Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 375567 |
| ensemblid | ENSG00000188730.5 |
| hgncid | 30200 |
| symbol | VWC2 |
| name | von Willebrand factor C domain containing 2 |
| refseq_nuc | NM_198570.5 |
| refseq_prot | NP_940972.2 |
| ensembl_nuc | ENST00000340652.5 |
| ensembl_prot | ENSP00000341819.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 49773638 |
| end | 49921950 |
| strand | + |
| ver | v1.2 |
| region | chr7:49773638-49921950 |
| region5000 | chr7:49768638-49926950 |
| regionname0 | VWC2_chr7_49773638_49921950 |
| regionname5000 | VWC2_chr7_49768638_49926950 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 325 | 119 | 29 | 25 | 36 | 5 | 23 | 23 | VWC2_chr7_49768638_49926950 | VWC2 | MPSST others(320): Show |
chr7 | 49768638 | 49926950 |
| a0002 | 0/1 | 325 | 106 | 38 | 25 | 19 | 7 | 16 | 15 | VWC2_chr7_49768638_49926950 | VWC2 | MPSST others(320): Show |
chr7 | 49768638 | 49926950 |
| a0003 | 0/0 | 325 | 27 | 12 | 1 | 9 | 0 | 5 | 8 | VWC2_chr7_49768638_49926950 | VWC2 | MPSST others(320): Show |
chr7 | 49768638 | 49926950 |
| a0004 | 0/0 | 325 | 4 | 1 | 3 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | MPSST others(320): Show |
chr7 | 49768638 | 49926950 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 975 | 119 | 29 | 25 | 36 | 5 | 23 | VWC2_chr7_49768638_49926950 | VWC2 | ATGCC others(970): Show |
chr7 | 49768638 | 49926950 | ||
| a0002c0002 | 0/1 | 975 | 105 | 37 | 25 | 19 | 7 | 16 | VWC2_chr7_49768638_49926950 | VWC2 | ATGCC others(970): Show |
chr7 | 49768638 | 49926950 | ||
| a0002c0006 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | ATGCC others(970): Show |
chr7 | 49768638 | 49926950 | ||
| a0003c0003 | 0/0 | 975 | 26 | 12 | 1 | 9 | 0 | 4 | VWC2_chr7_49768638_49926950 | VWC2 | ATGCC others(970): Show |
chr7 | 49768638 | 49926950 | ||
| a0003c0005 | 0/0 | 975 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | ATGCC others(970): Show |
chr7 | 49768638 | 49926950 | ||
| a0004c0004 | 0/0 | 975 | 4 | 1 | 3 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | ATGCC others(970): Show |
chr7 | 49768638 | 49926950 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 11326 | 25 | 6 | 4 | 9 | 1 | 5 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0002 | 0/0 | 11326 | 20 | 0 | 6 | 10 | 1 | 3 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0003 | 0/0 | 11327 | 10 | 3 | 2 | 4 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11322): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0004 | 1/0 | 11322 | 12 | 0 | 1 | 5 | 1 | 4 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11317): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0005 | 0/0 | 11318 | 10 | 1 | 6 | 1 | 0 | 2 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11313): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0006 | 0/0 | 11326 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0007 | 0/0 | 11323 | 6 | 0 | 1 | 0 | 0 | 5 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11318): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0008 | 0/0 | 11318 | 6 | 6 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11313): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0009 | 0/0 | 11326 | 3 | 0 | 1 | 0 | 1 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0010 | 0/0 | 11320 | 2 | 0 | 1 | 0 | 1 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11315): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0011 | 0/0 | 11327 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11322): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0013 | 0/0 | 11324 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11319): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0014 | 0/0 | 11328 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11323): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0015 | 0/0 | 11326 | 3 | 3 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0017 | 0/0 | 11326 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0019 | 0/0 | 11326 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0020 | 0/0 | 11326 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0021 | 0/0 | 11326 | 2 | 0 | 0 | 2 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0040 | 0/0 | 11326 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0041 | 0/0 | 11326 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0042 | 0/0 | 11326 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0043 | 0/0 | 11327 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11322): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0044 | 0/0 | 11326 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0051 | 0/0 | 11326 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0054 | 0/0 | 11326 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0056 | 0/0 | 11328 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11323): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0060 | 0/0 | 11326 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0063 | 0/0 | 11322 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11317): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0064 | 0/0 | 11322 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11317): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0067 | 0/0 | 11326 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0001c0001t0069 | 0/0 | 11326 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0001 | 0/0 | 11326 | 16 | 5 | 4 | 3 | 0 | 4 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0002 | 0/0 | 11326 | 19 | 0 | 4 | 8 | 5 | 2 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0003 | 0/0 | 11327 | 12 | 5 | 3 | 2 | 0 | 2 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11322): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0004 | 0/0 | 11322 | 6 | 1 | 1 | 3 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11317): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0005 | 0/0 | 11318 | 2 | 0 | 2 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11313): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0007 | 0/0 | 11323 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11318): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0009 | 0/0 | 11326 | 3 | 0 | 1 | 0 | 0 | 2 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0010 | 0/0 | 11320 | 4 | 0 | 3 | 0 | 1 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11315): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0013 | 0/0 | 11324 | 3 | 2 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11319): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0014 | 0/0 | 11328 | 3 | 3 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11323): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0019 | 0/0 | 11326 | 1 | 0 | 0 | 0 | 1 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0020 | 0/0 | 11326 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0022 | 0/0 | 11323 | 2 | 2 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11318): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0023 | 0/0 | 11326 | 2 | 2 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0024 | 0/0 | 11322 | 2 | 0 | 0 | 2 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11317): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0025 | 0/0 | 11322 | 2 | 1 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11317): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0026 | 0/0 | 11323 | 2 | 2 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11318): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0027 | 0/0 | 11322 | 2 | 0 | 2 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11317): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0028 | 0/0 | 11318 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11313): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0029 | 0/0 | 11326 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0030 | 0/0 | 11326 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0031 | 0/0 | 11322 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11317): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0032 | 0/0 | 11323 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11318): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0039 | 0/0 | 11326 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0045 | 0/0 | 11326 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0046 | 0/0 | 11326 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0047 | 0/0 | 11326 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0048 | 0/0 | 11327 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11322): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0049 | 0/0 | 11323 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11318): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0050 | 0/0 | 11326 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0052 | 0/0 | 11326 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0053 | 0/0 | 11326 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0055 | 0/0 | 11326 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0058 | 0/0 | 11327 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11322): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0059 | 0/0 | 11327 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11322): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0061 | 0/0 | 11326 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0062 | 0/0 | 11326 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0065 | 0/1 | 11322 | 1 | 0 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11317): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0066 | 0/0 | 11320 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11315): Show |
chr7 | 49768638 | 49926950 |
| a0002c0002t0068 | 0/0 | 11327 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11322): Show |
chr7 | 49768638 | 49926950 |
| a0002c0006t0057 | 0/0 | 11327 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11322): Show |
chr7 | 49768638 | 49926950 |
| a0003c0003t0006 | 0/0 | 11326 | 8 | 3 | 1 | 2 | 0 | 2 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0003c0003t0011 | 0/0 | 11327 | 4 | 3 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11322): Show |
chr7 | 49768638 | 49926950 |
| a0003c0003t0012 | 0/0 | 11322 | 4 | 3 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11317): Show |
chr7 | 49768638 | 49926950 |
| a0003c0003t0016 | 0/0 | 11326 | 2 | 1 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0003c0003t0017 | 0/0 | 11326 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0003c0003t0018 | 0/0 | 11318 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11313): Show |
chr7 | 49768638 | 49926950 |
| a0003c0003t0033 | 0/0 | 11326 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0003c0003t0034 | 0/0 | 11326 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0003c0003t0035 | 0/0 | 11318 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11313): Show |
chr7 | 49768638 | 49926950 |
| a0003c0003t0036 | 0/0 | 11327 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11322): Show |
chr7 | 49768638 | 49926950 |
| a0003c0003t0037 | 0/0 | 11326 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0003c0003t0038 | 0/0 | 11323 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11318): Show |
chr7 | 49768638 | 49926950 |
| a0003c0005t0018 | 0/0 | 11318 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11313): Show |
chr7 | 49768638 | 49926950 |
| a0004c0004t0001 | 0/0 | 11326 | 3 | 1 | 2 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11321): Show |
chr7 | 49768638 | 49926950 |
| a0004c0004t0003 | 0/0 | 11327 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | GCGCT others(11322): Show |
chr7 | 49768638 | 49926950 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0003g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0004g0162 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0005g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0005g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0005g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0005g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0007g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0007g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0007g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0007g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0007g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0007g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0008g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0008g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0008g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0008g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0009g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0009g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0009g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0010g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0010g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0011g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0013g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0014g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0015g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0015g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0015g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0017g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0019g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0020g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0021g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0021g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0040g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0041g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0042g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0043g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0044g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0051g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0054g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0056g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0060g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0063g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0064g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0067g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0001c0001t0069g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0004g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0004g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0005g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0005g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0007g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0009g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0009g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0010g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0010g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0010g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0010g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0013g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0013g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0013g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0014g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0014g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0014g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0019g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0020g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0022g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0022g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0023g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0023g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0024g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0024g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0025g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0025g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0026g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0026g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0027g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0027g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0028g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0029g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0030g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0031g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0032g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0039g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0045g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0046g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0047g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0048g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0049g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0050g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0052g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0053g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0055g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0058g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0059g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0061g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0062g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0065g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0066g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0002t0068g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0002c0006t0057g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0006g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0006g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0006g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0006g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0006g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0011g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0011g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0011g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0011g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0012g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0012g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0012g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0012g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0016g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0016g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0017g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0018g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0033g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0034g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0035g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0036g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0037g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0003t0038g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0003c0005t0018g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0004c0004t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0004c0004t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0004c0004t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| a0004c0004t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0021 | EUR | GBR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | GBR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG00280 | hp1 | a0002 | c0002 | t0019 | g0026 | EUR | FIN | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0032 | EUR | FIN | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG00323 | hp1 | a0001 | c0001 | t0009 | g0174 | EUR | FIN | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0074 | EUR | FIN | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG00423 | hp1 | a0001 | c0001 | t0044 | g0138 | EAS | CHS | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG00597 | hp1 | a0001 | c0001 | t0069 | g0176 | EAS | CHS | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | CHS | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | CHS | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG00733 | hp1 | a0002 | c0002 | t0007 | g0082 | AMR | PUR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0034 | AMR | PUR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0167 | AMR | PUR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | PUR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0031 | AMR | PUR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0155 | AMR | PUR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0158 | AMR | PUR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0035 | AMR | PUR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0157 | AMR | PUR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01074 | hp2 | a0003 | c0003 | t0006 | g0252 | AMR | PUR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01081 | hp1 | a0002 | c0002 | t0003 | g0006 | AMR | PUR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01081 | hp2 | a0001 | c0001 | t0064 | g0122 | AMR | PUR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0153 | AMR | PUR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01109 | hp2 | a0002 | c0002 | t0025 | g0066 | AMR | PUR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0051 | AMR | PUR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01167 | hp2 | a0002 | c0002 | t0010 | g0027 | AMR | PUR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01168 | hp1 | a0001 | c0001 | t0010 | g0114 | AMR | PUR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01168 | hp2 | a0002 | c0002 | t0045 | g0068 | AMR | PUR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01243 | hp1 | a0002 | c0002 | t0004 | g0017 | AMR | PUR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01243 | hp2 | a0001 | c0001 | t0063 | g0217 | AMR | PUR | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01255 | hp1 | a0004 | c0004 | t0001 | g0016 | AMR | CLM | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | CLM | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01256 | hp1 | a0002 | c0002 | t0009 | g0040 | AMR | CLM | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01256 | hp2 | a0002 | c0002 | t0010 | g0019 | AMR | CLM | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01258 | hp1 | a0004 | c0004 | t0001 | g0063 | AMR | CLM | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01258 | hp2 | a0002 | c0002 | t0010 | g0018 | AMR | CLM | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | CLM | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | CLM | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0081 | AMR | CLM | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01433 | hp1 | a0002 | c0002 | t0013 | g0214 | AMR | CLM | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01433 | hp2 | a0001 | c0001 | t0007 | g0172 | AMR | CLM | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01496 | hp1 | a0002 | c0002 | t0003 | g0023 | AMR | CLM | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01496 | hp2 | a0002 | c0002 | t0027 | g0015 | AMR | CLM | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0206 | EUR | IBS | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0079 | EUR | IBS | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01517 | hp1 | a0001 | c0001 | t0010 | g0111 | EUR | IBS | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0078 | EUR | IBS | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0161 | AMR | PEL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01928 | hp2 | a0001 | c0001 | t0005 | g0154 | AMR | PEL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01943 | hp1 | a0002 | c0002 | t0005 | g0037 | AMR | PEL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01978 | hp1 | a0004 | c0004 | t0003 | g0038 | AMR | PEL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | PEL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | PEL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01981 | hp2 | a0001 | c0001 | t0009 | g0175 | AMR | PEL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01993 | hp2 | a0002 | c0002 | t0039 | g0205 | AMR | PEL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02015 | hp2 | a0002 | c0002 | t0003 | g0083 | EAS | KHV | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02055 | hp1 | a0001 | c0001 | t0015 | g0187 | AFR | ACB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02055 | hp2 | a0003 | c0003 | t0011 | g0247 | AFR | ACB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02074 | hp1 | a0002 | c0002 | t0024 | g0077 | EAS | KHV | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0039 | EAS | KHV | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | KHV | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02135 | hp2 | a0003 | c0003 | t0006 | g0235 | EAS | KHV | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02145 | hp1 | a0003 | c0003 | t0016 | g0230 | AFR | ACB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02145 | hp2 | a0003 | c0003 | t0017 | g0242 | AFR | ACB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02148 | hp1 | a0001 | c0001 | t0005 | g0152 | AMR | PEL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02148 | hp2 | a0002 | c0002 | t0027 | g0069 | AMR | PEL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02257 | hp1 | a0002 | c0002 | t0003 | g0052 | AFR | ACB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02257 | hp2 | a0001 | c0001 | t0015 | g0182 | AFR | ACB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02258 | hp1 | a0002 | c0002 | t0014 | g0044 | AFR | ACB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0184 | AFR | ACB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02280 | hp1 | a0002 | c0002 | t0055 | g0211 | AFR | ACB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02280 | hp2 | a0002 | c0002 | t0003 | g0096 | AFR | ACB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02300 | hp1 | a0002 | c0002 | t0005 | g0080 | AMR | PEL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02300 | hp2 | a0001 | c0001 | t0043 | g0178 | AMR | PEL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0054 | AFR | ACB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02451 | hp2 | a0001 | c0001 | t0040 | g0003 | AFR | ACB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02602 | hp1 | a0002 | c0002 | t0058 | g0084 | SAS | PJL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0053 | AFR | GWD | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02615 | hp2 | a0003 | c0003 | t0006 | g0246 | AFR | GWD | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02630 | hp1 | a0002 | c0002 | t0022 | g0226 | AFR | GWD | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02698 | hp1 | a0001 | c0001 | t0009 | g0171 | SAS | PJL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02698 | hp2 | a0002 | c0002 | t0059 | g0085 | SAS | PJL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02717 | hp1 | a0002 | c0002 | t0026 | g0041 | AFR | GWD | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02717 | hp2 | a0002 | c0002 | t0004 | g0062 | AFR | GWD | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02723 | hp1 | a0002 | c0002 | t0068 | g0227 | AFR | GWD | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02723 | hp2 | a0002 | c0002 | t0025 | g0067 | AFR | GWD | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0190 | SAS | PJL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | PJL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02809 | hp2 | a0001 | c0001 | t0013 | g0219 | AFR | GWD | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02818 | hp1 | a0002 | c0002 | t0003 | g0049 | AFR | GWD | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02818 | hp2 | a0002 | c0002 | t0026 | g0254 | AFR | GWD | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | GWD | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02895 | hp2 | a0002 | c0002 | t0022 | g0048 | AFR | GWD | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02897 | hp1 | a0002 | c0002 | t0023 | g0047 | AFR | GWD | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0163 | AFR | GWD | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02922 | hp1 | a0001 | c0001 | t0051 | g0009 | AFR | ESN | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0195 | AFR | ESN | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02965 | hp1 | a0001 | c0001 | t0041 | g0007 | AFR | ESN | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02965 | hp2 | a0001 | c0001 | t0008 | g0186 | AFR | ESN | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0185 | AFR | ESN | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02970 | hp2 | a0002 | c0002 | t0048 | g0225 | AFR | ESN | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0093 | AFR | ESN | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02976 | hp2 | a0003 | c0003 | t0012 | g0250 | AFR | ESN | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03017 | hp1 | a0001 | c0001 | t0014 | g0168 | SAS | PJL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03041 | hp1 | a0001 | c0001 | t0017 | g0223 | AFR | GWD | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03098 | hp1 | a0003 | c0003 | t0011 | g0249 | AFR | MSL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03098 | hp2 | a0002 | c0002 | t0053 | g0095 | AFR | MSL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03130 | hp2 | a0003 | c0003 | t0012 | g0248 | AFR | ESN | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03139 | hp1 | a0003 | c0003 | t0011 | g0241 | AFR | ESN | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03139 | hp2 | a0001 | c0001 | t0054 | g0004 | AFR | ESN | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0222 | AFR | MSL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03209 | hp2 | a0002 | c0002 | t0014 | g0064 | AFR | MSL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03225 | hp1 | a0002 | c0002 | t0013 | g0046 | AFR | MSL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03239 | hp1 | a0002 | c0002 | t0004 | g0022 | SAS | PJL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03239 | hp2 | a0001 | c0001 | t0019 | g0173 | SAS | PJL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0221 | AFR | MSL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03453 | hp2 | a0002 | c0002 | t0050 | g0100 | AFR | MSL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03486 | hp1 | a0002 | c0002 | t0052 | g0224 | AFR | MSL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0198 | AFR | MSL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03490 | hp1 | a0002 | c0002 | t0009 | g0001 | SAS | PJL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03490 | hp2 | a0001 | c0001 | t0007 | g0103 | SAS | PJL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03491 | hp2 | a0001 | c0001 | t0007 | g0108 | SAS | PJL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03492 | hp1 | a0001 | c0001 | t0007 | g0107 | SAS | PJL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03492 | hp2 | a0002 | c0002 | t0009 | g0001 | SAS | PJL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03516 | hp1 | a0002 | c0002 | t0032 | g0102 | AFR | ESN | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03516 | hp2 | a0003 | c0003 | t0035 | g0245 | AFR | ESN | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03540 | hp1 | a0002 | c0002 | t0031 | g0099 | AFR | GWD | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03540 | hp2 | a0002 | c0002 | t0023 | g0210 | AFR | GWD | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0097 | SAS | PJL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0164 | SAS | PJL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0201 | SAS | PJL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | STU | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0073 | SAS | STU | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0104 | SAS | PJL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0116 | SAS | PJL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0076 | SAS | PJL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03710 | hp2 | a0001 | c0001 | t0007 | g0160 | SAS | PJL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03831 | hp1 | a0002 | c0002 | t0061 | g0061 | SAS | BEB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03831 | hp2 | a0001 | c0001 | t0007 | g0181 | SAS | BEB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0065 | SAS | BEB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03927 | hp2 | a0002 | c0002 | t0062 | g0086 | SAS | BEB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03942 | hp1 | a0002 | c0002 | t0003 | g0087 | SAS | BEB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03942 | hp2 | a0003 | c0003 | t0011 | g0228 | SAS | BEB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG04115 | hp1 | a0002 | c0002 | t0066 | g0091 | SAS | STU | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0060 | SAS | STU | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG04184 | hp1 | a0003 | c0003 | t0038 | g0239 | SAS | BEB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0128 | SAS | STU | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG04199 | hp2 | a0003 | c0003 | t0006 | g0234 | SAS | STU | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0013 | SAS | STU | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG04204 | hp2 | a0002 | c0002 | t0003 | g0075 | SAS | STU | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0165 | SAS | STU | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG04228 | hp2 | a0003 | c0005 | t0018 | g0240 | SAS | STU | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18522 | hp1 | a0002 | c0002 | t0049 | g0208 | AFR | YRI | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | YRI | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0134 | EAS | CHB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | CHB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | CHB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0140 | EAS | CHB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18906 | hp1 | a0003 | c0003 | t0006 | g0243 | AFR | YRI | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18906 | hp2 | a0002 | c0006 | t0057 | g0215 | AFR | YRI | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18945 | hp2 | a0001 | c0001 | t0042 | g0148 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0170 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18960 | hp1 | a0002 | c0002 | t0020 | g0036 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18961 | hp2 | a0003 | c0003 | t0037 | g0229 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18962 | hp2 | a0001 | c0001 | t0067 | g0204 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18964 | hp2 | a0003 | c0003 | t0018 | g0233 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18972 | hp1 | a0003 | c0003 | t0012 | g0231 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18972 | hp2 | a0001 | c0001 | t0021 | g0135 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18977 | hp2 | a0001 | c0001 | t0020 | g0143 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18978 | hp1 | a0003 | c0003 | t0016 | g0237 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18978 | hp2 | a0002 | c0002 | t0004 | g0089 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18979 | hp1 | a0002 | c0002 | t0003 | g0010 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19005 | hp2 | a0001 | c0001 | t0021 | g0112 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19010 | hp2 | a0003 | c0003 | t0033 | g0236 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19030 | hp1 | a0001 | c0001 | t0056 | g0125 | AFR | LWK | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19030 | hp2 | a0002 | c0002 | t0046 | g0050 | AFR | LWK | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0094 | AFR | LWK | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19043 | hp2 | a0002 | c0002 | t0003 | g0045 | AFR | LWK | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0106 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19060 | hp1 | a0002 | c0002 | t0004 | g0028 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19064 | hp1 | a0002 | c0002 | t0024 | g0216 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19066 | hp1 | a0003 | c0003 | t0036 | g0238 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19076 | hp2 | a0003 | c0003 | t0034 | g0232 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19079 | hp1 | a0002 | c0002 | t0004 | g0088 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19086 | hp1 | a0003 | c0003 | t0006 | g0220 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19240 | hp1 | a0003 | c0003 | t0012 | g0251 | AFR | YRI | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0197 | AFR | YRI | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA20129 | hp1 | a0002 | c0002 | t0013 | g0042 | AFR | ASW | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA20129 | hp2 | a0003 | c0003 | t0006 | g0244 | AFR | ASW | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0213 | EUR | TSI | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA20752 | hp2 | a0002 | c0002 | t0010 | g0025 | EUR | TSI | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA20905 | hp1 | a0003 | c0003 | t0006 | g0253 | SAS | GIH | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0117 | SAS | GIH | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG01123 | hp2 | a0002 | c0002 | t0003 | g0014 | AMR | CLM | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02486 | hp1 | a0002 | c0002 | t0003 | g0092 | AFR | ACB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02486 | hp2 | a0002 | c0002 | t0014 | g0043 | AFR | ACB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02559 | hp1 | a0002 | c0002 | t0047 | g0209 | AFR | ACB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG02559 | hp2 | a0001 | c0001 | t0015 | g0109 | AFR | ACB | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0057 | AFR | MSL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG03471 | hp2 | a0001 | c0001 | t0060 | g0105 | AFR | MSL | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG06807 | hp1 | a0002 | c0002 | t0030 | g0101 | AFR | USA | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0196 | AFR | USA | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0151 | AFR | USA | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA20300 | hp2 | a0002 | c0002 | t0029 | g0098 | AFR | USA | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA21309 | hp1 | a0002 | c0002 | t0028 | g0212 | AFR | LWK | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| NA21309 | hp2 | a0004 | c0004 | t0001 | g0070 | AFR | LWK | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0065 | g0059 | REF | REF | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0162 | REF | REF | VWC2_chr7_49768638_49926950 | VWC2 | chr7 | 49768638 | 49926950 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:49775794 | C | G | 3 | a0002 a0003 a0004 |
136 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(133): Show |
missense_variant | MODERATE | c.359C>G | p.Ala120Gly | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/4 | 938/11322 | 359/978 | 120/325 | chr7 | 49775794 | |||
| chr7:49775878 | C | T | 1 | a0003 | 27 | HG01074.hp2 HG02055.hp2 HG02135.hp2 others(24): Show |
missense_variant | MODERATE | c.443C>T | p.Pro148Leu | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/4 | 1022/11322 | 443/978 | 148/325 | chr7 | 49775878 | |||
| chr7:49802781 | A | C | 1 | a0004 | 4 | HG01255.hp1 HG01258.hp1 HG01978.hp1 others(1): Show |
missense_variant | MODERATE | c.767A>C | p.Gln256Pro | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/4 | 1346/11322 | 767/978 | 256/325 | chr7 | 49802781 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:49775585 | C | T | 1 | a0002c0006 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.150C>T | p.His50His | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/4 | 729/11322 | 150/978 | 50/325 | chr7 | 49775585 | |||
| chr7:49775897 | C | G | 2 | a0003c0003 a0003c0005 |
27 | HG01074.hp2 HG02055.hp2 HG02135.hp2 others(24): Show |
synonymous_variant | LOW | c.462C>G | p.Gly154Gly | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/4 | 1041/11322 | 462/978 | 154/325 | chr7 | 49775897 | |||
| chr7:49775966 | G | C | 1 | a0003c0005 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.531G>C | p.Pro177Pro | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/4 | 1110/11322 | 531/978 | 177/325 | chr7 | 49775966 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:49773689 | G | C | 5 | a0002c0002t0028 a0002c0002t0029 a0002c0002t0030 others(2): Show |
5 | HG03516.hp1 HG03540.hp1 HG06807.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-528G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 1/4 | 1747 | chr7 | 49773689 | ||||||
| chr7:49773706 | C | G | 1 | a0001c0001t0069 | 1 | HG00597.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-511C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 1/4 | chr7 | 49773706 | |||||||
| chr7:49773710 | C | T | 1 | a0002c0002t0068 | 1 | HG02723.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-507C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 1/4 | chr7 | 49773710 | |||||||
| chr7:49773713 | G | A | 16 | a0001c0001t0006 a0001c0001t0011 a0001c0001t0017 others(13): Show |
30 | HG01074.hp2 HG02055.hp2 HG02135.hp2 others(27): Show |
5_prime_UTR_variant | MODIFIER | c.-504G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 1/4 | 1723 | chr7 | 49773713 | ||||||
| chr7:49773840 | C | A | 1 | a0002c0002t0039 | 1 | HG01993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-377C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 1/4 | 1596 | chr7 | 49773840 | ||||||
| chr7:49773871 | C | T | 1 | a0001c0001t0067 | 1 | NA18962.hp2 | 5_prime_UTR_variant | MODIFIER | c.-346C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 1/4 | 1565 | chr7 | 49773871 | ||||||
| chr7:49773961 | C | A | 1 | a0001c0001t0040 | 1 | HG02451.hp2 | 5_prime_UTR_variant | MODIFIER | c.-256C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 1/4 | 1475 | chr7 | 49773961 | ||||||
| chr7:49912327 | T | G | 2 | a0001c0001t0019 a0002c0002t0019 |
2 | HG00280.hp1 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*142T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 142 | chr7 | 49912327 | ||||||
| chr7:49912620 | C | A | 65 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(62): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*435C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 435 | chr7 | 49912620 | ||||||
| chr7:49913024 | G | A | 1 | a0001c0001t0041 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*839G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 839 | chr7 | 49913024 | ||||||
| chr7:49913214 | A | G | 1 | a0003c0003t0037 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1029A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 1029 | chr7 | 49913214 | ||||||
| chr7:49913237 | T | C | 15 | a0001c0001t0002 a0001c0001t0020 a0001c0001t0021 others(12): Show |
54 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*1052T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 1052 | chr7 | 49913237 | ||||||
| chr7:49913350 | G | A | 1 | a0002c0002t0048 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1165G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 1165 | chr7 | 49913350 | ||||||
| chr7:49913518 | T | C | 66 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(63): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*1333T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 1333 | chr7 | 49913518 | ||||||
| chr7:49913543 | T | G | 9 | a0001c0001t0008 a0001c0001t0013 a0001c0001t0051 others(6): Show |
17 | HG01433.hp1 HG02630.hp1 HG02809.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1358T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 1358 | chr7 | 49913543 | ||||||
| chr7:49913717 | A | G | 47 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(44): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*1532A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 1532 | chr7 | 49913717 | ||||||
| chr7:49913862 | CTTAG | C | 3 | a0001c0001t0008 a0002c0002t0028 a0003c0003t0035 |
8 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1679_*1682delTAGT | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 1679 | INFO_REALIGN_3_PRIME | chr7 | 49913862 | |||||
| chr7:49913870 | G | C | 7 | a0001c0001t0015 a0001c0001t0017 a0001c0001t0019 others(4): Show |
9 | HG00280.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1685G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 1685 | chr7 | 49913870 | ||||||
| chr7:49913907 | C | T | 56 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(53): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*1722C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 1722 | chr7 | 49913907 | ||||||
| chr7:49913927 | G | A | 66 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(63): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*1742G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 1742 | chr7 | 49913927 | ||||||
| chr7:49913977 | T | G | 1 | a0002c0002t0055 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1792T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 1792 | chr7 | 49913977 | ||||||
| chr7:49914125 | G | A | 2 | a0002c0002t0022 a0002c0002t0049 |
3 | HG02630.hp1 HG02895.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1940G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 1940 | chr7 | 49914125 | ||||||
| chr7:49914689 | T | C | 1 | a0001c0001t0063 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2504T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 2504 | chr7 | 49914689 | ||||||
| chr7:49914709 | T | C | 2 | a0001c0001t0013 a0002c0002t0013 |
4 | HG01433.hp1 HG02809.hp2 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2524T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 2524 | chr7 | 49914709 | ||||||
| chr7:49914723 | T | C | 1 | a0001c0001t0064 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2538T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 2538 | chr7 | 49914723 | ||||||
| chr7:49914936 | T | C | 2 | a0002c0002t0029 a0002c0002t0052 |
2 | HG03486.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2751T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 2751 | chr7 | 49914936 | ||||||
| chr7:49915477 | C | A | 65 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(62): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*3292C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 3292 | chr7 | 49915477 | ||||||
| chr7:49915478 | G | C | 65 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(62): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*3293G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 3293 | chr7 | 49915478 | ||||||
| chr7:49915870 | T | G | 1 | a0001c0001t0056 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3685T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 3685 | chr7 | 49915870 | ||||||
| chr7:49915919 | T | C | 3 | a0001c0001t0020 a0001c0001t0021 a0002c0002t0020 |
4 | NA18960.hp1 NA18972.hp2 NA18977.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3734T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 3734 | chr7 | 49915919 | ||||||
| chr7:49916088 | C | A | 2 | a0002c0002t0039 a0002c0002t0053 |
2 | HG01993.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3903C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 3903 | chr7 | 49916088 | ||||||
| chr7:49916140 | T | C | 1 | a0002c0002t0025 | 2 | HG01109.hp2 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3955T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 3955 | chr7 | 49916140 | ||||||
| chr7:49916203 | A | T | 2 | a0002c0002t0046 a0002c0002t0047 |
2 | HG02559.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4018A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 4018 | chr7 | 49916203 | ||||||
| chr7:49916798 | A | G | 64 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(61): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*4613A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 4613 | chr7 | 49916798 | ||||||
| chr7:49917308 | G | A | 64 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(61): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*5123G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 5123 | chr7 | 49917308 | ||||||
| chr7:49917464 | C | T | 1 | a0002c0002t0066 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5279C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 5279 | chr7 | 49917464 | ||||||
| chr7:49917507 | C | T | 1 | a0002c0002t0062 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5322C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 5322 | chr7 | 49917507 | ||||||
| chr7:49917540 | C | A | 9 | a0001c0001t0008 a0001c0001t0013 a0001c0001t0051 others(6): Show |
17 | HG01433.hp1 HG02630.hp1 HG02809.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*5355C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 5355 | chr7 | 49917540 | ||||||
| chr7:49917635 | C | T | 1 | a0002c0002t0055 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5450C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 5450 | chr7 | 49917635 | ||||||
| chr7:49917675 | C | T | 65 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(62): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*5490C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 5490 | chr7 | 49917675 | ||||||
| chr7:49917812 | TAGAA | T | 6 | a0001c0001t0005 a0001c0001t0064 a0002c0002t0005 others(3): Show |
17 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*5632_*5635delAGAA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 5632 | INFO_REALIGN_3_PRIME | chr7 | 49917812 | |||||
| chr7:49917894 | A | G | 2 | a0002c0002t0022 a0002c0002t0049 |
3 | HG02630.hp1 HG02895.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5709A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 5709 | chr7 | 49917894 | ||||||
| chr7:49918133 | T | C | 2 | a0001c0001t0042 a0003c0003t0033 |
2 | NA18945.hp2 NA19010.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5948T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 5948 | chr7 | 49918133 | ||||||
| chr7:49918170 | C | T | 56 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(53): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*5985C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 5985 | chr7 | 49918170 | ||||||
| chr7:49918183 | G | C | 3 | a0001c0001t0009 a0002c0002t0009 a0002c0002t0058 |
7 | HG00323.hp1 HG01256.hp1 HG01981.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5998G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 5998 | chr7 | 49918183 | ||||||
| chr7:49918335 | A | T | 67 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(64): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*6150A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 6150 | chr7 | 49918335 | ||||||
| chr7:49918936 | C | G | 1 | a0002c0002t0024 | 2 | HG02074.hp1 NA19064.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6751C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 6751 | chr7 | 49918936 | ||||||
| chr7:49918948 | C | T | 1 | a0002c0002t0032 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6763C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 6763 | chr7 | 49918948 | ||||||
| chr7:49919012 | G | A | 12 | a0001c0001t0002 a0001c0001t0020 a0001c0001t0021 others(9): Show |
51 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*6827G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 6827 | chr7 | 49919012 | ||||||
| chr7:49919034 | A | G | 67 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(64): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*6849A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 6849 | chr7 | 49919034 | ||||||
| chr7:49919053 | T | TA | 52 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(49): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*6884dupA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 6885 | INFO_REALIGN_3_PRIME | chr7 | 49919053 | |||||
| chr7:49919053 | T | TAA | 14 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0013 others(11): Show |
39 | HG00735.hp1 HG01071.hp1 HG01081.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*6883_*6884dupAA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 6885 | INFO_REALIGN_3_PRIME | chr7 | 49919053 | |||||
| chr7:49919053 | T | TAAA | 3 | a0001c0001t0014 a0001c0001t0056 a0002c0002t0014 |
5 | HG02258.hp1 HG02486.hp2 HG03017.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6882_*6884dupAAA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 6885 | INFO_REALIGN_3_PRIME | chr7 | 49919053 | |||||
| chr7:49919302 | C | T | 48 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(45): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*7117C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 7117 | chr7 | 49919302 | ||||||
| chr7:49919312 | T | C | 9 | a0001c0001t0008 a0001c0001t0013 a0001c0001t0051 others(6): Show |
17 | HG01433.hp1 HG02630.hp1 HG02809.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*7127T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 7127 | chr7 | 49919312 | ||||||
| chr7:49919319 | A | T | 2 | a0002c0002t0022 a0002c0002t0049 |
3 | HG02630.hp1 HG02895.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7134A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 7134 | chr7 | 49919319 | ||||||
| chr7:49919360 | T | A | 1 | a0002c0002t0050 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7175T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 7175 | chr7 | 49919360 | ||||||
| chr7:49919395 | G | A | 1 | a0002c0002t0023 | 2 | HG02897.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7210G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 7210 | chr7 | 49919395 | ||||||
| chr7:49919403 | C | T | 1 | a0001c0001t0051 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7218C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 7218 | chr7 | 49919403 | ||||||
| chr7:49919733 | C | G | 1 | a0003c0003t0036 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7548C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 7548 | chr7 | 49919733 | ||||||
| chr7:49919761 | G | C | 2 | a0002c0002t0026 a0002c0002t0032 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7576G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 7576 | chr7 | 49919761 | ||||||
| chr7:49919901 | T | G | 1 | a0003c0003t0034 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7716T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 7716 | chr7 | 49919901 | ||||||
| chr7:49920034 | G | T | 1 | a0003c0003t0034 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7849G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 7849 | chr7 | 49920034 | ||||||
| chr7:49920036 | G | T | 1 | a0003c0003t0034 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7851G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 7851 | chr7 | 49920036 | ||||||
| chr7:49920077 | G | T | 67 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(64): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*7892G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 7892 | chr7 | 49920077 | ||||||
| chr7:49920189 | A | C | 1 | a0001c0001t0021 | 2 | NA18972.hp2 NA19005.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8004A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 8004 | chr7 | 49920189 | ||||||
| chr7:49920250 | C | T | 1 | a0002c0002t0023 | 2 | HG02897.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8065C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 8065 | chr7 | 49920250 | ||||||
| chr7:49920251 | T | A | 2 | a0002c0002t0026 a0002c0002t0032 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8066T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 8066 | chr7 | 49920251 | ||||||
| chr7:49920261 | GAA | G | 3 | a0001c0001t0010 a0002c0002t0010 a0002c0002t0066 |
7 | HG01167.hp2 HG01168.hp1 HG01256.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*8081_*8082delAA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 8081 | INFO_REALIGN_3_PRIME | chr7 | 49920261 | |||||
| chr7:49920282 | G | A | 2 | a0002c0002t0026 a0002c0002t0032 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8097G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 8097 | chr7 | 49920282 | ||||||
| chr7:49920506 | A | C | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*8321A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 8321 | chr7 | 49920506 | ||||||
| chr7:49920563 | G | A | 2 | a0002c0002t0026 a0002c0002t0032 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8378G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 8378 | chr7 | 49920563 | ||||||
| chr7:49920630 | C | T | 1 | a0002c0002t0049 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8445C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 8445 | chr7 | 49920630 | ||||||
| chr7:49920649 | A | C | 1 | a0003c0003t0034 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8464A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 8464 | chr7 | 49920649 | ||||||
| chr7:49920650 | C | T | 1 | a0003c0003t0034 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8465C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 8465 | chr7 | 49920650 | ||||||
| chr7:49920651 | T | A | 1 | a0003c0003t0034 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8466T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 8466 | chr7 | 49920651 | ||||||
| chr7:49920682 | T | C | 1 | a0002c0002t0050 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8497T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 8497 | chr7 | 49920682 | ||||||
| chr7:49920730 | T | TTAA | 67 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(64): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*8546_*8547insAAT | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 8547 | INFO_REALIGN_3_PRIME | chr7 | 49920730 | |||||
| chr7:49920768 | A | G | 1 | a0002c0002t0061 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8583A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 8583 | chr7 | 49920768 | ||||||
| chr7:49920825 | G | A | 1 | a0002c0002t0059 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8640G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 8640 | chr7 | 49920825 | ||||||
| chr7:49920862 | T | C | 3 | a0001c0001t0060 a0002c0002t0030 a0002c0002t0055 |
3 | HG02280.hp1 HG03471.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8677T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 8677 | chr7 | 49920862 | ||||||
| chr7:49921447 | A | G | 1 | a0002c0002t0047 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9262A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 9262 | chr7 | 49921447 | ||||||
| chr7:49921592 | A | C | 1 | a0001c0001t0044 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9407A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 9407 | chr7 | 49921592 | ||||||
| chr7:49921650 | G | T | 67 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(64): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*9465G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 9465 | chr7 | 49921650 | ||||||
| chr7:49921755 | CTCA | C | 7 | a0001c0001t0008 a0001c0001t0013 a0002c0002t0013 others(4): Show |
15 | HG01433.hp1 HG02630.hp1 HG02809.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*9572_*9574delCAT | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 9572 | INFO_REALIGN_3_PRIME | chr7 | 49921755 | |||||
| chr7:49921920 | G | T | 1 | a0002c0002t0068 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9735G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 4/4 | 9735 | chr7 | 49921920 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:49774399 | A | C | 35 | a0001c0001t0006g0221 a0001c0001t0011g0222 a0001c0001t0017g0223 others(32): Show |
35 | HG01074.hp2 HG02055.hp2 HG02135.hp2 others(32): Show |
intron_variant | MODIFIER | c.-104+286A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 1/3 | chr7 | 49774399 | |||||||
| chr7:49774410 | A | G | 3 | a0001c0001t0001g0218 a0001c0001t0013g0219 a0001c0001t0063g0217 |
3 | HG01243.hp2 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-104+297A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 1/3 | chr7 | 49774410 | |||||||
| chr7:49774418 | T | C | 3 | a0001c0001t0001g0218 a0001c0001t0013g0219 a0001c0001t0063g0217 |
3 | HG01243.hp2 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-104+305T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 1/3 | chr7 | 49774418 | |||||||
| chr7:49774449 | C | T | 1 | a0002c0002t0026g0254 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-104+336C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 1/3 | chr7 | 49774449 | |||||||
| chr7:49774501 | G | C | 2 | a0001c0001t0040g0003 a0001c0001t0054g0004 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-104+388G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 1/3 | chr7 | 49774501 | |||||||
| chr7:49774540 | A | C | 1 | a0002c0002t0024g0216 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-104+427A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 1/3 | chr7 | 49774540 | |||||||
| chr7:49774578 | T | C | 1 | a0003c0003t0006g0220 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-104+465T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 1/3 | chr7 | 49774578 | |||||||
| chr7:49774587 | G | A | 1 | a0002c0002t0002g0005 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-104+474G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 1/3 | chr7 | 49774587 | |||||||
| chr7:49774605 | G | T | 1 | a0003c0003t0006g0253 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-104+492G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 1/3 | chr7 | 49774605 | |||||||
| chr7:49774873 | A | G | 1 | a0002c0006t0057g0215 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-103-460A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 1/3 | chr7 | 49774873 | |||||||
| chr7:49774934 | C | A | 1 | a0002c0002t0003g0006 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-103-399C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 1/3 | chr7 | 49774934 | |||||||
| chr7:49774952 | G | A | 1 | a0001c0001t0041g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-103-381G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 1/3 | chr7 | 49774952 | |||||||
| chr7:49775082 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0051g0009 |
2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-103-251T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 1/3 | chr7 | 49775082 | |||||||
| chr7:49775163 | A | G | 2 | a0003c0003t0006g0252 a0003c0003t0006g0253 |
2 | HG01074.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-103-170A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 1/3 | chr7 | 49775163 | |||||||
| chr7:49775201 | C | T | 1 | a0001c0001t0041g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-103-132C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 1/3 | chr7 | 49775201 | |||||||
| chr7:49775257 | A | G | 1 | a0002c0002t0013g0214 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-103-76A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 1/3 | chr7 | 49775257 | |||||||
| chr7:49776176 | G | T | 1 | a0001c0001t0002g0213 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.696+45G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49776176 | |||||||
| chr7:49776279 | T | C | 1 | a0002c0002t0003g0010 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.696+148T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49776279 | |||||||
| chr7:49776315 | A | C | 28 | a0002c0002t0028g0212 a0003c0003t0006g0220 a0003c0003t0006g0234 others(25): Show |
28 | HG01074.hp2 HG02055.hp2 HG02135.hp2 others(25): Show |
intron_variant | MODIFIER | c.696+184A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49776315 | |||||||
| chr7:49776366 | A | G | 1 | a0002c0002t0055g0211 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.696+235A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49776366 | |||||||
| chr7:49776740 | C | T | 16 | a0002c0002t0022g0226 a0002c0002t0028g0212 a0002c0002t0048g0225 others(13): Show |
16 | HG02055.hp2 HG02145.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.696+609C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49776740 | |||||||
| chr7:49776813 | A | G | 2 | a0002c0002t0023g0210 a0002c0002t0047g0209 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.696+682A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49776813 | |||||||
| chr7:49776909 | A | G | 1 | a0002c0002t0049g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.696+778A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49776909 | |||||||
| chr7:49777159 | A | G | 1 | a0003c0005t0018g0240 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.696+1028A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49777159 | |||||||
| chr7:49777361 | A | G | 1 | a0001c0001t0001g0207 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.696+1230A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49777361 | |||||||
| chr7:49777461 | C | T | 1 | a0001c0001t0004g0206 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.696+1330C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49777461 | |||||||
| chr7:49777474 | C | T | 1 | a0002c0002t0039g0205 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.696+1343C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49777474 | |||||||
| chr7:49777722 | A | C | 1 | a0001c0001t0067g0204 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.696+1591A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49777722 | |||||||
| chr7:49778011 | G | C | 1 | a0002c0002t0001g0011 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.696+1880G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49778011 | |||||||
| chr7:49778222 | T | C | 1 | a0001c0001t0005g0012 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.696+2091T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49778222 | |||||||
| chr7:49778259 | T | C | 11 | a0003c0003t0006g0243 a0003c0003t0006g0244 a0003c0003t0006g0246 others(8): Show |
11 | HG02055.hp2 HG02145.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.696+2128T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49778259 | |||||||
| chr7:49778279 | T | G | 1 | a0002c0002t0028g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.696+2148T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49778279 | |||||||
| chr7:49778287 | A | G | 2 | a0002c0002t0022g0226 a0002c0002t0068g0227 |
2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.696+2156A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49778287 | |||||||
| chr7:49778361 | T | C | 28 | a0002c0002t0028g0212 a0003c0003t0006g0220 a0003c0003t0006g0234 others(25): Show |
28 | HG01074.hp2 HG02055.hp2 HG02135.hp2 others(25): Show |
intron_variant | MODIFIER | c.696+2230T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49778361 | |||||||
| chr7:49778438 | A | G | 12 | a0002c0002t0028g0212 a0003c0003t0006g0243 a0003c0003t0006g0244 others(9): Show |
12 | HG02055.hp2 HG02145.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.696+2307A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49778438 | |||||||
| chr7:49778531 | G | A | 138 | a0001c0001t0001g0008 a0001c0001t0051g0009 a0001c0001t0063g0217 others(135): Show |
139 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.696+2400G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49778531 | |||||||
| chr7:49778650 | A | G | 2 | a0002c0002t0022g0226 a0002c0002t0068g0227 |
2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.696+2519A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49778650 | |||||||
| chr7:49778721 | T | G | 132 | a0001c0001t0004g0104 a0001c0001t0007g0103 a0002c0002t0001g0011 others(129): Show |
133 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.696+2590T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49778721 | |||||||
| chr7:49778820 | A | G | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0002g0201 |
3 | HG03017.hp2 HG03669.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.696+2689A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49778820 | |||||||
| chr7:49778917 | C | T | 5 | a0002c0002t0029g0098 a0002c0002t0030g0101 a0002c0002t0031g0099 others(2): Show |
5 | HG03453.hp2 HG03516.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.696+2786C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49778917 | |||||||
| chr7:49778920 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0051g0009 a0001c0001t0063g0217 |
3 | HG01243.hp2 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.696+2789G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49778920 | |||||||
| chr7:49779038 | G | GGA | 67 | a0001c0001t0002g0200 a0001c0001t0004g0104 a0002c0002t0001g0076 others(64): Show |
68 | HG00323.hp2 HG00733.hp1 HG01074.hp2 others(65): Show |
intron_variant | MODIFIER | c.696+2928_696+2929d others(4): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49779038 | ||||||
| chr7:49779055 | G | C | 4 | a0002c0002t0022g0226 a0002c0002t0048g0225 a0002c0002t0052g0224 others(1): Show |
4 | HG02630.hp1 HG02723.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.696+2924G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49779055 | |||||||
| chr7:49779055 | G | GAC | 64 | a0001c0001t0007g0103 a0002c0002t0001g0011 a0002c0002t0001g0013 others(61): Show |
64 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.696+2925_696+2926i others(4): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49779055 | ||||||
| chr7:49779285 | T | A | 1 | a0002c0002t0001g0013 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.696+3154T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49779285 | |||||||
| chr7:49779300 | T | G | 4 | a0002c0002t0022g0226 a0002c0002t0048g0225 a0002c0002t0052g0224 others(1): Show |
4 | HG02630.hp1 HG02723.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.696+3169T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49779300 | |||||||
| chr7:49779584 | TA | T | 5 | a0001c0001t0001g0199 a0001c0001t0008g0195 a0001c0001t0008g0196 others(2): Show |
5 | HG02922.hp2 HG03041.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.696+3454delA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49779584 | |||||||
| chr7:49779585 | A | AT | 93 | a0001c0001t0007g0103 a0002c0002t0001g0011 a0002c0002t0001g0013 others(90): Show |
93 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.696+3465dupT | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49779585 | ||||||
| chr7:49779738 | T | C | 138 | a0001c0001t0001g0008 a0001c0001t0007g0103 a0001c0001t0051g0009 others(135): Show |
139 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.696+3607T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49779738 | |||||||
| chr7:49779760 | A | G | 1 | a0001c0001t0017g0223 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.696+3629A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49779760 | |||||||
| chr7:49779806 | G | A | 2 | a0003c0003t0016g0230 a0003c0003t0037g0229 |
2 | HG02145.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.696+3675G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49779806 | |||||||
| chr7:49779854 | C | A | 1 | a0002c0002t0039g0205 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.696+3723C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49779854 | |||||||
| chr7:49779866 | C | A | 134 | a0001c0001t0007g0103 a0002c0002t0001g0011 a0002c0002t0001g0013 others(131): Show |
135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.696+3735C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49779866 | |||||||
| chr7:49779900 | T | G | 8 | a0002c0002t0001g0020 a0002c0002t0002g0021 a0002c0002t0003g0014 others(5): Show |
8 | HG00099.hp1 HG01099.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.696+3769T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49779900 | |||||||
| chr7:49780000 | C | T | 1 | a0002c0002t0003g0006 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.696+3869C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49780000 | |||||||
| chr7:49780060 | A | G | 16 | a0003c0003t0006g0220 a0003c0003t0006g0234 a0003c0003t0006g0235 others(13): Show |
16 | HG01074.hp2 HG02135.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.696+3929A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49780060 | |||||||
| chr7:49780117 | G | A | 36 | a0002c0002t0001g0060 a0002c0002t0001g0076 a0002c0002t0002g0005 others(33): Show |
37 | HG00323.hp2 HG00733.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.696+3986G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49780117 | |||||||
| chr7:49780167 | C | T | 5 | a0002c0002t0022g0226 a0002c0002t0048g0225 a0002c0002t0052g0224 others(2): Show |
5 | HG02630.hp1 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.696+4036C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49780167 | |||||||
| chr7:49780168 | G | C | 1 | a0002c0002t0039g0205 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.696+4037G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49780168 | |||||||
| chr7:49780200 | A | G | 17 | a0002c0002t0022g0226 a0002c0002t0026g0254 a0002c0002t0028g0212 others(14): Show |
17 | HG02055.hp2 HG02145.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.696+4069A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49780200 | |||||||
| chr7:49780222 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0051g0009 |
2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.696+4091T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49780222 | |||||||
| chr7:49780740 | C | T | 1 | a0001c0001t0063g0217 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.696+4609C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49780740 | |||||||
| chr7:49780784 | C | G | 2 | a0002c0002t0003g0096 a0002c0002t0053g0095 |
2 | HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.696+4653C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49780784 | |||||||
| chr7:49780855 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0003g0002 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.696+4724G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49780855 | |||||||
| chr7:49781107 | G | C | 6 | a0001c0001t0001g0218 a0001c0001t0006g0221 a0001c0001t0011g0222 others(3): Show |
6 | HG02630.hp2 HG02809.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.696+4976G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49781107 | |||||||
| chr7:49781123 | T | C | 62 | a0001c0001t0007g0103 a0002c0002t0001g0011 a0002c0002t0001g0013 others(59): Show |
62 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.696+4992T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49781123 | |||||||
| chr7:49781209 | C | T | 1 | a0002c0002t0001g0060 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.696+5078C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49781209 | |||||||
| chr7:49781235 | A | G | 1 | a0002c0002t0002g0058 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.696+5104A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49781235 | |||||||
| chr7:49781584 | A | G | 1 | a0002c0002t0039g0205 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.696+5453A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49781584 | |||||||
| chr7:49781661 | G | T | 1 | a0002c0002t0023g0210 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.696+5530G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49781661 | |||||||
| chr7:49781723 | A | G | 3 | a0001c0001t0001g0218 a0001c0001t0013g0219 a0001c0001t0063g0217 |
3 | HG01243.hp2 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.696+5592A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49781723 | |||||||
| chr7:49781728 | G | A | 136 | a0001c0001t0001g0008 a0001c0001t0004g0106 a0001c0001t0051g0009 others(133): Show |
137 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.696+5597G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49781728 | |||||||
| chr7:49781740 | T | C | 1 | a0001c0001t0063g0217 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.696+5609T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49781740 | |||||||
| chr7:49781815 | C | A | 31 | a0002c0002t0001g0011 a0002c0002t0001g0013 a0002c0002t0001g0020 others(28): Show |
31 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.696+5684C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49781815 | |||||||
| chr7:49781865 | G | A | 1 | a0002c0002t0026g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.696+5734G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49781865 | |||||||
| chr7:49781917 | A | G | 1 | a0001c0001t0002g0194 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.696+5786A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49781917 | |||||||
| chr7:49781989 | A | T | 1 | a0001c0001t0001g0193 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.696+5858A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49781989 | |||||||
| chr7:49782154 | A | T | 38 | a0001c0001t0004g0106 a0002c0002t0001g0060 a0002c0002t0001g0076 others(35): Show |
39 | HG00323.hp2 HG00733.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.696+6023A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49782154 | |||||||
| chr7:49782386 | C | A | 2 | a0002c0002t0022g0226 a0002c0002t0068g0227 |
2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.696+6255C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49782386 | |||||||
| chr7:49782542 | TA | T | 37 | a0001c0001t0002g0191 a0001c0001t0003g0192 a0002c0002t0001g0011 others(34): Show |
37 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.696+6423delA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49782542 | ||||||
| chr7:49782569 | G | T | 1 | a0002c0002t0039g0205 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.696+6438G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49782569 | |||||||
| chr7:49782661 | A | G | 1 | a0002c0002t0003g0052 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.696+6530A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49782661 | |||||||
| chr7:49782690 | G | GA | 34 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0015g0109 others(31): Show |
34 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.696+6573dupA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49782690 | ||||||
| chr7:49782690 | GA | G | 28 | a0001c0001t0001g0199 a0001c0001t0063g0217 a0002c0002t0001g0051 others(25): Show |
28 | HG01167.hp1 HG01243.hp2 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.696+6573delA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49782690 | ||||||
| chr7:49782841 | A | G | 62 | a0001c0001t0001g0207 a0001c0001t0001g0218 a0001c0001t0002g0188 others(59): Show |
63 | HG00099.hp1 HG00323.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.696+6710A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49782841 | |||||||
| chr7:49782872 | G | GA | 8 | a0002c0002t0003g0045 a0002c0002t0013g0046 a0002c0002t0013g0214 others(5): Show |
8 | HG01433.hp1 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.696+6749dupA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49782872 | ||||||
| chr7:49782903 | C | T | 3 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0015g0187 |
3 | HG02055.hp1 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.696+6772C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49782903 | |||||||
| chr7:49783115 | A | C | 1 | a0001c0001t0004g0104 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.696+6984A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49783115 | |||||||
| chr7:49783255 | G | A | 1 | a0002c0002t0003g0023 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.696+7124G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49783255 | |||||||
| chr7:49783282 | G | C | 65 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0121 others(62): Show |
65 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.696+7151G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49783282 | |||||||
| chr7:49783325 | A | G | 7 | a0001c0001t0001g0124 a0001c0001t0002g0123 a0001c0001t0015g0109 others(4): Show |
7 | HG00099.hp2 HG00735.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.696+7194A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49783325 | |||||||
| chr7:49783375 | T | G | 36 | a0001c0001t0001g0126 a0001c0001t0006g0221 a0001c0001t0008g0185 others(33): Show |
36 | HG01433.hp1 HG01993.hp2 HG02145.hp2 others(33): Show |
intron_variant | MODIFIER | c.696+7244T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49783375 | |||||||
| chr7:49783476 | G | T | 3 | a0001c0001t0001g0183 a0001c0001t0003g0184 a0001c0001t0015g0182 |
3 | HG02257.hp2 HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.696+7345G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49783476 | |||||||
| chr7:49783630 | T | C | 3 | a0001c0001t0001g0199 a0001c0001t0060g0105 a0003c0003t0006g0244 |
3 | HG03041.hp2 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.696+7499T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49783630 | |||||||
| chr7:49783634 | G | T | 1 | a0002c0002t0002g0039 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.696+7503G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49783634 | |||||||
| chr7:49783815 | C | T | 3 | a0002c0002t0001g0024 a0002c0002t0004g0088 a0003c0003t0006g0220 |
3 | NA18960.hp2 NA19079.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.696+7684C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49783815 | |||||||
| chr7:49783816 | G | A | 1 | a0002c0002t0061g0061 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.696+7685G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49783816 | |||||||
| chr7:49783954 | G | A | 2 | a0001c0001t0003g0190 a0003c0003t0006g0234 |
2 | HG02735.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.696+7823G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49783954 | |||||||
| chr7:49783957 | C | T | 2 | a0002c0002t0048g0225 a0003c0003t0012g0251 |
2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.696+7826C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49783957 | |||||||
| chr7:49784157 | C | T | 1 | a0002c0002t0003g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.696+8026C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49784157 | |||||||
| chr7:49784171 | G | A | 2 | a0002c0002t0001g0054 a0002c0002t0003g0096 |
2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.696+8040G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49784171 | |||||||
| chr7:49784376 | A | C | 30 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0179 others(27): Show |
30 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.696+8245A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49784376 | |||||||
| chr7:49784403 | T | C | 6 | a0002c0002t0003g0049 a0002c0002t0030g0101 a0002c0002t0039g0205 others(3): Show |
6 | HG01993.hp2 HG02055.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.696+8272T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49784403 | |||||||
| chr7:49784430 | T | C | 6 | a0002c0002t0003g0049 a0002c0002t0030g0101 a0002c0002t0039g0205 others(3): Show |
6 | HG01993.hp2 HG02055.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.696+8299T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49784430 | |||||||
| chr7:49784498 | G | A | 1 | a0002c0002t0003g0014 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.696+8367G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49784498 | |||||||
| chr7:49784523 | G | T | 1 | a0002c0002t0066g0091 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.696+8392G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49784523 | |||||||
| chr7:49784867 | T | G | 63 | a0001c0001t0001g0008 a0001c0001t0001g0113 a0001c0001t0001g0127 others(60): Show |
63 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(60): Show |
intron_variant | MODIFIER | c.696+8736T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49784867 | |||||||
| chr7:49785188 | T | TATAATTA | 9 | a0001c0001t0001g0008 a0001c0001t0008g0185 a0001c0001t0008g0186 others(6): Show |
9 | HG02145.hp2 HG02615.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.696+9057_696+9058i others(9): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49785188 | |||||||
| chr7:49785212 | AC | A | 3 | a0001c0001t0041g0007 a0002c0002t0001g0054 a0002c0002t0003g0096 |
3 | HG02280.hp2 HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.696+9083delC | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49785212 | ||||||
| chr7:49785512 | T | G | 63 | a0001c0001t0001g0115 a0001c0001t0001g0136 a0001c0001t0001g0139 others(60): Show |
63 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.696+9381T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49785512 | |||||||
| chr7:49785572 | C | T | 9 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0002g0201 others(6): Show |
9 | HG03017.hp2 HG03669.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.696+9441C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49785572 | |||||||
| chr7:49785935 | A | T | 31 | a0001c0001t0001g0113 a0001c0001t0001g0127 a0001c0001t0001g0129 others(28): Show |
31 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.696+9804A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49785935 | |||||||
| chr7:49785947 | T | C | 4 | a0002c0002t0013g0042 a0002c0002t0022g0226 a0002c0002t0049g0208 others(1): Show |
4 | HG02630.hp1 HG03453.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.696+9816T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49785947 | |||||||
| chr7:49786119 | T | A | 9 | a0001c0001t0001g0008 a0001c0001t0008g0185 a0001c0001t0008g0186 others(6): Show |
9 | HG02145.hp2 HG02615.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.696+9988T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49786119 | |||||||
| chr7:49786345 | T | C | 170 | a0001c0001t0001g0008 a0001c0001t0001g0113 a0001c0001t0001g0115 others(167): Show |
170 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.696+10214T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49786345 | |||||||
| chr7:49786467 | T | C | 113 | a0001c0001t0001g0115 a0001c0001t0001g0136 a0001c0001t0001g0139 others(110): Show |
113 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.696+10336T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49786467 | |||||||
| chr7:49786680 | T | A | 112 | a0001c0001t0001g0115 a0001c0001t0001g0136 a0001c0001t0001g0139 others(109): Show |
112 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.696+10549T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49786680 | |||||||
| chr7:49786865 | T | G | 2 | a0001c0001t0041g0007 a0002c0002t0003g0096 |
2 | HG02280.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.696+10734T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49786865 | |||||||
| chr7:49786872 | G | A | 1 | a0001c0001t0002g0110 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.696+10741G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49786872 | |||||||
| chr7:49786954 | T | C | 28 | a0001c0001t0001g0008 a0001c0001t0001g0183 a0001c0001t0001g0199 others(25): Show |
28 | HG02145.hp2 HG02257.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.696+10823T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49786954 | |||||||
| chr7:49786993 | A | G | 1 | a0001c0001t0015g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.696+10862A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49786993 | |||||||
| chr7:49787208 | T | G | 59 | a0001c0001t0001g0008 a0001c0001t0001g0113 a0001c0001t0001g0127 others(56): Show |
59 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.696+11077T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49787208 | |||||||
| chr7:49787392 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.696+11261A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49787392 | |||||||
| chr7:49787473 | C | T | 1 | a0002c0002t0003g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.696+11342C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49787473 | |||||||
| chr7:49787605 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.696+11474G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49787605 | |||||||
| chr7:49787642 | C | T | 4 | a0002c0002t0013g0042 a0002c0002t0022g0226 a0002c0002t0049g0208 others(1): Show |
4 | HG02630.hp1 HG03453.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.696+11511C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49787642 | |||||||
| chr7:49787937 | G | T | 3 | a0002c0002t0048g0225 a0002c0006t0057g0215 a0003c0003t0012g0251 |
3 | HG02970.hp2 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.696+11806G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49787937 | |||||||
| chr7:49788014 | C | A | 1 | a0001c0001t0001g0127 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.696+11883C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49788014 | |||||||
| chr7:49788055 | C | T | 19 | a0001c0001t0001g0113 a0001c0001t0001g0127 a0001c0001t0001g0129 others(16): Show |
19 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.696+11924C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49788055 | |||||||
| chr7:49788164 | G | T | 1 | a0001c0001t0005g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.696+12033G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49788164 | |||||||
| chr7:49788332 | A | C | 1 | a0002c0002t0003g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.696+12201A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49788332 | |||||||
| chr7:49788391 | C | T | 59 | a0001c0001t0001g0008 a0001c0001t0001g0113 a0001c0001t0001g0127 others(56): Show |
59 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.696+12260C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49788391 | |||||||
| chr7:49788414 | C | T | 1 | a0002c0002t0003g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.696+12283C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49788414 | |||||||
| chr7:49788418 | A | G | 1 | a0002c0002t0003g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.696+12287A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49788418 | |||||||
| chr7:49788422 | C | G | 213 | a0001c0001t0001g0008 a0001c0001t0001g0113 a0001c0001t0001g0115 others(210): Show |
214 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.696+12291C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49788422 | |||||||
| chr7:49788445 | C | CTG | 12 | a0001c0001t0003g0118 a0001c0001t0003g0119 a0001c0001t0003g0120 others(9): Show |
12 | HG01993.hp2 HG02015.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.696+12337_696+1233 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49788445 | ||||||
| chr7:49788445 | CTG | C | 108 | a0001c0001t0001g0115 a0001c0001t0001g0136 a0001c0001t0001g0139 others(105): Show |
108 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.696+12337_696+1233 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49788445 | ||||||
| chr7:49788468 | T | A | 63 | a0001c0001t0001g0115 a0001c0001t0001g0136 a0001c0001t0001g0139 others(60): Show |
63 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.696+12337T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49788468 | |||||||
| chr7:49788468 | TGA | T | 18 | a0001c0001t0001g0113 a0001c0001t0001g0129 a0001c0001t0001g0130 others(15): Show |
18 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.696+12345_696+1234 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49788468 | ||||||
| chr7:49788470 | A | T | 41 | a0001c0001t0001g0008 a0001c0001t0001g0127 a0001c0001t0001g0183 others(38): Show |
41 | HG01993.hp2 HG02055.hp1 HG02055.hp2 others(38): Show |
intron_variant | MODIFIER | c.696+12339A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49788470 | |||||||
| chr7:49788556 | AGAGTGTG others(1): Show |
A | 6 | a0002c0002t0003g0049 a0002c0002t0030g0101 a0002c0002t0039g0205 others(3): Show |
6 | HG01993.hp2 HG02055.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.696+12433_696+1244 others(12): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49788556 | ||||||
| chr7:49788575 | A | G | 59 | a0001c0001t0001g0008 a0001c0001t0001g0113 a0001c0001t0001g0127 others(56): Show |
59 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.696+12444A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49788575 | |||||||
| chr7:49788581 | G | A | 1 | a0002c0002t0029g0098 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.696+12450G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49788581 | |||||||
| chr7:49788589 | C | T | 18 | a0001c0001t0003g0167 a0001c0001t0004g0169 a0001c0001t0004g0170 others(15): Show |
19 | HG00735.hp1 HG01074.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.696+12458C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49788589 | |||||||
| chr7:49788624 | TGTGA | T | 60 | a0001c0001t0001g0008 a0001c0001t0001g0113 a0001c0001t0001g0126 others(57): Show |
60 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.696+12501_696+1250 others(8): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49788624 | ||||||
| chr7:49788653 | ATGTGTGG others(23): Show |
A | 1 | a0002c0002t0052g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.696+12529_696+1255 others(34): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49788653 | ||||||
| chr7:49788692 | GGT | G | 172 | a0001c0001t0001g0008 a0001c0001t0001g0113 a0001c0001t0001g0115 others(169): Show |
172 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.696+12573_696+1257 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49788692 | ||||||
| chr7:49788736 | ATG | A | 20 | a0001c0001t0001g0183 a0001c0001t0001g0199 a0001c0001t0001g0218 others(17): Show |
20 | HG02257.hp1 HG02257.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.696+12614_696+1261 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49788736 | ||||||
| chr7:49788757 | T | TGGGGGTG others(5): Show |
1 | a0002c0002t0007g0082 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.696+12628_696+1263 others(16): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49788757 | ||||||
| chr7:49788773 | GGTGT | G | 19 | a0001c0001t0001g0183 a0001c0001t0001g0199 a0001c0001t0001g0218 others(16): Show |
19 | HG02257.hp1 HG02257.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.696+12645_696+1264 others(8): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49788773 | ||||||
| chr7:49788826 | A | G | 1 | a0002c0002t0010g0027 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.696+12695A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49788826 | |||||||
| chr7:49788834 | A | G | 2 | a0002c0002t0009g0001 a0002c0002t0059g0085 |
3 | HG02698.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.696+12703A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49788834 | |||||||
| chr7:49788868 | G | A | 1 | a0003c0003t0011g0247 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.696+12737G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49788868 | |||||||
| chr7:49788869 | T | G | 2 | a0001c0001t0002g0133 a0002c0002t0031g0099 |
2 | HG00609.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.696+12738T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49788869 | |||||||
| chr7:49788869 | T | TG | 22 | a0001c0001t0001g0113 a0001c0001t0001g0127 a0001c0001t0001g0129 others(19): Show |
22 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.696+12744dupG | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49788869 | ||||||
| chr7:49788907 | TGA | T | 3 | a0001c0001t0011g0222 a0001c0001t0051g0009 a0002c0002t0003g0052 |
3 | HG02257.hp1 HG02922.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.696+12780_696+1278 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49788907 | ||||||
| chr7:49788921 | G | A | 28 | a0001c0001t0001g0008 a0001c0001t0001g0183 a0001c0001t0001g0199 others(25): Show |
28 | HG02145.hp2 HG02257.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.696+12790G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49788921 | |||||||
| chr7:49788988 | TGA | T | 3 | a0002c0002t0048g0225 a0002c0006t0057g0215 a0003c0003t0012g0251 |
3 | HG02970.hp2 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.696+12859_696+1286 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49788988 | ||||||
| chr7:49788996 | G | A | 112 | a0001c0001t0001g0115 a0001c0001t0001g0136 a0001c0001t0001g0139 others(109): Show |
112 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.696+12865G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49788996 | |||||||
| chr7:49789020 | G | T | 19 | a0001c0001t0001g0183 a0001c0001t0001g0199 a0001c0001t0001g0218 others(16): Show |
19 | HG02257.hp1 HG02257.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.696+12889G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49789020 | |||||||
| chr7:49789039 | TGTGTGA | T | 19 | a0001c0001t0001g0183 a0001c0001t0001g0199 a0001c0001t0001g0218 others(16): Show |
19 | HG02257.hp1 HG02257.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.696+12914_696+1291 others(10): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49789039 | ||||||
| chr7:49789067 | CGTGA | C | 9 | a0001c0001t0001g0008 a0001c0001t0008g0185 a0001c0001t0008g0186 others(6): Show |
9 | HG02145.hp2 HG02615.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.696+12940_696+1294 others(8): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49789067 | ||||||
| chr7:49789097 | TGA | T | 4 | a0001c0001t0004g0164 a0001c0001t0004g0165 a0001c0001t0007g0181 others(1): Show |
4 | HG01361.hp2 HG03654.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.696+12975_696+1297 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49789097 | ||||||
| chr7:49789103 | A | C | 60 | a0001c0001t0001g0008 a0001c0001t0001g0113 a0001c0001t0001g0127 others(57): Show |
60 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.696+12972A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49789103 | |||||||
| chr7:49789104 | G | T | 3 | a0002c0002t0048g0225 a0002c0006t0057g0215 a0003c0003t0012g0251 |
3 | HG02970.hp2 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.696+12973G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49789104 | |||||||
| chr7:49789109 | TGA | T | 6 | a0001c0001t0001g0002 a0001c0001t0003g0002 a0001c0001t0042g0148 others(3): Show |
6 | HG01070.hp1 HG01071.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.696+12984_696+1298 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49789109 | ||||||
| chr7:49789115 | AGT | A | 58 | a0001c0001t0001g0008 a0001c0001t0001g0113 a0001c0001t0001g0127 others(55): Show |
58 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(55): Show |
intron_variant | MODIFIER | c.696+12987_696+1298 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49789115 | ||||||
| chr7:49789162 | TATGTGTG others(7): Show |
T | 1 | a0001c0001t0015g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.696+13041_696+1305 others(18): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49789162 | ||||||
| chr7:49789163 | ATG | A | 3 | a0002c0002t0004g0062 a0002c0002t0025g0066 a0002c0002t0025g0067 |
3 | HG01109.hp2 HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.696+13040_696+1304 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49789163 | ||||||
| chr7:49789172 | TTAGCA | T | 4 | a0003c0003t0006g0246 a0003c0003t0011g0249 a0003c0003t0012g0248 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.696+13043_696+1304 others(9): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49789172 | ||||||
| chr7:49789188 | T | C | 22 | a0001c0001t0001g0113 a0001c0001t0001g0127 a0001c0001t0001g0129 others(19): Show |
22 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.696+13057T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49789188 | |||||||
| chr7:49789204 | G | GGT | 21 | a0001c0001t0001g0113 a0001c0001t0001g0127 a0001c0001t0001g0129 others(18): Show |
21 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.696+13085_696+1308 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49789204 | ||||||
| chr7:49789207 | G | A | 1 | a0002c0002t0004g0089 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.696+13076G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49789207 | |||||||
| chr7:49789213 | G | A | 1 | a0003c0003t0016g0230 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.696+13082G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49789213 | |||||||
| chr7:49789239 | G | C | 2 | a0002c0002t0001g0055 a0002c0002t0001g0056 |
2 | NA19064.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.696+13108G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49789239 | |||||||
| chr7:49789246 | G | T | 20 | a0001c0001t0003g0163 a0001c0001t0003g0167 a0001c0001t0003g0192 others(17): Show |
21 | HG00735.hp1 HG01074.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.696+13115G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49789246 | |||||||
| chr7:49789256 | TGGGTGTG others(7): Show |
T | 1 | a0002c0002t0029g0098 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.696+13139_696+1315 others(18): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49789256 | ||||||
| chr7:49789268 | A | G | 59 | a0001c0001t0001g0008 a0001c0001t0001g0113 a0001c0001t0001g0127 others(56): Show |
59 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.696+13137A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49789268 | |||||||
| chr7:49789270 | CGG | C | 19 | a0001c0001t0001g0183 a0001c0001t0001g0199 a0001c0001t0001g0218 others(16): Show |
19 | HG02257.hp1 HG02257.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.696+13141_696+1314 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49789270 | ||||||
| chr7:49789272 | G | T | 40 | a0001c0001t0001g0008 a0001c0001t0001g0113 a0001c0001t0001g0127 others(37): Show |
40 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.696+13141G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49789272 | |||||||
| chr7:49789320 | G | GGT | 157 | a0001c0001t0001g0008 a0001c0001t0001g0113 a0001c0001t0001g0127 others(154): Show |
158 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.696+13197_696+1319 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49789320 | ||||||
| chr7:49789330 | G | T | 17 | a0001c0001t0001g0183 a0001c0001t0001g0199 a0001c0001t0003g0184 others(14): Show |
17 | HG02257.hp1 HG02257.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.696+13199G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49789330 | |||||||
| chr7:49789332 | T | G | 17 | a0001c0001t0001g0183 a0001c0001t0001g0199 a0001c0001t0003g0184 others(14): Show |
17 | HG02257.hp1 HG02257.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.696+13201T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49789332 | |||||||
| chr7:49789334 | C | G | 1 | a0001c0001t0001g0218 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.696+13203C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49789334 | |||||||
| chr7:49789334 | C | T | 26 | a0001c0001t0001g0008 a0001c0001t0001g0183 a0001c0001t0001g0199 others(23): Show |
26 | HG02145.hp2 HG02257.hp1 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.696+13203C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49789334 | |||||||
| chr7:49789340 | A | T | 19 | a0001c0001t0001g0183 a0001c0001t0001g0199 a0001c0001t0001g0218 others(16): Show |
19 | HG02257.hp1 HG02257.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.696+13209A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49789340 | |||||||
| chr7:49789352 | G | A | 28 | a0001c0001t0001g0008 a0001c0001t0001g0183 a0001c0001t0001g0199 others(25): Show |
28 | HG02145.hp2 HG02257.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.696+13221G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49789352 | |||||||
| chr7:49789419 | TCCC | T | 22 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0179 others(19): Show |
22 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.697-13288_697-1328 others(7): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49789419 | ||||||
| chr7:49789429 | G | A | 7 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0003c0003t0006g0246 others(4): Show |
7 | HG02145.hp2 HG02615.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.697-13282G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49789429 | |||||||
| chr7:49789468 | A | G | 1 | a0001c0001t0002g0147 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.697-13243A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49789468 | |||||||
| chr7:49789538 | C | T | 16 | a0001c0001t0001g0183 a0001c0001t0001g0199 a0001c0001t0001g0218 others(13): Show |
16 | HG02257.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.697-13173C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49789538 | |||||||
| chr7:49789621 | C | CT | 123 | a0001c0001t0001g0008 a0001c0001t0001g0115 a0001c0001t0001g0136 others(120): Show |
123 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.697-13084dupT | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49789621 | ||||||
| chr7:49789636 | G | A | 6 | a0002c0002t0003g0049 a0002c0002t0030g0101 a0002c0002t0039g0205 others(3): Show |
6 | HG01993.hp2 HG02055.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.697-13075G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49789636 | |||||||
| chr7:49789911 | G | A | 1 | a0002c0002t0039g0205 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.697-12800G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49789911 | |||||||
| chr7:49789951 | G | C | 66 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0179 others(63): Show |
67 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.697-12760G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49789951 | |||||||
| chr7:49790195 | A | G | 6 | a0001c0001t0001g0199 a0001c0001t0008g0195 a0001c0001t0008g0196 others(3): Show |
6 | HG02922.hp2 HG03041.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.697-12516A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49790195 | |||||||
| chr7:49790203 | G | A | 3 | a0002c0002t0048g0225 a0002c0006t0057g0215 a0003c0003t0012g0251 |
3 | HG02970.hp2 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.697-12508G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49790203 | |||||||
| chr7:49790651 | T | G | 217 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(214): Show |
218 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.697-12060T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49790651 | |||||||
| chr7:49790740 | G | A | 35 | a0001c0001t0001g0008 a0001c0001t0001g0113 a0001c0001t0001g0127 others(32): Show |
35 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.697-11971G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49790740 | |||||||
| chr7:49790882 | A | T | 1 | a0002c0006t0057g0215 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.697-11829A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49790882 | |||||||
| chr7:49790950 | A | C | 1 | a0003c0003t0012g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.697-11761A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49790950 | |||||||
| chr7:49790999 | G | C | 145 | a0001c0001t0001g0008 a0001c0001t0001g0113 a0001c0001t0001g0115 others(142): Show |
145 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.697-11712G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49790999 | |||||||
| chr7:49791076 | A | C | 144 | a0001c0001t0001g0008 a0001c0001t0001g0113 a0001c0001t0001g0115 others(141): Show |
144 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.697-11635A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49791076 | |||||||
| chr7:49791123 | C | T | 145 | a0001c0001t0001g0008 a0001c0001t0001g0113 a0001c0001t0001g0115 others(142): Show |
145 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.697-11588C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49791123 | |||||||
| chr7:49791860 | A | G | 58 | a0001c0001t0001g0115 a0001c0001t0001g0136 a0001c0001t0001g0139 others(55): Show |
58 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.697-10851A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49791860 | |||||||
| chr7:49791870 | G | A | 1 | a0003c0003t0018g0233 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.697-10841G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49791870 | |||||||
| chr7:49791922 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.697-10789T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49791922 | |||||||
| chr7:49792104 | C | A | 1 | a0003c0003t0006g0234 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.697-10607C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49792104 | |||||||
| chr7:49792199 | G | A | 7 | a0002c0002t0003g0049 a0002c0002t0030g0101 a0002c0002t0039g0205 others(4): Show |
7 | HG01993.hp2 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.697-10512G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49792199 | |||||||
| chr7:49792476 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(126): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.697-10235T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49792476 | |||||||
| chr7:49792708 | G | A | 3 | a0002c0002t0001g0020 a0002c0002t0002g0021 a0002c0002t0003g0006 |
3 | HG00099.hp1 HG01081.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.697-10003G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49792708 | |||||||
| chr7:49792714 | T | A | 37 | a0001c0001t0001g0113 a0001c0001t0001g0127 a0001c0001t0001g0129 others(34): Show |
37 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.697-9997T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49792714 | |||||||
| chr7:49793204 | T | C | 7 | a0002c0002t0003g0049 a0002c0002t0030g0101 a0002c0002t0039g0205 others(4): Show |
7 | HG01993.hp2 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.697-9507T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49793204 | |||||||
| chr7:49793276 | T | G | 115 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0121 others(112): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.697-9435T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49793276 | |||||||
| chr7:49793394 | T | A | 43 | a0001c0001t0001g0002 a0001c0001t0001g0121 a0001c0001t0001g0124 others(40): Show |
44 | HG00099.hp2 HG00597.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.697-9317T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49793394 | |||||||
| chr7:49793581 | CT | C | 16 | a0001c0001t0001g0183 a0001c0001t0001g0199 a0001c0001t0001g0218 others(13): Show |
16 | HG02257.hp2 HG02258.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.697-9122delT | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49793581 | ||||||
| chr7:49793663 | T | C | 2 | a0001c0001t0067g0204 a0002c0002t0002g0039 |
2 | HG02074.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.697-9048T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49793663 | |||||||
| chr7:49793713 | A | C | 1 | a0002c0002t0002g0058 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.697-8998A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49793713 | |||||||
| chr7:49793745 | T | G | 1 | a0002c0002t0003g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.697-8966T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49793745 | |||||||
| chr7:49793774 | T | C | 1 | a0001c0001t0041g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.697-8937T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49793774 | |||||||
| chr7:49793895 | C | A | 1 | a0002c0002t0055g0211 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.697-8816C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49793895 | |||||||
| chr7:49793938 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.697-8773C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49793938 | |||||||
| chr7:49794092 | C | T | 27 | a0001c0001t0006g0221 a0001c0001t0007g0103 a0001c0001t0007g0107 others(24): Show |
27 | HG00099.hp1 HG00323.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.697-8619C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49794092 | |||||||
| chr7:49794181 | A | T | 1 | a0001c0001t0054g0004 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.697-8530A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49794181 | |||||||
| chr7:49794183 | GCTAGCAA others(4): Show |
G | 1 | a0001c0001t0054g0004 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.697-8527_697-8517d others(13): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49794183 | |||||||
| chr7:49794208 | C | T | 1 | a0002c0002t0029g0098 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.697-8503C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49794208 | |||||||
| chr7:49794321 | G | A | 28 | a0001c0001t0001g0113 a0001c0001t0001g0127 a0001c0001t0001g0129 others(25): Show |
28 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.697-8390G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49794321 | |||||||
| chr7:49794412 | T | C | 1 | a0003c0003t0006g0234 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.697-8299T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49794412 | |||||||
| chr7:49794546 | A | C | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.697-8165A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49794546 | |||||||
| chr7:49794624 | T | C | 3 | a0002c0002t0048g0225 a0002c0006t0057g0215 a0003c0003t0012g0251 |
3 | HG02970.hp2 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.697-8087T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49794624 | |||||||
| chr7:49794656 | C | T | 1 | a0001c0001t0040g0003 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.697-8055C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49794656 | |||||||
| chr7:49794763 | G | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0121 a0001c0001t0001g0124 others(39): Show |
43 | HG00099.hp2 HG00597.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.697-7948G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49794763 | |||||||
| chr7:49794886 | C | A | 5 | a0001c0001t0001g0008 a0002c0002t0048g0225 a0002c0002t0053g0095 others(2): Show |
5 | HG02970.hp2 HG03098.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.697-7825C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49794886 | |||||||
| chr7:49794945 | C | T | 1 | a0001c0001t0041g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.697-7766C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49794945 | |||||||
| chr7:49795094 | A | G | 1 | a0002c0002t0003g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.697-7617A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49795094 | |||||||
| chr7:49795171 | T | G | 1 | a0001c0001t0069g0176 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.697-7540T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49795171 | |||||||
| chr7:49795632 | C | A | 1 | a0001c0001t0002g0110 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.697-7079C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49795632 | |||||||
| chr7:49795632 | C | T | 4 | a0001c0001t0001g0183 a0001c0001t0003g0184 a0001c0001t0015g0182 others(1): Show |
4 | HG02257.hp2 HG02258.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.697-7079C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49795632 | |||||||
| chr7:49795717 | A | G | 1 | a0001c0001t0069g0176 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.697-6994A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49795717 | |||||||
| chr7:49795945 | G | A | 3 | a0002c0002t0003g0045 a0002c0002t0014g0043 a0002c0002t0014g0044 |
3 | HG02258.hp1 HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.697-6766G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49795945 | |||||||
| chr7:49795961 | G | A | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.697-6750G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49795961 | |||||||
| chr7:49795967 | C | T | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.697-6744C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49795967 | |||||||
| chr7:49796172 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.697-6539A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49796172 | |||||||
| chr7:49796864 | A | C | 72 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0121 others(69): Show |
73 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.697-5847A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49796864 | |||||||
| chr7:49797054 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(126): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.697-5657T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49797054 | |||||||
| chr7:49797293 | C | A | 1 | a0002c0002t0001g0055 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.697-5418C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49797293 | |||||||
| chr7:49797351 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.697-5360A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49797351 | |||||||
| chr7:49797423 | A | C | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.697-5288A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49797423 | |||||||
| chr7:49797531 | T | A | 26 | a0001c0001t0006g0221 a0001c0001t0007g0103 a0001c0001t0007g0107 others(23): Show |
26 | HG00099.hp1 HG00323.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.697-5180T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49797531 | |||||||
| chr7:49797542 | G | A | 1 | a0002c0002t0002g0029 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.697-5169G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49797542 | |||||||
| chr7:49797578 | G | A | 3 | a0001c0001t0002g0188 a0001c0001t0002g0189 a0002c0002t0002g0005 |
3 | HG01123.hp1 NA18946.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.697-5133G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49797578 | |||||||
| chr7:49797638 | T | A | 1 | a0001c0001t0003g0190 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.697-5073T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49797638 | |||||||
| chr7:49797680 | A | T | 1 | a0002c0002t0002g0081 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.697-5031A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49797680 | |||||||
| chr7:49797742 | T | C | 1 | a0002c0002t0013g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.697-4969T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49797742 | |||||||
| chr7:49797747 | A | G | 20 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0002g0177 others(17): Show |
20 | HG00099.hp2 HG00597.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.697-4964A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49797747 | |||||||
| chr7:49797843 | A | G | 1 | a0002c0002t0003g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.697-4868A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49797843 | |||||||
| chr7:49797908 | C | T | 27 | a0001c0001t0006g0221 a0001c0001t0007g0103 a0001c0001t0007g0107 others(24): Show |
27 | HG00099.hp1 HG00323.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.697-4803C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49797908 | |||||||
| chr7:49798030 | G | T | 1 | a0003c0003t0011g0228 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.697-4681G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49798030 | |||||||
| chr7:49798040 | G | T | 1 | a0001c0001t0009g0175 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.697-4671G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49798040 | |||||||
| chr7:49798071 | T | C | 1 | a0002c0002t0003g0023 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.697-4640T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49798071 | |||||||
| chr7:49798186 | C | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(126): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.697-4525C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49798186 | |||||||
| chr7:49798254 | G | A | 72 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0121 others(69): Show |
73 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.697-4457G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49798254 | |||||||
| chr7:49798317 | C | T | 44 | a0001c0001t0001g0002 a0001c0001t0001g0121 a0001c0001t0001g0124 others(41): Show |
45 | HG00099.hp2 HG00597.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.697-4394C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49798317 | |||||||
| chr7:49798468 | G | A | 1 | a0001c0001t0007g0160 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.697-4243G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49798468 | |||||||
| chr7:49798579 | A | G | 26 | a0001c0001t0006g0221 a0001c0001t0007g0103 a0001c0001t0007g0107 others(23): Show |
26 | HG00099.hp1 HG00323.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.697-4132A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49798579 | |||||||
| chr7:49798595 | T | G | 2 | a0002c0002t0048g0225 a0003c0003t0012g0251 |
2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.697-4116T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49798595 | |||||||
| chr7:49798926 | T | C | 226 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.697-3785T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49798926 | |||||||
| chr7:49798939 | A | T | 1 | a0001c0001t0008g0198 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.697-3772A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49798939 | |||||||
| chr7:49798964 | T | C | 1 | a0001c0001t0007g0103 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.697-3747T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49798964 | |||||||
| chr7:49799047 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.697-3664C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49799047 | |||||||
| chr7:49799087 | G | A | 72 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0121 others(69): Show |
73 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.697-3624G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49799087 | |||||||
| chr7:49799277 | G | A | 1 | a0001c0001t0005g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.697-3434G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49799277 | |||||||
| chr7:49799521 | A | G | 1 | a0002c0002t0001g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.697-3190A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49799521 | |||||||
| chr7:49799568 | G | A | 1 | a0003c0003t0011g0241 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.697-3143G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49799568 | |||||||
| chr7:49799569 | C | A | 1 | a0003c0003t0011g0241 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.697-3142C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49799569 | |||||||
| chr7:49799706 | C | T | 26 | a0001c0001t0006g0221 a0001c0001t0007g0103 a0001c0001t0007g0107 others(23): Show |
26 | HG00099.hp1 HG00323.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.697-3005C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49799706 | |||||||
| chr7:49799720 | A | T | 4 | a0003c0003t0006g0246 a0003c0003t0011g0249 a0003c0003t0012g0248 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.697-2991A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49799720 | |||||||
| chr7:49799738 | T | C | 1 | a0003c0003t0006g0252 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.697-2973T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49799738 | |||||||
| chr7:49799839 | T | C | 4 | a0001c0001t0001g0183 a0001c0001t0003g0184 a0001c0001t0015g0182 others(1): Show |
4 | HG02257.hp2 HG02258.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.697-2872T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49799839 | |||||||
| chr7:49799869 | G | A | 52 | a0001c0001t0001g0002 a0001c0001t0001g0121 a0001c0001t0001g0124 others(49): Show |
53 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.697-2842G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49799869 | |||||||
| chr7:49799985 | T | C | 99 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0121 others(96): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.697-2726T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49799985 | |||||||
| chr7:49800115 | T | C | 9 | a0002c0002t0003g0049 a0002c0002t0013g0042 a0002c0002t0030g0101 others(6): Show |
9 | HG01993.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.697-2596T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49800115 | |||||||
| chr7:49800333 | C | T | 1 | a0002c0002t0001g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.697-2378C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49800333 | |||||||
| chr7:49800593 | C | G | 1 | a0002c0002t0014g0064 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.697-2118C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49800593 | |||||||
| chr7:49800848 | C | CA | 24 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0002g0149 others(21): Show |
24 | HG01361.hp1 HG01978.hp1 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.697-1840dupA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49800848 | ||||||
| chr7:49800848 | CA | C | 44 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0127 others(41): Show |
44 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.697-1840delA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49800848 | ||||||
| chr7:49800848 | CAA | C | 9 | a0001c0001t0001g0126 a0001c0001t0006g0221 a0001c0001t0040g0003 others(6): Show |
9 | HG02451.hp2 HG02559.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.697-1841_697-1840d others(4): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49800848 | ||||||
| chr7:49800848 | CAAAAAAA | C | 9 | a0002c0002t0003g0049 a0002c0002t0013g0042 a0002c0002t0030g0101 others(6): Show |
9 | HG01993.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.697-1846_697-1840d others(9): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49800848 | ||||||
| chr7:49801285 | A | G | 1 | a0001c0001t0044g0138 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.697-1426A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49801285 | |||||||
| chr7:49801321 | A | G | 54 | a0001c0001t0001g0115 a0001c0001t0001g0136 a0001c0001t0001g0139 others(51): Show |
54 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.697-1390A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49801321 | |||||||
| chr7:49801409 | G | T | 1 | a0002c0002t0068g0227 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.697-1302G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49801409 | |||||||
| chr7:49801523 | G | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(126): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.697-1188G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49801523 | |||||||
| chr7:49801532 | G | A | 1 | a0001c0001t0015g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.697-1179G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49801532 | |||||||
| chr7:49801620 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.697-1091G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49801620 | |||||||
| chr7:49801654 | G | A | 5 | a0001c0001t0009g0174 a0001c0001t0009g0175 a0002c0002t0001g0020 others(2): Show |
5 | HG00099.hp1 HG00323.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.697-1057G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49801654 | |||||||
| chr7:49801744 | T | C | 1 | a0003c0003t0037g0229 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.697-967T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49801744 | |||||||
| chr7:49801843 | G | A | 28 | a0001c0001t0006g0221 a0001c0001t0007g0103 a0001c0001t0007g0107 others(25): Show |
28 | HG00099.hp1 HG00323.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.697-868G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49801843 | |||||||
| chr7:49801897 | C | T | 2 | a0002c0002t0022g0226 a0002c0002t0049g0208 |
2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.697-814C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49801897 | |||||||
| chr7:49802038 | G | A | 2 | a0002c0002t0001g0055 a0002c0002t0001g0056 |
2 | NA19064.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.697-673G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49802038 | |||||||
| chr7:49802114 | CA | C | 25 | a0001c0001t0001g0113 a0001c0001t0001g0127 a0001c0001t0001g0129 others(22): Show |
25 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.697-589delA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49802114 | ||||||
| chr7:49802254 | G | A | 27 | a0001c0001t0006g0221 a0001c0001t0007g0103 a0001c0001t0007g0107 others(24): Show |
27 | HG00099.hp1 HG00323.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.697-457G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49802254 | |||||||
| chr7:49802331 | A | G | 1 | a0002c0002t0002g0039 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.697-380A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | chr7 | 49802331 | |||||||
| chr7:49802338 | AG | A | 10 | a0001c0001t0007g0103 a0001c0001t0007g0107 a0001c0001t0007g0108 others(7): Show |
10 | HG00099.hp1 HG00323.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.697-370delG | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 49802338 | ||||||
| chr7:49802844 | T | C | 2 | a0002c0002t0022g0226 a0002c0002t0049g0208 |
2 | HG02630.hp1 NA18522.hp1 |
splice_region_variant&intron_variant | LOW | c.826+4T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49802844 | |||||||
| chr7:49802965 | C | T | 27 | a0001c0001t0006g0221 a0001c0001t0007g0103 a0001c0001t0007g0107 others(24): Show |
27 | HG00099.hp1 HG00323.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.826+125C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49802965 | |||||||
| chr7:49803181 | C | T | 7 | a0002c0002t0003g0049 a0002c0002t0030g0101 a0002c0002t0039g0205 others(4): Show |
7 | HG01993.hp2 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+341C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49803181 | |||||||
| chr7:49803313 | C | T | 1 | a0002c0002t0003g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.826+473C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49803313 | |||||||
| chr7:49803325 | G | T | 2 | a0002c0002t0048g0225 a0003c0003t0012g0251 |
2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.826+485G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49803325 | |||||||
| chr7:49803387 | C | T | 1 | a0002c0002t0001g0011 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.826+547C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49803387 | |||||||
| chr7:49803559 | C | A | 27 | a0001c0001t0006g0221 a0001c0001t0007g0103 a0001c0001t0007g0107 others(24): Show |
27 | HG00099.hp1 HG00323.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.826+719C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49803559 | |||||||
| chr7:49803620 | T | A | 26 | a0001c0001t0001g0113 a0001c0001t0001g0127 a0001c0001t0001g0129 others(23): Show |
26 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.826+780T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49803620 | |||||||
| chr7:49803672 | G | A | 2 | a0002c0002t0046g0050 a0002c0002t0047g0209 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.826+832G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49803672 | |||||||
| chr7:49803722 | G | T | 1 | a0002c0002t0002g0035 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.826+882G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49803722 | |||||||
| chr7:49803811 | G | A | 1 | a0002c0002t0003g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.826+971G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49803811 | |||||||
| chr7:49803857 | C | G | 19 | a0001c0001t0006g0221 a0001c0001t0007g0103 a0001c0001t0007g0107 others(16): Show |
19 | HG00099.hp1 HG00323.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.826+1017C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49803857 | |||||||
| chr7:49803951 | G | A | 1 | a0002c0002t0055g0211 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.826+1111G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49803951 | |||||||
| chr7:49804172 | T | A | 1 | a0001c0001t0063g0217 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.826+1332T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49804172 | |||||||
| chr7:49804173 | A | T | 76 | a0001c0001t0001g0115 a0001c0001t0001g0136 a0001c0001t0001g0139 others(73): Show |
76 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.826+1333A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49804173 | |||||||
| chr7:49804194 | A | G | 2 | a0002c0002t0024g0216 a0003c0003t0033g0236 |
2 | NA19010.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.826+1354A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49804194 | |||||||
| chr7:49804331 | G | C | 1 | a0002c0002t0003g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.826+1491G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49804331 | |||||||
| chr7:49804361 | C | T | 1 | a0002c0002t0003g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.826+1521C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49804361 | |||||||
| chr7:49804404 | C | G | 1 | a0003c0003t0011g0228 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.826+1564C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49804404 | |||||||
| chr7:49804461 | G | C | 1 | a0002c0002t0013g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.826+1621G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49804461 | |||||||
| chr7:49804510 | C | T | 1 | a0002c0002t0003g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.826+1670C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49804510 | |||||||
| chr7:49804551 | T | G | 1 | a0003c0003t0011g0228 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.826+1711T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49804551 | |||||||
| chr7:49804665 | A | T | 1 | a0002c0002t0003g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.826+1825A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49804665 | |||||||
| chr7:49804681 | G | A | 8 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0003c0003t0006g0244 others(5): Show |
8 | HG02145.hp2 HG02615.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.826+1841G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49804681 | |||||||
| chr7:49804821 | C | T | 1 | a0001c0001t0003g0190 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.826+1981C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49804821 | |||||||
| chr7:49804883 | A | G | 7 | a0002c0002t0003g0049 a0002c0002t0030g0101 a0002c0002t0039g0205 others(4): Show |
7 | HG01993.hp2 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+2043A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49804883 | |||||||
| chr7:49805034 | A | G | 130 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(127): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.826+2194A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49805034 | |||||||
| chr7:49805041 | A | C | 1 | a0002c0002t0014g0064 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.826+2201A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49805041 | |||||||
| chr7:49805200 | T | C | 27 | a0001c0001t0006g0221 a0001c0001t0007g0103 a0001c0001t0007g0107 others(24): Show |
27 | HG00099.hp1 HG00323.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.826+2360T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49805200 | |||||||
| chr7:49805255 | G | T | 2 | a0002c0002t0022g0226 a0002c0002t0049g0208 |
2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.826+2415G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49805255 | |||||||
| chr7:49805419 | A | T | 1 | a0003c0003t0006g0243 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.826+2579A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49805419 | |||||||
| chr7:49805423 | T | C | 1 | a0003c0003t0006g0234 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.826+2583T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49805423 | |||||||
| chr7:49805579 | C | T | 17 | a0001c0001t0001g0183 a0001c0001t0001g0199 a0001c0001t0001g0218 others(14): Show |
17 | HG02257.hp2 HG02258.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.826+2739C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49805579 | |||||||
| chr7:49805883 | G | A | 1 | a0002c0002t0003g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.826+3043G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49805883 | |||||||
| chr7:49805914 | C | G | 9 | a0002c0002t0003g0049 a0002c0002t0013g0042 a0002c0002t0030g0101 others(6): Show |
9 | HG01993.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.826+3074C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49805914 | |||||||
| chr7:49806095 | T | TC | 15 | a0001c0001t0007g0160 a0001c0001t0008g0185 a0001c0001t0008g0186 others(12): Show |
15 | HG00099.hp1 HG00323.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.826+3257dupC | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49806095 | ||||||
| chr7:49806095 | T | TCC | 3 | a0001c0001t0007g0103 a0001c0001t0007g0107 a0001c0001t0007g0108 |
3 | HG03490.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.826+3256_826+3257d others(4): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49806095 | ||||||
| chr7:49806097 | C | T | 9 | a0002c0002t0003g0049 a0002c0002t0013g0042 a0002c0002t0030g0101 others(6): Show |
9 | HG01993.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.826+3257C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49806097 | |||||||
| chr7:49806098 | A | C | 28 | a0001c0001t0006g0221 a0001c0001t0007g0103 a0001c0001t0007g0107 others(25): Show |
28 | HG00099.hp1 HG00323.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.826+3258A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49806098 | |||||||
| chr7:49806243 | A | C | 27 | a0001c0001t0006g0221 a0001c0001t0007g0103 a0001c0001t0007g0107 others(24): Show |
27 | HG00099.hp1 HG00323.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.826+3403A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49806243 | |||||||
| chr7:49806393 | T | C | 1 | a0002c0006t0057g0215 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.826+3553T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49806393 | |||||||
| chr7:49806581 | T | G | 1 | a0002c0002t0001g0097 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.826+3741T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49806581 | |||||||
| chr7:49806591 | G | A | 27 | a0001c0001t0006g0221 a0001c0001t0007g0103 a0001c0001t0007g0107 others(24): Show |
27 | HG00099.hp1 HG00323.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.826+3751G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49806591 | |||||||
| chr7:49806610 | A | G | 1 | a0002c0002t0003g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.826+3770A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49806610 | |||||||
| chr7:49806621 | C | T | 5 | a0001c0001t0001g0008 a0002c0002t0048g0225 a0002c0002t0053g0095 others(2): Show |
5 | HG02970.hp2 HG03098.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.826+3781C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49806621 | |||||||
| chr7:49806752 | G | A | 1 | a0002c0002t0010g0025 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.826+3912G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49806752 | |||||||
| chr7:49806759 | T | G | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.826+3919T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49806759 | |||||||
| chr7:49806868 | T | G | 130 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(127): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.826+4028T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49806868 | |||||||
| chr7:49807100 | T | C | 2 | a0002c0002t0022g0226 a0002c0002t0049g0208 |
2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.826+4260T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49807100 | |||||||
| chr7:49807290 | C | T | 2 | a0002c0002t0022g0226 a0002c0002t0049g0208 |
2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.826+4450C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49807290 | |||||||
| chr7:49807456 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.826+4616C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49807456 | |||||||
| chr7:49807490 | C | T | 1 | a0001c0001t0041g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.826+4650C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49807490 | |||||||
| chr7:49807790 | T | A | 1 | a0002c0002t0019g0026 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.826+4950T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49807790 | |||||||
| chr7:49807920 | C | G | 3 | a0002c0002t0026g0041 a0002c0002t0026g0254 a0002c0002t0032g0102 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.826+5080C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49807920 | |||||||
| chr7:49808167 | C | T | 1 | a0002c0002t0003g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.826+5327C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49808167 | |||||||
| chr7:49808274 | T | G | 1 | a0001c0001t0007g0103 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.826+5434T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49808274 | |||||||
| chr7:49808513 | C | A | 27 | a0001c0001t0001g0113 a0001c0001t0001g0127 a0001c0001t0001g0129 others(24): Show |
27 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.826+5673C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49808513 | |||||||
| chr7:49808591 | G | T | 11 | a0001c0001t0001g0179 a0001c0001t0001g0202 a0001c0001t0001g0203 others(8): Show |
11 | HG02145.hp1 HG03017.hp2 HG03669.hp2 others(8): Show |
intron_variant | MODIFIER | c.826+5751G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49808591 | |||||||
| chr7:49808684 | A | G | 1 | a0003c0003t0012g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.826+5844A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49808684 | |||||||
| chr7:49808712 | A | G | 83 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0121 others(80): Show |
84 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.826+5872A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49808712 | |||||||
| chr7:49808846 | C | A | 1 | a0001c0001t0005g0012 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.826+6006C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49808846 | |||||||
| chr7:49808912 | G | T | 8 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0003c0003t0006g0244 others(5): Show |
8 | HG02145.hp2 HG02615.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.826+6072G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49808912 | |||||||
| chr7:49809008 | C | A | 7 | a0002c0002t0003g0049 a0002c0002t0030g0101 a0002c0002t0039g0205 others(4): Show |
7 | HG01993.hp2 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+6168C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49809008 | |||||||
| chr7:49809212 | C | T | 54 | a0001c0001t0001g0115 a0001c0001t0001g0136 a0001c0001t0001g0139 others(51): Show |
54 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.826+6372C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49809212 | |||||||
| chr7:49809238 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.826+6398T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49809238 | |||||||
| chr7:49809245 | A | G | 1 | a0001c0001t0002g0146 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.826+6405A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49809245 | |||||||
| chr7:49809360 | T | G | 2 | a0001c0001t0001g0008 a0002c0002t0053g0095 |
2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.826+6520T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49809360 | |||||||
| chr7:49809402 | G | A | 8 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0003c0003t0006g0244 others(5): Show |
8 | HG02145.hp2 HG02615.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.826+6562G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49809402 | |||||||
| chr7:49809465 | T | C | 1 | a0003c0003t0012g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.826+6625T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49809465 | |||||||
| chr7:49809605 | A | G | 1 | a0002c0002t0013g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.826+6765A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49809605 | |||||||
| chr7:49809651 | G | A | 1 | a0002c0002t0027g0069 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.826+6811G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49809651 | |||||||
| chr7:49809778 | A | G | 1 | a0002c0002t0029g0098 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.826+6938A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49809778 | |||||||
| chr7:49810060 | A | G | 20 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0002g0177 others(17): Show |
20 | HG00099.hp2 HG00597.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.826+7220A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49810060 | |||||||
| chr7:49810131 | G | A | 1 | a0002c0002t0003g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.826+7291G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49810131 | |||||||
| chr7:49810152 | T | G | 10 | a0001c0001t0001g0115 a0001c0001t0001g0136 a0001c0001t0002g0191 others(7): Show |
10 | HG00423.hp1 NA18612.hp2 NA18747.hp1 others(7): Show |
intron_variant | MODIFIER | c.826+7312T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49810152 | |||||||
| chr7:49810237 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.826+7397T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49810237 | |||||||
| chr7:49810253 | A | G | 30 | a0001c0001t0001g0113 a0001c0001t0001g0127 a0001c0001t0001g0129 others(27): Show |
30 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.826+7413A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49810253 | |||||||
| chr7:49810396 | A | G | 4 | a0001c0001t0001g0002 a0001c0001t0003g0002 a0001c0001t0003g0163 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+7556A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49810396 | |||||||
| chr7:49810508 | C | T | 8 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0003c0003t0006g0244 others(5): Show |
8 | HG02145.hp2 HG02615.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.826+7668C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49810508 | |||||||
| chr7:49810528 | A | C | 7 | a0002c0002t0003g0049 a0002c0002t0030g0101 a0002c0002t0039g0205 others(4): Show |
7 | HG01993.hp2 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+7688A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49810528 | |||||||
| chr7:49810554 | T | C | 25 | a0001c0001t0001g0113 a0001c0001t0001g0127 a0001c0001t0001g0129 others(22): Show |
25 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.826+7714T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49810554 | |||||||
| chr7:49810672 | T | C | 1 | a0002c0002t0023g0210 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.826+7832T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49810672 | |||||||
| chr7:49810677 | G | T | 1 | a0003c0003t0006g0234 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.826+7837G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49810677 | |||||||
| chr7:49810700 | G | A | 29 | a0001c0001t0001g0150 a0001c0001t0001g0156 a0001c0001t0001g0179 others(26): Show |
29 | HG00609.hp2 HG00741.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.826+7860G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49810700 | |||||||
| chr7:49811082 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0121 a0001c0001t0001g0124 others(52): Show |
56 | HG00099.hp2 HG00597.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.826+8242C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49811082 | |||||||
| chr7:49811084 | A | G | 1 | a0003c0003t0034g0232 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.826+8244A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49811084 | |||||||
| chr7:49811109 | A | G | 1 | a0002c0002t0055g0211 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.826+8269A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49811109 | |||||||
| chr7:49811123 | AG | A | 5 | a0003c0003t0006g0244 a0003c0003t0006g0246 a0003c0003t0011g0249 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.826+8284delG | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49811123 | |||||||
| chr7:49811204 | G | C | 2 | a0002c0002t0001g0020 a0002c0002t0002g0021 |
2 | HG00099.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.826+8364G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49811204 | |||||||
| chr7:49811205 | A | G | 6 | a0001c0001t0002g0123 a0001c0001t0002g0132 a0001c0001t0002g0213 others(3): Show |
6 | HG00323.hp2 HG00733.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.826+8365A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49811205 | |||||||
| chr7:49811518 | G | T | 1 | a0001c0001t0001g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.826+8678G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49811518 | |||||||
| chr7:49811599 | T | A | 1 | a0003c0003t0006g0235 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.826+8759T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49811599 | |||||||
| chr7:49811783 | G | A | 1 | a0002c0002t0001g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.826+8943G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49811783 | |||||||
| chr7:49811827 | G | C | 1 | a0002c0002t0003g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.826+8987G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49811827 | |||||||
| chr7:49811909 | A | G | 1 | a0002c0002t0005g0080 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.826+9069A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49811909 | |||||||
| chr7:49812043 | A | C | 4 | a0004c0004t0001g0016 a0004c0004t0001g0063 a0004c0004t0001g0070 others(1): Show |
4 | HG01255.hp1 HG01258.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+9203A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49812043 | |||||||
| chr7:49812050 | G | A | 2 | a0002c0002t0010g0018 a0002c0002t0010g0019 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.826+9210G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49812050 | |||||||
| chr7:49812322 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.826+9482A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49812322 | |||||||
| chr7:49812730 | G | C | 5 | a0001c0001t0001g0008 a0002c0002t0048g0225 a0002c0002t0053g0095 others(2): Show |
5 | HG02970.hp2 HG03098.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.826+9890G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49812730 | |||||||
| chr7:49812797 | T | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(108): Show |
112 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.826+9957T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49812797 | |||||||
| chr7:49812969 | T | C | 1 | a0002c0002t0001g0031 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.826+10129T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49812969 | |||||||
| chr7:49813042 | G | A | 1 | a0002c0002t0002g0030 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.826+10202G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49813042 | |||||||
| chr7:49813134 | A | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0121 a0001c0001t0001g0124 others(52): Show |
56 | HG00099.hp2 HG00597.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.826+10294A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49813134 | |||||||
| chr7:49813892 | C | T | 1 | a0002c0002t0001g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.826+11052C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49813892 | |||||||
| chr7:49814078 | T | C | 5 | a0001c0001t0003g0118 a0001c0001t0003g0119 a0001c0001t0003g0166 others(2): Show |
5 | HG02015.hp2 NA18944.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.826+11238T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49814078 | |||||||
| chr7:49814094 | G | A | 1 | a0001c0001t0006g0221 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.826+11254G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49814094 | |||||||
| chr7:49814761 | G | A | 4 | a0002c0002t0004g0062 a0002c0002t0025g0066 a0002c0002t0025g0067 others(1): Show |
4 | HG01109.hp2 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.826+11921G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49814761 | |||||||
| chr7:49814808 | GC | G | 8 | a0002c0002t0003g0049 a0002c0002t0030g0101 a0002c0002t0039g0205 others(5): Show |
8 | HG01993.hp2 HG02055.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.826+11971delC | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49814808 | ||||||
| chr7:49814964 | A | G | 30 | a0001c0001t0001g0113 a0001c0001t0001g0127 a0001c0001t0001g0129 others(27): Show |
30 | HG00280.hp1 HG00423.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.826+12124A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49814964 | |||||||
| chr7:49815047 | G | T | 1 | a0002c0002t0003g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.826+12207G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49815047 | |||||||
| chr7:49815108 | C | T | 1 | a0003c0003t0006g0235 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.826+12268C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49815108 | |||||||
| chr7:49815129 | C | T | 1 | a0002c0002t0053g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.826+12289C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49815129 | |||||||
| chr7:49815194 | C | T | 1 | a0001c0001t0063g0217 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.826+12354C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49815194 | |||||||
| chr7:49815199 | A | C | 31 | a0001c0001t0001g0115 a0001c0001t0001g0127 a0001c0001t0001g0129 others(28): Show |
31 | HG00280.hp1 HG00423.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.826+12359A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49815199 | |||||||
| chr7:49815255 | A | G | 1 | a0003c0003t0012g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.826+12415A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49815255 | |||||||
| chr7:49815265 | T | A | 12 | a0001c0001t0003g0167 a0001c0001t0007g0103 a0001c0001t0007g0107 others(9): Show |
13 | HG00323.hp1 HG00735.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.826+12425T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49815265 | |||||||
| chr7:49815480 | A | C | 228 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(225): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.826+12640A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49815480 | |||||||
| chr7:49815564 | G | A | 1 | a0001c0001t0060g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.826+12724G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49815564 | |||||||
| chr7:49815691 | C | T | 1 | a0001c0001t0002g0110 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.826+12851C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49815691 | |||||||
| chr7:49815717 | T | G | 1 | a0002c0002t0013g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.826+12877T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49815717 | |||||||
| chr7:49815823 | A | T | 2 | a0001c0001t0002g0132 a0002c0002t0002g0034 |
2 | HG00733.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.826+12983A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49815823 | |||||||
| chr7:49815914 | C | T | 28 | a0001c0001t0001g0156 a0001c0001t0001g0179 a0001c0001t0001g0193 others(25): Show |
28 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.826+13074C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49815914 | |||||||
| chr7:49816047 | T | C | 2 | a0001c0001t0003g0163 a0001c0001t0003g0192 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.826+13207T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49816047 | |||||||
| chr7:49816141 | G | A | 1 | a0002c0002t0062g0086 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.826+13301G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49816141 | |||||||
| chr7:49816175 | G | A | 1 | a0003c0003t0006g0246 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.826+13335G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49816175 | |||||||
| chr7:49816424 | A | G | 17 | a0001c0001t0001g0156 a0001c0001t0001g0193 a0001c0001t0005g0012 others(14): Show |
17 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.826+13584A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49816424 | |||||||
| chr7:49816439 | A | G | 226 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.826+13599A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49816439 | |||||||
| chr7:49816458 | A | G | 1 | a0002c0002t0045g0068 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.826+13618A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49816458 | |||||||
| chr7:49816468 | C | G | 1 | a0002c0002t0003g0075 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.826+13628C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49816468 | |||||||
| chr7:49816470 | A | G | 17 | a0001c0001t0001g0156 a0001c0001t0001g0193 a0001c0001t0005g0012 others(14): Show |
17 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.826+13630A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49816470 | |||||||
| chr7:49816500 | T | G | 1 | a0001c0001t0015g0182 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.826+13660T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49816500 | |||||||
| chr7:49816667 | C | A | 4 | a0001c0001t0001g0183 a0002c0002t0001g0053 a0002c0002t0001g0054 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+13827C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49816667 | |||||||
| chr7:49816699 | A | G | 211 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(208): Show |
212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.826+13859A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49816699 | |||||||
| chr7:49816708 | G | A | 11 | a0001c0001t0001g0179 a0001c0001t0001g0202 a0001c0001t0001g0203 others(8): Show |
11 | HG01261.hp1 HG02145.hp1 HG03017.hp2 others(8): Show |
intron_variant | MODIFIER | c.826+13868G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49816708 | |||||||
| chr7:49816807 | C | A | 1 | a0002c0002t0010g0025 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.826+13967C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49816807 | |||||||
| chr7:49817074 | A | G | 1 | a0002c0002t0029g0098 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.826+14234A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49817074 | |||||||
| chr7:49817372 | T | C | 1 | a0001c0001t0001g0207 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.826+14532T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49817372 | |||||||
| chr7:49817374 | G | A | 2 | a0002c0002t0001g0055 a0002c0002t0001g0056 |
2 | NA19064.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.826+14534G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49817374 | |||||||
| chr7:49817618 | T | C | 1 | a0001c0001t0002g0188 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.826+14778T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49817618 | |||||||
| chr7:49817734 | A | G | 2 | a0001c0001t0001g0008 a0002c0002t0053g0095 |
2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.826+14894A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49817734 | |||||||
| chr7:49817899 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.826+15059T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49817899 | |||||||
| chr7:49818197 | TC | T | 12 | a0001c0001t0001g0179 a0001c0001t0001g0202 a0001c0001t0001g0203 others(9): Show |
12 | HG01261.hp1 HG02145.hp1 HG03017.hp2 others(9): Show |
intron_variant | MODIFIER | c.826+15359delC | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49818197 | ||||||
| chr7:49818218 | A | C | 6 | a0001c0001t0001g0145 a0001c0001t0002g0147 a0001c0001t0002g0177 others(3): Show |
6 | HG01099.hp2 HG02300.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.826+15378A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49818218 | |||||||
| chr7:49818239 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.826+15399A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49818239 | |||||||
| chr7:49818264 | A | T | 118 | a0001c0001t0001g0115 a0001c0001t0001g0126 a0001c0001t0001g0127 others(115): Show |
119 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.826+15424A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49818264 | |||||||
| chr7:49818335 | A | G | 1 | a0002c0002t0013g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.826+15495A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49818335 | |||||||
| chr7:49818338 | G | A | 1 | a0003c0003t0006g0244 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.826+15498G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49818338 | |||||||
| chr7:49818399 | C | T | 2 | a0001c0001t0002g0147 a0002c0002t0002g0065 |
2 | HG02735.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.826+15559C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49818399 | |||||||
| chr7:49818779 | C | T | 17 | a0001c0001t0001g0156 a0001c0001t0001g0193 a0001c0001t0005g0012 others(14): Show |
17 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.826+15939C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49818779 | |||||||
| chr7:49818899 | A | C | 50 | a0001c0001t0001g0136 a0001c0001t0001g0139 a0001c0001t0001g0145 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.826+16059A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49818899 | |||||||
| chr7:49818925 | A | G | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.826+16085A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49818925 | |||||||
| chr7:49818948 | C | T | 12 | a0001c0001t0001g0179 a0001c0001t0001g0202 a0001c0001t0001g0203 others(9): Show |
12 | HG01261.hp1 HG02145.hp1 HG03017.hp2 others(9): Show |
intron_variant | MODIFIER | c.826+16108C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49818948 | |||||||
| chr7:49818982 | G | A | 1 | a0002c0002t0007g0082 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.826+16142G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49818982 | |||||||
| chr7:49819750 | G | T | 2 | a0001c0001t0004g0169 a0001c0001t0004g0170 |
2 | NA18946.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.826+16910G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49819750 | |||||||
| chr7:49819807 | G | A | 1 | a0002c0002t0002g0081 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.826+16967G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49819807 | |||||||
| chr7:49819878 | C | T | 1 | a0002c0002t0020g0036 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.826+17038C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49819878 | |||||||
| chr7:49819919 | G | T | 1 | a0003c0003t0006g0253 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.826+17079G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49819919 | |||||||
| chr7:49819962 | C | T | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.826+17122C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49819962 | |||||||
| chr7:49819984 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.826+17144G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49819984 | |||||||
| chr7:49820069 | GTCATTAC others(1): Show |
G | 224 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(221): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.826+17239_826+1724 others(12): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49820069 | ||||||
| chr7:49820155 | G | A | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.826+17315G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49820155 | |||||||
| chr7:49820214 | G | A | 220 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(217): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.826+17374G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49820214 | |||||||
| chr7:49820367 | C | T | 1 | a0002c0002t0003g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.826+17527C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49820367 | |||||||
| chr7:49820409 | CA | C | 5 | a0001c0001t0001g0199 a0001c0001t0001g0218 a0001c0001t0041g0007 others(2): Show |
5 | HG02630.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.826+17570delA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49820409 | |||||||
| chr7:49820512 | T | C | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.826+17672T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49820512 | |||||||
| chr7:49820569 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.826+17729A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49820569 | |||||||
| chr7:49820606 | C | T | 4 | a0001c0001t0001g0183 a0002c0002t0001g0053 a0002c0002t0001g0054 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+17766C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49820606 | |||||||
| chr7:49820758 | G | A | 2 | a0001c0001t0005g0012 a0003c0005t0018g0240 |
2 | HG02135.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.826+17918G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49820758 | |||||||
| chr7:49820934 | C | T | 67 | a0001c0001t0001g0115 a0001c0001t0001g0126 a0001c0001t0001g0127 others(64): Show |
68 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.826+18094C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49820934 | |||||||
| chr7:49820935 | G | A | 4 | a0001c0001t0001g0183 a0002c0002t0001g0053 a0002c0002t0001g0054 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+18095G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49820935 | |||||||
| chr7:49821006 | C | A | 7 | a0001c0001t0040g0003 a0001c0001t0054g0004 a0002c0002t0026g0041 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+18166C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49821006 | |||||||
| chr7:49821007 | C | T | 4 | a0001c0001t0001g0207 a0002c0002t0001g0057 a0002c0002t0003g0096 others(1): Show |
4 | HG02280.hp2 HG02895.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+18167C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49821007 | |||||||
| chr7:49821008 | T | C | 67 | a0001c0001t0001g0115 a0001c0001t0001g0126 a0001c0001t0001g0127 others(64): Show |
68 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.826+18168T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49821008 | |||||||
| chr7:49821016 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.826+18176C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49821016 | |||||||
| chr7:49821302 | G | A | 1 | a0002c0002t0002g0032 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.826+18462G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49821302 | |||||||
| chr7:49821481 | T | C | 15 | a0001c0001t0001g0126 a0001c0001t0007g0103 a0001c0001t0007g0107 others(12): Show |
16 | HG00323.hp1 HG01256.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.826+18641T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49821481 | |||||||
| chr7:49821552 | C | A | 1 | a0002c0002t0029g0098 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.826+18712C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49821552 | |||||||
| chr7:49821773 | T | G | 67 | a0001c0001t0001g0115 a0001c0001t0001g0126 a0001c0001t0001g0127 others(64): Show |
68 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.826+18933T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49821773 | |||||||
| chr7:49822610 | T | C | 4 | a0001c0001t0001g0183 a0002c0002t0001g0053 a0002c0002t0001g0054 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+19770T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49822610 | |||||||
| chr7:49823104 | T | C | 4 | a0001c0001t0001g0183 a0002c0002t0001g0053 a0002c0002t0001g0054 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+20264T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49823104 | |||||||
| chr7:49823172 | G | A | 204 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(201): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.826+20332G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49823172 | |||||||
| chr7:49823302 | G | C | 12 | a0001c0001t0001g0179 a0001c0001t0001g0202 a0001c0001t0001g0203 others(9): Show |
12 | HG01261.hp1 HG02145.hp1 HG03017.hp2 others(9): Show |
intron_variant | MODIFIER | c.826+20462G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49823302 | |||||||
| chr7:49823351 | G | A | 204 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(201): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.826+20511G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49823351 | |||||||
| chr7:49823421 | A | T | 66 | a0001c0001t0001g0115 a0001c0001t0001g0126 a0001c0001t0001g0127 others(63): Show |
67 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.826+20581A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49823421 | |||||||
| chr7:49823483 | G | A | 69 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0121 others(66): Show |
69 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.826+20643G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49823483 | |||||||
| chr7:49823505 | G | A | 1 | a0002c0002t0010g0027 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.826+20665G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49823505 | |||||||
| chr7:49823532 | A | G | 1 | a0001c0001t0043g0178 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.826+20692A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49823532 | |||||||
| chr7:49823814 | C | G | 17 | a0001c0001t0001g0156 a0001c0001t0001g0193 a0001c0001t0005g0012 others(14): Show |
17 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.826+20974C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49823814 | |||||||
| chr7:49823916 | A | G | 2 | a0001c0001t0001g0008 a0002c0002t0053g0095 |
2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.826+21076A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49823916 | |||||||
| chr7:49824195 | T | C | 11 | a0001c0001t0001g0179 a0001c0001t0001g0202 a0001c0001t0001g0203 others(8): Show |
11 | HG01261.hp1 HG02145.hp1 HG03017.hp2 others(8): Show |
intron_variant | MODIFIER | c.826+21355T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49824195 | |||||||
| chr7:49824410 | C | T | 1 | a0002c0002t0003g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.826+21570C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49824410 | |||||||
| chr7:49824538 | A | G | 224 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(221): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.826+21698A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49824538 | |||||||
| chr7:49824547 | T | G | 4 | a0001c0001t0002g0123 a0001c0001t0002g0213 a0002c0002t0002g0021 others(1): Show |
4 | HG00099.hp1 HG00323.hp2 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.826+21707T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49824547 | |||||||
| chr7:49824914 | T | C | 17 | a0001c0001t0001g0156 a0001c0001t0001g0193 a0001c0001t0005g0012 others(14): Show |
17 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.826+22074T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49824914 | |||||||
| chr7:49825506 | C | T | 2 | a0001c0001t0001g0008 a0002c0002t0053g0095 |
2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.826+22666C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49825506 | |||||||
| chr7:49825537 | T | C | 2 | a0001c0001t0002g0177 a0001c0001t0043g0178 |
2 | HG01099.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.826+22697T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49825537 | |||||||
| chr7:49825555 | G | T | 14 | a0001c0001t0007g0103 a0001c0001t0007g0107 a0001c0001t0007g0108 others(11): Show |
15 | HG00323.hp1 HG01256.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.826+22715G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49825555 | |||||||
| chr7:49825695 | G | A | 1 | a0002c0002t0013g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.826+22855G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49825695 | |||||||
| chr7:49825712 | A | G | 1 | a0001c0001t0005g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.826+22872A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49825712 | |||||||
| chr7:49825900 | T | C | 2 | a0002c0002t0003g0092 a0002c0002t0050g0100 |
2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.826+23060T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49825900 | |||||||
| chr7:49825902 | T | C | 4 | a0001c0001t0001g0183 a0002c0002t0001g0053 a0002c0002t0001g0054 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+23062T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49825902 | |||||||
| chr7:49826230 | G | A | 17 | a0001c0001t0001g0156 a0001c0001t0001g0193 a0001c0001t0005g0012 others(14): Show |
17 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.826+23390G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49826230 | |||||||
| chr7:49826233 | G | A | 1 | a0002c0002t0003g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.826+23393G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49826233 | |||||||
| chr7:49826324 | A | C | 1 | a0001c0001t0002g0201 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.826+23484A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49826324 | |||||||
| chr7:49826494 | C | T | 2 | a0001c0001t0001g0008 a0002c0002t0053g0095 |
2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.826+23654C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49826494 | |||||||
| chr7:49826689 | CTTG | C | 2 | a0002c0002t0024g0077 a0002c0002t0024g0216 |
2 | HG02074.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.826+23854_826+2385 others(7): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49826689 | ||||||
| chr7:49826834 | C | T | 4 | a0001c0001t0001g0183 a0002c0002t0001g0053 a0002c0002t0001g0054 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+23994C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49826834 | |||||||
| chr7:49826910 | T | A | 1 | a0002c0002t0068g0227 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.826+24070T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49826910 | |||||||
| chr7:49826980 | G | A | 1 | a0002c0002t0007g0082 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.826+24140G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49826980 | |||||||
| chr7:49826998 | A | T | 12 | a0001c0001t0001g0179 a0001c0001t0001g0202 a0001c0001t0001g0203 others(9): Show |
12 | HG01261.hp1 HG02145.hp1 HG03017.hp2 others(9): Show |
intron_variant | MODIFIER | c.826+24158A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49826998 | |||||||
| chr7:49827210 | T | C | 1 | a0002c0002t0003g0096 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.826+24370T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49827210 | |||||||
| chr7:49827242 | A | G | 1 | a0001c0001t0017g0223 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.826+24402A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49827242 | |||||||
| chr7:49827308 | T | TATA | 4 | a0001c0001t0001g0183 a0002c0002t0001g0053 a0002c0002t0001g0054 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+24471_826+2447 others(7): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49827308 | ||||||
| chr7:49827354 | C | A | 222 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.826+24514C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49827354 | |||||||
| chr7:49827356 | AATTTTTT others(7): Show |
A | 17 | a0001c0001t0001g0115 a0001c0001t0001g0127 a0001c0001t0001g0129 others(14): Show |
17 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.826+24519_826+2453 others(18): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49827356 | ||||||
| chr7:49827429 | T | TGGTATAA others(7): Show |
17 | a0001c0001t0001g0115 a0001c0001t0001g0127 a0001c0001t0001g0129 others(14): Show |
17 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.826+24589_826+2459 others(18): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49827429 | |||||||
| chr7:49827429 | T | TTATACCA others(38): Show |
203 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0121 others(200): Show |
204 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.826+24609_826+2461 others(49): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49827429 | ||||||
| chr7:49827514 | TTTTTA | T | 3 | a0002c0002t0004g0062 a0002c0002t0025g0066 a0002c0002t0025g0067 |
3 | HG01109.hp2 HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.826+24681_826+2468 others(9): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49827514 | ||||||
| chr7:49827645 | C | T | 222 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.826+24805C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49827645 | |||||||
| chr7:49828349 | A | G | 26 | a0001c0001t0001g0113 a0001c0001t0001g0121 a0001c0001t0001g0124 others(23): Show |
26 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.826+25509A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49828349 | |||||||
| chr7:49828514 | A | T | 1 | a0002c0002t0039g0205 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.826+25674A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49828514 | |||||||
| chr7:49828921 | T | C | 1 | a0001c0001t0007g0160 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.826+26081T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49828921 | |||||||
| chr7:49828968 | C | G | 1 | a0003c0003t0038g0239 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.826+26128C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49828968 | |||||||
| chr7:49829041 | A | T | 1 | a0001c0001t0002g0144 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.826+26201A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49829041 | |||||||
| chr7:49829057 | GTGGTCCC others(4): Show |
G | 1 | a0001c0001t0001g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.826+26218_826+2622 others(15): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49829057 | |||||||
| chr7:49829071 | G | T | 1 | a0001c0001t0001g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.826+26231G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49829071 | |||||||
| chr7:49829308 | C | T | 2 | a0002c0002t0010g0025 a0002c0002t0010g0027 |
2 | HG01167.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.826+26468C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49829308 | |||||||
| chr7:49829359 | G | T | 1 | a0001c0001t0004g0104 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.826+26519G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49829359 | |||||||
| chr7:49829427 | TC | T | 4 | a0001c0001t0001g0183 a0002c0002t0001g0053 a0002c0002t0001g0054 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+26588delC | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49829427 | |||||||
| chr7:49829443 | T | G | 224 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(221): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.826+26603T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49829443 | |||||||
| chr7:49829610 | C | T | 1 | a0001c0001t0005g0116 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.826+26770C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49829610 | |||||||
| chr7:49829668 | C | T | 4 | a0001c0001t0001g0002 a0001c0001t0003g0002 a0001c0001t0003g0163 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+26828C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49829668 | |||||||
| chr7:49829792 | C | T | 1 | a0002c0002t0061g0061 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.826+26952C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49829792 | |||||||
| chr7:49829821 | T | C | 222 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.826+26981T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49829821 | |||||||
| chr7:49829971 | G | A | 50 | a0001c0001t0001g0136 a0001c0001t0001g0139 a0001c0001t0001g0145 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.826+27131G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49829971 | |||||||
| chr7:49829996 | G | A | 1 | a0002c0002t0013g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.826+27156G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49829996 | |||||||
| chr7:49830175 | A | G | 17 | a0001c0001t0001g0115 a0001c0001t0001g0127 a0001c0001t0001g0129 others(14): Show |
17 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.826+27335A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49830175 | |||||||
| chr7:49830207 | C | G | 1 | a0001c0001t0002g0177 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.826+27367C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49830207 | |||||||
| chr7:49830256 | GA | G | 12 | a0001c0001t0001g0179 a0001c0001t0001g0202 a0001c0001t0001g0203 others(9): Show |
12 | HG01261.hp1 HG02145.hp1 HG03017.hp2 others(9): Show |
intron_variant | MODIFIER | c.826+27426delA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49830256 | ||||||
| chr7:49830298 | G | A | 1 | a0001c0001t0063g0217 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.826+27458G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49830298 | |||||||
| chr7:49830328 | G | A | 1 | a0002c0002t0002g0029 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.826+27488G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49830328 | |||||||
| chr7:49830430 | A | G | 224 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(221): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.826+27590A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49830430 | |||||||
| chr7:49830499 | G | A | 1 | a0001c0001t0003g0167 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.826+27659G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49830499 | |||||||
| chr7:49830512 | G | A | 4 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0002g0110 others(1): Show |
4 | HG00423.hp2 HG02056.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.826+27672G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49830512 | |||||||
| chr7:49830524 | T | A | 2 | a0001c0001t0001g0008 a0002c0002t0053g0095 |
2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.826+27684T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49830524 | |||||||
| chr7:49830591 | C | T | 7 | a0001c0001t0040g0003 a0001c0001t0054g0004 a0002c0002t0026g0041 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+27751C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49830591 | |||||||
| chr7:49830795 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.826+27955T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49830795 | |||||||
| chr7:49830967 | C | T | 4 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0197 others(1): Show |
4 | HG02965.hp2 HG02970.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.826+28127C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49830967 | |||||||
| chr7:49831176 | A | G | 1 | a0002c0002t0045g0068 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.826+28336A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49831176 | |||||||
| chr7:49831204 | G | A | 1 | a0002c0002t0013g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.826+28364G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49831204 | |||||||
| chr7:49831233 | A | C | 2 | a0002c0002t0046g0050 a0002c0002t0047g0209 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.826+28393A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49831233 | |||||||
| chr7:49831425 | G | C | 16 | a0001c0001t0001g0179 a0001c0001t0001g0202 a0001c0001t0001g0203 others(13): Show |
16 | HG01261.hp1 HG01993.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.826+28585G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49831425 | |||||||
| chr7:49831518 | G | A | 68 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0121 others(65): Show |
68 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.826+28678G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49831518 | |||||||
| chr7:49831893 | C | A | 5 | a0001c0001t0004g0106 a0001c0001t0004g0134 a0002c0002t0004g0028 others(2): Show |
5 | NA18612.hp1 NA18972.hp1 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.826+29053C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49831893 | |||||||
| chr7:49832123 | G | T | 1 | a0001c0001t0041g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.826+29283G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49832123 | |||||||
| chr7:49832245 | C | T | 4 | a0001c0001t0001g0183 a0002c0002t0001g0053 a0002c0002t0001g0054 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+29405C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49832245 | |||||||
| chr7:49832281 | T | G | 2 | a0001c0001t0004g0104 a0002c0002t0004g0022 |
2 | HG03239.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.826+29441T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49832281 | |||||||
| chr7:49832298 | A | G | 224 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(221): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.826+29458A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49832298 | |||||||
| chr7:49832361 | G | A | 4 | a0001c0001t0001g0183 a0002c0002t0001g0053 a0002c0002t0001g0054 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+29521G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49832361 | |||||||
| chr7:49832366 | G | C | 1 | a0001c0001t0002g0201 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.826+29526G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49832366 | |||||||
| chr7:49832408 | A | G | 2 | a0001c0001t0001g0008 a0002c0002t0053g0095 |
2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.826+29568A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49832408 | |||||||
| chr7:49832462 | T | C | 2 | a0001c0001t0009g0171 a0002c0002t0009g0001 |
3 | HG02698.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.826+29622T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49832462 | |||||||
| chr7:49832694 | T | A | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.826+29854T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49832694 | |||||||
| chr7:49832823 | C | T | 1 | a0001c0001t0011g0222 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.826+29983C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49832823 | |||||||
| chr7:49833008 | T | C | 11 | a0001c0001t0001g0179 a0001c0001t0001g0202 a0001c0001t0001g0203 others(8): Show |
11 | HG01261.hp1 HG02145.hp1 HG03017.hp2 others(8): Show |
intron_variant | MODIFIER | c.826+30168T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49833008 | |||||||
| chr7:49833027 | A | G | 1 | a0002c0002t0001g0024 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.826+30187A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49833027 | |||||||
| chr7:49833156 | C | T | 1 | a0002c0002t0001g0024 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.826+30316C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49833156 | |||||||
| chr7:49833422 | G | A | 1 | a0002c0002t0001g0020 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.826+30582G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49833422 | |||||||
| chr7:49833480 | C | T | 1 | a0001c0001t0010g0111 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.826+30640C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49833480 | |||||||
| chr7:49833529 | A | G | 224 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(221): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.826+30689A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49833529 | |||||||
| chr7:49833549 | G | A | 17 | a0001c0001t0001g0156 a0001c0001t0001g0193 a0001c0001t0005g0012 others(14): Show |
17 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.826+30709G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49833549 | |||||||
| chr7:49833730 | G | A | 1 | a0002c0002t0005g0080 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.826+30890G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49833730 | |||||||
| chr7:49833798 | A | G | 1 | a0002c0002t0066g0091 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.826+30958A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49833798 | |||||||
| chr7:49833867 | G | A | 17 | a0001c0001t0001g0115 a0001c0001t0001g0127 a0001c0001t0001g0129 others(14): Show |
17 | HG00280.hp1 HG00423.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.826+31027G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49833867 | |||||||
| chr7:49834176 | C | T | 1 | a0002c0002t0068g0227 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.826+31336C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49834176 | |||||||
| chr7:49834220 | T | A | 1 | a0002c0002t0014g0064 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.826+31380T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49834220 | |||||||
| chr7:49834281 | T | A | 1 | a0002c0002t0029g0098 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.826+31441T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49834281 | |||||||
| chr7:49834394 | G | A | 42 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0003g0002 others(39): Show |
42 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.826+31554G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49834394 | |||||||
| chr7:49834433 | A | G | 4 | a0001c0001t0001g0183 a0002c0002t0001g0053 a0002c0002t0001g0054 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+31593A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49834433 | |||||||
| chr7:49834637 | A | G | 25 | a0001c0001t0001g0113 a0001c0001t0001g0121 a0001c0001t0001g0124 others(22): Show |
25 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.826+31797A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49834637 | |||||||
| chr7:49834851 | C | T | 1 | a0001c0001t0014g0168 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.826+32011C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49834851 | |||||||
| chr7:49834852 | T | C | 2 | a0001c0001t0001g0008 a0002c0002t0053g0095 |
2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.826+32012T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49834852 | |||||||
| chr7:49834937 | A | C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(76): Show |
79 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.826+32097A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49834937 | |||||||
| chr7:49835029 | G | T | 1 | a0001c0001t0056g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.826+32189G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49835029 | |||||||
| chr7:49835489 | A | G | 220 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(217): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.826+32649A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49835489 | |||||||
| chr7:49835864 | C | T | 52 | a0001c0001t0001g0136 a0001c0001t0001g0139 a0001c0001t0001g0145 others(49): Show |
52 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.826+33024C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49835864 | |||||||
| chr7:49835913 | T | C | 4 | a0002c0002t0001g0020 a0002c0002t0003g0006 a0002c0002t0003g0014 others(1): Show |
4 | HG01081.hp1 HG01099.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.826+33073T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49835913 | |||||||
| chr7:49836091 | T | C | 220 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(217): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.826+33251T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49836091 | |||||||
| chr7:49836323 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.826+33483A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49836323 | |||||||
| chr7:49836421 | G | T | 5 | a0001c0001t0003g0184 a0001c0001t0011g0222 a0001c0001t0015g0109 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.826+33581G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49836421 | |||||||
| chr7:49836464 | G | GA | 89 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(86): Show |
89 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.826+33641dupA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49836464 | ||||||
| chr7:49836542 | G | A | 135 | a0001c0001t0001g0115 a0001c0001t0001g0126 a0001c0001t0001g0127 others(132): Show |
136 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.826+33702G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49836542 | |||||||
| chr7:49836566 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.826+33726G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49836566 | |||||||
| chr7:49836580 | A | G | 11 | a0001c0001t0001g0179 a0001c0001t0001g0202 a0001c0001t0001g0203 others(8): Show |
11 | HG01261.hp1 HG02145.hp1 HG03017.hp2 others(8): Show |
intron_variant | MODIFIER | c.826+33740A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49836580 | |||||||
| chr7:49836638 | C | CAATA | 12 | a0001c0001t0002g0144 a0001c0001t0040g0003 a0001c0001t0067g0204 others(9): Show |
12 | HG01071.hp2 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.826+33839_826+3384 others(8): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49836638 | ||||||
| chr7:49836638 | CAATA | C | 18 | a0001c0001t0001g0115 a0001c0001t0001g0207 a0001c0001t0002g0177 others(15): Show |
18 | HG00597.hp1 HG01099.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.826+33839_826+3384 others(8): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49836638 | ||||||
| chr7:49836638 | CAATAAAT others(1): Show |
C | 60 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(57): Show |
60 | HG00099.hp2 HG00609.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.826+33835_826+3384 others(12): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49836638 | ||||||
| chr7:49836638 | CAATAAAT others(5): Show |
C | 1 | a0001c0001t0008g0196 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.826+33831_826+3384 others(16): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49836638 | ||||||
| chr7:49836638 | CAATAAAT others(9): Show |
C | 34 | a0001c0001t0001g0126 a0001c0001t0001g0156 a0001c0001t0001g0193 others(31): Show |
35 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.826+33827_826+3384 others(20): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49836638 | ||||||
| chr7:49836641 | T | G | 1 | a0002c0002t0025g0067 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.826+33801T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49836641 | |||||||
| chr7:49836659 | A | C | 1 | a0002c0002t0001g0093 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.826+33819A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49836659 | |||||||
| chr7:49836748 | T | G | 2 | a0001c0001t0001g0008 a0002c0002t0053g0095 |
2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.826+33908T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49836748 | |||||||
| chr7:49836763 | A | T | 4 | a0001c0001t0001g0183 a0002c0002t0001g0053 a0002c0002t0001g0054 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+33923A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49836763 | |||||||
| chr7:49836800 | C | G | 4 | a0001c0001t0001g0183 a0002c0002t0001g0053 a0002c0002t0001g0054 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+33960C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49836800 | |||||||
| chr7:49836864 | C | T | 1 | a0001c0001t0006g0221 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.826+34024C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49836864 | |||||||
| chr7:49837010 | T | A | 2 | a0001c0001t0001g0008 a0002c0002t0053g0095 |
2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.826+34170T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49837010 | |||||||
| chr7:49837204 | A | G | 17 | a0001c0001t0001g0156 a0001c0001t0001g0193 a0001c0001t0005g0012 others(14): Show |
17 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.826+34364A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49837204 | |||||||
| chr7:49837377 | C | T | 2 | a0002c0002t0022g0226 a0002c0002t0049g0208 |
2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.826+34537C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49837377 | |||||||
| chr7:49837397 | C | T | 133 | a0001c0001t0001g0115 a0001c0001t0001g0126 a0001c0001t0001g0127 others(130): Show |
134 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.826+34557C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49837397 | |||||||
| chr7:49837400 | A | G | 1 | a0002c0002t0047g0209 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.826+34560A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49837400 | |||||||
| chr7:49837482 | T | G | 216 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(213): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.826+34642T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49837482 | |||||||
| chr7:49837522 | C | T | 1 | a0002c0002t0013g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.826+34682C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49837522 | |||||||
| chr7:49837563 | C | T | 1 | a0002c0002t0066g0091 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.826+34723C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49837563 | |||||||
| chr7:49837793 | G | A | 4 | a0001c0001t0001g0183 a0002c0002t0001g0053 a0002c0002t0001g0054 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+34953G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49837793 | |||||||
| chr7:49837936 | A | G | 1 | a0002c0002t0013g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.826+35096A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49837936 | |||||||
| chr7:49838189 | G | A | 10 | a0001c0001t0001g0179 a0001c0001t0001g0202 a0001c0001t0001g0203 others(7): Show |
10 | HG01261.hp1 HG02145.hp1 HG03017.hp2 others(7): Show |
intron_variant | MODIFIER | c.826+35349G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49838189 | |||||||
| chr7:49838219 | A | G | 11 | a0001c0001t0001g0179 a0001c0001t0001g0202 a0001c0001t0001g0203 others(8): Show |
11 | HG01261.hp1 HG02145.hp1 HG03017.hp2 others(8): Show |
intron_variant | MODIFIER | c.826+35379A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49838219 | |||||||
| chr7:49838239 | C | T | 4 | a0001c0001t0001g0183 a0002c0002t0001g0053 a0002c0002t0001g0054 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+35399C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49838239 | |||||||
| chr7:49838461 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.826+35621G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49838461 | |||||||
| chr7:49838496 | G | T | 4 | a0001c0001t0001g0183 a0002c0002t0001g0053 a0002c0002t0001g0054 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+35656G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49838496 | |||||||
| chr7:49838640 | G | A | 5 | a0001c0001t0001g0199 a0001c0001t0001g0218 a0001c0001t0041g0007 others(2): Show |
5 | HG02630.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.826+35800G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49838640 | |||||||
| chr7:49838679 | C | T | 4 | a0001c0001t0001g0183 a0002c0002t0001g0053 a0002c0002t0001g0054 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+35839C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49838679 | |||||||
| chr7:49838732 | A | G | 1 | a0003c0003t0012g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.826+35892A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49838732 | |||||||
| chr7:49838815 | G | A | 2 | a0001c0001t0002g0149 a0001c0001t0002g0200 |
2 | HG01981.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.826+35975G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49838815 | |||||||
| chr7:49838892 | C | T | 2 | a0001c0001t0001g0008 a0002c0002t0053g0095 |
2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.826+36052C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49838892 | |||||||
| chr7:49839051 | A | C | 1 | a0002c0002t0027g0069 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.826+36211A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49839051 | |||||||
| chr7:49839136 | A | G | 1 | a0002c0002t0004g0088 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.826+36296A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49839136 | |||||||
| chr7:49839171 | T | A | 2 | a0001c0001t0015g0109 a0001c0001t0051g0009 |
2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.826+36331T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49839171 | |||||||
| chr7:49839378 | T | C | 4 | a0001c0001t0001g0183 a0002c0002t0001g0053 a0002c0002t0001g0054 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+36538T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49839378 | |||||||
| chr7:49839526 | T | C | 4 | a0001c0001t0001g0183 a0002c0002t0001g0053 a0002c0002t0001g0054 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+36686T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49839526 | |||||||
| chr7:49839606 | C | CA | 5 | a0001c0001t0001g0199 a0001c0001t0001g0218 a0001c0001t0041g0007 others(2): Show |
5 | HG02630.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.826+36778dupA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49839606 | ||||||
| chr7:49839606 | CA | C | 36 | a0001c0001t0001g0002 a0001c0001t0003g0002 a0001c0001t0003g0118 others(33): Show |
36 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.826+36778delA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49839606 | ||||||
| chr7:49839751 | G | A | 1 | a0002c0002t0013g0046 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.826+36911G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49839751 | |||||||
| chr7:49839840 | A | G | 1 | a0002c0002t0013g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.826+37000A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49839840 | |||||||
| chr7:49839943 | G | A | 52 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0179 others(49): Show |
52 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.826+37103G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49839943 | |||||||
| chr7:49839985 | C | T | 2 | a0002c0002t0022g0226 a0002c0002t0049g0208 |
2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.826+37145C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49839985 | |||||||
| chr7:49840021 | G | A | 4 | a0001c0001t0001g0183 a0002c0002t0001g0053 a0002c0002t0001g0054 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+37181G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49840021 | |||||||
| chr7:49840055 | C | T | 4 | a0001c0001t0001g0183 a0002c0002t0001g0053 a0002c0002t0001g0054 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+37215C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49840055 | |||||||
| chr7:49840115 | T | C | 4 | a0001c0001t0001g0183 a0002c0002t0001g0053 a0002c0002t0001g0054 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+37275T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49840115 | |||||||
| chr7:49840125 | A | T | 1 | a0001c0001t0001g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.826+37285A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49840125 | |||||||
| chr7:49840242 | A | G | 1 | a0002c0002t0048g0225 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.826+37402A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49840242 | |||||||
| chr7:49840384 | C | T | 17 | a0001c0001t0001g0156 a0001c0001t0001g0193 a0001c0001t0005g0012 others(14): Show |
17 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.826+37544C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49840384 | |||||||
| chr7:49840526 | G | A | 1 | a0003c0003t0033g0236 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.826+37686G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49840526 | |||||||
| chr7:49840624 | C | T | 1 | a0001c0001t0007g0172 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.826+37784C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49840624 | |||||||
| chr7:49840732 | T | C | 1 | a0002c0002t0003g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.826+37892T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49840732 | |||||||
| chr7:49840793 | C | T | 1 | a0002c0002t0013g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.826+37953C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49840793 | |||||||
| chr7:49840794 | G | A | 10 | a0001c0001t0001g0179 a0001c0001t0001g0202 a0001c0001t0001g0203 others(7): Show |
10 | HG01261.hp1 HG02145.hp1 HG03017.hp2 others(7): Show |
intron_variant | MODIFIER | c.826+37954G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49840794 | |||||||
| chr7:49840848 | T | C | 216 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(213): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.826+38008T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49840848 | |||||||
| chr7:49840977 | C | T | 1 | a0002c0002t0003g0096 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.826+38137C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49840977 | |||||||
| chr7:49841012 | T | C | 1 | a0002c0002t0003g0049 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.826+38172T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49841012 | |||||||
| chr7:49841104 | T | C | 2 | a0002c0002t0022g0226 a0002c0002t0049g0208 |
2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.826+38264T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49841104 | |||||||
| chr7:49841302 | C | T | 1 | a0003c0003t0012g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.826+38462C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49841302 | |||||||
| chr7:49841309 | CT | C | 137 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0115 others(134): Show |
137 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.826+38485delT | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49841309 | ||||||
| chr7:49841309 | CTT | C | 6 | a0001c0001t0002g0142 a0001c0001t0003g0163 a0001c0001t0051g0009 others(3): Show |
6 | HG00280.hp2 HG01261.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.826+38484_826+3848 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49841309 | ||||||
| chr7:49841560 | G | A | 1 | a0001c0001t0014g0168 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.826+38720G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49841560 | |||||||
| chr7:49841584 | A | C | 17 | a0001c0001t0001g0002 a0001c0001t0003g0002 a0001c0001t0003g0118 others(14): Show |
17 | HG00733.hp2 HG00735.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.826+38744A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49841584 | |||||||
| chr7:49841619 | C | A | 17 | a0001c0001t0001g0113 a0001c0001t0001g0156 a0001c0001t0005g0012 others(14): Show |
17 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.826+38779C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49841619 | |||||||
| chr7:49841927 | C | T | 3 | a0001c0001t0010g0114 a0001c0001t0019g0173 a0002c0002t0019g0026 |
3 | HG00280.hp1 HG01168.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.826+39087C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49841927 | |||||||
| chr7:49841947 | T | C | 58 | a0001c0001t0001g0002 a0001c0001t0001g0126 a0001c0001t0001g0199 others(55): Show |
58 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.826+39107T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49841947 | |||||||
| chr7:49841958 | C | G | 47 | a0001c0001t0001g0002 a0001c0001t0001g0126 a0001c0001t0003g0002 others(44): Show |
47 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.826+39118C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49841958 | |||||||
| chr7:49842056 | C | T | 1 | a0001c0001t0051g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.826+39216C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49842056 | |||||||
| chr7:49842158 | G | A | 2 | a0002c0002t0029g0098 a0002c0002t0052g0224 |
2 | HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.826+39318G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49842158 | |||||||
| chr7:49842263 | A | G | 2 | a0002c0002t0039g0205 a0002c0002t0053g0095 |
2 | HG01993.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.826+39423A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49842263 | |||||||
| chr7:49842323 | C | G | 1 | a0001c0001t0042g0148 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.826+39483C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49842323 | |||||||
| chr7:49842330 | ATC | A | 4 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0197 others(1): Show |
4 | HG02965.hp2 HG02970.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.826+39492_826+3949 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49842330 | ||||||
| chr7:49843060 | C | T | 1 | a0001c0001t0041g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.826+40220C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49843060 | |||||||
| chr7:49843231 | T | A | 3 | a0002c0002t0022g0048 a0002c0002t0022g0226 a0002c0002t0049g0208 |
3 | HG02630.hp1 HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.826+40391T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49843231 | |||||||
| chr7:49843299 | T | G | 4 | a0002c0002t0026g0041 a0002c0002t0026g0254 a0002c0002t0032g0102 others(1): Show |
4 | HG02717.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.826+40459T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49843299 | |||||||
| chr7:49843512 | C | A | 1 | a0001c0001t0003g0167 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.826+40672C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49843512 | |||||||
| chr7:49843542 | A | C | 58 | a0001c0001t0001g0002 a0001c0001t0001g0126 a0001c0001t0001g0199 others(55): Show |
58 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.826+40702A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49843542 | |||||||
| chr7:49843565 | A | C | 2 | a0001c0001t0054g0004 a0003c0003t0006g0244 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.826+40725A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49843565 | |||||||
| chr7:49843580 | A | G | 1 | a0002c0002t0058g0084 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.826+40740A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49843580 | |||||||
| chr7:49843615 | T | C | 1 | a0002c0006t0057g0215 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.826+40775T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49843615 | |||||||
| chr7:49843707 | A | G | 3 | a0002c0002t0001g0093 a0002c0002t0014g0064 a0003c0003t0016g0230 |
3 | HG02145.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.826+40867A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49843707 | |||||||
| chr7:49843769 | C | A | 2 | a0002c0002t0029g0098 a0002c0002t0052g0224 |
2 | HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.826+40929C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49843769 | |||||||
| chr7:49843911 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.826+41071G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49843911 | |||||||
| chr7:49844024 | T | A | 4 | a0004c0004t0001g0016 a0004c0004t0001g0063 a0004c0004t0001g0070 others(1): Show |
4 | HG01255.hp1 HG01258.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+41184T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49844024 | |||||||
| chr7:49844153 | G | A | 104 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0121 others(101): Show |
105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.826+41313G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49844153 | |||||||
| chr7:49844217 | A | G | 1 | a0001c0001t0003g0190 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.826+41377A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49844217 | |||||||
| chr7:49844264 | C | T | 19 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(16): Show |
19 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.826+41424C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49844264 | |||||||
| chr7:49844365 | A | G | 2 | a0001c0001t0004g0169 a0001c0001t0004g0170 |
2 | NA18946.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.826+41525A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49844365 | |||||||
| chr7:49844485 | T | C | 47 | a0001c0001t0001g0002 a0001c0001t0001g0126 a0001c0001t0003g0002 others(44): Show |
47 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.826+41645T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49844485 | |||||||
| chr7:49844579 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.826+41739T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49844579 | |||||||
| chr7:49844748 | A | C | 1 | a0001c0001t0042g0148 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.826+41908A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49844748 | |||||||
| chr7:49844804 | T | C | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.826+41964T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49844804 | |||||||
| chr7:49844913 | C | A | 2 | a0002c0002t0029g0098 a0002c0002t0052g0224 |
2 | HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.826+42073C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49844913 | |||||||
| chr7:49844938 | C | T | 3 | a0002c0002t0026g0041 a0002c0002t0026g0254 a0002c0002t0032g0102 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.826+42098C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49844938 | |||||||
| chr7:49844989 | T | C | 16 | a0001c0001t0001g0156 a0001c0001t0005g0012 a0001c0001t0005g0116 others(13): Show |
16 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.826+42149T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49844989 | |||||||
| chr7:49845071 | G | A | 4 | a0004c0004t0001g0016 a0004c0004t0001g0063 a0004c0004t0001g0070 others(1): Show |
4 | HG01255.hp1 HG01258.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+42231G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49845071 | |||||||
| chr7:49845151 | C | G | 1 | a0003c0003t0006g0234 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.826+42311C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49845151 | |||||||
| chr7:49845265 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(19): Show |
22 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.826+42425C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49845265 | |||||||
| chr7:49845267 | T | C | 3 | a0001c0001t0003g0184 a0001c0001t0011g0222 a0002c0002t0003g0052 |
3 | HG02257.hp1 HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.826+42427T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49845267 | |||||||
| chr7:49845293 | G | GA | 11 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(8): Show |
11 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.826+42463dupA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49845293 | ||||||
| chr7:49845316 | T | C | 1 | a0001c0001t0051g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.826+42476T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49845316 | |||||||
| chr7:49845375 | A | C | 1 | a0001c0001t0001g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.826+42535A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49845375 | |||||||
| chr7:49845420 | G | A | 11 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(8): Show |
11 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.826+42580G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49845420 | |||||||
| chr7:49845651 | ACCAAC | A | 4 | a0001c0001t0013g0219 a0002c0002t0013g0042 a0002c0002t0013g0046 others(1): Show |
4 | HG01433.hp1 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+42813_826+4281 others(9): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49845651 | ||||||
| chr7:49845661 | G | A | 4 | a0001c0001t0013g0219 a0002c0002t0013g0042 a0002c0002t0013g0046 others(1): Show |
4 | HG01433.hp1 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+42821G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49845661 | |||||||
| chr7:49845662 | G | GAAGCAA | 4 | a0001c0001t0013g0219 a0002c0002t0013g0042 a0002c0002t0013g0046 others(1): Show |
4 | HG01433.hp1 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+42822_826+4282 others(10): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49845662 | |||||||
| chr7:49845664 | G | T | 4 | a0001c0001t0013g0219 a0002c0002t0013g0042 a0002c0002t0013g0046 others(1): Show |
4 | HG01433.hp1 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+42824G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49845664 | |||||||
| chr7:49845875 | G | A | 2 | a0001c0001t0001g0207 a0002c0002t0001g0057 |
2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.826+43035G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49845875 | |||||||
| chr7:49846047 | A | T | 2 | a0001c0001t0054g0004 a0003c0003t0006g0244 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.826+43207A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49846047 | |||||||
| chr7:49846258 | G | A | 1 | a0001c0001t0051g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.826+43418G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49846258 | |||||||
| chr7:49846258 | G | T | 11 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(8): Show |
11 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.826+43418G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49846258 | |||||||
| chr7:49846357 | T | G | 2 | a0003c0003t0016g0230 a0003c0003t0033g0236 |
2 | HG02145.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.826+43517T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49846357 | |||||||
| chr7:49846969 | T | G | 1 | a0001c0001t0051g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.826+44129T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49846969 | |||||||
| chr7:49847221 | AATATAAT others(7): Show |
A | 4 | a0001c0001t0013g0219 a0002c0002t0013g0042 a0002c0002t0013g0046 others(1): Show |
4 | HG01433.hp1 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+44397_826+4441 others(18): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49847221 | ||||||
| chr7:49847235 | TATATA | T | 4 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0197 others(1): Show |
4 | HG02965.hp2 HG02970.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.826+44408_826+4441 others(9): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49847235 | ||||||
| chr7:49847422 | C | A | 47 | a0001c0001t0001g0002 a0001c0001t0001g0126 a0001c0001t0003g0002 others(44): Show |
47 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.826+44582C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49847422 | |||||||
| chr7:49847457 | T | C | 188 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(185): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.826+44617T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49847457 | |||||||
| chr7:49847492 | G | T | 4 | a0002c0002t0026g0041 a0002c0002t0026g0254 a0002c0002t0032g0102 others(1): Show |
4 | HG02717.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.826+44652G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49847492 | |||||||
| chr7:49847700 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.826+44860G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49847700 | |||||||
| chr7:49847701 | G | C | 1 | a0001c0001t0003g0190 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.826+44861G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49847701 | |||||||
| chr7:49847705 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.826+44865G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49847705 | |||||||
| chr7:49847805 | G | A | 1 | a0003c0003t0006g0244 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.826+44965G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49847805 | |||||||
| chr7:49847840 | G | A | 1 | a0002c0002t0049g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.826+45000G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49847840 | |||||||
| chr7:49847905 | G | T | 1 | a0002c0002t0003g0049 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.826+45065G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49847905 | |||||||
| chr7:49847937 | A | C | 234 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.826+45097A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49847937 | |||||||
| chr7:49848077 | G | A | 1 | a0002c0002t0023g0210 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.826+45237G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49848077 | |||||||
| chr7:49848093 | T | G | 1 | a0002c0002t0022g0048 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.826+45253T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49848093 | |||||||
| chr7:49848149 | T | C | 18 | a0001c0001t0001g0156 a0001c0001t0005g0012 a0001c0001t0005g0116 others(15): Show |
18 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.826+45309T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49848149 | |||||||
| chr7:49848194 | G | A | 3 | a0002c0002t0022g0048 a0002c0002t0022g0226 a0002c0002t0049g0208 |
3 | HG02630.hp1 HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.826+45354G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49848194 | |||||||
| chr7:49848219 | A | G | 1 | a0001c0001t0051g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.826+45379A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49848219 | |||||||
| chr7:49848316 | G | A | 2 | a0001c0001t0054g0004 a0003c0003t0006g0244 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.826+45476G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49848316 | |||||||
| chr7:49848416 | G | A | 2 | a0002c0002t0039g0205 a0002c0002t0053g0095 |
2 | HG01993.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.826+45576G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49848416 | |||||||
| chr7:49848504 | C | G | 2 | a0002c0002t0029g0098 a0002c0002t0052g0224 |
2 | HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.826+45664C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49848504 | |||||||
| chr7:49848685 | C | T | 19 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(16): Show |
19 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.826+45845C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49848685 | |||||||
| chr7:49848855 | G | A | 1 | a0003c0003t0016g0230 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.826+46015G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49848855 | |||||||
| chr7:49849181 | G | A | 14 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(11): Show |
14 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.826+46341G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49849181 | |||||||
| chr7:49849190 | C | T | 2 | a0002c0002t0023g0047 a0002c0002t0023g0210 |
2 | HG02897.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.826+46350C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49849190 | |||||||
| chr7:49849211 | AC | A | 5 | a0001c0001t0001g0141 a0001c0001t0001g0150 a0001c0001t0069g0176 others(2): Show |
5 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.826+46372delC | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49849211 | |||||||
| chr7:49849245 | T | C | 14 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(11): Show |
14 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.826+46405T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49849245 | |||||||
| chr7:49849448 | G | T | 1 | a0001c0001t0005g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.826+46608G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49849448 | |||||||
| chr7:49849461 | C | T | 1 | a0001c0001t0051g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.826+46621C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49849461 | |||||||
| chr7:49849571 | C | T | 1 | a0001c0001t0006g0221 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.826+46731C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49849571 | |||||||
| chr7:49849673 | T | A | 6 | a0001c0001t0010g0111 a0002c0002t0010g0018 a0002c0002t0010g0019 others(3): Show |
6 | HG01167.hp2 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.826+46833T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49849673 | |||||||
| chr7:49849814 | A | AG | 6 | a0001c0001t0007g0103 a0001c0001t0007g0160 a0001c0001t0007g0172 others(3): Show |
6 | HG00733.hp1 HG01433.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.826+46975dupG | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49849814 | ||||||
| chr7:49849862 | A | G | 1 | a0001c0001t0051g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.826+47022A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49849862 | |||||||
| chr7:49849985 | G | GAGGAAGA others(28): Show |
1 | a0002c0002t0024g0216 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.826+47164_826+4719 others(39): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49849985 | ||||||
| chr7:49850211 | TC | T | 3 | a0001c0001t0002g0200 a0002c0002t0001g0024 a0003c0003t0006g0220 |
3 | NA18960.hp2 NA19086.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.826+47372delC | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49850211 | |||||||
| chr7:49850225 | ACTGTAGT others(3): Show |
A | 4 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0197 others(1): Show |
4 | HG02965.hp2 HG02970.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.826+47390_826+4739 others(14): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49850225 | ||||||
| chr7:49850242 | A | G | 1 | a0002c0002t0001g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.826+47402A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49850242 | |||||||
| chr7:49850291 | T | G | 2 | a0002c0002t0039g0205 a0002c0002t0053g0095 |
2 | HG01993.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.826+47451T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49850291 | |||||||
| chr7:49850301 | T | C | 20 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(17): Show |
20 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.826+47461T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49850301 | |||||||
| chr7:49850346 | T | C | 1 | a0003c0003t0038g0239 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.826+47506T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49850346 | |||||||
| chr7:49850555 | G | A | 18 | a0001c0001t0001g0156 a0001c0001t0005g0012 a0001c0001t0005g0116 others(15): Show |
18 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.826+47715G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49850555 | |||||||
| chr7:49850928 | C | A | 143 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(140): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.826+48088C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49850928 | |||||||
| chr7:49851134 | G | T | 143 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(140): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.826+48294G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49851134 | |||||||
| chr7:49851136 | G | A | 3 | a0002c0002t0026g0041 a0002c0002t0026g0254 a0002c0002t0032g0102 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.826+48296G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49851136 | |||||||
| chr7:49851269 | G | A | 5 | a0001c0001t0013g0219 a0001c0001t0051g0009 a0002c0002t0013g0042 others(2): Show |
5 | HG01433.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.826+48429G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49851269 | |||||||
| chr7:49851718 | C | G | 1 | a0004c0004t0001g0016 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.826+48878C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49851718 | |||||||
| chr7:49851843 | A | C | 4 | a0001c0001t0013g0219 a0002c0002t0013g0042 a0002c0002t0013g0046 others(1): Show |
4 | HG01433.hp1 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+49003A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49851843 | |||||||
| chr7:49851940 | C | T | 3 | a0001c0001t0001g0218 a0001c0001t0040g0003 a0003c0003t0006g0246 |
3 | HG02451.hp2 HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.826+49100C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49851940 | |||||||
| chr7:49852026 | C | T | 3 | a0002c0002t0026g0041 a0002c0002t0026g0254 a0002c0002t0032g0102 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.826+49186C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49852026 | |||||||
| chr7:49852268 | G | A | 3 | a0002c0002t0001g0020 a0002c0002t0003g0006 a0002c0002t0003g0014 |
3 | HG01081.hp1 HG01099.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.826+49428G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49852268 | |||||||
| chr7:49852311 | A | T | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.826+49471A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49852311 | |||||||
| chr7:49852345 | AAAG | A | 4 | a0001c0001t0002g0194 a0002c0002t0002g0030 a0002c0002t0002g0090 others(1): Show |
4 | NA18747.hp1 NA18944.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.826+49510_826+4951 others(7): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49852345 | ||||||
| chr7:49852355 | C | A | 16 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(13): Show |
16 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.826+49515C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49852355 | |||||||
| chr7:49852402 | C | T | 3 | a0002c0002t0026g0041 a0002c0002t0026g0254 a0002c0002t0032g0102 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.826+49562C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49852402 | |||||||
| chr7:49852448 | T | C | 223 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(220): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.826+49608T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49852448 | |||||||
| chr7:49852568 | G | A | 2 | a0001c0001t0004g0206 a0002c0002t0004g0017 |
2 | HG01243.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.826+49728G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49852568 | |||||||
| chr7:49852599 | A | G | 3 | a0002c0002t0026g0041 a0002c0002t0026g0254 a0002c0002t0032g0102 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.826+49759A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49852599 | |||||||
| chr7:49852600 | A | C | 2 | a0002c0002t0046g0050 a0002c0002t0047g0209 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.826+49760A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49852600 | |||||||
| chr7:49852689 | T | TG | 16 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(13): Show |
16 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.826+49854dupG | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49852689 | ||||||
| chr7:49852740 | C | T | 2 | a0002c0002t0023g0047 a0002c0002t0023g0210 |
2 | HG02897.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.826+49900C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49852740 | |||||||
| chr7:49852865 | G | A | 4 | a0001c0001t0013g0219 a0002c0002t0013g0042 a0002c0002t0013g0046 others(1): Show |
4 | HG01433.hp1 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+50025G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49852865 | |||||||
| chr7:49853102 | C | T | 1 | a0002c0002t0001g0013 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.826+50262C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49853102 | |||||||
| chr7:49853160 | G | A | 1 | a0002c0002t0001g0024 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.826+50320G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49853160 | |||||||
| chr7:49853172 | G | A | 1 | a0001c0001t0051g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.826+50332G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49853172 | |||||||
| chr7:49853264 | G | A | 5 | a0001c0001t0013g0219 a0001c0001t0051g0009 a0002c0002t0013g0042 others(2): Show |
5 | HG01433.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.826+50424G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49853264 | |||||||
| chr7:49853298 | G | A | 3 | a0002c0002t0026g0041 a0002c0002t0026g0254 a0002c0002t0032g0102 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.826+50458G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49853298 | |||||||
| chr7:49853552 | C | T | 18 | a0001c0001t0001g0156 a0001c0001t0005g0012 a0001c0001t0005g0116 others(15): Show |
18 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.826+50712C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49853552 | |||||||
| chr7:49853606 | G | A | 1 | a0002c0002t0001g0060 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.826+50766G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49853606 | |||||||
| chr7:49853692 | T | C | 1 | a0003c0003t0006g0244 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.826+50852T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49853692 | |||||||
| chr7:49853762 | C | T | 18 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(15): Show |
18 | HG02451.hp2 HG02615.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.826+50922C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49853762 | |||||||
| chr7:49853810 | A | G | 146 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(143): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.826+50970A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49853810 | |||||||
| chr7:49853837 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.826+50997T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49853837 | |||||||
| chr7:49853889 | G | A | 2 | a0001c0001t0054g0004 a0002c0002t0050g0100 |
2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.826+51049G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49853889 | |||||||
| chr7:49853980 | C | T | 45 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(42): Show |
45 | HG01261.hp1 HG01433.hp1 HG02280.hp1 others(42): Show |
intron_variant | MODIFIER | c.826+51140C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49853980 | |||||||
| chr7:49854049 | CT | C | 20 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(17): Show |
20 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.826+51215delT | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49854049 | ||||||
| chr7:49854074 | A | G | 4 | a0001c0001t0013g0219 a0002c0002t0013g0042 a0002c0002t0013g0046 others(1): Show |
4 | HG01433.hp1 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+51234A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49854074 | |||||||
| chr7:49854116 | G | T | 5 | a0001c0001t0015g0109 a0001c0001t0015g0182 a0001c0001t0015g0187 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.826+51276G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49854116 | |||||||
| chr7:49854173 | A | G | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.826+51333A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49854173 | |||||||
| chr7:49854185 | G | A | 20 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(17): Show |
20 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.826+51345G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49854185 | |||||||
| chr7:49854267 | T | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.826+51427T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49854267 | |||||||
| chr7:49854339 | C | T | 146 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(143): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.826+51499C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49854339 | |||||||
| chr7:49854398 | C | T | 44 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(41): Show |
44 | HG01261.hp1 HG01433.hp1 HG02280.hp1 others(41): Show |
intron_variant | MODIFIER | c.826+51558C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49854398 | |||||||
| chr7:49854401 | T | C | 212 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(209): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.826+51561T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49854401 | |||||||
| chr7:49854585 | T | C | 33 | a0001c0001t0001g0002 a0001c0001t0003g0002 a0001c0001t0003g0118 others(30): Show |
33 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.826+51745T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49854585 | |||||||
| chr7:49854630 | T | C | 20 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(17): Show |
20 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.826+51790T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49854630 | |||||||
| chr7:49854753 | G | A | 213 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(210): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.826+51913G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49854753 | |||||||
| chr7:49854766 | T | A | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.826+51926T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49854766 | |||||||
| chr7:49854840 | A | G | 1 | a0001c0001t0041g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.826+52000A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49854840 | |||||||
| chr7:49854961 | T | G | 18 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(15): Show |
18 | HG02451.hp2 HG02615.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.826+52121T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49854961 | |||||||
| chr7:49854979 | T | A | 1 | a0003c0003t0006g0244 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.826+52139T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49854979 | |||||||
| chr7:49855267 | T | A | 2 | a0001c0001t0007g0107 a0001c0001t0007g0108 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.826+52427T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49855267 | |||||||
| chr7:49855282 | G | A | 191 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.826+52442G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49855282 | |||||||
| chr7:49855313 | A | G | 18 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(15): Show |
18 | HG02451.hp2 HG02615.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.826+52473A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49855313 | |||||||
| chr7:49855395 | A | G | 1 | a0001c0001t0054g0004 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.826+52555A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49855395 | |||||||
| chr7:49855459 | G | C | 1 | a0001c0001t0009g0175 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.826+52619G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49855459 | |||||||
| chr7:49855504 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.826+52664G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49855504 | |||||||
| chr7:49855506 | T | C | 46 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(43): Show |
46 | HG01261.hp1 HG01433.hp1 HG02280.hp1 others(43): Show |
intron_variant | MODIFIER | c.826+52666T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49855506 | |||||||
| chr7:49855532 | C | A | 21 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(18): Show |
21 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.826+52692C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49855532 | |||||||
| chr7:49855727 | C | T | 1 | a0001c0001t0007g0181 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.826+52887C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49855727 | |||||||
| chr7:49855763 | C | G | 1 | a0001c0001t0051g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.826+52923C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49855763 | |||||||
| chr7:49855819 | C | T | 3 | a0001c0001t0013g0219 a0002c0002t0013g0046 a0002c0002t0013g0214 |
3 | HG01433.hp1 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.826+52979C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49855819 | |||||||
| chr7:49855826 | C | T | 2 | a0001c0001t0004g0169 a0001c0001t0004g0170 |
2 | NA18946.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.826+52986C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49855826 | |||||||
| chr7:49855828 | T | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(142): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.826+52988T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49855828 | |||||||
| chr7:49855934 | C | A | 1 | a0001c0001t0041g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.826+53094C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49855934 | |||||||
| chr7:49856281 | G | T | 3 | a0002c0002t0026g0041 a0002c0002t0026g0254 a0002c0002t0032g0102 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.826+53441G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49856281 | |||||||
| chr7:49856541 | T | C | 8 | a0001c0001t0010g0114 a0001c0001t0015g0109 a0001c0001t0015g0182 others(5): Show |
8 | HG00280.hp1 HG01168.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.826+53701T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49856541 | |||||||
| chr7:49856825 | C | T | 1 | a0003c0003t0006g0244 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.826+53985C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49856825 | |||||||
| chr7:49856869 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.826+54029C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49856869 | |||||||
| chr7:49856870 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(19): Show |
22 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.826+54030G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49856870 | |||||||
| chr7:49856881 | C | T | 2 | a0002c0002t0039g0205 a0002c0002t0053g0095 |
2 | HG01993.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.826+54041C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49856881 | |||||||
| chr7:49856949 | T | G | 5 | a0001c0001t0013g0219 a0001c0001t0051g0009 a0002c0002t0013g0042 others(2): Show |
5 | HG01433.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.826+54109T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49856949 | |||||||
| chr7:49857009 | C | CA | 10 | a0001c0001t0004g0140 a0001c0001t0007g0103 a0001c0001t0007g0107 others(7): Show |
10 | HG01243.hp1 HG03490.hp2 HG03491.hp2 others(7): Show |
intron_variant | MODIFIER | c.826+54201dupA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49857009 | ||||||
| chr7:49857009 | C | CAA | 8 | a0001c0001t0004g0106 a0001c0001t0007g0160 a0001c0001t0007g0172 others(5): Show |
8 | HG00733.hp1 HG01433.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.826+54200_826+5420 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49857009 | ||||||
| chr7:49857009 | C | CAAAAAAA others(2): Show |
5 | a0001c0001t0001g0156 a0001c0001t0005g0116 a0001c0001t0005g0157 others(2): Show |
5 | HG01070.hp2 HG01074.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.826+54193_826+5420 others(13): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49857009 | ||||||
| chr7:49857009 | C | CAAAAAAA others(3): Show |
5 | a0001c0001t0005g0012 a0001c0001t0005g0153 a0001c0001t0005g0154 others(2): Show |
5 | HG00741.hp2 HG01109.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.826+54192_826+5420 others(14): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49857009 | ||||||
| chr7:49857009 | C | CAAAAAAA others(4): Show |
3 | a0001c0001t0064g0122 a0002c0002t0027g0015 a0003c0005t0018g0240 |
3 | HG01081.hp2 HG01496.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.826+54191_826+5420 others(15): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49857009 | ||||||
| chr7:49857009 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0005g0152 a0002c0002t0027g0069 |
2 | HG02148.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.826+54190_826+5420 others(16): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49857009 | ||||||
| chr7:49857009 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0005g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.826+54186_826+5420 others(20): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49857009 | ||||||
| chr7:49857009 | CA | C | 17 | a0001c0001t0002g0144 a0001c0001t0008g0197 a0001c0001t0013g0219 others(14): Show |
17 | HG01433.hp1 HG02145.hp2 HG02602.hp2 others(14): Show |
intron_variant | MODIFIER | c.826+54201delA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49857009 | ||||||
| chr7:49857009 | CAA | C | 27 | a0001c0001t0002g0110 a0001c0001t0002g0123 a0001c0001t0002g0132 others(24): Show |
27 | HG00099.hp1 HG00733.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.826+54200_826+5420 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49857009 | ||||||
| chr7:49857009 | CAAA | C | 41 | a0001c0001t0002g0133 a0001c0001t0002g0137 a0001c0001t0002g0142 others(38): Show |
41 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.826+54199_826+5420 others(7): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49857009 | ||||||
| chr7:49857009 | CAAAA | C | 7 | a0001c0001t0001g0199 a0001c0001t0001g0218 a0001c0001t0015g0187 others(4): Show |
7 | HG02055.hp1 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.826+54198_826+5420 others(8): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49857009 | ||||||
| chr7:49857009 | CAAAAAA | C | 10 | a0001c0001t0001g0115 a0001c0001t0001g0136 a0001c0001t0003g0167 others(7): Show |
10 | HG00735.hp1 HG02055.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.826+54196_826+5420 others(10): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49857009 | ||||||
| chr7:49857009 | CAAAAAAA | C | 58 | a0001c0001t0001g0113 a0001c0001t0001g0121 a0001c0001t0001g0124 others(55): Show |
59 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.826+54195_826+5420 others(11): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49857009 | ||||||
| chr7:49857009 | CAAAAAAA others(1): Show |
C | 12 | a0001c0001t0001g0002 a0001c0001t0003g0002 a0001c0001t0003g0118 others(9): Show |
12 | HG01070.hp1 HG01071.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.826+54194_826+5420 others(12): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49857009 | ||||||
| chr7:49857009 | CAAAAAAA others(3): Show |
C | 15 | a0001c0001t0001g0008 a0001c0001t0001g0183 a0001c0001t0001g0202 others(12): Show |
15 | HG01261.hp1 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.826+54192_826+5420 others(14): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49857009 | ||||||
| chr7:49857009 | CAAAAAAA others(4): Show |
C | 4 | a0001c0001t0005g0117 a0001c0001t0060g0105 a0002c0002t0030g0101 others(1): Show |
4 | HG02280.hp1 HG03471.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+54191_826+5420 others(15): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49857009 | ||||||
| chr7:49857009 | CAAAAAAA others(7): Show |
C | 1 | a0003c0003t0011g0228 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.826+54188_826+5420 others(18): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49857009 | ||||||
| chr7:49857183 | C | T | 45 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(42): Show |
45 | HG01261.hp1 HG01433.hp1 HG02280.hp1 others(42): Show |
intron_variant | MODIFIER | c.826+54343C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49857183 | |||||||
| chr7:49857381 | T | C | 7 | a0001c0001t0013g0219 a0001c0001t0051g0009 a0001c0001t0054g0004 others(4): Show |
7 | HG01433.hp1 HG02809.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+54541T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49857381 | |||||||
| chr7:49857464 | G | C | 7 | a0001c0001t0013g0219 a0001c0001t0051g0009 a0001c0001t0054g0004 others(4): Show |
7 | HG01433.hp1 HG02809.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.827-54570G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49857464 | |||||||
| chr7:49857537 | T | C | 2 | a0001c0001t0054g0004 a0002c0002t0050g0100 |
2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.827-54497T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49857537 | |||||||
| chr7:49858002 | C | A | 4 | a0004c0004t0001g0016 a0004c0004t0001g0063 a0004c0004t0001g0070 others(1): Show |
4 | HG01255.hp1 HG01258.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-54032C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49858002 | |||||||
| chr7:49858014 | C | T | 2 | a0001c0001t0054g0004 a0002c0002t0050g0100 |
2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.827-54020C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49858014 | |||||||
| chr7:49858141 | C | A | 8 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(5): Show |
8 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.827-53893C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49858141 | |||||||
| chr7:49858256 | G | A | 1 | a0002c0002t0003g0049 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.827-53778G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49858256 | |||||||
| chr7:49858387 | G | T | 3 | a0002c0002t0026g0041 a0002c0002t0026g0254 a0002c0002t0032g0102 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.827-53647G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49858387 | |||||||
| chr7:49858403 | T | C | 20 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(17): Show |
20 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.827-53631T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49858403 | |||||||
| chr7:49858428 | G | C | 20 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(17): Show |
20 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.827-53606G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49858428 | |||||||
| chr7:49858551 | G | C | 2 | a0001c0001t0054g0004 a0002c0002t0050g0100 |
2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.827-53483G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49858551 | |||||||
| chr7:49858607 | T | C | 52 | a0001c0001t0002g0110 a0001c0001t0002g0123 a0001c0001t0002g0132 others(49): Show |
52 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.827-53427T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49858607 | |||||||
| chr7:49858610 | C | T | 52 | a0001c0001t0002g0110 a0001c0001t0002g0123 a0001c0001t0002g0132 others(49): Show |
52 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.827-53424C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49858610 | |||||||
| chr7:49858663 | C | T | 5 | a0001c0001t0015g0109 a0001c0001t0015g0182 a0001c0001t0015g0187 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.827-53371C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49858663 | |||||||
| chr7:49858708 | TA | T | 20 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(17): Show |
20 | HG01261.hp1 HG02451.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.827-53318delA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49858708 | ||||||
| chr7:49859134 | C | T | 2 | a0002c0002t0003g0096 a0003c0003t0011g0249 |
2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.827-52900C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49859134 | |||||||
| chr7:49859209 | G | T | 1 | a0004c0004t0001g0070 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.827-52825G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49859209 | |||||||
| chr7:49859640 | G | A | 7 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(4): Show |
7 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.827-52394G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49859640 | |||||||
| chr7:49859728 | T | C | 27 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(24): Show |
27 | HG01261.hp1 HG01433.hp1 HG02280.hp1 others(24): Show |
intron_variant | MODIFIER | c.827-52306T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49859728 | |||||||
| chr7:49859781 | C | T | 3 | a0001c0001t0001g0218 a0001c0001t0040g0003 a0003c0003t0006g0246 |
3 | HG02451.hp2 HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.827-52253C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49859781 | |||||||
| chr7:49859785 | T | C | 27 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(24): Show |
27 | HG01261.hp1 HG01433.hp1 HG02280.hp1 others(24): Show |
intron_variant | MODIFIER | c.827-52249T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49859785 | |||||||
| chr7:49859787 | CGT | C | 15 | a0001c0001t0001g0124 a0001c0001t0001g0130 a0001c0001t0001g0150 others(12): Show |
15 | HG00099.hp2 HG00609.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.827-52245_827-5224 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49859787 | ||||||
| chr7:49859788 | GTGCA | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(59): Show |
63 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.827-52245_827-5224 others(8): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49859788 | |||||||
| chr7:49859788 | GTGCACA | G | 56 | a0001c0001t0001g0193 a0001c0001t0002g0110 a0001c0001t0002g0123 others(53): Show |
56 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.827-52245_827-5224 others(10): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49859788 | |||||||
| chr7:49859788 | GTGCACAC others(1): Show |
G | 31 | a0001c0001t0001g0156 a0001c0001t0005g0012 a0001c0001t0005g0116 others(28): Show |
31 | HG00423.hp1 HG01074.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.827-52245_827-5223 others(12): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49859788 | |||||||
| chr7:49859788 | GTGCACAC others(3): Show |
G | 5 | a0001c0001t0002g0144 a0001c0001t0002g0159 a0001c0001t0010g0114 others(2): Show |
5 | HG00280.hp1 HG01168.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.827-52245_827-5223 others(14): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49859788 | |||||||
| chr7:49859788 | GTGCACAC others(5): Show |
G | 13 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(10): Show |
13 | HG01433.hp1 HG02451.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.827-52245_827-5223 others(16): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49859788 | |||||||
| chr7:49859788 | GTGCACAC others(7): Show |
G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(19): Show |
22 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.827-52245_827-5223 others(18): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49859788 | |||||||
| chr7:49859788 | GTGCACAC others(11): Show |
G | 8 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(5): Show |
8 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.827-52245_827-5222 others(22): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49859788 | |||||||
| chr7:49859789 | T | C | 39 | a0001c0001t0004g0106 a0001c0001t0004g0128 a0001c0001t0004g0134 others(36): Show |
39 | HG00733.hp1 HG01109.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.827-52245T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49859789 | |||||||
| chr7:49859790 | G | A | 1 | a0003c0003t0012g0251 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.827-52244G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49859790 | |||||||
| chr7:49859790 | G | GCA | 3 | a0001c0001t0007g0103 a0001c0001t0007g0160 a0001c0001t0007g0172 |
3 | HG01433.hp2 HG03490.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.827-52210_827-5220 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49859790 | ||||||
| chr7:49859792 | A | G | 30 | a0001c0001t0001g0124 a0001c0001t0001g0130 a0001c0001t0001g0150 others(27): Show |
30 | HG00099.hp2 HG00609.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.827-52242A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49859792 | |||||||
| chr7:49859794 | A | G | 76 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(73): Show |
77 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.827-52240A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49859794 | |||||||
| chr7:49859796 | A | G | 114 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(111): Show |
115 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.827-52238A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49859796 | |||||||
| chr7:49859798 | A | G | 40 | a0001c0001t0001g0156 a0001c0001t0001g0193 a0001c0001t0005g0012 others(37): Show |
40 | HG00423.hp1 HG01074.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.827-52236A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49859798 | |||||||
| chr7:49859800 | A | G | 7 | a0001c0001t0002g0144 a0001c0001t0002g0159 a0001c0001t0010g0114 others(4): Show |
7 | HG00280.hp1 HG01081.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.827-52234A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49859800 | |||||||
| chr7:49859802 | A | G | 13 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(10): Show |
13 | HG01433.hp1 HG02451.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.827-52232A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49859802 | |||||||
| chr7:49859804 | A | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(19): Show |
22 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.827-52230A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49859804 | |||||||
| chr7:49859808 | A | G | 8 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(5): Show |
8 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.827-52226A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49859808 | |||||||
| chr7:49859857 | T | C | 2 | a0001c0001t0054g0004 a0002c0002t0050g0100 |
2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.827-52177T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49859857 | |||||||
| chr7:49859994 | A | G | 1 | a0003c0003t0016g0237 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.827-52040A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49859994 | |||||||
| chr7:49860166 | T | G | 2 | a0001c0001t0054g0004 a0002c0002t0050g0100 |
2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.827-51868T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49860166 | |||||||
| chr7:49860185 | T | A | 1 | a0001c0001t0002g0200 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.827-51849T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49860185 | |||||||
| chr7:49860305 | A | G | 20 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(17): Show |
20 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.827-51729A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49860305 | |||||||
| chr7:49860439 | T | G | 20 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(17): Show |
20 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.827-51595T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49860439 | |||||||
| chr7:49860563 | T | C | 45 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(42): Show |
45 | HG01261.hp1 HG01433.hp1 HG02280.hp1 others(42): Show |
intron_variant | MODIFIER | c.827-51471T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49860563 | |||||||
| chr7:49860674 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.827-51360C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49860674 | |||||||
| chr7:49860792 | T | C | 45 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(42): Show |
45 | HG01261.hp1 HG01433.hp1 HG02280.hp1 others(42): Show |
intron_variant | MODIFIER | c.827-51242T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49860792 | |||||||
| chr7:49860811 | A | C | 1 | a0002c0002t0003g0023 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.827-51223A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49860811 | |||||||
| chr7:49860873 | C | A | 2 | a0002c0002t0022g0226 a0002c0002t0049g0208 |
2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.827-51161C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49860873 | |||||||
| chr7:49861011 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.827-51023G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49861011 | |||||||
| chr7:49861051 | T | G | 45 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(42): Show |
45 | HG01261.hp1 HG01433.hp1 HG02280.hp1 others(42): Show |
intron_variant | MODIFIER | c.827-50983T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49861051 | |||||||
| chr7:49861062 | G | A | 45 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(42): Show |
45 | HG01261.hp1 HG01433.hp1 HG02280.hp1 others(42): Show |
intron_variant | MODIFIER | c.827-50972G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49861062 | |||||||
| chr7:49861360 | G | T | 25 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(22): Show |
25 | HG01433.hp1 HG02451.hp2 HG02615.hp2 others(22): Show |
intron_variant | MODIFIER | c.827-50674G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49861360 | |||||||
| chr7:49861579 | A | C | 1 | a0001c0001t0001g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.827-50455A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49861579 | |||||||
| chr7:49862035 | A | G | 1 | a0002c0002t0003g0075 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.827-49999A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49862035 | |||||||
| chr7:49862254 | T | G | 8 | a0001c0001t0001g0179 a0001c0001t0001g0202 a0001c0001t0001g0203 others(5): Show |
8 | HG03017.hp2 HG03688.hp1 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.827-49780T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49862254 | |||||||
| chr7:49862279 | G | T | 15 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(12): Show |
15 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.827-49755G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49862279 | |||||||
| chr7:49862300 | C | CT | 23 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(20): Show |
23 | HG01433.hp1 HG02451.hp2 HG02615.hp2 others(20): Show |
intron_variant | MODIFIER | c.827-49727dupT | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49862300 | ||||||
| chr7:49862311 | T | G | 20 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(17): Show |
20 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.827-49723T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49862311 | |||||||
| chr7:49862319 | T | A | 20 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(17): Show |
20 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.827-49715T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49862319 | |||||||
| chr7:49862424 | G | A | 1 | a0001c0001t0054g0004 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.827-49610G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49862424 | |||||||
| chr7:49862653 | G | GT | 22 | a0001c0001t0001g0008 a0001c0001t0001g0130 a0001c0001t0001g0179 others(19): Show |
22 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.827-49371dupT | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49862653 | ||||||
| chr7:49862691 | A | G | 18 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(15): Show |
18 | HG02451.hp2 HG02615.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.827-49343A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49862691 | |||||||
| chr7:49862726 | G | GT | 8 | a0001c0001t0013g0219 a0002c0002t0004g0062 a0002c0002t0013g0042 others(5): Show |
8 | HG01433.hp1 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.827-49297dupT | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49862726 | ||||||
| chr7:49862726 | G | GTT | 8 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(5): Show |
8 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.827-49298_827-4929 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49862726 | ||||||
| chr7:49862726 | G | GTTT | 7 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(4): Show |
7 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.827-49299_827-4929 others(7): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49862726 | ||||||
| chr7:49862962 | G | T | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.827-49072G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49862962 | |||||||
| chr7:49863045 | A | G | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.827-48989A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49863045 | |||||||
| chr7:49863334 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.827-48700C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49863334 | |||||||
| chr7:49863346 | C | T | 10 | a0001c0001t0010g0114 a0001c0001t0015g0109 a0001c0001t0015g0182 others(7): Show |
10 | HG00280.hp1 HG01168.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.827-48688C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49863346 | |||||||
| chr7:49863379 | G | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(78): Show |
82 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.827-48655G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49863379 | |||||||
| chr7:49863534 | C | T | 1 | a0001c0001t0051g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.827-48500C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49863534 | |||||||
| chr7:49863587 | A | G | 1 | a0002c0002t0013g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.827-48447A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49863587 | |||||||
| chr7:49863916 | T | A | 18 | a0001c0001t0001g0156 a0001c0001t0005g0012 a0001c0001t0005g0116 others(15): Show |
18 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.827-48118T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49863916 | |||||||
| chr7:49864023 | G | A | 24 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(21): Show |
24 | HG01433.hp1 HG02451.hp2 HG02615.hp2 others(21): Show |
intron_variant | MODIFIER | c.827-48011G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49864023 | |||||||
| chr7:49864051 | C | T | 8 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(5): Show |
8 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.827-47983C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49864051 | |||||||
| chr7:49864055 | T | C | 3 | a0002c0002t0026g0041 a0002c0002t0026g0254 a0002c0002t0032g0102 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.827-47979T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49864055 | |||||||
| chr7:49864073 | TTTG | T | 3 | a0001c0001t0051g0009 a0002c0002t0002g0073 a0002c0002t0050g0100 |
3 | HG02922.hp1 HG03453.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.827-47942_827-4794 others(7): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49864073 | ||||||
| chr7:49864095 | C | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(17): Show |
20 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.827-47939C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49864095 | |||||||
| chr7:49864119 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.827-47915T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49864119 | |||||||
| chr7:49864123 | A | T | 3 | a0001c0001t0002g0188 a0001c0001t0002g0189 a0002c0002t0002g0005 |
3 | HG01123.hp1 NA18946.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.827-47911A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49864123 | |||||||
| chr7:49864258 | A | C | 5 | a0001c0001t0013g0219 a0002c0002t0013g0042 a0002c0002t0013g0046 others(2): Show |
5 | HG01433.hp1 HG02809.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.827-47776A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49864258 | |||||||
| chr7:49864271 | GGGA | G | 7 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(4): Show |
7 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.827-47758_827-4775 others(7): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49864271 | ||||||
| chr7:49864435 | A | T | 168 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(165): Show |
169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.827-47599A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49864435 | |||||||
| chr7:49864544 | A | G | 146 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(143): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.827-47490A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49864544 | |||||||
| chr7:49864603 | G | A | 212 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(209): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.827-47431G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49864603 | |||||||
| chr7:49864979 | A | G | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.827-47055A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49864979 | |||||||
| chr7:49865011 | ATT | A | 168 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(165): Show |
169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.827-47018_827-4701 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49865011 | ||||||
| chr7:49865017 | T | G | 168 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(165): Show |
169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.827-47017T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49865017 | |||||||
| chr7:49865063 | A | C | 1 | a0001c0001t0001g0136 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.827-46971A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49865063 | |||||||
| chr7:49865069 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.827-46965G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49865069 | |||||||
| chr7:49865115 | T | C | 2 | a0002c0002t0039g0205 a0002c0002t0053g0095 |
2 | HG01993.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.827-46919T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49865115 | |||||||
| chr7:49865140 | A | G | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.827-46894A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49865140 | |||||||
| chr7:49865427 | G | A | 1 | a0002c0002t0014g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.827-46607G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49865427 | |||||||
| chr7:49865505 | G | A | 1 | a0002c0002t0002g0073 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.827-46529G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49865505 | |||||||
| chr7:49865791 | A | C | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.827-46243A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49865791 | |||||||
| chr7:49865861 | C | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(17): Show |
20 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.827-46173C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49865861 | |||||||
| chr7:49866242 | G | A | 1 | a0002c0002t0003g0049 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.827-45792G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49866242 | |||||||
| chr7:49866328 | T | C | 8 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(5): Show |
8 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.827-45706T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49866328 | |||||||
| chr7:49866460 | G | A | 1 | a0001c0001t0004g0161 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.827-45574G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49866460 | |||||||
| chr7:49866511 | G | A | 3 | a0002c0002t0026g0041 a0002c0002t0026g0254 a0002c0002t0032g0102 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.827-45523G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49866511 | |||||||
| chr7:49866531 | C | G | 20 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(17): Show |
20 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.827-45503C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49866531 | |||||||
| chr7:49866531 | C | T | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.827-45503C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49866531 | |||||||
| chr7:49866560 | G | A | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.827-45474G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49866560 | |||||||
| chr7:49866566 | C | A | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.827-45468C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49866566 | |||||||
| chr7:49866567 | C | G | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.827-45467C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49866567 | |||||||
| chr7:49866569 | T | A | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.827-45465T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49866569 | |||||||
| chr7:49866570 | G | A | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.827-45464G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49866570 | |||||||
| chr7:49866571 | T | A | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.827-45463T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49866571 | |||||||
| chr7:49866902 | C | A | 1 | a0001c0001t0063g0217 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.827-45132C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49866902 | |||||||
| chr7:49866918 | C | A | 2 | a0001c0001t0005g0152 a0002c0002t0027g0069 |
2 | HG02148.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.827-45116C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49866918 | |||||||
| chr7:49867011 | G | A | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.827-45023G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49867011 | |||||||
| chr7:49867215 | C | T | 1 | a0002c0002t0014g0064 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.827-44819C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49867215 | |||||||
| chr7:49867600 | C | T | 1 | a0002c0002t0002g0035 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.827-44434C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49867600 | |||||||
| chr7:49867617 | A | T | 1 | a0003c0003t0033g0236 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.827-44417A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49867617 | |||||||
| chr7:49867824 | T | A | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.827-44210T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49867824 | |||||||
| chr7:49867840 | A | AT | 88 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(85): Show |
89 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.827-44190dupT | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49867840 | ||||||
| chr7:49867844 | TA | T | 52 | a0001c0001t0002g0110 a0001c0001t0002g0123 a0001c0001t0002g0132 others(49): Show |
52 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.827-44189delA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49867844 | |||||||
| chr7:49867845 | A | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(91): Show |
95 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.827-44189A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49867845 | |||||||
| chr7:49867877 | A | C | 1 | a0001c0001t0015g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.827-44157A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49867877 | |||||||
| chr7:49867903 | G | A | 1 | a0002c0002t0049g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.827-44131G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49867903 | |||||||
| chr7:49867921 | C | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(144): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.827-44113C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49867921 | |||||||
| chr7:49868158 | G | A | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.827-43876G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49868158 | |||||||
| chr7:49868228 | A | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.827-43806A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49868228 | |||||||
| chr7:49868445 | C | T | 2 | a0002c0002t0039g0205 a0002c0002t0053g0095 |
2 | HG01993.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.827-43589C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49868445 | |||||||
| chr7:49868494 | T | C | 5 | a0001c0001t0015g0109 a0001c0001t0015g0182 a0001c0001t0015g0187 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.827-43540T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49868494 | |||||||
| chr7:49868758 | C | T | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.827-43276C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49868758 | |||||||
| chr7:49868844 | C | G | 9 | a0001c0001t0010g0114 a0001c0001t0015g0109 a0001c0001t0015g0182 others(6): Show |
9 | HG00280.hp1 HG01168.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.827-43190C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49868844 | |||||||
| chr7:49868888 | G | A | 1 | a0003c0003t0037g0229 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.827-43146G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49868888 | |||||||
| chr7:49868910 | C | T | 4 | a0001c0001t0013g0219 a0002c0002t0013g0042 a0002c0002t0013g0046 others(1): Show |
4 | HG01433.hp1 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-43124C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49868910 | |||||||
| chr7:49869188 | G | A | 20 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(17): Show |
20 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.827-42846G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49869188 | |||||||
| chr7:49869318 | G | A | 168 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(165): Show |
169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.827-42716G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49869318 | |||||||
| chr7:49869415 | C | T | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.827-42619C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49869415 | |||||||
| chr7:49869429 | C | G | 7 | a0001c0001t0002g0149 a0001c0001t0002g0159 a0001c0001t0042g0148 others(4): Show |
7 | HG01361.hp2 HG01978.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.827-42605C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49869429 | |||||||
| chr7:49869466 | A | G | 5 | a0001c0001t0015g0109 a0001c0001t0015g0182 a0001c0001t0015g0187 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.827-42568A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49869466 | |||||||
| chr7:49869469 | A | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(17): Show |
20 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.827-42565A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49869469 | |||||||
| chr7:49869473 | A | G | 2 | a0002c0002t0022g0226 a0002c0002t0049g0208 |
2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.827-42561A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49869473 | |||||||
| chr7:49869509 | G | A | 3 | a0001c0001t0003g0184 a0001c0001t0011g0222 a0002c0002t0003g0052 |
3 | HG02257.hp1 HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.827-42525G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49869509 | |||||||
| chr7:49869681 | G | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(144): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.827-42353G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49869681 | |||||||
| chr7:49869784 | G | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(17): Show |
20 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.827-42250G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49869784 | |||||||
| chr7:49869818 | G | GT | 3 | a0001c0001t0002g0188 a0001c0001t0002g0189 a0002c0002t0002g0005 |
3 | HG01123.hp1 NA18946.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.827-42210dupT | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49869818 | ||||||
| chr7:49869855 | G | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(144): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.827-42179G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49869855 | |||||||
| chr7:49869888 | G | C | 1 | a0003c0003t0011g0228 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.827-42146G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49869888 | |||||||
| chr7:49870175 | C | A | 1 | a0002c0002t0002g0035 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.827-41859C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49870175 | |||||||
| chr7:49870227 | C | T | 4 | a0001c0001t0013g0219 a0002c0002t0013g0042 a0002c0002t0013g0046 others(1): Show |
4 | HG01433.hp1 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-41807C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49870227 | |||||||
| chr7:49870228 | G | A | 2 | a0002c0002t0029g0098 a0002c0002t0052g0224 |
2 | HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.827-41806G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49870228 | |||||||
| chr7:49870268 | C | T | 2 | a0002c0002t0025g0066 a0002c0002t0025g0067 |
2 | HG01109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.827-41766C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49870268 | |||||||
| chr7:49870295 | G | A | 18 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(15): Show |
18 | HG02451.hp2 HG02615.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.827-41739G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49870295 | |||||||
| chr7:49870348 | G | A | 1 | a0001c0001t0067g0204 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.827-41686G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49870348 | |||||||
| chr7:49870357 | G | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.827-41677G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49870357 | |||||||
| chr7:49870383 | C | T | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.827-41651C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49870383 | |||||||
| chr7:49870437 | T | C | 20 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(17): Show |
20 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.827-41597T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49870437 | |||||||
| chr7:49870543 | G | A | 37 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0121 others(34): Show |
38 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.827-41491G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49870543 | |||||||
| chr7:49870651 | G | T | 1 | a0002c0002t0001g0051 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.827-41383G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49870651 | |||||||
| chr7:49870681 | A | G | 3 | a0002c0002t0022g0048 a0002c0002t0022g0226 a0002c0002t0049g0208 |
3 | HG02630.hp1 HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.827-41353A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49870681 | |||||||
| chr7:49870762 | T | G | 3 | a0002c0002t0022g0048 a0002c0002t0022g0226 a0002c0002t0049g0208 |
3 | HG02630.hp1 HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.827-41272T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49870762 | |||||||
| chr7:49871117 | CA | C | 4 | a0001c0001t0013g0219 a0002c0002t0013g0042 a0002c0002t0013g0046 others(1): Show |
4 | HG01433.hp1 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-40916delA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49871117 | |||||||
| chr7:49871150 | T | A | 2 | a0001c0001t0064g0122 a0002c0002t0027g0015 |
2 | HG01081.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.827-40884T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49871150 | |||||||
| chr7:49871187 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(184): Show |
188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.827-40847C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49871187 | |||||||
| chr7:49871201 | T | C | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.827-40833T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49871201 | |||||||
| chr7:49871253 | G | A | 1 | a0001c0001t0014g0168 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.827-40781G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49871253 | |||||||
| chr7:49871354 | T | C | 1 | a0002c0002t0031g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.827-40680T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49871354 | |||||||
| chr7:49871375 | T | C | 1 | a0001c0001t0002g0200 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.827-40659T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49871375 | |||||||
| chr7:49871567 | A | G | 2 | a0002c0002t0025g0066 a0002c0002t0025g0067 |
2 | HG01109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.827-40467A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49871567 | |||||||
| chr7:49871830 | C | CATACATA others(17): Show |
13 | a0001c0001t0002g0191 a0001c0001t0002g0194 a0001c0001t0021g0112 others(10): Show |
13 | HG00423.hp1 HG02074.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.827-40193_827-4017 others(28): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49871830 | ||||||
| chr7:49871874 | TATA | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(18): Show |
21 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.827-40157_827-4015 others(7): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49871874 | ||||||
| chr7:49871907 | AAAC | A | 4 | a0001c0001t0002g0188 a0001c0001t0002g0189 a0002c0002t0002g0030 others(1): Show |
4 | HG02615.hp2 NA18944.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-40125_827-4012 others(7): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49871907 | ||||||
| chr7:49871907 | AAACACAC others(2): Show |
A | 3 | a0001c0001t0056g0125 a0002c0002t0003g0010 a0002c0002t0003g0096 |
3 | HG02280.hp2 NA18979.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.827-40125_827-4011 others(13): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49871907 | ||||||
| chr7:49871908 | A | AAC | 6 | a0001c0001t0007g0108 a0002c0002t0002g0029 a0002c0002t0002g0072 others(3): Show |
6 | HG02976.hp2 HG03491.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.827-40077_827-4007 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49871908 | ||||||
| chr7:49871908 | A | AACAC | 5 | a0001c0001t0007g0107 a0001c0001t0007g0160 a0002c0002t0025g0066 others(2): Show |
5 | HG01109.hp2 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.827-40079_827-4007 others(8): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49871908 | ||||||
| chr7:49871908 | A | AACACAC | 5 | a0001c0001t0007g0103 a0001c0001t0007g0172 a0001c0001t0007g0181 others(2): Show |
5 | HG00733.hp1 HG01433.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.827-40081_827-4007 others(10): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49871908 | ||||||
| chr7:49871908 | AAC | A | 37 | a0001c0001t0002g0110 a0001c0001t0002g0133 a0001c0001t0002g0137 others(34): Show |
37 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.827-40077_827-4007 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49871908 | ||||||
| chr7:49871908 | AACAC | A | 34 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0156 others(31): Show |
34 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.827-40079_827-4007 others(8): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49871908 | ||||||
| chr7:49871908 | AACACAC | A | 20 | a0001c0001t0001g0115 a0001c0001t0001g0130 a0001c0001t0001g0136 others(17): Show |
20 | HG01167.hp2 HG01256.hp2 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.827-40081_827-4007 others(10): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49871908 | ||||||
| chr7:49871908 | AACACACA others(1): Show |
A | 43 | a0001c0001t0001g0113 a0001c0001t0001g0121 a0001c0001t0001g0126 others(40): Show |
44 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.827-40083_827-4007 others(12): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49871908 | ||||||
| chr7:49871908 | AACACACA others(3): Show |
A | 27 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0003g0002 others(24): Show |
27 | HG00099.hp2 HG00741.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.827-40085_827-4007 others(14): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49871908 | ||||||
| chr7:49871908 | AACACACA others(5): Show |
A | 7 | a0002c0002t0003g0023 a0002c0002t0026g0041 a0002c0002t0026g0254 others(4): Show |
7 | HG01496.hp1 HG02602.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.827-40087_827-4007 others(16): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49871908 | ||||||
| chr7:49871908 | AACACACA others(7): Show |
A | 4 | a0002c0002t0001g0020 a0002c0002t0001g0093 a0002c0002t0022g0226 others(1): Show |
4 | HG01099.hp1 HG02630.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-40089_827-4007 others(18): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49871908 | ||||||
| chr7:49871908 | AACACACA others(9): Show |
A | 5 | a0001c0001t0015g0109 a0001c0001t0015g0182 a0001c0001t0015g0187 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.827-40091_827-4007 others(20): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49871908 | ||||||
| chr7:49871908 | AACACACA others(13): Show |
A | 5 | a0001c0001t0010g0114 a0001c0001t0019g0173 a0001c0001t0051g0009 others(2): Show |
5 | HG00280.hp1 HG01168.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.827-40095_827-4007 others(24): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49871908 | ||||||
| chr7:49871908 | AACACACA others(15): Show |
A | 20 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(17): Show |
20 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.827-40097_827-4007 others(26): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49871908 | ||||||
| chr7:49872256 | G | T | 4 | a0001c0001t0013g0219 a0002c0002t0013g0042 a0002c0002t0013g0046 others(1): Show |
4 | HG01433.hp1 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-39778G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49872256 | |||||||
| chr7:49872302 | T | C | 1 | a0001c0001t0051g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.827-39732T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49872302 | |||||||
| chr7:49872330 | C | T | 15 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(12): Show |
15 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.827-39704C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49872330 | |||||||
| chr7:49872536 | A | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(17): Show |
20 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.827-39498A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49872536 | |||||||
| chr7:49872604 | C | T | 1 | a0002c0002t0002g0032 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.827-39430C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49872604 | |||||||
| chr7:49872663 | T | C | 2 | a0001c0001t0004g0206 a0002c0002t0004g0017 |
2 | HG01243.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.827-39371T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49872663 | |||||||
| chr7:49872735 | G | A | 20 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(17): Show |
20 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.827-39299G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49872735 | |||||||
| chr7:49872751 | C | CA | 147 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(144): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.827-39268dupA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49872751 | ||||||
| chr7:49872830 | C | T | 11 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(8): Show |
11 | HG02630.hp1 HG02895.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.827-39204C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49872830 | |||||||
| chr7:49872838 | A | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.827-39196A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49872838 | |||||||
| chr7:49872915 | C | CA | 20 | a0001c0001t0001g0156 a0001c0001t0005g0012 a0001c0001t0005g0116 others(17): Show |
20 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.827-39097dupA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49872915 | ||||||
| chr7:49872915 | C | CAA | 9 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0196 others(6): Show |
9 | HG02630.hp1 HG02965.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.827-39098_827-3909 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49872915 | ||||||
| chr7:49872915 | C | CAAA | 50 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0137 others(47): Show |
50 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.827-39099_827-3909 others(7): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49872915 | ||||||
| chr7:49872915 | C | CAAAA | 25 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0002g0110 others(22): Show |
25 | HG00099.hp2 HG00735.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.827-39100_827-3909 others(8): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49872915 | ||||||
| chr7:49872915 | C | CAAAAA | 54 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0126 others(51): Show |
55 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.827-39101_827-3909 others(9): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49872915 | ||||||
| chr7:49872915 | C | CAAAAAA | 18 | a0001c0001t0001g0002 a0001c0001t0003g0002 a0001c0001t0003g0120 others(15): Show |
18 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.827-39102_827-3909 others(10): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49872915 | ||||||
| chr7:49872915 | CA | C | 19 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0203 others(16): Show |
19 | HG01261.hp1 HG01517.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.827-39097delA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49872915 | ||||||
| chr7:49872933 | A | G | 8 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(5): Show |
8 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.827-39101A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49872933 | |||||||
| chr7:49872934 | A | G | 4 | a0001c0001t0013g0219 a0002c0002t0013g0042 a0002c0002t0013g0046 others(1): Show |
4 | HG01433.hp1 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-39100A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49872934 | |||||||
| chr7:49872935 | A | T | 1 | a0002c0002t0001g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.827-39099A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49872935 | |||||||
| chr7:49872980 | C | T | 11 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(8): Show |
11 | HG02630.hp1 HG02895.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.827-39054C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49872980 | |||||||
| chr7:49873265 | T | G | 8 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(5): Show |
8 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.827-38769T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49873265 | |||||||
| chr7:49873365 | G | A | 4 | a0001c0001t0002g0142 a0002c0002t0002g0032 a0002c0002t0002g0078 others(1): Show |
4 | HG00280.hp2 HG01261.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-38669G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49873365 | |||||||
| chr7:49873365 | G | C | 1 | a0001c0001t0051g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.827-38669G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49873365 | |||||||
| chr7:49873447 | A | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(206): Show |
210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.827-38587A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49873447 | |||||||
| chr7:49873846 | A | G | 2 | a0001c0001t0004g0169 a0001c0001t0004g0170 |
2 | NA18946.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.827-38188A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49873846 | |||||||
| chr7:49873906 | T | TA | 11 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(8): Show |
11 | HG02630.hp1 HG02895.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.827-38116dupA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49873906 | ||||||
| chr7:49873906 | TA | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(168): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.827-38116delA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49873906 | ||||||
| chr7:49873919 | C | A | 8 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(5): Show |
8 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.827-38115C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49873919 | |||||||
| chr7:49873954 | C | T | 1 | a0001c0001t0002g0149 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.827-38080C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49873954 | |||||||
| chr7:49874081 | G | A | 1 | a0001c0001t0041g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.827-37953G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49874081 | |||||||
| chr7:49874108 | G | C | 1 | a0003c0003t0011g0228 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.827-37926G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49874108 | |||||||
| chr7:49874109 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.827-37925G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49874109 | |||||||
| chr7:49874180 | C | CCA | 8 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(5): Show |
8 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.827-37837_827-3783 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49874180 | ||||||
| chr7:49874432 | G | A | 2 | a0001c0001t0007g0107 a0001c0001t0007g0108 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.827-37602G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49874432 | |||||||
| chr7:49874446 | G | T | 2 | a0002c0002t0023g0047 a0002c0002t0023g0210 |
2 | HG02897.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.827-37588G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49874446 | |||||||
| chr7:49874535 | C | T | 1 | a0002c0002t0013g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.827-37499C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49874535 | |||||||
| chr7:49874542 | CTA | C | 10 | a0001c0001t0010g0111 a0001c0001t0011g0222 a0002c0002t0004g0062 others(7): Show |
10 | HG01167.hp2 HG01256.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.827-37486_827-3748 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49874542 | ||||||
| chr7:49874548 | A | ATG | 26 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(23): Show |
26 | HG02280.hp1 HG02451.hp1 HG02486.hp1 others(23): Show |
intron_variant | MODIFIER | c.827-37464_827-3746 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49874548 | ||||||
| chr7:49874548 | A | ATGTG | 5 | a0001c0001t0008g0195 a0001c0001t0008g0196 a0001c0001t0008g0198 others(2): Show |
5 | HG02922.hp1 HG02922.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.827-37466_827-3746 others(8): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49874548 | ||||||
| chr7:49874548 | ATG | A | 155 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.827-37464_827-3746 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49874548 | ||||||
| chr7:49874599 | G | A | 3 | a0001c0001t0010g0114 a0001c0001t0019g0173 a0002c0002t0019g0026 |
3 | HG00280.hp1 HG01168.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.827-37435G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49874599 | |||||||
| chr7:49874642 | T | G | 1 | a0002c0002t0002g0039 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.827-37392T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49874642 | |||||||
| chr7:49874754 | T | C | 5 | a0001c0001t0015g0109 a0001c0001t0015g0182 a0001c0001t0015g0187 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.827-37280T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49874754 | |||||||
| chr7:49874781 | G | A | 2 | a0001c0001t0004g0169 a0001c0001t0004g0170 |
2 | NA18946.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.827-37253G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49874781 | |||||||
| chr7:49874856 | CAG | C | 53 | a0001c0001t0002g0110 a0001c0001t0002g0123 a0001c0001t0002g0132 others(50): Show |
53 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.827-37173_827-3717 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49874856 | ||||||
| chr7:49874910 | G | A | 167 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(164): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.827-37124G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49874910 | |||||||
| chr7:49874985 | G | A | 8 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(5): Show |
8 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.827-37049G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49874985 | |||||||
| chr7:49875167 | C | T | 8 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(5): Show |
8 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.827-36867C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49875167 | |||||||
| chr7:49875298 | A | T | 3 | a0002c0002t0026g0041 a0002c0002t0026g0254 a0002c0002t0032g0102 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.827-36736A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49875298 | |||||||
| chr7:49875361 | T | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.827-36673T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49875361 | |||||||
| chr7:49875369 | C | CA | 5 | a0001c0001t0008g0185 a0001c0001t0041g0007 a0002c0002t0004g0028 others(2): Show |
5 | HG01258.hp2 HG02717.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.827-36637dupA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49875369 | ||||||
| chr7:49875369 | C | CAA | 5 | a0001c0001t0040g0003 a0002c0002t0022g0226 a0002c0002t0026g0254 others(2): Show |
5 | HG02451.hp2 HG02615.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.827-36638_827-3663 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49875369 | ||||||
| chr7:49875369 | C | CAAA | 18 | a0001c0001t0001g0008 a0001c0001t0001g0183 a0001c0001t0001g0199 others(15): Show |
18 | HG01168.hp2 HG01261.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.827-36639_827-3663 others(7): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49875369 | ||||||
| chr7:49875369 | C | CAAAA | 30 | a0001c0001t0001g0113 a0001c0001t0001g0121 a0001c0001t0001g0124 others(27): Show |
31 | HG00099.hp2 HG00609.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.827-36640_827-3663 others(8): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49875369 | ||||||
| chr7:49875369 | C | CAAAAA | 31 | a0001c0001t0001g0002 a0001c0001t0001g0115 a0001c0001t0001g0126 others(28): Show |
31 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.827-36641_827-3663 others(9): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49875369 | ||||||
| chr7:49875369 | C | CAAAAAA | 19 | a0001c0001t0001g0129 a0001c0001t0003g0190 a0001c0001t0009g0174 others(16): Show |
19 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(16): Show |
intron_variant | MODIFIER | c.827-36642_827-3663 others(10): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49875369 | ||||||
| chr7:49875369 | C | CAAAAAAA | 10 | a0001c0001t0002g0144 a0001c0001t0003g0120 a0001c0001t0003g0167 others(7): Show |
10 | HG00735.hp1 HG02015.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.827-36643_827-3663 others(11): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49875369 | ||||||
| chr7:49875369 | C | CAAAAAAA others(1): Show |
5 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0003g0166 others(2): Show |
5 | HG01168.hp1 HG02735.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.827-36644_827-3663 others(12): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49875369 | ||||||
| chr7:49875369 | C | CAAAAAAA others(2): Show |
17 | a0001c0001t0002g0133 a0001c0001t0002g0137 a0001c0001t0002g0149 others(14): Show |
17 | HG00597.hp2 HG00609.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.827-36645_827-3663 others(13): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49875369 | ||||||
| chr7:49875369 | C | CAAAAAAA others(3): Show |
19 | a0001c0001t0002g0110 a0001c0001t0002g0123 a0001c0001t0002g0132 others(16): Show |
19 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.827-36646_827-3663 others(14): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49875369 | ||||||
| chr7:49875369 | C | CAAAAAAA others(4): Show |
6 | a0001c0001t0021g0112 a0002c0002t0002g0072 a0002c0002t0003g0049 others(3): Show |
6 | HG02145.hp1 HG02818.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.827-36647_827-3663 others(15): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49875369 | ||||||
| chr7:49875369 | C | CAAAAAAA others(5): Show |
6 | a0001c0001t0002g0159 a0001c0001t0021g0135 a0001c0001t0044g0138 others(3): Show |
6 | HG00323.hp2 HG00423.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.827-36648_827-3663 others(16): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49875369 | ||||||
| chr7:49875369 | C | CAAAAAAA others(6): Show |
2 | a0001c0001t0002g0213 a0002c0002t0047g0209 |
2 | HG02559.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.827-36649_827-3663 others(17): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49875369 | ||||||
| chr7:49875369 | CA | C | 30 | a0001c0001t0004g0104 a0001c0001t0004g0106 a0001c0001t0004g0128 others(27): Show |
30 | HG00741.hp2 HG01070.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.827-36637delA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49875369 | ||||||
| chr7:49875369 | CAA | C | 7 | a0001c0001t0005g0157 a0001c0001t0007g0103 a0001c0001t0007g0107 others(4): Show |
7 | HG00733.hp1 HG01074.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.827-36638_827-3663 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49875369 | ||||||
| chr7:49875395 | A | AAAAAAAA others(8): Show |
1 | a0002c0002t0013g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.827-36637_827-3663 others(19): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49875395 | ||||||
| chr7:49875438 | G | GA | 21 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(18): Show |
21 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.827-36586dupA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49875438 | ||||||
| chr7:49875482 | T | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(172): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.827-36552T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49875482 | |||||||
| chr7:49875614 | G | A | 1 | a0001c0001t0051g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.827-36420G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49875614 | |||||||
| chr7:49875637 | C | T | 39 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0121 others(36): Show |
40 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.827-36397C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49875637 | |||||||
| chr7:49875994 | T | C | 18 | a0001c0001t0001g0156 a0001c0001t0005g0012 a0001c0001t0005g0116 others(15): Show |
18 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.827-36040T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49875994 | |||||||
| chr7:49876164 | A | G | 21 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(18): Show |
21 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.827-35870A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49876164 | |||||||
| chr7:49876179 | C | A | 4 | a0001c0001t0013g0219 a0002c0002t0013g0042 a0002c0002t0013g0046 others(1): Show |
4 | HG01433.hp1 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-35855C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49876179 | |||||||
| chr7:49876183 | T | G | 21 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(18): Show |
21 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.827-35851T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49876183 | |||||||
| chr7:49876359 | G | A | 4 | a0001c0001t0013g0219 a0002c0002t0013g0042 a0002c0002t0013g0046 others(1): Show |
4 | HG01433.hp1 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-35675G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49876359 | |||||||
| chr7:49876410 | T | C | 1 | a0002c0002t0002g0005 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.827-35624T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49876410 | |||||||
| chr7:49876454 | T | C | 1 | a0002c0002t0001g0031 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.827-35580T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49876454 | |||||||
| chr7:49876645 | T | C | 153 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.827-35389T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49876645 | |||||||
| chr7:49876864 | C | T | 9 | a0001c0001t0003g0184 a0001c0001t0011g0222 a0002c0002t0003g0052 others(6): Show |
9 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.827-35170C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49876864 | |||||||
| chr7:49877003 | G | A | 1 | a0003c0003t0036g0238 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.827-35031G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877003 | |||||||
| chr7:49877038 | T | C | 1 | a0002c0002t0001g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.827-34996T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877038 | |||||||
| chr7:49877151 | A | G | 5 | a0001c0001t0001g0183 a0002c0002t0001g0053 a0002c0002t0001g0054 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.827-34883A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877151 | |||||||
| chr7:49877462 | C | CAAA | 5 | a0001c0001t0020g0143 a0001c0001t0021g0112 a0002c0002t0002g0029 others(2): Show |
5 | NA18960.hp1 NA18977.hp2 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.827-34554_827-3455 others(7): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877462 | ||||||
| chr7:49877462 | C | CAAAAAAA others(5): Show |
1 | a0002c0002t0013g0046 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.827-34563_827-3455 others(16): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877462 | ||||||
| chr7:49877462 | CAAAAAAA | C | 5 | a0001c0001t0007g0103 a0001c0001t0007g0107 a0001c0001t0007g0108 others(2): Show |
5 | HG03490.hp2 HG03491.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.827-34558_827-3455 others(11): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877462 | ||||||
| chr7:49877473 | A | ATATATAT others(8): Show |
1 | a0001c0001t0007g0181 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.827-34561_827-3456 others(19): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877473 | |||||||
| chr7:49877475 | A | T | 1 | a0001c0001t0007g0181 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.827-34559A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877475 | |||||||
| chr7:49877475 | AAAAAAAA others(5): Show |
A | 1 | a0002c0002t0027g0015 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.827-34557_827-3454 others(16): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877475 | ||||||
| chr7:49877476 | AAAAAAAT others(4): Show |
A | 1 | a0001c0001t0005g0116 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.827-34556_827-3454 others(15): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877476 | ||||||
| chr7:49877476 | AAAAAAAT others(6): Show |
A | 2 | a0001c0001t0005g0158 a0002c0002t0050g0100 |
2 | HG01070.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.827-34556_827-3454 others(17): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877476 | ||||||
| chr7:49877477 | A | AATATATA others(7): Show |
1 | a0002c0002t0026g0254 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.827-34556_827-3455 others(18): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877477 | ||||||
| chr7:49877477 | A | AATATATA others(9): Show |
1 | a0002c0002t0032g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.827-34556_827-3455 others(20): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877477 | ||||||
| chr7:49877477 | A | ATATATAT others(6): Show |
1 | a0002c0002t0026g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.827-34557_827-3455 others(17): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877477 | |||||||
| chr7:49877477 | A | T | 1 | a0001c0001t0007g0181 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.827-34557A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877477 | |||||||
| chr7:49877477 | AAAAAATA others(5): Show |
A | 12 | a0001c0001t0005g0012 a0001c0001t0005g0117 a0001c0001t0005g0151 others(9): Show |
12 | HG00741.hp2 HG01074.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.827-34555_827-3454 others(16): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877477 | ||||||
| chr7:49877478 | AAAAATAT others(4): Show |
A | 1 | a0003c0003t0018g0233 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.827-34554_827-3454 others(15): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877478 | ||||||
| chr7:49877478 | AAAAATAT others(8): Show |
A | 1 | a0001c0001t0051g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.827-34554_827-3454 others(19): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877478 | ||||||
| chr7:49877479 | A | T | 4 | a0001c0001t0007g0181 a0002c0002t0026g0041 a0002c0002t0026g0254 others(1): Show |
4 | HG02717.hp1 HG02818.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-34555A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877479 | |||||||
| chr7:49877479 | AAAATAT | A | 8 | a0001c0001t0004g0104 a0001c0001t0004g0106 a0001c0001t0004g0134 others(5): Show |
8 | HG01928.hp1 HG03239.hp1 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.827-34553_827-3454 others(10): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877479 | ||||||
| chr7:49877479 | AAAATATA others(5): Show |
A | 1 | a0001c0001t0001g0156 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.827-34553_827-3454 others(16): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877479 | ||||||
| chr7:49877481 | A | AAAAAAAA others(5): Show |
2 | a0001c0001t0013g0219 a0002c0002t0013g0214 |
2 | HG01433.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.827-34552_827-3455 others(16): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAAAA others(4): Show |
1 | a0002c0002t0052g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.827-34552_827-3455 others(15): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0207 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.827-34552_827-3455 others(20): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAAAA others(23): Show |
1 | a0001c0001t0003g0190 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.827-34552_827-3455 others(34): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAAAA others(3): Show |
2 | a0002c0002t0013g0042 a0002c0002t0029g0098 |
2 | NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.827-34552_827-3455 others(14): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAAAA others(19): Show |
1 | a0001c0001t0001g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.827-34552_827-3455 others(30): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAAAA others(23): Show |
1 | a0002c0002t0058g0084 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.827-34552_827-3455 others(34): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAAAT others(12): Show |
1 | a0002c0002t0001g0057 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.827-34552_827-3455 others(23): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAAAT others(14): Show |
1 | a0001c0001t0040g0003 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.827-34552_827-3455 others(25): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAAAT others(16): Show |
1 | a0003c0003t0011g0241 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.827-34552_827-3455 others(27): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAAAT others(18): Show |
2 | a0002c0002t0003g0049 a0002c0002t0003g0096 |
2 | HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.827-34552_827-3455 others(29): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAAAT others(20): Show |
7 | a0001c0001t0001g0002 a0001c0001t0003g0002 a0002c0002t0003g0045 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.827-34552_827-3455 others(31): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAAAT others(22): Show |
8 | a0001c0001t0003g0163 a0001c0001t0003g0184 a0001c0001t0003g0192 others(5): Show |
8 | HG01099.hp1 HG02258.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.827-34552_827-3455 others(33): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAAAT others(24): Show |
7 | a0001c0001t0056g0125 a0002c0002t0003g0010 a0002c0002t0003g0014 others(4): Show |
7 | HG01123.hp2 HG02257.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.827-34552_827-3455 others(35): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAAAT others(26): Show |
1 | a0001c0001t0069g0176 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.827-34552_827-3455 others(37): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAAAT others(28): Show |
1 | a0001c0001t0001g0218 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.827-34552_827-3455 others(39): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAAAT others(30): Show |
2 | a0001c0001t0003g0167 a0002c0002t0014g0043 |
2 | HG00735.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.827-34552_827-3455 others(41): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAAAT others(36): Show |
1 | a0001c0001t0002g0123 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.827-34552_827-3455 others(47): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAATA others(23): Show |
1 | a0002c0002t0047g0209 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.827-34552_827-3455 others(34): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAATA others(27): Show |
1 | a0001c0001t0003g0166 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.827-34552_827-3455 others(38): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAATA others(9): Show |
1 | a0003c0003t0006g0235 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.827-34552_827-3455 others(20): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAATA others(11): Show |
1 | a0001c0001t0001g0130 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.827-34552_827-3455 others(22): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAATA others(15): Show |
2 | a0001c0001t0001g0145 a0001c0001t0002g0149 |
2 | HG01981.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.827-34552_827-3455 others(26): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAATA others(17): Show |
7 | a0001c0001t0009g0171 a0001c0001t0009g0174 a0002c0002t0001g0024 others(4): Show |
8 | HG00099.hp1 HG00323.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.827-34552_827-3455 others(28): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAATA others(19): Show |
5 | a0001c0001t0003g0118 a0002c0002t0002g0005 a0002c0002t0002g0035 others(2): Show |
5 | HG01071.hp2 HG01123.hp1 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.827-34552_827-3455 others(30): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAATA others(21): Show |
11 | a0001c0001t0001g0136 a0001c0001t0001g0150 a0001c0001t0001g0199 others(8): Show |
11 | HG00280.hp2 HG00597.hp2 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.827-34552_827-3455 others(32): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAATA others(23): Show |
7 | a0001c0001t0001g0129 a0001c0001t0002g0147 a0001c0001t0002g0177 others(4): Show |
7 | HG00423.hp2 HG01099.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.827-34552_827-3455 others(34): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAATA others(25): Show |
6 | a0001c0001t0002g0142 a0001c0001t0002g0146 a0002c0002t0001g0031 others(3): Show |
6 | HG00741.hp1 HG01081.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.827-34552_827-3455 others(36): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAATA others(27): Show |
5 | a0001c0001t0001g0141 a0001c0001t0002g0110 a0001c0001t0002g0144 others(2): Show |
5 | HG00733.hp2 HG02015.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.827-34552_827-3455 others(38): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAATA others(29): Show |
6 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0189 others(3): Show |
6 | HG00609.hp1 HG01255.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.827-34552_827-3455 others(40): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAATA others(31): Show |
5 | a0001c0001t0001g0115 a0001c0001t0002g0188 a0001c0001t0002g0213 others(2): Show |
5 | NA18962.hp1 NA18995.hp1 NA19064.hp2 others(2): Show |
intron_variant | MODIFIER | c.827-34552_827-3455 others(42): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAATA others(33): Show |
3 | a0002c0002t0002g0073 a0003c0003t0006g0220 a0003c0003t0006g0234 |
3 | HG03688.hp2 HG04199.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.827-34552_827-3455 others(44): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAATA others(37): Show |
1 | a0001c0001t0002g0200 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.827-34552_827-3455 others(48): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAATA others(27): Show |
1 | a0001c0001t0003g0120 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.827-34552_827-3455 others(38): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAAATA others(5): Show |
1 | a0001c0001t0004g0128 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.827-34552_827-3455 others(16): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAATAT others(16): Show |
1 | a0002c0002t0046g0050 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.827-34552_827-3455 others(27): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAATAT others(6): Show |
1 | a0001c0001t0001g0124 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.827-34552_827-3455 others(17): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAATAT others(8): Show |
1 | a0001c0001t0001g0131 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.827-34552_827-3455 others(19): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAATAT others(12): Show |
1 | a0003c0003t0017g0242 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.827-34552_827-3455 others(23): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAATAT others(14): Show |
1 | a0001c0001t0001g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.827-34552_827-3455 others(25): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAATAT others(16): Show |
6 | a0001c0001t0002g0191 a0001c0001t0009g0175 a0001c0001t0044g0138 others(3): Show |
6 | HG00423.hp1 HG01981.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.827-34552_827-3455 others(27): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAATAT others(18): Show |
1 | a0002c0002t0001g0013 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.827-34552_827-3455 others(29): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAATAT others(20): Show |
1 | a0002c0002t0002g0081 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.827-34552_827-3455 others(31): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAATAT others(22): Show |
1 | a0001c0001t0002g0137 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.827-34552_827-3455 others(33): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAATAT others(24): Show |
3 | a0002c0002t0002g0058 a0002c0002t0002g0071 a0002c0002t0002g0074 |
3 | HG00323.hp2 NA18612.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.827-34552_827-3455 others(35): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAATAT others(26): Show |
1 | a0001c0001t0001g0113 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.827-34552_827-3455 others(37): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAAATAT others(28): Show |
1 | a0002c0002t0002g0079 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.827-34552_827-3455 others(39): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAATATA others(7): Show |
2 | a0002c0002t0002g0090 a0003c0003t0034g0232 |
2 | NA19066.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.827-34552_827-3455 others(18): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAATATA others(9): Show |
3 | a0001c0001t0015g0182 a0001c0001t0015g0187 a0002c0002t0002g0033 |
3 | HG02055.hp1 HG02257.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.827-34552_827-3455 others(20): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAATATA others(11): Show |
3 | a0001c0001t0001g0193 a0001c0001t0002g0194 a0001c0001t0015g0109 |
3 | HG01943.hp2 HG02559.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.827-34552_827-3455 others(22): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAATATA others(21): Show |
1 | a0001c0001t0002g0159 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.827-34552_827-3455 others(32): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAAATATA others(5): Show |
1 | a0002c0002t0002g0039 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.827-34552_827-3455 others(16): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | AAATATAC others(4): Show |
1 | a0001c0001t0017g0223 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.827-34552_827-3455 others(15): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | A | T | 6 | a0001c0001t0004g0164 a0001c0001t0004g0165 a0001c0001t0007g0181 others(3): Show |
6 | HG02717.hp1 HG02818.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.827-34553A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877481 | |||||||
| chr7:49877481 | AATATATA others(3): Show |
A | 4 | a0002c0002t0001g0053 a0002c0002t0003g0092 a0003c0003t0006g0243 others(1): Show |
4 | HG02486.hp1 HG02615.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-34525_827-3451 others(14): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877481 | AATATATA others(5): Show |
A | 12 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0005g0154 others(9): Show |
12 | HG01928.hp2 HG02922.hp2 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.827-34527_827-3451 others(16): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49877481 | ||||||
| chr7:49877482 | ATATATAT others(2): Show |
A | 3 | a0001c0001t0060g0105 a0002c0002t0022g0048 a0002c0002t0048g0225 |
3 | HG02895.hp2 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.827-34551_827-3454 others(13): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877482 | |||||||
| chr7:49877482 | ATATATAT others(4): Show |
A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(8): Show |
11 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.827-34551_827-3454 others(15): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877482 | |||||||
| chr7:49877483 | T | A | 4 | a0001c0001t0001g0121 a0001c0001t0001g0127 a0002c0002t0039g0205 others(1): Show |
4 | HG01993.hp2 HG03098.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-34551T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877483 | |||||||
| chr7:49877483 | T | C | 4 | a0002c0002t0001g0093 a0002c0002t0014g0064 a0002c0002t0029g0098 others(1): Show |
4 | HG02976.hp1 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-34551T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877483 | |||||||
| chr7:49877485 | T | A | 3 | a0001c0001t0001g0127 a0002c0002t0039g0205 a0002c0002t0053g0095 |
3 | HG01993.hp2 HG03098.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.827-34549T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877485 | |||||||
| chr7:49877487 | T | A | 4 | a0001c0001t0042g0148 a0002c0002t0003g0083 a0002c0002t0039g0205 others(1): Show |
4 | HG01993.hp2 HG02015.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-34547T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877487 | |||||||
| chr7:49877487 | T | C | 6 | a0001c0001t0020g0143 a0001c0001t0021g0112 a0001c0001t0021g0135 others(3): Show |
6 | NA18960.hp1 NA18972.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.827-34547T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877487 | |||||||
| chr7:49877489 | T | A | 4 | a0002c0002t0003g0083 a0002c0002t0023g0047 a0002c0002t0023g0210 others(1): Show |
4 | HG02015.hp2 HG02145.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-34545T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877489 | |||||||
| chr7:49877489 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.827-34545T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877489 | |||||||
| chr7:49877491 | T | A | 4 | a0002c0002t0023g0047 a0002c0002t0023g0210 a0003c0003t0011g0247 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-34543T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877491 | |||||||
| chr7:49877491 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.827-34543T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877491 | |||||||
| chr7:49877493 | T | A | 6 | a0002c0002t0001g0053 a0002c0002t0003g0092 a0002c0002t0048g0225 others(3): Show |
6 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.827-34541T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877493 | |||||||
| chr7:49877493 | T | C | 3 | a0001c0001t0042g0148 a0002c0002t0039g0205 a0002c0002t0053g0095 |
3 | HG01993.hp2 HG03098.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.827-34541T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877493 | |||||||
| chr7:49877495 | T | A | 10 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(7): Show |
10 | HG02055.hp2 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.827-34539T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877495 | |||||||
| chr7:49877495 | T | C | 1 | a0002c0002t0003g0083 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.827-34539T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877495 | |||||||
| chr7:49877497 | T | A | 1 | a0001c0001t0008g0198 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.827-34537T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877497 | |||||||
| chr7:49877497 | T | C | 3 | a0002c0002t0023g0047 a0002c0002t0023g0210 a0003c0003t0016g0230 |
3 | HG02145.hp1 HG02897.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.827-34537T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877497 | |||||||
| chr7:49877507 | T | G | 5 | a0001c0001t0009g0171 a0001c0001t0009g0174 a0001c0001t0009g0175 others(2): Show |
6 | HG00323.hp1 HG01256.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.827-34527T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877507 | |||||||
| chr7:49877510 | A | G | 1 | a0003c0003t0006g0234 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.827-34524A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877510 | |||||||
| chr7:49877723 | C | G | 3 | a0001c0001t0020g0143 a0001c0001t0021g0112 a0001c0001t0021g0135 |
3 | NA18972.hp2 NA18977.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.827-34311C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877723 | |||||||
| chr7:49877805 | A | C | 2 | a0002c0002t0046g0050 a0002c0002t0047g0209 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.827-34229A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877805 | |||||||
| chr7:49877912 | G | T | 1 | a0003c0003t0006g0220 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.827-34122G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877912 | |||||||
| chr7:49877929 | T | C | 153 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.827-34105T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877929 | |||||||
| chr7:49877962 | C | A | 1 | a0002c0002t0003g0049 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.827-34072C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49877962 | |||||||
| chr7:49878080 | G | A | 25 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(22): Show |
25 | HG01261.hp1 HG01433.hp1 HG02280.hp1 others(22): Show |
intron_variant | MODIFIER | c.827-33954G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49878080 | |||||||
| chr7:49878104 | G | T | 153 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.827-33930G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49878104 | |||||||
| chr7:49878137 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.827-33897C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49878137 | |||||||
| chr7:49878398 | T | G | 1 | a0001c0001t0009g0174 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.827-33636T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49878398 | |||||||
| chr7:49878608 | T | C | 4 | a0001c0001t0013g0219 a0002c0002t0013g0042 a0002c0002t0013g0046 others(1): Show |
4 | HG01433.hp1 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-33426T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49878608 | |||||||
| chr7:49878610 | T | C | 18 | a0001c0001t0001g0156 a0001c0001t0005g0012 a0001c0001t0005g0116 others(15): Show |
18 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.827-33424T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49878610 | |||||||
| chr7:49878704 | A | G | 7 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0218 others(4): Show |
7 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.827-33330A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49878704 | |||||||
| chr7:49879072 | C | T | 1 | a0002c0002t0062g0086 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.827-32962C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49879072 | |||||||
| chr7:49879492 | A | G | 178 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(175): Show |
179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.827-32542A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49879492 | |||||||
| chr7:49879504 | A | G | 1 | a0001c0001t0063g0217 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.827-32530A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49879504 | |||||||
| chr7:49879535 | A | C | 5 | a0002c0002t0003g0096 a0002c0002t0048g0225 a0003c0003t0011g0241 others(2): Show |
5 | HG02055.hp2 HG02280.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.827-32499A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49879535 | |||||||
| chr7:49879712 | CT | C | 8 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(5): Show |
8 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.827-32319delT | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49879712 | ||||||
| chr7:49879712 | CTTTGGTT others(25): Show |
C | 3 | a0001c0001t0060g0105 a0002c0002t0030g0101 a0002c0002t0055g0211 |
3 | HG02280.hp1 HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.827-32318_827-3228 others(36): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49879712 | ||||||
| chr7:49879752 | A | T | 3 | a0001c0001t0060g0105 a0002c0002t0030g0101 a0002c0002t0055g0211 |
3 | HG02280.hp1 HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.827-32282A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49879752 | |||||||
| chr7:49879799 | G | T | 8 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(5): Show |
8 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.827-32235G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49879799 | |||||||
| chr7:49880426 | CTTTTG | C | 21 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(18): Show |
21 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.827-31598_827-3159 others(9): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49880426 | ||||||
| chr7:49880509 | C | T | 1 | a0002c0002t0061g0061 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.827-31525C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49880509 | |||||||
| chr7:49880581 | T | TTTTA | 8 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(5): Show |
8 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.827-31437_827-3143 others(8): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49880581 | ||||||
| chr7:49880632 | T | G | 3 | a0002c0002t0003g0096 a0003c0003t0011g0241 a0003c0003t0011g0249 |
3 | HG02280.hp2 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.827-31402T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49880632 | |||||||
| chr7:49880671 | G | T | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.827-31363G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49880671 | |||||||
| chr7:49880914 | G | A | 1 | a0002c0002t0001g0057 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.827-31120G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49880914 | |||||||
| chr7:49881416 | A | C | 153 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.827-30618A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49881416 | |||||||
| chr7:49881491 | G | A | 2 | a0001c0001t0005g0012 a0003c0005t0018g0240 |
2 | HG02135.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.827-30543G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49881491 | |||||||
| chr7:49881518 | C | G | 178 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(175): Show |
179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.827-30516C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49881518 | |||||||
| chr7:49881739 | G | T | 3 | a0002c0002t0026g0041 a0002c0002t0026g0254 a0002c0002t0032g0102 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.827-30295G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49881739 | |||||||
| chr7:49882188 | G | A | 1 | a0002c0002t0022g0048 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.827-29846G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49882188 | |||||||
| chr7:49882282 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.827-29752C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49882282 | |||||||
| chr7:49882286 | T | C | 1 | a0001c0001t0051g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.827-29748T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49882286 | |||||||
| chr7:49882332 | T | C | 2 | a0002c0002t0023g0047 a0002c0002t0023g0210 |
2 | HG02897.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.827-29702T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49882332 | |||||||
| chr7:49882405 | C | T | 2 | a0001c0001t0040g0003 a0003c0003t0006g0246 |
2 | HG02451.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.827-29629C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49882405 | |||||||
| chr7:49882532 | C | A | 2 | a0001c0001t0004g0206 a0002c0002t0004g0017 |
2 | HG01243.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.827-29502C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49882532 | |||||||
| chr7:49882826 | A | G | 21 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(18): Show |
21 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.827-29208A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49882826 | |||||||
| chr7:49882864 | T | TTTG | 8 | a0001c0001t0003g0184 a0001c0001t0015g0109 a0001c0001t0015g0182 others(5): Show |
8 | HG00280.hp1 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.827-29149_827-2914 others(7): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49882864 | ||||||
| chr7:49882927 | A | G | 13 | a0001c0001t0002g0191 a0001c0001t0002g0194 a0001c0001t0021g0112 others(10): Show |
13 | HG00423.hp1 HG02074.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.827-29107A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49882927 | |||||||
| chr7:49883251 | T | G | 2 | a0001c0001t0002g0177 a0001c0001t0043g0178 |
2 | HG01099.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.827-28783T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49883251 | |||||||
| chr7:49883367 | C | T | 1 | a0001c0001t0005g0116 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.827-28667C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49883367 | |||||||
| chr7:49883473 | T | C | 13 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(10): Show |
13 | HG02630.hp1 HG02895.hp2 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.827-28561T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49883473 | |||||||
| chr7:49883690 | C | T | 194 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.827-28344C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49883690 | |||||||
| chr7:49883761 | A | G | 153 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.827-28273A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49883761 | |||||||
| chr7:49883911 | T | G | 153 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.827-28123T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49883911 | |||||||
| chr7:49884037 | ACTC | A | 4 | a0001c0001t0013g0219 a0002c0002t0013g0042 a0002c0002t0013g0046 others(1): Show |
4 | HG01433.hp1 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-27995_827-2799 others(7): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49884037 | ||||||
| chr7:49884043 | A | G | 3 | a0002c0002t0026g0041 a0002c0002t0026g0254 a0002c0002t0032g0102 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.827-27991A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49884043 | |||||||
| chr7:49884099 | C | T | 34 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(31): Show |
34 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(31): Show |
intron_variant | MODIFIER | c.827-27935C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49884099 | |||||||
| chr7:49884214 | T | C | 212 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(209): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.827-27820T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49884214 | |||||||
| chr7:49884374 | G | A | 1 | a0002c0002t0013g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.827-27660G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49884374 | |||||||
| chr7:49884435 | A | G | 1 | a0001c0001t0002g0200 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.827-27599A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49884435 | |||||||
| chr7:49884461 | C | T | 152 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(149): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.827-27573C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49884461 | |||||||
| chr7:49884533 | T | C | 4 | a0001c0001t0002g0194 a0002c0002t0002g0030 a0002c0002t0002g0090 others(1): Show |
4 | NA18747.hp1 NA18944.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-27501T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49884533 | |||||||
| chr7:49884584 | A | G | 2 | a0002c0002t0029g0098 a0002c0002t0052g0224 |
2 | HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.827-27450A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49884584 | |||||||
| chr7:49884697 | C | T | 1 | a0002c0002t0022g0226 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.827-27337C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49884697 | |||||||
| chr7:49884724 | G | C | 174 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(171): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.827-27310G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49884724 | |||||||
| chr7:49884757 | A | G | 1 | a0001c0001t0054g0004 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.827-27277A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49884757 | |||||||
| chr7:49884758 | C | G | 1 | a0001c0001t0054g0004 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.827-27276C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49884758 | |||||||
| chr7:49884961 | A | G | 2 | a0002c0002t0025g0066 a0002c0002t0025g0067 |
2 | HG01109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.827-27073A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49884961 | |||||||
| chr7:49884979 | A | G | 2 | a0002c0002t0003g0092 a0003c0003t0006g0243 |
2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.827-27055A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49884979 | |||||||
| chr7:49885140 | A | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.827-26894A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49885140 | |||||||
| chr7:49885149 | T | C | 1 | a0003c0003t0006g0244 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.827-26885T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49885149 | |||||||
| chr7:49885314 | G | A | 1 | a0001c0001t0002g0110 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.827-26720G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49885314 | |||||||
| chr7:49885364 | G | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(18): Show |
21 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.827-26670G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49885364 | |||||||
| chr7:49885462 | G | A | 16 | a0001c0001t0001g0002 a0001c0001t0003g0002 a0001c0001t0003g0118 others(13): Show |
16 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.827-26572G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49885462 | |||||||
| chr7:49885464 | T | C | 174 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(171): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.827-26570T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49885464 | |||||||
| chr7:49885685 | T | C | 1 | a0001c0001t0064g0122 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.827-26349T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49885685 | |||||||
| chr7:49885836 | T | G | 1 | a0001c0001t0001g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.827-26198T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49885836 | |||||||
| chr7:49885855 | G | A | 2 | a0001c0001t0060g0105 a0002c0002t0055g0211 |
2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.827-26179G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49885855 | |||||||
| chr7:49885886 | A | G | 212 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(209): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.827-26148A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49885886 | |||||||
| chr7:49886055 | A | G | 21 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(18): Show |
21 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.827-25979A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49886055 | |||||||
| chr7:49886322 | TCAC | T | 17 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(14): Show |
17 | HG01433.hp1 HG02630.hp1 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.827-25708_827-2570 others(7): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49886322 | ||||||
| chr7:49886692 | T | C | 2 | a0002c0002t0001g0093 a0002c0002t0003g0049 |
2 | HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.827-25342T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49886692 | |||||||
| chr7:49887050 | C | T | 17 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(14): Show |
17 | HG01433.hp1 HG02630.hp1 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.827-24984C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49887050 | |||||||
| chr7:49887534 | A | ATTC | 194 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.827-24497_827-2449 others(7): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49887534 | ||||||
| chr7:49887563 | T | TCATTTGT others(44): Show |
8 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(5): Show |
8 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.827-24460_827-2445 others(55): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49887563 | ||||||
| chr7:49887575 | G | A | 212 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(209): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.827-24459G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49887575 | |||||||
| chr7:49887621 | T | A | 3 | a0002c0002t0022g0048 a0002c0002t0022g0226 a0002c0002t0049g0208 |
3 | HG02630.hp1 HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.827-24413T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49887621 | |||||||
| chr7:49887758 | C | T | 174 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(171): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.827-24276C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49887758 | |||||||
| chr7:49887817 | C | G | 2 | a0002c0002t0039g0205 a0002c0002t0053g0095 |
2 | HG01993.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.827-24217C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49887817 | |||||||
| chr7:49887984 | GCCCTTCA others(3): Show |
G | 8 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(5): Show |
8 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.827-24047_827-2403 others(14): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49887984 | ||||||
| chr7:49888294 | A | C | 2 | a0002c0002t0046g0050 a0002c0002t0047g0209 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.827-23740A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49888294 | |||||||
| chr7:49888498 | A | G | 1 | a0002c0002t0002g0029 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.827-23536A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49888498 | |||||||
| chr7:49888567 | C | A | 1 | a0001c0001t0001g0115 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.827-23467C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49888567 | |||||||
| chr7:49888638 | C | T | 1 | a0001c0001t0005g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.827-23396C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49888638 | |||||||
| chr7:49888735 | A | T | 17 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(14): Show |
17 | HG01433.hp1 HG02630.hp1 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.827-23299A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49888735 | |||||||
| chr7:49889323 | T | C | 53 | a0001c0001t0002g0110 a0001c0001t0002g0123 a0001c0001t0002g0132 others(50): Show |
53 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.827-22711T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49889323 | |||||||
| chr7:49889363 | A | G | 8 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(5): Show |
8 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.827-22671A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49889363 | |||||||
| chr7:49889958 | T | C | 17 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(14): Show |
17 | HG01433.hp1 HG02630.hp1 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.827-22076T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49889958 | |||||||
| chr7:49890069 | AT | A | 191 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.827-21962delT | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49890069 | ||||||
| chr7:49890114 | C | T | 1 | a0001c0001t0051g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.827-21920C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49890114 | |||||||
| chr7:49890668 | C | T | 1 | a0002c0002t0014g0064 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.827-21366C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49890668 | |||||||
| chr7:49890730 | CA | C | 5 | a0001c0001t0005g0158 a0002c0002t0002g0035 a0002c0002t0014g0064 others(2): Show |
5 | HG01070.hp2 HG01071.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.827-21290delA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49890730 | ||||||
| chr7:49890730 | CAA | C | 183 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(180): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.827-21291_827-2129 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49890730 | ||||||
| chr7:49890734 | A | C | 3 | a0002c0002t0026g0041 a0002c0002t0026g0254 a0002c0002t0032g0102 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.827-21300A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49890734 | |||||||
| chr7:49890735 | A | C | 1 | a0002c0002t0022g0048 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.827-21299A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49890735 | |||||||
| chr7:49890923 | T | TA | 53 | a0001c0001t0002g0110 a0001c0001t0002g0123 a0001c0001t0002g0132 others(50): Show |
53 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.827-21103dupA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49890923 | ||||||
| chr7:49890982 | T | A | 1 | a0001c0001t0054g0004 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.827-21052T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49890982 | |||||||
| chr7:49891038 | A | G | 191 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.827-20996A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49891038 | |||||||
| chr7:49891260 | G | A | 17 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(14): Show |
17 | HG01433.hp1 HG02630.hp1 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.827-20774G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49891260 | |||||||
| chr7:49891424 | C | G | 2 | a0001c0001t0002g0201 a0002c0002t0002g0073 |
2 | HG03669.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.827-20610C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49891424 | |||||||
| chr7:49891493 | G | A | 1 | a0002c0002t0002g0032 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.827-20541G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49891493 | |||||||
| chr7:49891602 | A | C | 3 | a0001c0001t0010g0114 a0001c0001t0019g0173 a0002c0002t0019g0026 |
3 | HG00280.hp1 HG01168.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.827-20432A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49891602 | |||||||
| chr7:49891679 | T | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(84): Show |
88 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.827-20355T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49891679 | |||||||
| chr7:49891687 | T | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.827-20347T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49891687 | |||||||
| chr7:49891835 | T | C | 1 | a0003c0003t0012g0251 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.827-20199T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49891835 | |||||||
| chr7:49892004 | A | G | 9 | a0001c0001t0010g0111 a0002c0002t0004g0062 a0002c0002t0010g0018 others(6): Show |
9 | HG01167.hp2 HG01256.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.827-20030A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49892004 | |||||||
| chr7:49892031 | A | AT | 6 | a0001c0001t0015g0182 a0001c0001t0020g0143 a0002c0002t0002g0032 others(3): Show |
6 | HG00280.hp2 HG01515.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.827-19972dupT | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49892031 | ||||||
| chr7:49892031 | AT | A | 95 | a0001c0001t0001g0136 a0001c0001t0001g0139 a0001c0001t0001g0156 others(92): Show |
96 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.827-19972delT | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49892031 | ||||||
| chr7:49892031 | ATT | A | 107 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(104): Show |
107 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.827-19973_827-1997 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49892031 | ||||||
| chr7:49892031 | ATTT | A | 6 | a0001c0001t0040g0003 a0002c0002t0001g0055 a0002c0002t0026g0254 others(3): Show |
6 | HG01168.hp2 HG01993.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.827-19974_827-1997 others(7): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49892031 | ||||||
| chr7:49892033 | T | TG | 4 | a0001c0001t0008g0186 a0001c0001t0008g0196 a0001c0001t0008g0198 others(1): Show |
4 | HG02965.hp2 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-20001_827-2000 others(5): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49892033 | |||||||
| chr7:49892034 | T | G | 7 | a0001c0001t0008g0195 a0002c0002t0013g0214 a0002c0002t0022g0048 others(4): Show |
7 | HG01433.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.827-20000T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49892034 | |||||||
| chr7:49892035 | T | G | 4 | a0001c0001t0013g0219 a0001c0001t0051g0009 a0002c0002t0013g0042 others(1): Show |
4 | HG02809.hp2 HG02922.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-19999T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49892035 | |||||||
| chr7:49892096 | G | A | 38 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0121 others(35): Show |
39 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.827-19938G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49892096 | |||||||
| chr7:49892468 | G | C | 174 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(171): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.827-19566G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49892468 | |||||||
| chr7:49892469 | G | A | 3 | a0002c0002t0003g0045 a0002c0002t0014g0043 a0002c0002t0014g0044 |
3 | HG02258.hp1 HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.827-19565G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49892469 | |||||||
| chr7:49892482 | T | C | 174 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(171): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.827-19552T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49892482 | |||||||
| chr7:49892955 | CACTT | C | 174 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(171): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.827-19077_827-1907 others(8): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49892955 | ||||||
| chr7:49893215 | T | C | 2 | a0001c0001t0040g0003 a0003c0003t0006g0246 |
2 | HG02451.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.827-18819T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49893215 | |||||||
| chr7:49893436 | C | T | 5 | a0001c0001t0001g0008 a0001c0001t0006g0221 a0001c0001t0060g0105 others(2): Show |
5 | HG02280.hp1 HG03225.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.827-18598C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49893436 | |||||||
| chr7:49893445 | A | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.827-18589A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49893445 | |||||||
| chr7:49893602 | C | G | 17 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(14): Show |
17 | HG01433.hp1 HG02630.hp1 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.827-18432C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49893602 | |||||||
| chr7:49893649 | T | TA | 173 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(170): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.827-18384dupA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49893649 | ||||||
| chr7:49893690 | A | G | 2 | a0002c0002t0004g0062 a0003c0003t0012g0248 |
2 | HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.827-18344A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49893690 | |||||||
| chr7:49893882 | A | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(84): Show |
88 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.827-18152A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49893882 | |||||||
| chr7:49893910 | A | G | 1 | a0001c0001t0004g0161 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.827-18124A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49893910 | |||||||
| chr7:49893995 | G | T | 1 | a0003c0003t0038g0239 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.827-18039G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49893995 | |||||||
| chr7:49894144 | G | A | 1 | a0002c0002t0027g0015 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.827-17890G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49894144 | |||||||
| chr7:49894160 | T | TTTTC | 191 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.827-17862_827-1785 others(8): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49894160 | ||||||
| chr7:49894317 | G | A | 17 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(14): Show |
17 | HG01433.hp1 HG02630.hp1 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.827-17717G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49894317 | |||||||
| chr7:49894393 | A | G | 109 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(106): Show |
110 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.827-17641A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49894393 | |||||||
| chr7:49894688 | G | A | 17 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(14): Show |
17 | HG01433.hp1 HG02630.hp1 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.827-17346G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49894688 | |||||||
| chr7:49895023 | A | G | 2 | a0002c0002t0029g0098 a0002c0002t0052g0224 |
2 | HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.827-17011A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49895023 | |||||||
| chr7:49895054 | A | G | 2 | a0002c0002t0029g0098 a0002c0002t0052g0224 |
2 | HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.827-16980A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49895054 | |||||||
| chr7:49895358 | C | T | 5 | a0001c0001t0015g0109 a0001c0001t0015g0182 a0001c0001t0015g0187 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.827-16676C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49895358 | |||||||
| chr7:49895424 | A | T | 3 | a0001c0001t0001g0124 a0002c0002t0001g0051 a0003c0003t0006g0252 |
3 | HG00099.hp2 HG01074.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.827-16610A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49895424 | |||||||
| chr7:49895731 | G | GCAT | 191 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.827-16302_827-1630 others(7): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49895731 | ||||||
| chr7:49895975 | G | A | 191 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.827-16059G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49895975 | |||||||
| chr7:49896009 | G | T | 2 | a0001c0001t0004g0169 a0001c0001t0004g0170 |
2 | NA18946.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.827-16025G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49896009 | |||||||
| chr7:49896044 | G | A | 1 | a0002c0002t0027g0069 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.827-15990G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49896044 | |||||||
| chr7:49896254 | T | G | 3 | a0002c0002t0022g0048 a0002c0002t0022g0226 a0002c0002t0049g0208 |
3 | HG02630.hp1 HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.827-15780T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49896254 | |||||||
| chr7:49896388 | G | A | 2 | a0002c0002t0024g0077 a0002c0002t0024g0216 |
2 | HG02074.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.827-15646G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49896388 | |||||||
| chr7:49896461 | T | A | 191 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.827-15573T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49896461 | |||||||
| chr7:49896750 | A | G | 17 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(14): Show |
17 | HG01433.hp1 HG02630.hp1 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.827-15284A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49896750 | |||||||
| chr7:49896848 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.827-15186C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49896848 | |||||||
| chr7:49896881 | A | AT | 7 | a0001c0001t0004g0106 a0001c0001t0005g0012 a0002c0002t0004g0062 others(4): Show |
7 | HG02135.hp1 HG02717.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.827-15128dupT | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49896881 | ||||||
| chr7:49896881 | AT | A | 7 | a0001c0001t0007g0108 a0001c0001t0007g0181 a0001c0001t0013g0219 others(4): Show |
7 | HG01256.hp2 HG01433.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.827-15128delT | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49896881 | ||||||
| chr7:49896881 | ATT | A | 25 | a0001c0001t0001g0127 a0001c0001t0001g0139 a0001c0001t0001g0145 others(22): Show |
25 | HG00597.hp2 HG01099.hp2 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.827-15129_827-1512 others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49896881 | ||||||
| chr7:49896881 | ATTT | A | 138 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.827-15130_827-1512 others(7): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49896881 | ||||||
| chr7:49896881 | ATTTT | A | 24 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(21): Show |
24 | HG01168.hp2 HG01261.hp1 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.827-15131_827-1512 others(8): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49896881 | ||||||
| chr7:49897500 | T | A | 1 | a0002c0002t0002g0081 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.827-14534T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49897500 | |||||||
| chr7:49897540 | T | G | 2 | a0002c0002t0039g0205 a0002c0002t0053g0095 |
2 | HG01993.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.827-14494T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49897540 | |||||||
| chr7:49897694 | A | T | 4 | a0001c0001t0013g0219 a0002c0002t0013g0042 a0002c0002t0013g0046 others(1): Show |
4 | HG01433.hp1 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-14340A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49897694 | |||||||
| chr7:49897800 | T | TA | 3 | a0002c0002t0026g0041 a0002c0002t0026g0254 a0002c0002t0032g0102 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.827-14228dupA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49897800 | ||||||
| chr7:49898049 | G | A | 2 | a0001c0001t0001g0183 a0002c0002t0001g0054 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.827-13985G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49898049 | |||||||
| chr7:49898051 | G | A | 2 | a0001c0001t0001g0183 a0002c0002t0001g0054 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.827-13983G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49898051 | |||||||
| chr7:49898121 | G | A | 2 | a0001c0001t0002g0110 a0001c0001t0002g0144 |
2 | HG02056.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.827-13913G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49898121 | |||||||
| chr7:49898129 | G | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.827-13905G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49898129 | |||||||
| chr7:49898147 | A | G | 1 | a0001c0001t0051g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.827-13887A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49898147 | |||||||
| chr7:49898293 | C | G | 1 | a0002c0002t0001g0013 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.827-13741C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49898293 | |||||||
| chr7:49898307 | A | T | 1 | a0001c0001t0007g0172 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.827-13727A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49898307 | |||||||
| chr7:49898310 | G | A | 4 | a0001c0001t0003g0167 a0002c0002t0026g0041 a0002c0002t0026g0254 others(1): Show |
4 | HG00735.hp1 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-13724G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49898310 | |||||||
| chr7:49898313 | G | GT | 17 | a0001c0001t0005g0012 a0001c0001t0005g0116 a0001c0001t0005g0117 others(14): Show |
17 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.827-13710dupT | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49898313 | ||||||
| chr7:49898325 | A | T | 3 | a0002c0002t0026g0041 a0002c0002t0026g0254 a0002c0002t0032g0102 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.827-13709A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49898325 | |||||||
| chr7:49898380 | G | A | 2 | a0002c0002t0039g0205 a0002c0002t0053g0095 |
2 | HG01993.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.827-13654G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49898380 | |||||||
| chr7:49898514 | T | A | 191 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.827-13520T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49898514 | |||||||
| chr7:49898604 | C | A | 8 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(5): Show |
8 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.827-13430C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49898604 | |||||||
| chr7:49898846 | A | G | 3 | a0002c0002t0026g0041 a0002c0002t0026g0254 a0002c0002t0032g0102 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.827-13188A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49898846 | |||||||
| chr7:49898904 | C | T | 17 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(14): Show |
17 | HG01433.hp1 HG02630.hp1 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.827-13130C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49898904 | |||||||
| chr7:49898946 | G | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.827-13088G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49898946 | |||||||
| chr7:49898979 | T | C | 1 | a0002c0002t0068g0227 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.827-13055T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49898979 | |||||||
| chr7:49898997 | C | A | 1 | a0003c0003t0012g0251 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.827-13037C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49898997 | |||||||
| chr7:49899078 | C | A | 191 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.827-12956C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49899078 | |||||||
| chr7:49899146 | A | G | 1 | a0001c0001t0054g0004 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.827-12888A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49899146 | |||||||
| chr7:49899324 | C | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(85): Show |
89 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.827-12710C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49899324 | |||||||
| chr7:49899447 | C | A | 3 | a0002c0002t0026g0041 a0002c0002t0026g0254 a0002c0002t0032g0102 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.827-12587C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49899447 | |||||||
| chr7:49899551 | T | C | 234 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.827-12483T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49899551 | |||||||
| chr7:49899630 | C | A | 2 | a0001c0001t0001g0207 a0002c0002t0001g0057 |
2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.827-12404C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49899630 | |||||||
| chr7:49899646 | C | T | 2 | a0002c0002t0010g0018 a0002c0002t0010g0019 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.827-12388C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49899646 | |||||||
| chr7:49899764 | G | A | 53 | a0001c0001t0002g0110 a0001c0001t0002g0123 a0001c0001t0002g0132 others(50): Show |
53 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.827-12270G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49899764 | |||||||
| chr7:49899805 | G | T | 1 | a0001c0001t0005g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.827-12229G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49899805 | |||||||
| chr7:49899863 | T | C | 1 | a0001c0001t0010g0114 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.827-12171T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49899863 | |||||||
| chr7:49899938 | T | C | 3 | a0002c0002t0026g0041 a0002c0002t0026g0254 a0002c0002t0032g0102 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.827-12096T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49899938 | |||||||
| chr7:49900039 | C | T | 2 | a0001c0001t0051g0009 a0002c0002t0050g0100 |
2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.827-11995C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49900039 | |||||||
| chr7:49900184 | T | G | 191 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.827-11850T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49900184 | |||||||
| chr7:49900658 | A | G | 15 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(12): Show |
15 | HG01433.hp1 HG02630.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.827-11376A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49900658 | |||||||
| chr7:49900689 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.827-11345C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49900689 | |||||||
| chr7:49900734 | G | A | 191 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.827-11300G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49900734 | |||||||
| chr7:49900911 | T | C | 3 | a0002c0002t0026g0041 a0002c0002t0026g0254 a0002c0002t0032g0102 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.827-11123T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49900911 | |||||||
| chr7:49901011 | C | A | 5 | a0001c0001t0015g0109 a0001c0001t0015g0182 a0001c0001t0015g0187 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.827-11023C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49901011 | |||||||
| chr7:49901500 | A | C | 4 | a0001c0001t0002g0142 a0002c0002t0002g0032 a0002c0002t0002g0078 others(1): Show |
4 | HG00280.hp2 HG01261.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-10534A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49901500 | |||||||
| chr7:49901735 | G | A | 3 | a0002c0002t0026g0041 a0002c0002t0026g0254 a0002c0002t0032g0102 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.827-10299G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49901735 | |||||||
| chr7:49901747 | GA | G | 3 | a0002c0002t0022g0048 a0002c0002t0022g0226 a0002c0002t0049g0208 |
3 | HG02630.hp1 HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.827-10282delA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49901747 | ||||||
| chr7:49901758 | C | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0183 others(18): Show |
21 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.827-10276C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49901758 | |||||||
| chr7:49901830 | G | C | 1 | a0001c0001t0004g0161 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.827-10204G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49901830 | |||||||
| chr7:49901870 | G | GAACACTG others(19): Show |
18 | a0001c0001t0005g0012 a0001c0001t0005g0117 a0001c0001t0005g0151 others(15): Show |
18 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.827-10146_827-1012 others(30): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49901870 | ||||||
| chr7:49901870 | G | GAACACTG others(45): Show |
1 | a0001c0001t0005g0116 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.827-10121_827-1012 others(56): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49901870 | ||||||
| chr7:49901870 | G | GAACACTG others(123): Show |
1 | a0001c0001t0008g0196 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.827-10121_827-1012 others(134): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49901870 | ||||||
| chr7:49901870 | G | GAACACTG others(175): Show |
2 | a0001c0001t0008g0185 a0001c0001t0008g0186 |
2 | HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.827-10121_827-1012 others(186): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49901870 | ||||||
| chr7:49901870 | G | GAACACTG others(201): Show |
4 | a0001c0001t0008g0195 a0001c0001t0008g0197 a0001c0001t0008g0198 others(1): Show |
4 | HG02922.hp2 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-10121_827-1012 others(212): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49901870 | ||||||
| chr7:49901870 | G | GAACACTG others(253): Show |
1 | a0002c0002t0028g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.827-10121_827-1012 others(264): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49901870 | ||||||
| chr7:49901887 | A | T | 1 | a0003c0003t0012g0248 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.827-10147A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49901887 | |||||||
| chr7:49901896 | T | G | 1 | a0002c0002t0050g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.827-10138T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49901896 | |||||||
| chr7:49902109 | T | C | 174 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(171): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.827-9925T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49902109 | |||||||
| chr7:49902146 | A | G | 1 | a0002c0002t0003g0083 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.827-9888A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49902146 | |||||||
| chr7:49902187 | G | T | 1 | a0001c0001t0051g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.827-9847G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49902187 | |||||||
| chr7:49902225 | A | G | 1 | a0001c0001t0009g0174 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.827-9809A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49902225 | |||||||
| chr7:49902352 | C | A | 1 | a0001c0001t0005g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.827-9682C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49902352 | |||||||
| chr7:49902406 | C | A | 8 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(5): Show |
8 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.827-9628C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49902406 | |||||||
| chr7:49902508 | C | T | 1 | a0002c0002t0007g0082 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.827-9526C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49902508 | |||||||
| chr7:49902554 | C | CA | 39 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0121 others(36): Show |
40 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.827-9465dupA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49902554 | ||||||
| chr7:49902554 | CA | C | 17 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(14): Show |
17 | HG00323.hp2 HG01433.hp1 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.827-9465delA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49902554 | ||||||
| chr7:49902599 | G | A | 2 | a0002c0002t0029g0098 a0002c0002t0052g0224 |
2 | HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.827-9435G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49902599 | |||||||
| chr7:49902659 | T | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(159): Show |
163 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.827-9375T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49902659 | |||||||
| chr7:49902675 | A | G | 191 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.827-9359A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49902675 | |||||||
| chr7:49902691 | T | A | 2 | a0002c0002t0002g0078 a0002c0002t0002g0079 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.827-9343T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49902691 | |||||||
| chr7:49902700 | T | C | 2 | a0002c0002t0004g0062 a0003c0003t0012g0248 |
2 | HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.827-9334T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49902700 | |||||||
| chr7:49902760 | T | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.827-9274T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49902760 | |||||||
| chr7:49902922 | A | G | 1 | a0001c0001t0056g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.827-9112A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49902922 | |||||||
| chr7:49902927 | C | A | 4 | a0001c0001t0013g0219 a0002c0002t0013g0042 a0002c0002t0013g0046 others(1): Show |
4 | HG01433.hp1 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-9107C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49902927 | |||||||
| chr7:49903072 | C | T | 1 | a0001c0001t0002g0149 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.827-8962C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49903072 | |||||||
| chr7:49903137 | C | T | 3 | a0002c0002t0022g0048 a0002c0002t0022g0226 a0002c0002t0049g0208 |
3 | HG02630.hp1 HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.827-8897C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49903137 | |||||||
| chr7:49903689 | C | T | 1 | a0002c0002t0055g0211 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.827-8345C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49903689 | |||||||
| chr7:49903806 | T | C | 17 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(14): Show |
17 | HG01433.hp1 HG02630.hp1 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.827-8228T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49903806 | |||||||
| chr7:49903940 | A | G | 8 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(5): Show |
8 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.827-8094A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49903940 | |||||||
| chr7:49904077 | A | G | 1 | a0001c0001t0002g0200 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.827-7957A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49904077 | |||||||
| chr7:49904138 | G | T | 10 | a0001c0001t0005g0151 a0001c0001t0005g0152 a0001c0001t0005g0153 others(7): Show |
10 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.827-7896G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49904138 | |||||||
| chr7:49904143 | C | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(76): Show |
80 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.827-7891C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49904143 | |||||||
| chr7:49904237 | A | C | 3 | a0002c0002t0022g0048 a0002c0002t0022g0226 a0002c0002t0049g0208 |
3 | HG02630.hp1 HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.827-7797A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49904237 | |||||||
| chr7:49904253 | C | T | 3 | a0001c0001t0013g0219 a0002c0002t0013g0046 a0002c0002t0013g0214 |
3 | HG01433.hp1 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.827-7781C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49904253 | |||||||
| chr7:49904373 | C | T | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0002c0002t0062g0086 |
3 | HG03017.hp2 HG03927.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.827-7661C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49904373 | |||||||
| chr7:49904736 | A | AT | 162 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0115 others(159): Show |
163 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.827-7281dupT | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49904736 | ||||||
| chr7:49904736 | A | ATT | 6 | a0001c0001t0002g0133 a0001c0001t0002g0146 a0001c0001t0002g0200 others(3): Show |
6 | HG00609.hp1 HG02055.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.827-7282_827-7281d others(4): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49904736 | ||||||
| chr7:49904736 | AT | A | 11 | a0001c0001t0007g0107 a0001c0001t0013g0219 a0002c0002t0004g0088 others(8): Show |
11 | HG01433.hp1 HG02717.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.827-7281delT | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49904736 | ||||||
| chr7:49904798 | C | T | 1 | a0001c0001t0002g0191 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.827-7236C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49904798 | |||||||
| chr7:49904853 | A | G | 191 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.827-7181A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49904853 | |||||||
| chr7:49904925 | G | A | 1 | a0003c0003t0012g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.827-7109G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49904925 | |||||||
| chr7:49905238 | A | G | 1 | a0002c0002t0025g0067 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.827-6796A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49905238 | |||||||
| chr7:49905279 | G | C | 17 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(14): Show |
17 | HG01433.hp1 HG02630.hp1 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.827-6755G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49905279 | |||||||
| chr7:49905595 | C | T | 3 | a0001c0001t0003g0184 a0001c0001t0011g0222 a0002c0002t0003g0052 |
3 | HG02257.hp1 HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.827-6439C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49905595 | |||||||
| chr7:49905767 | C | T | 1 | a0001c0001t0002g0180 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.827-6267C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49905767 | |||||||
| chr7:49905792 | A | G | 2 | a0002c0002t0029g0098 a0002c0002t0052g0224 |
2 | HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.827-6242A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49905792 | |||||||
| chr7:49905839 | C | T | 2 | a0001c0001t0004g0104 a0002c0002t0004g0022 |
2 | HG03239.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.827-6195C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49905839 | |||||||
| chr7:49906177 | C | T | 1 | a0002c0002t0001g0031 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.827-5857C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49906177 | |||||||
| chr7:49906214 | A | C | 2 | a0002c0002t0039g0205 a0002c0002t0053g0095 |
2 | HG01993.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.827-5820A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49906214 | |||||||
| chr7:49906245 | T | G | 2 | a0002c0002t0048g0225 a0003c0003t0011g0247 |
2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.827-5789T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49906245 | |||||||
| chr7:49906287 | C | A | 1 | a0002c0002t0003g0083 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.827-5747C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49906287 | |||||||
| chr7:49906345 | T | G | 17 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(14): Show |
17 | HG01433.hp1 HG02630.hp1 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.827-5689T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49906345 | |||||||
| chr7:49906376 | C | T | 2 | a0002c0002t0029g0098 a0002c0002t0052g0224 |
2 | HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.827-5658C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49906376 | |||||||
| chr7:49906401 | C | T | 17 | a0001c0001t0005g0012 a0001c0001t0005g0116 a0001c0001t0005g0117 others(14): Show |
17 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.827-5633C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49906401 | |||||||
| chr7:49906517 | T | C | 1 | a0001c0001t0007g0172 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.827-5517T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49906517 | |||||||
| chr7:49906616 | G | T | 2 | a0002c0002t0025g0066 a0002c0002t0025g0067 |
2 | HG01109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.827-5418G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49906616 | |||||||
| chr7:49906674 | T | G | 191 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.827-5360T>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49906674 | |||||||
| chr7:49906824 | AT | A | 51 | a0001c0001t0002g0110 a0001c0001t0002g0123 a0001c0001t0002g0132 others(48): Show |
51 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.827-5206delT | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49906824 | ||||||
| chr7:49906835 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.827-5199T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49906835 | |||||||
| chr7:49906910 | T | C | 2 | a0002c0002t0029g0098 a0002c0002t0052g0224 |
2 | HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.827-5124T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49906910 | |||||||
| chr7:49907121 | A | C | 2 | a0002c0002t0029g0098 a0002c0002t0052g0224 |
2 | HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.827-4913A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49907121 | |||||||
| chr7:49907175 | T | C | 1 | a0001c0001t0004g0206 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.827-4859T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49907175 | |||||||
| chr7:49907242 | A | C | 17 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(14): Show |
17 | HG01433.hp1 HG02630.hp1 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.827-4792A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49907242 | |||||||
| chr7:49907667 | A | G | 17 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(14): Show |
17 | HG01433.hp1 HG02630.hp1 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.827-4367A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49907667 | |||||||
| chr7:49907680 | T | A | 174 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(171): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.827-4354T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49907680 | |||||||
| chr7:49907715 | G | A | 174 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(171): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.827-4319G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49907715 | |||||||
| chr7:49907857 | G | A | 17 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(14): Show |
17 | HG01433.hp1 HG02630.hp1 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.827-4177G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49907857 | |||||||
| chr7:49908132 | C | T | 1 | a0004c0004t0001g0070 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.827-3902C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49908132 | |||||||
| chr7:49908542 | T | A | 1 | a0001c0001t0004g0161 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.827-3492T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49908542 | |||||||
| chr7:49908640 | C | T | 1 | a0002c0002t0049g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.827-3394C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49908640 | |||||||
| chr7:49909212 | A | T | 3 | a0002c0002t0022g0048 a0002c0002t0022g0226 a0002c0002t0049g0208 |
3 | HG02630.hp1 HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.827-2822A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49909212 | |||||||
| chr7:49909230 | T | C | 1 | a0001c0001t0005g0116 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.827-2804T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49909230 | |||||||
| chr7:49909291 | T | C | 1 | a0001c0001t0002g0137 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.827-2743T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49909291 | |||||||
| chr7:49909324 | T | C | 174 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(171): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.827-2710T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49909324 | |||||||
| chr7:49909350 | A | G | 1 | a0001c0001t0051g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.827-2684A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49909350 | |||||||
| chr7:49909359 | CA | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.827-2671delA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49909359 | ||||||
| chr7:49909647 | A | T | 5 | a0001c0001t0001g0183 a0002c0002t0001g0053 a0002c0002t0001g0054 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.827-2387A>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49909647 | |||||||
| chr7:49909722 | G | T | 6 | a0001c0001t0001g0179 a0002c0002t0001g0060 a0002c0002t0001g0076 others(3): Show |
6 | HG03688.hp1 HG03710.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.827-2312G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49909722 | |||||||
| chr7:49909747 | C | T | 7 | a0001c0001t0015g0109 a0001c0001t0015g0182 a0001c0001t0015g0187 others(4): Show |
7 | HG00280.hp1 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.827-2287C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49909747 | |||||||
| chr7:49909825 | T | C | 174 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(171): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.827-2209T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49909825 | |||||||
| chr7:49909921 | T | C | 4 | a0001c0001t0013g0219 a0002c0002t0013g0042 a0002c0002t0013g0046 others(1): Show |
4 | HG01433.hp1 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-2113T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49909921 | |||||||
| chr7:49909946 | T | C | 11 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(8): Show |
11 | HG02630.hp1 HG02895.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.827-2088T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49909946 | |||||||
| chr7:49909995 | G | A | 1 | a0001c0001t0014g0168 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.827-2039G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49909995 | |||||||
| chr7:49910163 | C | T | 5 | a0001c0001t0015g0109 a0001c0001t0015g0182 a0001c0001t0015g0187 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.827-1871C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49910163 | |||||||
| chr7:49910173 | C | G | 1 | a0002c0002t0022g0226 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.827-1861C>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49910173 | |||||||
| chr7:49910210 | G | C | 17 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0195 others(14): Show |
17 | HG01433.hp1 HG02630.hp1 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.827-1824G>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49910210 | |||||||
| chr7:49910388 | C | T | 38 | a0001c0001t0001g0002 a0001c0001t0003g0002 a0001c0001t0003g0118 others(35): Show |
38 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.827-1646C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49910388 | |||||||
| chr7:49910505 | C | T | 2 | a0002c0002t0004g0062 a0003c0003t0012g0248 |
2 | HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.827-1529C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49910505 | |||||||
| chr7:49910605 | TA | T | 191 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.827-1420delA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49910605 | ||||||
| chr7:49910705 | G | T | 1 | a0003c0003t0016g0230 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.827-1329G>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49910705 | |||||||
| chr7:49910706 | C | A | 1 | a0003c0003t0016g0230 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.827-1328C>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49910706 | |||||||
| chr7:49910847 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.827-1187C>T | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49910847 | |||||||
| chr7:49910899 | A | G | 191 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.827-1135A>G | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49910899 | |||||||
| chr7:49911208 | G | A | 1 | a0002c0002t0022g0048 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.827-826G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49911208 | |||||||
| chr7:49911212 | G | A | 1 | a0004c0004t0001g0070 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.827-822G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49911212 | |||||||
| chr7:49911386 | G | A | 1 | a0001c0001t0002g0132 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.827-648G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49911386 | |||||||
| chr7:49911480 | C | CA | 138 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.827-531dupA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49911480 | ||||||
| chr7:49911480 | C | CAA | 19 | a0001c0001t0001g0179 a0001c0001t0001g0202 a0001c0001t0001g0203 others(16): Show |
19 | HG00741.hp1 HG01123.hp1 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.827-532_827-531dup others(2): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49911480 | ||||||
| chr7:49911480 | CA | C | 15 | a0001c0001t0001g0141 a0001c0001t0005g0012 a0001c0001t0005g0116 others(12): Show |
15 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.827-531delA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49911480 | ||||||
| chr7:49911739 | T | A | 211 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(208): Show |
212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.827-295T>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49911739 | |||||||
| chr7:49911822 | G | A | 3 | a0002c0002t0026g0041 a0002c0002t0026g0254 a0002c0002t0032g0102 |
3 | HG02717.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.827-212G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49911822 | |||||||
| chr7:49911878 | T | C | 2 | a0002c0002t0039g0205 a0002c0002t0053g0095 |
2 | HG01993.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.827-156T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49911878 | |||||||
| chr7:49911912 | A | AATACACG others(5): Show |
1 | a0002c0002t0001g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.827-121_827-120ins others(12): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49911912 | ||||||
| chr7:49911916 | A | C | 1 | a0002c0002t0001g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.827-118A>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49911916 | |||||||
| chr7:49911918 | T | C | 1 | a0002c0002t0001g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.827-116T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49911918 | |||||||
| chr7:49911923 | G | A | 1 | a0002c0002t0001g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.827-111G>A | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49911923 | |||||||
| chr7:49911923 | G | GCA | 20 | a0001c0001t0005g0012 a0001c0001t0005g0116 a0001c0001t0005g0117 others(17): Show |
20 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.827-88_827-87dupCA | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49911923 | ||||||
| chr7:49911923 | G | GCACA | 10 | a0001c0001t0002g0194 a0001c0001t0013g0219 a0001c0001t0051g0009 others(7): Show |
10 | HG01433.hp1 HG02809.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.827-90_827-87dupCA others(2): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49911923 | ||||||
| chr7:49911923 | G | GCACACAC others(1): Show |
51 | a0001c0001t0001g0115 a0001c0001t0001g0121 a0001c0001t0001g0124 others(48): Show |
52 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.827-94_827-87dupCA others(6): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49911923 | ||||||
| chr7:49911923 | G | GCACACAC others(3): Show |
16 | a0001c0001t0001g0139 a0001c0001t0001g0193 a0001c0001t0001g0199 others(13): Show |
16 | HG00741.hp1 HG01361.hp1 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.827-96_827-87dupCA others(8): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49911923 | ||||||
| chr7:49911923 | G | GCACACAC others(5): Show |
21 | a0001c0001t0001g0002 a0001c0001t0002g0110 a0001c0001t0002g0132 others(18): Show |
21 | HG00609.hp1 HG00733.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.827-98_827-87dupCA others(10): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49911923 | ||||||
| chr7:49911923 | G | GCACACAC others(7): Show |
60 | a0001c0001t0001g0179 a0001c0001t0001g0183 a0001c0001t0001g0202 others(57): Show |
60 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.827-100_827-87dupC others(13): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49911923 | ||||||
| chr7:49911923 | G | GCACACAC others(9): Show |
15 | a0001c0001t0001g0203 a0001c0001t0002g0147 a0001c0001t0006g0221 others(12): Show |
15 | HG01099.hp1 HG01123.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.827-102_827-87dupC others(15): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49911923 | ||||||
| chr7:49911923 | G | GCACACAC others(11): Show |
7 | a0001c0001t0001g0008 a0001c0001t0003g0184 a0001c0001t0011g0222 others(4): Show |
7 | HG02257.hp1 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.827-104_827-87dupC others(17): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49911923 | ||||||
| chr7:49911923 | G | GCACACAC others(13): Show |
2 | a0002c0002t0001g0011 a0002c0002t0003g0023 |
2 | HG01261.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.827-106_827-87dupC others(19): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49911923 | ||||||
| chr7:49911923 | G | GCGCACAC others(1): Show |
4 | a0001c0001t0001g0113 a0002c0002t0022g0226 a0002c0002t0046g0050 others(1): Show |
4 | HG02630.hp1 NA18522.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-110_827-109ins others(8): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49911923 | ||||||
| chr7:49911923 | G | GCGCACAC others(3): Show |
1 | a0002c0002t0022g0048 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.827-110_827-109ins others(10): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49911923 | ||||||
| chr7:49911923 | G | GCGCGCAC others(11): Show |
1 | a0001c0001t0054g0004 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.827-110_827-109ins others(18): Show |
VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 49911923 | ||||||
| chr7:49911948 | T | C | 193 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0113 others(190): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.827-86T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49911948 | |||||||
| chr7:49911950 | T | C | 2 | a0002c0002t0002g0005 a0002c0002t0003g0075 |
2 | HG01123.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.827-84T>C | VWC2 | ENSG00000188730.5 | transcript | ENST00000340652.5 | protein_coding | 3/3 | chr7 | 49911950 |