Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51322 |
| ensemblid | ENSG00000095787.26 |
| hgncid | 17327 |
| symbol | WAC |
| name | WW domain containing adaptor with coiled-coil |
| refseq_nuc | NM_016628.5 |
| refseq_prot | NP_057712.2 |
| ensembl_nuc | ENST00000354911.9 |
| ensembl_prot | ENSP00000346986.4 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 28533118 |
| end | 28623112 |
| strand | + |
| ver | v1.2 |
| region | chr10:28533118-28623112 |
| region5000 | chr10:28528118-28628112 |
| regionname0 | WAC_chr10_28533118_28623112 |
| regionname5000 | WAC_chr10_28528118_28628112 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 647 | 317 | 83 | 67 | 126 | 12 | 27 | 88 | WAC_chr10_28528118_28628112 | WAC | MVMYA others(642): Show |
chr10 | 28528118 | 28628112 |
| a0002 | 0/0 | 647 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | MVMYA others(642): Show |
chr10 | 28528118 | 28628112 |
| a0003 | 0/0 | 647 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | MVMYA others(642): Show |
chr10 | 28528118 | 28628112 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1941 | 302 | 71 | 65 | 126 | 12 | 26 | WAC_chr10_28528118_28628112 | WAC | ATGGT others(1936): Show |
chr10 | 28528118 | 28628112 | ||
| a0001c0002 | 0/0 | 1941 | 10 | 9 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | ATGGT others(1936): Show |
chr10 | 28528118 | 28628112 | ||
| a0001c0004 | 0/0 | 1941 | 3 | 2 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | ATGGT others(1936): Show |
chr10 | 28528118 | 28628112 | ||
| a0001c0005 | 0/0 | 1941 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | ATGGT others(1936): Show |
chr10 | 28528118 | 28628112 | ||
| a0001c0007 | 0/0 | 1941 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | ATGGT others(1936): Show |
chr10 | 28528118 | 28628112 | ||
| a0002c0003 | 0/0 | 1941 | 4 | 3 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | ATGGT others(1936): Show |
chr10 | 28528118 | 28628112 | ||
| a0003c0006 | 0/0 | 1941 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | ATGGT others(1936): Show |
chr10 | 28528118 | 28628112 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5909 | 69 | 19 | 22 | 21 | 0 | 7 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5904): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0002 | 0/0 | 5908 | 41 | 1 | 9 | 26 | 3 | 2 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5903): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0003 | 0/0 | 5910 | 24 | 1 | 1 | 18 | 0 | 4 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5905): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0004 | 0/0 | 5910 | 19 | 5 | 7 | 0 | 3 | 4 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5905): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0005 | 1/0 | 5912 | 18 | 4 | 4 | 5 | 0 | 4 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5907): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0006 | 0/0 | 5908 | 15 | 12 | 3 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5903): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0007 | 0/0 | 5910 | 13 | 2 | 2 | 9 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5905): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0008 | 0/0 | 5913 | 6 | 3 | 2 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5908): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0010 | 0/0 | 5909 | 8 | 3 | 0 | 4 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5904): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0011 | 0/0 | 5910 | 6 | 0 | 0 | 6 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5905): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0012 | 0/0 | 5907 | 6 | 0 | 1 | 3 | 2 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5902): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0013 | 0/0 | 5911 | 5 | 2 | 0 | 3 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5906): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0014 | 0/0 | 5906 | 4 | 4 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5901): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0015 | 0/0 | 5908 | 4 | 0 | 0 | 4 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5903): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0016 | 0/0 | 5910 | 3 | 0 | 3 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5905): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0017 | 0/0 | 5910 | 3 | 0 | 3 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5905): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0018 | 0/0 | 5907 | 3 | 3 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5902): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0019 | 0/0 | 5909 | 3 | 3 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5904): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0020 | 0/0 | 5909 | 2 | 1 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5904): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0021 | 0/0 | 5908 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5903): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0022 | 0/0 | 5907 | 2 | 0 | 0 | 2 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5902): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0023 | 0/0 | 5908 | 2 | 0 | 0 | 2 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5903): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0024 | 0/0 | 5909 | 2 | 0 | 0 | 2 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5904): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0025 | 0/0 | 5911 | 2 | 0 | 0 | 2 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5906): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0026 | 0/0 | 5907 | 2 | 0 | 1 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5902): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0027 | 0/0 | 5908 | 2 | 0 | 0 | 2 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5903): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0028 | 0/0 | 5909 | 2 | 0 | 0 | 2 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5904): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0029 | 0/0 | 5909 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5904): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0030 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5906): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0031 | 0/0 | 5909 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5904): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0032 | 0/0 | 5910 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5905): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0033 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5906): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0034 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5906): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0035 | 0/0 | 5912 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5907): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0036 | 0/0 | 5909 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5904): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0037 | 0/0 | 5910 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5905): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0039 | 0/0 | 5909 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5904): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0040 | 0/0 | 5909 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5904): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0042 | 0/0 | 5909 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5904): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0043 | 0/0 | 5910 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5905): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0044 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5906): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0045 | 0/0 | 5909 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5904): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0046 | 0/0 | 5909 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5904): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0047 | 0/0 | 5908 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5903): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0048 | 0/0 | 5913 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5908): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0049 | 0/0 | 5912 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5907): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0050 | 0/0 | 5909 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5904): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0051 | 0/0 | 5908 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5903): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0052 | 0/0 | 5908 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5903): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0053 | 0/0 | 5907 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5902): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0054 | 0/0 | 5909 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5904): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0055 | 0/0 | 5912 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5907): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0056 | 0/0 | 5909 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5904): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0057 | 0/0 | 5908 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5903): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0058 | 0/0 | 5908 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5903): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0059 | 0/0 | 5908 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5903): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0060 | 0/0 | 5909 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5904): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0061 | 0/0 | 5909 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5904): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0062 | 0/0 | 5908 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5903): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0063 | 0/1 | 5912 | 1 | 0 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5907): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0064 | 0/0 | 5909 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5904): Show |
chr10 | 28528118 | 28628112 |
| a0001c0001t0065 | 0/0 | 5909 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5904): Show |
chr10 | 28528118 | 28628112 |
| a0001c0002t0009 | 0/0 | 5905 | 9 | 8 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5900): Show |
chr10 | 28528118 | 28628112 |
| a0001c0002t0038 | 0/0 | 5908 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5903): Show |
chr10 | 28528118 | 28628112 |
| a0001c0004t0001 | 0/0 | 5909 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5904): Show |
chr10 | 28528118 | 28628112 |
| a0001c0004t0021 | 0/0 | 5908 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5903): Show |
chr10 | 28528118 | 28628112 |
| a0001c0004t0041 | 0/0 | 5909 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5904): Show |
chr10 | 28528118 | 28628112 |
| a0001c0005t0004 | 0/0 | 5910 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5905): Show |
chr10 | 28528118 | 28628112 |
| a0001c0007t0004 | 0/0 | 5910 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5905): Show |
chr10 | 28528118 | 28628112 |
| a0002c0003t0008 | 0/0 | 5913 | 4 | 3 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5908): Show |
chr10 | 28528118 | 28628112 |
| a0003c0006t0005 | 0/0 | 5912 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | GAGTT others(5907): Show |
chr10 | 28528118 | 28628112 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0238 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0006g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0006g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0006g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0006g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0006g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0006g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0006g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0006g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0006g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0006g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0006g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0006g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0006g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0006g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0007g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0007g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0007g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0007g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0007g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0007g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0007g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0007g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0007g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0007g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0007g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0007g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0008g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0008g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0008g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0008g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0008g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0008g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0010g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0010g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0010g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0010g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0010g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0010g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0010g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0010g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0011g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0011g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0011g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0011g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0011g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0011g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0012g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0012g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0012g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0012g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0012g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0012g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0013g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0013g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0013g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0013g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0013g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0014g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0014g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0014g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0014g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0015g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0015g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0015g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0015g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0016g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0016g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0016g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0017g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0017g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0017g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0018g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0018g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0018g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0019g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0019g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0019g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0020g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0020g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0021g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0022g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0022g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0023g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0023g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0024g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0024g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0025g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0025g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0026g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0026g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0027g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0027g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0028g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0028g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0029g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0030g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0031g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0032g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0033g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0034g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0035g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0036g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0037g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0039g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0040g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0042g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0043g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0044g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0045g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0046g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0047g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0048g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0049g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0050g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0051g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0052g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0053g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0054g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0055g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0056g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0057g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0058g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0059g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0060g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0061g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0062g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0063g0064 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0064g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0065g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0002t0009g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0002t0009g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0002t0009g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0002t0009g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0002t0009g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0002t0009g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0002t0009g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0002t0009g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0002t0009g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0002t0038g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0004t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0004t0021g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0004t0041g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0005t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0007t0004g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0002c0003t0008g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0002c0003t0008g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0002c0003t0008g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0002c0003t0008g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0003c0006t0005g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0047 | EUR | GBR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00099 | hp2 | a0001 | c0001 | t0010 | g0276 | EUR | GBR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00140 | hp1 | a0001 | c0001 | t0039 | g0156 | EUR | GBR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0269 | EUR | GBR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | FIN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0277 | EUR | FIN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0270 | EUR | FIN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00323 | hp2 | a0001 | c0001 | t0012 | g0048 | EUR | FIN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | CHS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00438 | hp2 | a0001 | c0001 | t0035 | g0225 | EAS | CHS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00558 | hp2 | a0001 | c0001 | t0005 | g0243 | EAS | CHS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | CHS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | CHS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00609 | hp1 | a0001 | c0001 | t0010 | g0289 | EAS | CHS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | CHS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00621 | hp2 | a0001 | c0001 | t0025 | g0245 | EAS | CHS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00639 | hp1 | a0001 | c0001 | t0016 | g0312 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | CHS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00673 | hp2 | a0001 | c0001 | t0022 | g0152 | EAS | CHS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00733 | hp1 | a0001 | c0001 | t0008 | g0234 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00735 | hp2 | a0001 | c0002 | t0009 | g0005 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0257 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0278 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01069 | hp1 | a0001 | c0004 | t0021 | g0132 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0251 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0261 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0298 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01106 | hp2 | a0001 | c0001 | t0006 | g0304 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0146 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01109 | hp2 | a0001 | c0001 | t0062 | g0065 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0318 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01168 | hp2 | a0001 | c0001 | t0042 | g0275 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01175 | hp1 | a0001 | c0001 | t0016 | g0310 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01192 | hp2 | a0001 | c0001 | t0016 | g0311 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01243 | hp2 | a0001 | c0001 | t0006 | g0303 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0239 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01256 | hp1 | a0001 | c0001 | t0058 | g0054 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0265 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01257 | hp1 | a0001 | c0001 | t0026 | g0053 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0264 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01346 | hp1 | a0001 | c0001 | t0020 | g0137 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0272 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0235 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01361 | hp2 | a0001 | c0001 | t0037 | g0260 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01496 | hp1 | a0001 | c0001 | t0017 | g0078 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01515 | hp1 | a0001 | c0001 | t0056 | g0266 | EUR | IBS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01515 | hp2 | a0001 | c0001 | t0012 | g0063 | EUR | IBS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0163 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0240 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01891 | hp2 | a0001 | c0005 | t0004 | g0220 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01928 | hp2 | a0001 | c0001 | t0017 | g0077 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0081 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01943 | hp1 | a0001 | c0001 | t0017 | g0105 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01981 | hp1 | a0001 | c0001 | t0045 | g0280 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0268 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02004 | hp2 | a0001 | c0001 | t0008 | g0230 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02040 | hp1 | a0001 | c0001 | t0015 | g0267 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02040 | hp2 | a0001 | c0001 | t0007 | g0114 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02055 | hp1 | a0001 | c0004 | t0001 | g0127 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02055 | hp2 | a0001 | c0002 | t0009 | g0009 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02071 | hp2 | a0001 | c0001 | t0008 | g0248 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02074 | hp2 | a0001 | c0001 | t0005 | g0244 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02083 | hp1 | a0001 | c0001 | t0011 | g0207 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02083 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02129 | hp1 | a0001 | c0001 | t0064 | g0307 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02129 | hp2 | a0001 | c0001 | t0030 | g0135 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02132 | hp1 | a0001 | c0001 | t0011 | g0169 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02132 | hp2 | a0001 | c0001 | t0012 | g0031 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02135 | hp2 | a0001 | c0001 | t0007 | g0180 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02145 | hp2 | a0001 | c0001 | t0014 | g0255 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CDX | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CDX | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0229 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02273 | hp1 | a0001 | c0001 | t0012 | g0317 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02273 | hp2 | a0001 | c0001 | t0007 | g0143 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02293 | hp1 | a0001 | c0001 | t0059 | g0055 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02451 | hp2 | a0001 | c0001 | t0010 | g0290 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02572 | hp1 | a0001 | c0002 | t0009 | g0103 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0301 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02630 | hp1 | a0001 | c0002 | t0009 | g0004 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02647 | hp1 | a0001 | c0001 | t0033 | g0153 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02647 | hp2 | a0001 | c0002 | t0009 | g0008 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02698 | hp1 | a0001 | c0001 | t0026 | g0061 | SAS | PJL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0262 | SAS | PJL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02717 | hp1 | a0001 | c0001 | t0020 | g0071 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02717 | hp2 | a0001 | c0001 | t0018 | g0191 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02723 | hp1 | a0001 | c0001 | t0019 | g0162 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02723 | hp2 | a0002 | c0003 | t0008 | g0231 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0224 | SAS | PJL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02809 | hp2 | a0001 | c0002 | t0009 | g0003 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0305 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0247 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02886 | hp2 | a0001 | c0002 | t0009 | g0006 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02895 | hp1 | a0001 | c0001 | t0010 | g0308 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02895 | hp2 | a0001 | c0001 | t0014 | g0256 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02896 | hp1 | a0002 | c0003 | t0008 | g0068 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02896 | hp2 | a0001 | c0002 | t0009 | g0007 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0309 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02897 | hp2 | a0001 | c0002 | t0038 | g0010 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02922 | hp1 | a0001 | c0001 | t0013 | g0193 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02922 | hp2 | a0001 | c0001 | t0050 | g0294 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02965 | hp1 | a0001 | c0001 | t0053 | g0104 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0295 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0302 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02970 | hp2 | a0001 | c0001 | t0032 | g0106 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0252 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0076 | SAS | PJL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03017 | hp2 | a0001 | c0001 | t0065 | g0185 | SAS | PJL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03041 | hp1 | a0001 | c0001 | t0047 | g0306 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03041 | hp2 | a0001 | c0001 | t0055 | g0227 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03098 | hp1 | a0001 | c0001 | t0034 | g0273 | AFR | MSL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0296 | AFR | MSL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03130 | hp2 | a0001 | c0001 | t0018 | g0190 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0293 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03209 | hp1 | a0001 | c0001 | t0013 | g0204 | AFR | MSL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0236 | AFR | MSL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0233 | SAS | PJL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03239 | hp2 | a0001 | c0001 | t0031 | g0165 | SAS | PJL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0226 | AFR | MSL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0297 | AFR | MSL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03486 | hp2 | a0001 | c0001 | t0019 | g0117 | AFR | MSL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0299 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0258 | SAS | PJL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | BEB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0073 | SAS | BEB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03834 | hp2 | a0001 | c0007 | t0004 | g0263 | SAS | BEB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03927 | hp1 | a0001 | c0001 | t0061 | g0291 | SAS | BEB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0283 | SAS | BEB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG04115 | hp1 | a0001 | c0001 | t0005 | g0237 | SAS | STU | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | STU | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG04184 | hp1 | a0001 | c0001 | t0005 | g0246 | SAS | BEB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0089 | SAS | BEB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0098 | SAS | STU | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | STU | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG04204 | hp1 | a0001 | c0001 | t0057 | g0036 | SAS | STU | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | STU | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG04228 | hp1 | a0003 | c0006 | t0005 | g0241 | SAS | STU | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | STU | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0203 | AFR | YRI | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0148 | AFR | YRI | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18612 | hp1 | a0001 | c0001 | t0007 | g0173 | EAS | CHB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18612 | hp2 | a0001 | c0001 | t0025 | g0249 | EAS | CHB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18747 | hp1 | a0001 | c0001 | t0011 | g0168 | EAS | CHB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | CHB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18906 | hp1 | a0001 | c0002 | t0009 | g0074 | AFR | YRI | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18906 | hp2 | a0001 | c0001 | t0048 | g0253 | AFR | YRI | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18940 | hp1 | a0001 | c0001 | t0010 | g0285 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18941 | hp2 | a0001 | c0001 | t0024 | g0149 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18947 | hp1 | a0001 | c0001 | t0044 | g0075 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18948 | hp2 | a0001 | c0001 | t0023 | g0189 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18952 | hp2 | a0001 | c0001 | t0007 | g0216 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18954 | hp2 | a0001 | c0001 | t0007 | g0171 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18959 | hp1 | a0001 | c0001 | t0028 | g0020 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18960 | hp1 | a0001 | c0001 | t0024 | g0178 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18964 | hp2 | a0001 | c0001 | t0011 | g0167 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18965 | hp1 | a0001 | c0001 | t0007 | g0210 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18965 | hp2 | a0001 | c0001 | t0015 | g0101 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18972 | hp1 | a0001 | c0001 | t0011 | g0134 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18975 | hp1 | a0001 | c0001 | t0021 | g0181 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18978 | hp2 | a0001 | c0001 | t0027 | g0030 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18988 | hp2 | a0001 | c0001 | t0060 | g0113 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18989 | hp2 | a0001 | c0001 | t0007 | g0176 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18990 | hp1 | a0001 | c0001 | t0022 | g0183 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18990 | hp2 | a0001 | c0001 | t0015 | g0100 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18992 | hp1 | a0001 | c0001 | t0012 | g0056 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18994 | hp1 | a0001 | c0001 | t0028 | g0060 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18994 | hp2 | a0001 | c0001 | t0007 | g0159 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18995 | hp1 | a0001 | c0001 | t0013 | g0205 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18998 | hp1 | a0001 | c0001 | t0046 | g0151 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19002 | hp1 | a0001 | c0001 | t0012 | g0025 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19003 | hp2 | a0001 | c0001 | t0010 | g0287 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19005 | hp2 | a0001 | c0001 | t0007 | g0131 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19007 | hp1 | a0001 | c0001 | t0015 | g0099 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | LWK | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0222 | AFR | LWK | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19057 | hp1 | a0001 | c0001 | t0051 | g0286 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19058 | hp2 | a0001 | c0001 | t0011 | g0107 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19062 | hp1 | a0001 | c0001 | t0049 | g0242 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19068 | hp1 | a0001 | c0001 | t0013 | g0122 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19074 | hp1 | a0001 | c0001 | t0023 | g0126 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19074 | hp2 | a0001 | c0001 | t0054 | g0094 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19077 | hp2 | a0001 | c0001 | t0005 | g0250 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19089 | hp1 | a0001 | c0001 | t0052 | g0041 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19089 | hp2 | a0001 | c0001 | t0029 | g0066 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19090 | hp1 | a0001 | c0001 | t0013 | g0160 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19090 | hp2 | a0001 | c0001 | t0036 | g0042 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19091 | hp1 | a0001 | c0001 | t0043 | g0109 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19091 | hp2 | a0001 | c0001 | t0027 | g0024 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0221 | AFR | YRI | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19240 | hp2 | a0001 | c0001 | t0018 | g0192 | AFR | YRI | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ASW | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0300 | AFR | ASW | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0014 | EUR | TSI | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA20752 | hp2 | a0001 | c0001 | t0040 | g0174 | EUR | TSI | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0274 | SAS | GIH | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | GIH | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01123 | hp2 | a0002 | c0003 | t0008 | g0223 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02109 | hp1 | a0001 | c0001 | t0014 | g0254 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0292 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0279 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0228 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03471 | hp1 | a0001 | c0001 | t0019 | g0206 | AFR | MSL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03471 | hp2 | a0001 | c0001 | t0014 | g0070 | AFR | MSL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG06807 | hp1 | a0001 | c0001 | t0010 | g0271 | AFR | USA | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG06807 | hp2 | a0001 | c0004 | t0041 | g0154 | AFR | USA | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18955 | hp2 | a0001 | c0001 | t0010 | g0288 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0097 | AFR | USA | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | USA | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | LWK | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA21309 | hp2 | a0002 | c0003 | t0008 | g0232 | AFR | LWK | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0063 | g0064 | REF | REF | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0238 | REF | REF | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:28608191 | A | G | 1 | a0002 | 4 | HG01123.hp2 HG02723.hp2 HG02896.hp1 others(1): Show |
missense_variant | MODERATE | c.925A>G | p.Thr309Ala | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/14 | 1387/5912 | 925/1944 | 309/647 | chr10 | 28608191 | |||
| chr10:28617687 | A | G | 1 | a0003 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.1777A>G | p.Met593Val | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/14 | 2239/5912 | 1777/1944 | 593/647 | chr10 | 28617687 | |||
| chr10:28623110 | T | G | 1 | a0001 | 1 | HG02922.hp2 | splice_region_variant | LOW | c.*3504T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | chr10 | 28623110 | |||||||
| chr10:28623110 | TAATC | T | 1 | a0001 | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
splice_region_variant | LOW | c.*3505_*3508delAATC | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | chr10 | 28623110 | |||||||
| chr10:28623112 | A | G | 1 | a0001 | 16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
splice_region_variant | LOW | c.*3506A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | chr10 | 28623112 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:28595923 | A | G | 1 | a0001c0007 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.801A>G | p.Pro267Pro | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/14 | 1263/5912 | 801/1944 | 267/647 | chr10 | 28595923 | |||
| chr10:28610784 | G | A | 1 | a0001c0005 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.1251G>A | p.Thr417Thr | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 9/14 | 1713/5912 | 1251/1944 | 417/647 | chr10 | 28610784 | |||
| chr10:28611841 | T | G | 1 | a0001c0004 | 3 | HG01069.hp1 HG02055.hp1 HG06807.hp2 |
synonymous_variant | LOW | c.1356T>G | p.Ser452Ser | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/14 | 1818/5912 | 1356/1944 | 452/647 | chr10 | 28611841 | |||
| chr10:28617776 | A | G | 1 | a0001c0002 | 10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
synonymous_variant | LOW | c.1866A>G | p.Arg622Arg | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/14 | 2328/5912 | 1866/1944 | 622/647 | chr10 | 28617776 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:28533160 | A | G | 1 | a0001c0001t0065 | 1 | HG03017.hp2 | 5_prime_UTR_variant | MODIFIER | c.-420A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 1/14 | 420 | chr10 | 28533160 | ||||||
| chr10:28533177 | C | G | 1 | a0001c0001t0065 | 1 | HG03017.hp2 | 5_prime_UTR_variant | MODIFIER | c.-403C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 1/14 | 403 | chr10 | 28533177 | ||||||
| chr10:28533178 | G | A | 1 | a0001c0001t0065 | 1 | HG03017.hp2 | 5_prime_UTR_variant | MODIFIER | c.-402G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 1/14 | 402 | chr10 | 28533178 | ||||||
| chr10:28533270 | A | G | 1 | a0001c0001t0064 | 1 | HG02129.hp1 | 5_prime_UTR_variant | MODIFIER | c.-310A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 1/14 | 310 | chr10 | 28533270 | ||||||
| chr10:28533287 | C | T | 1 | a0001c0001t0019 | 3 | HG02723.hp1 HG03471.hp1 HG03486.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-293C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 1/14 | chr10 | 28533287 | |||||||
| chr10:28619710 | T | G | 3 | a0001c0001t0011 a0001c0001t0029 a0001c0001t0030 |
8 | HG02083.hp1 HG02129.hp2 HG02132.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*104T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 104 | chr10 | 28619710 | ||||||
| chr10:28619734 | C | T | 1 | a0001c0001t0062 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*128C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 128 | chr10 | 28619734 | ||||||
| chr10:28619773 | T | C | 1 | a0001c0001t0014 | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*167T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 167 | chr10 | 28619773 | ||||||
| chr10:28619813 | G | T | 1 | a0001c0001t0061 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*207G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 207 | chr10 | 28619813 | ||||||
| chr10:28619960 | T | A | 7 | a0001c0001t0016 a0001c0001t0017 a0001c0001t0031 others(4): Show |
11 | HG00438.hp2 HG00639.hp1 HG01175.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*354T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 354 | chr10 | 28619960 | ||||||
| chr10:28619960 | TA | T | 15 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0014 others(12): Show |
45 | HG00099.hp2 HG00609.hp1 HG00621.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*373delA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 373 | INFO_REALIGN_3_PRIME | chr10 | 28619960 | |||||
| chr10:28619960 | TAA | T | 10 | a0001c0001t0002 a0001c0001t0026 a0001c0001t0027 others(7): Show |
53 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*372_*373delAA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 372 | INFO_REALIGN_3_PRIME | chr10 | 28619960 | |||||
| chr10:28619960 | TAAA | T | 1 | a0001c0001t0012 | 6 | HG00323.hp2 HG01515.hp2 HG02132.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*371_*373delAAA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 371 | INFO_REALIGN_3_PRIME | chr10 | 28619960 | |||||
| chr10:28619961 | A | T | 1 | a0001c0001t0001 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*355A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 355 | chr10 | 28619961 | ||||||
| chr10:28620043 | C | T | 1 | a0001c0001t0056 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*437C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 437 | chr10 | 28620043 | ||||||
| chr10:28620347 | T | G | 1 | a0001c0001t0036 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*741T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 741 | chr10 | 28620347 | ||||||
| chr10:28620370 | GT | G | 61 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(58): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*766delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 766 | INFO_REALIGN_3_PRIME | chr10 | 28620370 | |||||
| chr10:28620454 | T | A | 1 | a0001c0001t0036 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*848T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 848 | chr10 | 28620454 | ||||||
| chr10:28620598 | G | A | 1 | a0001c0001t0057 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*992G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 992 | chr10 | 28620598 | ||||||
| chr10:28620676 | G | A | 3 | a0001c0001t0006 a0001c0001t0014 a0001c0001t0050 |
20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1070G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1070 | chr10 | 28620676 | ||||||
| chr10:28620716 | A | G | 1 | a0001c0001t0036 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1110A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1110 | chr10 | 28620716 | ||||||
| chr10:28620717 | G | A | 1 | a0001c0001t0036 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1111G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1111 | chr10 | 28620717 | ||||||
| chr10:28620748 | C | A | 1 | a0001c0001t0036 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1142C>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1142 | chr10 | 28620748 | ||||||
| chr10:28620750 | A | G | 1 | a0001c0001t0047 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1144A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1144 | chr10 | 28620750 | ||||||
| chr10:28620921 | A | G | 1 | a0001c0001t0046 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1315A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1315 | chr10 | 28620921 | ||||||
| chr10:28620996 | A | G | 1 | a0001c0001t0045 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1390A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1390 | chr10 | 28620996 | ||||||
| chr10:28620997 | T | A | 1 | a0001c0001t0048 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1391T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1391 | chr10 | 28620997 | ||||||
| chr10:28621090 | A | G | 5 | a0001c0001t0003 a0001c0001t0015 a0001c0001t0017 others(2): Show |
33 | HG00597.hp1 HG00597.hp2 HG01496.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1484A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1484 | chr10 | 28621090 | ||||||
| chr10:28621127 | T | A | 1 | a0001c0001t0045 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1521T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1521 | chr10 | 28621127 | ||||||
| chr10:28621154 | A | C | 1 | a0001c0001t0045 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1548A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1548 | chr10 | 28621154 | ||||||
| chr10:28621163 | TTTC | T | 3 | a0001c0001t0022 a0001c0001t0053 a0001c0002t0009 |
12 | HG00673.hp2 HG00735.hp2 HG02055.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1572_*1574delCTT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1572 | INFO_REALIGN_3_PRIME | chr10 | 28621163 | |||||
| chr10:28621166 | C | T | 62 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(59): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
3_prime_UTR_variant | MODIFIER | c.*1560C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1560 | chr10 | 28621166 | ||||||
| chr10:28621169 | C | T | 3 | a0001c0001t0022 a0001c0001t0053 a0001c0002t0009 |
12 | HG00673.hp2 HG00735.hp2 HG02055.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1563C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1563 | chr10 | 28621169 | ||||||
| chr10:28621178 | C | CT | 9 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0026 others(6): Show |
51 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1580dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1581 | INFO_REALIGN_3_PRIME | chr10 | 28621178 | |||||
| chr10:28621181 | T | C | 1 | a0001c0001t0037 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1575T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1575 | chr10 | 28621181 | ||||||
| chr10:28621186 | TC | T | 5 | a0001c0001t0021 a0001c0001t0042 a0001c0001t0043 others(2): Show |
5 | HG01069.hp1 HG01168.hp2 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1581delC | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1581 | chr10 | 28621186 | ||||||
| chr10:28621187 | C | T | 57 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(54): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
3_prime_UTR_variant | MODIFIER | c.*1581C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1581 | chr10 | 28621187 | ||||||
| chr10:28621215 | A | AT | 4 | a0001c0001t0008 a0001c0001t0048 a0001c0001t0055 others(1): Show |
12 | HG00733.hp1 HG01123.hp2 HG02004.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1629dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1630 | INFO_REALIGN_3_PRIME | chr10 | 28621215 | |||||
| chr10:28621215 | AT | A | 25 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(22): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*1629delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1629 | INFO_REALIGN_3_PRIME | chr10 | 28621215 | |||||
| chr10:28621215 | ATT | A | 26 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(23): Show |
129 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*1628_*1629delTT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1628 | INFO_REALIGN_3_PRIME | chr10 | 28621215 | |||||
| chr10:28621268 | C | T | 1 | a0001c0001t0014 | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1662C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1662 | chr10 | 28621268 | ||||||
| chr10:28621270 | G | A | 1 | a0001c0001t0036 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1664G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1664 | chr10 | 28621270 | ||||||
| chr10:28621320 | T | C | 1 | a0001c0001t0045 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1714T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1714 | chr10 | 28621320 | ||||||
| chr10:28621379 | T | A | 1 | a0001c0001t0058 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1773T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1773 | chr10 | 28621379 | ||||||
| chr10:28621443 | G | T | 11 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0026 others(8): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1837G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1837 | chr10 | 28621443 | ||||||
| chr10:28621568 | GT | G | 2 | a0001c0002t0009 a0001c0002t0038 |
10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1965delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1965 | INFO_REALIGN_3_PRIME | chr10 | 28621568 | |||||
| chr10:28621570 | T | C | 2 | a0001c0002t0009 a0001c0002t0038 |
10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1964T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1964 | chr10 | 28621570 | ||||||
| chr10:28621575 | C | A | 2 | a0001c0002t0009 a0001c0002t0038 |
10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1969C>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1969 | chr10 | 28621575 | ||||||
| chr10:28621594 | A | G | 1 | a0001c0001t0065 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1988A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1988 | chr10 | 28621594 | ||||||
| chr10:28621786 | C | T | 46 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(43): Show |
206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*2180C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2180 | chr10 | 28621786 | ||||||
| chr10:28621789 | T | A | 1 | a0001c0001t0036 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2183T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2183 | chr10 | 28621789 | ||||||
| chr10:28621995 | G | A | 61 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(58): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*2389G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2389 | chr10 | 28621995 | ||||||
| chr10:28622050 | T | C | 46 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(43): Show |
206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*2444T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2444 | chr10 | 28622050 | ||||||
| chr10:28622208 | A | G | 1 | a0001c0001t0032 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2602A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2602 | chr10 | 28622208 | ||||||
| chr10:28622374 | T | C | 26 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0011 others(23): Show |
122 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*2768T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2768 | chr10 | 28622374 | ||||||
| chr10:28622425 | G | GC | 17 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(14): Show |
32 | HG00140.hp1 HG00621.hp2 HG01069.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2838dupC | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2839 | INFO_REALIGN_3_PRIME | chr10 | 28622425 | |||||
| chr10:28622425 | G | GCC | 19 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(16): Show |
48 | HG00140.hp2 HG00558.hp1 HG00673.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*2837_*2838dupCC | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2839 | INFO_REALIGN_3_PRIME | chr10 | 28622425 | |||||
| chr10:28622425 | G | GCCC | 16 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(13): Show |
34 | HG00621.hp1 HG00673.hp1 HG00741.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2836_*2838dupCCC | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2839 | INFO_REALIGN_3_PRIME | chr10 | 28622425 | |||||
| chr10:28622425 | G | GCCCC | 15 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(12): Show |
18 | HG00099.hp2 HG00609.hp1 HG01106.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2835_*2838dupCCCC | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2839 | INFO_REALIGN_3_PRIME | chr10 | 28622425 | |||||
| chr10:28622425 | G | GCCCCC | 10 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(7): Show |
20 | HG00735.hp1 HG00738.hp1 HG00741.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2834_*2838dupCCCC others(1): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2839 | INFO_REALIGN_3_PRIME | chr10 | 28622425 | |||||
| chr10:28622425 | G | GCCCCCCC others(5): Show |
1 | a0001c0001t0002 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2827_*2838dupCCCC others(8): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2839 | INFO_REALIGN_3_PRIME | chr10 | 28622425 | |||||
| chr10:28622425 | G | GGCCCCCC others(3): Show |
1 | a0001c0001t0002 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2819_*2820insGCCC others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2820 | chr10 | 28622425 | ||||||
| chr10:28622425 | GC | G | 17 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(14): Show |
43 | HG00438.hp2 HG00558.hp2 HG00642.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*2838delC | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2838 | INFO_REALIGN_3_PRIME | chr10 | 28622425 | |||||
| chr10:28622425 | GCC | G | 13 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(10): Show |
30 | HG00609.hp2 HG00639.hp2 HG00642.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2837_*2838delCC | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2837 | INFO_REALIGN_3_PRIME | chr10 | 28622425 | |||||
| chr10:28622425 | GCCC | G | 13 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(10): Show |
15 | HG00735.hp2 HG01123.hp2 HG01891.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2836_*2838delCCC | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2836 | INFO_REALIGN_3_PRIME | chr10 | 28622425 | |||||
| chr10:28622425 | GCCCCCCC others(4): Show |
G | 3 | a0001c0004t0001 a0001c0004t0021 a0001c0004t0041 |
3 | HG01069.hp1 HG02055.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2828_*2838delCCCC others(7): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2828 | INFO_REALIGN_3_PRIME | chr10 | 28622425 | |||||
| chr10:28622437 | C | T | 1 | a0001c0001t0064 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2831C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2831 | chr10 | 28622437 | ||||||
| chr10:28622442 | C | G | 1 | a0001c0001t0047 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2836C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2836 | chr10 | 28622442 | ||||||
| chr10:28622444 | C | G | 2 | a0001c0001t0036 a0001c0004t0041 |
2 | HG06807.hp2 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2838C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2838 | chr10 | 28622444 | ||||||
| chr10:28622445 | G | T | 1 | a0001c0001t0036 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2839G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2839 | chr10 | 28622445 | ||||||
| chr10:28622462 | GTC | G | 1 | a0001c0001t0018 | 3 | HG02717.hp2 HG03130.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2860_*2861delCT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2860 | INFO_REALIGN_3_PRIME | chr10 | 28622462 | |||||
| chr10:28622539 | G | T | 1 | a0001c0001t0040 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2933G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2933 | chr10 | 28622539 | ||||||
| chr10:28622564 | T | A | 1 | a0001c0001t0036 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2958T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2958 | chr10 | 28622564 | ||||||
| chr10:28622566 | T | C | 1 | a0001c0001t0062 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2960T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2960 | chr10 | 28622566 | ||||||
| chr10:28622693 | T | C | 1 | a0001c0001t0059 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3087T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 3087 | chr10 | 28622693 | ||||||
| chr10:28622793 | A | G | 1 | a0001c0001t0054 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3187A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 3187 | chr10 | 28622793 | ||||||
| chr10:28622909 | A | G | 1 | a0001c0001t0039 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3303A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 3303 | chr10 | 28622909 | ||||||
| chr10:28622968 | A | G | 1 | a0001c0001t0027 | 2 | NA18978.hp2 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3362A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 3362 | chr10 | 28622968 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:28533630 | C | T | 1 | a0001c0001t0003g0320 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.41+10C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 1/13 | chr10 | 28533630 | |||||||
| chr10:28533659 | G | GGGCGGC | 8 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(5): Show |
8 | HG00735.hp2 HG02055.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.41+45_41+50dupCGGC others(2): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 28533659 | ||||||
| chr10:28533777 | G | T | 1 | a0001c0001t0001g0319 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.41+157G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 1/13 | chr10 | 28533777 | |||||||
| chr10:28533812 | C | T | 1 | a0001c0001t0005g0318 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.42-186C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 1/13 | chr10 | 28533812 | |||||||
| chr10:28533840 | C | T | 1 | a0001c0001t0012g0317 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.42-158C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 1/13 | chr10 | 28533840 | |||||||
| chr10:28533924 | G | A | 1 | a0001c0001t0005g0318 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.42-74G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 1/13 | chr10 | 28533924 | |||||||
| chr10:28533978 | C | T | 4 | a0001c0001t0002g0313 a0001c0001t0002g0314 a0001c0001t0002g0315 others(1): Show |
4 | NA18967.hp1 NA18998.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-20C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 1/13 | chr10 | 28533978 | |||||||
| chr10:28534053 | G | T | 3 | a0001c0001t0016g0310 a0001c0001t0016g0311 a0001c0001t0016g0312 |
3 | HG00639.hp1 HG01175.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.78+19G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534053 | |||||||
| chr10:28534057 | A | G | 2 | a0001c0001t0004g0309 a0001c0001t0010g0308 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.78+23A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534057 | |||||||
| chr10:28534197 | G | A | 59 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.78+163G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534197 | |||||||
| chr10:28534340 | A | T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.78+306A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534340 | |||||||
| chr10:28534343 | A | T | 1 | a0001c0001t0047g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.78+309A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534343 | |||||||
| chr10:28534409 | G | T | 15 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(12): Show |
16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.78+375G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534409 | |||||||
| chr10:28534452 | T | G | 1 | a0001c0001t0029g0066 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.78+418T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534452 | |||||||
| chr10:28534520 | C | T | 7 | a0001c0001t0010g0285 a0001c0001t0010g0287 a0001c0001t0010g0288 others(4): Show |
7 | HG00609.hp1 HG02451.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+486C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534520 | |||||||
| chr10:28534641 | A | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.78+607A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534641 | |||||||
| chr10:28534787 | T | A | 1 | a0001c0001t0001g0067 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.78+753T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534787 | |||||||
| chr10:28534835 | A | T | 1 | a0001c0001t0001g0284 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.79-727A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534835 | |||||||
| chr10:28534920 | A | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.79-642A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534920 | |||||||
| chr10:28534955 | G | C | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.79-607G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534955 | |||||||
| chr10:28535046 | A | T | 1 | a0001c0001t0004g0283 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.79-516A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28535046 | |||||||
| chr10:28535118 | GT | G | 187 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(184): Show |
188 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.79-427delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 28535118 | ||||||
| chr10:28535154 | T | C | 59 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.79-408T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28535154 | |||||||
| chr10:28535161 | GCTTA | G | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0005t0004g0220 |
3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.79-400_79-397delCT others(2): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28535161 | |||||||
| chr10:28535332 | TG | T | 5 | a0001c0001t0001g0069 a0001c0001t0014g0070 a0001c0001t0014g0254 others(2): Show |
5 | HG00639.hp2 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.79-227delG | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 28535332 | ||||||
| chr10:28535334 | G | GT | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0282 |
3 | HG01123.hp1 HG02559.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.79-228_79-227insT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28535334 | |||||||
| chr10:28535335 | G | T | 218 | a0001c0001t0001g0067 a0001c0001t0001g0072 a0001c0001t0001g0108 others(215): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.79-227G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28535335 | |||||||
| chr10:28535353 | G | A | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.79-209G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28535353 | |||||||
| chr10:28535461 | T | C | 1 | a0001c0001t0002g0013 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.79-101T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28535461 | |||||||
| chr10:28535484 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.79-78A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28535484 | |||||||
| chr10:28535887 | A | AT | 25 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0047 others(22): Show |
25 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.274+140dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28535887 | ||||||
| chr10:28536013 | G | A | 7 | a0001c0001t0010g0285 a0001c0001t0010g0287 a0001c0001t0010g0288 others(4): Show |
7 | HG00609.hp1 HG02451.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+256G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28536013 | |||||||
| chr10:28536086 | C | G | 59 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.274+329C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28536086 | |||||||
| chr10:28536243 | A | G | 1 | a0001c0001t0048g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.274+486A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28536243 | |||||||
| chr10:28536245 | TA | T | 280 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(277): Show |
281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.274+503delA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28536245 | ||||||
| chr10:28536279 | T | A | 1 | a0001c0001t0001g0072 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.274+522T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28536279 | |||||||
| chr10:28536313 | A | G | 4 | a0001c0001t0014g0070 a0001c0001t0014g0254 a0001c0001t0014g0255 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+556A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28536313 | |||||||
| chr10:28536382 | TTTCAGTT others(18): Show |
T | 1 | a0001c0001t0048g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.274+635_274+659del others(25): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28536382 | ||||||
| chr10:28536760 | C | T | 122 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(119): Show |
122 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.274+1003C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28536760 | |||||||
| chr10:28536956 | G | A | 19 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(16): Show |
20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.274+1199G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28536956 | |||||||
| chr10:28537340 | C | T | 1 | a0001c0001t0032g0106 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.274+1583C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28537340 | |||||||
| chr10:28537462 | C | G | 6 | a0001c0001t0004g0277 a0001c0001t0004g0278 a0001c0001t0004g0279 others(3): Show |
6 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.274+1705C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28537462 | |||||||
| chr10:28537499 | A | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+1742A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28537499 | |||||||
| chr10:28537630 | C | T | 1 | a0001c0001t0007g0216 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.274+1873C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28537630 | |||||||
| chr10:28537654 | A | T | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG00735.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.274+1897A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28537654 | |||||||
| chr10:28537901 | G | C | 1 | a0001c0001t0011g0107 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.274+2144G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28537901 | |||||||
| chr10:28537901 | G | T | 1 | a0001c0001t0001g0213 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.274+2144G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28537901 | |||||||
| chr10:28537919 | G | A | 1 | a0001c0001t0004g0257 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.274+2162G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28537919 | |||||||
| chr10:28537958 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.274+2201C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28537958 | |||||||
| chr10:28538022 | C | G | 15 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(12): Show |
16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.274+2265C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538022 | |||||||
| chr10:28538063 | T | G | 59 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.274+2306T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538063 | |||||||
| chr10:28538076 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.274+2319C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538076 | |||||||
| chr10:28538167 | A | T | 1 | a0001c0001t0001g0069 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.274+2410A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538167 | |||||||
| chr10:28538323 | C | T | 1 | a0001c0001t0047g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274+2566C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538323 | |||||||
| chr10:28538324 | G | A | 1 | a0001c0001t0045g0280 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.274+2567G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538324 | |||||||
| chr10:28538407 | C | G | 7 | a0001c0001t0010g0285 a0001c0001t0010g0287 a0001c0001t0010g0288 others(4): Show |
7 | HG00609.hp1 HG02451.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+2650C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538407 | |||||||
| chr10:28538538 | T | C | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+2781T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538538 | |||||||
| chr10:28538581 | C | CA | 56 | a0001c0001t0001g0281 a0001c0001t0002g0011 a0001c0001t0002g0013 others(53): Show |
56 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.274+2844dupA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28538581 | ||||||
| chr10:28538581 | CA | C | 209 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(206): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.274+2844delA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28538581 | ||||||
| chr10:28538663 | G | A | 1 | a0001c0001t0002g0313 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.274+2906G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538663 | |||||||
| chr10:28538695 | G | T | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0005t0004g0220 |
3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.274+2938G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538695 | |||||||
| chr10:28538810 | G | A | 2 | a0001c0001t0002g0047 a0001c0001t0012g0048 |
2 | HG00099.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.274+3053G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538810 | |||||||
| chr10:28538866 | T | TA | 17 | a0001c0001t0002g0014 a0001c0001t0006g0002 a0001c0001t0006g0292 others(14): Show |
18 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.274+3127dupA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28538866 | ||||||
| chr10:28538866 | TA | T | 199 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.274+3127delA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28538866 | ||||||
| chr10:28538866 | TAA | T | 7 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0004g0309 others(4): Show |
7 | HG01167.hp1 HG01943.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+3126_274+3127d others(4): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28538866 | ||||||
| chr10:28538914 | C | T | 63 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(60): Show |
63 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.274+3157C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538914 | |||||||
| chr10:28538958 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.274+3201C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538958 | |||||||
| chr10:28539014 | A | G | 1 | a0001c0001t0002g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.274+3257A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539014 | |||||||
| chr10:28539055 | G | T | 58 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(55): Show |
58 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.274+3298G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539055 | |||||||
| chr10:28539145 | C | T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+3388C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539145 | |||||||
| chr10:28539173 | A | G | 1 | a0001c0001t0048g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.274+3416A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539173 | |||||||
| chr10:28539216 | C | T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+3459C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539216 | |||||||
| chr10:28539308 | C | T | 1 | a0001c0001t0011g0207 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.274+3551C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539308 | |||||||
| chr10:28539352 | G | C | 1 | a0001c0001t0003g0076 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.274+3595G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539352 | |||||||
| chr10:28539398 | G | T | 1 | a0001c0001t0001g0067 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.274+3641G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539398 | |||||||
| chr10:28539425 | A | G | 1 | a0001c0001t0047g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274+3668A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539425 | |||||||
| chr10:28539553 | C | T | 15 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(12): Show |
16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.274+3796C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539553 | |||||||
| chr10:28539554 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.274+3797G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539554 | |||||||
| chr10:28539571 | G | T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+3814G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539571 | |||||||
| chr10:28539572 | GT | G | 284 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(281): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.274+3826delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28539572 | ||||||
| chr10:28539597 | T | C | 295 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(292): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.274+3840T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539597 | |||||||
| chr10:28539838 | C | T | 62 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(59): Show |
62 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.274+4081C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539838 | |||||||
| chr10:28540003 | T | A | 1 | a0001c0001t0002g0049 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.274+4246T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28540003 | |||||||
| chr10:28540178 | T | G | 1 | a0001c0001t0001g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.274+4421T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28540178 | |||||||
| chr10:28540330 | A | T | 2 | a0001c0001t0004g0279 a0001c0001t0042g0275 |
2 | HG01168.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.274+4573A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28540330 | |||||||
| chr10:28540602 | A | C | 1 | a0001c0001t0004g0274 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.274+4845A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28540602 | |||||||
| chr10:28540608 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.274+4851G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28540608 | |||||||
| chr10:28540669 | G | A | 1 | a0001c0001t0004g0283 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.274+4912G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28540669 | |||||||
| chr10:28540870 | CTTCA | C | 3 | a0001c0001t0006g0002 a0001c0001t0006g0304 a0001c0001t0006g0305 |
4 | HG01106.hp2 HG01884.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+5116_274+5119d others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28540870 | ||||||
| chr10:28541106 | A | C | 15 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(12): Show |
16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.274+5349A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541106 | |||||||
| chr10:28541179 | T | C | 68 | a0001c0001t0003g0073 a0001c0001t0003g0076 a0001c0001t0003g0079 others(65): Show |
68 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.274+5422T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541179 | |||||||
| chr10:28541368 | A | G | 2 | a0001c0001t0004g0279 a0001c0001t0042g0275 |
2 | HG01168.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.274+5611A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541368 | |||||||
| chr10:28541404 | T | G | 121 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(118): Show |
121 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.274+5647T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541404 | |||||||
| chr10:28541415 | G | GT | 6 | a0001c0001t0002g0013 a0001c0001t0002g0033 a0001c0001t0002g0037 others(3): Show |
6 | HG00609.hp2 HG01069.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.274+5662dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28541415 | ||||||
| chr10:28541415 | G | GTT | 26 | a0001c0001t0002g0015 a0001c0001t0002g0019 a0001c0001t0002g0021 others(23): Show |
26 | HG00323.hp2 HG00673.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.274+5661_274+5662d others(4): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28541415 | ||||||
| chr10:28541415 | G | GTTT | 14 | a0001c0001t0002g0014 a0001c0001t0002g0016 a0001c0001t0002g0018 others(11): Show |
14 | HG01167.hp2 HG01358.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.274+5660_274+5662d others(5): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28541415 | ||||||
| chr10:28541415 | G | GTTTT | 5 | a0001c0001t0002g0012 a0001c0001t0002g0026 a0001c0001t0002g0035 others(2): Show |
5 | HG00099.hp1 HG00280.hp1 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.274+5659_274+5662d others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28541415 | ||||||
| chr10:28541415 | G | GTTTTT | 7 | a0001c0001t0002g0011 a0001c0001t0002g0017 a0001c0001t0002g0059 others(4): Show |
7 | HG01109.hp2 HG01175.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.274+5662_274+5663i others(7): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28541415 | ||||||
| chr10:28541415 | GTTT | G | 4 | a0001c0001t0003g0083 a0001c0001t0004g0221 a0001c0001t0004g0222 others(1): Show |
4 | HG01891.hp2 NA18971.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+5660_274+5662d others(5): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28541415 | ||||||
| chr10:28541415 | GTTTTGTT others(2): Show |
G | 7 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
7 | HG02055.hp1 NA18969.hp1 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+5663_274+5671d others(11): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28541415 | ||||||
| chr10:28541415 | GTTTTGTT others(10): Show |
G | 1 | a0001c0001t0012g0063 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.274+5663_274+5679d others(19): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28541415 | ||||||
| chr10:28541416 | T | TG | 12 | a0001c0001t0001g0119 a0001c0001t0001g0128 a0001c0001t0001g0129 others(9): Show |
12 | HG00642.hp1 HG01934.hp2 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.274+5659_274+5660i others(3): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541416 | |||||||
| chr10:28541417 | T | G | 166 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(163): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.274+5660T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541417 | |||||||
| chr10:28541417 | TTTG | T | 6 | a0001c0001t0014g0255 a0001c0002t0009g0003 a0001c0002t0009g0004 others(3): Show |
6 | HG02145.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.274+5663_274+5665d others(5): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28541417 | ||||||
| chr10:28541418 | T | G | 5 | a0001c0001t0001g0155 a0001c0001t0003g0081 a0001c0001t0004g0257 others(2): Show |
5 | HG00738.hp1 HG01934.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.274+5661T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541418 | |||||||
| chr10:28541418 | TTG | T | 29 | a0001c0001t0001g0120 a0001c0001t0001g0133 a0001c0001t0001g0136 others(26): Show |
29 | HG00140.hp1 HG00673.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.274+5663_274+5664d others(4): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28541418 | ||||||
| chr10:28541419 | T | G | 3 | a0001c0001t0017g0077 a0001c0001t0017g0078 a0001c0001t0017g0105 |
3 | HG01496.hp1 HG01928.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.274+5662T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541419 | |||||||
| chr10:28541419 | TG | T | 102 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(99): Show |
103 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.274+5663delG | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541419 | |||||||
| chr10:28541420 | G | GT | 8 | a0001c0001t0005g0224 a0001c0001t0005g0235 a0001c0001t0005g0252 others(5): Show |
8 | HG00438.hp2 HG00621.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.274+5689dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28541420 | ||||||
| chr10:28541420 | G | T | 129 | a0001c0001t0001g0108 a0001c0001t0001g0119 a0001c0001t0001g0128 others(126): Show |
129 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.274+5663G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541420 | |||||||
| chr10:28541426 | T | G | 7 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
7 | HG02055.hp1 NA18969.hp1 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+5669T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541426 | |||||||
| chr10:28541432 | T | G | 1 | a0001c0001t0048g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.274+5675T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541432 | |||||||
| chr10:28541436 | T | G | 1 | a0001c0001t0048g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.274+5679T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541436 | |||||||
| chr10:28541461 | C | G | 1 | a0001c0001t0053g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.274+5704C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541461 | |||||||
| chr10:28541501 | A | G | 59 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.274+5744A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541501 | |||||||
| chr10:28541609 | T | C | 1 | a0001c0001t0001g0164 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.274+5852T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541609 | |||||||
| chr10:28541615 | A | G | 1 | a0001c0001t0004g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.274+5858A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541615 | |||||||
| chr10:28541861 | G | T | 15 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(12): Show |
16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.274+6104G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541861 | |||||||
| chr10:28541928 | C | G | 2 | a0001c0001t0003g0091 a0001c0001t0003g0102 |
2 | NA18959.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.274+6171C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541928 | |||||||
| chr10:28541969 | C | T | 10 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(7): Show |
10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.274+6212C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541969 | |||||||
| chr10:28542071 | T | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+6314T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28542071 | |||||||
| chr10:28542112 | T | A | 3 | a0001c0001t0003g0079 a0001c0001t0003g0080 a0001c0001t0003g0259 |
3 | HG00597.hp2 HG02056.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.274+6355T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28542112 | |||||||
| chr10:28542137 | A | G | 1 | a0001c0001t0013g0205 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.274+6380A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28542137 | |||||||
| chr10:28542173 | C | T | 59 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.274+6416C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28542173 | |||||||
| chr10:28542251 | A | T | 1 | a0001c0001t0003g0320 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.274+6494A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28542251 | |||||||
| chr10:28542317 | T | G | 19 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(16): Show |
20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.274+6560T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28542317 | |||||||
| chr10:28542536 | C | T | 1 | a0001c0001t0013g0204 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.274+6779C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28542536 | |||||||
| chr10:28542635 | T | C | 3 | a0001c0001t0004g0265 a0001c0001t0037g0260 a0001c0001t0056g0266 |
3 | HG01256.hp2 HG01361.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.274+6878T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28542635 | |||||||
| chr10:28542640 | C | T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+6883C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28542640 | |||||||
| chr10:28543161 | C | T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+7404C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543161 | |||||||
| chr10:28543182 | G | C | 4 | a0001c0001t0001g0108 a0001c0001t0001g0128 a0001c0001t0001g0129 others(1): Show |
4 | HG01358.hp2 HG01928.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+7425G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543182 | |||||||
| chr10:28543264 | A | G | 1 | a0001c0001t0007g0203 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.274+7507A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543264 | |||||||
| chr10:28543322 | AT | A | 59 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.274+7569delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28543322 | ||||||
| chr10:28543404 | T | G | 1 | a0001c0001t0007g0131 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.274+7647T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543404 | |||||||
| chr10:28543437 | A | G | 15 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(12): Show |
16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.274+7680A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543437 | |||||||
| chr10:28543632 | A | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+7875A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543632 | |||||||
| chr10:28543648 | A | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+7891A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543648 | |||||||
| chr10:28543709 | C | T | 4 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(1): Show |
4 | HG02155.hp2 NA18967.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+7952C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543709 | |||||||
| chr10:28543783 | A | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+8026A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543783 | |||||||
| chr10:28543813 | C | T | 8 | a0001c0001t0001g0118 a0001c0001t0001g0196 a0001c0001t0001g0197 others(5): Show |
8 | HG01192.hp1 HG01243.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+8056C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543813 | |||||||
| chr10:28543872 | G | GT | 32 | a0001c0001t0004g0257 a0001c0001t0004g0258 a0001c0001t0004g0261 others(29): Show |
32 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.274+8121dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28543872 | ||||||
| chr10:28543891 | G | C | 67 | a0001c0001t0003g0076 a0001c0001t0003g0079 a0001c0001t0003g0080 others(64): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.274+8134G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543891 | |||||||
| chr10:28543965 | C | T | 10 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(7): Show |
10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.274+8208C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543965 | |||||||
| chr10:28543969 | A | G | 1 | a0001c0001t0001g0195 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.274+8212A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543969 | |||||||
| chr10:28544013 | G | T | 10 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(7): Show |
10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.274+8256G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28544013 | |||||||
| chr10:28544089 | G | T | 4 | a0002c0003t0008g0068 a0002c0003t0008g0223 a0002c0003t0008g0231 others(1): Show |
4 | HG01123.hp2 HG02723.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.274+8332G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28544089 | |||||||
| chr10:28544187 | C | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+8430C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28544187 | |||||||
| chr10:28544229 | T | C | 34 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(31): Show |
34 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.274+8472T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28544229 | |||||||
| chr10:28544248 | C | T | 7 | a0001c0001t0010g0285 a0001c0001t0010g0287 a0001c0001t0010g0288 others(4): Show |
7 | HG00609.hp1 HG02451.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+8491C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28544248 | |||||||
| chr10:28544254 | G | T | 8 | a0001c0001t0001g0119 a0001c0001t0001g0161 a0001c0001t0001g0194 others(5): Show |
8 | HG00642.hp1 HG02109.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+8497G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28544254 | |||||||
| chr10:28544471 | C | T | 1 | a0001c0001t0048g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.274+8714C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28544471 | |||||||
| chr10:28544965 | C | T | 10 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(7): Show |
10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.274+9208C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28544965 | |||||||
| chr10:28545040 | CA | C | 93 | a0001c0001t0001g0164 a0001c0001t0002g0011 a0001c0001t0002g0012 others(90): Show |
93 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.274+9303delA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28545040 | ||||||
| chr10:28545040 | CAA | C | 31 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(28): Show |
32 | HG00735.hp2 HG01099.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.274+9302_274+9303d others(4): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28545040 | ||||||
| chr10:28545040 | CAAA | C | 118 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(115): Show |
118 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.274+9301_274+9303d others(5): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28545040 | ||||||
| chr10:28545049 | A | C | 1 | a0001c0001t0013g0160 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.274+9292A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28545049 | |||||||
| chr10:28545266 | C | T | 2 | a0001c0001t0005g0250 a0001c0001t0025g0249 |
2 | NA18612.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.274+9509C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28545266 | |||||||
| chr10:28545324 | C | T | 1 | a0001c0001t0002g0038 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.274+9567C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28545324 | |||||||
| chr10:28545580 | C | T | 1 | a0001c0001t0012g0063 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.274+9823C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28545580 | |||||||
| chr10:28545611 | T | A | 1 | a0001c0001t0002g0011 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.274+9854T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28545611 | |||||||
| chr10:28545759 | A | G | 4 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(1): Show |
4 | HG02155.hp2 NA18967.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+10002A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28545759 | |||||||
| chr10:28545874 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.274+10117C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28545874 | |||||||
| chr10:28545999 | C | G | 3 | a0001c0001t0006g0002 a0001c0001t0006g0304 a0001c0001t0006g0305 |
4 | HG01106.hp2 HG01884.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+10242C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28545999 | |||||||
| chr10:28546172 | G | A | 1 | a0001c0001t0006g0293 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.274+10415G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28546172 | |||||||
| chr10:28546344 | G | A | 2 | a0001c0001t0004g0309 a0001c0001t0010g0308 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.274+10587G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28546344 | |||||||
| chr10:28546534 | G | A | 285 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.274+10777G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28546534 | |||||||
| chr10:28546670 | TTAAA | T | 3 | a0001c0001t0018g0190 a0001c0001t0018g0191 a0001c0001t0018g0192 |
3 | HG02717.hp2 HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.274+10919_274+1092 others(8): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28546670 | ||||||
| chr10:28546721 | C | T | 4 | a0001c0001t0014g0070 a0001c0001t0014g0254 a0001c0001t0014g0255 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+10964C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28546721 | |||||||
| chr10:28546867 | CT | C | 82 | a0001c0001t0001g0200 a0001c0001t0003g0076 a0001c0001t0003g0079 others(79): Show |
82 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.274+11122delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28546867 | ||||||
| chr10:28547158 | G | T | 203 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(200): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.274+11401G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547158 | |||||||
| chr10:28547185 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.274+11428T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547185 | |||||||
| chr10:28547245 | G | A | 20 | a0001c0001t0004g0222 a0001c0001t0006g0002 a0001c0001t0006g0292 others(17): Show |
21 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.274+11488G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547245 | |||||||
| chr10:28547302 | A | G | 81 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(78): Show |
82 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.274+11545A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547302 | |||||||
| chr10:28547326 | G | A | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+11569G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547326 | |||||||
| chr10:28547364 | G | A | 6 | a0001c0001t0001g0067 a0001c0001t0001g0110 a0001c0001t0001g0166 others(3): Show |
6 | HG01255.hp1 HG01257.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+11607G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547364 | |||||||
| chr10:28547436 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.274+11679G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547436 | |||||||
| chr10:28547541 | A | T | 10 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(7): Show |
10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.274+11784A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547541 | |||||||
| chr10:28547770 | C | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+12013C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547770 | |||||||
| chr10:28547780 | A | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+12023A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547780 | |||||||
| chr10:28547833 | T | C | 1 | a0001c0001t0002g0018 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.274+12076T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547833 | |||||||
| chr10:28547847 | C | CT | 10 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(7): Show |
10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.274+12096dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28547847 | ||||||
| chr10:28547854 | C | G | 10 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(7): Show |
10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.274+12097C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547854 | |||||||
| chr10:28547869 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.274+12112G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547869 | |||||||
| chr10:28547915 | C | CT | 182 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.274+12173dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28547915 | ||||||
| chr10:28547915 | CT | C | 11 | a0001c0001t0064g0307 a0001c0002t0009g0003 a0001c0002t0009g0004 others(8): Show |
11 | HG00735.hp2 HG02055.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.274+12173delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28547915 | ||||||
| chr10:28547918 | T | TC | 7 | a0001c0001t0011g0107 a0001c0001t0011g0134 a0001c0001t0011g0167 others(4): Show |
7 | HG02083.hp1 HG02129.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+12161_274+1216 others(5): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547918 | |||||||
| chr10:28547950 | C | T | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0005t0004g0220 |
3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.274+12193C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547950 | |||||||
| chr10:28547951 | G | A | 59 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.274+12194G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547951 | |||||||
| chr10:28547962 | T | C | 9 | a0001c0001t0001g0119 a0001c0001t0001g0161 a0001c0001t0001g0194 others(6): Show |
9 | HG00642.hp1 HG02109.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.274+12205T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547962 | |||||||
| chr10:28548014 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.274+12257G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28548014 | |||||||
| chr10:28548216 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.274+12459G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28548216 | |||||||
| chr10:28548248 | T | C | 1 | a0001c0001t0013g0160 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.274+12491T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28548248 | |||||||
| chr10:28548294 | G | A | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+12537G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28548294 | |||||||
| chr10:28548457 | C | G | 1 | a0001c0001t0001g0072 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.274+12700C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28548457 | |||||||
| chr10:28548567 | C | T | 15 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(12): Show |
16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.274+12810C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28548567 | |||||||
| chr10:28548682 | G | A | 285 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.274+12925G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28548682 | |||||||
| chr10:28548797 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.274+13040A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28548797 | |||||||
| chr10:28549038 | G | A | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+13281G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549038 | |||||||
| chr10:28549058 | C | G | 193 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(190): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.274+13301C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549058 | |||||||
| chr10:28549158 | CAA | C | 59 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.274+13403_274+1340 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28549158 | ||||||
| chr10:28549201 | G | C | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+13444G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549201 | |||||||
| chr10:28549273 | A | G | 1 | a0001c0001t0007g0159 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.274+13516A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549273 | |||||||
| chr10:28549389 | A | G | 1 | a0001c0001t0008g0230 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.274+13632A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549389 | |||||||
| chr10:28549404 | T | C | 1 | a0001c0001t0007g0171 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.274+13647T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549404 | |||||||
| chr10:28549506 | C | G | 1 | a0001c0001t0047g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274+13749C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549506 | |||||||
| chr10:28549520 | T | C | 4 | a0001c0001t0003g0081 a0001c0001t0017g0077 a0001c0001t0017g0078 others(1): Show |
4 | HG01496.hp1 HG01928.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+13763T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549520 | |||||||
| chr10:28549643 | T | C | 295 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(292): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.274+13886T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549643 | |||||||
| chr10:28549763 | T | C | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+14006T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549763 | |||||||
| chr10:28549890 | C | T | 1 | a0001c0001t0010g0290 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.274+14133C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549890 | |||||||
| chr10:28549891 | G | A | 1 | a0001c0001t0005g0251 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.274+14134G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549891 | |||||||
| chr10:28549938 | A | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+14181A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549938 | |||||||
| chr10:28550110 | G | A | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+14353G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28550110 | |||||||
| chr10:28550123 | C | G | 7 | a0001c0001t0010g0285 a0001c0001t0010g0287 a0001c0001t0010g0288 others(4): Show |
7 | HG00609.hp1 HG02451.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+14366C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28550123 | |||||||
| chr10:28550166 | C | CA | 224 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0108 others(221): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.274+14423dupA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28550166 | ||||||
| chr10:28550291 | C | CT | 20 | a0001c0001t0004g0221 a0001c0001t0004g0257 a0001c0001t0004g0258 others(17): Show |
20 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.274+14546dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28550291 | ||||||
| chr10:28550343 | T | C | 1 | a0001c0001t0002g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.274+14586T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28550343 | |||||||
| chr10:28550550 | G | A | 4 | a0001c0001t0014g0070 a0001c0001t0014g0254 a0001c0001t0014g0255 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+14793G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28550550 | |||||||
| chr10:28550597 | T | C | 22 | a0001c0001t0003g0073 a0001c0001t0003g0079 a0001c0001t0003g0080 others(19): Show |
22 | HG00597.hp1 HG00597.hp2 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.274+14840T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28550597 | |||||||
| chr10:28550768 | T | C | 7 | a0001c0001t0010g0285 a0001c0001t0010g0287 a0001c0001t0010g0288 others(4): Show |
7 | HG00609.hp1 HG02451.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+15011T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28550768 | |||||||
| chr10:28550901 | G | A | 2 | a0001c0001t0005g0224 a0001c0001t0005g0233 |
2 | HG02738.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.274+15144G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28550901 | |||||||
| chr10:28551124 | T | G | 203 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(200): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.274+15367T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551124 | |||||||
| chr10:28551185 | A | C | 193 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(190): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.274+15428A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551185 | |||||||
| chr10:28551195 | C | T | 18 | a0001c0001t0004g0257 a0001c0001t0004g0258 a0001c0001t0004g0261 others(15): Show |
18 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.274+15438C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551195 | |||||||
| chr10:28551459 | G | T | 3 | a0001c0001t0004g0265 a0001c0001t0037g0260 a0001c0001t0056g0266 |
3 | HG01256.hp2 HG01361.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.274+15702G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551459 | |||||||
| chr10:28551586 | A | G | 1 | a0001c0001t0053g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.274+15829A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551586 | |||||||
| chr10:28551784 | T | TTG | 8 | a0001c0001t0001g0194 a0001c0001t0004g0222 a0001c0001t0005g0235 others(5): Show |
8 | HG00733.hp1 HG01361.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+16061_274+1606 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28551784 | ||||||
| chr10:28551784 | T | TTGTG | 33 | a0001c0001t0001g0116 a0001c0001t0001g0119 a0001c0001t0001g0155 others(30): Show |
33 | HG00140.hp1 HG00642.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.274+16059_274+1606 others(8): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28551784 | ||||||
| chr10:28551784 | T | TTGTGTG | 28 | a0001c0001t0001g0133 a0001c0001t0001g0138 a0001c0001t0003g0080 others(25): Show |
28 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.274+16057_274+1606 others(10): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28551784 | ||||||
| chr10:28551784 | T | TTGTGTGT others(1): Show |
39 | a0001c0001t0001g0069 a0001c0001t0001g0118 a0001c0001t0001g0121 others(36): Show |
39 | HG00323.hp1 HG00597.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.274+16055_274+1606 others(12): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28551784 | ||||||
| chr10:28551784 | T | TTGTGTGT others(3): Show |
49 | a0001c0001t0001g0067 a0001c0001t0001g0108 a0001c0001t0001g0110 others(46): Show |
49 | HG00140.hp2 HG00558.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.274+16053_274+1606 others(14): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28551784 | ||||||
| chr10:28551784 | T | TTGTGTGT others(5): Show |
19 | a0001c0001t0001g0128 a0001c0001t0001g0140 a0001c0001t0001g0141 others(16): Show |
19 | HG00438.hp1 HG01099.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.274+16051_274+1606 others(16): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28551784 | ||||||
| chr10:28551784 | T | TTGTGTGT others(7): Show |
12 | a0001c0001t0001g0072 a0001c0001t0007g0171 a0001c0001t0010g0285 others(9): Show |
12 | HG00609.hp1 HG00639.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.274+16049_274+1606 others(18): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28551784 | ||||||
| chr10:28551784 | T | TTGTGTGT others(9): Show |
2 | a0001c0001t0001g0172 a0001c0001t0013g0160 |
2 | NA18940.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.274+16047_274+1606 others(20): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28551784 | ||||||
| chr10:28551784 | TTGTGTG | T | 53 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(50): Show |
53 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.274+16057_274+1606 others(10): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28551784 | ||||||
| chr10:28551784 | TTGTGTGT others(1): Show |
T | 3 | a0001c0001t0002g0018 a0001c0001t0002g0037 a0001c0001t0034g0273 |
3 | HG00609.hp2 HG03098.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.274+16055_274+1606 others(12): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28551784 | ||||||
| chr10:28551784 | TTGTGTGT others(9): Show |
T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+16047_274+1606 others(20): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28551784 | ||||||
| chr10:28551813 | TGTGTG | T | 4 | a0001c0001t0002g0017 a0001c0001t0002g0040 a0001c0001t0002g0050 others(1): Show |
4 | HG00621.hp1 HG04115.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.274+16057_274+1606 others(9): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551813 | |||||||
| chr10:28551816 | G | T | 13 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(10): Show |
14 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.274+16059G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551816 | |||||||
| chr10:28551818 | G | C | 13 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(10): Show |
14 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.274+16061G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551818 | |||||||
| chr10:28551818 | G | T | 5 | a0001c0001t0014g0070 a0001c0001t0014g0254 a0001c0001t0014g0255 others(2): Show |
5 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.274+16061G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551818 | |||||||
| chr10:28551819 | T | TC | 4 | a0001c0001t0014g0070 a0001c0001t0014g0254 a0001c0001t0014g0255 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+16062_274+1606 others(5): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551819 | |||||||
| chr10:28551819 | T | TGTGTGTG others(4): Show |
3 | a0001c0001t0001g0139 a0001c0001t0004g0258 a0001c0001t0061g0291 |
3 | HG03704.hp1 HG03704.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.274+16062_274+1606 others(15): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551819 | |||||||
| chr10:28551819 | T | TGTGTGTG others(6): Show |
2 | a0001c0001t0003g0092 a0001c0001t0047g0306 |
2 | HG03041.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.274+16062_274+1606 others(17): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551819 | |||||||
| chr10:28551820 | T | C | 1 | a0001c0001t0050g0294 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.274+16063T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551820 | |||||||
| chr10:28551820 | TTC | T | 13 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(10): Show |
14 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.274+16065_274+1606 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28551820 | ||||||
| chr10:28551821 | T | C | 5 | a0001c0001t0002g0017 a0001c0001t0002g0040 a0001c0001t0002g0050 others(2): Show |
5 | HG00621.hp1 HG02965.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.274+16064T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551821 | |||||||
| chr10:28551822 | C | T | 16 | a0001c0001t0001g0139 a0001c0001t0001g0158 a0001c0001t0002g0017 others(13): Show |
16 | HG00621.hp1 HG02109.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.274+16065C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551822 | |||||||
| chr10:28551823 | T | C | 6 | a0001c0001t0001g0139 a0001c0001t0001g0158 a0001c0001t0023g0189 others(3): Show |
6 | HG03041.hp1 HG03704.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+16066T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551823 | |||||||
| chr10:28551974 | G | A | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+16217G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551974 | |||||||
| chr10:28552285 | G | A | 285 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.274+16528G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28552285 | |||||||
| chr10:28552364 | G | C | 1 | a0001c0001t0018g0190 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.274+16607G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28552364 | |||||||
| chr10:28552550 | T | C | 1 | a0001c0001t0004g0257 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.274+16793T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28552550 | |||||||
| chr10:28552560 | A | G | 1 | a0001c0001t0004g0257 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.274+16803A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28552560 | |||||||
| chr10:28552629 | T | C | 1 | a0001c0001t0015g0101 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.274+16872T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28552629 | |||||||
| chr10:28552730 | C | T | 1 | a0001c0001t0008g0248 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.274+16973C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28552730 | |||||||
| chr10:28552822 | CAGTG | C | 114 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(111): Show |
114 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.274+17068_274+1707 others(8): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28552822 | ||||||
| chr10:28552823 | A | G | 15 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(12): Show |
16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.274+17066A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28552823 | |||||||
| chr10:28552840 | G | A | 24 | a0001c0001t0004g0257 a0001c0001t0004g0258 a0001c0001t0004g0261 others(21): Show |
24 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(21): Show |
intron_variant | MODIFIER | c.274+17083G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28552840 | |||||||
| chr10:28552845 | C | CT | 26 | a0001c0001t0003g0087 a0001c0001t0005g0235 a0001c0001t0005g0246 others(23): Show |
27 | HG00609.hp1 HG00621.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.274+17111dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28552845 | ||||||
| chr10:28552845 | CT | C | 42 | a0001c0001t0001g0128 a0001c0001t0001g0138 a0001c0001t0001g0157 others(39): Show |
42 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.274+17111delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28552845 | ||||||
| chr10:28552845 | CTT | C | 151 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(148): Show |
151 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.274+17110_274+1711 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28552845 | ||||||
| chr10:28552845 | CTTT | C | 11 | a0001c0001t0001g0119 a0001c0001t0001g0161 a0001c0001t0002g0019 others(8): Show |
11 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.274+17109_274+1711 others(7): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28552845 | ||||||
| chr10:28552845 | CTTTTTTT others(4): Show |
C | 1 | a0001c0002t0009g0004 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.274+17101_274+1711 others(15): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28552845 | ||||||
| chr10:28552872 | T | G | 1 | a0001c0001t0001g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.274+17115T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28552872 | |||||||
| chr10:28552969 | A | G | 4 | a0001c0001t0014g0070 a0001c0001t0014g0254 a0001c0001t0014g0255 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+17212A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28552969 | |||||||
| chr10:28553103 | A | G | 124 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(121): Show |
124 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.274+17346A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28553103 | |||||||
| chr10:28553263 | A | ATAAT | 285 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.274+17507_274+1750 others(8): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28553263 | ||||||
| chr10:28553338 | T | C | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+17581T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28553338 | |||||||
| chr10:28553348 | C | G | 204 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(201): Show |
204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.274+17591C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28553348 | |||||||
| chr10:28553545 | C | T | 285 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.274+17788C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28553545 | |||||||
| chr10:28553706 | A | G | 1 | a0001c0002t0009g0103 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.274+17949A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28553706 | |||||||
| chr10:28553762 | A | G | 1 | a0001c0001t0005g0251 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.274+18005A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28553762 | |||||||
| chr10:28553765 | G | A | 1 | a0001c0001t0004g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.274+18008G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28553765 | |||||||
| chr10:28553789 | T | C | 1 | a0001c0001t0004g0258 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.274+18032T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28553789 | |||||||
| chr10:28553824 | G | A | 1 | a0001c0001t0065g0185 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.274+18067G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28553824 | |||||||
| chr10:28553853 | A | G | 1 | a0001c0001t0020g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.274+18096A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28553853 | |||||||
| chr10:28553914 | G | A | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0209 |
3 | HG02155.hp2 NA18967.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.274+18157G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28553914 | |||||||
| chr10:28554093 | C | T | 123 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(120): Show |
123 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.274+18336C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554093 | |||||||
| chr10:28554113 | C | T | 2 | a0001c0001t0007g0159 a0001c0001t0013g0205 |
2 | NA18994.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.274+18356C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554113 | |||||||
| chr10:28554194 | A | G | 1 | a0001c0001t0005g0244 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.274+18437A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554194 | |||||||
| chr10:28554430 | C | T | 4 | a0001c0001t0015g0099 a0001c0001t0015g0100 a0001c0001t0015g0101 others(1): Show |
4 | HG02040.hp1 NA18965.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+18673C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554430 | |||||||
| chr10:28554483 | A | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+18726A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554483 | |||||||
| chr10:28554532 | A | G | 1 | a0001c0001t0062g0065 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.274+18775A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554532 | |||||||
| chr10:28554549 | G | A | 59 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.274+18792G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554549 | |||||||
| chr10:28554577 | G | GCCATGAT others(312): Show |
1 | a0001c0001t0005g0236 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.274+18835_274+1883 others(323): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28554577 | ||||||
| chr10:28554594 | C | T | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0005t0004g0220 |
3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.274+18837C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554594 | |||||||
| chr10:28554611 | C | T | 2 | a0001c0001t0004g0221 a0001c0005t0004g0220 |
2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.274+18854C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554611 | |||||||
| chr10:28554717 | A | G | 19 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(16): Show |
20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.274+18960A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554717 | |||||||
| chr10:28554857 | G | T | 35 | a0001c0001t0003g0076 a0001c0001t0003g0079 a0001c0001t0003g0080 others(32): Show |
35 | HG00597.hp1 HG00597.hp2 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.274+19100G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554857 | |||||||
| chr10:28554923 | A | T | 1 | a0001c0001t0002g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.274+19166A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554923 | |||||||
| chr10:28554925 | T | C | 69 | a0001c0001t0003g0073 a0001c0001t0003g0076 a0001c0001t0003g0079 others(66): Show |
69 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.274+19168T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554925 | |||||||
| chr10:28555004 | G | C | 81 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(78): Show |
82 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.274+19247G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28555004 | |||||||
| chr10:28555014 | G | A | 59 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.274+19257G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28555014 | |||||||
| chr10:28555160 | T | A | 2 | a0001c0001t0008g0228 a0001c0001t0008g0229 |
2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.274+19403T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28555160 | |||||||
| chr10:28555213 | A | G | 1 | a0001c0001t0053g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.274+19456A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28555213 | |||||||
| chr10:28555334 | A | T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+19577A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28555334 | |||||||
| chr10:28555437 | AT | A | 285 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.274+19690delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28555437 | ||||||
| chr10:28555465 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0208 |
2 | HG00741.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.274+19708G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28555465 | |||||||
| chr10:28555498 | TGGTG | T | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0005t0004g0220 |
3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.274+19744_274+1974 others(8): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28555498 | ||||||
| chr10:28555506 | G | A | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+19749G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28555506 | |||||||
| chr10:28555513 | G | A | 2 | a0001c0001t0008g0228 a0001c0001t0008g0229 |
2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.274+19756G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28555513 | |||||||
| chr10:28555692 | C | T | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0005t0004g0220 |
3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.274+19935C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28555692 | |||||||
| chr10:28555762 | G | A | 6 | a0001c0001t0001g0119 a0001c0001t0001g0161 a0001c0001t0001g0194 others(3): Show |
6 | HG00642.hp1 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.274+20005G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28555762 | |||||||
| chr10:28555903 | A | G | 4 | a0001c0001t0001g0108 a0001c0001t0001g0128 a0001c0001t0001g0129 others(1): Show |
4 | HG01358.hp2 HG01928.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+20146A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28555903 | |||||||
| chr10:28556229 | CTT | C | 6 | a0001c0001t0004g0277 a0001c0001t0004g0278 a0001c0001t0004g0279 others(3): Show |
6 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.274+20473_274+2047 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28556229 | |||||||
| chr10:28556312 | A | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+20555A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28556312 | |||||||
| chr10:28556388 | A | AT | 17 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0155 others(14): Show |
17 | HG00140.hp1 HG01167.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.274+20658dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | ||||||
| chr10:28556388 | A | ATT | 56 | a0001c0001t0001g0069 a0001c0001t0001g0110 a0001c0001t0001g0116 others(53): Show |
56 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.274+20657_274+2065 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | ||||||
| chr10:28556388 | A | ATTT | 43 | a0001c0001t0001g0072 a0001c0001t0001g0115 a0001c0001t0001g0121 others(40): Show |
43 | HG00558.hp1 HG00735.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.274+20656_274+2065 others(7): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | ||||||
| chr10:28556388 | A | ATTTT | 9 | a0001c0001t0001g0067 a0001c0001t0001g0108 a0001c0001t0001g0147 others(6): Show |
9 | HG00673.hp2 HG01257.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.274+20655_274+2065 others(8): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | ||||||
| chr10:28556388 | A | ATTTTT | 17 | a0001c0001t0001g0213 a0001c0001t0004g0279 a0001c0001t0004g0283 others(14): Show |
17 | HG00099.hp2 HG00735.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.274+20654_274+2065 others(9): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | ||||||
| chr10:28556388 | A | ATTTTTT | 10 | a0001c0001t0001g0128 a0001c0001t0002g0018 a0001c0001t0002g0052 others(7): Show |
10 | HG00280.hp2 HG00741.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.274+20653_274+2065 others(10): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | ||||||
| chr10:28556388 | A | ATTTTTTT | 23 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0019 others(20): Show |
23 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.274+20652_274+2065 others(11): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | ||||||
| chr10:28556388 | A | ATTTTTTT others(1): Show |
27 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(24): Show |
27 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.274+20651_274+2065 others(12): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | ||||||
| chr10:28556388 | A | ATTTTTTT others(2): Show |
14 | a0001c0001t0002g0016 a0001c0001t0002g0029 a0001c0001t0002g0045 others(11): Show |
14 | HG00738.hp2 HG01175.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.274+20650_274+2065 others(13): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | ||||||
| chr10:28556388 | A | ATTTTTTT others(3): Show |
9 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0033 others(6): Show |
9 | HG00673.hp1 HG00733.hp2 HG03831.hp1 others(6): Show |
intron_variant | MODIFIER | c.274+20649_274+2065 others(14): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | ||||||
| chr10:28556388 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0002g0037 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.274+20648_274+2065 others(15): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | ||||||
| chr10:28556388 | AT | A | 24 | a0001c0001t0003g0076 a0001c0001t0003g0079 a0001c0001t0003g0085 others(21): Show |
24 | HG00597.hp1 HG00597.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.274+20658delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | ||||||
| chr10:28556388 | ATT | A | 21 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(18): Show |
21 | HG01496.hp1 HG01891.hp2 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.274+20657_274+2065 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | ||||||
| chr10:28556388 | ATTTTTTT others(4): Show |
A | 2 | a0001c0001t0002g0022 a0001c0001t0031g0165 |
2 | HG02080.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.274+20648_274+2065 others(15): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | ||||||
| chr10:28556388 | ATTTTTTT others(9): Show |
A | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+20643_274+2065 others(20): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | ||||||
| chr10:28556564 | A | T | 1 | a0001c0001t0002g0028 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.274+20807A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28556564 | |||||||
| chr10:28556663 | A | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+20906A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28556663 | |||||||
| chr10:28556866 | G | A | 285 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.274+21109G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28556866 | |||||||
| chr10:28557065 | G | GT | 30 | a0001c0001t0002g0015 a0001c0001t0002g0022 a0001c0001t0003g0090 others(27): Show |
30 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.274+21319dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28557065 | ||||||
| chr10:28557065 | G | GTT | 6 | a0001c0001t0004g0277 a0001c0001t0004g0278 a0001c0001t0004g0279 others(3): Show |
6 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.274+21318_274+2131 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28557065 | ||||||
| chr10:28557223 | C | T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+21466C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28557223 | |||||||
| chr10:28557326 | A | G | 1 | a0001c0001t0047g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274+21569A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28557326 | |||||||
| chr10:28557583 | G | A | 223 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(220): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.274+21826G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28557583 | |||||||
| chr10:28557617 | C | G | 15 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(12): Show |
16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.274+21860C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28557617 | |||||||
| chr10:28557652 | C | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+21895C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28557652 | |||||||
| chr10:28557740 | G | T | 1 | a0001c0001t0010g0289 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.274+21983G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28557740 | |||||||
| chr10:28557888 | C | T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+22131C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28557888 | |||||||
| chr10:28557990 | C | T | 1 | a0001c0001t0059g0055 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.274+22233C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28557990 | |||||||
| chr10:28557993 | G | A | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0005t0004g0220 |
3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.274+22236G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28557993 | |||||||
| chr10:28558148 | A | G | 123 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(120): Show |
123 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.274+22391A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28558148 | |||||||
| chr10:28558239 | A | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+22482A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28558239 | |||||||
| chr10:28558342 | A | G | 1 | a0001c0002t0009g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.274+22585A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28558342 | |||||||
| chr10:28558371 | C | A | 68 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(65): Show |
68 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.274+22614C>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28558371 | |||||||
| chr10:28558427 | TG | T | 9 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(6): Show |
9 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.274+22673delG | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28558427 | ||||||
| chr10:28558727 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.274+22970A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28558727 | |||||||
| chr10:28558753 | C | G | 1 | a0001c0001t0047g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274+22996C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28558753 | |||||||
| chr10:28558768 | T | C | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+23011T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28558768 | |||||||
| chr10:28558788 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.274+23031G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28558788 | |||||||
| chr10:28558931 | C | T | 10 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(7): Show |
10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.274+23174C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28558931 | |||||||
| chr10:28559050 | G | A | 15 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(12): Show |
16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.274+23293G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559050 | |||||||
| chr10:28559100 | A | G | 1 | a0001c0001t0012g0063 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.274+23343A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559100 | |||||||
| chr10:28559135 | G | GGTGTGTG others(7): Show |
1 | a0001c0001t0001g0144 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.274+23378_274+2337 others(18): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559135 | |||||||
| chr10:28559135 | G | GGTGTGTG others(9): Show |
1 | a0001c0001t0001g0116 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.274+23378_274+2337 others(20): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559135 | |||||||
| chr10:28559135 | G | GGTGTGTG others(11): Show |
3 | a0001c0001t0001g0155 a0001c0001t0001g0186 a0001c0001t0001g0187 |
3 | HG02451.hp1 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.274+23378_274+2337 others(22): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559135 | |||||||
| chr10:28559135 | G | GGTGTGTG others(15): Show |
1 | a0001c0001t0001g0188 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.274+23378_274+2337 others(26): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559135 | |||||||
| chr10:28559135 | GAT | G | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0005t0004g0220 |
3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.274+23379_274+2338 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559135 | |||||||
| chr10:28559136 | A | ATG | 25 | a0001c0001t0003g0076 a0001c0001t0003g0081 a0001c0001t0003g0088 others(22): Show |
26 | HG00558.hp2 HG00621.hp2 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.274+23407_274+2340 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | ||||||
| chr10:28559136 | A | ATGTG | 26 | a0001c0001t0003g0079 a0001c0001t0003g0080 a0001c0001t0003g0082 others(23): Show |
26 | HG00597.hp1 HG00597.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.274+23405_274+2340 others(8): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | ||||||
| chr10:28559136 | A | ATGTGTG | 27 | a0001c0001t0004g0148 a0001c0001t0004g0257 a0001c0001t0004g0258 others(24): Show |
27 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.274+23403_274+2340 others(10): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | ||||||
| chr10:28559136 | A | ATGTGTGT others(1): Show |
11 | a0001c0001t0006g0297 a0001c0001t0010g0285 a0001c0001t0010g0287 others(8): Show |
11 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.274+23401_274+2340 others(12): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | ||||||
| chr10:28559136 | A | ATGTGTGT others(3): Show |
8 | a0001c0001t0001g0142 a0001c0001t0001g0145 a0001c0001t0001g0179 others(5): Show |
8 | HG00558.hp1 HG00741.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.274+23399_274+2340 others(14): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | ||||||
| chr10:28559136 | A | ATGTGTGT others(5): Show |
26 | a0001c0001t0001g0108 a0001c0001t0001g0111 a0001c0001t0001g0112 others(23): Show |
26 | HG01243.hp1 HG01243.hp2 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.274+23397_274+2340 others(16): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | ||||||
| chr10:28559136 | A | ATGTGTGT others(7): Show |
34 | a0001c0001t0001g0115 a0001c0001t0001g0133 a0001c0001t0001g0136 others(31): Show |
34 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.274+23395_274+2340 others(18): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | ||||||
| chr10:28559136 | A | ATGTGTGT others(9): Show |
40 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0118 others(37): Show |
40 | HG00639.hp2 HG00735.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.274+23393_274+2340 others(20): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | ||||||
| chr10:28559136 | A | ATGTGTGT others(11): Show |
13 | a0001c0001t0001g0125 a0001c0001t0001g0158 a0001c0001t0001g0166 others(10): Show |
13 | HG01255.hp1 HG01884.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.274+23391_274+2340 others(22): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | ||||||
| chr10:28559136 | A | ATGTGTGT others(13): Show |
6 | a0001c0001t0001g0067 a0001c0001t0001g0110 a0001c0001t0001g0170 others(3): Show |
6 | HG01109.hp1 HG01257.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+23389_274+2340 others(24): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | ||||||
| chr10:28559136 | A | ATGTGTGT others(15): Show |
2 | a0001c0001t0001g0212 a0001c0001t0046g0151 |
2 | HG01934.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.274+23387_274+2340 others(26): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | ||||||
| chr10:28559136 | A | ATTGTGTG others(6): Show |
1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+23380_274+2338 others(17): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | ||||||
| chr10:28559136 | A | G | 6 | a0001c0001t0001g0116 a0001c0001t0001g0144 a0001c0001t0001g0155 others(3): Show |
6 | HG01081.hp1 HG02451.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+23379A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559136 | |||||||
| chr10:28559136 | ATG | A | 3 | a0001c0001t0004g0265 a0001c0001t0037g0260 a0001c0001t0056g0266 |
3 | HG01256.hp2 HG01361.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.274+23407_274+2340 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | ||||||
| chr10:28559136 | ATGTGTGT others(5): Show |
A | 59 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.274+23397_274+2340 others(16): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | ||||||
| chr10:28559166 | A | G | 3 | a0001c0001t0006g0002 a0001c0001t0006g0304 a0001c0001t0006g0305 |
4 | HG01106.hp2 HG01884.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+23409A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559166 | |||||||
| chr10:28559167 | A | T | 3 | a0001c0001t0006g0002 a0001c0001t0006g0304 a0001c0001t0006g0305 |
4 | HG01106.hp2 HG01884.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+23410A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559167 | |||||||
| chr10:28559170 | C | G | 3 | a0001c0001t0006g0002 a0001c0001t0006g0304 a0001c0001t0006g0305 |
4 | HG01106.hp2 HG01884.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+23413C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559170 | |||||||
| chr10:28559172 | G | GTGTGTAA others(2): Show |
2 | a0001c0001t0006g0002 a0001c0001t0006g0304 |
3 | HG01106.hp2 HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.274+23415_274+2341 others(13): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559172 | |||||||
| chr10:28559172 | G | GTGTGTGT others(4): Show |
1 | a0001c0001t0006g0305 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.274+23415_274+2341 others(15): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559172 | |||||||
| chr10:28559173 | A | C | 3 | a0001c0001t0006g0002 a0001c0001t0006g0304 a0001c0001t0006g0305 |
4 | HG01106.hp2 HG01884.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+23416A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559173 | |||||||
| chr10:28559399 | T | A | 285 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.274+23642T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559399 | |||||||
| chr10:28559718 | T | C | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-23681T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559718 | |||||||
| chr10:28559774 | A | T | 1 | a0001c0001t0048g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.275-23625A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559774 | |||||||
| chr10:28559855 | G | C | 1 | a0001c0001t0007g0163 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.275-23544G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559855 | |||||||
| chr10:28559860 | A | G | 50 | a0001c0001t0001g0067 a0001c0001t0001g0072 a0001c0001t0001g0110 others(47): Show |
50 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.275-23539A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559860 | |||||||
| chr10:28559874 | G | A | 1 | a0001c0001t0010g0290 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.275-23525G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559874 | |||||||
| chr10:28560073 | G | A | 2 | a0001c0001t0002g0011 a0001c0001t0002g0012 |
2 | HG00280.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.275-23326G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28560073 | |||||||
| chr10:28560094 | C | T | 10 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(7): Show |
10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.275-23305C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28560094 | |||||||
| chr10:28560111 | A | G | 286 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(283): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.275-23288A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28560111 | |||||||
| chr10:28560273 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.275-23126A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28560273 | |||||||
| chr10:28560397 | C | T | 1 | a0001c0001t0003g0086 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.275-23002C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28560397 | |||||||
| chr10:28560398 | G | A | 1 | a0001c0001t0053g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.275-23001G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28560398 | |||||||
| chr10:28560496 | C | T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-22903C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28560496 | |||||||
| chr10:28560534 | A | T | 1 | a0001c0001t0030g0135 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.275-22865A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28560534 | |||||||
| chr10:28560621 | A | G | 59 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.275-22778A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28560621 | |||||||
| chr10:28561003 | G | A | 59 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.275-22396G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28561003 | |||||||
| chr10:28561319 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.275-22080A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28561319 | |||||||
| chr10:28561328 | C | G | 1 | a0001c0001t0020g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.275-22071C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28561328 | |||||||
| chr10:28561371 | T | C | 1 | a0001c0001t0035g0225 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.275-22028T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28561371 | |||||||
| chr10:28561497 | G | GT | 58 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(55): Show |
58 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.275-21892dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28561497 | ||||||
| chr10:28561539 | C | T | 1 | a0001c0001t0047g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.275-21860C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28561539 | |||||||
| chr10:28561577 | G | C | 1 | a0001c0001t0005g0252 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.275-21822G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28561577 | |||||||
| chr10:28561649 | G | A | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-21750G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28561649 | |||||||
| chr10:28561652 | G | A | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-21747G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28561652 | |||||||
| chr10:28561654 | C | T | 1 | a0001c0001t0004g0258 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.275-21745C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28561654 | |||||||
| chr10:28561682 | C | G | 1 | a0001c0001t0045g0280 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.275-21717C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28561682 | |||||||
| chr10:28561823 | T | C | 1 | a0001c0001t0022g0183 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.275-21576T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28561823 | |||||||
| chr10:28562025 | T | C | 59 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.275-21374T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28562025 | |||||||
| chr10:28562026 | G | C | 1 | a0001c0001t0026g0053 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.275-21373G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28562026 | |||||||
| chr10:28562267 | G | A | 155 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(152): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.275-21132G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28562267 | |||||||
| chr10:28562313 | C | T | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0005t0004g0220 |
3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.275-21086C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28562313 | |||||||
| chr10:28562423 | T | G | 10 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(7): Show |
10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.275-20976T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28562423 | |||||||
| chr10:28562633 | G | A | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-20766G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28562633 | |||||||
| chr10:28562794 | G | A | 1 | a0001c0001t0061g0291 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.275-20605G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28562794 | |||||||
| chr10:28562908 | G | A | 1 | a0001c0001t0023g0126 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.275-20491G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28562908 | |||||||
| chr10:28563175 | GA | G | 6 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0023 others(3): Show |
6 | NA18948.hp1 NA18955.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.275-20223delA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28563175 | |||||||
| chr10:28563497 | T | C | 1 | a0001c0001t0007g0131 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.275-19902T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28563497 | |||||||
| chr10:28563625 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.275-19774G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28563625 | |||||||
| chr10:28563744 | C | CT | 57 | a0001c0001t0001g0108 a0001c0001t0001g0111 a0001c0001t0001g0118 others(54): Show |
58 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.275-19626dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | ||||||
| chr10:28563744 | C | CTT | 43 | a0001c0001t0001g0072 a0001c0001t0001g0133 a0001c0001t0001g0136 others(40): Show |
43 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.275-19627_275-1962 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | ||||||
| chr10:28563744 | C | CTTT | 28 | a0001c0001t0001g0067 a0001c0001t0001g0112 a0001c0001t0001g0115 others(25): Show |
28 | HG00558.hp1 HG00735.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.275-19628_275-1962 others(7): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | ||||||
| chr10:28563744 | C | CTTTT | 11 | a0001c0001t0001g0110 a0001c0001t0001g0164 a0001c0001t0001g0166 others(8): Show |
11 | HG01255.hp1 HG01934.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.275-19629_275-1962 others(8): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | ||||||
| chr10:28563744 | C | CTTTTTTT | 19 | a0001c0001t0002g0013 a0001c0001t0002g0016 a0001c0001t0002g0017 others(16): Show |
19 | HG00099.hp1 HG00323.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.275-19632_275-1962 others(11): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | ||||||
| chr10:28563744 | C | CTTTTTTT others(1): Show |
16 | a0001c0001t0001g0282 a0001c0001t0002g0014 a0001c0001t0002g0015 others(13): Show |
16 | HG00673.hp1 HG00733.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.275-19633_275-1962 others(12): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | ||||||
| chr10:28563744 | C | CTTTTTTT others(2): Show |
14 | a0001c0001t0002g0022 a0001c0001t0002g0026 a0001c0001t0002g0027 others(11): Show |
14 | HG00609.hp2 HG00621.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.275-19634_275-1962 others(13): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | ||||||
| chr10:28563744 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0002g0038 a0001c0001t0012g0031 a0001c0001t0036g0042 |
3 | HG02132.hp2 NA19085.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.275-19635_275-1962 others(14): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | ||||||
| chr10:28563744 | C | CTTTTTTT others(4): Show |
3 | a0001c0001t0002g0023 a0001c0001t0012g0063 a0001c0001t0059g0055 |
3 | HG01515.hp2 HG02293.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.275-19636_275-1962 others(15): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | ||||||
| chr10:28563744 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0002g0043 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.275-19637_275-1962 others(16): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | ||||||
| chr10:28563744 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0002g0034 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.275-19639_275-1962 others(18): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | ||||||
| chr10:28563744 | CT | C | 9 | a0001c0001t0005g0318 a0001c0001t0006g0292 a0001c0001t0006g0300 others(6): Show |
9 | HG00609.hp1 HG01168.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.275-19626delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | ||||||
| chr10:28563744 | CTTTTTTT others(2): Show |
C | 12 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0002t0009g0003 others(9): Show |
12 | HG00735.hp2 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.275-19634_275-1962 others(13): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | ||||||
| chr10:28563744 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0054g0094 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.275-19636_275-1962 others(15): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | ||||||
| chr10:28563744 | CTTTTTTT others(6): Show |
C | 28 | a0001c0001t0001g0116 a0001c0001t0001g0188 a0001c0001t0004g0148 others(25): Show |
28 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.275-19638_275-1962 others(17): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | ||||||
| chr10:28563774 | G | T | 2 | a0001c0001t0002g0011 a0001c0001t0002g0012 |
2 | HG00280.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.275-19625G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28563774 | |||||||
| chr10:28563842 | C | T | 1 | a0001c0001t0023g0189 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.275-19557C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28563842 | |||||||
| chr10:28563874 | A | C | 219 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(216): Show |
220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.275-19525A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28563874 | |||||||
| chr10:28564382 | G | A | 2 | a0001c0001t0008g0228 a0001c0001t0008g0229 |
2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.275-19017G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28564382 | |||||||
| chr10:28564620 | T | C | 1 | a0001c0001t0020g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.275-18779T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28564620 | |||||||
| chr10:28564841 | T | A | 1 | a0001c0002t0009g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.275-18558T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28564841 | |||||||
| chr10:28564864 | T | G | 1 | a0001c0001t0001g0184 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.275-18535T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28564864 | |||||||
| chr10:28564894 | T | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-18505T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28564894 | |||||||
| chr10:28564907 | G | T | 3 | a0002c0003t0008g0068 a0002c0003t0008g0231 a0002c0003t0008g0232 |
3 | HG02723.hp2 HG02896.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.275-18492G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28564907 | |||||||
| chr10:28564927 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.275-18472C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28564927 | |||||||
| chr10:28564933 | G | A | 286 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(283): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.275-18466G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28564933 | |||||||
| chr10:28565010 | C | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-18389C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28565010 | |||||||
| chr10:28565106 | CT | C | 295 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(292): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.275-18286delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28565106 | ||||||
| chr10:28565153 | T | C | 3 | a0001c0004t0001g0127 a0001c0004t0021g0132 a0001c0004t0041g0154 |
3 | HG01069.hp1 HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.275-18246T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28565153 | |||||||
| chr10:28565185 | C | A | 281 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(278): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.275-18214C>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28565185 | |||||||
| chr10:28565186 | C | T | 1 | a0001c0001t0004g0258 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.275-18213C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28565186 | |||||||
| chr10:28565605 | A | G | 1 | a0001c0001t0008g0230 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.275-17794A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28565605 | |||||||
| chr10:28565711 | A | G | 203 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(200): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.275-17688A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28565711 | |||||||
| chr10:28566063 | C | T | 59 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.275-17336C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28566063 | |||||||
| chr10:28566166 | A | G | 1 | a0001c0001t0020g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.275-17233A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28566166 | |||||||
| chr10:28566167 | C | A | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-17232C>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28566167 | |||||||
| chr10:28566386 | A | T | 3 | a0001c0001t0004g0265 a0001c0001t0037g0260 a0001c0001t0056g0266 |
3 | HG01256.hp2 HG01361.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.275-17013A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28566386 | |||||||
| chr10:28566507 | C | T | 1 | a0001c0001t0003g0098 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.275-16892C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28566507 | |||||||
| chr10:28566872 | A | C | 2 | a0001c0001t0008g0228 a0001c0001t0008g0229 |
2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.275-16527A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28566872 | |||||||
| chr10:28566952 | G | GT | 61 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(58): Show |
61 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.275-16434dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28566952 | ||||||
| chr10:28567090 | A | G | 19 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(16): Show |
20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.275-16309A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28567090 | |||||||
| chr10:28567214 | C | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.275-16185C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28567214 | |||||||
| chr10:28567399 | C | T | 1 | a0001c0001t0036g0042 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.275-16000C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28567399 | |||||||
| chr10:28567523 | A | T | 1 | a0001c0001t0001g0177 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.275-15876A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28567523 | |||||||
| chr10:28567610 | A | G | 1 | a0001c0001t0020g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.275-15789A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28567610 | |||||||
| chr10:28567808 | G | A | 1 | a0001c0001t0002g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.275-15591G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28567808 | |||||||
| chr10:28567890 | G | A | 121 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(118): Show |
121 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.275-15509G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28567890 | |||||||
| chr10:28567914 | C | T | 4 | a0001c0001t0014g0070 a0001c0001t0014g0254 a0001c0001t0014g0255 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-15485C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28567914 | |||||||
| chr10:28568001 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0208 |
2 | HG00741.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.275-15398G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568001 | |||||||
| chr10:28568082 | G | A | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0005t0004g0220 |
3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.275-15317G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568082 | |||||||
| chr10:28568204 | T | C | 36 | a0001c0001t0003g0073 a0001c0001t0003g0076 a0001c0001t0003g0079 others(33): Show |
36 | HG00597.hp1 HG00597.hp2 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.275-15195T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568204 | |||||||
| chr10:28568249 | C | T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-15150C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568249 | |||||||
| chr10:28568385 | G | T | 1 | a0001c0001t0001g0213 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.275-15014G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568385 | |||||||
| chr10:28568444 | G | A | 3 | a0001c0001t0004g0309 a0001c0001t0010g0308 a0001c0001t0032g0106 |
3 | HG02895.hp1 HG02897.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.275-14955G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568444 | |||||||
| chr10:28568445 | G | A | 285 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.275-14954G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568445 | |||||||
| chr10:28568521 | C | T | 3 | a0001c0001t0003g0083 a0001c0001t0003g0085 a0001c0001t0003g0087 |
3 | NA18971.hp1 NA18972.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.275-14878C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568521 | |||||||
| chr10:28568531 | C | T | 15 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(12): Show |
16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.275-14868C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568531 | |||||||
| chr10:28568814 | C | T | 15 | a0001c0001t0002g0013 a0001c0001t0002g0016 a0001c0001t0002g0028 others(12): Show |
15 | HG00735.hp2 HG01069.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.275-14585C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568814 | |||||||
| chr10:28568825 | G | A | 1 | a0001c0001t0006g0292 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.275-14574G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568825 | |||||||
| chr10:28568878 | C | G | 1 | a0001c0001t0047g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.275-14521C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568878 | |||||||
| chr10:28568886 | A | G | 18 | a0001c0001t0004g0257 a0001c0001t0004g0258 a0001c0001t0004g0261 others(15): Show |
18 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.275-14513A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568886 | |||||||
| chr10:28568931 | A | G | 19 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(16): Show |
20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.275-14468A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568931 | |||||||
| chr10:28568958 | A | G | 4 | a0001c0001t0014g0070 a0001c0001t0014g0254 a0001c0001t0014g0255 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-14441A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568958 | |||||||
| chr10:28568991 | A | G | 3 | a0001c0001t0013g0193 a0001c0001t0013g0204 a0001c0001t0034g0273 |
3 | HG02922.hp1 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.275-14408A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568991 | |||||||
| chr10:28569534 | G | A | 3 | a0001c0001t0001g0136 a0001c0001t0001g0218 a0001c0001t0020g0137 |
3 | HG01346.hp1 HG03831.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.275-13865G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28569534 | |||||||
| chr10:28569628 | G | A | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-13771G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28569628 | |||||||
| chr10:28569649 | C | T | 204 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(201): Show |
204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.275-13750C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28569649 | |||||||
| chr10:28569813 | T | A | 1 | a0001c0001t0005g0236 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.275-13586T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28569813 | |||||||
| chr10:28569904 | AT | A | 3 | a0001c0001t0011g0107 a0001c0001t0011g0134 a0001c0001t0011g0167 |
3 | NA18964.hp2 NA18972.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.275-13492delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28569904 | ||||||
| chr10:28569915 | C | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-13484C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28569915 | |||||||
| chr10:28569960 | C | T | 58 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(55): Show |
58 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.275-13439C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28569960 | |||||||
| chr10:28569971 | C | T | 9 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(6): Show |
9 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.275-13428C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28569971 | |||||||
| chr10:28570050 | A | T | 286 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(283): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.275-13349A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570050 | |||||||
| chr10:28570063 | G | A | 204 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(201): Show |
204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.275-13336G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570063 | |||||||
| chr10:28570150 | C | T | 285 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.275-13249C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570150 | |||||||
| chr10:28570380 | G | T | 15 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(12): Show |
16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.275-13019G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570380 | |||||||
| chr10:28570383 | A | G | 1 | a0001c0001t0055g0227 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.275-13016A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570383 | |||||||
| chr10:28570389 | C | A | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0005t0004g0220 |
3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.275-13010C>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570389 | |||||||
| chr10:28570431 | C | G | 285 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.275-12968C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570431 | |||||||
| chr10:28570435 | C | G | 2 | a0001c0001t0027g0024 a0001c0001t0027g0030 |
2 | NA18978.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.275-12964C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570435 | |||||||
| chr10:28570626 | T | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-12773T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570626 | |||||||
| chr10:28570633 | A | G | 5 | a0001c0001t0008g0226 a0002c0003t0008g0068 a0002c0003t0008g0223 others(2): Show |
5 | HG01123.hp2 HG02723.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.275-12766A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570633 | |||||||
| chr10:28570643 | T | C | 4 | a0001c0001t0014g0070 a0001c0001t0014g0254 a0001c0001t0014g0255 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-12756T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570643 | |||||||
| chr10:28570889 | A | G | 1 | a0001c0001t0039g0156 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.275-12510A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570889 | |||||||
| chr10:28570926 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.275-12473G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570926 | |||||||
| chr10:28570946 | CT | C | 12 | a0001c0001t0002g0016 a0001c0001t0002g0023 a0001c0001t0002g0057 others(9): Show |
12 | HG01358.hp1 HG01978.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.275-12425delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28570946 | ||||||
| chr10:28570946 | CTT | C | 44 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(41): Show |
44 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.275-12426_275-1242 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28570946 | ||||||
| chr10:28570946 | CTTT | C | 35 | a0001c0001t0001g0120 a0001c0001t0001g0197 a0001c0001t0001g0199 others(32): Show |
35 | HG00673.hp2 HG00733.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.275-12427_275-1242 others(7): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28570946 | ||||||
| chr10:28570946 | CTTTT | C | 166 | a0001c0001t0001g0072 a0001c0001t0001g0108 a0001c0001t0001g0110 others(163): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.275-12428_275-1242 others(8): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28570946 | ||||||
| chr10:28570946 | CTTTTT | C | 8 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0112 others(5): Show |
8 | HG00639.hp2 HG01257.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.275-12429_275-1242 others(9): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28570946 | ||||||
| chr10:28570946 | CTTTTTTT others(2): Show |
C | 15 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(12): Show |
16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.275-12433_275-1242 others(13): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28570946 | ||||||
| chr10:28570946 | CTTTTTTT others(3): Show |
C | 5 | a0001c0001t0004g0277 a0001c0001t0014g0070 a0001c0001t0014g0254 others(2): Show |
5 | HG00280.hp2 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.275-12434_275-1242 others(14): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28570946 | ||||||
| chr10:28571076 | C | T | 1 | a0001c0001t0036g0042 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.275-12323C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28571076 | |||||||
| chr10:28571147 | C | T | 1 | a0001c0002t0009g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.275-12252C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28571147 | |||||||
| chr10:28571161 | C | T | 1 | a0001c0001t0026g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.275-12238C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28571161 | |||||||
| chr10:28571171 | C | T | 4 | a0001c0001t0014g0070 a0001c0001t0014g0254 a0001c0001t0014g0255 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-12228C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28571171 | |||||||
| chr10:28571195 | G | A | 2 | a0001c0001t0002g0047 a0001c0001t0012g0048 |
2 | HG00099.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.275-12204G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28571195 | |||||||
| chr10:28571254 | T | G | 10 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(7): Show |
10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.275-12145T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28571254 | |||||||
| chr10:28571289 | C | T | 59 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.275-12110C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28571289 | |||||||
| chr10:28571525 | C | T | 19 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(16): Show |
20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.275-11874C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28571525 | |||||||
| chr10:28571635 | C | G | 1 | a0001c0001t0003g0098 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.275-11764C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28571635 | |||||||
| chr10:28571635 | C | T | 1 | a0001c0001t0004g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.275-11764C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28571635 | |||||||
| chr10:28571830 | A | G | 10 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(7): Show |
10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.275-11569A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28571830 | |||||||
| chr10:28571901 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.275-11498T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28571901 | |||||||
| chr10:28572013 | G | T | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0005t0004g0220 |
3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.275-11386G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28572013 | |||||||
| chr10:28572036 | C | T | 1 | a0001c0001t0046g0151 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.275-11363C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28572036 | |||||||
| chr10:28572173 | C | T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-11226C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28572173 | |||||||
| chr10:28572174 | TA | T | 203 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(200): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.275-11221delA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28572174 | ||||||
| chr10:28572291 | C | T | 1 | a0001c0001t0008g0226 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.275-11108C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28572291 | |||||||
| chr10:28572337 | C | CA | 95 | a0001c0001t0001g0182 a0001c0001t0001g0212 a0001c0001t0001g0218 others(92): Show |
96 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.275-11045dupA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28572337 | ||||||
| chr10:28572337 | C | CAA | 10 | a0001c0001t0003g0085 a0001c0001t0003g0089 a0001c0001t0003g0090 others(7): Show |
10 | HG01192.hp2 HG01928.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.275-11046_275-1104 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28572337 | ||||||
| chr10:28572337 | CA | C | 13 | a0001c0001t0001g0147 a0001c0001t0001g0213 a0001c0001t0008g0226 others(10): Show |
13 | HG01123.hp2 HG02004.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.275-11045delA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28572337 | ||||||
| chr10:28572365 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.275-11034A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28572365 | |||||||
| chr10:28572464 | G | C | 1 | a0001c0001t0020g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.275-10935G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28572464 | |||||||
| chr10:28572548 | A | T | 15 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(12): Show |
16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.275-10851A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28572548 | |||||||
| chr10:28572799 | G | A | 4 | a0002c0003t0008g0068 a0002c0003t0008g0223 a0002c0003t0008g0231 others(1): Show |
4 | HG01123.hp2 HG02723.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.275-10600G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28572799 | |||||||
| chr10:28572833 | A | T | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0005t0004g0220 |
3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.275-10566A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28572833 | |||||||
| chr10:28573118 | A | AT | 135 | a0001c0001t0001g0067 a0001c0001t0001g0072 a0001c0001t0001g0110 others(132): Show |
135 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.275-10272dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28573118 | ||||||
| chr10:28573118 | A | ATT | 150 | a0001c0001t0001g0069 a0001c0001t0001g0108 a0001c0001t0001g0111 others(147): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.275-10273_275-1027 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28573118 | ||||||
| chr10:28573172 | C | G | 1 | a0001c0001t0007g0163 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.275-10227C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28573172 | |||||||
| chr10:28573212 | T | G | 1 | a0001c0001t0047g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.275-10187T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28573212 | |||||||
| chr10:28573223 | C | T | 67 | a0001c0001t0003g0076 a0001c0001t0003g0079 a0001c0001t0003g0080 others(64): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.275-10176C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28573223 | |||||||
| chr10:28573259 | C | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-10140C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28573259 | |||||||
| chr10:28573332 | C | G | 1 | a0001c0001t0004g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.275-10067C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28573332 | |||||||
| chr10:28573339 | C | T | 8 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(5): Show |
8 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.275-10060C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28573339 | |||||||
| chr10:28573360 | T | A | 4 | a0001c0001t0014g0070 a0001c0001t0014g0254 a0001c0001t0014g0255 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-10039T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28573360 | |||||||
| chr10:28573583 | C | T | 4 | a0001c0001t0014g0070 a0001c0001t0014g0254 a0001c0001t0014g0255 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-9816C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28573583 | |||||||
| chr10:28573746 | A | G | 1 | a0001c0001t0053g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.275-9653A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28573746 | |||||||
| chr10:28573866 | C | G | 3 | a0001c0001t0005g0250 a0001c0001t0025g0249 a0001c0001t0035g0225 |
3 | HG00438.hp2 NA18612.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.275-9533C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28573866 | |||||||
| chr10:28573926 | A | G | 1 | a0002c0003t0008g0232 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.275-9473A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28573926 | |||||||
| chr10:28573977 | C | G | 1 | a0001c0001t0013g0205 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.275-9422C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28573977 | |||||||
| chr10:28574026 | T | A | 1 | a0001c0001t0046g0151 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.275-9373T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574026 | |||||||
| chr10:28574112 | GTTTTTA | G | 120 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(117): Show |
120 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.275-9281_275-9276d others(8): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28574112 | ||||||
| chr10:28574117 | T | C | 1 | a0001c0001t0002g0014 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.275-9282T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574117 | |||||||
| chr10:28574216 | C | T | 3 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0037 |
3 | HG00609.hp2 NA18962.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.275-9183C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574216 | |||||||
| chr10:28574230 | C | T | 1 | a0001c0002t0009g0103 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.275-9169C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574230 | |||||||
| chr10:28574381 | C | T | 10 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(7): Show |
10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.275-9018C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574381 | |||||||
| chr10:28574383 | G | A | 22 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0049 others(19): Show |
22 | HG00280.hp1 HG00621.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.275-9016G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574383 | |||||||
| chr10:28574443 | C | A | 1 | a0001c0001t0010g0290 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.275-8956C>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574443 | |||||||
| chr10:28574444 | G | A | 35 | a0001c0001t0003g0076 a0001c0001t0003g0079 a0001c0001t0003g0080 others(32): Show |
35 | HG00597.hp1 HG00597.hp2 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.275-8955G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574444 | |||||||
| chr10:28574605 | G | C | 1 | a0001c0001t0013g0205 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.275-8794G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574605 | |||||||
| chr10:28574642 | C | G | 4 | a0002c0003t0008g0068 a0002c0003t0008g0223 a0002c0003t0008g0231 others(1): Show |
4 | HG01123.hp2 HG02723.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.275-8757C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574642 | |||||||
| chr10:28574736 | G | A | 1 | a0001c0001t0012g0025 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.275-8663G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574736 | |||||||
| chr10:28574758 | A | G | 3 | a0001c0001t0002g0014 a0001c0001t0002g0039 a0001c0001t0057g0036 |
3 | HG03831.hp1 HG04204.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.275-8641A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574758 | |||||||
| chr10:28574867 | T | C | 7 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
7 | NA18969.hp1 NA18984.hp1 NA18998.hp1 others(4): Show |
intron_variant | MODIFIER | c.275-8532T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574867 | |||||||
| chr10:28574879 | C | G | 121 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(118): Show |
121 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.275-8520C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574879 | |||||||
| chr10:28574923 | G | C | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-8476G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574923 | |||||||
| chr10:28574954 | G | C | 1 | a0001c0001t0008g0234 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.275-8445G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574954 | |||||||
| chr10:28574958 | C | G | 1 | a0001c0001t0048g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.275-8441C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574958 | |||||||
| chr10:28574960 | A | G | 1 | a0001c0001t0003g0088 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.275-8439A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574960 | |||||||
| chr10:28574986 | TG | T | 59 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.275-8411delG | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28574986 | ||||||
| chr10:28575026 | G | A | 285 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.275-8373G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28575026 | |||||||
| chr10:28575058 | T | G | 36 | a0001c0001t0003g0076 a0001c0001t0003g0079 a0001c0001t0003g0080 others(33): Show |
36 | HG00597.hp1 HG00597.hp2 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.275-8341T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28575058 | |||||||
| chr10:28575244 | C | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-8155C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28575244 | |||||||
| chr10:28575777 | G | A | 285 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.275-7622G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28575777 | |||||||
| chr10:28575782 | G | T | 58 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(55): Show |
58 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.275-7617G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28575782 | |||||||
| chr10:28575818 | C | T | 6 | a0001c0001t0001g0120 a0001c0001t0007g0159 a0001c0001t0007g0216 others(3): Show |
6 | HG00673.hp2 HG01975.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.275-7581C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28575818 | |||||||
| chr10:28575826 | C | T | 1 | a0001c0001t0002g0027 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.275-7573C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28575826 | |||||||
| chr10:28576118 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.275-7281C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28576118 | |||||||
| chr10:28576443 | C | T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-6956C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28576443 | |||||||
| chr10:28576600 | G | T | 4 | a0001c0001t0014g0070 a0001c0001t0014g0254 a0001c0001t0014g0255 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-6799G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28576600 | |||||||
| chr10:28576813 | T | C | 2 | a0001c0001t0001g0197 a0001c0001t0001g0198 |
2 | HG01192.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.275-6586T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28576813 | |||||||
| chr10:28576911 | A | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-6488A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28576911 | |||||||
| chr10:28577325 | G | GT | 6 | a0001c0001t0002g0052 a0001c0001t0003g0259 a0001c0001t0005g0246 others(3): Show |
6 | HG01167.hp2 HG02056.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.275-6066dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28577325 | ||||||
| chr10:28577407 | A | C | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-5992A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28577407 | |||||||
| chr10:28577449 | A | G | 1 | a0001c0001t0010g0289 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.275-5950A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28577449 | |||||||
| chr10:28577683 | A | G | 1 | a0001c0001t0035g0225 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.275-5716A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28577683 | |||||||
| chr10:28577764 | C | T | 1 | a0001c0001t0053g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.275-5635C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28577764 | |||||||
| chr10:28577779 | A | G | 6 | a0001c0001t0004g0277 a0001c0001t0004g0278 a0001c0001t0004g0279 others(3): Show |
6 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.275-5620A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28577779 | |||||||
| chr10:28577949 | G | A | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0005t0004g0220 |
3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.275-5450G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28577949 | |||||||
| chr10:28578031 | T | C | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-5368T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28578031 | |||||||
| chr10:28578155 | TCAAAA | T | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0005t0004g0220 |
3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.275-5228_275-5224d others(7): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28578155 | ||||||
| chr10:28578284 | A | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-5115A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28578284 | |||||||
| chr10:28578291 | C | G | 121 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(118): Show |
121 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.275-5108C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28578291 | |||||||
| chr10:28578293 | T | G | 1 | a0001c0001t0007g0180 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.275-5106T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28578293 | |||||||
| chr10:28578406 | A | C | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-4993A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28578406 | |||||||
| chr10:28578468 | C | T | 58 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(55): Show |
58 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.275-4931C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28578468 | |||||||
| chr10:28578711 | C | A | 2 | a0001c0001t0002g0047 a0001c0001t0012g0048 |
2 | HG00099.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.275-4688C>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28578711 | |||||||
| chr10:28578818 | T | C | 1 | a0001c0001t0002g0033 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.275-4581T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28578818 | |||||||
| chr10:28579014 | C | G | 15 | a0001c0001t0003g0080 a0001c0001t0003g0082 a0001c0001t0003g0083 others(12): Show |
15 | HG00597.hp1 HG02056.hp1 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.275-4385C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28579014 | |||||||
| chr10:28579026 | A | G | 155 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(152): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.275-4373A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28579026 | |||||||
| chr10:28579074 | C | G | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0005t0004g0220 |
3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.275-4325C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28579074 | |||||||
| chr10:28579174 | A | AT | 45 | a0001c0001t0001g0140 a0001c0001t0002g0038 a0001c0001t0002g0047 others(42): Show |
45 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.275-4210dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28579174 | ||||||
| chr10:28579174 | AT | A | 24 | a0001c0001t0001g0186 a0001c0001t0004g0148 a0001c0001t0004g0268 others(21): Show |
25 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.275-4210delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28579174 | ||||||
| chr10:28579248 | G | A | 1 | a0001c0001t0042g0275 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.275-4151G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28579248 | |||||||
| chr10:28579474 | G | C | 1 | a0001c0001t0001g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.275-3925G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28579474 | |||||||
| chr10:28579630 | G | A | 1 | a0001c0001t0002g0033 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.275-3769G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28579630 | |||||||
| chr10:28579685 | ACAAT | A | 4 | a0001c0001t0014g0070 a0001c0001t0014g0254 a0001c0001t0014g0255 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-3711_275-3708d others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28579685 | ||||||
| chr10:28579699 | C | G | 1 | a0001c0001t0002g0062 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.275-3700C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28579699 | |||||||
| chr10:28579734 | T | C | 8 | a0001c0001t0001g0108 a0001c0001t0001g0128 a0001c0001t0001g0129 others(5): Show |
8 | HG01358.hp2 HG01928.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-3665T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28579734 | |||||||
| chr10:28579892 | T | C | 204 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(201): Show |
204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.275-3507T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28579892 | |||||||
| chr10:28579973 | TGTTA | T | 62 | a0001c0001t0001g0067 a0001c0001t0001g0072 a0001c0001t0001g0110 others(59): Show |
62 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.275-3422_275-3419d others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28579973 | ||||||
| chr10:28580056 | A | C | 1 | a0001c0001t0014g0070 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.275-3343A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28580056 | |||||||
| chr10:28580254 | CT | C | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0005t0004g0220 |
3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.275-3144delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28580254 | |||||||
| chr10:28580255 | T | C | 282 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(279): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.275-3144T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28580255 | |||||||
| chr10:28580352 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.275-3047A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28580352 | |||||||
| chr10:28580357 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.275-3042G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28580357 | |||||||
| chr10:28580611 | T | C | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-2788T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28580611 | |||||||
| chr10:28580749 | T | C | 1 | a0001c0001t0048g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.275-2650T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28580749 | |||||||
| chr10:28580800 | T | C | 26 | a0001c0001t0004g0148 a0001c0001t0004g0257 a0001c0001t0004g0258 others(23): Show |
26 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.275-2599T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28580800 | |||||||
| chr10:28580922 | A | T | 59 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.275-2477A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28580922 | |||||||
| chr10:28581238 | C | CT | 6 | a0001c0001t0005g0224 a0001c0001t0005g0236 a0001c0001t0005g0243 others(3): Show |
6 | HG00558.hp2 HG00621.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.275-2129dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28581238 | ||||||
| chr10:28581238 | CT | C | 10 | a0001c0001t0005g0233 a0001c0001t0005g0235 a0001c0001t0005g0250 others(7): Show |
10 | HG00438.hp2 HG00733.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.275-2129delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28581238 | ||||||
| chr10:28581238 | CTTTTTT | C | 18 | a0001c0001t0001g0140 a0001c0001t0001g0142 a0001c0001t0001g0166 others(15): Show |
18 | HG00741.hp1 HG01167.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.275-2134_275-2129d others(8): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28581238 | ||||||
| chr10:28581238 | CTTTTTTT | C | 218 | a0001c0001t0001g0067 a0001c0001t0001g0072 a0001c0001t0001g0108 others(215): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.275-2135_275-2129d others(9): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28581238 | ||||||
| chr10:28581238 | CTTTTTTT others(1): Show |
C | 36 | a0001c0001t0001g0069 a0001c0001t0001g0125 a0001c0001t0002g0040 others(33): Show |
37 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.275-2136_275-2129d others(10): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28581238 | ||||||
| chr10:28581238 | CTTTTTTT others(2): Show |
C | 8 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(5): Show |
8 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.275-2137_275-2129d others(11): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28581238 | ||||||
| chr10:28581238 | CTTTTTTT others(3): Show |
C | 1 | a0001c0002t0009g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.275-2138_275-2129d others(12): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28581238 | ||||||
| chr10:28581238 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0058 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.275-2140_275-2129d others(14): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28581238 | ||||||
| chr10:28581238 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0004g0257 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.275-2144_275-2129d others(18): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28581238 | ||||||
| chr10:28581238 | CTTTTTTT others(13): Show |
C | 1 | a0001c0001t0001g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.275-2148_275-2129d others(22): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28581238 | ||||||
| chr10:28581254 | T | C | 1 | a0001c0001t0024g0178 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.275-2145T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28581254 | |||||||
| chr10:28581369 | C | T | 3 | a0001c0001t0002g0059 a0001c0001t0012g0063 a0001c0001t0062g0065 |
3 | HG01109.hp2 HG01175.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.275-2030C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28581369 | |||||||
| chr10:28581561 | T | G | 123 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(120): Show |
123 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.275-1838T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28581561 | |||||||
| chr10:28581573 | G | C | 2 | a0001c0002t0009g0005 a0001c0002t0009g0009 |
2 | HG00735.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.275-1826G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28581573 | |||||||
| chr10:28581636 | A | C | 1 | a0001c0001t0001g0172 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.275-1763A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28581636 | |||||||
| chr10:28581636 | A | G | 1 | a0001c0001t0053g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.275-1763A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28581636 | |||||||
| chr10:28581823 | A | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-1576A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28581823 | |||||||
| chr10:28582013 | T | C | 1 | a0001c0002t0009g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.275-1386T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28582013 | |||||||
| chr10:28582316 | A | T | 18 | a0001c0001t0004g0257 a0001c0001t0004g0258 a0001c0001t0004g0261 others(15): Show |
18 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.275-1083A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28582316 | |||||||
| chr10:28582356 | T | TA | 3 | a0001c0001t0001g0120 a0001c0001t0007g0159 a0001c0001t0013g0205 |
3 | HG01975.hp1 NA18994.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.275-1042dupA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28582356 | ||||||
| chr10:28582378 | A | C | 1 | a0001c0001t0062g0065 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.275-1021A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28582378 | |||||||
| chr10:28582387 | A | G | 1 | a0001c0001t0032g0106 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.275-1012A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28582387 | |||||||
| chr10:28582963 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.275-436G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28582963 | |||||||
| chr10:28583552 | C | A | 1 | a0001c0001t0007g0216 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.381+47C>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28583552 | |||||||
| chr10:28583552 | C | CA | 214 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(211): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.381+63dupA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 28583552 | ||||||
| chr10:28583552 | C | CAA | 11 | a0001c0001t0001g0129 a0001c0001t0001g0164 a0001c0001t0001g0170 others(8): Show |
11 | HG00438.hp1 HG01256.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.381+62_381+63dupAA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 28583552 | ||||||
| chr10:28583611 | T | A | 4 | a0001c0001t0014g0070 a0001c0001t0014g0254 a0001c0001t0014g0255 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+106T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28583611 | |||||||
| chr10:28583612 | T | A | 6 | a0001c0001t0014g0070 a0001c0001t0014g0254 a0001c0001t0014g0255 others(3): Show |
6 | HG02109.hp1 HG02129.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+107T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28583612 | |||||||
| chr10:28583627 | C | T | 6 | a0001c0002t0009g0003 a0001c0002t0009g0005 a0001c0002t0009g0007 others(3): Show |
6 | HG00735.hp2 HG02055.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+122C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28583627 | |||||||
| chr10:28583666 | A | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.381+161A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28583666 | |||||||
| chr10:28583707 | G | C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0208 |
2 | HG00741.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.381+202G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28583707 | |||||||
| chr10:28583829 | G | A | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.381+324G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28583829 | |||||||
| chr10:28583875 | CATTT | C | 4 | a0001c0001t0014g0070 a0001c0001t0014g0254 a0001c0001t0014g0255 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+374_381+377del others(4): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 28583875 | ||||||
| chr10:28584273 | C | T | 121 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(118): Show |
121 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.381+768C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28584273 | |||||||
| chr10:28584276 | G | A | 204 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(201): Show |
204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.381+771G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28584276 | |||||||
| chr10:28584301 | A | G | 1 | a0001c0001t0002g0021 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.381+796A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28584301 | |||||||
| chr10:28584548 | T | A | 1 | a0001c0001t0006g0296 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.381+1043T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28584548 | |||||||
| chr10:28584584 | T | C | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.381+1079T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28584584 | |||||||
| chr10:28584624 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.381+1119A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28584624 | |||||||
| chr10:28584634 | C | T | 1 | a0001c0001t0012g0025 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.381+1129C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28584634 | |||||||
| chr10:28584670 | C | T | 5 | a0001c0001t0001g0123 a0001c0001t0004g0221 a0001c0001t0004g0222 others(2): Show |
5 | HG01891.hp2 NA18969.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+1165C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28584670 | |||||||
| chr10:28585172 | C | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.381+1667C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28585172 | |||||||
| chr10:28585262 | A | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.381+1757A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28585262 | |||||||
| chr10:28585297 | A | G | 203 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(200): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.381+1792A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28585297 | |||||||
| chr10:28585331 | G | T | 285 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.381+1826G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28585331 | |||||||
| chr10:28585348 | C | T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.381+1843C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28585348 | |||||||
| chr10:28585602 | G | A | 286 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(283): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.381+2097G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28585602 | |||||||
| chr10:28585688 | G | A | 20 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(17): Show |
21 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.381+2183G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28585688 | |||||||
| chr10:28585704 | G | C | 20 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(17): Show |
21 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.381+2199G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28585704 | |||||||
| chr10:28585908 | C | T | 1 | a0001c0001t0004g0268 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.381+2403C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28585908 | |||||||
| chr10:28585986 | T | G | 19 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(16): Show |
20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.381+2481T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28585986 | |||||||
| chr10:28586039 | A | G | 1 | a0001c0001t0003g0093 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.381+2534A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28586039 | |||||||
| chr10:28586314 | G | A | 2 | a0001c0001t0008g0228 a0001c0001t0008g0229 |
2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.381+2809G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28586314 | |||||||
| chr10:28586466 | T | C | 59 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.381+2961T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28586466 | |||||||
| chr10:28586714 | A | T | 1 | a0001c0001t0001g0138 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.382-3022A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28586714 | |||||||
| chr10:28586763 | T | C | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.382-2973T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28586763 | |||||||
| chr10:28586797 | AAAAT | A | 10 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(7): Show |
10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.382-2938_382-2935d others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28586797 | |||||||
| chr10:28587021 | G | A | 6 | a0001c0001t0004g0277 a0001c0001t0004g0278 a0001c0001t0004g0279 others(3): Show |
6 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-2715G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28587021 | |||||||
| chr10:28587168 | AATT | A | 59 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.382-2564_382-2562d others(5): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 28587168 | ||||||
| chr10:28587194 | A | G | 1 | a0001c0001t0048g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.382-2542A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28587194 | |||||||
| chr10:28587391 | G | A | 1 | a0001c0001t0007g0173 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.382-2345G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28587391 | |||||||
| chr10:28587758 | C | G | 1 | a0001c0001t0024g0178 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.382-1978C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28587758 | |||||||
| chr10:28587876 | G | C | 1 | a0001c0001t0005g0236 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.382-1860G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28587876 | |||||||
| chr10:28587924 | C | CT | 204 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(201): Show |
204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.382-1802dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 28587924 | ||||||
| chr10:28587972 | T | G | 1 | a0001c0001t0005g0247 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.382-1764T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28587972 | |||||||
| chr10:28588007 | G | C | 2 | a0001c0001t0002g0051 a0001c0001t0028g0060 |
2 | NA18994.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.382-1729G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28588007 | |||||||
| chr10:28588170 | G | A | 1 | a0001c0001t0008g0230 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.382-1566G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28588170 | |||||||
| chr10:28588236 | G | A | 1 | a0001c0001t0052g0041 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.382-1500G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28588236 | |||||||
| chr10:28588332 | C | T | 1 | a0001c0001t0003g0097 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.382-1404C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28588332 | |||||||
| chr10:28588359 | T | G | 1 | a0001c0001t0044g0075 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.382-1377T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28588359 | |||||||
| chr10:28588416 | A | G | 34 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(31): Show |
34 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.382-1320A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28588416 | |||||||
| chr10:28588647 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.382-1089C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28588647 | |||||||
| chr10:28588767 | T | C | 1 | a0001c0001t0047g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.382-969T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28588767 | |||||||
| chr10:28588787 | C | T | 1 | a0001c0001t0020g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.382-949C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28588787 | |||||||
| chr10:28588830 | G | A | 1 | a0001c0001t0003g0076 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.382-906G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28588830 | |||||||
| chr10:28588933 | T | C | 10 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(7): Show |
10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.382-803T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28588933 | |||||||
| chr10:28589070 | A | G | 1 | a0001c0001t0053g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.382-666A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28589070 | |||||||
| chr10:28589133 | A | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.382-603A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28589133 | |||||||
| chr10:28589381 | A | G | 15 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(12): Show |
16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.382-355A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28589381 | |||||||
| chr10:28589450 | T | C | 1 | a0001c0001t0002g0052 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.382-286T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28589450 | |||||||
| chr10:28589546 | A | C | 1 | a0001c0001t0026g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.382-190A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28589546 | |||||||
| chr10:28589865 | A | T | 1 | a0001c0001t0054g0094 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.497+14A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 5/13 | chr10 | 28589865 | |||||||
| chr10:28589920 | A | G | 2 | a0001c0001t0002g0045 a0001c0001t0002g0046 |
2 | HG00733.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.497+69A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 5/13 | chr10 | 28589920 | |||||||
| chr10:28589977 | G | A | 1 | a0001c0001t0010g0276 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.497+126G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 5/13 | chr10 | 28589977 | |||||||
| chr10:28590028 | A | G | 4 | a0001c0001t0003g0081 a0001c0001t0017g0077 a0001c0001t0017g0078 others(1): Show |
4 | HG01496.hp1 HG01928.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+177A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 5/13 | chr10 | 28590028 | |||||||
| chr10:28590088 | A | G | 1 | a0001c0001t0010g0271 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.497+237A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 5/13 | chr10 | 28590088 | |||||||
| chr10:28590182 | A | G | 4 | a0001c0001t0014g0070 a0001c0001t0014g0254 a0001c0001t0014g0255 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+331A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 5/13 | chr10 | 28590182 | |||||||
| chr10:28590311 | CA | C | 67 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(64): Show |
68 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.498-385delA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 28590311 | ||||||
| chr10:28590311 | CAA | C | 19 | a0001c0001t0001g0128 a0001c0001t0001g0138 a0001c0001t0001g0150 others(16): Show |
19 | HG01069.hp1 HG01891.hp2 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.498-386_498-385del others(2): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 28590311 | ||||||
| chr10:28590311 | CAAA | C | 189 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(186): Show |
189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.498-387_498-385del others(3): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 28590311 | ||||||
| chr10:28590311 | CAAAA | C | 6 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0217 others(3): Show |
6 | HG01192.hp1 HG01261.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.498-388_498-385del others(4): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 28590311 | ||||||
| chr10:28590381 | A | C | 1 | a0001c0001t0001g0212 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.498-339A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 5/13 | chr10 | 28590381 | |||||||
| chr10:28590549 | G | A | 2 | a0001c0001t0008g0228 a0001c0001t0008g0229 |
2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.498-171G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 5/13 | chr10 | 28590549 | |||||||
| chr10:28590909 | A | G | 59 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.610+77A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28590909 | |||||||
| chr10:28590944 | C | T | 1 | a0001c0001t0012g0063 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.610+112C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28590944 | |||||||
| chr10:28591186 | A | G | 1 | a0001c0001t0004g0278 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.610+354A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28591186 | |||||||
| chr10:28591231 | A | G | 69 | a0001c0001t0003g0073 a0001c0001t0003g0076 a0001c0001t0003g0079 others(66): Show |
69 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.610+399A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28591231 | |||||||
| chr10:28591317 | TC | T | 19 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(16): Show |
20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.610+486delC | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28591317 | |||||||
| chr10:28591372 | A | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.610+540A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28591372 | |||||||
| chr10:28591375 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.610+543A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28591375 | |||||||
| chr10:28591465 | C | A | 285 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.610+633C>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28591465 | |||||||
| chr10:28591833 | CA | C | 58 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0014 others(55): Show |
58 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.610+1028delA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28591833 | ||||||
| chr10:28591833 | CAA | C | 17 | a0001c0001t0002g0013 a0001c0001t0003g0085 a0001c0001t0010g0285 others(14): Show |
17 | HG00735.hp2 HG01069.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.610+1027_610+1028d others(4): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28591833 | ||||||
| chr10:28591833 | CAAA | C | 43 | a0001c0001t0003g0076 a0001c0001t0003g0079 a0001c0001t0003g0080 others(40): Show |
43 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.610+1026_610+1028d others(5): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28591833 | ||||||
| chr10:28591833 | CAAAA | C | 26 | a0001c0001t0003g0073 a0001c0001t0004g0148 a0001c0001t0004g0221 others(23): Show |
26 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.610+1025_610+1028d others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28591833 | ||||||
| chr10:28591833 | CAAAAAAA others(1): Show |
C | 16 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(13): Show |
17 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.610+1021_610+1028d others(10): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28591833 | ||||||
| chr10:28591833 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0007g0173 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.610+1018_610+1028d others(13): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28591833 | ||||||
| chr10:28591833 | CAAAAAAA others(5): Show |
C | 119 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(116): Show |
119 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.610+1017_610+1028d others(14): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28591833 | ||||||
| chr10:28591833 | CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0121 a0001c0001t0001g0201 |
2 | NA19057.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.610+1016_610+1028d others(15): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28591833 | ||||||
| chr10:28591860 | A | T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.610+1028A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28591860 | |||||||
| chr10:28592063 | T | C | 69 | a0001c0001t0003g0073 a0001c0001t0003g0076 a0001c0001t0003g0079 others(66): Show |
69 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.610+1231T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28592063 | |||||||
| chr10:28592247 | G | A | 10 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(7): Show |
10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.610+1415G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28592247 | |||||||
| chr10:28592328 | A | G | 8 | a0001c0001t0006g0292 a0001c0001t0006g0295 a0001c0001t0006g0296 others(5): Show |
8 | HG01243.hp2 HG02486.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.610+1496A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28592328 | |||||||
| chr10:28592354 | T | G | 1 | a0001c0001t0005g0252 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.610+1522T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28592354 | |||||||
| chr10:28592451 | G | A | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.610+1619G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28592451 | |||||||
| chr10:28592458 | C | T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.610+1626C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28592458 | |||||||
| chr10:28592475 | T | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.610+1643T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28592475 | |||||||
| chr10:28592535 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.610+1703C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28592535 | |||||||
| chr10:28592942 | G | A | 1 | a0001c0001t0012g0025 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.610+2110G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28592942 | |||||||
| chr10:28593082 | A | G | 1 | a0001c0001t0002g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.610+2250A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28593082 | |||||||
| chr10:28593110 | T | G | 2 | a0001c0001t0010g0288 a0001c0001t0010g0289 |
2 | HG00609.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.610+2278T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28593110 | |||||||
| chr10:28593152 | G | A | 285 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.610+2320G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28593152 | |||||||
| chr10:28593596 | C | T | 1 | a0001c0002t0009g0103 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.611-2137C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28593596 | |||||||
| chr10:28593637 | G | A | 3 | a0002c0003t0008g0068 a0002c0003t0008g0231 a0002c0003t0008g0232 |
3 | HG02723.hp2 HG02896.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.611-2096G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28593637 | |||||||
| chr10:28593655 | C | A | 1 | a0001c0001t0047g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.611-2078C>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28593655 | |||||||
| chr10:28593695 | G | A | 1 | a0001c0001t0017g0078 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.611-2038G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28593695 | |||||||
| chr10:28593730 | C | CA | 14 | a0001c0001t0002g0050 a0001c0001t0008g0226 a0001c0001t0008g0228 others(11): Show |
14 | HG00621.hp1 HG01123.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.611-1990dupA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28593730 | ||||||
| chr10:28593730 | CA | C | 205 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(202): Show |
205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.611-1990delA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28593730 | ||||||
| chr10:28593869 | A | G | 1 | a0001c0001t0005g0250 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.611-1864A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28593869 | |||||||
| chr10:28594139 | G | A | 205 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(202): Show |
205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.611-1594G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28594139 | |||||||
| chr10:28594168 | TTTTG | T | 58 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(55): Show |
58 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.611-1561_611-1558d others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28594168 | ||||||
| chr10:28594298 | T | C | 3 | a0001c0001t0006g0295 a0001c0001t0006g0299 a0001c0001t0006g0300 |
3 | HG02965.hp2 HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.611-1435T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28594298 | |||||||
| chr10:28594355 | T | A | 1 | a0001c0001t0008g0230 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.611-1378T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28594355 | |||||||
| chr10:28594408 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.611-1325A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28594408 | |||||||
| chr10:28594486 | T | C | 1 | a0001c0001t0002g0037 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.611-1247T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28594486 | |||||||
| chr10:28595214 | A | T | 1 | a0001c0001t0054g0094 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.611-519A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28595214 | |||||||
| chr10:28595385 | T | A | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.611-348T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28595385 | |||||||
| chr10:28595396 | A | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.611-337A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28595396 | |||||||
| chr10:28595420 | AT | A | 11 | a0001c0001t0001g0072 a0001c0001t0001g0121 a0001c0001t0001g0123 others(8): Show |
11 | HG00558.hp1 HG01192.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.611-301delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28595420 | ||||||
| chr10:28595420 | ATT | A | 59 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.611-302_611-301del others(2): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28595420 | ||||||
| chr10:28595431 | T | G | 5 | a0001c0001t0005g0243 a0001c0001t0025g0245 a0001c0001t0035g0225 others(2): Show |
5 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(2): Show |
intron_variant | MODIFIER | c.611-302T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28595431 | |||||||
| chr10:28595433 | G | A | 285 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.611-300G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28595433 | |||||||
| chr10:28595566 | T | A | 1 | a0001c0001t0047g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.611-167T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28595566 | |||||||
| chr10:28595700 | C | G | 2 | a0001c0001t0001g0158 a0001c0001t0043g0109 |
2 | NA19000.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.611-33C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28595700 | |||||||
| chr10:28596142 | A | G | 2 | a0001c0001t0005g0235 a0001c0001t0005g0247 |
2 | HG01361.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.919+101A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28596142 | |||||||
| chr10:28596313 | G | A | 1 | a0001c0001t0004g0274 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.919+272G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28596313 | |||||||
| chr10:28596392 | TCTTAATA | T | 3 | a0001c0001t0007g0216 a0001c0001t0022g0152 a0001c0001t0022g0183 |
3 | HG00673.hp2 NA18952.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.919+359_919+365del others(7): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28596392 | ||||||
| chr10:28596484 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.919+443G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28596484 | |||||||
| chr10:28596583 | T | G | 1 | a0001c0001t0005g0244 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.919+542T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28596583 | |||||||
| chr10:28596604 | T | A | 1 | a0001c0001t0002g0015 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.919+563T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28596604 | |||||||
| chr10:28596670 | A | C | 1 | a0001c0001t0012g0317 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.919+629A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28596670 | |||||||
| chr10:28596693 | A | G | 5 | a0001c0001t0001g0119 a0001c0001t0001g0161 a0001c0001t0019g0117 others(2): Show |
5 | HG00642.hp1 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+652A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28596693 | |||||||
| chr10:28596745 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.919+704G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28596745 | |||||||
| chr10:28596746 | T | C | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.919+705T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28596746 | |||||||
| chr10:28596859 | C | G | 3 | a0001c0001t0001g0196 a0001c0001t0001g0199 a0001c0001t0001g0219 |
3 | HG01243.hp1 HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.919+818C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28596859 | |||||||
| chr10:28597056 | CAT | C | 15 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(12): Show |
16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.919+1016_919+1017d others(4): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28597056 | |||||||
| chr10:28597066 | G | A | 15 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(12): Show |
16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.919+1025G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28597066 | |||||||
| chr10:28597067 | CATGTAAT others(8): Show |
C | 1 | a0001c0001t0012g0031 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.919+1032_919+1046d others(17): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28597067 | ||||||
| chr10:28597118 | T | G | 3 | a0001c0001t0003g0092 a0001c0001t0003g0096 a0001c0001t0044g0075 |
3 | HG02523.hp1 NA18943.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.919+1077T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28597118 | |||||||
| chr10:28597225 | A | C | 9 | a0001c0001t0001g0119 a0001c0001t0001g0161 a0001c0001t0001g0194 others(6): Show |
9 | HG00642.hp1 HG02109.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+1184A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28597225 | |||||||
| chr10:28597409 | A | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.919+1368A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28597409 | |||||||
| chr10:28597518 | A | G | 1 | a0001c0001t0020g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.919+1477A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28597518 | |||||||
| chr10:28597608 | A | G | 67 | a0001c0001t0003g0076 a0001c0001t0003g0079 a0001c0001t0003g0080 others(64): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.919+1567A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28597608 | |||||||
| chr10:28597697 | G | A | 70 | a0001c0001t0003g0076 a0001c0001t0003g0079 a0001c0001t0003g0080 others(67): Show |
70 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.919+1656G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28597697 | |||||||
| chr10:28597757 | G | A | 1 | a0001c0002t0009g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.919+1716G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28597757 | |||||||
| chr10:28597882 | G | C | 4 | a0001c0001t0006g0297 a0001c0001t0006g0298 a0001c0001t0006g0302 others(1): Show |
4 | HG01099.hp2 HG02129.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+1841G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28597882 | |||||||
| chr10:28598128 | C | T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.919+2087C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28598128 | |||||||
| chr10:28598153 | T | A | 1 | a0001c0001t0001g0141 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.919+2112T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28598153 | |||||||
| chr10:28598158 | C | T | 2 | a0001c0001t0004g0309 a0001c0001t0010g0308 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.919+2117C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28598158 | |||||||
| chr10:28598263 | C | T | 122 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(119): Show |
122 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.919+2222C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28598263 | |||||||
| chr10:28598339 | T | G | 4 | a0001c0001t0014g0070 a0001c0001t0014g0254 a0001c0001t0014g0255 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+2298T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28598339 | |||||||
| chr10:28598348 | CTT | C | 15 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(12): Show |
16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.919+2309_919+2310d others(4): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28598348 | ||||||
| chr10:28598431 | A | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.919+2390A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28598431 | |||||||
| chr10:28598746 | C | G | 1 | a0001c0001t0001g0166 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.919+2705C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28598746 | |||||||
| chr10:28598788 | G | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG00735.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.919+2747G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28598788 | |||||||
| chr10:28598991 | A | T | 1 | a0001c0001t0005g0236 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.919+2950A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28598991 | |||||||
| chr10:28599087 | AT | A | 59 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.919+3054delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28599087 | ||||||
| chr10:28599133 | C | T | 1 | a0001c0001t0008g0230 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.919+3092C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28599133 | |||||||
| chr10:28599221 | A | G | 2 | a0001c0001t0004g0270 a0001c0001t0010g0271 |
2 | HG00323.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.919+3180A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28599221 | |||||||
| chr10:28599510 | A | G | 1 | a0001c0001t0001g0125 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.919+3469A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28599510 | |||||||
| chr10:28599616 | G | C | 9 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(6): Show |
9 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.919+3575G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28599616 | |||||||
| chr10:28599672 | G | A | 3 | a0001c0001t0016g0310 a0001c0001t0016g0311 a0001c0001t0016g0312 |
3 | HG00639.hp1 HG01175.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.919+3631G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28599672 | |||||||
| chr10:28599762 | T | C | 2 | a0001c0001t0004g0261 a0001c0001t0008g0226 |
2 | HG01099.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.919+3721T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28599762 | |||||||
| chr10:28599911 | G | C | 285 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.919+3870G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28599911 | |||||||
| chr10:28599960 | A | C | 285 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.919+3919A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28599960 | |||||||
| chr10:28600227 | TACTC | T | 121 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(118): Show |
121 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.919+4189_919+4192d others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28600227 | ||||||
| chr10:28600268 | AGTC | A | 15 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(12): Show |
16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.919+4230_919+4232d others(5): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28600268 | ||||||
| chr10:28600309 | A | G | 2 | a0001c0001t0004g0221 a0001c0005t0004g0220 |
2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.919+4268A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28600309 | |||||||
| chr10:28600759 | A | G | 1 | a0001c0001t0053g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.919+4718A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28600759 | |||||||
| chr10:28600945 | G | A | 4 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0115 others(1): Show |
4 | HG02145.hp1 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+4904G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28600945 | |||||||
| chr10:28600967 | T | C | 1 | a0001c0001t0012g0317 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.919+4926T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28600967 | |||||||
| chr10:28601119 | A | G | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0005t0004g0220 |
3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.919+5078A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28601119 | |||||||
| chr10:28601139 | T | A | 317 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(314): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.919+5098T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28601139 | |||||||
| chr10:28601231 | C | T | 121 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(118): Show |
121 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.919+5190C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28601231 | |||||||
| chr10:28601390 | A | G | 1 | a0001c0001t0010g0276 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.919+5349A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28601390 | |||||||
| chr10:28601648 | C | G | 1 | a0001c0001t0002g0027 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.919+5607C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28601648 | |||||||
| chr10:28601680 | C | T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.919+5639C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28601680 | |||||||
| chr10:28601755 | G | T | 3 | a0001c0004t0001g0127 a0001c0004t0021g0132 a0001c0004t0041g0154 |
3 | HG01069.hp1 HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.919+5714G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28601755 | |||||||
| chr10:28601942 | A | C | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.919+5901A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28601942 | |||||||
| chr10:28602046 | C | T | 1 | a0001c0001t0053g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.919+6005C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28602046 | |||||||
| chr10:28602245 | A | G | 68 | a0001c0001t0003g0073 a0001c0001t0003g0076 a0001c0001t0003g0079 others(65): Show |
68 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.920-5941A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28602245 | |||||||
| chr10:28602507 | A | G | 10 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(7): Show |
10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.920-5679A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28602507 | |||||||
| chr10:28602743 | G | A | 1 | a0001c0001t0020g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.920-5443G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28602743 | |||||||
| chr10:28602798 | G | A | 1 | a0001c0001t0005g0252 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.920-5388G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28602798 | |||||||
| chr10:28603207 | G | A | 3 | a0001c0001t0013g0193 a0001c0001t0013g0204 a0001c0001t0034g0273 |
3 | HG02922.hp1 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.920-4979G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603207 | |||||||
| chr10:28603255 | T | C | 1 | a0001c0001t0013g0122 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.920-4931T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603255 | |||||||
| chr10:28603426 | G | T | 1 | a0001c0001t0003g0098 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.920-4760G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603426 | |||||||
| chr10:28603704 | A | G | 1 | a0001c0002t0009g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.920-4482A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603704 | |||||||
| chr10:28603826 | C | T | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0005t0004g0220 |
3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.920-4360C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603826 | |||||||
| chr10:28603846 | A | G | 1 | a0001c0001t0048g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.920-4340A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603846 | |||||||
| chr10:28603938 | AAAAAATA others(39): Show |
A | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0005t0004g0220 |
3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.920-4246_920-4201d others(48): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603938 | ||||||
| chr10:28603940 | A | T | 1 | a0001c0001t0005g0247 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.920-4246A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603940 | |||||||
| chr10:28603942 | A | T | 1 | a0001c0001t0005g0247 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.920-4244A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603942 | |||||||
| chr10:28603942 | AATATATA others(13): Show |
A | 2 | a0001c0001t0001g0219 a0001c0001t0002g0040 |
2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.920-4233_920-4214d others(22): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603942 | ||||||
| chr10:28603942 | AATATATA others(15): Show |
A | 9 | a0001c0001t0001g0120 a0001c0001t0001g0172 a0001c0001t0001g0177 others(6): Show |
9 | HG01069.hp1 HG01123.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.920-4233_920-4212d others(24): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603942 | ||||||
| chr10:28603942 | AATATATA others(17): Show |
A | 40 | a0001c0001t0001g0069 a0001c0001t0001g0111 a0001c0001t0001g0112 others(37): Show |
40 | HG00639.hp2 HG00673.hp2 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.920-4233_920-4210d others(26): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603942 | ||||||
| chr10:28603942 | AATATATA others(19): Show |
A | 1 | a0001c0001t0012g0025 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.920-4233_920-4208d others(28): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603942 | ||||||
| chr10:28603942 | AATATATA others(23): Show |
A | 3 | a0001c0001t0006g0297 a0001c0001t0014g0255 a0001c0001t0014g0256 |
3 | HG02145.hp2 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.920-4233_920-4204d others(32): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603942 | ||||||
| chr10:28603942 | AATATATA others(25): Show |
A | 11 | a0001c0001t0006g0002 a0001c0001t0006g0293 a0001c0001t0006g0295 others(8): Show |
12 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.920-4233_920-4202d others(34): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603942 | ||||||
| chr10:28603943 | ATATATAT others(8): Show |
A | 4 | a0001c0001t0003g0081 a0001c0001t0003g0092 a0001c0001t0044g0075 others(1): Show |
4 | HG01934.hp2 HG03927.hp1 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.920-4242_920-4228d others(17): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603943 | |||||||
| chr10:28603943 | ATATATAT others(10): Show |
A | 2 | a0001c0001t0004g0279 a0001c0001t0042g0275 |
2 | HG01168.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.920-4242_920-4226d others(19): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603943 | |||||||
| chr10:28603943 | ATATATAT others(11): Show |
A | 4 | a0001c0001t0001g0121 a0001c0001t0001g0138 a0001c0001t0001g0199 others(1): Show |
4 | HG01243.hp1 HG02572.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-4233_920-4216d others(20): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603943 | ||||||
| chr10:28603943 | ATATATAT others(12): Show |
A | 17 | a0001c0001t0001g0119 a0001c0001t0001g0147 a0001c0001t0001g0161 others(14): Show |
17 | HG00280.hp2 HG00597.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.920-4242_920-4224d others(21): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603943 | |||||||
| chr10:28603943 | ATATATAT others(14): Show |
A | 32 | a0001c0001t0001g0067 a0001c0001t0001g0110 a0001c0001t0001g0133 others(29): Show |
32 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.920-4242_920-4222d others(23): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603943 | |||||||
| chr10:28603943 | ATATATAT others(16): Show |
A | 55 | a0001c0001t0001g0108 a0001c0001t0001g0116 a0001c0001t0001g0118 others(52): Show |
55 | HG00140.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.920-4242_920-4220d others(25): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603943 | |||||||
| chr10:28603943 | ATATATAT others(18): Show |
A | 63 | a0001c0001t0001g0072 a0001c0001t0001g0145 a0001c0001t0001g0179 others(60): Show |
63 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.920-4242_920-4218d others(27): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603943 | |||||||
| chr10:28603943 | ATATATAT others(20): Show |
A | 1 | a0001c0001t0047g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.920-4242_920-4216d others(29): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603943 | |||||||
| chr10:28603943 | ATATATAT others(24): Show |
A | 5 | a0001c0001t0006g0292 a0001c0001t0010g0276 a0001c0001t0014g0070 others(2): Show |
5 | HG00099.hp2 HG02109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.920-4242_920-4212d others(33): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603943 | |||||||
| chr10:28603943 | ATATATAT others(26): Show |
A | 1 | a0001c0001t0006g0300 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.920-4242_920-4210d others(35): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603943 | |||||||
| chr10:28603943 | ATATATAT others(30): Show |
A | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.920-4242_920-4206d others(39): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603943 | |||||||
| chr10:28603944 | T | A | 31 | a0001c0001t0001g0150 a0001c0001t0001g0157 a0001c0001t0001g0175 others(28): Show |
31 | HG00735.hp1 HG00735.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.920-4242T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603944 | |||||||
| chr10:28603945 | ATATATAT others(6): Show |
A | 2 | a0001c0001t0003g0082 a0001c0001t0003g0320 |
2 | NA18954.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.920-4240_920-4228d others(15): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603945 | |||||||
| chr10:28603945 | ATATATAT others(9): Show |
A | 5 | a0001c0001t0001g0150 a0001c0001t0001g0157 a0001c0001t0001g0175 others(2): Show |
5 | HG02647.hp1 HG02647.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.920-4233_920-4218d others(18): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603945 | ||||||
| chr10:28603945 | ATATATAT others(10): Show |
A | 10 | a0001c0001t0001g0188 a0001c0001t0001g0214 a0001c0001t0001g0215 others(7): Show |
10 | HG00735.hp1 HG01975.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.920-4240_920-4224d others(19): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603945 | |||||||
| chr10:28603946 | T | A | 13 | a0001c0001t0003g0096 a0001c0001t0004g0148 a0001c0001t0013g0204 others(10): Show |
13 | HG00735.hp2 HG01496.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.920-4240T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603946 | |||||||
| chr10:28603947 | ATATATGT others(4): Show |
A | 2 | a0001c0001t0017g0078 a0001c0001t0019g0117 |
2 | HG01496.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.920-4238_920-4228d others(13): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603947 | |||||||
| chr10:28603947 | ATATATGT others(8): Show |
A | 8 | a0001c0001t0003g0096 a0001c0001t0004g0148 a0001c0001t0013g0204 others(5): Show |
8 | HG00735.hp2 HG01928.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.920-4238_920-4224d others(17): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603947 | |||||||
| chr10:28603948 | T | A | 3 | a0001c0001t0024g0178 a0001c0001t0034g0273 a0001c0002t0009g0074 |
3 | HG03098.hp1 NA18906.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.920-4238T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603948 | |||||||
| chr10:28603949 | ATATGTAT others(6): Show |
A | 1 | a0001c0001t0024g0178 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.920-4236_920-4224d others(15): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603949 | |||||||
| chr10:28603957 | G | A | 1 | a0001c0001t0003g0086 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.920-4229G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603957 | |||||||
| chr10:28603958 | T | A | 1 | a0001c0002t0009g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.920-4228T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603958 | |||||||
| chr10:28603960 | T | A | 7 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0092 others(4): Show |
7 | HG01934.hp2 HG03098.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.920-4226T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603960 | |||||||
| chr10:28603961 | G | A | 14 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0086 others(11): Show |
14 | HG01168.hp2 HG01496.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.920-4225G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603961 | |||||||
| chr10:28603961 | GTA | G | 15 | a0001c0001t0005g0001 a0001c0001t0005g0235 a0001c0001t0005g0237 others(12): Show |
16 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.920-4199_920-4198d others(4): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603961 | ||||||
| chr10:28603962 | T | A | 10 | a0001c0001t0001g0121 a0001c0001t0001g0138 a0001c0001t0001g0150 others(7): Show |
10 | HG01243.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.920-4224T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603962 | |||||||
| chr10:28603963 | A | ATATATAT others(19): Show |
1 | a0001c0001t0005g0233 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.920-4200_920-4199i others(28): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603963 | ||||||
| chr10:28603963 | A | G | 1 | a0002c0003t0008g0223 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.920-4223A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603963 | |||||||
| chr10:28603964 | T | A | 40 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0138 others(37): Show |
40 | HG00642.hp1 HG00735.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.920-4222T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603964 | |||||||
| chr10:28603965 | A | ATATATAT others(17): Show |
1 | a0001c0001t0005g0224 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.920-4200_920-4199i others(26): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603965 | ||||||
| chr10:28603966 | T | A | 73 | a0001c0001t0001g0067 a0001c0001t0001g0110 a0001c0001t0001g0119 others(70): Show |
73 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.920-4220T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603966 | |||||||
| chr10:28603968 | T | A | 152 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0108 others(149): Show |
152 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.920-4218T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603968 | |||||||
| chr10:28603970 | T | A | 191 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(188): Show |
191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.920-4216T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603970 | |||||||
| chr10:28603972 | T | A | 160 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(157): Show |
160 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.920-4214T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603972 | |||||||
| chr10:28603974 | T | A | 122 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0111 others(119): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.920-4212T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603974 | |||||||
| chr10:28603975 | ATATATAT others(7): Show |
A | 2 | a0001c0001t0005g0236 a0001c0001t0005g0252 |
2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.920-4197_920-4184d others(16): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603975 | ||||||
| chr10:28603976 | T | A | 87 | a0001c0001t0001g0072 a0001c0001t0001g0130 a0001c0001t0001g0145 others(84): Show |
88 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.920-4210T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603976 | |||||||
| chr10:28603977 | A | G | 1 | a0002c0003t0008g0223 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.920-4209A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603977 | |||||||
| chr10:28603978 | T | A | 61 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(58): Show |
62 | HG00280.hp1 HG00323.hp2 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.920-4208T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603978 | |||||||
| chr10:28603978 | T | C | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG00735.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.920-4208T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603978 | |||||||
| chr10:28603980 | T | A | 19 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(16): Show |
20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.920-4206T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603980 | |||||||
| chr10:28603982 | T | A | 20 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(17): Show |
21 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.920-4204T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603982 | |||||||
| chr10:28603984 | T | A | 16 | a0001c0001t0006g0002 a0001c0001t0006g0293 a0001c0001t0006g0295 others(13): Show |
17 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.920-4202T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603984 | |||||||
| chr10:28603986 | T | A | 4 | a0001c0001t0014g0070 a0001c0001t0014g0254 a0001c0001t0014g0255 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-4200T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603986 | |||||||
| chr10:28603988 | T | A | 4 | a0001c0001t0014g0070 a0001c0001t0014g0254 a0001c0001t0014g0255 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-4198T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603988 | |||||||
| chr10:28603989 | G | A | 291 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(288): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.920-4197G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603989 | |||||||
| chr10:28603991 | A | G | 2 | a0001c0001t0005g0224 a0001c0001t0005g0233 |
2 | HG02738.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.920-4195A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603991 | |||||||
| chr10:28604125 | T | C | 1 | a0001c0001t0020g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.920-4061T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604125 | |||||||
| chr10:28604177 | C | T | 62 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(59): Show |
62 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.920-4009C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604177 | |||||||
| chr10:28604182 | T | G | 7 | a0001c0001t0010g0285 a0001c0001t0010g0287 a0001c0001t0010g0288 others(4): Show |
7 | HG00609.hp1 HG02451.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.920-4004T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604182 | |||||||
| chr10:28604196 | G | C | 5 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0023 others(2): Show |
5 | NA18948.hp1 NA18964.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.920-3990G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604196 | |||||||
| chr10:28604198 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.920-3988C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604198 | |||||||
| chr10:28604238 | G | GT | 14 | a0001c0001t0001g0141 a0001c0001t0001g0172 a0001c0001t0001g0175 others(11): Show |
14 | HG00438.hp1 HG00621.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.920-3934dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28604238 | ||||||
| chr10:28604266 | A | G | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0005t0004g0220 |
3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.920-3920A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604266 | |||||||
| chr10:28604368 | C | T | 1 | a0001c0001t0005g0236 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.920-3818C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604368 | |||||||
| chr10:28604442 | TACA | T | 34 | a0001c0001t0003g0073 a0001c0001t0003g0076 a0001c0001t0003g0079 others(31): Show |
34 | HG00597.hp1 HG00597.hp2 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.920-3739_920-3737d others(5): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28604442 | ||||||
| chr10:28604507 | A | G | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0005t0004g0220 |
3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.920-3679A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604507 | |||||||
| chr10:28604562 | T | C | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.920-3624T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604562 | |||||||
| chr10:28604625 | G | A | 68 | a0001c0001t0003g0076 a0001c0001t0003g0079 a0001c0001t0003g0080 others(65): Show |
68 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.920-3561G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604625 | |||||||
| chr10:28604685 | G | A | 223 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(220): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.920-3501G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604685 | |||||||
| chr10:28604790 | A | C | 19 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(16): Show |
20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.920-3396A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604790 | |||||||
| chr10:28604796 | T | C | 2 | a0001c0001t0010g0287 a0001c0001t0051g0286 |
2 | NA19003.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.920-3390T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604796 | |||||||
| chr10:28604999 | G | A | 1 | a0001c0002t0009g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.920-3187G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604999 | |||||||
| chr10:28605139 | C | T | 1 | a0001c0001t0014g0256 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.920-3047C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28605139 | |||||||
| chr10:28605181 | A | G | 26 | a0001c0001t0004g0148 a0001c0001t0004g0257 a0001c0001t0004g0258 others(23): Show |
26 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.920-3005A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28605181 | |||||||
| chr10:28605306 | A | G | 1 | a0001c0001t0048g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.920-2880A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28605306 | |||||||
| chr10:28605318 | C | T | 69 | a0001c0001t0003g0073 a0001c0001t0003g0076 a0001c0001t0003g0079 others(66): Show |
69 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.920-2868C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28605318 | |||||||
| chr10:28605366 | G | A | 121 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(118): Show |
121 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.920-2820G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28605366 | |||||||
| chr10:28605650 | G | A | 2 | a0001c0001t0006g0301 a0001c0001t0006g0303 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.920-2536G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28605650 | |||||||
| chr10:28605725 | C | T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.920-2461C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28605725 | |||||||
| chr10:28605893 | A | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.920-2293A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28605893 | |||||||
| chr10:28605937 | G | A | 10 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(7): Show |
10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.920-2249G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28605937 | |||||||
| chr10:28606055 | GT | G | 281 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(278): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.920-2117delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28606055 | ||||||
| chr10:28606058 | T | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0219 |
2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.920-2128T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28606058 | |||||||
| chr10:28606120 | C | T | 4 | a0001c0001t0014g0070 a0001c0001t0014g0254 a0001c0001t0014g0255 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-2066C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28606120 | |||||||
| chr10:28606240 | C | T | 1 | a0001c0001t0040g0174 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.920-1946C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28606240 | |||||||
| chr10:28606288 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.920-1898A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28606288 | |||||||
| chr10:28606315 | C | T | 9 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0052 others(6): Show |
9 | HG00280.hp1 HG01109.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-1871C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28606315 | |||||||
| chr10:28606316 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.920-1870G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28606316 | |||||||
| chr10:28606320 | G | A | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.920-1866G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28606320 | |||||||
| chr10:28606433 | A | G | 1 | a0001c0001t0020g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.920-1753A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28606433 | |||||||
| chr10:28606437 | T | A | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.920-1749T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28606437 | |||||||
| chr10:28606457 | C | T | 1 | a0001c0001t0003g0079 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.920-1729C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28606457 | |||||||
| chr10:28607015 | C | T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.920-1171C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28607015 | |||||||
| chr10:28607017 | G | A | 123 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(120): Show |
123 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.920-1169G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28607017 | |||||||
| chr10:28607121 | C | T | 1 | a0001c0001t0020g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.920-1065C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28607121 | |||||||
| chr10:28607488 | G | A | 285 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.920-698G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28607488 | |||||||
| chr10:28607699 | G | T | 1 | a0001c0001t0002g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.920-487G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28607699 | |||||||
| chr10:28608108 | A | G | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0005t0004g0220 |
3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.920-78A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28608108 | |||||||
| chr10:28608121 | C | T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.920-65C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28608121 | |||||||
| chr10:28608158 | T | G | 8 | a0001c0001t0001g0118 a0001c0001t0001g0196 a0001c0001t0001g0197 others(5): Show |
8 | HG01192.hp1 HG01243.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.920-28T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28608158 | |||||||
| chr10:28608719 | G | A | 1 | a0001c0001t0005g0243 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1165+288G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28608719 | |||||||
| chr10:28608756 | G | A | 203 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(200): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.1165+325G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28608756 | |||||||
| chr10:28608990 | G | A | 19 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(16): Show |
20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.1165+559G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28608990 | |||||||
| chr10:28609128 | G | A | 4 | a0001c0001t0014g0070 a0001c0001t0014g0254 a0001c0001t0014g0255 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1165+697G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28609128 | |||||||
| chr10:28609133 | G | A | 1 | a0001c0002t0009g0103 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1165+702G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28609133 | |||||||
| chr10:28609168 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1165+737C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28609168 | |||||||
| chr10:28609298 | G | A | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1165+867G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28609298 | |||||||
| chr10:28609327 | C | T | 1 | a0001c0001t0005g0236 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1165+896C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28609327 | |||||||
| chr10:28609448 | T | C | 3 | a0001c0001t0011g0134 a0001c0001t0011g0167 a0001c0001t0029g0066 |
3 | NA18964.hp2 NA18972.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1165+1017T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28609448 | |||||||
| chr10:28609495 | T | TA | 33 | a0001c0001t0004g0148 a0001c0001t0004g0257 a0001c0001t0004g0258 others(30): Show |
33 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.1165+1065dupA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 28609495 | ||||||
| chr10:28609608 | G | C | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1166-1091G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28609608 | |||||||
| chr10:28609746 | C | T | 203 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(200): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.1166-953C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28609746 | |||||||
| chr10:28609926 | C | CT | 95 | a0001c0001t0001g0170 a0001c0001t0002g0013 a0001c0001t0002g0014 others(92): Show |
96 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.1166-752dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 28609926 | ||||||
| chr10:28609926 | C | CTT | 15 | a0001c0001t0002g0037 a0001c0001t0002g0040 a0001c0001t0003g0089 others(12): Show |
15 | HG00609.hp2 HG01243.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1166-753_1166-752d others(4): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 28609926 | ||||||
| chr10:28609926 | C | CTTT | 8 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(5): Show |
8 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1166-754_1166-752d others(5): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 28609926 | ||||||
| chr10:28609926 | CT | C | 21 | a0001c0001t0001g0069 a0001c0001t0001g0121 a0001c0001t0001g0123 others(18): Show |
21 | HG00639.hp2 HG01167.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.1166-752delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 28609926 | ||||||
| chr10:28610170 | C | T | 193 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(190): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1166-529C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28610170 | |||||||
| chr10:28610277 | T | C | 2 | a0001c0001t0005g0224 a0001c0001t0005g0233 |
2 | HG02738.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1166-422T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28610277 | |||||||
| chr10:28610283 | T | A | 1 | a0001c0001t0047g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1166-416T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28610283 | |||||||
| chr10:28610306 | G | A | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1166-393G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28610306 | |||||||
| chr10:28610394 | T | C | 285 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1166-305T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28610394 | |||||||
| chr10:28610541 | G | T | 19 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(16): Show |
20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.1166-158G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28610541 | |||||||
| chr10:28610855 | G | T | 1 | a0001c0001t0001g0200 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1288+34G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 9/13 | chr10 | 28610855 | |||||||
| chr10:28610856 | C | T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1288+35C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 9/13 | chr10 | 28610856 | |||||||
| chr10:28610889 | T | C | 2 | a0001c0001t0002g0050 a0001c0001t0002g0062 |
2 | HG00621.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.1288+68T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 9/13 | chr10 | 28610889 | |||||||
| chr10:28610912 | A | AT | 193 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(190): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1288+102dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 28610912 | ||||||
| chr10:28610918 | T | C | 10 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(7): Show |
10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1288+97T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 9/13 | chr10 | 28610918 | |||||||
| chr10:28610984 | A | G | 1 | a0001c0001t0020g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1288+163A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 9/13 | chr10 | 28610984 | |||||||
| chr10:28611072 | G | A | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1288+251G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 9/13 | chr10 | 28611072 | |||||||
| chr10:28611397 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1289-377G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 9/13 | chr10 | 28611397 | |||||||
| chr10:28611727 | G | T | 1 | a0001c0001t0002g0032 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1289-47G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 9/13 | chr10 | 28611727 | |||||||
| chr10:28612083 | A | C | 36 | a0001c0001t0003g0073 a0001c0001t0003g0076 a0001c0001t0003g0079 others(33): Show |
36 | HG00597.hp1 HG00597.hp2 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.1437+161A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28612083 | |||||||
| chr10:28612180 | A | C | 1 | a0001c0001t0001g0195 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1437+258A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28612180 | |||||||
| chr10:28612221 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1437+299A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28612221 | |||||||
| chr10:28612379 | A | G | 1 | a0001c0001t0002g0058 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1437+457A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28612379 | |||||||
| chr10:28612692 | TC | T | 58 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(55): Show |
58 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1437+773delC | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr10 | 28612692 | ||||||
| chr10:28612700 | G | C | 2 | a0001c0001t0002g0011 a0001c0001t0002g0012 |
2 | HG00280.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1437+778G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28612700 | |||||||
| chr10:28613052 | C | T | 1 | a0001c0001t0005g0246 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1437+1130C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613052 | |||||||
| chr10:28613056 | A | G | 1 | a0001c0001t0003g0098 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1437+1134A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613056 | |||||||
| chr10:28613142 | C | T | 1 | a0001c0001t0058g0054 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1437+1220C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613142 | |||||||
| chr10:28613170 | C | T | 19 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(16): Show |
20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.1437+1248C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613170 | |||||||
| chr10:28613194 | C | T | 1 | a0001c0001t0002g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1437+1272C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613194 | |||||||
| chr10:28613222 | C | T | 1 | a0001c0001t0047g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1437+1300C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613222 | |||||||
| chr10:28613253 | G | T | 1 | a0001c0001t0047g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1438-1314G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613253 | |||||||
| chr10:28613294 | A | T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1438-1273A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613294 | |||||||
| chr10:28613299 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1438-1268G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613299 | |||||||
| chr10:28613332 | C | T | 206 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(203): Show |
206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.1438-1235C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613332 | |||||||
| chr10:28613339 | C | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1438-1228C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613339 | |||||||
| chr10:28613543 | T | C | 1 | a0001c0001t0033g0153 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1438-1024T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613543 | |||||||
| chr10:28613689 | T | G | 123 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(120): Show |
123 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.1438-878T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613689 | |||||||
| chr10:28613711 | C | G | 3 | a0001c0001t0001g0196 a0001c0001t0001g0199 a0001c0001t0001g0219 |
3 | HG01243.hp1 HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1438-856C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613711 | |||||||
| chr10:28613924 | A | G | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1438-643A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613924 | |||||||
| chr10:28614191 | C | T | 1 | a0001c0001t0046g0151 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1438-376C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28614191 | |||||||
| chr10:28614233 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1438-334G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28614233 | |||||||
| chr10:28614246 | C | T | 6 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | NA18969.hp1 NA18984.hp1 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.1438-321C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28614246 | |||||||
| chr10:28614271 | A | G | 1 | a0001c0001t0006g0293 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1438-296A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28614271 | |||||||
| chr10:28614307 | G | GTGTTAGC others(5): Show |
2 | a0001c0001t0001g0182 a0001c0001t0045g0280 |
2 | HG00642.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1438-258_1438-257i others(14): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr10 | 28614307 | ||||||
| chr10:28614345 | G | A | 4 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0115 others(1): Show |
4 | HG02145.hp1 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1438-222G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28614345 | |||||||
| chr10:28614395 | A | AGTTTCTT others(6): Show |
1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1438-168_1438-167i others(15): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr10 | 28614395 | ||||||
| chr10:28614471 | G | GTCTTCTT others(7): Show |
285 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1438-96_1438-95ins others(14): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28614471 | |||||||
| chr10:28614735 | A | G | 1 | a0001c0001t0005g0236 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1556+50A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 11/13 | chr10 | 28614735 | |||||||
| chr10:28614839 | C | T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1556+154C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 11/13 | chr10 | 28614839 | |||||||
| chr10:28614842 | G | A | 206 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(203): Show |
206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.1556+157G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 11/13 | chr10 | 28614842 | |||||||
| chr10:28615000 | C | G | 6 | a0001c0001t0001g0067 a0001c0001t0001g0110 a0001c0001t0001g0166 others(3): Show |
6 | HG01255.hp1 HG01257.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.1556+315C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 11/13 | chr10 | 28615000 | |||||||
| chr10:28615158 | C | T | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1556+473C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 11/13 | chr10 | 28615158 | |||||||
| chr10:28615761 | C | G | 5 | a0001c0001t0001g0116 a0001c0001t0001g0155 a0001c0001t0001g0186 others(2): Show |
5 | HG02451.hp1 HG02976.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1557-412C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 11/13 | chr10 | 28615761 | |||||||
| chr10:28616150 | A | G | 69 | a0001c0001t0003g0073 a0001c0001t0003g0076 a0001c0001t0003g0079 others(66): Show |
69 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.1557-23A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 11/13 | chr10 | 28616150 | |||||||
| chr10:28616520 | T | C | 5 | a0001c0001t0008g0226 a0002c0003t0008g0068 a0002c0003t0008g0223 others(2): Show |
5 | HG01123.hp2 HG02723.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1746+158T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 12/13 | chr10 | 28616520 | |||||||
| chr10:28616751 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1746+389A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 12/13 | chr10 | 28616751 | |||||||
| chr10:28616824 | T | A | 1 | a0001c0001t0020g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1746+462T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 12/13 | chr10 | 28616824 | |||||||
| chr10:28617082 | C | G | 2 | a0001c0001t0002g0047 a0001c0001t0012g0048 |
2 | HG00099.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.1747-575C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 12/13 | chr10 | 28617082 | |||||||
| chr10:28617090 | C | CA | 9 | a0001c0001t0001g0170 a0001c0001t0001g0281 a0001c0001t0002g0022 others(6): Show |
9 | HG00735.hp2 HG01361.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.1747-558dupA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 28617090 | ||||||
| chr10:28617105 | C | G | 1 | a0001c0001t0002g0015 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1747-552C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 12/13 | chr10 | 28617105 | |||||||
| chr10:28617217 | T | C | 1 | a0001c0001t0020g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1747-440T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 12/13 | chr10 | 28617217 | |||||||
| chr10:28617252 | GT | G | 4 | a0001c0001t0003g0081 a0001c0001t0017g0077 a0001c0001t0017g0078 others(1): Show |
4 | HG01496.hp1 HG01928.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1747-402delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 28617252 | ||||||
| chr10:28617442 | T | C | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0005t0004g0220 |
3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1747-215T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 12/13 | chr10 | 28617442 | |||||||
| chr10:28617518 | G | A | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1747-139G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 12/13 | chr10 | 28617518 | |||||||
| chr10:28617897 | A | T | 1 | a0001c0001t0002g0033 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1874+113A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28617897 | |||||||
| chr10:28617960 | C | T | 1 | a0001c0001t0008g0230 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1874+176C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28617960 | |||||||
| chr10:28618020 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1874+236G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28618020 | |||||||
| chr10:28618221 | T | C | 286 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(283): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1874+437T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28618221 | |||||||
| chr10:28618267 | A | G | 19 | a0001c0001t0006g0002 a0001c0001t0006g0292 a0001c0001t0006g0293 others(16): Show |
20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.1874+483A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28618267 | |||||||
| chr10:28618366 | A | AG | 206 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(203): Show |
206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.1874+584dupG | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 28618366 | ||||||
| chr10:28618491 | C | T | 4 | a0001c0001t0003g0081 a0001c0001t0017g0077 a0001c0001t0017g0078 others(1): Show |
4 | HG01496.hp1 HG01928.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1874+707C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28618491 | |||||||
| chr10:28619066 | G | A | 1 | a0001c0001t0064g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1875-471G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28619066 | |||||||
| chr10:28619069 | A | G | 3 | a0001c0001t0004g0265 a0001c0001t0037g0260 a0001c0001t0056g0266 |
3 | HG01256.hp2 HG01361.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1875-468A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28619069 | |||||||
| chr10:28619104 | C | T | 2 | a0001c0001t0007g0180 a0001c0001t0024g0178 |
2 | HG02135.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.1875-433C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28619104 | |||||||
| chr10:28619183 | G | C | 1 | a0001c0001t0001g0120 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1875-354G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28619183 | |||||||
| chr10:28619184 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1875-353C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28619184 | |||||||
| chr10:28619212 | G | A | 37 | a0001c0001t0001g0069 a0001c0001t0001g0108 a0001c0001t0001g0120 others(34): Show |
37 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.1875-325G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28619212 | |||||||
| chr10:28619214 | A | T | 10 | a0001c0002t0009g0003 a0001c0002t0009g0004 a0001c0002t0009g0005 others(7): Show |
10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1875-323A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28619214 | |||||||
| chr10:28619245 | C | A | 285 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1875-292C>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28619245 | |||||||
| chr10:28619261 | C | T | 3 | a0001c0001t0014g0254 a0001c0001t0014g0255 a0001c0001t0014g0256 |
3 | HG02109.hp1 HG02145.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1875-276C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28619261 | |||||||
| chr10:28619413 | T | A | 196 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(193): Show |
196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1875-124T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28619413 | |||||||
| chr10:28619510 | G | T | 6 | a0001c0001t0002g0013 a0001c0001t0002g0016 a0001c0001t0002g0028 others(3): Show |
6 | HG01069.hp2 HG01358.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.1875-27G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28619510 |