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98242531 | ||||||
| chr2:98242601
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2673+5871G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98242601 | ||||||
| chr2:98242639
|
T | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2673+5909T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98242639 | ||||||
| chr2:98242802
|
A | G | 2 | a0002c0012t0004g0007a0002c0016t0020g0031 | 2 | HG01358.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2673+6072A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98242802 | ||||||
| chr2:98242814
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2673+6084A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98242814 | ||||||
| chr2:98242873
|
T | C | 1 | a0002c0002t0021g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2673+6143T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98242873 | ||||||
| chr2:98242945
|
T | C | 2 | a0011c0015t0001g0112a0011c0022t0003g0038 | 2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.2673+6215T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98242945 | ||||||
| chr2:98243205
|
C | A | 144 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.2673+6475C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98243205 | ||||||
| chr2:98243308
|
C | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2673+6578C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98243308 | ||||||
| chr2:98243421
|
T | C | 182 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(179): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.2673+6691T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98243421 | ||||||
| chr2:98243426
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2673+6696C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98243426 | ||||||
| chr2:98243637
|
T | TG | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2674-6681_2674-668 others(5): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98243637 | ||||||
| chr2:98243652
|
C | T | 1 | a0003c0003t0003g0073 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2674-6666C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98243652 | ||||||
| chr2:98243670
|
C | T | 7 | a0002c0002t0002g0001a0002c0002t0002g0087a0002c0002t0002g0108others(4): Show | 7 | HG00597.hp1 HG02080.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.2674-6648C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98243670 | ||||||
| chr2:98244099
|
C | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2674-6219C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98244099 | ||||||
| chr2:98244398
|
AT | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2674-5917delT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr2 | 98244398 | |||||
| chr2:98244408
|
A | C | 11 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0004g0003others(8): Show | 11 | HG01261.hp2 HG01358.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2674-5910A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98244408 | ||||||
| chr2:98244441
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2674-5877G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98244441 | ||||||
| chr2:98244594
|
C | T | 144 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.2674-5724C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98244594 | ||||||
| chr2:98244622
|
G | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2674-5696G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98244622 | ||||||
| chr2:98244710
|
T | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2674-5608T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98244710 | ||||||
| chr2:98244908
|
TCA | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2674-5409_2674-540 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98244908 | ||||||
| chr2:98244936
|
C | G | 1 | a0001c0004t0003g0020 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2674-5382C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98244936 | ||||||
| chr2:98245003
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2674-5315A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98245003 | ||||||
| chr2:98245041
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2674-5277T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98245041 | ||||||
| chr2:98245389
|
C | A | 2 | a0002c0012t0004g0007a0002c0016t0020g0031 | 2 | HG01358.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2674-4929C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98245389 | ||||||
| chr2:98245634
|
A | G | 181 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(178): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.2674-4684A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98245634 | ||||||
| chr2:98245643
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2674-4675G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98245643 | ||||||
| chr2:98245646
|
A | G | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2674-4672A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98245646 | ||||||
| chr2:98245687
|
A | AGTATTCT | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2674-4629_2674-462 others(11): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr2 | 98245687 | |||||
| chr2:98245751
|
C | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2674-4567C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98245751 | ||||||
| chr2:98245875
|
A | T | 4 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0021g0006others(1): Show | 4 | HG01261.hp2 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2674-4443A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98245875 | ||||||
| chr2:98245918
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2674-4400C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98245918 | ||||||
| chr2:98246020
|
A | C | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2674-4298A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98246020 | ||||||
| chr2:98246030
|
C | A | 1 | a0001c0001t0001g0204 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2674-4288C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98246030 | ||||||
| chr2:98246272
|
T | A | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2674-4046T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98246272 | ||||||
| chr2:98246431
|
G | A | 1 | a0002c0002t0004g0022 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2674-3887G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98246431 | ||||||
| chr2:98246455
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2674-3863G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98246455 | ||||||
| chr2:98246519
|
A | G | 8 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0004g0005others(5): Show | 8 | HG01261.hp2 HG01358.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2674-3799A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98246519 | ||||||
| chr2:98246659
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2674-3659A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98246659 | ||||||
| chr2:98246719
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2674-3599G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98246719 | ||||||
| chr2:98246893
|
CT | C | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2674-3418delT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr2 | 98246893 | |||||
| chr2:98246909
|
A | G | 1 | a0002c0002t0002g0168 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2674-3409A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98246909 | ||||||
| chr2:98246978
|
T | G | 1 | a0001c0001t0001g0160 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2674-3340T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98246978 | ||||||
| chr2:98247060
|
T | C | 182 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(179): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.2674-3258T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98247060 | ||||||
| chr2:98247061
|
G | A | 16 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0004g0003others(13): Show | 16 | HG01261.hp2 HG01358.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2674-3257G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98247061 | ||||||
| chr2:98247067
|
G | A | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2674-3251G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98247067 | ||||||
| chr2:98247177
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2674-3141T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98247177 | ||||||
| chr2:98247186
|
C | T | 1 | a0005c0008t0003g0235 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2674-3132C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98247186 | ||||||
| chr2:98247519
|
A | T | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.2674-2799A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98247519 | ||||||
| chr2:98247549
|
G | C | 227 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(224): Show | 227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.2674-2769G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98247549 | ||||||
| chr2:98247818
|
A | G | 144 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.2674-2500A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98247818 | ||||||
| chr2:98248409
|
A | T | 1 | a0001c0001t0001g0211 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2674-1909A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98248409 | ||||||
| chr2:98248481
|
T | G | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2674-1837T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98248481 | ||||||
| chr2:98248668
|
G | A | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2674-1650G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98248668 | ||||||
| chr2:98248727
|
T | C | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2674-1591T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98248727 | ||||||
| chr2:98248733
|
A | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2674-1585A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98248733 | ||||||
| chr2:98248815
|
CTCTTTCT others(7): Show |
C | 1 | a0001c0004t0003g0010 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2674-1493_2674-148 others(18): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr2 | 98248815 | |||||
| chr2:98248821
|
CTTTTTCT others(4): Show |
C | 1 | a0003c0003t0005g0069 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2674-1494_2674-148 others(15): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr2 | 98248821 | |||||
| chr2:98248823
|
TTTTC | T | 3 | a0002c0006t0004g0237a0007c0009t0002g0139a0007c0009t0002g0140 | 3 | HG01123.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2674-1437_2674-143 others(8): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr2 | 98248823 | |||||
| chr2:98248823
|
TTTTCTTT others(5): Show |
T | 2 | a0002c0002t0002g0219a0002c0002t0008g0196 | 2 | HG00280.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.2674-1445_2674-143 others(16): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr2 | 98248823 | |||||
| chr2:98248824
|
TTTCTTTC others(4): Show |
T | 1 | a0003c0003t0003g0048 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2674-1491_2674-148 others(15): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr2 | 98248824 | |||||
| chr2:98248825
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2674-1493T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98248825 | ||||||
| chr2:98248835
|
CTTTCTTT others(35): Show |
C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2674-1481_2674-144 others(46): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr2 | 98248835 | |||||
| chr2:98248855
|
CTTTCTTT others(19): Show |
C | 5 | a0003c0003t0003g0071a0006c0007t0009g0080a0008c0010t0009g0239others(2): Show | 5 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2674-1461_2674-143 others(30): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr2 | 98248855 | |||||
| chr2:98248859
|
CTTTCTTT others(15): Show |
C | 4 | a0001c0004t0003g0020a0002c0002t0004g0003a0003c0003t0003g0060others(1): Show | 4 | HG02717.hp2 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2674-1457_2674-143 others(26): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr2 | 98248859 | |||||
| chr2:98248863
|
CTTTCTTT others(11): Show |
C | 13 | a0001c0001t0001g0083a0001c0001t0001g0109a0001c0001t0001g0115others(10): Show | 13 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(10): Show |
intron_variant | MODIFIER | c.2674-1453_2674-143 others(22): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr2 | 98248863 | |||||
| chr2:98248867
|
CTTTCTTT others(7): Show |
C | 44 | a0001c0001t0001g0090a0001c0001t0001g0105a0001c0001t0001g0117others(41): Show | 44 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.2674-1449_2674-143 others(18): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr2 | 98248867 | |||||
| chr2:98248871
|
CTTTCTTT others(3): Show |
C | 62 | a0001c0001t0001g0088a0001c0001t0001g0106a0001c0001t0001g0127others(59): Show | 62 | HG00544.hp1 HG00544.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.2674-1445_2674-143 others(14): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr2 | 98248871 | |||||
| chr2:98248875
|
CTTTCTT | C | 34 | a0001c0001t0001g0082a0001c0001t0001g0089a0001c0001t0001g0131others(31): Show | 34 | HG00323.hp2 HG00609.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.2674-1441_2674-143 others(10): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr2 | 98248875 | |||||
| chr2:98248876
|
T | TCTTTCTT others(11): Show |
1 | a0001c0001t0001g0211 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2674-1442_2674-144 others(22): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98248876 | ||||||
| chr2:98248879
|
CTT | C | 28 | a0001c0001t0001g0130a0001c0001t0001g0204a0001c0001t0002g0212others(25): Show | 28 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.2674-1437_2674-143 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr2 | 98248879 | |||||
| chr2:98248881
|
T | TTCTTTC | 5 | a0001c0001t0003g0236a0001c0001t0013g0028a0002c0002t0002g0001others(2): Show | 5 | HG03098.hp2 HG03209.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.2674-1434_2674-143 others(10): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr2 | 98248881 | |||||
| chr2:98248881
|
T | TTCTTTCT others(3): Show |
2 | a0002c0002t0002g0087a0002c0002t0002g0108 | 2 | HG00597.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.2674-1434_2674-143 others(14): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr2 | 98248881 | |||||
| chr2:98248885
|
C | CTT | 25 | a0001c0001t0003g0232a0002c0002t0002g0095a0002c0002t0002g0110others(22): Show | 25 | HG00408.hp1 HG00621.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.2674-1432_2674-143 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr2 | 98248885 | |||||
| chr2:98248885
|
C | T | 201 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(198): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.2674-1433C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98248885 | ||||||
| chr2:98248888
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2674-1430T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98248888 | ||||||
| chr2:98248889
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2674-1429T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98248889 | ||||||
| chr2:98248891
|
C | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2674-1427C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98248891 | ||||||
| chr2:98248895
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2674-1423T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98248895 | ||||||
| chr2:98248907
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2674-1411C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98248907 | ||||||
| chr2:98248913
|
CTCCT | C | 18 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(15): Show | 18 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(15): Show |
intron_variant | MODIFIER | c.2674-1389_2674-138 others(8): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr2 | 98248913 | |||||
| chr2:98249386
|
C | T | 231 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(228): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2674-932C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98249386 | ||||||
| chr2:98249635
|
G | A | 16 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0004g0003others(13): Show | 16 | HG01261.hp2 HG01358.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2674-683G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98249635 | ||||||
| chr2:98249846
|
G | A | 3 | a0001c0001t0001g0161a0001c0001t0001g0206a0003c0003t0003g0070 | 3 | HG00673.hp2 HG02155.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.2674-472G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98249846 | ||||||
| chr2:98250014
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2674-304G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98250014 | ||||||
| chr2:98250037
|
A | C | 16 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0004g0003others(13): Show | 16 | HG01261.hp2 HG01358.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2674-281A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98250037 | ||||||
| chr2:98250094
|
G | A | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.2674-224G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98250094 | ||||||
| chr2:98250312
|
A | G | 43 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(40): Show | 43 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(40): Show |
splice_region_variant&intron_variant | LOW | c.2674-6A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98250312 | ||||||
| chr2:98250517
|
CT | C | 7 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(4): Show | 7 | HG00140.hp1 HG01515.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.2792+95delT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 98250517 | |||||
| chr2:98250696
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2792+260A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98250696 | ||||||
| chr2:98251564
|
C | A | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.2792+1128C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98251564 | ||||||
| chr2:98251835
|
T | C | 182 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(179): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.2792+1399T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98251835 | ||||||
| chr2:98251891
|
G | T | 1 | a0002c0019t0011g0228 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2792+1455G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98251891 | ||||||
| chr2:98252034
|
C | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2792+1598C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98252034 | ||||||
| chr2:98252185
|
G | A | 38 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(35): Show | 38 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.2792+1749G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98252185 | ||||||
| chr2:98252213
|
A | G | 3 | a0002c0002t0004g0003a0002c0002t0004g0004a0006c0007t0019g0059 | 3 | HG03139.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2792+1777A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98252213 | ||||||
| chr2:98252237
|
G | A | 1 | a0002c0002t0004g0022 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2792+1801G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98252237 | ||||||
| chr2:98252301
|
A | G | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2792+1865A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98252301 | ||||||
| chr2:98252361
|
C | A | 182 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(179): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.2792+1925C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98252361 | ||||||
| chr2:98252434
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2792+1998G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98252434 | ||||||
| chr2:98252462
|
G | A | 1 | a0004c0005t0002g0107 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2792+2026G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98252462 | ||||||
| chr2:98252477
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2792+2041T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98252477 | ||||||
| chr2:98252515
|
C | T | 144 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.2792+2079C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98252515 | ||||||
| chr2:98252703
|
C | T | 2 | a0002c0012t0011g0226a0002c0019t0011g0228 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2792+2267C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98252703 | ||||||
| chr2:98253012
|
T | C | 1 | a0002c0002t0002g0123 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2792+2576T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98253012 | ||||||
| chr2:98253075
|
A | G | 1 | a0004c0005t0002g0107 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2792+2639A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98253075 | ||||||
| chr2:98253146
|
C | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2792+2710C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98253146 | ||||||
| chr2:98253255
|
T | C | 1 | a0006c0007t0019g0059 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2792+2819T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98253255 | ||||||
| chr2:98253256
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2792+2820T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98253256 | ||||||
| chr2:98253272
|
G | A | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.2792+2836G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98253272 | ||||||
| chr2:98253349
|
A | G | 2 | a0001c0001t0003g0236a0001c0001t0013g0028 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2793-2775A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98253349 | ||||||
| chr2:98253451
|
A | G | 43 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(40): Show | 43 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.2793-2673A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98253451 | ||||||
| chr2:98253532
|
C | T | 3 | a0002c0002t0002g0116a0002c0002t0002g0174a0002c0002t0002g0180 | 3 | HG00735.hp1 HG01099.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.2793-2592C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98253532 | ||||||
| chr2:98253592
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2793-2532C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98253592 | ||||||
| chr2:98253667
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2793-2457T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98253667 | ||||||
| chr2:98254089
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2793-2035T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98254089 | ||||||
| chr2:98254290
|
A | G | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2793-1834A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98254290 | ||||||
| chr2:98254308
|
A | G | 1 | a0002c0002t0004g0022 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2793-1816A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98254308 | ||||||
| chr2:98254329
|
C | T | 5 | a0001c0001t0001g0127a0001c0001t0001g0144a0001c0001t0001g0145others(2): Show | 5 | HG01123.hp2 HG02717.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.2793-1795C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98254329 | ||||||
| chr2:98254574
|
A | G | 182 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(179): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.2793-1550A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98254574 | ||||||
| chr2:98254612
|
G | C | 16 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0004g0003others(13): Show | 16 | HG01261.hp2 HG01358.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2793-1512G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98254612 | ||||||
| chr2:98254748
|
G | A | 16 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0004g0003others(13): Show | 16 | HG01261.hp2 HG01358.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2793-1376G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98254748 | ||||||
| chr2:98254802
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2793-1322A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98254802 | ||||||
| chr2:98254896
|
C | T | 1 | a0003c0017t0005g0056 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2793-1228C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98254896 | ||||||
| chr2:98254916
|
C | T | 2 | a0002c0002t0004g0036a0002c0002t0004g0037 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2793-1208C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98254916 | ||||||
| chr2:98254973
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2793-1151A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98254973 | ||||||
| chr2:98255015
|
GTTTTTTG others(3): Show |
G | 2 | a0002c0012t0004g0007a0002c0016t0020g0031 | 2 | HG01358.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2793-1101_2793-109 others(14): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 98255015 | |||||
| chr2:98255044
|
C | T | 16 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0004g0003others(13): Show | 16 | HG01261.hp2 HG01358.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2793-1080C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98255044 | ||||||
| chr2:98255180
|
A | ATTTTTT | 4 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0024g0008others(1): Show | 4 | HG01261.hp2 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2793-943_2793-942i others(8): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 98255180 | |||||
| chr2:98255180
|
A | ATTTTTTT others(2): Show |
6 | a0002c0002t0004g0004a0002c0002t0004g0005a0002c0012t0004g0007others(3): Show | 6 | HG01358.hp1 HG02109.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2793-943_2793-942i others(11): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 98255180 | |||||
| chr2:98255180
|
ATATTTTT others(4): Show |
A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2793-942_2793-932d others(13): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 98255180 | |||||
| chr2:98255182
|
A | AT | 12 | a0001c0001t0001g0137a0001c0001t0002g0212a0001c0001t0016g0152others(9): Show | 12 | HG00733.hp2 HG01070.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.2793-913dupT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 98255182 | |||||
| chr2:98255182
|
A | ATT | 138 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0089others(135): Show | 138 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.2793-914_2793-913d others(4): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 98255182 | |||||
| chr2:98255182
|
A | ATTT | 20 | a0001c0001t0001g0083a0001c0001t0001g0127a0001c0001t0001g0133others(17): Show | 20 | HG00423.hp1 HG00423.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.2793-915_2793-913d others(5): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 98255182 | |||||
| chr2:98255182
|
A | T | 16 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0004g0003others(13): Show | 16 | HG01261.hp2 HG01358.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2793-942A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98255182 | ||||||
| chr2:98255252
|
G | A | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.2793-872G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98255252 | ||||||
| chr2:98255324
|
A | G | 21 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0004g0003others(18): Show | 21 | HG00140.hp1 HG01261.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.2793-800A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98255324 | ||||||
| chr2:98255328
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2793-796G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98255328 | ||||||
| chr2:98255331
|
T | C | 231 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(228): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2793-793T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98255331 | ||||||
| chr2:98255411
|
T | TGCAGGC | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.2793-713_2793-712i others(8): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98255411 | ||||||
| chr2:98255414
|
T | TCTGTC | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.2793-710_2793-709i others(7): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98255414 | ||||||
| chr2:98255415
|
G | A | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.2793-709G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98255415 | ||||||
| chr2:98255576
|
A | C | 144 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.2793-548A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98255576 | ||||||
| chr2:98255799
|
A | G | 3 | a0002c0002t0004g0032a0002c0002t0004g0036a0002c0002t0004g0037 | 3 | HG01070.hp1 HG01071.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.2793-325A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98255799 | ||||||
| chr2:98255828
|
G | T | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2793-296G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98255828 | ||||||
| chr2:98256049
|
G | A | 1 | a0002c0002t0021g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2793-75G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 20/27 | chr2 | 98256049 | ||||||
| chr2:98256199
|
C | CT | 174 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(171): Show | 174 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.2843+36dupT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 98256199 | |||||
| chr2:98256199
|
C | CTT | 7 | a0001c0001t0001g0142a0002c0012t0011g0226a0002c0019t0011g0228others(4): Show | 7 | HG00140.hp1 HG02280.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.2843+35_2843+36dup others(2): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 98256199 | |||||
| chr2:98256525
|
A | G | 2 | a0002c0012t0004g0007a0002c0016t0020g0031 | 2 | HG01358.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2843+351A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98256525 | ||||||
| chr2:98256633
|
C | G | 2 | a0001c0004t0003g0025a0001c0004t0003g0026 | 2 | NA18951.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.2843+459C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98256633 | ||||||
| chr2:98256654
|
T | C | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2843+480T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98256654 | ||||||
| chr2:98257023
|
G | T | 143 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(140): Show | 143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.2843+849G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98257023 | ||||||
| chr2:98257090
|
A | G | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2843+916A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98257090 | ||||||
| chr2:98257136
|
G | A | 143 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(140): Show | 143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.2843+962G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98257136 | ||||||
| chr2:98257165
|
C | CA | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2843+991_2843+992i others(3): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98257165 | ||||||
| chr2:98257274
|
G | T | 2 | a0002c0002t0003g0024a0002c0002t0003g0027 | 2 | HG01261.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2843+1100G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98257274 | ||||||
| chr2:98257289
|
C | A | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2843+1115C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98257289 | ||||||
| chr2:98257293
|
T | C | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.2843+1119T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98257293 | ||||||
| chr2:98257372
|
G | A | 1 | a0010c0013t0002g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2843+1198G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98257372 | ||||||
| chr2:98257553
|
C | CT | 6 | a0004c0005t0002g0098a0010c0013t0002g0104a0010c0013t0002g0141others(3): Show | 6 | HG00140.hp1 HG01515.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.2843+1390dupT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 98257553 | |||||
| chr2:98257816
|
C | A | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.2843+1642C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98257816 | ||||||
| chr2:98257817
|
G | A | 2 | a0002c0002t0004g0005a0008c0010t0004g0227 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2843+1643G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98257817 | ||||||
| chr2:98257946
|
G | A | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2843+1772G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98257946 | ||||||
| chr2:98258022
|
G | T | 182 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(179): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.2843+1848G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98258022 | ||||||
| chr2:98258025
|
CTT | C | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2843+1855_2843+185 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 98258025 | |||||
| chr2:98258026
|
T | G | 17 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0004g0003others(14): Show | 17 | HG01243.hp2 HG01261.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.2843+1852T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98258026 | ||||||
| chr2:98258057
|
C | T | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.2843+1883C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98258057 | ||||||
| chr2:98258082
|
C | G | 1 | a0002c0002t0008g0196 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2843+1908C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98258082 | ||||||
| chr2:98258091
|
C | T | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.2843+1917C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98258091 | ||||||
| chr2:98258287
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2843+2113A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98258287 | ||||||
| chr2:98258341
|
G | A | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.2843+2167G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98258341 | ||||||
| chr2:98258388
|
GA | G | 17 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0004g0003others(14): Show | 17 | HG01243.hp2 HG01261.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.2843+2223delA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 98258388 | |||||
| chr2:98258413
|
G | A | 2 | a0002c0002t0004g0002a0015c0029t0004g0046 | 2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2843+2239G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98258413 | ||||||
| chr2:98258491
|
A | C | 1 | a0001c0001t0001g0158 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2843+2317A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98258491 | ||||||
| chr2:98258495
|
C | A | 17 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0004g0003others(14): Show | 17 | HG01243.hp2 HG01261.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.2843+2321C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98258495 | ||||||
| chr2:98258757
|
A | G | 2 | a0002c0002t0004g0003a0002c0002t0004g0004 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2843+2583A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98258757 | ||||||
| chr2:98258847
|
G | C | 1 | a0001c0001t0006g0198 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2843+2673G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98258847 | ||||||
| chr2:98259166
|
G | A | 2 | a0001c0001t0001g0170a0001c0004t0003g0017 | 2 | HG02004.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.2843+2992G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98259166 | ||||||
| chr2:98259373
|
C | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2843+3199C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98259373 | ||||||
| chr2:98259447
|
T | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2843+3273T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98259447 | ||||||
| chr2:98259582
|
G | C | 2 | a0002c0002t0004g0003a0002c0002t0004g0004 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2843+3408G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98259582 | ||||||
| chr2:98259584
|
A | G | 1 | a0002c0002t0004g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2843+3410A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98259584 | ||||||
| chr2:98259985
|
C | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2843+3811C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98259985 | ||||||
| chr2:98260208
|
T | C | 1 | a0001c0001t0015g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2843+4034T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98260208 | ||||||
| chr2:98260406
|
A | T | 3 | a0001c0001t0007g0146a0001c0001t0007g0147a0001c0001t0007g0148 | 3 | NA18945.hp2 NA18963.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.2843+4232A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98260406 | ||||||
| chr2:98260587
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2843+4413G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98260587 | ||||||
| chr2:98260588
|
C | T | 4 | a0002c0002t0004g0003a0002c0002t0004g0004a0006c0007t0019g0059others(1): Show | 4 | HG01243.hp2 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2843+4414C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98260588 | ||||||
| chr2:98260898
|
G | A | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.2843+4724G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98260898 | ||||||
| chr2:98260949
|
C | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2843+4775C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98260949 | ||||||
| chr2:98261183
|
C | T | 1 | a0019c0024t0001g0103 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2843+5009C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98261183 | ||||||
| chr2:98261258
|
T | A | 4 | a0002c0002t0004g0003a0002c0002t0004g0004a0006c0007t0019g0059others(1): Show | 4 | HG01243.hp2 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2843+5084T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98261258 | ||||||
| chr2:98261392
|
C | T | 1 | a0001c0001t0006g0198 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2843+5218C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98261392 | ||||||
| chr2:98261393
|
G | A | 5 | a0002c0002t0004g0022a0002c0012t0011g0226a0002c0019t0011g0228others(2): Show | 5 | HG02280.hp2 HG02922.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2843+5219G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98261393 | ||||||
| chr2:98261569
|
G | C | 4 | a0002c0002t0004g0003a0002c0002t0004g0004a0006c0007t0019g0059others(1): Show | 4 | HG01243.hp2 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2843+5395G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98261569 | ||||||
| chr2:98261584
|
C | G | 1 | a0024c0034t0022g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2843+5410C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98261584 | ||||||
| chr2:98261935
|
C | T | 1 | a0003c0003t0003g0072 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2843+5761C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98261935 | ||||||
| chr2:98262215
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2843+6041C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98262215 | ||||||
| chr2:98262240
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2843+6066T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98262240 | ||||||
| chr2:98262516
|
G | C | 2 | a0002c0012t0011g0226a0002c0019t0011g0228 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2843+6342G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98262516 | ||||||
| chr2:98262534
|
C | T | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2843+6360C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98262534 | ||||||
| chr2:98263096
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2843+6922A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98263096 | ||||||
| chr2:98263179
|
G | C | 4 | a0001c0001t0003g0232a0001c0001t0010g0128a0001c0004t0013g0029others(1): Show | 4 | HG03209.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2843+7005G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98263179 | ||||||
| chr2:98263189
|
A | G | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.2843+7015A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98263189 | ||||||
| chr2:98263355
|
C | T | 92 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(89): Show | 92 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.2843+7181C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98263355 | ||||||
| chr2:98263478
|
T | A | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2844-7204T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98263478 | ||||||
| chr2:98263677
|
A | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | NA19056.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.2844-7005A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98263677 | ||||||
| chr2:98263724
|
G | T | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.2844-6958G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98263724 | ||||||
| chr2:98263738
|
G | A | 4 | a0002c0002t0002g0087a0002c0002t0002g0110a0002c0002t0004g0003others(1): Show | 4 | HG00597.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2844-6944G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98263738 | ||||||
| chr2:98263997
|
C | A | 2 | a0002c0002t0004g0005a0008c0010t0004g0227 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2844-6685C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98263997 | ||||||
| chr2:98264019
|
G | A | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2844-6663G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98264019 | ||||||
| chr2:98264174
|
C | A | 6 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(3): Show | 6 | HG01891.hp1 HG02056.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.2844-6508C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98264174 | ||||||
| chr2:98264202
|
AT | A | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2844-6472delT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 98264202 | |||||
| chr2:98264348
|
G | T | 12 | a0002c0002t0001g0190a0002c0002t0002g0116a0002c0002t0002g0174others(9): Show | 12 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.2844-6334G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98264348 | ||||||
| chr2:98264382
|
C | A | 4 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0021g0006others(1): Show | 4 | HG01261.hp2 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2844-6300C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98264382 | ||||||
| chr2:98264400
|
C | G | 1 | a0001c0001t0001g0188 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2844-6282C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98264400 | ||||||
| chr2:98264406
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2844-6276G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98264406 | ||||||
| chr2:98264437
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2844-6245A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98264437 | ||||||
| chr2:98264581
|
T | C | 2 | a0002c0012t0004g0007a0002c0016t0020g0031 | 2 | HG01358.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2844-6101T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98264581 | ||||||
| chr2:98264994
|
A | ATGTTTTA others(1): Show |
57 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(54): Show | 57 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.2844-5688_2844-568 others(12): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98264994 | ||||||
| chr2:98264995
|
G | T | 57 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(54): Show | 57 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.2844-5687G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98264995 | ||||||
| chr2:98264997
|
C | A | 57 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(54): Show | 57 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.2844-5685C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98264997 | ||||||
| chr2:98264998
|
A | T | 57 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(54): Show | 57 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.2844-5684A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98264998 | ||||||
| chr2:98265006
|
A | T | 57 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(54): Show | 57 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.2844-5676A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98265006 | ||||||
| chr2:98265011
|
A | T | 57 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(54): Show | 57 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.2844-5671A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98265011 | ||||||
| chr2:98265081
|
C | T | 96 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(93): Show | 96 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.2844-5601C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98265081 | ||||||
| chr2:98265093
|
A | G | 96 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(93): Show | 96 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.2844-5589A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98265093 | ||||||
| chr2:98265119
|
T | C | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2844-5563T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98265119 | ||||||
| chr2:98265150
|
A | G | 92 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(89): Show | 92 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.2844-5532A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98265150 | ||||||
| chr2:98265191
|
G | A | 1 | a0005c0008t0003g0235 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2844-5491G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98265191 | ||||||
| chr2:98265224
|
C | T | 1 | a0002c0002t0002g0095 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2844-5458C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98265224 | ||||||
| chr2:98265289
|
C | T | 1 | a0002c0002t0021g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2844-5393C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98265289 | ||||||
| chr2:98265505
|
C | A | 17 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0004g0003others(14): Show | 17 | HG01243.hp2 HG01261.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.2844-5177C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98265505 | ||||||
| chr2:98265510
|
G | A | 1 | a0004c0005t0002g0093 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2844-5172G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98265510 | ||||||
| chr2:98265511
|
C | T | 2 | a0002c0012t0011g0226a0002c0019t0011g0228 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2844-5171C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98265511 | ||||||
| chr2:98265512
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2844-5170G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98265512 | ||||||
| chr2:98265591
|
C | T | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2844-5091C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98265591 | ||||||
| chr2:98265650
|
A | C | 1 | a0001c0001t0002g0212 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2844-5032A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98265650 | ||||||
| chr2:98265667
|
A | C | 6 | a0004c0005t0002g0100a0004c0005t0002g0101a0004c0005t0002g0125others(3): Show | 6 | HG00408.hp1 HG00609.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.2844-5015A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98265667 | ||||||
| chr2:98265722
|
T | G | 1 | a0001c0001t0001g0144 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2844-4960T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98265722 | ||||||
| chr2:98265729
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2844-4953T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98265729 | ||||||
| chr2:98265730
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2844-4952G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98265730 | ||||||
| chr2:98265733
|
G | A | 5 | a0001c0001t0001g0144a0002c0002t0003g0024a0002c0002t0003g0027others(2): Show | 5 | HG01261.hp2 HG03041.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2844-4949G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98265733 | ||||||
| chr2:98265742
|
G | C | 1 | a0001c0001t0001g0144 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2844-4940G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98265742 | ||||||
| chr2:98265818
|
G | GT | 4 | a0002c0002t0001g0190a0002c0002t0008g0177a0002c0002t0008g0196others(1): Show | 4 | HG00609.hp1 HG01123.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2844-4858dupT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 98265818 | |||||
| chr2:98265870
|
C | T | 1 | a0024c0034t0022g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2844-4812C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98265870 | ||||||
| chr2:98265919
|
A | T | 57 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(54): Show | 57 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.2844-4763A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98265919 | ||||||
| chr2:98265968
|
C | T | 4 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0021g0006others(1): Show | 4 | HG01261.hp2 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2844-4714C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98265968 | ||||||
| chr2:98266071
|
T | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2844-4611T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98266071 | ||||||
| chr2:98266207
|
G | A | 5 | a0001c0001t0002g0212a0002c0002t0002g0221a0002c0002t0002g0222others(2): Show | 5 | HG00741.hp1 HG01070.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.2844-4475G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98266207 | ||||||
| chr2:98266269
|
G | A | 1 | a0002c0002t0003g0024 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2844-4413G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98266269 | ||||||
| chr2:98266293
|
T | G | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2844-4389T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98266293 | ||||||
| chr2:98266327
|
C | T | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.2844-4355C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98266327 | ||||||
| chr2:98266420
|
C | T | 1 | a0001c0001t0006g0198 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2844-4262C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98266420 | ||||||
| chr2:98266449
|
C | T | 2 | a0002c0002t0003g0024a0002c0002t0003g0027 | 2 | HG01261.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2844-4233C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98266449 | ||||||
| chr2:98266521
|
C | T | 5 | a0002c0002t0004g0022a0002c0012t0011g0226a0002c0019t0011g0228others(2): Show | 5 | HG02280.hp2 HG02922.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2844-4161C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98266521 | ||||||
| chr2:98266587
|
G | A | 2 | a0002c0012t0011g0226a0002c0019t0011g0228 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2844-4095G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98266587 | ||||||
| chr2:98266621
|
G | A | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2844-4061G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98266621 | ||||||
| chr2:98266653
|
C | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2844-4029C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98266653 | ||||||
| chr2:98266823
|
T | A | 17 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0004g0003others(14): Show | 17 | HG01243.hp2 HG01261.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.2844-3859T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98266823 | ||||||
| chr2:98266837
|
G | A | 1 | a0001c0004t0004g0023 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2844-3845G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98266837 | ||||||
| chr2:98266861
|
G | A | 2 | a0007c0009t0002g0139a0007c0009t0002g0140 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2844-3821G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98266861 | ||||||
| chr2:98266876
|
T | G | 1 | a0022c0023t0002g0154 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2844-3806T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98266876 | ||||||
| chr2:98266882
|
T | C | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2844-3800T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98266882 | ||||||
| chr2:98266924
|
T | G | 1 | a0001c0001t0001g0215 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2844-3758T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98266924 | ||||||
| chr2:98266929
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2844-3753G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98266929 | ||||||
| chr2:98266974
|
C | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2844-3708C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98266974 | ||||||
| chr2:98267019
|
C | T | 1 | a0001c0001t0001g0176 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2844-3663C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98267019 | ||||||
| chr2:98267049
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2844-3633A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98267049 | ||||||
| chr2:98267191
|
G | A | 1 | a0004c0005t0002g0107 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2844-3491G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98267191 | ||||||
| chr2:98267220
|
C | T | 1 | a0002c0002t0004g0022 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2844-3462C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98267220 | ||||||
| chr2:98267258
|
G | T | 57 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(54): Show | 57 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.2844-3424G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98267258 | ||||||
| chr2:98267305
|
CAT | C | 4 | a0001c0001t0001g0136a0001c0001t0001g0170a0001c0001t0001g0209others(1): Show | 4 | HG01167.hp2 HG01981.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.2844-3376_2844-337 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98267305 | ||||||
| chr2:98267311
|
GT | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2844-3365delT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 98267311 | |||||
| chr2:98267376
|
C | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2844-3306C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98267376 | ||||||
| chr2:98267396
|
C | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2844-3286C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98267396 | ||||||
| chr2:98267397
|
G | A | 1 | a0003c0003t0003g0055 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2844-3285G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98267397 | ||||||
| chr2:98267419
|
C | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2844-3263C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98267419 | ||||||
| chr2:98267431
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2844-3251G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98267431 | ||||||
| chr2:98267867
|
A | G | 2 | a0001c0001t0001g0149a0001c0001t0001g0153 | 2 | HG01099.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.2844-2815A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98267867 | ||||||
| chr2:98267889
|
C | T | 1 | a0002c0002t0004g0022 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2844-2793C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98267889 | ||||||
| chr2:98267891
|
A | G | 2 | a0002c0002t0004g0005a0008c0010t0004g0227 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2844-2791A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98267891 | ||||||
| chr2:98268009
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2844-2673G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98268009 | ||||||
| chr2:98268213
|
C | T | 1 | a0005c0008t0003g0234 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2844-2469C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98268213 | ||||||
| chr2:98268223
|
C | G | 1 | a0001c0001t0001g0186 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2844-2459C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98268223 | ||||||
| chr2:98268617
|
A | C | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.2844-2065A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98268617 | ||||||
| chr2:98268679
|
C | CT | 7 | a0001c0001t0001g0142a0001c0001t0023g0009a0001c0004t0004g0018others(4): Show | 7 | HG01071.hp1 HG01081.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2844-1990dupT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 98268679 | |||||
| chr2:98268679
|
CT | C | 60 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(57): Show | 60 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.2844-1990delT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 98268679 | |||||
| chr2:98268722
|
T | C | 1 | a0023c0031t0014g0097 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2844-1960T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98268722 | ||||||
| chr2:98268862
|
A | G | 2 | a0007c0009t0002g0091a0007c0009t0002g0092 | 2 | HG01071.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.2844-1820A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98268862 | ||||||
| chr2:98269007
|
G | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2844-1675G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98269007 | ||||||
| chr2:98269141
|
G | C | 57 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(54): Show | 57 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.2844-1541G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98269141 | ||||||
| chr2:98269185
|
T | C | 4 | a0002c0002t0001g0190a0002c0002t0008g0177a0002c0002t0008g0196others(1): Show | 4 | HG00609.hp1 HG01123.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2844-1497T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98269185 | ||||||
| chr2:98269211
|
C | T | 2 | a0001c0001t0001g0089a0003c0003t0003g0073 | 2 | HG01346.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2844-1471C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98269211 | ||||||
| chr2:98269462
|
G | A | 96 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(93): Show | 96 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.2844-1220G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98269462 | ||||||
| chr2:98269479
|
C | T | 1 | a0025c0033t0006g0214 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2844-1203C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98269479 | ||||||
| chr2:98269751
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2844-931G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98269751 | ||||||
| chr2:98269846
|
T | A | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2844-836T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98269846 | ||||||
| chr2:98269881
|
G | A | 2 | a0002c0002t0004g0005a0008c0010t0004g0227 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2844-801G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98269881 | ||||||
| chr2:98269969
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2844-713G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98269969 | ||||||
| chr2:98270203
|
A | G | 96 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(93): Show | 96 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.2844-479A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98270203 | ||||||
| chr2:98270308
|
C | A | 1 | a0002c0019t0011g0228 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2844-374C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98270308 | ||||||
| chr2:98270479
|
C | T | 1 | a0014c0030t0002g0120 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2844-203C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98270479 | ||||||
| chr2:98270653
|
G | C | 96 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(93): Show | 96 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.2844-29G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98270653 | ||||||
| chr2:98270657
|
G | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2844-25G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98270657 | ||||||
| chr2:98270669
|
C | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2844-13C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 21/27 | chr2 | 98270669 | ||||||
| chr2:98270892
|
C | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+9C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98270892 | ||||||
| chr2:98270915
|
C | T | 2 | a0002c0012t0011g0226a0002c0019t0011g0228 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3045+32C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98270915 | ||||||
| chr2:98270979
|
C | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+96C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98270979 | ||||||
| chr2:98271105
|
G | GA | 59 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(56): Show | 59 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.3045+232dupA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr2 | 98271105 | |||||
| chr2:98271105
|
GA | G | 5 | a0008c0010t0009g0239a0008c0010t0009g0240a0010c0013t0002g0104others(2): Show | 5 | HG00140.hp1 HG01515.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.3045+232delA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr2 | 98271105 | |||||
| chr2:98271223
|
C | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+340C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98271223 | ||||||
| chr2:98271341
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+458A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98271341 | ||||||
| chr2:98271378
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+495G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98271378 | ||||||
| chr2:98271414
|
G | A | 2 | a0002c0002t0004g0002a0015c0029t0004g0046 | 2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3045+531G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98271414 | ||||||
| chr2:98271535
|
A | G | 1 | a0022c0023t0002g0154 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3045+652A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98271535 | ||||||
| chr2:98271617
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+734G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98271617 | ||||||
| chr2:98271732
|
TTTG | T | 6 | a0001c0001t0001g0115a0001c0001t0001g0156a0001c0001t0001g0158others(3): Show | 6 | HG00544.hp1 HG00597.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.3045+852_3045+854d others(5): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr2 | 98271732 | |||||
| chr2:98271822
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+939T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98271822 | ||||||
| chr2:98271847
|
T | C | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.3045+964T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98271847 | ||||||
| chr2:98271928
|
G | T | 17 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0004g0003others(14): Show | 17 | HG01243.hp2 HG01261.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.3045+1045G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98271928 | ||||||
| chr2:98271976
|
C | T | 3 | a0001c0001t0001g0193a0001c0001t0001g0208a0001c0001t0001g0216 | 3 | NA18939.hp2 NA18948.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.3045+1093C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98271976 | ||||||
| chr2:98272019
|
T | C | 1 | a0002c0002t0024g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3045+1136T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98272019 | ||||||
| chr2:98272107
|
C | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+1224C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98272107 | ||||||
| chr2:98272254
|
T | G | 4 | a0001c0001t0001g0144a0001c0001t0001g0145a0003c0003t0003g0060others(1): Show | 4 | HG02717.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3045+1371T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98272254 | ||||||
| chr2:98272594
|
C | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+1711C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98272594 | ||||||
| chr2:98272604
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+1721G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98272604 | ||||||
| chr2:98272617
|
C | T | 1 | a0002c0016t0020g0031 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3045+1734C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98272617 | ||||||
| chr2:98272909
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+2026T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98272909 | ||||||
| chr2:98272912
|
T | C | 1 | a0003c0003t0003g0049 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3045+2029T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98272912 | ||||||
| chr2:98273044
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+2161G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98273044 | ||||||
| chr2:98273145
|
C | T | 2 | a0001c0004t0004g0018a0001c0004t0004g0023 | 2 | HG01257.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3045+2262C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98273145 | ||||||
| chr2:98273173
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+2290A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98273173 | ||||||
| chr2:98273253
|
T | G | 17 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0004g0003others(14): Show | 17 | HG01243.hp2 HG01261.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.3045+2370T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98273253 | ||||||
| chr2:98273333
|
T | A | 1 | a0002c0006t0004g0021 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3045+2450T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98273333 | ||||||
| chr2:98273498
|
G | T | 190 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0089others(187): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.3045+2615G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98273498 | ||||||
| chr2:98273516
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+2633G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98273516 | ||||||
| chr2:98273550
|
C | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+2667C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98273550 | ||||||
| chr2:98273599
|
G | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+2716G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98273599 | ||||||
| chr2:98273737
|
C | T | 1 | a0002c0002t0021g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3045+2854C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98273737 | ||||||
| chr2:98273792
|
A | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+2909A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98273792 | ||||||
| chr2:98273904
|
T | C | 4 | a0001c0001t0001g0130a0003c0003t0003g0066a0003c0003t0003g0074others(1): Show | 4 | HG00673.hp1 NA18977.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.3045+3021T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98273904 | ||||||
| chr2:98274102
|
A | G | 96 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(93): Show | 96 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.3045+3219A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98274102 | ||||||
| chr2:98274128
|
C | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+3245C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98274128 | ||||||
| chr2:98274193
|
G | A | 1 | a0003c0003t0003g0049 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3045+3310G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98274193 | ||||||
| chr2:98274282
|
T | C | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.3045+3399T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98274282 | ||||||
| chr2:98274300
|
A | G | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.3045+3417A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98274300 | ||||||
| chr2:98274566
|
G | A | 2 | a0002c0002t0001g0094a0002c0002t0001g0102 | 2 | HG00639.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.3045+3683G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98274566 | ||||||
| chr2:98274633
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+3750G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98274633 | ||||||
| chr2:98274719
|
G | A | 2 | a0002c0012t0011g0226a0002c0019t0011g0228 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3045+3836G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98274719 | ||||||
| chr2:98274766
|
C | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+3883C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98274766 | ||||||
| chr2:98274977
|
T | A | 59 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(56): Show | 59 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.3045+4094T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98274977 | ||||||
| chr2:98274991
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+4108G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98274991 | ||||||
| chr2:98275024
|
C | A | 3 | a0002c0002t0004g0003a0002c0002t0004g0004a0006c0007t0019g0059 | 3 | HG03139.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3045+4141C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98275024 | ||||||
| chr2:98275033
|
G | A | 1 | a0002c0002t0002g0168 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3045+4150G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98275033 | ||||||
| chr2:98275056
|
T | C | 96 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(93): Show | 96 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.3045+4173T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98275056 | ||||||
| chr2:98275173
|
G | A | 2 | a0002c0002t0001g0094a0002c0002t0001g0102 | 2 | HG00639.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.3045+4290G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98275173 | ||||||
| chr2:98275290
|
C | T | 1 | a0014c0030t0002g0120 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3045+4407C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98275290 | ||||||
| chr2:98275317
|
G | A | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3045+4434G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98275317 | ||||||
| chr2:98275318
|
C | T | 1 | a0001c0004t0003g0017 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3045+4435C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98275318 | ||||||
| chr2:98275450
|
G | A | 2 | a0002c0012t0011g0226a0002c0019t0011g0228 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3045+4567G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98275450 | ||||||
| chr2:98275454
|
GAGGCCCG others(4): Show |
G | 2 | a0002c0002t0004g0005a0008c0010t0004g0227 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3045+4574_3045+458 others(15): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr2 | 98275454 | |||||
| chr2:98275516
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+4633G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98275516 | ||||||
| chr2:98275643
|
C | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+4760C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98275643 | ||||||
| chr2:98275644
|
A | G | 96 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(93): Show | 96 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.3045+4761A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98275644 | ||||||
| chr2:98275846
|
G | A | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3045+4963G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98275846 | ||||||
| chr2:98275886
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3045+5003G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98275886 | ||||||
| chr2:98275891
|
G | A | 1 | a0001c0004t0003g0013 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3045+5008G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98275891 | ||||||
| chr2:98275947
|
A | G | 5 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120others(2): Show | 5 | HG00140.hp1 HG01515.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.3045+5064A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98275947 | ||||||
| chr2:98275976
|
G | A | 1 | a0002c0002t0002g0163 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3045+5093G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98275976 | ||||||
| chr2:98276125
|
C | CTG | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+5242_3045+524 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98276125 | ||||||
| chr2:98276154
|
C | T | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.3045+5271C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98276154 | ||||||
| chr2:98276252
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+5369T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98276252 | ||||||
| chr2:98276337
|
A | G | 57 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(54): Show | 57 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.3045+5454A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98276337 | ||||||
| chr2:98276379
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3045+5496C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98276379 | ||||||
| chr2:98276485
|
A | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+5602A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98276485 | ||||||
| chr2:98276569
|
GTGGGCTG others(181): Show |
G | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3045+5726_3045+591 others(4): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr2 | 98276569 | |||||
| chr2:98276656
|
G | A | 2 | a0002c0012t0011g0226a0002c0019t0011g0228 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3045+5773G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98276656 | ||||||
| chr2:98276703
|
G | A | 2 | a0001c0001t0001g0130a0003c0003t0003g0066 | 2 | HG00673.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.3045+5820G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98276703 | ||||||
| chr2:98276750
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+5867A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98276750 | ||||||
| chr2:98276906
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.3045+6023C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98276906 | ||||||
| chr2:98277030
|
G | T | 1 | a0002c0002t0002g0108 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3045+6147G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98277030 | ||||||
| chr2:98277041
|
G | GC | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+6161dupC | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr2 | 98277041 | |||||
| chr2:98277183
|
C | G | 96 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(93): Show | 96 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.3045+6300C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98277183 | ||||||
| chr2:98277268
|
C | G | 2 | a0002c0002t0004g0039a0002c0002t0004g0041 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3045+6385C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98277268 | ||||||
| chr2:98277298
|
C | T | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.3045+6415C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98277298 | ||||||
| chr2:98277435
|
A | T | 1 | a0002c0016t0020g0031 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3045+6552A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98277435 | ||||||
| chr2:98277668
|
T | C | 1 | a0003c0003t0003g0072 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3045+6785T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98277668 | ||||||
| chr2:98277698
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+6815G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98277698 | ||||||
| chr2:98277743
|
G | A | 1 | a0002c0002t0002g0162 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.3045+6860G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98277743 | ||||||
| chr2:98277820
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3045+6937T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98277820 | ||||||
| chr2:98277824
|
T | C | 96 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(93): Show | 96 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.3045+6941T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98277824 | ||||||
| chr2:98277896
|
A | G | 4 | a0001c0004t0004g0018a0001c0004t0004g0023a0007c0009t0002g0091others(1): Show | 4 | HG01071.hp1 HG01081.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.3045+7013A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98277896 | ||||||
| chr2:98277963
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+7080T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98277963 | ||||||
| chr2:98278032
|
A | G | 5 | a0002c0002t0002g0162a0002c0002t0002g0164a0002c0002t0002g0194others(2): Show | 5 | NA18941.hp1 NA18946.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.3045+7149A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98278032 | ||||||
| chr2:98278145
|
G | A | 96 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(93): Show | 96 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.3045+7262G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98278145 | ||||||
| chr2:98278241
|
C | T | 2 | a0002c0002t0004g0003a0002c0002t0004g0004 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3045+7358C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98278241 | ||||||
| chr2:98278550
|
A | AGCTAGAA others(12): Show |
5 | a0002c0002t0003g0024a0002c0002t0003g0027a0002c0002t0004g0022others(2): Show | 5 | HG01261.hp2 HG03041.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3045+7669_3045+768 others(23): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr2 | 98278550 | |||||
| chr2:98278552
|
C | G | 1 | a0001c0001t0001g0088 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3045+7669C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98278552 | ||||||
| chr2:98278630
|
G | A | 1 | a0025c0033t0006g0214 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3045+7747G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98278630 | ||||||
| chr2:98278687
|
T | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+7804T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98278687 | ||||||
| chr2:98278751
|
G | T | 1 | a0002c0002t0002g0111 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3045+7868G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98278751 | ||||||
| chr2:98278816
|
G | A | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.3045+7933G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98278816 | ||||||
| chr2:98278938
|
T | C | 2 | a0002c0012t0011g0226a0002c0019t0011g0228 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3045+8055T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98278938 | ||||||
| chr2:98278959
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3045+8076T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98278959 | ||||||
| chr2:98278993
|
A | G | 11 | a0004c0005t0002g0093a0004c0005t0002g0098a0004c0005t0002g0099others(8): Show | 11 | HG00408.hp1 HG00609.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.3045+8110A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98278993 | ||||||
| chr2:98279105
|
GA | G | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.3045+8224delA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr2 | 98279105 | |||||
| chr2:98279538
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3045+8655G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98279538 | ||||||
| chr2:98279575
|
T | C | 39 | a0002c0002t0002g0173a0002c0002t0003g0024a0002c0002t0003g0027others(36): Show | 39 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.3045+8692T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98279575 | ||||||
| chr2:98279701
|
C | T | 2 | a0001c0001t0001g0089a0003c0003t0003g0073 | 2 | HG01346.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.3045+8818C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98279701 | ||||||
| chr2:98279703
|
T | A | 1 | a0001c0001t0001g0115 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3045+8820T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98279703 | ||||||
| chr2:98279738
|
G | A | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3045+8855G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98279738 | ||||||
| chr2:98280127
|
C | T | 5 | a0001c0001t0001g0130a0003c0003t0003g0066a0003c0003t0003g0074others(2): Show | 5 | HG00673.hp1 NA18977.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.3045+9244C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98280127 | ||||||
| chr2:98280289
|
G | A | 1 | a0008c0010t0009g0239 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3045+9406G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98280289 | ||||||
| chr2:98280337
|
C | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+9454C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98280337 | ||||||
| chr2:98280344
|
A | G | 57 | a0001c0001t0002g0212a0002c0002t0001g0094a0002c0002t0001g0102others(54): Show | 57 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.3045+9461A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98280344 | ||||||
| chr2:98280350
|
AAG | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+9479_3045+948 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr2 | 98280350 | |||||
| chr2:98280430
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3045+9547G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98280430 | ||||||
| chr2:98280468
|
G | C | 2 | a0002c0012t0011g0226a0002c0019t0011g0228 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3045+9585G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98280468 | ||||||
| chr2:98280477
|
C | G | 40 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0137others(37): Show | 40 | HG00673.hp1 HG00735.hp2 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.3045+9594C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98280477 | ||||||
| chr2:98280506
|
C | G | 2 | a0001c0001t0001g0089a0003c0003t0003g0073 | 2 | HG01346.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.3045+9623C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98280506 | ||||||
| chr2:98280711
|
G | A | 77 | a0001c0001t0002g0212a0002c0002t0001g0190a0002c0002t0002g0001others(74): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.3046-9800G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98280711 | ||||||
| chr2:98280720
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-9791T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98280720 | ||||||
| chr2:98280729
|
G | A | 2 | a0002c0002t0003g0024a0002c0002t0003g0027 | 2 | HG01261.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3046-9782G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98280729 | ||||||
| chr2:98280767
|
G | C | 1 | a0008c0010t0004g0227 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3046-9744G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98280767 | ||||||
| chr2:98280840
|
G | A | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3046-9671G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98280840 | ||||||
| chr2:98281019
|
G | A | 2 | a0002c0002t0004g0005a0008c0010t0004g0227 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3046-9492G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98281019 | ||||||
| chr2:98281062
|
G | T | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.3046-9449G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98281062 | ||||||
| chr2:98281203
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3046-9308G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98281203 | ||||||
| chr2:98281303
|
C | G | 1 | a0003c0032t0003g0062 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3046-9208C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98281303 | ||||||
| chr2:98281338
|
G | A | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.3046-9173G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98281338 | ||||||
| chr2:98281455
|
A | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-9056A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98281455 | ||||||
| chr2:98281489
|
G | A | 1 | a0003c0003t0003g0076 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.3046-9022G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98281489 | ||||||
| chr2:98281543
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-8968T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98281543 | ||||||
| chr2:98281555
|
A | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-8956A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98281555 | ||||||
| chr2:98281556
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-8955T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98281556 | ||||||
| chr2:98281579
|
T | C | 77 | a0001c0001t0002g0212a0002c0002t0001g0190a0002c0002t0002g0001others(74): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.3046-8932T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98281579 | ||||||
| chr2:98281631
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-8880T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98281631 | ||||||
| chr2:98281637
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-8874A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98281637 | ||||||
| chr2:98281647
|
C | A | 55 | a0001c0001t0002g0212a0002c0002t0001g0190a0002c0002t0002g0001others(52): Show | 55 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.3046-8864C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98281647 | ||||||
| chr2:98281737
|
G | A | 1 | a0024c0034t0022g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3046-8774G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98281737 | ||||||
| chr2:98281757
|
G | A | 77 | a0001c0001t0002g0212a0002c0002t0001g0190a0002c0002t0002g0001others(74): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.3046-8754G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98281757 | ||||||
| chr2:98281870
|
C | T | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3046-8641C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98281870 | ||||||
| chr2:98282122
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-8389G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98282122 | ||||||
| chr2:98282141
|
G | C | 55 | a0001c0001t0002g0212a0002c0002t0001g0190a0002c0002t0002g0001others(52): Show | 55 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.3046-8370G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98282141 | ||||||
| chr2:98282180
|
G | T | 2 | a0002c0002t0004g0005a0008c0010t0004g0227 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3046-8331G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98282180 | ||||||
| chr2:98282209
|
A | G | 55 | a0001c0001t0002g0212a0002c0002t0001g0190a0002c0002t0002g0001others(52): Show | 55 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.3046-8302A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98282209 | ||||||
| chr2:98282212
|
C | G | 1 | a0001c0004t0003g0026 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.3046-8299C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98282212 | ||||||
| chr2:98282246
|
C | T | 1 | a0024c0034t0022g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3046-8265C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98282246 | ||||||
| chr2:98282277
|
A | AACCCAAT others(10): Show |
4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3046-8234_3046-823 others(21): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98282277 | ||||||
| chr2:98282279
|
A | G | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3046-8232A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98282279 | ||||||
| chr2:98282280
|
G | C | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3046-8231G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98282280 | ||||||
| chr2:98282432
|
C | CT | 27 | a0001c0001t0001g0135a0001c0001t0001g0151a0001c0001t0001g0156others(24): Show | 27 | HG00280.hp1 HG01071.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.3046-8056dupT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr2 | 98282432 | |||||
| chr2:98282432
|
CTTTTTT | C | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.3046-8061_3046-805 others(10): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr2 | 98282432 | |||||
| chr2:98282458
|
G | A | 4 | a0001c0001t0001g0149a0001c0001t0001g0153a0001c0001t0001g0176others(1): Show | 4 | HG01099.hp2 HG02698.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.3046-8053G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98282458 | ||||||
| chr2:98282522
|
C | A | 4 | a0001c0004t0004g0018a0001c0004t0004g0023a0007c0009t0002g0091others(1): Show | 4 | HG01071.hp1 HG01081.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.3046-7989C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98282522 | ||||||
| chr2:98282569
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-7942T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98282569 | ||||||
| chr2:98282585
|
C | T | 1 | a0003c0003t0003g0065 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.3046-7926C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98282585 | ||||||
| chr2:98282645
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-7866G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98282645 | ||||||
| chr2:98282802
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3046-7709G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98282802 | ||||||
| chr2:98282804
|
G | A | 2 | a0002c0002t0002g0087a0002c0002t0002g0110 | 2 | HG00597.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.3046-7707G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98282804 | ||||||
| chr2:98282864
|
G | A | 64 | a0001c0001t0002g0212a0001c0004t0004g0018a0001c0004t0004g0023others(61): Show | 64 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.3046-7647G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98282864 | ||||||
| chr2:98283076
|
A | T | 1 | a0001c0001t0001g0176 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3046-7435A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98283076 | ||||||
| chr2:98283085
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3046-7426G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98283085 | ||||||
| chr2:98283617
|
C | T | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.3046-6894C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98283617 | ||||||
| chr2:98283699
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-6812T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98283699 | ||||||
| chr2:98283935
|
T | G | 1 | a0001c0001t0001g0183 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3046-6576T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98283935 | ||||||
| chr2:98283956
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-6555T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98283956 | ||||||
| chr2:98283995
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3046-6516C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98283995 | ||||||
| chr2:98284052
|
A | T | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.3046-6459A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98284052 | ||||||
| chr2:98284287
|
C | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-6224C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98284287 | ||||||
| chr2:98284346
|
G | T | 4 | a0002c0012t0004g0007a0002c0012t0011g0226a0002c0016t0020g0031others(1): Show | 4 | HG01358.hp1 HG02109.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.3046-6165G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98284346 | ||||||
| chr2:98284712
|
G | A | 3 | a0001c0001t0003g0034a0009c0011t0001g0171a0009c0011t0001g0213 | 3 | HG01255.hp2 HG01258.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.3046-5799G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98284712 | ||||||
| chr2:98284863
|
C | T | 8 | a0002c0002t0002g0116a0002c0002t0002g0174a0002c0002t0002g0180others(5): Show | 8 | HG00280.hp2 HG00735.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.3046-5648C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98284863 | ||||||
| chr2:98284872
|
G | A | 98 | a0001c0001t0002g0212a0001c0004t0004g0018a0001c0004t0004g0023others(95): Show | 98 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.3046-5639G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98284872 | ||||||
| chr2:98285007
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-5504G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98285007 | ||||||
| chr2:98285080
|
A | G | 1 | a0001c0001t0002g0212 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3046-5431A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98285080 | ||||||
| chr2:98285138
|
C | G | 55 | a0001c0001t0002g0212a0002c0002t0001g0190a0002c0002t0002g0001others(52): Show | 55 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.3046-5373C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98285138 | ||||||
| chr2:98285280
|
C | T | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.3046-5231C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98285280 | ||||||
| chr2:98285281
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3046-5230G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98285281 | ||||||
| chr2:98285363
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-5148T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98285363 | ||||||
| chr2:98285418
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-5093A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98285418 | ||||||
| chr2:98285869
|
A | G | 1 | a0023c0031t0014g0097 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3046-4642A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98285869 | ||||||
| chr2:98285995
|
T | C | 6 | a0001c0001t0001g0083a0001c0001t0003g0047a0001c0001t0003g0238others(3): Show | 6 | HG02486.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3046-4516T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98285995 | ||||||
| chr2:98286087
|
C | G | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3046-4424C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98286087 | ||||||
| chr2:98286103
|
A | AT | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-4402dupT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr2 | 98286103 | |||||
| chr2:98286109
|
T | C | 55 | a0001c0001t0002g0212a0002c0002t0001g0190a0002c0002t0002g0001others(52): Show | 55 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.3046-4402T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98286109 | ||||||
| chr2:98286185
|
G | A | 1 | a0002c0002t0024g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3046-4326G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98286185 | ||||||
| chr2:98286197
|
T | C | 55 | a0001c0001t0002g0212a0002c0002t0001g0190a0002c0002t0002g0001others(52): Show | 55 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.3046-4314T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98286197 | ||||||
| chr2:98286279
|
GTACTGGC others(4): Show |
G | 15 | a0002c0002t0001g0190a0002c0002t0002g0116a0002c0002t0002g0174others(12): Show | 15 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.3046-4231_3046-422 others(15): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98286279 | ||||||
| chr2:98286470
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-4041A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98286470 | ||||||
| chr2:98286714
|
G | A | 1 | a0002c0002t0024g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3046-3797G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98286714 | ||||||
| chr2:98286715
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-3796G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98286715 | ||||||
| chr2:98287331
|
A | G | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0023g0009 | 3 | HG02896.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3046-3180A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98287331 | ||||||
| chr2:98287421
|
C | A | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.3046-3090C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98287421 | ||||||
| chr2:98287570
|
A | G | 1 | a0002c0002t0024g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3046-2941A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98287570 | ||||||
| chr2:98287572
|
A | T | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3046-2939A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98287572 | ||||||
| chr2:98287837
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-2674G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98287837 | ||||||
| chr2:98287887
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-2624T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98287887 | ||||||
| chr2:98287899
|
A | T | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.3046-2612A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98287899 | ||||||
| chr2:98288031
|
G | T | 4 | a0002c0002t0004g0003a0002c0002t0004g0004a0006c0007t0019g0059others(1): Show | 4 | HG01243.hp2 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3046-2480G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98288031 | ||||||
| chr2:98288077
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-2434A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98288077 | ||||||
| chr2:98288116
|
A | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0203 | 2 | HG00621.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.3046-2395A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98288116 | ||||||
| chr2:98288391
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-2120A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98288391 | ||||||
| chr2:98288549
|
A | G | 147 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0089others(144): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.3046-1962A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98288549 | ||||||
| chr2:98288650
|
A | G | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3046-1861A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98288650 | ||||||
| chr2:98288744
|
C | T | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3046-1767C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98288744 | ||||||
| chr2:98288830
|
C | T | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3046-1681C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98288830 | ||||||
| chr2:98288853
|
T | A | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3046-1658T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98288853 | ||||||
| chr2:98288876
|
C | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-1635C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98288876 | ||||||
| chr2:98289041
|
G | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-1470G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98289041 | ||||||
| chr2:98289091
|
C | T | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.3046-1420C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98289091 | ||||||
| chr2:98289168
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3046-1343C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98289168 | ||||||
| chr2:98289265
|
C | A | 3 | a0002c0002t0002g0095a0002c0002t0002g0096a0002c0002t0002g0217 | 3 | NA18993.hp2 NA19000.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.3046-1246C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98289265 | ||||||
| chr2:98289290
|
G | C | 6 | a0001c0001t0001g0083a0001c0001t0003g0047a0001c0001t0003g0238others(3): Show | 6 | HG02486.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3046-1221G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98289290 | ||||||
| chr2:98289466
|
T | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-1045T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98289466 | ||||||
| chr2:98289596
|
T | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-915T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98289596 | ||||||
| chr2:98289703
|
T | C | 2 | a0002c0002t0003g0024a0002c0002t0003g0027 | 2 | HG01261.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3046-808T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98289703 | ||||||
| chr2:98290098
|
A | C | 1 | a0001c0001t0001g0216 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3046-413A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98290098 | ||||||
| chr2:98290242
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-269G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98290242 | ||||||
| chr2:98290420
|
C | T | 1 | a0002c0002t0021g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3046-91C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98290420 | ||||||
| chr2:98290421
|
A | C | 1 | a0002c0002t0004g0022 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3046-90A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98290421 | ||||||
| chr2:98290450
|
A | C | 1 | a0002c0002t0021g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3046-61A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98290450 | ||||||
| chr2:98290492
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3046-19T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98290492 | ||||||
| chr2:98290626
|
GT | G | 6 | a0001c0001t0001g0138a0001c0001t0023g0009a0002c0002t0004g0037others(3): Show | 6 | HG00140.hp1 HG01070.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.3157+17delT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr2 | 98290626 | |||||
| chr2:98290879
|
A | T | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3157+257A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98290879 | ||||||
| chr2:98291012
|
A | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3157+390A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98291012 | ||||||
| chr2:98291096
|
T | C | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3157+474T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98291096 | ||||||
| chr2:98291269
|
T | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3157+647T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98291269 | ||||||
| chr2:98291278
|
C | T | 2 | a0001c0004t0003g0025a0001c0004t0003g0026 | 2 | NA18951.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.3157+656C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98291278 | ||||||
| chr2:98291599
|
T | A | 1 | a0003c0032t0003g0062 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3157+977T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98291599 | ||||||
| chr2:98291717
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3157+1095G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98291717 | ||||||
| chr2:98291834
|
C | A | 12 | a0001c0001t0002g0212a0002c0002t0002g0162a0002c0002t0002g0164others(9): Show | 12 | HG00741.hp1 HG01070.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.3157+1212C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98291834 | ||||||
| chr2:98292081
|
T | TA | 41 | a0001c0001t0002g0212a0001c0001t0006g0181a0002c0002t0002g0001others(38): Show | 41 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.3157+1483dupA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr2 | 98292081 | |||||
| chr2:98292081
|
TA | T | 9 | a0001c0001t0001g0132a0001c0001t0001g0193a0001c0001t0001g0208others(6): Show | 9 | HG00323.hp2 HG01257.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.3157+1483delA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr2 | 98292081 | |||||
| chr2:98292101
|
A | C | 2 | a0002c0002t0004g0005a0008c0010t0004g0227 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3157+1479A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98292101 | ||||||
| chr2:98292229
|
C | T | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.3157+1607C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98292229 | ||||||
| chr2:98292285
|
T | C | 9 | a0001c0004t0004g0018a0001c0004t0004g0023a0002c0002t0003g0024others(6): Show | 9 | HG01071.hp1 HG01081.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.3157+1663T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98292285 | ||||||
| chr2:98292373
|
T | C | 6 | a0001c0001t0001g0083a0001c0001t0003g0047a0001c0001t0003g0238others(3): Show | 6 | HG02486.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3157+1751T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98292373 | ||||||
| chr2:98292388
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3157+1766G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98292388 | ||||||
| chr2:98292397
|
T | C | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3157+1775T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98292397 | ||||||
| chr2:98292420
|
G | GGACAGA | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3157+1798_3157+179 others(10): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98292420 | ||||||
| chr2:98292431
|
C | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3157+1809C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98292431 | ||||||
| chr2:98292539
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3157+1917A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98292539 | ||||||
| chr2:98292571
|
A | C | 1 | a0008c0010t0009g0240 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3157+1949A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98292571 | ||||||
| chr2:98292869
|
C | G | 3 | a0001c0001t0001g0167a0003c0003t0001g0199a0003c0003t0001g0201 | 3 | NA18959.hp2 NA19009.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.3157+2247C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98292869 | ||||||
| chr2:98293189
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3157+2567C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98293189 | ||||||
| chr2:98293248
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.3157+2626G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98293248 | ||||||
| chr2:98293443
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3157+2821T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98293443 | ||||||
| chr2:98293778
|
A | G | 37 | a0001c0001t0002g0212a0002c0002t0002g0001a0002c0002t0002g0087others(34): Show | 37 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.3157+3156A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98293778 | ||||||
| chr2:98293825
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3157+3203T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98293825 | ||||||
| chr2:98293903
|
T | G | 5 | a0001c0001t0001g0136a0001c0001t0001g0165a0001c0001t0001g0170others(2): Show | 5 | HG01167.hp2 HG01361.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.3157+3281T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98293903 | ||||||
| chr2:98293906
|
G | C | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3157+3284G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98293906 | ||||||
| chr2:98294013
|
C | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3157+3391C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98294013 | ||||||
| chr2:98294014
|
G | A | 1 | a0001c0004t0003g0020 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3157+3392G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98294014 | ||||||
| chr2:98294098
|
T | C | 2 | a0001c0001t0001g0089a0003c0003t0003g0073 | 2 | HG01346.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.3157+3476T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98294098 | ||||||
| chr2:98294152
|
A | T | 1 | a0001c0001t0001g0166 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3157+3530A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98294152 | ||||||
| chr2:98294184
|
T | TCA | 9 | a0001c0001t0001g0153a0001c0001t0023g0009a0002c0002t0004g0011others(6): Show | 9 | HG00609.hp1 HG01123.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.3157+3581_3157+358 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr2 | 98294184 | |||||
| chr2:98294203
|
C | A | 2 | a0001c0001t0003g0232a0001c0001t0003g0236 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3157+3581C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98294203 | ||||||
| chr2:98294203
|
C | CA | 27 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0105others(24): Show | 27 | HG00544.hp1 HG00621.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.3157+3608dupA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr2 | 98294203 | |||||
| chr2:98294203
|
C | CAA | 35 | a0001c0001t0001g0089a0001c0001t0001g0106a0001c0001t0001g0114others(32): Show | 35 | HG00423.hp2 HG00544.hp2 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.3157+3607_3157+360 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr2 | 98294203 | |||||
| chr2:98294203
|
CA | C | 15 | a0001c0001t0001g0183a0001c0001t0001g0208a0001c0004t0004g0018others(12): Show | 15 | HG01071.hp1 HG01081.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.3157+3608delA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr2 | 98294203 | |||||
| chr2:98294204
|
A | AC | 67 | a0001c0001t0001g0083a0001c0001t0001g0207a0001c0001t0001g0215others(64): Show | 67 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.3157+3582_3157+358 others(5): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98294204 | ||||||
| chr2:98294205
|
A | C | 12 | a0001c0001t0001g0166a0001c0001t0003g0034a0002c0002t0003g0024others(9): Show | 12 | HG01255.hp2 HG01258.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.3157+3583A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98294205 | ||||||
| chr2:98294206
|
A | C | 41 | a0001c0001t0002g0212a0002c0002t0002g0001a0002c0002t0002g0087others(38): Show | 41 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.3157+3584A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98294206 | ||||||
| chr2:98294207
|
A | C | 2 | a0002c0002t0004g0011a0010c0013t0002g0104 | 2 | HG02896.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3157+3585A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98294207 | ||||||
| chr2:98294208
|
A | C | 37 | a0001c0001t0002g0212a0002c0002t0002g0001a0002c0002t0002g0087others(34): Show | 37 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.3157+3586A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98294208 | ||||||
| chr2:98294325
|
T | TA | 9 | a0001c0004t0004g0018a0001c0004t0004g0023a0002c0002t0003g0024others(6): Show | 9 | HG01071.hp1 HG01081.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.3158-3574dupA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr2 | 98294325 | |||||
| chr2:98294390
|
C | T | 9 | a0001c0004t0004g0018a0001c0004t0004g0023a0002c0002t0003g0024others(6): Show | 9 | HG01071.hp1 HG01081.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.3158-3517C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98294390 | ||||||
| chr2:98294395
|
A | G | 59 | a0001c0001t0002g0212a0002c0002t0001g0190a0002c0002t0002g0001others(56): Show | 59 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.3158-3512A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98294395 | ||||||
| chr2:98294745
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3158-3162T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98294745 | ||||||
| chr2:98294775
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3158-3132G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98294775 | ||||||
| chr2:98294820
|
C | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3158-3087C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98294820 | ||||||
| chr2:98294971
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3158-2936G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98294971 | ||||||
| chr2:98295008
|
A | G | 4 | a0002c0002t0004g0003a0002c0002t0004g0004a0006c0007t0019g0059others(1): Show | 4 | HG01243.hp2 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3158-2899A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98295008 | ||||||
| chr2:98295060
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3158-2847A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98295060 | ||||||
| chr2:98295155
|
G | A | 1 | a0001c0001t0023g0009 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3158-2752G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98295155 | ||||||
| chr2:98295160
|
C | T | 4 | a0002c0002t0004g0003a0002c0002t0004g0004a0006c0007t0019g0059others(1): Show | 4 | HG01243.hp2 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3158-2747C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98295160 | ||||||
| chr2:98295184
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.3158-2723C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98295184 | ||||||
| chr2:98295274
|
G | A | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.3158-2633G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98295274 | ||||||
| chr2:98295526
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3158-2381A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98295526 | ||||||
| chr2:98295563
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3158-2344C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98295563 | ||||||
| chr2:98295649
|
T | TG | 188 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0089others(185): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.3158-2257dupG | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr2 | 98295649 | |||||
| chr2:98295744
|
C | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3158-2163C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98295744 | ||||||
| chr2:98295761
|
C | T | 4 | a0002c0002t0004g0003a0002c0002t0004g0004a0006c0007t0019g0059others(1): Show | 4 | HG01243.hp2 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3158-2146C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98295761 | ||||||
| chr2:98295808
|
G | A | 75 | a0001c0001t0002g0212a0001c0004t0004g0018a0001c0004t0004g0023others(72): Show | 75 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.3158-2099G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98295808 | ||||||
| chr2:98295876
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3158-2031C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98295876 | ||||||
| chr2:98295880
|
A | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3158-2027A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98295880 | ||||||
| chr2:98296224
|
G | A | 6 | a0001c0004t0004g0018a0001c0004t0004g0023a0002c0002t0004g0022others(3): Show | 6 | HG01071.hp1 HG01081.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.3158-1683G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98296224 | ||||||
| chr2:98296289
|
C | T | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3158-1618C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98296289 | ||||||
| chr2:98296290
|
G | A | 4 | a0003c0003t0003g0048a0003c0003t0003g0055a0016c0028t0002g0085others(1): Show | 4 | HG02056.hp1 HG02165.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.3158-1617G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98296290 | ||||||
| chr2:98296319
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3158-1588A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98296319 | ||||||
| chr2:98296410
|
G | GA | 96 | a0001c0001t0002g0212a0001c0004t0004g0018a0001c0004t0004g0023others(93): Show | 96 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.3158-1494dupA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr2 | 98296410 | |||||
| chr2:98296659
|
C | T | 1 | a0025c0033t0006g0214 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3158-1248C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98296659 | ||||||
| chr2:98297001
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3158-906G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98297001 | ||||||
| chr2:98297014
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3158-893T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98297014 | ||||||
| chr2:98297085
|
A | AT | 6 | a0001c0001t0001g0082a0001c0001t0001g0109a0001c0001t0001g0122others(3): Show | 6 | HG00408.hp2 HG00621.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.3158-809dupT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr2 | 98297085 | |||||
| chr2:98297168
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3158-739A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98297168 | ||||||
| chr2:98297676
|
C | T | 2 | a0002c0012t0011g0226a0002c0019t0011g0228 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3158-231C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 23/27 | chr2 | 98297676 | ||||||
| chr2:98298036
|
C | G | 2 | a0001c0001t0003g0232a0001c0001t0003g0236 | 2 | HG03098.hp2 HG03209.hp2 |
splice_region_variant&intron_variant | LOW | c.3282+5C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98298036 | ||||||
| chr2:98298081
|
T | G | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3282+50T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98298081 | ||||||
| chr2:98298096
|
C | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3282+65C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98298096 | ||||||
| chr2:98298137
|
C | T | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3282+106C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98298137 | ||||||
| chr2:98298367
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3282+336A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98298367 | ||||||
| chr2:98298373
|
G | GATTCT | 57 | a0001c0001t0001g0089a0001c0001t0001g0115a0001c0001t0001g0118others(54): Show | 57 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.3282+410_3282+414d others(7): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 98298373 | |||||
| chr2:98298373
|
G | GATTCTAT others(3): Show |
29 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0109others(26): Show | 29 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.3282+405_3282+414d others(12): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 98298373 | |||||
| chr2:98298373
|
G | GATTCTAT others(8): Show |
17 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(14): Show | 17 | HG00423.hp2 HG02155.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.3282+400_3282+414d others(17): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 98298373 | |||||
| chr2:98298373
|
G | GATTCTAT others(13): Show |
3 | a0002c0002t0001g0094a0003c0003t0003g0052a0003c0017t0005g0056 | 3 | HG00639.hp2 HG02080.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.3282+395_3282+414d others(22): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 98298373 | |||||
| chr2:98298373
|
GATTCT | G | 37 | a0001c0001t0001g0090a0001c0001t0001g0105a0001c0001t0001g0106others(34): Show | 37 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.3282+410_3282+414d others(7): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 98298373 | |||||
| chr2:98298373
|
GATTCTAT others(3): Show |
G | 9 | a0001c0001t0001g0186a0001c0001t0003g0034a0001c0004t0003g0010others(6): Show | 9 | HG00733.hp2 HG01081.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.3282+405_3282+414d others(12): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 98298373 | |||||
| chr2:98298373
|
GATTCTAT others(8): Show |
G | 19 | a0001c0001t0001g0161a0001c0004t0004g0018a0001c0004t0004g0023others(16): Show | 19 | HG00140.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.3282+400_3282+414d others(17): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 98298373 | |||||
| chr2:98298373
|
GATTCTAT others(13): Show |
G | 8 | a0002c0002t0002g0173a0002c0002t0004g0014a0002c0002t0004g0035others(5): Show | 8 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.3282+395_3282+414d others(22): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 98298373 | |||||
| chr2:98298373
|
GATTCTAT others(18): Show |
G | 1 | a0001c0001t0001g0206 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3282+390_3282+414d others(27): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 98298373 | |||||
| chr2:98298436
|
T | G | 1 | a0002c0012t0011g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3282+405T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98298436 | ||||||
| chr2:98298438
|
T | C | 1 | a0002c0012t0011g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3282+407T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98298438 | ||||||
| chr2:98298438
|
TATTCTAT others(3): Show |
T | 1 | a0010c0013t0002g0141 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3282+410_3282+419d others(12): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 98298438 | |||||
| chr2:98298441
|
T | G | 11 | a0001c0001t0003g0034a0001c0004t0004g0018a0001c0004t0004g0023others(8): Show | 11 | HG01071.hp1 HG01081.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.3282+410T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98298441 | ||||||
| chr2:98298441
|
T | TCTATG | 4 | a0001c0001t0001g0137a0008c0010t0004g0227a0009c0011t0001g0171others(1): Show | 4 | HG01168.hp1 HG01255.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3282+412_3282+416d others(7): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 98298441 | |||||
| chr2:98298443
|
T | C | 8 | a0001c0004t0004g0018a0001c0004t0004g0023a0002c0002t0004g0022others(5): Show | 8 | HG01071.hp1 HG01081.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.3282+412T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98298443 | ||||||
| chr2:98298443
|
T | TATGCCAT others(3): Show |
1 | a0002c0016t0020g0031 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3282+430_3282+439d others(12): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 98298443 | |||||
| chr2:98298446
|
G | T | 2 | a0003c0003t0003g0060a0010c0013t0002g0104 | 2 | HG02717.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.3282+415G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98298446 | ||||||
| chr2:98298448
|
C | T | 2 | a0003c0003t0003g0060a0010c0013t0002g0104 | 2 | HG02717.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.3282+417C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98298448 | ||||||
| chr2:98298451
|
G | T | 1 | a0003c0003t0003g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3282+420G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98298451 | ||||||
| chr2:98298453
|
C | T | 1 | a0003c0003t0003g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3282+422C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98298453 | ||||||
| chr2:98298471
|
C | G | 1 | a0003c0003t0003g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3282+440C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98298471 | ||||||
| chr2:98298476
|
C | G | 1 | a0003c0003t0003g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3282+445C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98298476 | ||||||
| chr2:98298621
|
G | A | 3 | a0002c0002t0004g0005a0002c0002t0024g0008a0008c0010t0004g0227 | 3 | HG02647.hp2 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3282+590G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98298621 | ||||||
| chr2:98298727
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3282+696G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98298727 | ||||||
| chr2:98298800
|
G | A | 1 | a0002c0002t0002g0222 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.3282+769G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98298800 | ||||||
| chr2:98298847
|
A | G | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.3282+816A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98298847 | ||||||
| chr2:98298918
|
A | G | 3 | a0002c0002t0004g0005a0002c0002t0024g0008a0008c0010t0004g0227 | 3 | HG02647.hp2 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3282+887A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98298918 | ||||||
| chr2:98299042
|
C | T | 1 | a0004c0005t0002g0107 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3282+1011C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98299042 | ||||||
| chr2:98299050
|
G | A | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3282+1019G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98299050 | ||||||
| chr2:98299256
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3283-823T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98299256 | ||||||
| chr2:98299388
|
A | T | 14 | a0002c0002t0001g0190a0002c0002t0002g0116a0002c0002t0002g0174others(11): Show | 14 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.3283-691A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98299388 | ||||||
| chr2:98299443
|
C | T | 4 | a0001c0001t0001g0144a0001c0001t0001g0145a0003c0003t0003g0060others(1): Show | 4 | HG02717.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3283-636C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98299443 | ||||||
| chr2:98299810
|
C | G | 1 | a0002c0002t0002g0116 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3283-269C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98299810 | ||||||
| chr2:98300019
|
A | T | 5 | a0001c0001t0002g0212a0002c0002t0002g0221a0002c0002t0002g0222others(2): Show | 5 | HG00741.hp1 HG01070.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.3283-60A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | chr2 | 98300019 | ||||||
| chr2:98300279
|
C | A | 1 | a0001c0001t0023g0009 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3420+63C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98300279 | ||||||
| chr2:98300447
|
A | G | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3420+231A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98300447 | ||||||
| chr2:98300463
|
G | T | 1 | a0001c0001t0001g0090 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3420+247G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98300463 | ||||||
| chr2:98300531
|
C | T | 2 | a0001c0004t0013g0029a0002c0002t0004g0033 | 2 | HG00140.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3420+315C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98300531 | ||||||
| chr2:98300718
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3420+502G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98300718 | ||||||
| chr2:98300944
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3420+728G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98300944 | ||||||
| chr2:98301029
|
G | A | 1 | a0005c0008t0003g0235 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3420+813G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98301029 | ||||||
| chr2:98301053
|
G | A | 1 | a0002c0002t0008g0177 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3420+837G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98301053 | ||||||
| chr2:98301395
|
CT | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3420+1180delT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98301395 | ||||||
| chr2:98301610
|
C | G | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.3420+1394C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98301610 | ||||||
| chr2:98301670
|
C | T | 1 | a0003c0003t0003g0073 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3420+1454C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98301670 | ||||||
| chr2:98301691
|
G | C | 72 | a0001c0001t0002g0212a0002c0002t0001g0190a0002c0002t0002g0001others(69): Show | 72 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.3420+1475G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98301691 | ||||||
| chr2:98301751
|
C | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3420+1535C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98301751 | ||||||
| chr2:98301835
|
T | C | 1 | a0005c0008t0003g0235 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3420+1619T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98301835 | ||||||
| chr2:98302006
|
T | G | 1 | a0002c0006t0004g0019 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3421-1696T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98302006 | ||||||
| chr2:98302183
|
T | C | 2 | a0002c0002t0004g0003a0002c0002t0004g0004 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3421-1519T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98302183 | ||||||
| chr2:98302193
|
C | CT | 72 | a0001c0001t0002g0212a0002c0002t0001g0190a0002c0002t0002g0001others(69): Show | 72 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.3421-1508dupT | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 98302193 | |||||
| chr2:98302195
|
G | T | 75 | a0001c0001t0002g0212a0002c0002t0001g0190a0002c0002t0002g0001others(72): Show | 75 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.3421-1507G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98302195 | ||||||
| chr2:98302348
|
A | C | 6 | a0001c0001t0001g0114a0001c0001t0001g0151a0001c0001t0001g0161others(3): Show | 6 | HG00673.hp2 HG02155.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.3421-1354A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98302348 | ||||||
| chr2:98302567
|
A | T | 1 | a0001c0001t0001g0157 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3421-1135A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98302567 | ||||||
| chr2:98302756
|
A | G | 77 | a0001c0001t0002g0212a0002c0002t0001g0190a0002c0002t0002g0001others(74): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.3421-946A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98302756 | ||||||
| chr2:98302865
|
C | A | 2 | a0006c0007t0019g0059a0020c0026t0002g0210 | 2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3421-837C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98302865 | ||||||
| chr2:98302882
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3421-820A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98302882 | ||||||
| chr2:98303125
|
G | A | 4 | a0002c0002t0004g0032a0002c0002t0004g0036a0002c0002t0004g0037others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.3421-577G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98303125 | ||||||
| chr2:98303226
|
A | G | 77 | a0001c0001t0002g0212a0002c0002t0001g0190a0002c0002t0002g0001others(74): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.3421-476A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98303226 | ||||||
| chr2:98303277
|
G | T | 2 | a0006c0007t0012g0050a0006c0007t0012g0051 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3421-425G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98303277 | ||||||
| chr2:98303357
|
G | A | 39 | a0001c0001t0001g0089a0001c0001t0001g0105a0001c0001t0001g0106others(36): Show | 39 | HG00423.hp2 HG00544.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.3421-345G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98303357 | ||||||
| chr2:98303396
|
A | G | 1 | a0003c0003t0003g0068 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3421-306A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98303396 | ||||||
| chr2:98303397
|
TAGAA | T | 72 | a0001c0001t0002g0212a0002c0002t0001g0190a0002c0002t0002g0001others(69): Show | 72 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.3421-302_3421-299d others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 98303397 | |||||
| chr2:98303421
|
G | GGT | 19 | a0001c0001t0001g0122a0001c0001t0001g0155a0001c0001t0001g0167others(16): Show | 19 | HG00673.hp1 HG01071.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.3421-246_3421-245d others(4): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 98303421 | |||||
| chr2:98303421
|
G | GGTGT | 5 | a0001c0001t0001g0127a0001c0004t0004g0018a0001c0004t0004g0023others(2): Show | 5 | HG00639.hp2 HG01123.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.3421-248_3421-245d others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 98303421 | |||||
| chr2:98303421
|
G | GGTGTGT | 5 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(2): Show | 5 | HG00140.hp1 HG01891.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3421-250_3421-245d others(8): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 98303421 | |||||
| chr2:98303421
|
G | GGTGTGTG others(1): Show |
3 | a0002c0012t0004g0007a0002c0012t0011g0226a0010c0013t0002g0104 | 3 | HG02109.hp2 HG03225.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3421-252_3421-245d others(10): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 98303421 | |||||
| chr2:98303421
|
G | GGTGTGTG others(3): Show |
1 | a0002c0002t0021g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3421-254_3421-245d others(12): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 98303421 | |||||
| chr2:98303421
|
G | GGTGTGTG others(5): Show |
1 | a0002c0019t0011g0228 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3421-256_3421-245d others(14): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 98303421 | |||||
| chr2:98303421
|
G | GGTGTGTG others(9): Show |
1 | a0002c0016t0020g0031 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3421-260_3421-245d others(18): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 98303421 | |||||
| chr2:98303421
|
GGT | G | 6 | a0001c0001t0006g0198a0002c0002t0004g0003a0002c0002t0004g0004others(3): Show | 6 | HG02056.hp1 HG02165.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.3421-246_3421-245d others(4): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 98303421 | |||||
| chr2:98303421
|
GGTGT | G | 10 | a0001c0001t0001g0156a0001c0001t0002g0212a0001c0001t0023g0009others(7): Show | 10 | HG00741.hp1 HG01070.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.3421-248_3421-245d others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 98303421 | |||||
| chr2:98303421
|
GGTGTGT | G | 63 | a0002c0002t0001g0190a0002c0002t0002g0001a0002c0002t0002g0087others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.3421-250_3421-245d others(8): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 98303421 | |||||
| chr2:98303609
|
A | G | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3421-93A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98303609 | ||||||
| chr2:98303625
|
T | C | 1 | a0001c0001t0001g0216 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3421-77T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 25/27 | chr2 | 98303625 | ||||||
| chr2:98304008
|
C | T | 1 | a0003c0003t0001g0202 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3521+206C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98304008 | ||||||
| chr2:98304017
|
T | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3521+215T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98304017 | ||||||
| chr2:98304209
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.3521+407C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98304209 | ||||||
| chr2:98304332
|
C | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3521+530C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98304332 | ||||||
| chr2:98304493
|
G | T | 1 | a0001c0001t0001g0184 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3521+691G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98304493 | ||||||
| chr2:98304687
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3521+885G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98304687 | ||||||
| chr2:98304916
|
A | G | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.3521+1114A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98304916 | ||||||
| chr2:98304925
|
C | T | 4 | a0002c0012t0004g0007a0002c0012t0011g0226a0002c0016t0020g0031others(1): Show | 4 | HG01358.hp1 HG02109.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.3521+1123C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98304925 | ||||||
| chr2:98304980
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3521+1178A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98304980 | ||||||
| chr2:98305025
|
G | A | 1 | a0005c0020t0003g0230 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3521+1223G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98305025 | ||||||
| chr2:98305037
|
G | A | 1 | a0002c0002t0002g0217 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.3521+1235G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98305037 | ||||||
| chr2:98305097
|
G | A | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3521+1295G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98305097 | ||||||
| chr2:98305161
|
G | A | 1 | a0025c0033t0006g0214 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3521+1359G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98305161 | ||||||
| chr2:98305192
|
T | C | 237 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(234): Show | 237 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.3521+1390T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98305192 | ||||||
| chr2:98305209
|
C | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3521+1407C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98305209 | ||||||
| chr2:98305363
|
G | A | 55 | a0001c0001t0002g0212a0002c0002t0001g0190a0002c0002t0002g0001others(52): Show | 55 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.3521+1561G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98305363 | ||||||
| chr2:98305384
|
G | A | 2 | a0001c0004t0003g0044a0005c0008t0003g0231 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3521+1582G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98305384 | ||||||
| chr2:98305539
|
C | T | 4 | a0002c0012t0004g0007a0002c0012t0011g0226a0002c0016t0020g0031others(1): Show | 4 | HG01358.hp1 HG02109.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.3521+1737C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98305539 | ||||||
| chr2:98305556
|
T | C | 3 | a0001c0001t0001g0167a0003c0003t0001g0199a0003c0003t0001g0201 | 3 | NA18959.hp2 NA19009.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.3521+1754T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98305556 | ||||||
| chr2:98305585
|
C | A | 1 | a0006c0007t0004g0067 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3521+1783C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98305585 | ||||||
| chr2:98305672
|
G | T | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.3521+1870G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98305672 | ||||||
| chr2:98305675
|
G | A | 2 | a0008c0010t0009g0239a0008c0010t0009g0240 | 2 | HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3521+1873G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98305675 | ||||||
| chr2:98305737
|
C | G | 4 | a0002c0012t0004g0007a0002c0012t0011g0226a0002c0016t0020g0031others(1): Show | 4 | HG01358.hp1 HG02109.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.3521+1935C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98305737 | ||||||
| chr2:98305846
|
C | A | 1 | a0002c0002t0004g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3521+2044C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98305846 | ||||||
| chr2:98306162
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3521+2360G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98306162 | ||||||
| chr2:98306195
|
GC | G | 6 | a0002c0002t0004g0005a0002c0002t0004g0011a0002c0002t0024g0008others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.3521+2400delC | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr2 | 98306195 | |||||
| chr2:98306934
|
A | C | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3521+3132A>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98306934 | ||||||
| chr2:98306993
|
G | A | 4 | a0002c0002t0004g0003a0002c0002t0004g0004a0006c0007t0019g0059others(1): Show | 4 | HG01243.hp2 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3521+3191G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98306993 | ||||||
| chr2:98307094
|
G | A | 3 | a0001c0001t0001g0183a0001c0001t0001g0192a0001c0004t0001g0220 | 3 | HG00735.hp2 HG01952.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.3521+3292G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98307094 | ||||||
| chr2:98307154
|
A | G | 80 | a0001c0001t0002g0212a0001c0004t0004g0018a0001c0004t0004g0023others(77): Show | 80 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.3521+3352A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98307154 | ||||||
| chr2:98307259
|
C | G | 4 | a0002c0002t0004g0003a0002c0002t0004g0004a0006c0007t0019g0059others(1): Show | 4 | HG01243.hp2 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3521+3457C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98307259 | ||||||
| chr2:98307294
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3521+3492G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98307294 | ||||||
| chr2:98307325
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3521+3523T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98307325 | ||||||
| chr2:98307345
|
C | A | 56 | a0001c0001t0001g0138a0001c0001t0002g0212a0002c0002t0001g0190others(53): Show | 56 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.3521+3543C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98307345 | ||||||
| chr2:98307361
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3521+3559T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98307361 | ||||||
| chr2:98307490
|
A | G | 95 | a0001c0001t0001g0138a0001c0001t0002g0212a0001c0004t0004g0018others(92): Show | 95 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.3521+3688A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98307490 | ||||||
| chr2:98307496
|
C | T | 95 | a0001c0001t0001g0138a0001c0001t0002g0212a0001c0004t0004g0018others(92): Show | 95 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.3521+3694C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98307496 | ||||||
| chr2:98307534
|
T | C | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.3521+3732T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98307534 | ||||||
| chr2:98307590
|
T | C | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3521+3788T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98307590 | ||||||
| chr2:98307627
|
A | G | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.3521+3825A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98307627 | ||||||
| chr2:98307775
|
A | T | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.3521+3973A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98307775 | ||||||
| chr2:98307806
|
T | TTA | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.3521+4006_3521+400 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr2 | 98307806 | |||||
| chr2:98307838
|
A | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3522-3981A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98307838 | ||||||
| chr2:98307911
|
A | G | 72 | a0001c0001t0001g0138a0001c0001t0002g0212a0001c0004t0004g0018others(69): Show | 72 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.3522-3908A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98307911 | ||||||
| chr2:98308107
|
T | C | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.3522-3712T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98308107 | ||||||
| chr2:98308132
|
T | C | 9 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(6): Show | 9 | HG01243.hp2 HG02056.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.3522-3687T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98308132 | ||||||
| chr2:98308351
|
G | A | 2 | a0001c0001t0003g0232a0001c0001t0003g0236 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3522-3468G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98308351 | ||||||
| chr2:98308388
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3522-3431G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98308388 | ||||||
| chr2:98308458
|
T | C | 93 | a0001c0001t0001g0138a0001c0001t0002g0212a0001c0004t0004g0018others(90): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.3522-3361T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98308458 | ||||||
| chr2:98308460
|
T | C | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.3522-3359T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98308460 | ||||||
| chr2:98308784
|
A | G | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.3522-3035A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98308784 | ||||||
| chr2:98309167
|
C | CA | 13 | a0001c0001t0001g0127a0001c0001t0001g0144a0001c0001t0001g0145others(10): Show | 13 | HG00323.hp2 HG01123.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.3522-2638dupA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr2 | 98309167 | |||||
| chr2:98309199
|
C | G | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3522-2620C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98309199 | ||||||
| chr2:98309228
|
A | T | 5 | a0002c0012t0011g0226a0002c0016t0020g0031a0002c0019t0011g0228others(2): Show | 5 | HG01358.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.3522-2591A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98309228 | ||||||
| chr2:98309311
|
G | T | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3522-2508G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98309311 | ||||||
| chr2:98309426
|
G | A | 2 | a0004c0005t0002g0098a0023c0031t0014g0097 | 2 | NA18951.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.3522-2393G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98309426 | ||||||
| chr2:98309642
|
T | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0218 | 2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.3522-2177T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98309642 | ||||||
| chr2:98309817
|
T | G | 13 | a0002c0002t0002g0173a0002c0002t0004g0030a0002c0002t0004g0032others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.3522-2002T>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98309817 | ||||||
| chr2:98309832
|
C | T | 3 | a0002c0002t0008g0086a0002c0002t0008g0177a0002c0002t0008g0196 | 3 | HG00609.hp1 NA18983.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.3522-1987C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98309832 | ||||||
| chr2:98309881
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0016g0152 | 2 | NA18941.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.3522-1938G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98309881 | ||||||
| chr2:98309949
|
G | C | 12 | a0002c0002t0002g0116a0002c0002t0002g0174a0002c0002t0002g0180others(9): Show | 12 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.3522-1870G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98309949 | ||||||
| chr2:98310152
|
C | T | 1 | a0002c0006t0004g0016 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3522-1667C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98310152 | ||||||
| chr2:98310390
|
A | T | 1 | a0001c0001t0001g0144 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3522-1429A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98310390 | ||||||
| chr2:98310393
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3522-1426G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98310393 | ||||||
| chr2:98310393
|
G | C | 1 | a0001c0001t0001g0115 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3522-1426G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98310393 | ||||||
| chr2:98310486
|
G | A | 4 | a0006c0007t0009g0080a0008c0010t0009g0239a0008c0010t0009g0240others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3522-1333G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98310486 | ||||||
| chr2:98310725
|
C | T | 2 | a0016c0028t0002g0085a0017c0027t0002g0084 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.3522-1094C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98310725 | ||||||
| chr2:98311216
|
G | A | 1 | a0006c0007t0019g0059 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3522-603G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98311216 | ||||||
| chr2:98311383
|
G | A | 3 | a0010c0013t0002g0104a0010c0013t0002g0141a0014c0030t0002g0120 | 3 | HG00140.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3522-436G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98311383 | ||||||
| chr2:98311622
|
C | T | 13 | a0001c0001t0002g0212a0002c0002t0002g0162a0002c0002t0002g0164others(10): Show | 13 | HG00621.hp2 HG00741.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.3522-197C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | chr2 | 98311622 | ||||||
| chr2:98312132
|
G | T | 1 | a0007c0009t0002g0092 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3736-68G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 27/27 | chr2 | 98312132 |