Item | Value |
---|---|
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 | 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 | MEKSG others(1289): Show |
chr2 | 98082167 | 98318299 |
a0002 | 0/0 | 1294 | 63 | 13 | 20 | 22 | 7 | 1 | 18 | VWA3B_chr2_98082167_98318299 | VWA3B | MEKSG others(1289): Show |
chr2 | 98082167 | 98318299 |
a0003 | 0/0 | 1294 | 30 | 10 | 4 | 14 | 1 | 1 | 10 | VWA3B_chr2_98082167_98318299 | VWA3B | MEKSG others(1289): Show |
chr2 | 98082167 | 98318299 |
a0004 | 0/0 | 1294 | 10 | 0 | 1 | 9 | 0 | 0 | 8 | VWA3B_chr2_98082167_98318299 | VWA3B | MEKSG others(1289): Show |
chr2 | 98082167 | 98318299 |
a0005 | 0/0 | 1294 | 6 | 5 | 0 | 1 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | MEKSG others(1289): Show |
chr2 | 98082167 | 98318299 |
a0006 | 0/0 | 1294 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | MEKSG others(1289): Show |
chr2 | 98082167 | 98318299 |
a0007 | 0/0 | 1294 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | MEKSG others(1289): Show |
chr2 | 98082167 | 98318299 |
a0008 | 0/0 | 1294 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | MEKSG others(1289): Show |
chr2 | 98082167 | 98318299 |
a0009 | 0/0 | 1294 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | MEKSG others(1289): Show |
chr2 | 98082167 | 98318299 |
a0010 | 0/0 | 218 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | MEKSG others(213): Show |
chr2 | 98082167 | 98318299 |
a0011 | 0/0 | 1294 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | MEKSG others(1289): Show |
chr2 | 98082167 | 98318299 |
a0012 | 0/0 | 1294 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | MEKSG others(1289): Show |
chr2 | 98082167 | 98318299 |
a0013 | 1/0 | 1294 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | MEKSG others(1289): Show |
chr2 | 98082167 | 98318299 |
a0014 | 0/0 | 371 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | MEKSG others(366): Show |
chr2 | 98082167 | 98318299 |
a0015 | 0/0 | 1294 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | MEKSG others(1289): Show |
chr2 | 98082167 | 98318299 |
a0016 | 0/0 | 742 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | MEKSG others(737): Show |
chr2 | 98082167 | 98318299 |
a0017 | 0/0 | 1294 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | MEKSG others(1289): Show |
chr2 | 98082167 | 98318299 |
a0018 | 0/0 | 1294 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | MEKSG others(1289): Show |
chr2 | 98082167 | 98318299 |
a0019 | 0/0 | 1294 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | MEKSG others(1289): Show |
chr2 | 98082167 | 98318299 |
a0020 | 0/0 | 1294 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | MEKSG others(1289): Show |
chr2 | 98082167 | 98318299 |
a0021 | 0/0 | 571 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | MEKSG others(566): Show |
chr2 | 98082167 | 98318299 |
a0022 | 0/0 | 1294 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | MEKSG others(1289): Show |
chr2 | 98082167 | 98318299 |
a0023 | 0/0 | 1294 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | MEKSG others(1289): Show |
chr2 | 98082167 | 98318299 |
a0024 | 0/0 | 1294 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | MEKSG others(1289): Show |
chr2 | 98082167 | 98318299 |
a0025 | 0/0 | 1294 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | MEKSG others(1289): Show |
chr2 | 98082167 | 98318299 |
a0026 | 0/0 | 1294 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | MEKSG others(1289): Show |
chr2 | 98082167 | 98318299 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3882 | 85 | 16 | 15 | 41 | 3 | 9 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0001c0004 | 0/0 | 3882 | 11 | 3 | 4 | 3 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0002c0002 | 0/0 | 3882 | 53 | 10 | 16 | 20 | 6 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0002c0006 | 0/0 | 3882 | 6 | 0 | 3 | 2 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0002c0012 | 0/0 | 3882 | 2 | 2 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0002c0016 | 0/0 | 3882 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0002c0019 | 0/0 | 3882 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0003c0003 | 0/0 | 3882 | 28 | 9 | 4 | 14 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0003c0017 | 0/0 | 3882 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0003c0032 | 0/0 | 3882 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0004c0005 | 0/0 | 3882 | 10 | 0 | 1 | 9 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0005c0007 | 0/0 | 3882 | 6 | 5 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0006c0008 | 0/0 | 3882 | 5 | 5 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0006c0020 | 0/0 | 3882 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0007c0009 | 0/0 | 3882 | 4 | 0 | 4 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0008c0010 | 0/0 | 3882 | 3 | 3 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0009c0015 | 0/0 | 3882 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0009c0022 | 0/0 | 3882 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0010c0035 | 0/0 | 3882 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0010c0036 | 0/0 | 3882 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0011c0011 | 0/0 | 3882 | 2 | 0 | 2 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0012c0013 | 0/0 | 3882 | 2 | 0 | 0 | 0 | 1 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0013c0025 | 1/0 | 3882 | 1 | 0 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0014c0030 | 0/0 | 3882 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0015c0024 | 0/0 | 3882 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0016c0026 | 0/0 | 3882 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0017c0027 | 0/0 | 3882 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0018c0028 | 0/0 | 3882 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0019c0014 | 0/0 | 3882 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0020c0029 | 0/0 | 3882 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0021c0018 | 0/0 | 3882 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0022c0023 | 0/0 | 3882 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0023c0034 | 0/0 | 3882 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0024c0031 | 0/0 | 3882 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0025c0033 | 0/0 | 3882 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
chr2 | 98082167 | 98318299 | ||
a0026c0021 | 0/0 | 3882 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | ATGGA others(3877): Show |
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 | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0001c0001t0002 | 0/0 | 5064 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0001c0001t0003 | 0/0 | 5064 | 6 | 5 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0001c0001t0005 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0001c0001t0006 | 0/0 | 5064 | 2 | 0 | 0 | 2 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0001c0001t0007 | 0/0 | 5064 | 3 | 0 | 0 | 3 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0001c0001t0010 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0001c0001t0013 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0001c0001t0015 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0001c0001t0016 | 0/0 | 5065 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5060): Show |
chr2 | 98082167 | 98318299 |
a0001c0001t0023 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | GGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0001c0004t0001 | 0/0 | 5064 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0001c0004t0003 | 0/0 | 5064 | 7 | 1 | 2 | 3 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0001c0004t0004 | 0/0 | 5064 | 2 | 1 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0001c0004t0013 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0002c0002t0001 | 0/0 | 5064 | 3 | 0 | 2 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0002c0002t0002 | 0/0 | 5064 | 26 | 0 | 8 | 16 | 2 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0002c0002t0003 | 0/0 | 5064 | 2 | 1 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0002c0002t0004 | 0/0 | 5064 | 17 | 7 | 5 | 0 | 4 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0002c0002t0008 | 0/0 | 5064 | 3 | 0 | 0 | 3 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0002c0002t0021 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0002c0002t0024 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | GGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0002c0006t0002 | 0/0 | 5064 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0002c0006t0004 | 0/0 | 5064 | 5 | 0 | 3 | 2 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0002c0012t0004 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0002c0012t0011 | 0/0 | 5066 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5061): Show |
chr2 | 98082167 | 98318299 |
a0002c0016t0020 | 0/0 | 5066 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5061): Show |
chr2 | 98082167 | 98318299 |
a0002c0019t0011 | 0/0 | 5066 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5061): Show |
chr2 | 98082167 | 98318299 |
a0003c0003t0001 | 0/0 | 5064 | 3 | 0 | 0 | 3 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0003c0003t0003 | 0/0 | 5064 | 18 | 4 | 4 | 9 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0003c0003t0005 | 0/0 | 5064 | 5 | 5 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0003c0003t0006 | 0/0 | 5064 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0003c0003t0018 | 0/0 | 5064 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0003c0017t0005 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0003c0032t0003 | 0/0 | 5064 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0004c0005t0002 | 0/0 | 5064 | 10 | 0 | 1 | 9 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0005c0007t0002 | 0/0 | 5064 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0005c0007t0004 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0005c0007t0009 | 0/0 | 5065 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5060): Show |
chr2 | 98082167 | 98318299 |
a0005c0007t0012 | 0/0 | 5064 | 2 | 2 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0005c0007t0019 | 0/0 | 5029 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5024): Show |
chr2 | 98082167 | 98318299 |
a0006c0008t0003 | 0/0 | 5064 | 5 | 5 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0006c0020t0003 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0007c0009t0002 | 0/0 | 5064 | 4 | 0 | 4 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0008c0010t0004 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0008c0010t0009 | 0/0 | 5065 | 2 | 2 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5060): Show |
chr2 | 98082167 | 98318299 |
a0009c0015t0001 | 0/0 | 5064 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0009c0022t0003 | 0/0 | 5064 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0010c0035t0004 | 0/0 | 5064 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0010c0036t0003 | 0/0 | 5064 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0011c0011t0001 | 0/0 | 5064 | 2 | 0 | 2 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0012c0013t0002 | 0/0 | 5064 | 2 | 0 | 0 | 0 | 1 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0013c0025t0001 | 1/0 | 5064 | 1 | 0 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0014c0030t0002 | 0/0 | 5064 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0015c0024t0001 | 0/0 | 5064 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0016c0026t0002 | 0/0 | 5064 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0017c0027t0002 | 0/0 | 5064 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0018c0028t0002 | 0/0 | 5064 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0019c0014t0017 | 0/0 | 5065 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5060): Show |
chr2 | 98082167 | 98318299 |
a0020c0029t0004 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0021c0018t0010 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0022c0023t0002 | 0/0 | 5064 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0023c0034t0022 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0024c0031t0014 | 0/0 | 5064 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0025c0033t0006 | 0/0 | 5064 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
a0026c0021t0003 | 0/0 | 5064 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | AGAGG others(5059): Show |
chr2 | 98082167 | 98318299 |
actghapid | grch38/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 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0172 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0002g0204 | 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 |
a0001c0001t0003g0045 | 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 |
a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0006g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0007g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0010g0134 | 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 |
a0001c0001t0015g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0001c0001t0016g0146 | 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 |
a0001c0004t0001g0221 | 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 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0002c0002t0001g0182 | 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 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0002c0002t0002g0160 | 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 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0002c0002t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0002c0002t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
a0002c0002t0002g0225 | 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 |
a0002c0002t0008g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0002c0002t0008g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0002c0002t0008g0217 | 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 |
a0002c0006t0002g0109 | 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 |
a0003c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0003c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0003c0003t0001g0194 | 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 |
a0003c0003t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0003c0003t0003g0051 | 0/0 | 1 | 1 | 0 | 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 |
a0003c0003t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0003c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0003c0003t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0003c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0003c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0003c0003t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0003c0003t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0003c0003t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0003c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 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 |
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 |
a0003c0003t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0003c0003t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0003c0003t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0003c0003t0006g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0003c0003t0018g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0003c0017t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0003c0032t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0004c0005t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0004c0005t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0004c0005t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0004c0005t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0004c0005t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0004c0005t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0004c0005t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0004c0005t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0004c0005t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0005c0007t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0005c0007t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0005c0007t0009g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0005c0007t0012g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0005c0007t0012g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0005c0007t0019g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0006c0008t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0006c0008t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0006c0008t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0006c0008t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0006c0008t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0006c0020t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0007c0009t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0007c0009t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0007c0009t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0007c0009t0002g0131 | 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 |
a0009c0015t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0009c0022t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0010c0035t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0010c0036t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0011c0011t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0011c0011t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0012c0013t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0012c0013t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0013c0025t0001g0170 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0014c0030t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0015c0024t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0016c0026t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0017c0027t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0018c0028t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0019c0014t0017g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0020c0029t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0021c0018t0010g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0022c0023t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0023c0034t0022g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0024c0031t0014g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0025c0033t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
a0026c0021t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | g0116 | 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 | a0009 | c0015 | t0001 | g0108 | EUR | FIN | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG00280 | hp2 | a0002 | c0002 | t0002 | g0220 | EUR | FIN | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG00323 | hp1 | a0009 | c0022 | t0003 | g0038 | EUR | FIN | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG00323 | hp2 | a0002 | c0006 | t0002 | g0109 | EUR | FIN | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG00408 | hp1 | a0004 | c0005 | t0002 | g0177 | EAS | CHS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG00423 | hp1 | a0003 | c0003 | t0018 | g0078 | EAS | CHS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0218 | EAS | CHS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG00609 | hp1 | a0002 | c0002 | t0008 | g0171 | EAS | CHS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG00609 | hp2 | a0010 | 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 | g0164 | EAS | CHS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0089 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG00673 | hp1 | a0003 | c0003 | t0003 | g0065 | EAS | CHS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0199 | 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 | g0168 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG00741 | hp1 | a0002 | c0002 | t0002 | g0224 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0212 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG01070 | hp1 | a0002 | c0002 | t0004 | g0036 | 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 | g0086 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG01071 | hp2 | a0002 | c0002 | t0004 | g0037 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG01081 | hp1 | a0007 | c0009 | t0002 | g0087 | 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 | g0210 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG01167 | hp1 | a0015 | c0024 | t0001 | g0099 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG01168 | hp2 | a0002 | c0002 | t0002 | g0112 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG01175 | hp2 | a0003 | c0003 | t0003 | g0067 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG01243 | hp1 | a0002 | c0002 | t0002 | g0225 | AMR | PUR | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG01243 | hp2 | a0016 | c0026 | t0002 | g0202 | 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 | a0011 | c0011 | t0001 | g0205 | AMR | CLM | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG01257 | hp1 | a0007 | c0009 | t0002 | g0131 | 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 | g0130 | AMR | CLM | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG01258 | hp2 | a0011 | c0011 | t0001 | g0166 | AMR | CLM | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG01261 | hp1 | a0003 | c0003 | t0003 | g0070 | 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 | g0102 | AMR | CLM | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG01346 | hp2 | a0003 | c0003 | t0003 | g0071 | 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 | g0050 | AMR | CLM | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0161 | 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 | g0098 | AMR | CLM | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG01515 | hp1 | a0012 | c0013 | t0002 | g0135 | EUR | IBS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0167 | 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 | g0113 | 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 | g0169 | EUR | IBS | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG01891 | hp1 | a0005 | c0007 | t0009 | g0081 | AFR | ACB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG01891 | hp2 | a0005 | c0007 | t0004 | g0066 | AFR | ACB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG01952 | hp1 | a0001 | c0004 | t0001 | g0221 | AMR | PEL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG02056 | hp1 | a0017 | c0027 | t0002 | g0215 | 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 | g0074 | EAS | KHV | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG02080 | hp2 | a0002 | c0002 | t0002 | g0103 | EAS | KHV | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CDX | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CDX | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CDX | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG02165 | hp2 | a0018 | c0028 | t0002 | g0216 | EAS | CDX | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0128 | 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 | g0223 | 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 | g0204 | 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 | g0055 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG02572 | hp2 | a0019 | c0014 | t0017 | g0122 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG02615 | hp1 | a0006 | 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 | g0046 | 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 | g0178 | SAS | PJL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG02717 | hp1 | a0003 | c0003 | t0005 | g0080 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG02717 | hp2 | a0003 | c0003 | t0003 | g0056 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG02723 | hp1 | a0020 | c0029 | t0004 | g0047 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG02723 | hp2 | a0003 | c0003 | t0003 | g0054 | 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 | g0198 | SAS | PJL | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG02886 | hp1 | a0003 | c0003 | t0005 | g0075 | 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 | a0006 | c0020 | t0003 | g0231 | 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 | g0150 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG02897 | hp2 | a0006 | c0008 | t0003 | g0230 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG02922 | hp1 | a0005 | c0007 | t0012 | g0053 | 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 | g0051 | 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 | a0005 | c0007 | t0012 | g0052 | 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 | a0006 | 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 | g0127 | AFR | ESN | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG03139 | hp2 | a0005 | 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 | a0006 | c0008 | t0003 | g0229 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG03540 | hp2 | a0021 | c0018 | t0010 | g0124 | AFR | GWD | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0139 | 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 | g0180 | SAS | BEB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG03927 | hp2 | a0022 | c0023 | t0002 | g0148 | SAS | BEB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG03942 | hp1 | a0003 | c0032 | t0003 | g0061 | SAS | BEB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | STU | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG04228 | hp2 | a0012 | c0013 | t0002 | g0100 | SAS | STU | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18522 | hp1 | a0001 | c0001 | t0010 | g0134 | 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 | g0117 | EAS | CHB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18612 | hp2 | a0003 | c0003 | t0003 | g0068 | EAS | CHB | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18906 | hp1 | a0023 | c0034 | t0022 | g0079 | AFR | YRI | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18906 | hp2 | a0006 | c0008 | t0003 | g0234 | AFR | YRI | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18939 | hp1 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0186 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18941 | hp2 | a0001 | c0001 | t0016 | g0146 | 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 | g0097 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18945 | hp1 | a0001 | c0001 | t0006 | g0173 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18945 | hp2 | a0001 | c0001 | t0007 | g0140 | 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 | g0160 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18948 | hp1 | a0004 | c0005 | t0002 | g0096 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18951 | hp1 | a0024 | c0031 | t0014 | g0092 | 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 | g0183 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18959 | hp2 | a0003 | c0003 | t0001 | g0191 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18962 | hp2 | a0002 | c0002 | t0002 | g0119 | 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 | g0141 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18977 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18977 | hp2 | a0003 | c0003 | t0003 | g0072 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18983 | hp1 | a0001 | c0001 | t0006 | g0190 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18983 | hp2 | a0002 | c0002 | t0008 | g0188 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18985 | hp1 | a0004 | c0005 | t0002 | g0120 | 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 | g0149 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0159 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18989 | hp1 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18992 | hp1 | a0002 | c0002 | t0002 | g0158 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18992 | hp2 | a0003 | c0003 | t0003 | g0069 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18993 | hp2 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18995 | hp2 | a0002 | c0002 | t0008 | g0217 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18998 | hp2 | a0004 | c0005 | t0002 | g0088 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18999 | hp1 | a0004 | c0005 | t0002 | g0121 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA19000 | hp1 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA19007 | hp2 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA19009 | hp2 | a0003 | c0003 | t0001 | g0194 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA19064 | hp2 | a0010 | c0036 | t0003 | g0063 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA19065 | hp1 | a0003 | c0003 | t0006 | g0193 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA19065 | hp2 | a0004 | c0005 | t0002 | g0095 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA19066 | hp2 | a0003 | c0003 | t0003 | g0073 | 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 | g0195 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA19080 | hp1 | a0001 | c0001 | t0007 | g0142 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA19080 | hp2 | a0004 | c0005 | t0002 | g0093 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA19085 | hp1 | a0002 | c0002 | t0002 | g0181 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA19087 | hp1 | a0003 | c0003 | t0003 | g0062 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA19087 | hp2 | a0005 | c0007 | t0002 | g0174 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA19088 | hp1 | a0003 | c0003 | t0001 | g0192 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA19088 | hp2 | a0004 | c0005 | t0002 | g0094 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA19090 | hp1 | a0025 | c0033 | t0006 | g0206 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0189 | EUR | TSI | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
NA20752 | hp2 | a0026 | 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 | g0084 | 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 | g0123 | AMR | CLM | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
HG02109 | hp1 | a0003 | c0003 | t0005 | g0060 | 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 | g0045 | 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 | g0138 | 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 | a0001 | c0001 | t0001 | g0172 | REF | REF | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
homoSapiens | grch38p0 | a0013 | c0025 | t0001 | g0170 | REF | REF | VWA3B_chr2_98082167_98318299 | VWA3B | chr2 | 98082167 | 98318299 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:98093183 | C | A | 1 | a0019 | 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 | a0021 | 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 | a0003 a0005 a0010 others(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 | a0010 | 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 | a0011 | 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 | a0024 | 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 | a0010 | 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 | a0006 a0008 |
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 | a0023 | 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 | a0020 | 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 | a0017 a0018 |
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 | a0009 a0022 a0026 |
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 | a0021 | 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 | a0001 a0003 a0006 others(12): Show |
149 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(146): 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 | a0016 | 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 | a0018 | 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 | a0015 | 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 | a0023 | 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 | a0001 a0003 a0006 others(8): Show |
141 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(138): 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 | a0012 a0014 |
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 | a0001 a0002 a0003 others(21): Show |
236 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(233): 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 | a0004 a0010 a0024 |
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 | a0001 a0002 a0005 others(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 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:98093221 | T | C | 4 | a0001c0004 a0002c0006 a0002c0016 others(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 | a0021c0018 | 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 | a0002c0012 a0002c0016 a0002c0019 |
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 | a0006c0020 | 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 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:98087167 | A | G | 2 | a0001c0001t0023 a0002c0002t0024 |
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 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0013 others(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 | a0001c0001t0023 a0002c0002t0024 |
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 | a0024c0031t0014 | 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 | a0023c0034t0022 | 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 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0013 others(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 | a0002c0012t0011 a0002c0016t0020 a0002c0019t0011 |
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 | a0001c0001t0002 a0001c0004t0004 a0002c0002t0002 others(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 | a0001c0001t0005 a0001c0001t0015 a0003c0003t0005 others(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 | a0001c0001t0006 a0003c0003t0006 a0003c0003t0018 others(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 | a0005c0007t0019 | 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 | a0001c0001t0002 a0001c0004t0004 a0002c0002t0002 others(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 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:98087409 | C | T | 4 | a0001c0001t0003g0238 a0002c0006t0004g0237 a0008c0010t0009g0239 others(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 | a0001c0001t0003g0232 a0001c0001t0003g0236 a0001c0001t0003g0238 others(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 | a0001c0001t0003g0012 a0001c0001t0003g0034 a0001c0001t0003g0045 others(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 | a0003c0003t0003g0049 a0003c0003t0003g0050 a0003c0003t0003g0051 others(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 | a0001c0001t0003g0045 a0001c0001t0005g0046 a0003c0003t0003g0048 others(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 | a0001c0001t0003g0012 a0001c0001t0003g0034 a0001c0001t0003g0045 others(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 | a0001c0001t0001g0219 a0002c0002t0002g0218 a0002c0002t0008g0217 others(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 | a0005c0007t0012g0053 | 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 | a0003c0003t0018g0078 a0004c0005t0002g0095 |
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 | a0001c0001t0001g0084 | 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 | a0001c0001t0023g0009 a0002c0002t0004g0002 a0002c0002t0004g0003 others(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 | a0001c0001t0023g0009 a0002c0002t0024g0008 |
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 | a0001c0001t0003g0012 a0001c0001t0003g0034 a0001c0001t0003g0045 others(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 | a0001c0004t0001g0221 a0002c0002t0002g0222 a0002c0002t0002g0223 others(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 | a0002c0002t0002g0220 | 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 | a0001c0001t0003g0012 a0001c0001t0003g0034 a0001c0001t0003g0045 others(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 | a0001c0001t0001g0085 | 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 | a0001c0001t0001g0219 a0002c0002t0002g0218 a0002c0002t0008g0217 others(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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0085 a0001c0001t0001g0101 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0126 others(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 | a0003c0003t0005g0080 a0005c0007t0009g0081 a0023c0034t0022g0079 |
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 | a0002c0002t0002g0213 | 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 | a0001c0001t0001g0219 a0002c0002t0002g0218 a0002c0002t0008g0217 others(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 | a0001c0001t0003g0012 a0001c0001t0003g0034 a0001c0001t0013g0028 others(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 | a0003c0003t0018g0078 | 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 | a0001c0001t0003g0012 a0001c0001t0013g0028 a0001c0001t0023g0009 others(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 | a0004c0005t0002g0121 | 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 | a0002c0002t0021g0006 a0002c0012t0004g0007 a0005c0007t0009g0081 |
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 | a0001c0001t0001g0147 a0001c0001t0001g0149 a0022c0023t0002g0148 |
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 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0126 others(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 | GTATA | 2 | a0001c0001t0010g0134 a0003c0003t0005g0075 |
2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-32-204_-32-201dup others(4): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 98092816 | ||||||
chr2:98092816 | G | GTATATA | 9 | a0001c0001t0001g0082 a0001c0001t0001g0198 a0001c0001t0001g0199 others(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 | a0001c0001t0001g0203 a0001c0001t0002g0204 a0002c0002t0002g0224 others(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 | a0001c0001t0001g0207 a0001c0001t0013g0028 a0011c0011t0001g0205 others(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 | a0002c0002t0002g0225 | 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 | G | GTATGTA | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-32-242_-32-241ins others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 98092816 | ||||||
chr2:98092816 | GTA | G | 37 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0157 a0001c0004t0003g0020 others(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 | a0001c0001t0003g0045 a0001c0001t0005g0046 a0001c0004t0003g0013 others(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 | a0001c0001t0003g0012 a0002c0002t0004g0030 a0002c0016t0020g0031 |
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 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0002c0002t0004g0011 |
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 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0152 a0017c0027t0002g0215 others(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 | a0001c0001t0003g0232 a0001c0001t0003g0238 a0002c0019t0011g0228 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0003c0003t0005g0080 | 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 | a0001c0001t0001g0139 a0001c0001t0007g0140 a0001c0001t0007g0141 others(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 | a0001c0001t0001g0138 | 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 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
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 | a0001c0001t0001g0208 | 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 | |||||||
chr2:98092860 | A | ATATATG | 2 | a0001c0001t0001g0209 a0002c0002t0002g0210 |
2 | HG01099.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-32-201_-32-200ins others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98092860 | |||||||
chr2:98092860 | A | ATATG | 2 | a0001c0001t0001g0211 a0002c0002t0002g0212 |
2 | HG00741.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.-32-201_-32-200ins others(4): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 1/27 | chr2 | 98092860 | |||||||
chr2:98092899 | A | G | 11 | a0001c0001t0001g0082 a0001c0001t0001g0161 a0001c0001t0001g0175 others(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 | a0001c0001t0003g0012 a0001c0001t0003g0045 a0001c0001t0003g0236 others(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 | a0003c0003t0001g0191 a0003c0003t0001g0192 a0003c0003t0001g0194 others(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 | a0001c0001t0001g0143 | 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 | a0016c0026t0002g0202 | 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 | a0003c0003t0003g0048 a0003c0003t0003g0050 a0003c0003t0003g0051 others(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 | a0001c0001t0003g0012 a0001c0001t0003g0045 a0001c0001t0003g0236 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | a0003c0017t0005g0055 | 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 | a0001c0001t0006g0173 a0001c0001t0006g0190 |
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 | a0009c0022t0003g0038 | 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 | a0002c0002t0002g0222 a0002c0002t0002g0223 a0002c0002t0002g0224 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0128 a0001c0001t0001g0129 others(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 | a0001c0001t0003g0238 a0008c0010t0009g0239 a0008c0010t0009g0240 |
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 | a0001c0004t0003g0025 a0001c0004t0003g0026 |
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 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0128 others(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 | a0003c0017t0005g0055 | 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 | a0003c0003t0003g0067 a0003c0003t0003g0070 a0003c0003t0003g0071 others(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 | a0003c0003t0003g0067 a0003c0003t0003g0070 a0003c0003t0003g0071 others(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 | a0001c0001t0023g0009 a0002c0002t0024g0008 |
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 | a0016c0026t0002g0202 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0003c0003t0001g0191 a0003c0003t0001g0192 a0003c0003t0001g0194 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0149 a0001c0001t0016g0146 |
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 | a0001c0001t0001g0083 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
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 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(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 | a0002c0002t0002g0158 a0002c0002t0002g0160 a0002c0002t0002g0186 |
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 | a0001c0001t0015g0127 | 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 | a0001c0004t0003g0017 a0002c0006t0004g0021 |
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 | a0003c0003t0001g0191 a0003c0003t0001g0192 a0003c0003t0001g0194 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0006c0008t0003g0229 | 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 | a0002c0002t0002g0159 | 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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0003g0012 a0001c0001t0003g0045 a0001c0001t0003g0236 others(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 | a0011c0011t0001g0166 | 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 | a0001c0001t0003g0012 a0001c0001t0003g0236 a0001c0001t0013g0028 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0136 a0001c0001t0001g0137 others(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 | a0001c0004t0003g0010 a0001c0004t0004g0018 |
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 | a0001c0001t0001g0083 a0002c0012t0011g0226 |
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 | a0001c0001t0001g0178 a0001c0001t0003g0034 a0001c0001t0003g0236 others(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 | a0001c0001t0003g0232 a0001c0001t0003g0238 a0002c0019t0011g0228 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0083 a0002c0012t0011g0226 |
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 | a0002c0002t0002g0158 a0002c0002t0002g0160 a0002c0002t0002g0186 |
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 | a0001c0001t0001g0185 a0001c0001t0001g0200 a0002c0002t0002g0213 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0003c0003t0003g0069 | 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 | a0001c0001t0003g0232 a0001c0001t0003g0238 a0002c0002t0004g0030 others(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 | a0003c0003t0018g0078 | 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 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
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 | a0001c0001t0001g0179 | 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 | a0001c0001t0001g0180 | 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 | a0001c0001t0001g0180 | 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 | a0001c0001t0001g0147 | 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 | a0001c0001t0001g0162 | 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 | a0003c0003t0001g0191 a0003c0003t0001g0192 a0003c0003t0001g0194 others(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 | a0001c0001t0001g0180 | 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 | a0002c0002t0004g0030 a0002c0002t0004g0032 a0002c0002t0004g0033 others(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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0083 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0165 others(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 | a0002c0002t0002g0222 a0002c0002t0002g0223 a0002c0002t0002g0224 others(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 | a0001c0001t0010g0134 | 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 | a0002c0002t0002g0181 | 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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0128 others(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 | a0001c0001t0003g0045 a0001c0001t0005g0046 a0020c0029t0004g0047 |
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 | a0002c0006t0002g0109 a0009c0015t0001g0108 |
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 | a0001c0001t0001g0083 a0001c0001t0003g0045 a0001c0001t0003g0236 others(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 | a0002c0002t0004g0002 a0002c0002t0004g0005 a0002c0002t0021g0006 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0128 a0001c0001t0001g0129 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0003g0012 a0001c0001t0003g0045 a0001c0001t0003g0236 others(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 | a0002c0002t0004g0030 a0002c0002t0004g0032 a0002c0002t0004g0033 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0002c0002t0002g0181 | 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 | a0002c0002t0002g0189 | 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 | a0002c0002t0002g0222 a0002c0002t0002g0223 a0002c0002t0002g0224 others(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 | a0014c0030t0002g0116 | 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 | a0001c0001t0001g0083 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0024c0031t0014g0092 | 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 | a0001c0001t0010g0134 | 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 | a0003c0003t0001g0191 a0003c0003t0001g0192 a0003c0003t0001g0194 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0184 |
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 | a0001c0001t0003g0012 a0001c0001t0003g0045 a0001c0001t0003g0236 others(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 | a0003c0003t0001g0191 a0003c0003t0001g0192 a0003c0003t0001g0194 others(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 | a0003c0003t0001g0191 a0003c0003t0001g0192 a0003c0003t0001g0194 others(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 | a0001c0001t0003g0012 a0001c0001t0003g0045 a0001c0001t0003g0236 others(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 | a0001c0001t0001g0207 | 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 | a0008c0010t0009g0239 a0008c0010t0009g0240 |
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 | a0001c0001t0001g0176 | 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 | a0016c0026t0002g0202 | 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 | a0001c0001t0001g0083 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | a0003c0003t0005g0060 | 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 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0150 others(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 | a0002c0002t0004g0003 a0002c0002t0004g0004 |
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 | a0019c0014t0017g0122 | 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 | a0016c0026t0002g0202 | 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 | a0001c0001t0003g0236 a0001c0001t0013g0028 a0002c0002t0003g0024 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0002c0002t0002g0189 | 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 | a0001c0001t0003g0012 a0001c0001t0003g0045 a0001c0001t0003g0236 others(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 | a0001c0001t0023g0009 a0002c0002t0024g0008 |
2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.291+117T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | chr2 | 98115863 | |||||||
chr2:98115920 | GA | G | 2 | a0001c0001t0001g0083 a0002c0012t0011g0226 |
2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.291+176delA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 98115920 | ||||||
chr2:98116120 | A | G | 1 | a0001c0001t0006g0190 | 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 | a0001c0004t0003g0017 a0002c0006t0004g0021 |
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 | a0001c0001t0023g0009 a0002c0002t0024g0008 |
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 | a0001c0001t0001g0083 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0115 | 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 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0128 others(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 | a0002c0006t0002g0109 a0002c0006t0004g0237 a0009c0015t0001g0108 |
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 | a0003c0003t0003g0073 | 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 | a0001c0001t0001g0083 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | a0002c0002t0002g0164 | 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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0006c0008t0003g0235 | 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 | a0002c0002t0004g0030 a0002c0002t0004g0032 a0002c0002t0004g0033 others(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 | a0002c0002t0002g0210 | 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 | a0001c0001t0001g0083 a0001c0001t0001g0165 a0002c0002t0001g0182 others(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 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0001t0001g0152 a0002c0012t0011g0226 |
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 | a0001c0001t0001g0136 | 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 | a0002c0002t0004g0030 a0002c0002t0004g0032 a0002c0002t0004g0033 others(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 | a0004c0005t0002g0088 a0004c0005t0002g0093 a0004c0005t0002g0094 others(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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0015c0024t0001g0099 | 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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0016c0026t0002g0202 | 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 | a0001c0001t0001g0083 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0002c0002t0002g0210 | 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 | a0001c0001t0001g0083 a0002c0012t0011g0226 |
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 | a0002c0002t0004g0002 a0002c0002t0004g0005 a0002c0002t0021g0006 others(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 | a0001c0001t0003g0012 a0001c0001t0003g0045 a0001c0001t0003g0236 others(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 | |||||||
chr2:98121839 | AGTCT | A | 2 | a0001c0001t0001g0083 a0002c0012t0011g0226 |
2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.702+382_702+385del others(4): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98121839 | |||||||
chr2:98121855 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0209 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0019c0014t0017g0122 | 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 | a0001c0001t0001g0101 a0001c0001t0001g0209 |
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 | a0003c0003t0003g0068 | 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 | a0012c0013t0002g0100 | 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 | a0003c0003t0003g0069 | 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 | a0001c0001t0001g0083 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0002c0002t0002g0164 | 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 | a0001c0001t0001g0197 a0004c0005t0002g0088 a0004c0005t0002g0093 others(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 | a0001c0001t0003g0232 a0001c0001t0003g0238 a0006c0008t0003g0229 others(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 | a0003c0032t0003g0061 | 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 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0003g0012 others(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 | a0019c0014t0017g0122 | 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 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0003g0012 others(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 | a0004c0005t0002g0177 | 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 | a0014c0030t0002g0116 | 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 | a0003c0032t0003g0061 | 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 | a0003c0003t0003g0050 | 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 | a0002c0002t0004g0036 a0002c0002t0004g0037 |
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 | a0001c0001t0001g0083 a0001c0001t0001g0128 a0001c0001t0001g0129 others(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 | a0003c0003t0001g0191 | 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 | a0003c0003t0001g0191 a0003c0003t0001g0192 a0003c0003t0001g0194 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0136 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0184 |
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 | a0001c0004t0001g0221 a0001c0004t0003g0010 a0001c0004t0003g0013 others(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 | a0003c0003t0003g0067 a0003c0003t0003g0070 a0003c0003t0003g0071 others(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 | a0002c0002t0004g0032 a0026c0021t0003g0042 |
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 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0003g0012 others(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 | a0001c0001t0001g0197 a0004c0005t0002g0120 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0184 |
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 | a0002c0002t0002g0164 | 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 | a0003c0003t0003g0073 a0025c0033t0006g0206 |
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 | a0001c0001t0003g0045 a0001c0001t0005g0046 a0020c0029t0004g0047 |
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 | |||||||
chr2:98127592 | GC | G | 2 | a0001c0001t0005g0046 a0020c0029t0004g0047 |
2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.703-646delC | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 5/27 | chr2 | 98127592 | |||||||
chr2:98127593 | C | CG | 25 | a0001c0001t0001g0083 a0001c0001t0001g0107 a0001c0001t0001g0113 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0133 a0001c0001t0001g0161 others(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 | a0001c0001t0003g0045 a0002c0012t0011g0226 a0003c0003t0001g0191 |
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 | 41 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0125 others(38): Show |
41 | HG00609.hp1 HG00639.hp2 HG01070.hp1 others(38): 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 | a0001c0001t0001g0132 a0001c0001t0001g0138 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0128 a0001c0001t0001g0129 others(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 | a0001c0001t0003g0045 | 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 | a0001c0001t0005g0046 a0002c0012t0011g0226 a0020c0029t0004g0047 |
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 | a0003c0003t0005g0080 | 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 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0003g0012 others(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 | a0007c0009t0002g0086 a0007c0009t0002g0087 a0012c0013t0002g0100 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0001c0001t0010g0134 a0021c0018t0010g0124 |
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 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0138 a0002c0002t0002g0222 a0002c0002t0002g0223 others(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 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(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 | a0001c0001t0001g0139 a0001c0001t0010g0134 a0005c0007t0012g0052 others(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 | a0003c0003t0003g0048 a0003c0003t0003g0051 a0003c0003t0003g0054 others(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 | a0001c0001t0003g0045 a0001c0001t0003g0236 a0001c0001t0013g0028 others(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 | a0002c0002t0004g0003 a0002c0002t0004g0004 a0002c0002t0021g0006 others(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 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0003g0012 others(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 | a0003c0003t0001g0191 | 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 | a0002c0002t0004g0030 a0002c0002t0004g0032 a0002c0002t0004g0033 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0136 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0132 others(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 | a0001c0001t0001g0083 a0003c0003t0001g0192 a0003c0003t0001g0194 others(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 | a0001c0001t0001g0085 a0002c0019t0011g0228 a0003c0003t0003g0074 others(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 | a0003c0003t0003g0049 a0003c0003t0003g0056 a0003c0003t0003g0065 others(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 | a0001c0001t0001g0133 a0001c0001t0001g0197 a0003c0003t0003g0076 others(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 | a0004c0005t0002g0088 a0004c0005t0002g0120 |
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 | a0001c0001t0001g0178 a0001c0004t0003g0017 a0001c0004t0004g0023 others(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 | AGTGT | 2 | a0002c0006t0004g0015 a0002c0006t0004g0016 |
2 | NA18946.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.872+848_872+851dup others(4): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 98129224 | ||||||
chr2:98129224 | A | AGTGTGTG others(1): Show |
2 | a0001c0001t0001g0104 a0002c0002t0002g0103 |
2 | HG00408.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.872+844_872+851dup others(8): 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 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
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 | a0001c0001t0001g0115 a0001c0001t0001g0208 a0002c0002t0002g0105 others(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 | a0001c0001t0001g0107 a0002c0002t0002g0001 |
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 | a0001c0001t0023g0009 a0001c0004t0013g0029 a0002c0002t0002g0091 others(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 | a0001c0001t0001g0101 a0001c0001t0001g0209 a0001c0004t0003g0025 others(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 | a0001c0001t0003g0045 a0002c0002t0004g0002 a0002c0002t0004g0003 others(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 | a0002c0002t0004g0002 a0002c0002t0004g0003 a0002c0002t0004g0004 others(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 | a0002c0002t0004g0002 a0002c0002t0021g0006 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0004t0001g0221 | 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 | a0001c0004t0001g0221 | 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 | a0002c0002t0004g0030 a0002c0002t0004g0032 a0002c0002t0004g0033 others(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 | a0003c0003t0003g0056 a0005c0007t0004g0066 a0023c0034t0022g0079 |
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 | a0001c0001t0001g0157 a0001c0001t0001g0199 |
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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0114 | 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 | a0002c0002t0004g0032 a0026c0021t0003g0042 |
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 | a0002c0006t0002g0109 a0009c0015t0001g0108 |
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 | a0001c0001t0001g0207 | 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 | a0001c0001t0001g0111 | 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 | a0001c0001t0001g0136 | 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 | a0001c0004t0003g0017 a0002c0006t0004g0021 |
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 | a0003c0003t0003g0068 | 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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0001c0001t0003g0045 a0001c0001t0003g0236 a0001c0001t0005g0046 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0002c0002t0008g0171 | 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 | a0012c0013t0002g0100 | 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 | a0003c0003t0003g0056 | 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 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0002c0002t0008g0171 a0002c0002t0008g0188 |
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 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0002c0002t0002g0220 | 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 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0128 others(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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | a0004c0005t0002g0120 | 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 | a0001c0001t0001g0145 | 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 | a0003c0003t0003g0073 a0025c0033t0006g0206 |
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 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0002c0002t0002g0223 | 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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0199 others(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 | a0001c0001t0001g0114 a0001c0001t0001g0136 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0133 a0001c0001t0001g0137 a0001c0001t0001g0150 others(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 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0003g0012 others(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 | a0001c0001t0003g0232 a0003c0003t0003g0072 a0003c0003t0018g0078 others(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 | a0001c0001t0001g0133 a0001c0001t0003g0238 a0002c0002t0004g0030 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0003c0003t0003g0048 a0003c0003t0003g0050 a0003c0003t0003g0051 others(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 | a0003c0003t0003g0048 a0003c0003t0003g0051 a0003c0003t0003g0054 others(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 | a0004c0005t0002g0120 | 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 | a0001c0001t0001g0200 | 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 | a0002c0002t0002g0119 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.988+1676G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98135615 | |||||||
chr2:98135673 | CGTT | C | 2 | a0004c0005t0002g0095 a0004c0005t0002g0121 |
2 | NA18999.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.988+1738_988+1740d others(5): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 98135673 | ||||||
chr2:98136576 | C | T | 2 | a0001c0001t0003g0236 a0001c0001t0013g0028 |
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 | a0001c0001t0003g0236 a0001c0001t0013g0028 a0001c0001t0023g0009 others(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 | a0001c0001t0003g0045 a0001c0001t0003g0236 a0001c0001t0005g0046 others(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 | a0001c0004t0001g0221 | 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 | a0001c0001t0001g0200 | 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 | a0002c0002t0001g0098 | 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 | a0003c0003t0003g0062 a0003c0003t0003g0065 |
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 | a0001c0001t0001g0178 | 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 | a0019c0014t0017g0122 | 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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | a0001c0001t0003g0045 a0001c0001t0003g0236 a0001c0001t0005g0046 others(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 | a0001c0001t0003g0045 a0001c0001t0003g0236 a0001c0001t0005g0046 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0128 others(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 | a0001c0001t0001g0110 | 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 | a0003c0003t0005g0075 | 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 | a0002c0002t0004g0030 a0002c0002t0004g0032 a0002c0002t0004g0033 others(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 | a0001c0001t0003g0045 a0001c0001t0003g0236 a0001c0001t0005g0046 others(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 | a0002c0002t0004g0002 a0002c0002t0004g0005 a0002c0002t0021g0006 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0149 a0001c0001t0016g0146 |
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 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0003c0003t0001g0191 a0003c0003t0001g0192 a0003c0003t0001g0194 others(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 | a0010c0036t0003g0063 | 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 | a0001c0001t0001g0165 | 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 | a0003c0003t0003g0056 | 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 | a0001c0001t0003g0045 a0001c0001t0003g0236 a0001c0001t0005g0046 others(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 | a0001c0004t0003g0025 a0001c0004t0003g0026 |
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 | a0001c0004t0003g0025 a0001c0004t0003g0026 |
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 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0128 others(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 | a0001c0001t0001g0195 | 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 | a0001c0004t0003g0017 a0002c0006t0004g0021 |
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 | a0001c0001t0023g0009 a0002c0002t0024g0008 |
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 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0128 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0180 | 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 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0016c0026t0002g0202 | 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 | a0001c0001t0001g0133 a0003c0003t0001g0191 a0003c0003t0001g0192 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0187 | 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 | a0016c0026t0002g0202 | 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 | a0001c0001t0001g0187 | 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 | a0007c0009t0002g0130 a0007c0009t0002g0131 |
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 | a0001c0004t0001g0221 | 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 | a0001c0001t0001g0126 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0003g0045 a0001c0001t0003g0236 a0001c0001t0005g0046 others(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 | a0001c0001t0001g0133 a0001c0001t0003g0232 a0001c0001t0003g0238 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0011c0011t0001g0205 | 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 | a0001c0001t0003g0045 a0001c0001t0003g0236 a0001c0001t0005g0046 others(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 | a0001c0001t0001g0104 a0001c0001t0001g0118 a0001c0001t0001g0128 others(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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0002c0002t0004g0030 a0002c0002t0004g0032 a0002c0002t0004g0033 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0003g0012 others(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 | a0019c0014t0017g0122 | 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 | a0001c0004t0003g0017 a0002c0006t0004g0021 |
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 | a0002c0002t0002g0105 | 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 | a0001c0001t0003g0012 a0001c0001t0003g0236 a0001c0001t0013g0028 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0128 others(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 | a0001c0001t0001g0133 a0001c0001t0003g0045 a0001c0001t0003g0232 others(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 | a0001c0001t0007g0140 a0001c0001t0007g0141 a0001c0001t0007g0142 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
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 | a0001c0001t0001g0083 a0001c0001t0023g0009 a0002c0002t0024g0008 others(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 | a0004c0005t0002g0177 | 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 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0128 others(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 | a0001c0004t0003g0044 a0003c0003t0003g0050 |
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 | a0001c0001t0001g0083 a0001c0001t0023g0009 a0002c0002t0024g0008 others(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 | a0001c0001t0001g0203 | 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 | 65 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0101 others(62): Show |
65 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(62): 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 | a0003c0003t0003g0048 a0003c0003t0003g0054 a0003c0003t0005g0058 others(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 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0003g0232 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0138 a0001c0001t0001g0139 others(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 | a0002c0002t0002g0112 | 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 | a0001c0001t0001g0083 a0001c0001t0023g0009 a0002c0002t0024g0008 others(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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0001c0001t0001g0083 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | a0011c0011t0001g0166 | 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 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0019c0014t0017g0122 |
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 | a0014c0030t0002g0116 | 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 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0019c0014t0017g0122 |
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 | a0001c0001t0003g0236 a0001c0001t0013g0028 a0002c0002t0003g0024 others(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 | a0007c0009t0002g0086 a0007c0009t0002g0087 |
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 | a0006c0008t0003g0229 a0006c0008t0003g0230 a0006c0008t0003g0233 others(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 | a0006c0008t0003g0229 a0006c0008t0003g0230 a0006c0008t0003g0233 others(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 | a0002c0002t0004g0036 a0002c0002t0004g0037 |
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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | a0001c0001t0001g0101 a0001c0001t0001g0209 |
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 | a0001c0001t0023g0009 a0002c0002t0024g0008 |
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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | a0001c0001t0023g0009 a0002c0002t0024g0008 a0016c0026t0002g0202 |
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 | a0002c0002t0002g0090 a0002c0002t0002g0091 |
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 | a0005c0007t0009g0081 | 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 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
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 | a0006c0008t0003g0229 a0006c0008t0003g0230 a0006c0008t0003g0233 others(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 | a0001c0001t0001g0167 a0001c0001t0001g0169 a0002c0002t0002g0168 others(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 | a0023c0034t0022g0079 | 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 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0019c0014t0017g0122 |
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 | a0001c0001t0001g0082 a0001c0001t0001g0195 |
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 | a0001c0001t0001g0126 a0001c0001t0001g0179 |
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 | a0001c0001t0001g0114 | 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 | a0001c0001t0003g0045 a0001c0001t0005g0046 a0020c0029t0004g0047 |
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 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0128 others(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 | 73 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0101 others(70): Show |
73 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(70): 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 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0128 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | a0003c0003t0018g0078 | 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 | a0020c0029t0004g0047 | 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 | 191 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(188): Show |
191 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.989-5810C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98157041 | |||||||
chr2:98157429 | C | CATATA | 2 | a0001c0001t0007g0141 a0001c0001t0007g0142 |
2 | NA18963.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.989-5413_989-5409d others(7): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 98157429 | ||||||
chr2:98157959 | T | A | 4 | a0006c0008t0003g0229 a0006c0008t0003g0230 a0006c0008t0003g0233 others(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 | a0004c0005t0002g0102 | 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 | a0001c0001t0001g0083 a0001c0001t0023g0009 a0002c0002t0024g0008 others(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 | 79 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0101 others(76): Show |
79 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(76): 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | 79 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0101 others(76): Show |
79 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.989-4196C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | chr2 | 98158655 | |||||||
chr2:98158710 | TG | T | 191 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(188): Show |
191 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(188): 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 | 79 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0101 others(76): Show |
79 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(76): 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 | a0003c0003t0003g0067 | 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 | |||||||
chr2:98159185 | CTG | C | 2 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.989-3663_989-3662d others(4): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 98159185 | ||||||
chr2:98159222 | C | T | 1 | a0016c0026t0002g0202 | 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 | a0001c0001t0001g0085 | 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 | a0001c0001t0001g0133 a0001c0001t0001g0207 a0002c0002t0004g0036 others(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 | a0001c0001t0001g0126 | 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 | a0001c0001t0001g0083 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | 81 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0101 others(78): Show |
81 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(78): 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 | a0001c0001t0001g0083 a0001c0001t0001g0118 a0001c0001t0001g0169 others(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 | a0010c0035t0004g0064 a0010c0036t0003g0063 |
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 | a0001c0001t0001g0125 | 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 | a0001c0001t0001g0133 a0001c0001t0001g0207 a0002c0002t0004g0036 others(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 | a0003c0003t0005g0075 | 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 | a0026c0021t0003g0042 | 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 | a0011c0011t0001g0205 | 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 | 79 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0101 others(76): Show |
79 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(76): 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 | a0001c0001t0001g0113 a0002c0002t0002g0112 |
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 | a0001c0001t0001g0083 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0111 a0001c0001t0001g0138 a0001c0001t0001g0139 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | 166 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(163): Show |
166 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(163): 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 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0019c0014t0017g0122 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0006c0008t0003g0229 a0006c0008t0003g0233 a0006c0008t0003g0234 others(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 | a0001c0001t0001g0083 a0001c0001t0023g0009 a0002c0002t0004g0002 others(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 | a0006c0008t0003g0229 a0006c0008t0003g0230 a0006c0008t0003g0233 others(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 | a0001c0001t0001g0133 a0001c0001t0001g0149 a0001c0001t0001g0207 others(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 | 168 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(165): Show |
168 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(165): 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 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0128 others(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 | a0001c0001t0001g0083 a0001c0001t0023g0009 a0002c0002t0024g0008 others(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 | a0002c0002t0001g0182 | 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 | a0016c0026t0002g0202 | 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 | a0002c0002t0002g0112 | 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 | a0023c0034t0022g0079 | 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 | a0001c0004t0003g0017 a0002c0006t0004g0021 |
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 | a0001c0001t0001g0198 | 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 | a0023c0034t0022g0079 | 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 | a0001c0001t0001g0133 a0001c0001t0001g0207 a0002c0002t0004g0036 others(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 | a0003c0003t0003g0074 | 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 | a0023c0034t0022g0079 | 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 | a0002c0002t0004g0002 a0002c0002t0004g0005 a0002c0002t0021g0006 |
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 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0003g0012 others(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 | a0023c0034t0022g0079 | 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 | a0016c0026t0002g0202 | 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 | 72 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0101 others(69): Show |
72 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(69): 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 | a0003c0003t0003g0062 | 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 | a0002c0002t0002g0159 | 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 | a0006c0008t0003g0229 a0006c0008t0003g0230 a0006c0008t0003g0233 others(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 | a0003c0003t0018g0078 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0133 a0001c0001t0001g0207 a0002c0002t0004g0036 others(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 | a0023c0034t0022g0079 | 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 | a0001c0001t0001g0179 | 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 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0019c0014t0017g0122 |
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 | a0001c0001t0001g0196 a0003c0032t0003g0061 a0006c0008t0003g0229 others(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 |
64 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0101 others(61): Show |
64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): 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 | a0001c0001t0001g0126 a0001c0001t0001g0176 a0001c0001t0001g0179 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0128 a0001c0001t0001g0129 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0132 a0001c0001t0001g0133 others(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 | a0001c0001t0001g0151 a0001c0001t0003g0236 a0001c0001t0013g0028 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0150 a0001c0001t0003g0232 |
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 | a0007c0009t0002g0086 a0007c0009t0002g0087 |
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 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0023c0034t0022g0079 | 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 | 165 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(162): Show |
165 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(162): 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 | a0007c0009t0002g0086 a0007c0009t0002g0087 |
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 | a0004c0005t0002g0088 a0004c0005t0002g0093 a0004c0005t0002g0094 others(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 | a0001c0004t0003g0013 a0001c0004t0003g0020 a0001c0004t0003g0025 others(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 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0003g0232 others(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 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0003g0232 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0133 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0185 a0001c0001t0001g0198 others(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 | a0002c0002t0004g0032 a0026c0021t0003g0042 |
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 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0104 others(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 | a0001c0001t0003g0045 a0001c0001t0005g0046 a0001c0001t0023g0009 others(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 | a0001c0001t0001g0175 a0001c0001t0001g0211 a0001c0004t0001g0221 |
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 | a0001c0001t0001g0110 | 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 | a0023c0034t0022g0079 | 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 | a0002c0002t0008g0171 | 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 | a0006c0008t0003g0229 a0006c0008t0003g0230 a0006c0008t0003g0233 others(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 | a0001c0001t0001g0126 | 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 | 81 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0101 others(78): Show |
81 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(78): 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0001c0001t0001g0082 a0001c0001t0001g0126 a0001c0001t0001g0133 others(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 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0183 others(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 | a0001c0001t0001g0107 a0002c0002t0004g0032 a0002c0006t0004g0016 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0150 a0001c0001t0001g0151 others(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 | 23 | a0001c0001t0001g0123 a0001c0001t0001g0132 a0001c0004t0003g0020 others(20): Show |
23 | HG00639.hp2 HG01070.hp1 HG01071.hp2 others(20): 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 | a0001c0001t0001g0138 a0001c0001t0001g0156 a0001c0001t0003g0232 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0129 others(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 | a0001c0001t0001g0084 a0006c0008t0003g0229 a0006c0008t0003g0230 others(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 | a0019c0014t0017g0122 | 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 | a0018c0028t0002g0216 | 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 | a0006c0008t0003g0229 a0006c0008t0003g0230 a0006c0008t0003g0233 others(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 | a0002c0002t0004g0002 a0002c0002t0004g0005 a0002c0002t0021g0006 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | 75 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0101 others(72): Show |
75 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(72): 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 | a0023c0034t0022g0079 | 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 | a0016c0026t0002g0202 | 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 | a0006c0008t0003g0234 | 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 | 161 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(158): Show |
161 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(158): 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 | a0005c0007t0004g0066 | 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 | a0003c0003t0003g0072 a0003c0003t0003g0076 |
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 | a0023c0034t0022g0079 | 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 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0019c0014t0017g0122 |
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 | a0001c0001t0001g0133 a0001c0001t0001g0207 a0002c0002t0004g0036 others(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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1115-8722A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98172294 | |||||||
chr2:98172377 | 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 | a0001c0001t0001g0214 | 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 | a0001c0004t0003g0017 a0002c0006t0004g0015 a0002c0006t0004g0016 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0128 a0001c0001t0001g0129 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0128 others(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 | a0001c0001t0003g0045 a0001c0001t0005g0046 a0020c0029t0004g0047 |
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 | 82 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0101 others(79): Show |
82 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1115-7125C>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98173891 | |||||||
chr2:98173971 | G | GA | 82 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0101 others(79): Show |
82 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(79): 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 | a0001c0001t0001g0083 a0001c0001t0023g0009 a0002c0002t0004g0005 others(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 | a0002c0002t0002g0090 a0002c0002t0002g0091 |
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 | a0001c0001t0001g0133 a0001c0001t0001g0207 a0002c0002t0004g0036 others(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 | a0001c0001t0001g0219 | 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 | a0002c0012t0011g0226 a0002c0019t0011g0228 |
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 | a0002c0002t0002g0212 | 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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | a0001c0001t0001g0187 | 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 | 163 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(160): Show |
163 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(160): 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 | a0002c0002t0004g0002 a0002c0002t0021g0006 |
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 | a0001c0001t0001g0203 | 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 | a0001c0001t0003g0236 a0001c0001t0013g0028 a0002c0002t0003g0024 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0136 a0001c0001t0001g0137 others(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 | a0003c0003t0003g0068 a0003c0003t0003g0069 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0003c0003t0018g0078 | 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 | a0002c0002t0004g0005 a0002c0012t0011g0226 a0002c0019t0011g0228 others(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 | a0001c0001t0006g0190 | 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 | a0016c0026t0002g0202 | 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 | a0001c0001t0006g0190 | 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 | a0023c0034t0022g0079 | 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 | a0002c0002t0002g0181 | 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 | a0003c0003t0003g0048 a0003c0003t0003g0054 a0003c0003t0005g0057 others(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 | a0005c0007t0004g0066 | 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 | a0001c0001t0001g0114 a0001c0001t0001g0214 |
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 | a0023c0034t0022g0079 | 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 | a0001c0001t0001g0152 a0001c0001t0001g0155 a0001c0001t0001g0156 others(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 | a0001c0001t0001g0153 | 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 | 86 | a0001c0001t0001g0084 a0001c0001t0001g0113 a0001c0001t0001g0114 others(83): Show |
86 | HG00423.hp1 HG00639.hp1 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.1115-1687C>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98179329 | |||||||
chr2:98179410 | T | TG | 215 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(212): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): 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 | a0001c0001t0001g0084 | 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 | a0002c0002t0004g0004 a0005c0007t0019g0059 |
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 | 197 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0104 others(194): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): 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 | a0001c0001t0001g0138 a0003c0003t0003g0070 a0003c0003t0003g0077 others(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 | a0003c0003t0001g0191 | 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 | a0003c0003t0001g0191 | 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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0004g0005 others(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 | a0001c0001t0001g0149 a0001c0001t0001g0167 a0001c0001t0001g0169 others(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 | a0002c0002t0002g0212 | 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 | a0002c0002t0002g0210 | 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 | a0001c0001t0001g0113 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0110 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0187 a0002c0002t0003g0024 others(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 | a0003c0003t0001g0191 | 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 | a0003c0003t0001g0191 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0101 a0001c0001t0001g0104 others(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 | a0002c0006t0002g0109 a0002c0012t0004g0007 a0002c0016t0020g0031 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0002c0006t0002g0109 | 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 | a0002c0006t0002g0109 | 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | 78 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0123 others(75): Show |
78 | HG00423.hp1 HG00639.hp1 HG00735.hp2 others(75): 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 | a0004c0005t0002g0097 | 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 | a0001c0001t0001g0085 a0001c0001t0001g0107 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0083 a0002c0002t0003g0024 a0002c0002t0003g0027 others(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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0001c0001t0005g0046 a0003c0003t0003g0048 a0003c0003t0003g0054 others(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 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
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 | a0001c0001t0003g0238 a0002c0002t0004g0002 a0005c0007t0004g0066 others(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 | a0001c0001t0001g0083 a0002c0002t0003g0024 a0002c0002t0003g0027 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0128 a0001c0001t0001g0129 others(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 | a0001c0001t0001g0083 a0001c0001t0003g0238 a0002c0002t0003g0024 others(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 | a0001c0001t0003g0232 a0001c0004t0013g0029 |
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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0004g0005 others(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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0010c0036t0003g0063 | 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 | 12 | a0001c0001t0001g0125 a0001c0001t0001g0136 a0001c0001t0001g0137 others(9): Show |
12 | HG01099.hp2 HG02698.hp2 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.1115-33A>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 8/27 | chr2 | 98180983 | |||||||
chr2:98181281 | C | T | 146 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0101 others(143): Show |
146 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(143): 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 | a0002c0006t0002g0109 | 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0001c0001t0001g0083 a0001c0001t0001g0107 a0001c0001t0001g0110 others(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 | a0005c0007t0019g0059 | 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 | a0001c0001t0005g0046 | 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 | a0001c0001t0005g0046 | 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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0083 a0001c0001t0003g0238 a0002c0012t0004g0007 others(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 | a0004c0005t0002g0093 | 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 | a0001c0004t0003g0013 a0001c0004t0003g0025 a0001c0004t0003g0026 |
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 | a0001c0001t0001g0126 a0001c0004t0013g0029 a0002c0002t0004g0002 others(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 | a0001c0001t0001g0083 a0001c0001t0003g0238 a0002c0016t0020g0031 others(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 | a0018c0028t0002g0216 | 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 | a0017c0027t0002g0215 | 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 | a0001c0001t0001g0152 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0110 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0117 others(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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0001c0001t0001g0083 a0001c0001t0003g0238 a0005c0007t0004g0066 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0001t0001g0083 a0001c0001t0003g0238 a0002c0012t0004g0007 others(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 | 222 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(219): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): 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 | a0002c0002t0002g0158 a0002c0002t0002g0160 a0002c0002t0002g0163 others(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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0001c0001t0007g0140 a0001c0001t0007g0141 a0001c0001t0007g0142 |
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 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0132 others(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 | a0002c0002t0004g0003 a0002c0002t0004g0004 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0003c0003t0003g0051 others(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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0001c0001t0001g0175 | 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 | a0001c0001t0001g0165 | 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | 204 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(201): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1312-1881G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 9/27 | chr2 | 98186094 | |||||||
chr2:98186158 | A | AT | 182 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(179): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): 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 | a0001c0001t0001g0114 a0001c0001t0001g0128 a0001c0001t0001g0129 others(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 | a0002c0002t0003g0024 a0002c0002t0003g0027 |
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 | a0002c0002t0004g0003 a0002c0002t0004g0004 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0019c0014t0017g0122 | 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 | 222 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(219): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): 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 | a0001c0001t0001g0082 a0001c0001t0001g0101 a0001c0001t0001g0104 others(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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0023c0034t0022g0079 | 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0001c0001t0001g0083 a0001c0001t0003g0238 a0002c0012t0004g0007 others(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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0001c0001t0001g0113 a0002c0002t0002g0112 a0003c0003t0003g0051 others(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 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0003g0012 others(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 | 53 | a0001c0001t0001g0113 a0001c0001t0001g0123 a0001c0001t0001g0128 others(50): Show |
53 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(50): 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 | a0001c0001t0001g0175 a0001c0001t0001g0184 a0001c0001t0001g0207 others(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 | a0002c0012t0011g0226 a0003c0003t0003g0048 a0007c0009t0002g0086 others(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 | a0002c0002t0003g0027 a0002c0002t0004g0005 a0008c0010t0004g0227 |
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 | a0003c0003t0006g0193 | 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 | a0002c0002t0004g0003 a0002c0002t0004g0004 a0002c0002t0021g0006 |
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 | a0001c0001t0001g0083 a0001c0001t0001g0132 a0001c0001t0001g0165 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0110 a0001c0001t0001g0144 a0001c0001t0001g0150 others(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 | a0001c0001t0001g0167 a0001c0001t0001g0169 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | 228 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(225): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0001c0001t0001g0083 a0001c0001t0003g0238 a0002c0012t0004g0007 others(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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1466+210T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98188339 | |||||||
chr2:98188587 | TGTG | T | 2 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1466+461_1466+463d others(5): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 98188587 | ||||||
chr2:98188638 | G | A | 2 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0001c0001t0005g0046 | 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 | a0001c0001t0001g0083 a0001c0001t0003g0238 a0002c0012t0004g0007 others(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 | a0016c0026t0002g0202 | 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 | a0004c0005t0002g0088 | 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0012c0013t0002g0100 | 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0001c0001t0001g0110 a0001c0001t0001g0144 a0002c0002t0001g0089 others(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 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
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 | 87 | a0001c0001t0001g0107 a0001c0001t0001g0113 a0001c0001t0001g0114 others(84): Show |
87 | HG00423.hp1 HG00544.hp2 HG00639.hp1 others(84): 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 | a0001c0001t0001g0132 | 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 | a0001c0001t0001g0126 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1467-2145A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 10/27 | chr2 | 98190753 | |||||||
chr2:98190821 | G | A | 1 | a0016c0026t0002g0202 | 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | 228 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(225): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): 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 | a0001c0001t0003g0045 a0006c0008t0003g0229 a0020c0029t0004g0047 |
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 | a0003c0003t0003g0069 | 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 | 222 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(219): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): 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 | a0001c0001t0003g0045 a0006c0008t0003g0229 a0020c0029t0004g0047 |
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 | a0001c0001t0001g0083 a0001c0001t0003g0238 a0002c0012t0004g0007 others(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 | a0001c0001t0001g0209 | 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 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
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 | a0016c0026t0002g0202 | 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 | a0001c0001t0001g0083 a0001c0001t0003g0238 a0002c0012t0004g0007 others(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 | a0003c0003t0003g0050 | 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 | a0002c0002t0002g0163 | 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 | a0001c0001t0001g0083 a0001c0001t0003g0238 a0002c0012t0004g0007 others(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 | 222 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(219): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): 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 | a0001c0001t0001g0203 | 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 | a0002c0002t0004g0003 a0002c0002t0004g0004 a0002c0002t0021g0006 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0117 others(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 | a0003c0003t0003g0050 | 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 | a0012c0013t0002g0135 | 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | 141 | a0001c0001t0001g0084 a0001c0001t0001g0107 a0001c0001t0001g0110 others(138): Show |
141 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(138): 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 | a0003c0003t0003g0067 | 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 | a0001c0001t0003g0236 a0001c0001t0013g0028 |
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 | a0002c0002t0004g0003 a0002c0002t0004g0004 a0002c0002t0021g0006 |
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 | a0002c0002t0008g0171 a0002c0002t0008g0188 |
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 | a0004c0005t0002g0088 a0004c0005t0002g0095 a0004c0005t0002g0096 others(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 | a0001c0001t0001g0139 a0002c0002t0004g0002 |
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 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0101 others(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 | a0002c0002t0002g0105 | 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 | a0006c0008t0003g0230 a0006c0020t0003g0231 |
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 | a0008c0010t0009g0239 a0008c0010t0009g0240 a0019c0014t0017g0122 |
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 | a0001c0001t0001g0125 | 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | 202 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0085 others(199): Show |
202 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(199): 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 | a0010c0036t0003g0063 | 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0125 a0001c0001t0001g0136 a0001c0001t0001g0137 others(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 | a0003c0003t0003g0051 | 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | 162 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0085 others(159): Show |
162 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(159): 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 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0003g0236 others(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 | ||||||
chr2:98199097 | A | AT | 2 | a0001c0004t0003g0020 a0003c0003t0003g0071 |
2 | HG01346.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1737+4605_1737+460 others(5): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98199097 | |||||||
chr2:98199518 | G | A | 2 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | 209 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0085 others(206): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): 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 | a0001c0001t0001g0209 | 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 | a0001c0001t0001g0145 a0001c0001t0001g0203 |
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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0001c0001t0001g0123 a0001c0004t0004g0023 a0007c0009t0002g0086 others(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 | a0002c0012t0004g0007 a0002c0016t0020g0031 a0008c0010t0009g0239 others(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 | 99 | a0001c0001t0001g0083 a0001c0001t0001g0107 a0001c0001t0001g0113 others(96): Show |
99 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(96): 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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0138 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0101 a0001c0001t0001g0104 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0012c0013t0002g0135 | 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0178 | 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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0003c0003t0003g0069 | 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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0101 others(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 | a0002c0012t0004g0007 a0002c0016t0020g0031 |
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 | a0002c0012t0004g0007 a0002c0016t0020g0031 |
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 | a0002c0012t0004g0007 a0002c0016t0020g0031 |
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 | a0002c0012t0004g0007 a0002c0016t0020g0031 |
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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | a0003c0003t0006g0193 a0007c0009t0002g0130 a0007c0009t0002g0131 others(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 | a0001c0001t0001g0203 | 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 | a0016c0026t0002g0202 | 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 | a0018c0028t0002g0216 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(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 | a0002c0002t0004g0003 a0002c0002t0004g0004 a0002c0002t0004g0030 others(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 | a0002c0002t0004g0003 a0002c0002t0004g0004 a0002c0002t0004g0030 others(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 | a0001c0001t0001g0214 a0002c0002t0004g0003 a0002c0002t0004g0004 others(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 | a0001c0001t0001g0184 | 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 | 1 | a0003c0032t0003g0061 | 1 | HG03942.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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | 145 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(142): Show |
145 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(142): 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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0004g0002 others(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 | a0002c0002t0004g0005 a0008c0010t0004g0227 |
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 | a0002c0002t0002g0212 a0002c0002t0003g0024 a0002c0002t0003g0027 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0021c0018t0010g0124 | 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 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | 182 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(179): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1738-7336T>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98204594 | |||||||
chr2:98204639 | C | T | 182 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(179): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): 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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0001c0001t0005g0046 a0001c0001t0015g0127 a0003c0003t0003g0048 others(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 | a0005c0007t0012g0053 | 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 | 182 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(179): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): 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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | 1 | a0001c0001t0001g0198 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1738-6263T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98205667 | |||||||
chr2:98205770 | A | C | 182 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(179): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): 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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | 144 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(141): Show |
144 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(141): 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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0003c0003t0005g0075 | 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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0001c0001t0001g0104 a0001c0001t0001g0118 |
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 | a0007c0009t0002g0086 a0007c0009t0002g0087 |
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 | a0001c0001t0001g0114 a0001c0001t0001g0214 a0003c0003t0003g0050 |
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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0002c0012t0004g0007 a0002c0016t0020g0031 |
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 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0101 others(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 | a0002c0002t0001g0089 a0002c0002t0001g0098 a0002c0002t0002g0001 others(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 | a0003c0003t0003g0067 | 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 | a0003c0003t0003g0056 | 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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0022c0023t0002g0148 | 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 | 181 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0002c0002t0002g0159 | 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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0001c0001t0001g0200 | 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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | |||||||
chr2:98208579 | TC | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0169 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1738-3350delC | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | chr2 | 98208579 | |||||||
chr2:98208581 | A | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0169 |
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 | 143 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(140): Show |
143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): 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 | a0001c0001t0001g0219 | 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 | a0002c0002t0004g0002 a0020c0029t0004g0047 |
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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | 143 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(140): Show |
143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): 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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0001c0001t0001g0154 | 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 | a0002c0002t0002g0105 | 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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0002c0002t0002g0212 a0002c0002t0004g0035 a0002c0002t0004g0039 others(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 | |||||||
chr2:98210492 | CGTG | C | 2 | a0002c0006t0004g0016 a0002c0006t0004g0021 |
2 | HG00733.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.1738-1435_1738-143 others(7): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | 98210492 | ||||||
chr2:98210555 | C | A | 1 | a0016c0026t0002g0202 | 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 | a0003c0003t0001g0194 | 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 | 226 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(223): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): 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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0001c0004t0004g0023 a0007c0009t0002g0086 a0007c0009t0002g0087 |
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 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | 181 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): 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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0021c0018t0010g0124 | 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 | a0002c0002t0002g0212 a0002c0002t0003g0024 a0002c0002t0003g0027 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0001c0001t0001g0198 | 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 | 181 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1836+746A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 13/27 | chr2 | 98212774 | |||||||
chr2:98212978 | T | C | 6 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 |
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 | a0002c0002t0004g0005 a0008c0010t0004g0227 |
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 | a0002c0002t0002g0212 a0002c0002t0003g0024 a0002c0002t0003g0027 others(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 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0003g0012 others(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 | a0002c0002t0004g0003 a0002c0002t0004g0004 |
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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | a0002c0012t0011g0226 a0002c0019t0011g0228 |
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 | a0002c0012t0011g0226 a0002c0019t0011g0228 |
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 | a0001c0001t0003g0232 a0001c0001t0010g0134 a0001c0004t0013g0029 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0001c0001t0001g0115 | 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 | a0002c0002t0001g0098 | 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 | 228 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(225): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): 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 | a0001c0001t0001g0183 a0001c0001t0001g0187 a0001c0001t0001g0208 |
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 | a0001c0001t0001g0132 | 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 | a0002c0002t0002g0212 a0002c0002t0004g0005 a0002c0002t0004g0030 others(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 | a0001c0001t0001g0139 | 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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0011c0011t0001g0205 others(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 | a0002c0012t0004g0007 a0002c0016t0020g0031 |
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 | a0002c0002t0002g0212 a0002c0002t0003g0024 a0002c0002t0003g0027 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0001c0001t0001g0085 | 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0002c0002t0004g0005 a0005c0007t0009g0081 a0008c0010t0004g0227 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0138 a0001c0001t0001g0139 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0101 others(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 | 33 | a0001c0001t0001g0107 a0001c0001t0001g0110 a0001c0001t0001g0111 others(30): Show |
33 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(30): 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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0033 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0150 others(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 | a0001c0001t0001g0133 a0001c0001t0003g0034 a0011c0011t0001g0166 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | 175 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(172): Show |
175 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(172): 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 | a0006c0008t0003g0233 | 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 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0003g0012 others(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 | 181 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): 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 | a0001c0001t0001g0114 a0001c0001t0001g0214 a0001c0004t0003g0013 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0001c0001t0001g0199 | 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 | a0001c0004t0004g0023 a0007c0009t0002g0086 a0007c0009t0002g0087 |
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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0001c0001t0001g0149 a0001c0001t0001g0196 a0001c0001t0016g0146 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | 143 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(140): Show |
143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): 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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | |||||||
chr2:98219148 | A | AT | 2 | a0008c0010t0009g0239 a0008c0010t0009g0240 |
2 | HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2019+1120_2019+112 others(5): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98219148 | |||||||
chr2:98219152 | A | T | 2 | a0008c0010t0009g0239 a0008c0010t0009g0240 |
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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | 142 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(139): Show |
142 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(139): 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 | a0009c0015t0001g0108 a0009c0022t0003g0038 |
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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0002c0002t0002g0160 a0005c0007t0002g0174 |
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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0004g0040 others(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 | 188 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(185): Show |
188 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(185): 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 | a0001c0001t0001g0199 a0002c0002t0002g0186 a0002c0002t0004g0002 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | 143 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(140): Show |
143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): 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 | a0001c0001t0007g0140 a0001c0001t0007g0141 a0001c0001t0007g0142 |
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 | a0001c0001t0001g0143 a0001c0001t0001g0147 |
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 | a0004c0005t0002g0088 | 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 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0005c0007t0012g0052 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0022c0023t0002g0148 | 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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0021g0006 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0203 a0001c0001t0001g0219 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0016c0026t0002g0202 | 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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0002c0002t0004g0003 a0002c0002t0004g0004 a0005c0007t0009g0081 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0104 a0001c0001t0001g0118 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0001c0001t0001g0114 | 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 | 143 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(140): Show |
143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): 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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0033 others(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 | a0001c0001t0001g0084 | 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 | a0001c0001t0001g0214 | 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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0001c0001t0001g0178 | 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 | a0001c0001t0003g0045 | 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 | 143 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(140): Show |
143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): 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 | a0002c0002t0004g0011 a0005c0007t0009g0081 |
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 | a0001c0001t0005g0046 a0001c0001t0015g0127 a0003c0003t0003g0048 others(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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0002c0002t0002g0212 a0002c0002t0003g0024 a0002c0002t0003g0027 others(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 | 143 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(140): Show |
143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | 143 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(140): Show |
143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.2019+5033A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98223061 | |||||||
chr2:98223145 | A | T | 2 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | 140 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(137): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): 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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | a0010c0036t0003g0063 | 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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | 181 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): 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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0002c0012t0011g0226 a0002c0019t0011g0228 |
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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0001c0001t0001g0153 | 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 | 220 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(217): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): 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 | a0008c0010t0009g0239 a0008c0010t0009g0240 |
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 | a0002c0002t0002g0212 a0002c0002t0003g0024 a0002c0002t0003g0027 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0001c0001t0005g0046 a0001c0001t0015g0127 a0003c0003t0003g0048 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0001c0004t0003g0025 a0001c0004t0003g0026 |
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 | 143 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(140): Show |
143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0021g0006 others(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 | 181 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): 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 | a0002c0002t0001g0089 a0002c0002t0001g0098 a0002c0002t0002g0001 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0001c0001t0001g0180 | 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 | a0001c0001t0007g0140 a0001c0001t0007g0141 a0001c0001t0007g0142 |
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 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0144 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0101 others(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 | a0003c0003t0006g0193 | 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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | 143 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(140): Show |
143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): 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 | a0004c0005t0002g0094 | 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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0021g0006 others(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 | a0002c0002t0004g0005 a0008c0010t0004g0227 |
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 | 228 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(225): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.2020-331G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 14/27 | chr2 | 98227871 | |||||||
chr2:98228112 | A | G | 149 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(146): Show |
149 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(146): 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 | a0002c0002t0001g0089 a0002c0002t0001g0098 a0002c0002t0002g0001 others(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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0021g0006 others(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 | 148 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(145): Show |
148 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(145): 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 | a0001c0001t0001g0209 | 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 | a0002c0002t0004g0005 a0008c0010t0004g0227 |
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 | a0002c0002t0003g0024 a0002c0002t0003g0027 |
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 | a0002c0002t0001g0089 a0002c0002t0001g0098 a0015c0024t0001g0099 |
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 | a0006c0008t0003g0234 | 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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | 228 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(225): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): 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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0021g0006 others(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 | 143 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(140): Show |
143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.2151-280G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 15/27 | chr2 | 98229770 | |||||||
chr2:98229838 | T | C | 143 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(140): Show |
143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.2151-212T>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 15/27 | chr2 | 98229838 | |||||||
chr2:98229942 | A | T | 225 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(222): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): 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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | 1 | a0001c0001t0001g0198 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2151-42C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 15/27 | chr2 | 98230008 | |||||||
chr2:98230400 | G | A | 2 | a0002c0002t0004g0036 a0002c0002t0004g0037 |
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 | a0001c0001t0003g0232 a0001c0001t0010g0134 a0001c0004t0013g0029 others(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 | |||||||
chr2:98230537 | CA | C | 2 | a0002c0012t0011g0226 a0002c0019t0011g0228 |
2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2308+331delA | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 16/27 | chr2 | 98230537 | |||||||
chr2:98230831 | G | A | 44 | a0002c0002t0001g0089 a0002c0002t0001g0098 a0002c0002t0002g0001 others(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 | a0002c0002t0004g0003 a0002c0002t0004g0004 |
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 | a0002c0002t0004g0011 a0002c0006t0004g0016 a0002c0006t0004g0021 others(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 | a0002c0002t0001g0089 a0002c0002t0001g0098 a0002c0002t0002g0001 others(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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0001c0001t0001g0157 a0001c0001t0001g0199 a0003c0003t0003g0068 others(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 | 148 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(145): Show |
148 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(145): 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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | 181 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): 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 | a0003c0003t0003g0051 | 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 | a0002c0002t0004g0003 a0002c0002t0004g0004 |
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 | a0002c0002t0002g0213 | 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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0002c0012t0011g0226 a0002c0019t0011g0228 |
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 | a0002c0012t0004g0007 a0002c0016t0020g0031 |
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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0002c0002t0008g0188 | 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 | 181 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): 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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0021g0006 others(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 | 148 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(145): Show |
148 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(145): 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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0002c0002t0004g0005 a0008c0010t0004g0227 |
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 | 226 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(223): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): 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 | a0001c0001t0001g0123 a0001c0001t0001g0138 a0001c0001t0001g0139 others(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 | a0002c0002t0004g0002 a0020c0029t0004g0047 |
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 | a0001c0001t0001g0157 | 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 | 143 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(140): Show |
143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.2428+343C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 17/27 | chr2 | 98235110 | |||||||
chr2:98235168 | C | T | 181 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): 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 | a0007c0009t0002g0130 a0007c0009t0002g0131 a0012c0013t0002g0100 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0002c0002t0004g0003 a0002c0002t0004g0004 |
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 | 147 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(144): Show |
147 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(144): 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 | a0002c0002t0002g0212 a0002c0002t0003g0024 a0002c0002t0003g0027 others(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 | 181 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): 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 | a0001c0001t0001g0104 | 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 | a0002c0012t0011g0226 a0002c0019t0011g0228 |
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 | a0001c0001t0006g0173 | 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 | 148 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(145): Show |
148 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.2673+171C>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98236901 | |||||||
chr2:98236910 | G | T | 154 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(151): Show |
154 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(151): 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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0021g0006 others(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 | 148 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(145): Show |
148 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(145): 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 | a0001c0001t0003g0236 a0001c0001t0013g0028 |
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 | a0002c0002t0002g0091 | 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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0004g0003 others(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 | 154 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(151): Show |
154 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(151): 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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | a0001c0001t0001g0176 | 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 | a0002c0002t0002g0164 | 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 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0150 others(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 | a0003c0003t0003g0067 | 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 | 148 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(145): Show |
148 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(145): 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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | 148 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(145): Show |
148 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(145): 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 | a0002c0012t0011g0226 a0002c0019t0011g0228 |
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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0002c0002t0001g0089 a0002c0002t0001g0098 a0002c0002t0002g0001 others(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 | a0021c0018t0010g0124 | 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 | a0016c0026t0002g0202 | 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 | a0002c0012t0004g0007 a0002c0016t0020g0031 |
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 | 225 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(222): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): 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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | 181 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): 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 | a0002c0002t0004g0011 a0002c0006t0004g0016 a0002c0006t0004g0021 others(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 | a0003c0003t0003g0067 | 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 | a0001c0001t0003g0236 a0001c0001t0013g0028 |
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 | 142 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(139): Show |
142 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(139): 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 | a0002c0002t0003g0024 a0002c0002t0003g0027 |
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 | a0001c0001t0002g0204 a0002c0002t0002g0001 a0002c0002t0002g0090 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | 135 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(132): Show |
135 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(132): 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 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0150 a0001c0001t0001g0151 others(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 | 182 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(179): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.2673+4995A>G | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98241725 | |||||||
chr2:98241763 | A | G | 149 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(146): Show |
149 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(146): 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 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(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 | a0001c0001t0010g0134 | 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 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0012t0004g0007 a0002c0016t0020g0031 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0009c0015t0001g0108 a0009c0022t0003g0038 |
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 | 143 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(140): Show |
143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | 181 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): 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 | a0001c0001t0001g0184 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0003c0003t0003g0071 | 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 | a0002c0002t0002g0001 a0002c0002t0002g0103 a0002c0002t0002g0105 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0004g0003 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | 143 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(140): Show |
143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0012t0004g0007 a0002c0016t0020g0031 |
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 | 180 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(177): Show |
180 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(177): 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0021g0006 others(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 | a0001c0001t0001g0162 | 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0001c0001t0001g0196 | 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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0004g0005 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0002c0002t0002g0163 | 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 | a0001c0001t0001g0155 | 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 | 181 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): 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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0004g0003 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0006c0008t0003g0235 | 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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | 226 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(223): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.2674-2769G>C | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 19/27 | chr2 | 98247549 | |||||||
chr2:98247818 | A | G | 143 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(140): Show |
143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): 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 | a0001c0001t0001g0203 | 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0003c0003t0005g0075 | 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 | a0002c0006t0004g0237 a0007c0009t0002g0130 a0007c0009t0002g0131 |
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 | a0002c0002t0002g0220 a0002c0002t0008g0188 |
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 | a0001c0001t0001g0165 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0003c0003t0003g0069 a0005c0007t0009g0081 a0008c0010t0009g0239 others(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 | a0001c0004t0003g0020 a0002c0002t0004g0003 a0003c0003t0003g0056 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0104 a0001c0001t0001g0111 others(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 | 43 | a0001c0001t0001g0085 a0001c0001t0001g0101 a0001c0001t0001g0113 others(40): Show |
43 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(40): 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 | a0001c0001t0001g0107 a0001c0001t0001g0123 a0001c0001t0001g0128 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0129 others(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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0125 a0001c0001t0001g0196 a0001c0001t0002g0204 others(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 | a0001c0001t0003g0236 a0001c0001t0013g0028 a0002c0002t0002g0001 others(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 | a0002c0002t0002g0103 a0002c0002t0002g0218 |
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 | a0001c0001t0003g0232 a0002c0002t0002g0090 a0002c0002t0002g0105 others(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 | 200 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(197): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0203 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0147 | 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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | 230 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(227): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): 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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0004g0003 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0199 a0003c0003t0003g0068 |
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 | a0001c0001t0001g0147 | 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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0004g0003 others(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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | 181 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0002c0002t0004g0003 a0002c0002t0004g0004 a0005c0007t0019g0059 |
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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | 181 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0004c0005t0002g0102 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | 143 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(140): Show |
143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): 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 | a0002c0012t0011g0226 a0002c0019t0011g0228 |
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 | a0002c0002t0002g0119 | 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 | a0004c0005t0002g0102 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0005c0007t0019g0059 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0001c0001t0003g0236 a0001c0001t0013g0028 |
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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0002c0002t0002g0112 a0002c0002t0002g0168 a0002c0002t0002g0210 |
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 | a0001c0001t0001g0180 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0143 | 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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0138 a0001c0001t0001g0139 others(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 | 181 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): 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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0004g0003 others(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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0004g0003 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0003c0017t0005g0055 | 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 | a0002c0002t0004g0036 a0002c0002t0004g0037 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0012t0004g0007 a0002c0016t0020g0031 |
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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0004g0003 others(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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0024g0008 others(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 | a0002c0002t0004g0004 a0002c0002t0004g0005 a0002c0012t0004g0007 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0133 a0001c0001t0002g0204 a0001c0001t0016g0146 others(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 | 137 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(134): Show |
137 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(134): 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 | a0001c0001t0001g0083 a0001c0001t0001g0123 a0001c0001t0001g0126 others(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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0004g0003 others(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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0004g0003 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | 230 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(227): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): 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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | 143 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(140): Show |
143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): 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 | a0002c0002t0004g0032 a0002c0002t0004g0036 a0002c0002t0004g0037 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | 173 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(170): Show |
173 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(170): 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 | a0001c0001t0001g0136 a0002c0012t0011g0226 a0002c0019t0011g0228 others(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 | a0002c0012t0004g0007 a0002c0016t0020g0031 |
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 | a0001c0004t0003g0025 a0001c0004t0003g0026 |
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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | 142 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(139): Show |
142 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(139): 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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | 142 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(139): Show |
142 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(139): 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0003g0024 a0002c0002t0003g0027 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0012c0013t0002g0100 | 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 | a0004c0005t0002g0094 a0012c0013t0002g0100 a0012c0013t0002g0135 others(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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0002c0002t0004g0005 a0008c0010t0004g0227 |
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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | 181 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): 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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0004g0003 others(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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0002c0002t0008g0188 | 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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0004g0003 others(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 | a0002c0002t0004g0002 a0020c0029t0004g0047 |
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 | a0001c0001t0001g0154 | 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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0004g0003 others(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 | a0002c0002t0004g0003 a0002c0002t0004g0004 |
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 | a0001c0001t0006g0190 | 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 | a0001c0001t0001g0165 a0001c0004t0003g0017 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0004g0003 a0002c0002t0004g0004 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0015g0127 | 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 | a0001c0001t0007g0140 a0001c0001t0007g0141 a0001c0001t0007g0142 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0004g0003 a0002c0002t0004g0004 a0005c0007t0019g0059 others(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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0015c0024t0001g0099 | 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 | a0002c0002t0004g0003 a0002c0002t0004g0004 a0005c0007t0019g0059 others(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 | a0001c0001t0006g0190 | 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 | a0002c0002t0004g0022 a0002c0012t0011g0226 a0002c0019t0011g0228 others(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 | a0002c0002t0004g0003 a0002c0002t0004g0004 a0005c0007t0019g0059 others(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 | a0023c0034t0022g0079 | 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 | a0003c0003t0003g0070 | 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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0114 | 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 | a0002c0012t0011g0226 a0002c0019t0011g0228 |
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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0003g0232 a0001c0001t0010g0134 a0001c0004t0013g0029 others(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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0002c0002t0002g0106 a0002c0002t0002g0218 a0002c0002t0004g0003 others(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 | a0002c0002t0004g0005 a0008c0010t0004g0227 |
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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0002c0002t0001g0182 a0002c0002t0002g0112 a0002c0002t0002g0168 others(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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0021g0006 others(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 | a0001c0001t0001g0180 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0012t0004g0007 a0002c0016t0020g0031 |
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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0006c0008t0003g0235 | 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 | a0002c0002t0002g0090 | 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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0004g0003 others(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 | a0004c0005t0002g0088 | 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 | a0002c0012t0011g0226 a0002c0019t0011g0228 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0001c0001t0002g0204 | 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 | a0004c0005t0002g0095 a0004c0005t0002g0096 a0004c0005t0002g0097 others(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 | a0001c0001t0001g0138 | 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 | a0001c0001t0001g0138 | 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 | a0001c0001t0001g0138 | 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 | a0001c0001t0001g0138 a0002c0002t0003g0024 a0002c0002t0003g0027 others(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 | a0001c0001t0001g0138 | 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 | a0002c0002t0001g0182 a0002c0002t0008g0171 a0002c0002t0008g0188 others(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 | a0023c0034t0022g0079 | 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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0021g0006 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0002g0204 a0002c0002t0002g0222 a0002c0002t0002g0223 others(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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0001c0001t0006g0190 | 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 | a0002c0002t0003g0024 a0002c0002t0003g0027 |
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 | a0002c0002t0004g0022 a0002c0012t0011g0226 a0002c0019t0011g0228 others(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 | a0002c0012t0011g0226 a0002c0019t0011g0228 |
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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0004g0003 others(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 | a0007c0009t0002g0130 a0007c0009t0002g0131 |
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 | a0022c0023t0002g0148 | 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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0001c0001t0001g0207 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | |||||||
chr2:98267049 | A | G | 3 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0004c0005t0002g0102 | 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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0001c0001t0001g0129 a0001c0001t0001g0165 a0001c0001t0001g0201 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0003c0003t0003g0054 | 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 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0143 a0001c0001t0001g0147 |
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 | a0002c0002t0004g0005 a0008c0010t0004g0227 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0006c0008t0003g0234 | 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 | a0001c0001t0001g0178 | 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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0001c0001t0001g0136 a0001c0001t0023g0009 a0001c0004t0004g0018 others(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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0024c0031t0014g0092 | 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 | a0007c0009t0002g0086 a0007c0009t0002g0087 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0002c0002t0001g0182 a0002c0002t0008g0171 a0002c0002t0008g0188 others(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 | a0001c0001t0001g0084 a0003c0003t0003g0071 |
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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0025c0033t0006g0206 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0002c0002t0004g0005 a0008c0010t0004g0227 |
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 | a0001c0001t0001g0153 | 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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0014c0030t0002g0116 | 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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0012t0011g0226 a0002c0019t0011g0228 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0008c0010t0009g0239 a0008c0010t0009g0240 a0012c0013t0002g0100 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0004g0002 a0020c0029t0004g0047 |
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 | a0022c0023t0002g0148 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0111 a0001c0001t0001g0152 a0001c0001t0001g0154 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0004g0003 others(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 | |||||||
chr2:98271938 | A | AGAGGT | 2 | a0012c0013t0002g0135 a0014c0030t0002g0116 |
2 | HG00140.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.3045+1057_3045+106 others(9): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr2 | 98271938 | ||||||
chr2:98271976 | C | T | 3 | a0001c0001t0001g0185 a0001c0001t0001g0200 a0001c0001t0001g0208 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0003c0003t0003g0056 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0004t0004g0018 a0001c0004t0004g0023 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0004g0003 others(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 | 189 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0101 others(186): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0125 a0003c0003t0003g0065 a0003c0003t0003g0072 others(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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0002c0002t0001g0089 a0002c0002t0001g0098 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0012t0011g0226 a0002c0019t0011g0228 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0004g0003 a0002c0002t0004g0004 a0005c0007t0019g0059 |
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 | a0002c0002t0002g0163 | 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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0002c0002t0001g0089 a0002c0002t0001g0098 |
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 | a0014c0030t0002g0116 | 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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0002c0012t0011g0226 a0002c0019t0011g0228 |
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 | a0002c0002t0004g0005 a0008c0010t0004g0227 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0001c0001t0001g0183 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 others(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 | a0002c0002t0002g0159 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0001c0001t0001g0178 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0002c0012t0011g0226 a0002c0019t0011g0228 |
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 | a0001c0001t0001g0125 a0003c0003t0003g0065 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0125 | 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 | a0002c0002t0002g0103 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0002c0002t0004g0039 a0002c0002t0004g0041 |
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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0003c0003t0003g0070 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0002g0158 | 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 | a0001c0001t0001g0123 | 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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0001c0004t0004g0018 a0001c0004t0004g0023 a0007c0009t0002g0086 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0002g0158 a0002c0002t0002g0160 a0002c0002t0002g0186 others(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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0002c0002t0004g0003 a0002c0002t0004g0004 |
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 | a0002c0002t0003g0024 a0002c0002t0003g0027 a0002c0002t0004g0022 others(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 | a0001c0001t0001g0219 | 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 | a0025c0033t0006g0206 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0002g0105 | 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0002c0012t0011g0226 a0002c0019t0011g0228 |
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 | a0001c0001t0001g0203 | 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 | a0004c0005t0002g0088 a0004c0005t0002g0093 a0004c0005t0002g0094 others(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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0001c0001t0001g0084 | 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 | a0002c0002t0002g0212 a0002c0002t0003g0024 a0002c0002t0003g0027 others(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 | a0001c0001t0001g0084 a0003c0003t0003g0071 |
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 | a0001c0001t0001g0111 | 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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | a0001c0001t0001g0125 a0003c0003t0003g0065 a0003c0003t0003g0072 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0002g0204 a0002c0002t0001g0089 a0002c0002t0001g0098 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0012t0011g0226 a0002c0019t0011g0228 |
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 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0132 others(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 | a0001c0001t0001g0084 a0003c0003t0003g0071 |
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 | a0001c0001t0002g0204 a0002c0002t0001g0182 a0002c0002t0002g0001 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0003g0024 a0002c0002t0003g0027 |
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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0002c0002t0004g0005 a0008c0010t0004g0227 |
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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0001c0001t0001g0178 | 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 | a0003c0032t0003g0061 | 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0002g0204 a0002c0002t0001g0182 a0002c0002t0002g0001 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0002g0204 a0002c0002t0001g0182 a0002c0002t0002g0001 others(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 | a0023c0034t0022g0079 | 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 | a0001c0001t0002g0204 a0002c0002t0001g0182 a0002c0002t0002g0001 others(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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0002g0204 a0002c0002t0001g0182 a0002c0002t0002g0001 others(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 | a0002c0002t0004g0005 a0008c0010t0004g0227 |
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 | a0001c0001t0002g0204 a0002c0002t0001g0182 a0002c0002t0002g0001 others(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 | a0023c0034t0022g0079 | 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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0001c0001t0001g0128 a0001c0001t0001g0144 a0001c0001t0001g0152 others(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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | 3 | a0001c0001t0001g0143 a0001c0001t0001g0147 a0001c0001t0001g0198 |
3 | HG01099.hp2 HG02698.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.3046-8053G>A | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 22/27 | chr2 | 98282458 | |||||||
chr2:98282522 | C | A | 4 | a0001c0004t0004g0018 a0001c0004t0004g0023 a0007c0009t0002g0086 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0003c0003t0003g0062 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0196 | 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 | a0002c0002t0002g0106 a0002c0002t0002g0218 |
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 | a0001c0001t0002g0204 a0001c0004t0004g0018 a0001c0004t0004g0023 others(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 | |||||||
chr2:98283085 | G | A | 1 | a0001c0001t0001g0180 | 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0175 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0139 | 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0012t0004g0007 a0002c0012t0011g0226 a0002c0016t0020g0031 others(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 | a0001c0001t0003g0034 a0011c0011t0001g0166 a0011c0011t0001g0205 |
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 | a0002c0002t0002g0112 a0002c0002t0002g0168 a0002c0002t0002g0189 others(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 | a0001c0001t0002g0204 a0001c0004t0004g0018 a0001c0004t0004g0023 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0002g0204 | 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 | a0001c0001t0002g0204 a0002c0002t0001g0182 a0002c0002t0002g0001 others(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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0001c0001t0001g0132 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0024c0031t0014g0092 | 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 | a0001c0001t0001g0083 a0001c0001t0003g0045 a0001c0001t0003g0238 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0002g0204 a0002c0002t0001g0182 a0002c0002t0002g0001 others(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 | a0001c0001t0002g0204 a0002c0002t0001g0182 a0002c0002t0002g0001 others(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 | a0002c0002t0001g0182 a0002c0002t0002g0112 a0002c0002t0002g0168 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0023g0009 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0167 a0001c0001t0001g0169 |
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 | a0002c0002t0004g0003 a0002c0002t0004g0004 a0005c0007t0019g0059 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0082 a0001c0001t0001g0195 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | 146 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0101 others(143): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): 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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0001c0001t0001g0111 | 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 | a0002c0002t0002g0090 a0002c0002t0002g0091 a0002c0002t0002g0213 |
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 | a0001c0001t0001g0083 a0001c0001t0003g0045 a0001c0001t0003g0238 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0003g0024 a0002c0002t0003g0027 |
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 | a0001c0001t0001g0208 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0132 a0001c0001t0023g0009 a0002c0002t0004g0036 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0004t0003g0025 a0001c0004t0003g0026 |
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 | a0003c0032t0003g0061 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0002g0204 a0002c0002t0002g0158 a0002c0002t0002g0160 others(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 | a0001c0001t0002g0204 a0001c0001t0006g0173 a0002c0002t0002g0001 others(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 | a0001c0001t0001g0151 a0001c0001t0001g0185 a0001c0001t0001g0200 others(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 | a0002c0002t0004g0005 a0008c0010t0004g0227 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0001c0004t0004g0018 a0001c0004t0004g0023 a0002c0002t0003g0024 others(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 | a0001c0001t0001g0083 a0001c0001t0003g0045 a0001c0001t0003g0238 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0209 a0003c0003t0001g0191 a0003c0003t0001g0192 |
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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0113 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0002g0204 a0002c0002t0002g0001 a0002c0002t0002g0090 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0129 a0001c0001t0001g0161 a0001c0001t0001g0165 others(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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0084 a0003c0003t0003g0071 |
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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0147 a0001c0001t0023g0009 a0002c0002t0004g0011 others(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 | a0001c0001t0003g0232 a0001c0001t0003g0236 |
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 | a0001c0001t0001g0082 a0001c0001t0001g0101 a0001c0001t0001g0113 others(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 | 34 | a0001c0001t0001g0084 a0001c0001t0001g0107 a0001c0001t0001g0110 others(31): Show |
34 | HG00423.hp2 HG00544.hp2 HG01123.hp2 others(31): 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 | a0001c0001t0001g0175 a0001c0001t0001g0200 a0001c0004t0004g0018 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0198 a0001c0001t0001g0207 others(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 | a0001c0001t0001g0162 a0001c0001t0003g0034 a0002c0002t0003g0024 others(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 | a0001c0001t0002g0204 a0002c0002t0002g0001 a0002c0002t0002g0090 others(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 | a0002c0002t0004g0011 a0012c0013t0002g0100 |
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 | a0001c0001t0002g0204 a0002c0002t0002g0001 a0002c0002t0002g0090 others(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 | a0001c0004t0004g0018 a0001c0004t0004g0023 a0002c0002t0003g0024 others(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 | a0001c0004t0004g0018 a0001c0004t0004g0023 a0002c0002t0003g0024 others(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 | a0001c0001t0002g0204 a0002c0002t0001g0182 a0002c0002t0002g0001 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0132 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0085 | 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 | a0002c0002t0004g0003 a0002c0002t0004g0004 a0005c0007t0019g0059 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0004g0003 a0002c0002t0004g0004 a0005c0007t0019g0059 others(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 | a0001c0001t0001g0113 | 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0126 | 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 | 187 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0101 others(184): Show |
187 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(184): 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0004g0003 a0002c0002t0004g0004 a0005c0007t0019g0059 others(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 | a0001c0001t0002g0204 a0001c0004t0004g0018 a0001c0004t0004g0023 others(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 | a0001c0001t0001g0207 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0004t0004g0018 a0001c0004t0004g0023 a0002c0002t0004g0022 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0003c0003t0003g0048 a0003c0003t0003g0054 a0017c0027t0002g0215 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0002g0204 a0001c0004t0004g0018 a0001c0004t0004g0023 others(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 | a0025c0033t0006g0206 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0082 a0001c0001t0001g0104 a0001c0001t0001g0118 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0012t0011g0226 a0002c0019t0011g0228 |
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 | a0001c0001t0003g0232 a0001c0001t0003g0236 |
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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | 56 | a0001c0001t0001g0084 a0001c0001t0001g0111 a0001c0001t0001g0114 others(53): Show |
56 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(53): 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 | a0001c0001t0001g0082 a0001c0001t0001g0104 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0150 a0001c0001t0001g0151 others(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 | a0002c0002t0001g0089 a0003c0003t0003g0074 a0003c0017t0005g0055 |
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 | a0001c0001t0001g0085 a0001c0001t0001g0101 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0178 a0001c0001t0003g0034 a0001c0004t0003g0010 others(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 | a0001c0001t0001g0157 a0001c0004t0004g0018 a0001c0004t0004g0023 others(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 | a0002c0002t0002g0212 a0002c0002t0004g0014 a0002c0002t0004g0035 others(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 | a0001c0001t0001g0199 | 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 | T | TATGCC | 2 | a0002c0012t0004g0007 a0002c0019t0011g0228 |
2 | HG02109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.3282+409_3282+410i others(7): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 98298438 | ||||||
chr2:98298438 | TATTCTAT others(3): Show |
T | 1 | a0012c0013t0002g0135 | 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 | a0001c0001t0003g0034 a0001c0004t0004g0018 a0001c0004t0004g0023 others(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 | a0001c0001t0001g0133 a0008c0010t0004g0227 a0011c0011t0001g0166 others(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 | a0001c0004t0004g0018 a0001c0004t0004g0023 a0002c0002t0004g0022 others(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 | a0003c0003t0003g0056 a0012c0013t0002g0100 |
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 | a0003c0003t0003g0056 a0012c0013t0002g0100 |
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 | a0003c0003t0003g0056 | 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 | a0003c0003t0003g0056 | 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 | a0003c0003t0003g0056 | 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 | a0003c0003t0003g0056 | 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 | a0002c0002t0004g0005 a0002c0002t0024g0008 a0008c0010t0004g0227 |
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 | a0001c0001t0001g0179 | 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0002c0002t0004g0005 a0002c0002t0024g0008 a0008c0010t0004g0227 |
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 | a0004c0005t0002g0102 | 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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0001g0182 a0002c0002t0002g0112 a0002c0002t0002g0168 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0003c0003t0003g0056 others(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 | a0002c0002t0002g0112 | 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 | a0001c0001t0002g0204 a0002c0002t0002g0222 a0002c0002t0002g0223 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0001c0001t0001g0085 | 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 | a0001c0004t0013g0029 a0002c0002t0004g0033 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0006c0008t0003g0235 | 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 | a0002c0002t0008g0171 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0003c0003t0003g0071 | 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 | a0001c0001t0002g0204 a0002c0002t0001g0182 a0002c0002t0002g0001 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0006c0008t0003g0235 | 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 | a0002c0002t0004g0003 a0002c0002t0004g0004 |
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 | a0001c0001t0002g0204 a0002c0002t0001g0182 a0002c0002t0002g0001 others(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 | a0001c0001t0002g0204 a0002c0002t0001g0182 a0002c0002t0002g0001 others(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 | a0001c0001t0001g0110 a0001c0001t0001g0144 a0001c0001t0001g0157 others(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 | a0001c0001t0001g0153 | 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 | a0001c0001t0002g0204 a0002c0002t0001g0182 a0002c0002t0002g0001 others(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 | a0005c0007t0019g0059 a0016c0026t0002g0202 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0002t0004g0032 a0002c0002t0004g0036 a0002c0002t0004g0037 others(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 | a0001c0001t0002g0204 a0002c0002t0001g0182 a0002c0002t0002g0001 others(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 | a0005c0007t0012g0052 a0005c0007t0012g0053 |
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 | 38 | a0001c0001t0001g0084 a0001c0001t0001g0101 a0001c0001t0001g0107 others(35): Show |
38 | HG00423.hp2 HG00544.hp2 HG00639.hp1 others(35): 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 | a0003c0003t0003g0067 | 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 | a0001c0001t0002g0204 a0002c0002t0001g0182 a0002c0002t0002g0001 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0149 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0123 a0001c0004t0004g0018 a0001c0004t0004g0023 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0002c0012t0004g0007 a0002c0012t0011g0226 a0012c0013t0002g0100 |
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 | a0001c0001t0006g0190 a0002c0002t0004g0003 a0002c0002t0004g0004 others(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 | a0001c0001t0001g0152 a0001c0001t0002g0204 a0001c0001t0023g0009 others(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 | a0002c0002t0001g0182 a0002c0002t0002g0001 a0002c0002t0002g0090 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0001c0001t0001g0208 | 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 | a0003c0003t0001g0194 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0113 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0176 | 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 | a0001c0001t0001g0111 | 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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0002c0012t0004g0007 a0002c0012t0011g0226 a0002c0016t0020g0031 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0006c0020t0003g0231 | 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 | a0002c0002t0002g0213 | 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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0025c0033t0006g0206 | 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 | 236 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(233): Show |
236 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(233): 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0002g0204 a0002c0002t0001g0182 a0002c0002t0002g0001 others(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 | a0001c0004t0003g0044 a0006c0008t0003g0230 |
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 | a0002c0012t0004g0007 a0002c0012t0011g0226 a0002c0016t0020g0031 others(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 | a0001c0001t0001g0209 a0003c0003t0001g0191 a0003c0003t0001g0192 |
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 | a0005c0007t0004g0066 | 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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0008c0010t0009g0239 a0008c0010t0009g0240 |
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 | a0002c0012t0004g0007 a0002c0012t0011g0226 a0002c0016t0020g0031 others(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 | a0001c0001t0001g0123 | 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 | a0002c0002t0004g0005 a0002c0002t0004g0011 a0002c0002t0024g0008 others(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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0002c0002t0004g0003 a0002c0002t0004g0004 a0005c0007t0019g0059 others(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 | a0001c0001t0001g0175 a0001c0001t0001g0184 a0001c0004t0001g0221 |
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 | a0001c0001t0002g0204 a0001c0004t0004g0018 a0001c0004t0004g0023 others(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 | a0002c0002t0004g0003 a0002c0002t0004g0004 a0005c0007t0019g0059 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0132 a0001c0001t0002g0204 a0002c0002t0001g0182 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0132 a0001c0001t0002g0204 a0001c0004t0004g0018 others(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 | a0001c0001t0001g0132 a0001c0001t0002g0204 a0001c0004t0004g0018 others(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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0132 a0001c0001t0002g0204 a0001c0004t0004g0018 others(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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0002c0002t0004g0003 a0002c0002t0004g0004 a0002c0002t0004g0005 others(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 | a0001c0001t0003g0232 a0001c0001t0003g0236 |
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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | |||||||
chr2:98308456 | CAT | C | 2 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.3522-3360_3522-335 others(6): Show |
VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr2 | 98308456 | ||||||
chr2:98308458 | T | C | 93 | a0001c0001t0001g0132 a0001c0001t0002g0204 a0001c0004t0004g0018 others(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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0138 a0001c0001t0001g0139 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0002c0012t0011g0226 a0002c0016t0020g0031 a0002c0019t0011g0228 others(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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0004c0005t0002g0094 a0024c0031t0014g0092 |
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 | a0001c0001t0001g0114 a0001c0001t0001g0214 |
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 | a0002c0002t0002g0212 a0002c0002t0004g0030 a0002c0002t0004g0032 others(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 | a0002c0002t0008g0171 a0002c0002t0008g0188 a0002c0002t0008g0217 |
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 | a0001c0001t0001g0149 a0001c0001t0016g0146 |
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 | a0002c0002t0002g0112 a0002c0002t0002g0168 a0002c0002t0002g0189 others(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 | a0001c0001t0001g0138 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0001g0111 | 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 | a0005c0007t0009g0081 a0008c0010t0009g0239 a0008c0010t0009g0240 others(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 | a0017c0027t0002g0215 a0018c0028t0002g0216 |
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 | a0005c0007t0019g0059 | 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 | a0012c0013t0002g0100 a0012c0013t0002g0135 a0014c0030t0002g0116 |
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 | a0001c0001t0002g0204 a0002c0002t0002g0158 a0002c0002t0002g0160 others(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 | a0007c0009t0002g0087 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3736-68G>T | VWA3B | ENSG00000168658.20 | transcript | ENST00000477737.6 | protein_coding | 27/27 | chr2 | 98312132 |