| geneid | 5108 |
|---|---|
| ensemblid | ENSG00000078674.20 |
| hgncid | 8727 |
| symbol | PCM1 |
| name | pericentriolar material 1 |
| refseq_nuc | NM_006197.4 |
| refseq_prot | NP_006188.4 |
| ensembl_nuc | ENST00000325083.13 |
| ensembl_prot | ENSP00000327077.8 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 17922988 |
| end | 18029948 |
| strand | + |
| ver | v1.2 |
| region | chr8:17922988-18029948 |
| region5000 | chr8:17917988-18034948 |
| regionname0 | PCM1_chr8_17922988_18029948 |
| regionname5000 | PCM1_chr8_17917988_18034948 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 2024 | 103 | 13 | 15 | 51 | 6 | 16 | 43 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002 | 0/0 | 2024 | 84 | 27 | 23 | 19 | 6 | 9 | 12 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003 | 0/0 | 2024 | 70 | 2 | 12 | 52 | 3 | 1 | 39 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0004 | 0/0 | 2024 | 36 | 12 | 9 | 12 | 2 | 1 | 8 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0005 | 0/0 | 2024 | 20 | 20 | 0 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0006 | 0/0 | 2024 | 8 | 0 | 0 | 8 | 0 | 0 | 4 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0007 | 0/0 | 2024 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0008 | 0/0 | 2024 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0009 | 0/0 | 2024 | 4 | 0 | 0 | 3 | 1 | 0 | 3 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0010 | 0/0 | 2024 | 4 | 0 | 0 | 0 | 0 | 4 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0011 | 0/0 | 2035 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0012 | 0/0 | 2024 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0013 | 0/0 | 2024 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0014 | 0/0 | 2024 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0015 | 0/0 | 2024 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0016 | 0/0 | 2024 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0017 | 0/0 | 2024 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0018 | 0/0 | 2024 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0019 | 0/0 | 2024 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0020 | 0/0 | 2024 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0021 | 0/0 | 2024 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0022 | 0/0 | 2024 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0023 | 0/0 | 2024 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0024 | 0/0 | 2024 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0025 | 0/0 | 2024 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0026 | 0/0 | 2024 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0027 | 0/0 | 2024 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0028 | 0/0 | 2024 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0029 | 0/0 | 2024 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0030 | 0/0 | 2024 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0031 | 0/0 | 1729 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0032 | 0/0 | 2024 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 6075 | 99 | 12 | 15 | 48 | 6 | 16 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0002 | 0/0 | 6075 | 60 | 14 | 22 | 10 | 6 | 8 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0003 | 0/0 | 6075 | 52 | 2 | 9 | 38 | 3 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0004 | 0/0 | 6075 | 33 | 9 | 9 | 12 | 2 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0005 | 0/0 | 6075 | 20 | 20 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0006 | 0/0 | 6075 | 11 | 0 | 3 | 8 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0007 | 0/0 | 6075 | 9 | 1 | 0 | 7 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0008 | 0/0 | 6075 | 8 | 0 | 0 | 8 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0009 | 0/0 | 6075 | 7 | 7 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0010 | 0/0 | 6075 | 5 | 0 | 0 | 5 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0011 | 0/0 | 6075 | 5 | 5 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0012 | 0/0 | 6075 | 4 | 0 | 0 | 3 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0013 | 0/0 | 6075 | 4 | 0 | 0 | 3 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0014 | 0/0 | 6075 | 4 | 0 | 0 | 0 | 0 | 4 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0015 | 0/0 | 6075 | 3 | 0 | 0 | 3 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0016 | 0/0 | 6075 | 3 | 3 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0017 | 0/0 | 6075 | 3 | 2 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0018 | 0/0 | 6108 | 3 | 0 | 0 | 3 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0019 | 0/0 | 6075 | 2 | 0 | 0 | 2 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0020 | 0/0 | 6075 | 2 | 1 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0021 | 0/0 | 6075 | 2 | 2 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0022 | 0/0 | 6075 | 2 | 0 | 2 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0023 | 0/0 | 6075 | 2 | 2 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0024 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0025 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0026 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0027 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0028 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0029 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0030 | 0/0 | 6075 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0031 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0032 | 0/0 | 6075 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0033 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0034 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0035 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0036 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0037 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0038 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0039 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0040 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0041 | 0/0 | 6075 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0042 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0043 | 0/0 | 6075 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0044 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0045 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0046 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0047 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| c0048 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 2578 | 74 | 11 | 10 | 35 | 3 | 14 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0002 | 0/0 | 2571 | 41 | 0 | 9 | 30 | 2 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0003 | 0/0 | 2570 | 38 | 14 | 9 | 12 | 2 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0004 | 0/0 | 2568 | 33 | 4 | 3 | 20 | 2 | 4 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0005 | 0/0 | 2569 | 30 | 8 | 12 | 3 | 3 | 4 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0006 | 0/0 | 2579 | 15 | 0 | 1 | 13 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0007 | 0/0 | 2570 | 13 | 0 | 0 | 13 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0008 | 0/0 | 2568 | 8 | 8 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0009 | 0/0 | 2576 | 7 | 0 | 0 | 6 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0010 | 0/0 | 2578 | 6 | 0 | 2 | 0 | 4 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0011 | 0/0 | 2572 | 6 | 1 | 1 | 4 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0012 | 0/0 | 2570 | 6 | 1 | 4 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0013 | 0/0 | 2571 | 5 | 0 | 0 | 5 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0014 | 0/0 | 2569 | 5 | 5 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0015 | 0/0 | 2567 | 5 | 5 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0016 | 0/0 | 2575 | 5 | 5 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0017 | 0/0 | 2575 | 4 | 4 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0018 | 0/0 | 2576 | 3 | 3 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0019 | 0/0 | 2578 | 3 | 0 | 0 | 3 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0020 | 0/0 | 2575 | 3 | 2 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0021 | 0/0 | 2569 | 3 | 0 | 2 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0022 | 0/0 | 2571 | 2 | 0 | 0 | 0 | 0 | 2 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0023 | 0/0 | 2571 | 2 | 0 | 0 | 0 | 0 | 2 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0024 | 0/0 | 2578 | 2 | 0 | 0 | 2 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0025 | 0/0 | 2577 | 2 | 0 | 0 | 2 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0026 | 0/0 | 2569 | 2 | 1 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0027 | 0/0 | 2568 | 2 | 2 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0028 | 0/0 | 2571 | 2 | 1 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0029 | 0/0 | 2567 | 2 | 1 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0030 | 0/0 | 2579 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0031 | 0/0 | 2571 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0032 | 0/0 | 2567 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0033 | 0/0 | 2570 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0034 | 0/0 | 2570 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0035 | 0/0 | 2576 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0036 | 0/0 | 2568 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0037 | 0/0 | 2578 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0038 | 0/0 | 2578 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0039 | 0/1 | 2579 | 1 | 0 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0040 | 0/0 | 2577 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0041 | 0/0 | 2569 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0042 | 0/0 | 2577 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0043 | 0/0 | 2576 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0044 | 0/0 | 2569 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0045 | 0/0 | 2569 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0046 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0047 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0048 | 0/0 | 2567 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0049 | 0/0 | 2570 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0050 | 0/0 | 2570 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0051 | 0/0 | 2576 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0052 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0053 | 0/0 | 2573 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0054 | 0/0 | 2571 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0055 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0056 | 0/0 | 2575 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0057 | 0/0 | 2567 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0058 | 0/0 | 2568 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0059 | 0/0 | 2569 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0060 | 0/0 | 2569 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0061 | 0/0 | 2579 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0062 | 0/0 | 2579 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0063 | 0/0 | 2576 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0064 | 0/0 | 2572 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0065 | 0/0 | 2571 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0066 | 0/0 | 2571 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0067 | 0/0 | 2569 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| t0068 | 0/0 | 2570 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0009 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0063 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 6075 | 99 | 12 | 15 | 48 | 6 | 16 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0001c0024 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0001c0026 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0001c0047 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0001c0048 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0002 | 0/0 | 6075 | 60 | 14 | 22 | 10 | 6 | 8 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0007 | 0/0 | 6075 | 9 | 1 | 0 | 7 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0009 | 0/0 | 6075 | 7 | 7 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0017 | 0/0 | 6075 | 3 | 2 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0019 | 0/0 | 6075 | 2 | 0 | 0 | 2 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0021 | 0/0 | 6075 | 2 | 2 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0034 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0003 | 0/0 | 6075 | 52 | 2 | 9 | 38 | 3 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0006 | 0/0 | 6075 | 11 | 0 | 3 | 8 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0012 | 0/0 | 6075 | 4 | 0 | 0 | 3 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0038 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0040 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0044 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0004c0004 | 0/0 | 6075 | 33 | 9 | 9 | 12 | 2 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0004c0016 | 0/0 | 6075 | 3 | 3 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0005c0005 | 0/0 | 6075 | 20 | 20 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0006c0008 | 0/0 | 6075 | 8 | 0 | 0 | 8 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0007c0011 | 0/0 | 6075 | 5 | 5 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0008c0010 | 0/0 | 6075 | 5 | 0 | 0 | 5 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0009c0013 | 0/0 | 6075 | 4 | 0 | 0 | 3 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0010c0014 | 0/0 | 6075 | 4 | 0 | 0 | 0 | 0 | 4 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0011c0018 | 0/0 | 6108 | 3 | 0 | 0 | 3 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0012c0015 | 0/0 | 6075 | 3 | 0 | 0 | 3 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0013c0023 | 0/0 | 6075 | 2 | 2 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0014c0020 | 0/0 | 6075 | 2 | 1 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0015c0022 | 0/0 | 6075 | 2 | 0 | 2 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0016c0046 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0017c0027 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0018c0028 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0019c0025 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0020c0045 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0021c0043 | 0/0 | 6075 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0022c0029 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0023c0042 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0024c0033 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0025c0036 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0026c0032 | 0/0 | 6075 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0027c0031 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0028c0035 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0029c0037 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0030c0041 | 0/0 | 6075 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0031c0039 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0032c0030 | 0/0 | 6075 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 8652 | 64 | 6 | 10 | 30 | 3 | 14 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0001c0001t0002 | 0/0 | 8645 | 2 | 0 | 0 | 2 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0001c0001t0004 | 0/0 | 8642 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0001c0001t0006 | 0/0 | 8653 | 13 | 0 | 1 | 11 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0001c0001t0010 | 0/0 | 8652 | 5 | 0 | 2 | 0 | 3 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0001c0001t0017 | 0/0 | 8649 | 2 | 2 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0001c0001t0018 | 0/0 | 8650 | 3 | 3 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0001c0001t0024 | 0/0 | 8652 | 2 | 0 | 0 | 2 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0001c0001t0035 | 0/0 | 8650 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0001c0001t0037 | 0/0 | 8652 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0001c0001t0038 | 0/0 | 8652 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0001c0001t0039 | 0/1 | 8653 | 1 | 0 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0001c0001t0040 | 0/0 | 8651 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0001c0001t0061 | 0/0 | 8653 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0001c0001t0062 | 0/0 | 8653 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0001c0024t0017 | 0/0 | 8649 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0001c0026t0001 | 0/0 | 8652 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0001c0047t0006 | 0/0 | 8653 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0001c0048t0006 | 0/0 | 8653 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0002t0004 | 0/0 | 8642 | 17 | 3 | 2 | 7 | 2 | 3 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0002t0005 | 0/0 | 8643 | 26 | 6 | 11 | 2 | 3 | 4 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0002t0012 | 0/0 | 8644 | 5 | 1 | 3 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0002t0021 | 0/0 | 8643 | 3 | 0 | 2 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0002t0028 | 0/0 | 8645 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0002t0029 | 0/0 | 8641 | 2 | 1 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0002t0047 | 0/0 | 8642 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0002t0048 | 0/0 | 8641 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0002t0053 | 0/0 | 8647 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0002t0059 | 0/0 | 8643 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0002t0060 | 0/0 | 8643 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0002t0066 | 0/0 | 8645 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0007t0001 | 0/0 | 8652 | 2 | 0 | 0 | 2 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0007t0004 | 0/0 | 8642 | 5 | 1 | 0 | 4 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0007t0005 | 0/0 | 8643 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0007t0030 | 0/0 | 8653 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0009t0005 | 0/0 | 8643 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0009t0016 | 0/0 | 8649 | 3 | 3 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0009t0051 | 0/0 | 8650 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0009t0052 | 0/0 | 8648 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0009t0063 | 0/0 | 8650 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0017t0003 | 0/0 | 8644 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0017t0031 | 0/0 | 8645 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0017t0032 | 0/0 | 8641 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0019t0004 | 0/0 | 8642 | 2 | 0 | 0 | 2 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0021t0020 | 0/0 | 8649 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0021t0027 | 0/0 | 8642 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0002c0034t0057 | 0/0 | 8641 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0003t0002 | 0/0 | 8645 | 29 | 0 | 7 | 20 | 2 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0003t0007 | 0/0 | 8644 | 6 | 0 | 0 | 6 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0003t0009 | 0/0 | 8650 | 5 | 0 | 0 | 5 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0003t0011 | 0/0 | 8646 | 5 | 1 | 1 | 3 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0003t0013 | 0/0 | 8645 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0003t0026 | 0/0 | 8643 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0003t0036 | 0/0 | 8642 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0003t0043 | 0/0 | 8650 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0003t0046 | 0/0 | 8642 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0003t0064 | 0/0 | 8646 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0003t0065 | 0/0 | 8645 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0006t0002 | 0/0 | 8645 | 5 | 0 | 2 | 3 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0006t0007 | 0/0 | 8644 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0006t0011 | 0/0 | 8646 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0006t0013 | 0/0 | 8645 | 3 | 0 | 0 | 3 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0006t0054 | 0/0 | 8645 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0012t0002 | 0/0 | 8645 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0012t0009 | 0/0 | 8650 | 2 | 0 | 0 | 1 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0012t0020 | 0/0 | 8649 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0038t0067 | 0/0 | 8643 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0040t0013 | 0/0 | 8645 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0003c0044t0007 | 0/0 | 8644 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0004c0004t0003 | 0/0 | 8644 | 30 | 8 | 8 | 11 | 2 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0004c0004t0028 | 0/0 | 8645 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0004c0004t0049 | 0/0 | 8644 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0004c0004t0050 | 0/0 | 8644 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0004c0016t0003 | 0/0 | 8644 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0004c0016t0008 | 0/0 | 8642 | 2 | 2 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0005c0005t0008 | 0/0 | 8642 | 6 | 6 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0005c0005t0014 | 0/0 | 8643 | 5 | 5 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0005c0005t0015 | 0/0 | 8641 | 5 | 5 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0005c0005t0027 | 0/0 | 8642 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0005c0005t0041 | 0/0 | 8643 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0005c0005t0044 | 0/0 | 8643 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0005c0005t0055 | 0/0 | 8642 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0006c0008t0007 | 0/0 | 8644 | 5 | 0 | 0 | 5 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0006c0008t0033 | 0/0 | 8644 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0006c0008t0034 | 0/0 | 8644 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0006c0008t0068 | 0/0 | 8644 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0007c0011t0001 | 0/0 | 8652 | 2 | 2 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0007c0011t0003 | 0/0 | 8644 | 3 | 3 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0008c0010t0004 | 0/0 | 8642 | 4 | 0 | 0 | 4 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0008c0010t0058 | 0/0 | 8642 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0009c0013t0001 | 0/0 | 8652 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0009c0013t0002 | 0/0 | 8645 | 2 | 0 | 0 | 2 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0009c0013t0010 | 0/0 | 8652 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0010c0014t0022 | 0/0 | 8645 | 2 | 0 | 0 | 0 | 0 | 2 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0010c0014t0023 | 0/0 | 8645 | 2 | 0 | 0 | 0 | 0 | 2 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0011c0018t0019 | 0/0 | 8685 | 3 | 0 | 0 | 3 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0012c0015t0025 | 0/0 | 8651 | 2 | 0 | 0 | 2 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0012c0015t0042 | 0/0 | 8651 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0013c0023t0001 | 0/0 | 8652 | 2 | 2 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0014c0020t0004 | 0/0 | 8642 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0014c0020t0020 | 0/0 | 8649 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0015c0022t0004 | 0/0 | 8642 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0015c0022t0012 | 0/0 | 8644 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0016c0046t0002 | 0/0 | 8645 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0017c0027t0001 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0018c0028t0001 | 0/0 | 8652 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0019c0025t0017 | 0/0 | 8649 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0020c0045t0003 | 0/0 | 8644 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0021c0043t0004 | 0/0 | 8642 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0022c0029t0045 | 0/0 | 8643 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0023c0042t0016 | 0/0 | 8649 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0024c0033t0003 | 0/0 | 8644 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0025c0036t0004 | 0/0 | 8642 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0026c0032t0003 | 0/0 | 8644 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0027c0031t0056 | 0/0 | 8649 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0028c0035t0005 | 0/0 | 8643 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0029c0037t0016 | 0/0 | 8649 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0030c0041t0026 | 0/0 | 8643 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0031c0039t0002 | 0/0 | 8645 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| a0032c0030t0005 | 0/0 | 8643 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | copy fasta | chr8 | 17917988 | 18034948 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0063 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0006g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0006g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0006g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0006g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0006g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0006g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0006g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0006g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0006g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0010g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0010g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0010g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0010g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0010g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0017g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0017g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0018g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0018g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0018g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0024g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0024g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0035g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0037g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0038g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0039g0009 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0040g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0061g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0001t0062g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0024t0017g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0026t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0047t0006g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0001c0048t0006g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0004g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0004g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0004g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0004g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0004g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0004g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0005g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0012g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0012g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0012g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0012g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0012g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0021g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0021g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0021g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0028g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0029g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0029g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0047g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0048g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0053g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0059g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0060g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0002t0066g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0007t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0007t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0007t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0007t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0007t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0007t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0007t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0007t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0007t0030g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0009t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0009t0016g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0009t0016g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0009t0016g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0009t0051g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0009t0052g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0009t0063g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0017t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0017t0031g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0017t0032g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0019t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0019t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0021t0020g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0021t0027g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0002c0034t0057g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0007g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0007g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0007g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0007g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0007g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0007g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0009g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0009g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0009g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0009g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0009g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0011g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0011g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0011g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0011g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0011g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0013g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0026g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0036g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0043g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0046g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0064g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0003t0065g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0006t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0006t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0006t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0006t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0006t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0006t0007g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0006t0011g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0006t0013g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0006t0013g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0006t0013g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0006t0054g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0012t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0012t0009g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0012t0009g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0012t0020g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0038t0067g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0040t0013g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0003c0044t0007g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0003g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0028g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0049g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0004t0050g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0016t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0016t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0004c0016t0008g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0005c0005t0008g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0005c0005t0008g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0005c0005t0008g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0005c0005t0008g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0005c0005t0008g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0005c0005t0008g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0005c0005t0014g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0005c0005t0014g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0005c0005t0014g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0005c0005t0014g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0005c0005t0014g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0005c0005t0015g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0005c0005t0015g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0005c0005t0015g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0005c0005t0015g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0005c0005t0015g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0005c0005t0027g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0005c0005t0041g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0005c0005t0044g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0005c0005t0055g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0006c0008t0007g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0006c0008t0007g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0006c0008t0007g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0006c0008t0007g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0006c0008t0007g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0006c0008t0033g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0006c0008t0034g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0006c0008t0068g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0007c0011t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0007c0011t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0007c0011t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0007c0011t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0007c0011t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0008c0010t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0008c0010t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0008c0010t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0008c0010t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0008c0010t0058g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0009c0013t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0009c0013t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0009c0013t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0009c0013t0010g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0010c0014t0022g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0010c0014t0022g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0010c0014t0023g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0010c0014t0023g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0011c0018t0019g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0011c0018t0019g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0011c0018t0019g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0012c0015t0025g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0012c0015t0025g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0012c0015t0042g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0013c0023t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0013c0023t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0014c0020t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0014c0020t0020g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0015c0022t0004g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0015c0022t0012g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0016c0046t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0017c0027t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0018c0028t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0019c0025t0017g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0020c0045t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0021c0043t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0022c0029t0045g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0023c0042t0016g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0024c0033t0003g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0025c0036t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0026c0032t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0027c0031t0056g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0028c0035t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0029c0037t0016g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0030c0041t0026g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0031c0039t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| a0032c0030t0005g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0036 | g0262 | EUR | GBR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00099 | hp2 | a0003 | c0003 | t0002 | g0156 | EUR | GBR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00140 | hp1 | a0004 | c0004 | t0003 | g0132 | EUR | GBR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00140 | hp2 | a0002 | c0002 | t0021 | g0309 | EUR | GBR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00280 | hp1 | a0001 | c0001 | t0010 | g0013 | EUR | FIN | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00280 | hp2 | a0002 | c0002 | t0005 | g0301 | EUR | FIN | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00323 | hp1 | a0002 | c0002 | t0004 | g0311 | EUR | FIN | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00323 | hp2 | a0004 | c0004 | t0003 | g0145 | EUR | FIN | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00423 | hp1 | a0001 | c0001 | t0006 | g0056 | EAS | CHS | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00423 | hp2 | a0003 | c0003 | t0002 | g0280 | EAS | CHS | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00438 | hp1 | a0004 | c0004 | t0050 | g0130 | EAS | CHS | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00544 | hp1 | a0002 | c0002 | t0004 | g0192 | EAS | CHS | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00544 | hp2 | a0003 | c0003 | t0002 | g0245 | EAS | CHS | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00558 | hp2 | a0003 | c0003 | t0007 | g0219 | EAS | CHS | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00597 | hp1 | a0003 | c0003 | t0009 | g0348 | EAS | CHS | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00609 | hp1 | a0006 | c0008 | t0033 | g0277 | EAS | CHS | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00609 | hp2 | a0003 | c0006 | t0013 | g0250 | EAS | CHS | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00621 | hp1 | a0002 | c0002 | t0005 | g0281 | EAS | CHS | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00639 | hp1 | a0003 | c0003 | t0002 | g0264 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00639 | hp2 | a0030 | c0041 | t0026 | g0270 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00642 | hp1 | a0001 | c0001 | t0010 | g0014 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00642 | hp2 | a0032 | c0030 | t0005 | g0186 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00738 | hp1 | a0002 | c0002 | t0059 | g0291 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG00741 | hp2 | a0002 | c0002 | t0005 | g0288 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01069 | hp1 | a0002 | c0002 | t0021 | g0195 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01069 | hp2 | a0015 | c0022 | t0004 | g0295 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01070 | hp1 | a0003 | c0003 | t0002 | g0265 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01070 | hp2 | a0015 | c0022 | t0012 | g0314 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01074 | hp1 | a0002 | c0002 | t0048 | g0205 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01074 | hp2 | a0002 | c0002 | t0005 | g0316 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01081 | hp1 | a0001 | c0001 | t0037 | g0087 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01081 | hp2 | a0002 | c0002 | t0005 | g0284 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01099 | hp1 | a0002 | c0017 | t0031 | g0321 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01099 | hp2 | a0003 | c0003 | t0011 | g0003 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01106 | hp1 | a0002 | c0002 | t0012 | g0319 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01109 | hp1 | a0002 | c0002 | t0004 | g0180 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01109 | hp2 | a0002 | c0002 | t0005 | g0283 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01167 | hp1 | a0002 | c0002 | t0005 | g0315 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01167 | hp2 | a0004 | c0004 | t0003 | g0140 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01168 | hp1 | a0002 | c0002 | t0021 | g0308 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01168 | hp2 | a0003 | c0003 | t0002 | g0268 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01169 | hp1 | a0004 | c0004 | t0003 | g0137 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01169 | hp2 | a0003 | c0003 | t0002 | g0267 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01192 | hp1 | a0002 | c0002 | t0005 | g0300 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01192 | hp2 | a0003 | c0003 | t0002 | g0003 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01243 | hp1 | a0003 | c0003 | t0002 | g0158 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01243 | hp2 | a0002 | c0002 | t0005 | g0297 | AMR | PUR | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01255 | hp1 | a0001 | c0001 | t0006 | g0019 | AMR | CLM | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01255 | hp2 | a0002 | c0002 | t0066 | g0317 | AMR | CLM | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01256 | hp1 | a0003 | c0003 | t0002 | g0159 | AMR | CLM | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01256 | hp2 | a0002 | c0002 | t0005 | g0312 | AMR | CLM | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01257 | hp1 | a0002 | c0002 | t0012 | g0310 | AMR | CLM | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01257 | hp2 | a0026 | c0032 | t0003 | g0118 | AMR | CLM | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01261 | hp1 | a0002 | c0002 | t0005 | g0306 | AMR | CLM | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01261 | hp2 | a0004 | c0004 | t0003 | g0133 | AMR | CLM | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01361 | hp1 | a0004 | c0004 | t0003 | g0120 | AMR | CLM | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01361 | hp2 | a0002 | c0002 | t0004 | g0287 | AMR | CLM | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01433 | hp2 | a0004 | c0004 | t0003 | g0122 | AMR | CLM | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01496 | hp1 | a0001 | c0001 | t0010 | g0015 | AMR | CLM | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01496 | hp2 | a0004 | c0004 | t0003 | g0121 | AMR | CLM | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01515 | hp2 | a0009 | c0013 | t0010 | g0305 | EUR | IBS | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01516 | hp1 | a0002 | c0002 | t0005 | g0292 | EUR | IBS | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01516 | hp2 | a0001 | c0001 | t0010 | g0011 | EUR | IBS | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01517 | hp1 | a0002 | c0002 | t0005 | g0293 | EUR | IBS | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01517 | hp2 | a0001 | c0001 | t0010 | g0010 | EUR | IBS | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01884 | hp1 | a0004 | c0004 | t0003 | g0351 | AFR | ACB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01884 | hp2 | a0007 | c0011 | t0003 | g0151 | AFR | ACB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01891 | hp1 | a0005 | c0005 | t0015 | g0162 | AFR | ACB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01891 | hp2 | a0005 | c0005 | t0014 | g0171 | AFR | ACB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01928 | hp2 | a0003 | c0006 | t0054 | g0227 | AMR | PEL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01934 | hp1 | a0001 | c0001 | t0038 | g0073 | AMR | PEL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01934 | hp2 | a0003 | c0003 | t0046 | g0259 | AMR | PEL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01952 | hp2 | a0004 | c0004 | t0028 | g0119 | AMR | PEL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01978 | hp1 | a0002 | c0002 | t0005 | g0294 | AMR | PEL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01981 | hp1 | a0003 | c0006 | t0002 | g0252 | AMR | PEL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG01993 | hp2 | a0003 | c0006 | t0002 | g0228 | AMR | PEL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02004 | hp2 | a0002 | c0002 | t0005 | g0318 | AMR | PEL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02027 | hp1 | a0003 | c0003 | t0007 | g0274 | EAS | KHV | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02027 | hp2 | a0002 | c0002 | t0004 | g0320 | EAS | KHV | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02040 | hp2 | a0003 | c0006 | t0013 | g0251 | EAS | KHV | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02056 | hp1 | a0002 | c0019 | t0004 | g0337 | EAS | KHV | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02056 | hp2 | a0003 | c0006 | t0013 | g0247 | EAS | KHV | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02071 | hp1 | a0002 | c0002 | t0004 | g0185 | EAS | KHV | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02071 | hp2 | a0003 | c0003 | t0002 | g0229 | EAS | KHV | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02074 | hp1 | a0003 | c0003 | t0002 | g0217 | EAS | KHV | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02074 | hp2 | a0001 | c0026 | t0001 | g0065 | EAS | KHV | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02083 | hp1 | a0004 | c0004 | t0003 | g0141 | EAS | KHV | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02129 | hp1 | a0003 | c0003 | t0002 | g0231 | EAS | KHV | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02129 | hp2 | a0004 | c0004 | t0003 | g0126 | EAS | KHV | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02132 | hp1 | a0003 | c0003 | t0007 | g0257 | EAS | KHV | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02132 | hp2 | a0002 | c0002 | t0004 | g0184 | EAS | KHV | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02135 | hp1 | a0008 | c0010 | t0058 | g0211 | EAS | KHV | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02135 | hp2 | a0006 | c0008 | t0068 | g0273 | EAS | KHV | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02145 | hp1 | a0001 | c0001 | t0018 | g0110 | AFR | ACB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02145 | hp2 | a0002 | c0002 | t0047 | g0206 | AFR | ACB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02257 | hp1 | a0004 | c0004 | t0003 | g0117 | AFR | ACB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02257 | hp2 | a0002 | c0017 | t0032 | g0322 | AFR | ACB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02258 | hp1 | a0005 | c0005 | t0008 | g0332 | AFR | ACB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02258 | hp2 | a0005 | c0005 | t0014 | g0176 | AFR | ACB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02273 | hp1 | a0002 | c0002 | t0060 | g0212 | AMR | PEL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02273 | hp2 | a0004 | c0004 | t0003 | g0129 | AMR | PEL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02280 | hp1 | a0004 | c0004 | t0003 | g0353 | AFR | ACB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02300 | hp1 | a0004 | c0004 | t0003 | g0115 | AMR | PEL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02300 | hp2 | a0002 | c0002 | t0012 | g0155 | AMR | PEL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02451 | hp1 | a0003 | c0003 | t0026 | g0271 | AFR | ACB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02451 | hp2 | a0027 | c0031 | t0056 | g0139 | AFR | ACB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02523 | hp1 | a0002 | c0002 | t0004 | g0196 | EAS | KHV | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02523 | hp2 | a0006 | c0008 | t0034 | g0282 | EAS | KHV | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02572 | hp1 | a0002 | c0002 | t0004 | g0187 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02572 | hp2 | a0005 | c0005 | t0044 | g0335 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02602 | hp2 | a0021 | c0043 | t0004 | g0197 | SAS | PJL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02615 | hp1 | a0002 | c0002 | t0005 | g0285 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02615 | hp2 | a0004 | c0004 | t0003 | g0357 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02622 | hp1 | a0002 | c0007 | t0004 | g0004 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02622 | hp2 | a0028 | c0035 | t0005 | g0298 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02630 | hp1 | a0005 | c0005 | t0027 | g0170 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02630 | hp2 | a0004 | c0004 | t0049 | g0356 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02647 | hp1 | a0005 | c0005 | t0008 | g0169 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02647 | hp2 | a0029 | c0037 | t0016 | g0360 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02683 | hp2 | a0003 | c0012 | t0009 | g0349 | SAS | PJL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02698 | hp2 | a0010 | c0014 | t0022 | g0331 | SAS | PJL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02717 | hp1 | a0001 | c0001 | t0017 | g0105 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02717 | hp2 | a0005 | c0005 | t0008 | g0168 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02723 | hp2 | a0023 | c0042 | t0016 | g0361 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02809 | hp1 | a0002 | c0009 | t0005 | g0304 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02809 | hp2 | a0005 | c0005 | t0014 | g0160 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02818 | hp1 | a0005 | c0005 | t0014 | g0175 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02818 | hp2 | a0002 | c0009 | t0016 | g0365 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02886 | hp1 | a0004 | c0004 | t0003 | g0135 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02886 | hp2 | a0001 | c0001 | t0018 | g0106 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02895 | hp1 | a0001 | c0001 | t0018 | g0112 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02895 | hp2 | a0013 | c0023 | t0001 | g0154 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02896 | hp1 | a0002 | c0009 | t0016 | g0359 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02896 | hp2 | a0014 | c0020 | t0020 | g0098 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02897 | hp1 | a0002 | c0009 | t0052 | g0358 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02897 | hp2 | a0013 | c0023 | t0001 | g0153 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02965 | hp1 | a0002 | c0034 | t0057 | g0325 | AFR | ESN | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02965 | hp2 | a0002 | c0002 | t0005 | g0313 | AFR | ESN | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02970 | hp1 | a0002 | c0002 | t0005 | g0299 | AFR | ESN | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02970 | hp2 | a0002 | c0002 | t0004 | g0198 | AFR | ESN | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02976 | hp1 | a0004 | c0016 | t0003 | g0131 | AFR | ESN | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02976 | hp2 | a0022 | c0029 | t0045 | g0279 | AFR | ESN | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03017 | hp2 | a0010 | c0014 | t0022 | g0330 | SAS | PJL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03041 | hp1 | a0002 | c0002 | t0028 | g0323 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03041 | hp2 | a0005 | c0005 | t0008 | g0334 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03098 | hp2 | a0002 | c0002 | t0005 | g0327 | AFR | MSL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03130 | hp1 | a0004 | c0004 | t0003 | g0352 | AFR | ESN | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03130 | hp2 | a0019 | c0025 | t0017 | g0109 | AFR | ESN | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03139 | hp1 | a0005 | c0005 | t0015 | g0173 | AFR | ESN | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03139 | hp2 | a0001 | c0024 | t0017 | g0107 | AFR | ESN | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03195 | hp1 | a0005 | c0005 | t0015 | g0165 | AFR | ESN | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03195 | hp2 | a0007 | c0011 | t0003 | g0152 | AFR | ESN | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03209 | hp1 | a0002 | c0021 | t0020 | g0103 | AFR | MSL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03209 | hp2 | a0002 | c0017 | t0003 | g0104 | AFR | MSL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03225 | hp1 | a0002 | c0002 | t0005 | g0296 | AFR | MSL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03225 | hp2 | a0004 | c0016 | t0008 | g0138 | AFR | MSL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03239 | hp1 | a0002 | c0002 | t0012 | g0286 | SAS | PJL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03453 | hp1 | a0005 | c0005 | t0041 | g0161 | AFR | MSL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03453 | hp2 | a0002 | c0009 | t0051 | g0364 | AFR | MSL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03490 | hp1 | a0002 | c0002 | t0004 | g0204 | SAS | PJL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03490 | hp2 | a0002 | c0002 | t0004 | g0002 | SAS | PJL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03492 | hp1 | a0002 | c0002 | t0005 | g0002 | SAS | PJL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03516 | hp1 | a0007 | c0011 | t0003 | g0172 | AFR | ESN | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03516 | hp2 | a0002 | c0002 | t0004 | g0328 | AFR | ESN | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03540 | hp1 | a0007 | c0011 | t0001 | g0149 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03540 | hp2 | a0002 | c0002 | t0005 | g0326 | AFR | GWD | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03579 | hp1 | a0001 | c0001 | t0035 | g0111 | AFR | MSL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03579 | hp2 | a0024 | c0033 | t0003 | g0350 | AFR | MSL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03688 | hp1 | a0002 | c0002 | t0004 | g0199 | SAS | STU | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03831 | hp1 | a0002 | c0002 | t0005 | g0182 | SAS | BEB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03831 | hp2 | a0001 | c0001 | t0062 | g0093 | SAS | BEB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03834 | hp2 | a0010 | c0014 | t0023 | g0354 | SAS | BEB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03942 | hp1 | a0001 | c0001 | t0006 | g0094 | SAS | BEB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03942 | hp2 | a0002 | c0002 | t0005 | g0302 | SAS | BEB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG04115 | hp1 | a0004 | c0004 | t0003 | g0142 | SAS | STU | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | STU | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG04184 | hp1 | a0002 | c0007 | t0030 | g0179 | SAS | BEB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | STU | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG04204 | hp2 | a0002 | c0002 | t0005 | g0303 | SAS | STU | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG04228 | hp1 | a0010 | c0014 | t0023 | g0355 | SAS | STU | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | STU | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18522 | hp1 | a0001 | c0001 | t0017 | g0108 | AFR | YRI | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18522 | hp2 | a0002 | c0021 | t0027 | g0102 | AFR | YRI | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18612 | hp1 | a0004 | c0004 | t0003 | g0114 | EAS | CHB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18612 | hp2 | a0006 | c0008 | t0007 | g0272 | EAS | CHB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18747 | hp1 | a0014 | c0020 | t0004 | g0070 | EAS | CHB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18747 | hp2 | a0003 | c0003 | t0002 | g0239 | EAS | CHB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18906 | hp1 | a0004 | c0004 | t0003 | g0136 | AFR | YRI | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18906 | hp2 | a0005 | c0005 | t0008 | g0333 | AFR | YRI | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18939 | hp2 | a0003 | c0003 | t0009 | g0347 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18941 | hp2 | a0003 | c0012 | t0020 | g0338 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18942 | hp1 | a0002 | c0007 | t0004 | g0201 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18942 | hp2 | a0003 | c0006 | t0007 | g0218 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18943 | hp1 | a0009 | c0013 | t0002 | g0214 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18943 | hp2 | a0001 | c0001 | t0006 | g0049 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18944 | hp1 | a0003 | c0003 | t0002 | g0216 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18944 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18945 | hp1 | a0004 | c0004 | t0003 | g0124 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18945 | hp2 | a0003 | c0003 | t0002 | g0220 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18947 | hp1 | a0003 | c0003 | t0002 | g0275 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18947 | hp2 | a0001 | c0048 | t0006 | g0081 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18948 | hp2 | a0001 | c0001 | t0040 | g0076 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18949 | hp2 | a0004 | c0004 | t0003 | g0128 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18950 | hp2 | a0003 | c0003 | t0013 | g0248 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18956 | hp2 | a0009 | c0013 | t0002 | g0148 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18959 | hp1 | a0003 | c0044 | t0007 | g0234 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18959 | hp2 | a0002 | c0002 | t0004 | g0181 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18960 | hp2 | a0003 | c0003 | t0002 | g0243 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18961 | hp1 | a0008 | c0010 | t0004 | g0209 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18962 | hp1 | a0001 | c0001 | t0024 | g0048 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18962 | hp2 | a0006 | c0008 | t0007 | g0263 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18963 | hp1 | a0003 | c0003 | t0007 | g0258 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18963 | hp2 | a0002 | c0007 | t0001 | g0033 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18965 | hp1 | a0018 | c0028 | t0001 | g0097 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18965 | hp2 | a0003 | c0012 | t0009 | g0340 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18966 | hp1 | a0001 | c0001 | t0006 | g0020 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18966 | hp2 | a0002 | c0002 | t0005 | g0290 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18970 | hp1 | a0003 | c0012 | t0002 | g0341 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18970 | hp2 | a0003 | c0003 | t0009 | g0226 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18972 | hp1 | a0004 | c0004 | t0003 | g0125 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18972 | hp2 | a0003 | c0003 | t0011 | g0255 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18975 | hp1 | a0031 | c0039 | t0002 | g0222 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18975 | hp2 | a0002 | c0007 | t0004 | g0203 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18977 | hp1 | a0012 | c0015 | t0025 | g0343 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18978 | hp1 | a0003 | c0003 | t0064 | g0254 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18978 | hp2 | a0001 | c0001 | t0006 | g0101 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18979 | hp1 | a0012 | c0015 | t0025 | g0342 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18979 | hp2 | a0001 | c0001 | t0006 | g0079 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18981 | hp1 | a0011 | c0018 | t0019 | g0190 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18982 | hp1 | a0006 | c0008 | t0007 | g0276 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18982 | hp2 | a0011 | c0018 | t0019 | g0188 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18983 | hp1 | a0006 | c0008 | t0007 | g0266 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18983 | hp2 | a0011 | c0018 | t0019 | g0189 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18984 | hp1 | a0002 | c0002 | t0004 | g0194 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18986 | hp2 | a0003 | c0003 | t0043 | g0345 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18987 | hp1 | a0003 | c0003 | t0002 | g0233 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18992 | hp1 | a0003 | c0003 | t0065 | g0238 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18992 | hp2 | a0001 | c0001 | t0006 | g0026 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18993 | hp1 | a0002 | c0007 | t0005 | g0202 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18995 | hp1 | a0004 | c0004 | t0003 | g0144 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18995 | hp2 | a0012 | c0015 | t0042 | g0344 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18998 | hp2 | a0003 | c0003 | t0011 | g0178 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18999 | hp1 | a0001 | c0001 | t0024 | g0085 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA18999 | hp2 | a0004 | c0004 | t0003 | g0116 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19001 | hp1 | a0003 | c0003 | t0002 | g0256 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19001 | hp2 | a0001 | c0001 | t0061 | g0024 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19004 | hp1 | a0004 | c0004 | t0003 | g0113 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19006 | hp1 | a0001 | c0047 | t0006 | g0069 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19006 | hp2 | a0003 | c0003 | t0002 | g0236 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19007 | hp1 | a0003 | c0003 | t0007 | g0269 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19011 | hp1 | a0008 | c0010 | t0004 | g0207 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19011 | hp2 | a0003 | c0003 | t0002 | g0230 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19030 | hp1 | a0002 | c0002 | t0053 | g0289 | AFR | LWK | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19030 | hp2 | a0003 | c0003 | t0011 | g0329 | AFR | LWK | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19043 | hp1 | a0002 | c0002 | t0029 | g0324 | AFR | LWK | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19043 | hp2 | a0004 | c0016 | t0008 | g0134 | AFR | LWK | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19055 | hp1 | a0016 | c0046 | t0002 | g0244 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19057 | hp1 | a0004 | c0004 | t0003 | g0123 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19057 | hp2 | a0003 | c0003 | t0002 | g0237 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19058 | hp1 | a0003 | c0006 | t0002 | g0177 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19058 | hp2 | a0002 | c0019 | t0004 | g0213 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19060 | hp2 | a0008 | c0010 | t0004 | g0210 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19063 | hp1 | a0008 | c0010 | t0004 | g0208 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19063 | hp2 | a0001 | c0001 | t0006 | g0062 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19064 | hp2 | a0003 | c0003 | t0009 | g0346 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19066 | hp1 | a0003 | c0040 | t0013 | g0249 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19066 | hp2 | a0025 | c0036 | t0004 | g0193 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19068 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19068 | hp2 | a0003 | c0003 | t0009 | g0339 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19072 | hp1 | a0002 | c0002 | t0029 | g0183 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19072 | hp2 | a0003 | c0006 | t0002 | g0260 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19074 | hp1 | a0006 | c0008 | t0007 | g0261 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19074 | hp2 | a0003 | c0003 | t0002 | g0221 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19077 | hp1 | a0002 | c0007 | t0004 | g0200 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19077 | hp2 | a0002 | c0007 | t0001 | g0253 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19078 | hp1 | a0003 | c0003 | t0002 | g0241 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19080 | hp1 | a0003 | c0003 | t0002 | g0240 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19080 | hp2 | a0001 | c0001 | t0006 | g0053 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19081 | hp1 | a0009 | c0013 | t0001 | g0215 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19082 | hp1 | a0003 | c0038 | t0067 | g0235 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19084 | hp1 | a0003 | c0003 | t0011 | g0223 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19085 | hp1 | a0003 | c0003 | t0002 | g0224 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19085 | hp2 | a0003 | c0003 | t0002 | g0242 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19086 | hp1 | a0004 | c0004 | t0003 | g0143 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19086 | hp2 | a0002 | c0007 | t0004 | g0278 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19087 | hp1 | a0001 | c0001 | t0006 | g0080 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19087 | hp2 | a0003 | c0006 | t0011 | g0246 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19088 | hp1 | a0003 | c0006 | t0002 | g0225 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19090 | hp1 | a0020 | c0045 | t0003 | g0127 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19090 | hp2 | a0003 | c0003 | t0007 | g0232 | EAS | JPT | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19240 | hp1 | a0002 | c0009 | t0016 | g0362 | AFR | YRI | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA19240 | hp2 | a0005 | c0005 | t0014 | g0163 | AFR | YRI | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA20129 | hp1 | a0004 | c0004 | t0003 | g0336 | AFR | ASW | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ASW | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | TSI | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA20752 | hp2 | a0003 | c0003 | t0002 | g0157 | EUR | TSI | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA20805 | hp1 | a0002 | c0002 | t0004 | g0191 | EUR | TSI | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | TSI | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02109 | hp1 | a0002 | c0009 | t0063 | g0363 | AFR | ACB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02109 | hp2 | a0005 | c0005 | t0015 | g0164 | AFR | ACB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02486 | hp2 | a0005 | c0005 | t0015 | g0166 | AFR | ACB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG02559 | hp2 | a0005 | c0005 | t0055 | g0167 | AFR | ACB | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03471 | hp1 | a0017 | c0027 | t0001 | g0061 | AFR | MSL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| HG03471 | hp2 | a0005 | c0005 | t0008 | g0174 | AFR | MSL | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA21309 | hp1 | a0007 | c0011 | t0001 | g0150 | AFR | LWK | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| NA21309 | hp2 | a0002 | c0002 | t0012 | g0307 | AFR | LWK | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0039 | g0009 | REF | REF | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0063 | REF | REF | PCM1_chr8_17917988_18034948 | PCM1 | chr8 | 17917988 | 18034948 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:17937267
|
C | T | 1 | a0013 | 2 | HG02895.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.230C>T | p.Thr77Ile | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/39 | 521/8652 | 230/6075 | 77/2024 | chr8 | 17937267 | ||
| chr8:17938869
|
A | G | 1 | a0016 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.472A>G | p.Thr158Ala | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 5/39 | 763/8652 | 472/6075 | 158/2024 | chr8 | 17938869 | ||
| chr8:17938873
|
A | G | 27 | a0002a0003a0004others(24): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
missense_variant | MODERATE | c.476A>G | p.Asn159Ser | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 5/39 | 767/8652 | 476/6075 | 159/2024 | chr8 | 17938873 | ||
| chr8:17938924
|
C | A | 1 | a0008 | 5 | HG02135.hp1 NA18961.hp1 NA19011.hp1 others(2): Show |
missense_variant | MODERATE | c.527C>A | p.Ala176Asp | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 5/39 | 818/8652 | 527/6075 | 176/2024 | chr8 | 17938924 | ||
| chr8:17947186
|
G | A | 1 | a0012 | 3 | NA18977.hp1 NA18979.hp1 NA18995.hp2 |
missense_variant&splice_region_variant | MODERATE | c.784G>A | p.Ala262Thr | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/39 | 1075/8652 | 784/6075 | 262/2024 | chr8 | 17947186 | ||
| chr8:17953001
|
C | A | 1 | a0019 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.1103C>A | p.Ala368Glu | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/39 | 1394/8652 | 1103/6075 | 368/2024 | chr8 | 17953001 | ||
| chr8:17953081
|
G | A | 2 | a0007a0013 | 7 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
missense_variant | MODERATE | c.1183G>A | p.Glu395Lys | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/39 | 1474/8652 | 1183/6075 | 395/2024 | chr8 | 17953081 | ||
| chr8:17955536
|
C | T | 1 | a0020 | 1 | NA19090.hp1 | missense_variant | MODERATE | c.1355C>T | p.Pro452Leu | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 10/39 | 1646/8652 | 1355/6075 | 452/2024 | chr8 | 17955536 | ||
| chr8:17955628
|
C | T | 1 | a0018 | 1 | NA18965.hp1 | missense_variant | MODERATE | c.1447C>T | p.His483Tyr | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 10/39 | 1738/8652 | 1447/6075 | 483/2024 | chr8 | 17955628 | ||
| chr8:17957405
|
C | G | 1 | a0021 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.1788C>G | p.Asn596Lys | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 12/39 | 2079/8652 | 1788/6075 | 596/2024 | chr8 | 17957405 | ||
| chr8:17957406
|
A | G | 28 | a0002a0003a0004others(25): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
missense_variant | MODERATE | c.1789A>G | p.Met597Val | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 12/39 | 2080/8652 | 1789/6075 | 597/2024 | chr8 | 17957406 | ||
| chr8:17957415
|
T | C | 1 | a0022 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.1798T>C | p.Ser600Pro | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 12/39 | 2089/8652 | 1798/6075 | 600/2024 | chr8 | 17957415 | ||
| chr8:17957546
|
G | A | 1 | a0017 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.1811G>A | p.Arg604Gln | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/39 | 2102/8652 | 1811/6075 | 604/2024 | chr8 | 17957546 | ||
| chr8:17957573
|
T | G | 1 | a0032 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.1838T>G | p.Ile613Ser | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/39 | 2129/8652 | 1838/6075 | 613/2024 | chr8 | 17957573 | ||
| chr8:17957601
|
G | T | 1 | a0023 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1866G>T | p.Glu622Asp | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/39 | 2157/8652 | 1866/6075 | 622/2024 | chr8 | 17957601 | ||
| chr8:17960044
|
G | T | 6 | a0003a0006a0012others(3): Show | 84 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(81): Show |
missense_variant | MODERATE | c.2071G>T | p.Ala691Ser | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 14/39 | 2362/8652 | 2071/6075 | 691/2024 | chr8 | 17960044 | ||
| chr8:17962119
|
C | G | 1 | a0030 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.2408C>G | p.Thr803Ser | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 16/39 | 2699/8652 | 2408/6075 | 803/2024 | chr8 | 17962119 | ||
| chr8:17962155
|
C | G | 1 | a0024 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.2444C>G | p.Ser815Cys | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 16/39 | 2735/8652 | 2444/6075 | 815/2024 | chr8 | 17962155 | ||
| chr8:17963249
|
G | T | 1 | a0005 | 20 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(17): Show |
missense_variant | MODERATE | c.2612G>T | p.Gly871Val | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 17/39 | 2903/8652 | 2612/6075 | 871/2024 | chr8 | 17963249 | ||
| chr8:17963281
|
A | G | 1 | a0025 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.2644A>G | p.Arg882Gly | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 17/39 | 2935/8652 | 2644/6075 | 882/2024 | chr8 | 17963281 | ||
| chr8:17972640
|
G | C | 1 | a0029 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.3896G>C | p.Ser1299Thr | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/39 | 4187/8652 | 3896/6075 | 1299/2024 | chr8 | 17972640 | ||
| chr8:17991638
|
C | T | 6 | a0004a0006a0020others(3): Show | 48 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(45): Show |
missense_variant | MODERATE | c.4628C>T | p.Thr1543Ile | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/39 | 4919/8652 | 4628/6075 | 1543/2024 | chr8 | 17991638 | ||
| chr8:18009676
|
A | T | 1 | a0010 | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
missense_variant | MODERATE | c.5092A>T | p.Ile1698Leu | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 31/39 | 5383/8652 | 5092/6075 | 1698/2024 | chr8 | 18009676 | ||
| chr8:18009702
|
G | C | 1 | a0028 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.5118G>C | p.Arg1706Ser | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 31/39 | 5409/8652 | 5118/6075 | 1706/2024 | chr8 | 18009702 | ||
| chr8:18010637
|
C | G | 1 | a0031 | 1 | NA18975.hp1 | stop_gained | HIGH | c.5189C>G | p.Ser1730* | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 32/39 | 5480/8652 | 5189/6075 | 1730/2024 | chr8 | 18010637 | ||
| chr8:18011308
|
A | C | 1 | a0015 | 2 | HG01069.hp2 HG01070.hp2 |
missense_variant | MODERATE | c.5292A>C | p.Arg1764Ser | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 33/39 | 5583/8652 | 5292/6075 | 1764/2024 | chr8 | 18011308 | ||
| chr8:18013989
|
C | T | 1 | a0026 | 1 | HG01257.hp2 | missense_variant | MODERATE | c.5537C>T | p.Thr1846Ile | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 35/39 | 5828/8652 | 5537/6075 | 1846/2024 | chr8 | 18013989 | ||
| chr8:18014624
|
T | G | 1 | a0027 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.5625T>G | p.Asn1875Lys | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/39 | 5916/8652 | 5625/6075 | 1875/2024 | chr8 | 18014624 | ||
| chr8:18014745
|
C | CCTAGAGT others(26): Show |
1 | a0011 | 3 | NA18981.hp1 NA18982.hp2 NA18983.hp2 |
conservative_inframe_insertion | MODERATE | c.5749_5781dupAGAGTC others(27): Show |
p.Arg1917_Thr1927dup | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/39 | 6073/8652 | 5782/6075 | 1928/2024 | INFO_REALIGN_3_PRIME | chr8 | 18014745 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:17935664
|
A | C | 1 | a0001c0048 | 1 | NA18947.hp2 | synonymous_variant | LOW | c.54A>C | p.Pro18Pro | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 3/39 | 345/8652 | 54/6075 | 18/2024 | chr8 | 17935664 | ||
| chr8:17937190
|
G | A | 1 | a0001c0024 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.153G>A | p.Lys51Lys | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/39 | 444/8652 | 153/6075 | 51/2024 | chr8 | 17937190 | ||
| chr8:17937247
|
A | G | 1 | a0001c0047 | 1 | NA19006.hp1 | synonymous_variant | LOW | c.210A>G | p.Pro70Pro | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/39 | 501/8652 | 210/6075 | 70/2024 | chr8 | 17937247 | ||
| chr8:17937283
|
G | A | 2 | a0002c0019a0003c0012 | 6 | HG02056.hp1 HG02683.hp2 NA18941.hp2 others(3): Show |
synonymous_variant | LOW | c.246G>A | p.Thr82Thr | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/39 | 537/8652 | 246/6075 | 82/2024 | chr8 | 17937283 | ||
| chr8:17938874
|
C | T | 39 | a0002c0002a0002c0007a0002c0009others(36): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
synonymous_variant | LOW | c.477C>T | p.Asn159Asn | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 5/39 | 768/8652 | 477/6075 | 159/2024 | chr8 | 17938874 | ||
| chr8:17953002
|
A | G | 1 | a0019c0025 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.1104A>G | p.Ala368Ala | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/39 | 1395/8652 | 1104/6075 | 368/2024 | chr8 | 17953002 | ||
| chr8:17957378
|
A | G | 1 | a0003c0044 | 1 | NA18959.hp1 | synonymous_variant | LOW | c.1761A>G | p.Arg587Arg | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 12/39 | 2052/8652 | 1761/6075 | 587/2024 | chr8 | 17957378 | ||
| chr8:17960417
|
A | G | 3 | a0002c0009a0023c0042a0029c0037 | 9 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(6): Show |
synonymous_variant | LOW | c.2295A>G | p.Ala765Ala | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/39 | 2586/8652 | 2295/6075 | 765/2024 | chr8 | 17960417 | ||
| chr8:17962063
|
C | T | 10 | a0002c0002a0002c0019a0002c0034others(7): Show | 77 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
synonymous_variant | LOW | c.2352C>T | p.Pro784Pro | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 16/39 | 2643/8652 | 2352/6075 | 784/2024 | chr8 | 17962063 | ||
| chr8:17963205
|
A | T | 14 | a0002c0017a0002c0021a0003c0003others(11): Show | 109 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(106): Show |
synonymous_variant | LOW | c.2568A>T | p.Leu856Leu | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 17/39 | 2859/8652 | 2568/6075 | 856/2024 | chr8 | 17963205 | ||
| chr8:17963268
|
T | C | 1 | a0002c0034 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.2631T>C | p.Thr877Thr | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 17/39 | 2922/8652 | 2631/6075 | 877/2024 | chr8 | 17963268 | ||
| chr8:17964628
|
C | T | 1 | a0002c0021 | 2 | HG03209.hp1 NA18522.hp2 |
synonymous_variant | LOW | c.2715C>T | p.Asp905Asp | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 18/39 | 3006/8652 | 2715/6075 | 905/2024 | chr8 | 17964628 | ||
| chr8:17972512
|
A | G | 1 | a0003c0040 | 1 | NA19066.hp1 | synonymous_variant | LOW | c.3768A>G | p.Glu1256Glu | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/39 | 4059/8652 | 3768/6075 | 1256/2024 | chr8 | 17972512 | ||
| chr8:17985994
|
A | G | 1 | a0001c0026 | 1 | HG02074.hp2 | synonymous_variant | LOW | c.4317A>G | p.Glu1439Glu | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/39 | 4608/8652 | 4317/6075 | 1439/2024 | chr8 | 17985994 | ||
| chr8:18011284
|
G | C | 2 | a0003c0006a0003c0040 | 12 | HG00609.hp2 HG01928.hp2 HG01981.hp1 others(9): Show |
synonymous_variant | LOW | c.5268G>C | p.Val1756Val | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 33/39 | 5559/8652 | 5268/6075 | 1756/2024 | chr8 | 18011284 | ||
| chr8:18011290
|
T | C | 1 | a0004c0016 | 3 | HG02976.hp1 HG03225.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.5274T>C | p.Asp1758Asp | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 33/39 | 5565/8652 | 5274/6075 | 1758/2024 | chr8 | 18011290 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:17923012
|
G | A | 1 | a0002c0007t0030 | 1 | HG04184.hp1 | 5_prime_UTR_variant | MODIFIER | c.-267G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/39 | 12599 | chr8 | 17923012 | |||||
| chr8:17923105
|
T | A | 2 | a0002c0017t0031a0002c0017t0032 | 2 | HG01099.hp1 HG02257.hp2 |
5_prime_UTR_variant | MODIFIER | c.-174T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/39 | 12506 | chr8 | 17923105 | |||||
| chr8:17923147
|
C | A | 1 | a0006c0008t0033 | 1 | HG00609.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-132C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/39 | chr8 | 17923147 | ||||||
| chr8:17924743
|
G | C | 1 | a0006c0008t0034 | 1 | HG02523.hp2 | 5_prime_UTR_variant | MODIFIER | c.-60G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/39 | 10868 | chr8 | 17924743 | |||||
| chr8:18027820
|
C | G | 1 | a0006c0008t0068 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*158C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 158 | chr8 | 18027820 | |||||
| chr8:18027859
|
T | A | 1 | a0001c0001t0035 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*197T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 197 | chr8 | 18027859 | |||||
| chr8:18027862
|
G | GT | 7 | a0001c0001t0061a0001c0001t0062a0002c0002t0066others(4): Show | 7 | HG01255.hp2 HG02109.hp1 HG03831.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*213dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 214 | INFO_REALIGN_3_PRIME | chr8 | 18027862 | ||||
| chr8:18027862
|
GT | G | 6 | a0001c0001t0017a0001c0001t0018a0001c0001t0035others(3): Show | 9 | HG00099.hp1 HG02145.hp1 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*213delT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 213 | INFO_REALIGN_3_PRIME | chr8 | 18027862 | ||||
| chr8:18027875
|
T | C | 5 | a0003c0003t0013a0003c0006t0013a0003c0040t0013others(2): Show | 9 | HG00609.hp2 HG02040.hp2 HG02056.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*213T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 213 | chr8 | 18027875 | |||||
| chr8:18027897
|
C | G | 98 | a0001c0001t0002a0001c0001t0004a0001c0001t0017others(95): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
3_prime_UTR_variant | MODIFIER | c.*235C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 235 | chr8 | 18027897 | |||||
| chr8:18027898
|
A | AT | 25 | a0001c0001t0004a0002c0002t0004a0002c0002t0005others(22): Show | 81 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*243dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 244 | INFO_REALIGN_3_PRIME | chr8 | 18027898 | ||||
| chr8:18027939
|
G | A | 1 | a0002c0034t0057 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*277G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 277 | chr8 | 18027939 | |||||
| chr8:18028096
|
C | T | 1 | a0027c0031t0056 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*434C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 434 | chr8 | 18028096 | |||||
| chr8:18028099
|
A | G | 1 | a0005c0005t0055 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*437A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 437 | chr8 | 18028099 | |||||
| chr8:18028121
|
C | A | 1 | a0001c0001t0037 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*459C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 459 | chr8 | 18028121 | |||||
| chr8:18028144
|
G | A | 1 | a0005c0005t0041 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*482G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 482 | chr8 | 18028144 | |||||
| chr8:18028170
|
C | T | 1 | a0003c0006t0054 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*508C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 508 | chr8 | 18028170 | |||||
| chr8:18028244
|
ATATT | A | 2 | a0010c0014t0022a0010c0014t0023 | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*587_*590delTATT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 587 | INFO_REALIGN_3_PRIME | chr8 | 18028244 | ||||
| chr8:18028316
|
TATC | T | 98 | a0001c0001t0002a0001c0001t0004a0001c0001t0017others(95): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
3_prime_UTR_variant | MODIFIER | c.*658_*660delATC | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 658 | INFO_REALIGN_3_PRIME | chr8 | 18028316 | ||||
| chr8:18028353
|
A | G | 23 | a0001c0001t0002a0002c0002t0053a0003c0003t0002others(20): Show | 72 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*691A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 691 | chr8 | 18028353 | |||||
| chr8:18028382
|
A | G | 1 | a0001c0001t0062 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*720A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 720 | chr8 | 18028382 | |||||
| chr8:18028398
|
A | C | 91 | a0001c0001t0002a0001c0001t0004a0002c0002t0004others(88): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*736A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 736 | chr8 | 18028398 | |||||
| chr8:18028411
|
G | A | 1 | a0012c0015t0042 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*749G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 749 | chr8 | 18028411 | |||||
| chr8:18028517
|
G | A | 93 | a0001c0001t0002a0001c0001t0004a0001c0001t0017others(90): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*855G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 855 | chr8 | 18028517 | |||||
| chr8:18028658
|
GTGAT | G | 75 | a0001c0001t0002a0001c0001t0004a0002c0002t0004others(72): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*1002_*1005delGATT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1002 | INFO_REALIGN_3_PRIME | chr8 | 18028658 | ||||
| chr8:18028667
|
T | C | 1 | a0002c0017t0031 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1005T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1005 | chr8 | 18028667 | |||||
| chr8:18028668
|
T | A | 1 | a0002c0017t0031 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1006T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1006 | chr8 | 18028668 | |||||
| chr8:18028710
|
A | G | 1 | a0002c0002t0060 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1048A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1048 | chr8 | 18028710 | |||||
| chr8:18028802
|
G | C | 1 | a0008c0010t0058 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1140G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1140 | chr8 | 18028802 | |||||
| chr8:18028836
|
T | C | 93 | a0001c0001t0002a0001c0001t0004a0001c0001t0038others(90): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*1174T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1174 | chr8 | 18028836 | |||||
| chr8:18028837
|
G | A | 1 | a0002c0002t0021 | 3 | HG00140.hp2 HG01069.hp1 HG01168.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1175G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1175 | chr8 | 18028837 | |||||
| chr8:18028841
|
A | G | 11 | a0002c0002t0028a0002c0017t0003a0004c0004t0003others(8): Show | 42 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1179A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1179 | chr8 | 18028841 | |||||
| chr8:18028906
|
C | A | 1 | a0003c0003t0043 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1244C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1244 | chr8 | 18028906 | |||||
| chr8:18028918
|
G | A | 4 | a0004c0016t0008a0005c0005t0008a0005c0005t0044others(1): Show | 10 | HG02258.hp1 HG02559.hp2 HG02572.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1256G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1256 | chr8 | 18028918 | |||||
| chr8:18028933
|
C | G | 1 | a0005c0005t0044 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1271C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1271 | chr8 | 18028933 | |||||
| chr8:18028989
|
A | G | 2 | a0002c0017t0031a0002c0017t0032 | 2 | HG01099.hp1 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1327A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1327 | chr8 | 18028989 | |||||
| chr8:18029067
|
C | T | 1 | a0002c0002t0059 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1405C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1405 | chr8 | 18029067 | |||||
| chr8:18029126
|
C | G | 2 | a0002c0017t0031a0002c0017t0032 | 2 | HG01099.hp1 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1464C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1464 | chr8 | 18029126 | |||||
| chr8:18029156
|
C | CA | 30 | a0001c0001t0006a0001c0001t0017a0001c0001t0039others(27): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1520dupA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1521 | INFO_REALIGN_3_PRIME | chr8 | 18029156 | ||||
| chr8:18029156
|
C | CAA | 14 | a0001c0001t0018a0001c0001t0035a0002c0002t0012others(11): Show | 25 | HG00639.hp2 HG01070.hp2 HG01106.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1519_*1520dupAA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1521 | INFO_REALIGN_3_PRIME | chr8 | 18029156 | ||||
| chr8:18029156
|
CA | C | 21 | a0001c0001t0040a0002c0002t0029a0002c0009t0052others(18): Show | 62 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1520delA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1520 | INFO_REALIGN_3_PRIME | chr8 | 18029156 | ||||
| chr8:18029215
|
A | G | 3 | a0001c0001t0010a0001c0001t0039a0009c0013t0010 | 7 | HG00280.hp1 HG00642.hp1 HG01496.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1553A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1553 | chr8 | 18029215 | |||||
| chr8:18029238
|
T | A | 31 | a0001c0001t0004a0002c0002t0004a0002c0002t0005others(28): Show | 89 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*1576T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1576 | chr8 | 18029238 | |||||
| chr8:18029278
|
T | C | 1 | a0005c0005t0041 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1616T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1616 | chr8 | 18029278 | |||||
| chr8:18029283
|
G | C | 1 | a0002c0002t0066 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1621G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1621 | chr8 | 18029283 | |||||
| chr8:18029339
|
C | T | 1 | a0004c0004t0050 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1677C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1677 | chr8 | 18029339 | |||||
| chr8:18029366
|
A | T | 1 | a0001c0001t0024 | 2 | NA18962.hp1 NA18999.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1704A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1704 | chr8 | 18029366 | |||||
| chr8:18029395
|
T | C | 9 | a0002c0021t0027a0004c0016t0008a0005c0005t0008others(6): Show | 23 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1733T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1733 | chr8 | 18029395 | |||||
| chr8:18029405
|
ACACT | A | 12 | a0002c0017t0031a0002c0017t0032a0002c0021t0027others(9): Show | 26 | HG01099.hp1 HG01891.hp1 HG01891.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1746_*1749delCTCA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1746 | INFO_REALIGN_3_PRIME | chr8 | 18029405 | ||||
| chr8:18029553
|
T | C | 2 | a0010c0014t0022a0010c0014t0023 | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1891T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1891 | chr8 | 18029553 | |||||
| chr8:18029574
|
A | G | 27 | a0001c0001t0004a0002c0002t0004a0002c0002t0005others(24): Show | 83 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*1912A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1912 | chr8 | 18029574 | |||||
| chr8:18029580
|
CTTAT | C | 30 | a0001c0001t0004a0002c0002t0004a0002c0002t0005others(27): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*1921_*1924delATTT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1921 | INFO_REALIGN_3_PRIME | chr8 | 18029580 | ||||
| chr8:18029594
|
G | A | 1 | a0010c0014t0022 | 2 | HG02698.hp2 HG03017.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1932G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1932 | chr8 | 18029594 | |||||
| chr8:18029641
|
A | G | 6 | a0002c0009t0016a0002c0009t0051a0002c0009t0052others(3): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1979A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 1979 | chr8 | 18029641 | |||||
| chr8:18029696
|
T | C | 11 | a0002c0002t0028a0002c0017t0003a0004c0004t0003others(8): Show | 42 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2034T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 2034 | chr8 | 18029696 | |||||
| chr8:18029823
|
T | C | 1 | a0004c0004t0049 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2161T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 2161 | chr8 | 18029823 | |||||
| chr8:18029833
|
G | C | 9 | a0002c0021t0027a0004c0016t0008a0005c0005t0008others(6): Show | 23 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2171G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 2171 | chr8 | 18029833 | |||||
| chr8:18029905
|
G | A | 23 | a0001c0001t0002a0002c0002t0053a0003c0003t0002others(20): Show | 72 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*2243G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 39/39 | 2243 | chr8 | 18029905 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:17923343
|
T | C | 1 | a0002c0007t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-91+155T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17923343 | ||||||
| chr8:17923410
|
C | T | 10 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(7): Show | 10 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-91+222C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17923410 | ||||||
| chr8:17923422
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-91+234G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17923422 | ||||||
| chr8:17923480
|
G | T | 2 | a0010c0014t0023g0354a0010c0014t0023g0355 | 2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-91+292G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17923480 | ||||||
| chr8:17923493
|
G | T | 18 | a0002c0019t0004g0337a0003c0003t0009g0339a0003c0003t0009g0346others(15): Show | 18 | HG00597.hp1 HG01884.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.-91+305G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17923493 | ||||||
| chr8:17923503
|
C | G | 212 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.-91+315C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17923503 | ||||||
| chr8:17923519
|
C | T | 4 | a0005c0005t0008g0332a0005c0005t0008g0333a0005c0005t0008g0334others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-91+331C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17923519 | ||||||
| chr8:17923576
|
T | C | 212 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.-91+388T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17923576 | ||||||
| chr8:17923603
|
T | C | 208 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.-91+415T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17923603 | ||||||
| chr8:17923659
|
G | A | 6 | a0007c0011t0001g0149a0007c0011t0001g0150a0007c0011t0003g0151others(3): Show | 6 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-91+471G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17923659 | ||||||
| chr8:17923680
|
A | T | 1 | a0002c0007t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-91+492A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17923680 | ||||||
| chr8:17923748
|
T | C | 221 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.-91+560T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17923748 | ||||||
| chr8:17923806
|
C | G | 6 | a0002c0002t0004g0328a0002c0002t0005g0326a0002c0002t0005g0327others(3): Show | 6 | HG02965.hp1 HG03041.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-91+618C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17923806 | ||||||
| chr8:17923816
|
C | T | 2 | a0002c0017t0031g0321a0002c0017t0032g0322 | 2 | HG01099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-91+628C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17923816 | ||||||
| chr8:17923873
|
G | C | 7 | a0002c0007t0004g0004a0007c0011t0001g0149a0007c0011t0001g0150others(4): Show | 7 | HG01884.hp2 HG02622.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-91+685G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17923873 | ||||||
| chr8:17923892
|
A | G | 221 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.-91+704A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17923892 | ||||||
| chr8:17923893
|
C | T | 1 | a0009c0013t0002g0148 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-91+705C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17923893 | ||||||
| chr8:17923967
|
C | A | 1 | a0002c0002t0012g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-90-746C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17923967 | ||||||
| chr8:17923996
|
T | G | 4 | a0003c0003t0002g0156a0003c0003t0002g0157a0003c0003t0002g0158others(1): Show | 4 | HG00099.hp2 HG01243.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.-90-717T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17923996 | ||||||
| chr8:17924007
|
G | GTTTT | 205 | a0002c0002t0004g0180a0002c0002t0004g0181a0002c0002t0004g0184others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.-90-702_-90-699dup others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr8 | 17924007 | |||||
| chr8:17924112
|
C | T | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90-601C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17924112 | ||||||
| chr8:17924198
|
C | A | 21 | a0005c0005t0008g0168a0005c0005t0008g0169a0005c0005t0008g0174others(18): Show | 21 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.-90-515C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17924198 | ||||||
| chr8:17924219
|
T | A | 1 | a0007c0011t0001g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-90-494T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17924219 | ||||||
| chr8:17924301
|
A | C | 213 | a0001c0001t0001g0146a0001c0001t0001g0147a0002c0002t0004g0002others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.-90-412A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17924301 | ||||||
| chr8:17924341
|
A | T | 39 | a0002c0002t0004g0287a0002c0002t0004g0311a0002c0002t0004g0320others(36): Show | 39 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.-90-372A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17924341 | ||||||
| chr8:17924458
|
A | G | 2 | a0005c0005t0014g0175a0005c0005t0014g0176 | 2 | HG02258.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-90-255A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17924458 | ||||||
| chr8:17924466
|
C | A | 1 | a0003c0006t0002g0177 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-90-247C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17924466 | ||||||
| chr8:17924542
|
A | G | 10 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(7): Show | 10 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-90-171A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17924542 | ||||||
| chr8:17924580
|
T | C | 10 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(7): Show | 10 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-90-133T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17924580 | ||||||
| chr8:17924625
|
C | T | 265 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-90-88C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17924625 | ||||||
| chr8:17924649
|
T | G | 210 | a0001c0001t0001g0146a0002c0002t0004g0002a0002c0002t0004g0180others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.-90-64T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 1/38 | chr8 | 17924649 | ||||||
| chr8:17924882
|
C | G | 1 | a0006c0008t0034g0282 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-23+102C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17924882 | ||||||
| chr8:17924903
|
T | G | 11 | a0002c0002t0028g0323a0002c0009t0016g0359a0002c0009t0016g0362others(8): Show | 11 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-23+123T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17924903 | ||||||
| chr8:17924918
|
C | G | 33 | a0004c0004t0003g0113a0004c0004t0003g0114a0004c0004t0003g0115others(30): Show | 33 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.-23+138C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17924918 | ||||||
| chr8:17924935
|
C | T | 1 | a0002c0002t0005g0281 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-23+155C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17924935 | ||||||
| chr8:17924968
|
G | T | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23+188G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17924968 | ||||||
| chr8:17925116
|
C | T | 1 | a0004c0004t0003g0145 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-23+336C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17925116 | ||||||
| chr8:17925118
|
C | G | 206 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.-23+338C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17925118 | ||||||
| chr8:17925177
|
T | A | 3 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102 | 3 | HG03209.hp1 HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-23+397T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17925177 | ||||||
| chr8:17925183
|
T | C | 34 | a0002c0007t0004g0004a0004c0004t0003g0113a0004c0004t0003g0114others(31): Show | 34 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.-23+403T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17925183 | ||||||
| chr8:17925253
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-23+473G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17925253 | ||||||
| chr8:17925359
|
G | A | 82 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(79): Show | 82 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.-23+579G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17925359 | ||||||
| chr8:17925504
|
T | G | 11 | a0001c0001t0001g0012a0001c0001t0010g0010a0001c0001t0010g0011others(8): Show | 11 | HG00280.hp1 HG00642.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.-23+724T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17925504 | ||||||
| chr8:17925540
|
A | G | 10 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(7): Show | 10 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-23+760A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17925540 | ||||||
| chr8:17925591
|
C | G | 6 | a0007c0011t0001g0149a0007c0011t0001g0150a0007c0011t0003g0151others(3): Show | 6 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-23+811C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17925591 | ||||||
| chr8:17925612
|
G | A | 32 | a0004c0004t0003g0113a0004c0004t0003g0114a0004c0004t0003g0115others(29): Show | 32 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.-23+832G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17925612 | ||||||
| chr8:17925697
|
C | T | 1 | a0001c0001t0010g0015 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-23+917C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17925697 | ||||||
| chr8:17925753
|
C | T | 1 | a0002c0002t0060g0212 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-23+973C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17925753 | ||||||
| chr8:17925760
|
C | G | 1 | a0001c0001t0001g0147 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-23+980C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17925760 | ||||||
| chr8:17925775
|
T | G | 19 | a0002c0019t0004g0213a0002c0019t0004g0337a0003c0003t0009g0339others(16): Show | 19 | HG00597.hp1 HG01884.hp1 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.-23+995T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17925775 | ||||||
| chr8:17925821
|
A | T | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+1041A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17925821 | ||||||
| chr8:17925834
|
C | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+1054C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17925834 | ||||||
| chr8:17925998
|
G | GT | 21 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0006g0101others(18): Show | 21 | HG00423.hp2 HG01099.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.-23+1231dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17925998 | |||||
| chr8:17925999
|
T | G | 82 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(79): Show | 82 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.-23+1219T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17925999 | ||||||
| chr8:17926000
|
T | G | 1 | a0002c0002t0004g0320 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-23+1220T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17926000 | ||||||
| chr8:17926004
|
T | G | 19 | a0002c0019t0004g0213a0002c0019t0004g0337a0003c0003t0009g0339others(16): Show | 19 | HG00597.hp1 HG01884.hp1 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.-23+1224T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17926004 | ||||||
| chr8:17926328
|
T | C | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23+1548T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17926328 | ||||||
| chr8:17926346
|
A | T | 1 | a0001c0001t0001g0146 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-23+1566A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17926346 | ||||||
| chr8:17926472
|
A | G | 4 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102others(1): Show | 4 | HG02896.hp2 HG03209.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+1692A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17926472 | ||||||
| chr8:17926502
|
A | G | 1 | a0006c0008t0034g0282 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-23+1722A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17926502 | ||||||
| chr8:17926619
|
T | A | 42 | a0002c0007t0001g0253a0003c0003t0002g0216a0003c0003t0002g0217others(39): Show | 42 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.-23+1839T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17926619 | ||||||
| chr8:17926624
|
A | C | 3 | a0002c0021t0020g0103a0002c0021t0027g0102a0014c0020t0020g0098 | 3 | HG02896.hp2 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-23+1844A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17926624 | ||||||
| chr8:17926624
|
A | G | 1 | a0002c0017t0003g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-23+1844A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17926624 | ||||||
| chr8:17926634
|
C | T | 14 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(11): Show | 14 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-23+1854C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17926634 | ||||||
| chr8:17926644
|
C | T | 1 | a0018c0028t0001g0097 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-23+1864C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17926644 | ||||||
| chr8:17926694
|
A | G | 86 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.-23+1914A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17926694 | ||||||
| chr8:17926768
|
G | A | 83 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-23+1988G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17926768 | ||||||
| chr8:17926791
|
A | G | 1 | a0006c0008t0033g0277 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-23+2011A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17926791 | ||||||
| chr8:17926905
|
T | C | 90 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(87): Show | 90 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.-23+2125T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17926905 | ||||||
| chr8:17926912
|
G | C | 6 | a0007c0011t0001g0149a0007c0011t0001g0150a0007c0011t0003g0151others(3): Show | 6 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-23+2132G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17926912 | ||||||
| chr8:17926962
|
A | G | 13 | a0004c0004t0003g0132a0004c0004t0003g0133a0004c0004t0003g0135others(10): Show | 13 | HG00140.hp1 HG00323.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.-23+2182A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17926962 | ||||||
| chr8:17926977
|
C | A | 266 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(263): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.-23+2197C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17926977 | ||||||
| chr8:17927015
|
G | A | 1 | a0002c0007t0030g0179 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-23+2235G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927015 | ||||||
| chr8:17927107
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-23+2327C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927107 | ||||||
| chr8:17927117
|
C | T | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+2337C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927117 | ||||||
| chr8:17927124
|
A | AT | 25 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0095others(22): Show | 25 | HG00423.hp2 HG00741.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.-23+2363dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17927124 | |||||
| chr8:17927124
|
A | ATTTTTTT others(11): Show |
3 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354 | 3 | HG02698.hp2 HG03017.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-23+2346_-23+2363d others(20): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17927124 | |||||
| chr8:17927124
|
A | ATTTTTTT others(14): Show |
1 | a0010c0014t0023g0355 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-23+2363_-23+2364i others(23): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17927124 | |||||
| chr8:17927124
|
ATT | A | 10 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(7): Show | 10 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-23+2362_-23+2363d others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17927124 | |||||
| chr8:17927197
|
G | A | 6 | a0007c0011t0001g0149a0007c0011t0001g0150a0007c0011t0003g0151others(3): Show | 6 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-23+2417G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927197 | ||||||
| chr8:17927259
|
C | T | 6 | a0003c0003t0013g0248a0003c0006t0011g0246a0003c0006t0013g0247others(3): Show | 6 | HG00609.hp2 HG02040.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.-23+2479C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927259 | ||||||
| chr8:17927277
|
C | T | 5 | a0002c0002t0012g0319a0010c0014t0022g0330a0010c0014t0022g0331others(2): Show | 5 | HG01106.hp1 HG02698.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23+2497C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927277 | ||||||
| chr8:17927278
|
G | A | 1 | a0004c0004t0049g0356 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-23+2498G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927278 | ||||||
| chr8:17927320
|
G | A | 266 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(263): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.-23+2540G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927320 | ||||||
| chr8:17927361
|
T | C | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+2581T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927361 | ||||||
| chr8:17927402
|
A | G | 1 | a0005c0005t0014g0176 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-23+2622A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927402 | ||||||
| chr8:17927447
|
C | G | 1 | a0002c0002t0005g0318 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-23+2667C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927447 | ||||||
| chr8:17927573
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-23+2793G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927573 | ||||||
| chr8:17927575
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-23+2795T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927575 | ||||||
| chr8:17927625
|
A | C | 6 | a0007c0011t0001g0149a0007c0011t0001g0150a0007c0011t0003g0151others(3): Show | 6 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-23+2845A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927625 | ||||||
| chr8:17927638
|
C | T | 2 | a0002c0002t0005g0316a0002c0002t0066g0317 | 2 | HG01074.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.-23+2858C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927638 | ||||||
| chr8:17927651
|
A | G | 83 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-23+2871A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927651 | ||||||
| chr8:17927665
|
C | G | 2 | a0002c0002t0004g0002a0002c0002t0005g0002 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-23+2885C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927665 | ||||||
| chr8:17927671
|
C | T | 2 | a0002c0017t0031g0321a0002c0017t0032g0322 | 2 | HG01099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-23+2891C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927671 | ||||||
| chr8:17927676
|
T | A | 14 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(11): Show | 14 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-23+2896T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927676 | ||||||
| chr8:17927695
|
C | T | 2 | a0013c0023t0001g0153a0013c0023t0001g0154 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-23+2915C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927695 | ||||||
| chr8:17927708
|
G | A | 3 | a0003c0003t0002g0256a0003c0003t0011g0255a0003c0003t0064g0254 | 3 | NA18972.hp2 NA18978.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.-23+2928G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927708 | ||||||
| chr8:17927711
|
C | T | 1 | a0002c0002t0004g0320 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-23+2931C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927711 | ||||||
| chr8:17927712
|
G | A | 1 | a0002c0002t0004g0180 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-23+2932G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927712 | ||||||
| chr8:17927749
|
A | C | 87 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(84): Show | 87 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.-23+2969A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927749 | ||||||
| chr8:17927757
|
A | G | 267 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(264): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.-23+2977A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927757 | ||||||
| chr8:17927796
|
G | A | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+3016G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927796 | ||||||
| chr8:17927807
|
C | T | 1 | a0006c0008t0007g0276 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-23+3027C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927807 | ||||||
| chr8:17927829
|
G | A | 1 | a0002c0007t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-23+3049G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927829 | ||||||
| chr8:17927863
|
TA | T | 247 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0083others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.-23+3103delA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17927863 | |||||
| chr8:17927863
|
TAA | T | 19 | a0001c0001t0018g0112a0002c0002t0004g0311a0002c0002t0005g0312others(16): Show | 19 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+3102_-23+3103d others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17927863 | |||||
| chr8:17927909
|
C | T | 1 | a0004c0016t0008g0138 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-23+3129C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927909 | ||||||
| chr8:17927915
|
A | G | 4 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102others(1): Show | 4 | HG02896.hp2 HG03209.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+3135A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927915 | ||||||
| chr8:17927916
|
T | C | 1 | a0005c0005t0014g0160 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-23+3136T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927916 | ||||||
| chr8:17927936
|
T | C | 33 | a0004c0004t0003g0113a0004c0004t0003g0114a0004c0004t0003g0115others(30): Show | 33 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.-23+3156T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17927936 | ||||||
| chr8:17927938
|
T | TA | 55 | a0001c0001t0001g0006a0001c0001t0001g0083a0001c0001t0006g0019others(52): Show | 55 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.-23+3174dupA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17927938 | |||||
| chr8:17927938
|
T | TAA | 14 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102others(11): Show | 14 | HG01099.hp2 HG01192.hp2 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.-23+3173_-23+3174d others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17927938 | |||||
| chr8:17927938
|
TA | T | 10 | a0002c0002t0012g0310a0005c0005t0008g0332a0005c0005t0008g0333others(7): Show | 10 | HG01257.hp1 HG01891.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-23+3174delA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17927938 | |||||
| chr8:17927952
|
A | AAC | 7 | a0002c0009t0016g0362a0002c0009t0016g0365a0002c0009t0051g0364others(4): Show | 7 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-23+3173_-23+3174i others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17927952 | |||||
| chr8:17928094
|
C | G | 1 | a0001c0001t0010g0015 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-23+3314C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17928094 | ||||||
| chr8:17928157
|
T | C | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23+3377T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17928157 | ||||||
| chr8:17928262
|
A | G | 4 | a0005c0005t0008g0168a0005c0005t0008g0169a0005c0005t0008g0174others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+3482A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17928262 | ||||||
| chr8:17928281
|
C | T | 83 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-23+3501C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17928281 | ||||||
| chr8:17928558
|
C | G | 1 | a0004c0004t0003g0357 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-23+3778C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17928558 | ||||||
| chr8:17928611
|
TCC | T | 61 | a0002c0007t0001g0253a0003c0003t0002g0003a0003c0003t0002g0156others(58): Show | 61 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-23+3833_-23+3834d others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17928611 | |||||
| chr8:17928613
|
C | T | 16 | a0002c0007t0004g0278a0003c0003t0002g0239a0003c0003t0002g0240others(13): Show | 16 | HG00423.hp2 HG00544.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23+3833C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17928613 | ||||||
| chr8:17928616
|
C | CT | 6 | a0001c0001t0001g0016a0001c0001t0001g0082a0001c0001t0001g0090others(3): Show | 6 | HG00642.hp1 HG02273.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.-23+3864dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17928616 | |||||
| chr8:17928616
|
CT | C | 22 | a0001c0001t0001g0025a0001c0001t0001g0146a0001c0001t0006g0026others(19): Show | 22 | HG00423.hp2 HG00544.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.-23+3864delT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17928616 | |||||
| chr8:17928616
|
CTT | C | 18 | a0002c0002t0005g0182a0002c0002t0005g0281a0002c0002t0021g0308others(15): Show | 18 | HG00140.hp2 HG00621.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-23+3863_-23+3864d others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17928616 | |||||
| chr8:17928616
|
CTTT | C | 103 | a0001c0001t0018g0110a0002c0002t0004g0002a0002c0002t0004g0180others(100): Show | 103 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.-23+3862_-23+3864d others(5): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17928616 | |||||
| chr8:17928616
|
CTTTT | C | 49 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(46): Show | 49 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.-23+3861_-23+3864d others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17928616 | |||||
| chr8:17928616
|
CTTTTTTT | C | 9 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0051g0364others(6): Show | 9 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-23+3858_-23+3864d others(9): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17928616 | |||||
| chr8:17928616
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02602.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.-23+3854_-23+3864d others(13): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17928616 | |||||
| chr8:17928616
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-23+3850_-23+3864d others(17): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17928616 | |||||
| chr8:17928618
|
T | C | 61 | a0002c0007t0001g0253a0003c0003t0002g0003a0003c0003t0002g0156others(58): Show | 61 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-23+3838T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17928618 | ||||||
| chr8:17928622
|
T | A | 2 | a0004c0004t0003g0128a0020c0045t0003g0127 | 2 | NA18949.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-23+3842T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17928622 | ||||||
| chr8:17928623
|
T | A | 28 | a0004c0004t0003g0113a0004c0004t0003g0114a0004c0004t0003g0115others(25): Show | 28 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.-23+3843T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17928623 | ||||||
| chr8:17928624
|
T | A | 3 | a0004c0004t0003g0129a0004c0004t0003g0137a0004c0004t0003g0140 | 3 | HG01167.hp2 HG01169.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.-23+3844T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17928624 | ||||||
| chr8:17928644
|
T | A | 1 | a0002c0007t0030g0179 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-23+3864T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17928644 | ||||||
| chr8:17928655
|
G | A | 33 | a0004c0004t0003g0113a0004c0004t0003g0114a0004c0004t0003g0115others(30): Show | 33 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.-23+3875G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17928655 | ||||||
| chr8:17928656
|
G | A | 1 | a0002c0002t0005g0285 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-23+3876G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17928656 | ||||||
| chr8:17928694
|
C | T | 1 | a0006c0008t0068g0273 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-23+3914C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17928694 | ||||||
| chr8:17928695
|
T | A | 1 | a0004c0004t0003g0114 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-23+3915T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17928695 | ||||||
| chr8:17928695
|
T | G | 267 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(264): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.-23+3915T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17928695 | ||||||
| chr8:17928717
|
T | C | 269 | a0001c0001t0001g0146a0001c0001t0017g0105a0001c0001t0017g0108others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.-23+3937T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17928717 | ||||||
| chr8:17928829
|
G | A | 1 | a0004c0004t0003g0115 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-23+4049G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17928829 | ||||||
| chr8:17928838
|
A | G | 7 | a0005c0005t0014g0163a0005c0005t0015g0162a0005c0005t0015g0164others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-23+4058A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17928838 | ||||||
| chr8:17928895
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-23+4115G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17928895 | ||||||
| chr8:17928924
|
A | G | 1 | a0005c0005t0014g0176 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-23+4144A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17928924 | ||||||
| chr8:17928926
|
C | T | 34 | a0002c0007t0004g0004a0004c0004t0003g0113a0004c0004t0003g0114others(31): Show | 34 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.-23+4146C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17928926 | ||||||
| chr8:17929001
|
A | G | 2 | a0002c0002t0047g0206a0002c0002t0048g0205 | 2 | HG01074.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.-23+4221A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17929001 | ||||||
| chr8:17929007
|
G | A | 268 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(265): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.-23+4227G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17929007 | ||||||
| chr8:17929098
|
T | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 6 | NA18944.hp2 NA18948.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.-23+4318T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17929098 | ||||||
| chr8:17929158
|
A | G | 1 | a0002c0007t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-23+4378A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17929158 | ||||||
| chr8:17929250
|
C | G | 1 | a0003c0006t0002g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-23+4470C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17929250 | ||||||
| chr8:17929305
|
T | C | 1 | a0002c0007t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-23+4525T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17929305 | ||||||
| chr8:17929309
|
G | A | 268 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(265): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.-23+4529G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17929309 | ||||||
| chr8:17929317
|
G | A | 10 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(7): Show | 10 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-23+4537G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17929317 | ||||||
| chr8:17929349
|
C | T | 1 | a0002c0002t0028g0323 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-23+4569C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17929349 | ||||||
| chr8:17929476
|
G | A | 1 | a0002c0002t0005g0182 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-23+4696G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17929476 | ||||||
| chr8:17929496
|
T | C | 98 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(95): Show | 98 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.-23+4716T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17929496 | ||||||
| chr8:17929514
|
C | G | 10 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(7): Show | 10 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-23+4734C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17929514 | ||||||
| chr8:17929516
|
C | T | 4 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102others(1): Show | 4 | HG02896.hp2 HG03209.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+4736C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17929516 | ||||||
| chr8:17929657
|
C | T | 1 | a0001c0048t0006g0081 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-23+4877C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17929657 | ||||||
| chr8:17929709
|
G | T | 1 | a0003c0003t0002g0237 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-23+4929G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17929709 | ||||||
| chr8:17929731
|
C | T | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+4951C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17929731 | ||||||
| chr8:17929760
|
C | G | 3 | a0002c0017t0031g0321a0002c0017t0032g0322a0007c0011t0003g0152 | 3 | HG01099.hp1 HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-23+4980C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17929760 | ||||||
| chr8:17929925
|
C | T | 14 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(11): Show | 14 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-23+5145C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17929925 | ||||||
| chr8:17929961
|
T | C | 1 | a0007c0011t0003g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-23+5181T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17929961 | ||||||
| chr8:17930027
|
A | G | 220 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.-23+5247A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17930027 | ||||||
| chr8:17930101
|
C | CT | 10 | a0001c0001t0001g0027a0001c0001t0001g0078a0001c0001t0006g0079others(7): Show | 10 | HG00438.hp2 HG00544.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.-23+5341dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17930101 | |||||
| chr8:17930101
|
CT | C | 96 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(93): Show | 96 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.-23+5341delT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17930101 | |||||
| chr8:17930101
|
CTT | C | 46 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(43): Show | 46 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.-23+5340_-23+5341d others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17930101 | |||||
| chr8:17930121
|
T | G | 4 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102others(1): Show | 4 | HG02896.hp2 HG03209.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+5341T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17930121 | ||||||
| chr8:17930130
|
G | C | 3 | a0012c0015t0025g0342a0012c0015t0025g0343a0012c0015t0042g0344 | 3 | NA18977.hp1 NA18979.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-23+5350G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17930130 | ||||||
| chr8:17930136
|
C | T | 1 | a0002c0002t0029g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-23+5356C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17930136 | ||||||
| chr8:17930142
|
C | T | 1 | a0004c0016t0003g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-23+5362C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17930142 | ||||||
| chr8:17930250
|
G | A | 1 | a0004c0004t0003g0116 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-22-5339G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17930250 | ||||||
| chr8:17930254
|
C | G | 15 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(12): Show | 15 | HG01884.hp2 HG02145.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.-22-5335C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17930254 | ||||||
| chr8:17930269
|
T | G | 1 | a0001c0001t0006g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-22-5320T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17930269 | ||||||
| chr8:17930298
|
T | C | 3 | a0003c0003t0007g0274a0006c0008t0007g0276a0006c0008t0068g0273 | 3 | HG02027.hp1 HG02135.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.-22-5291T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17930298 | ||||||
| chr8:17930299
|
T | A | 83 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-22-5290T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17930299 | ||||||
| chr8:17930304
|
C | T | 1 | a0006c0008t0007g0276 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-22-5285C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17930304 | ||||||
| chr8:17930328
|
C | T | 6 | a0003c0003t0013g0248a0003c0006t0011g0246a0003c0006t0013g0247others(3): Show | 6 | HG00609.hp2 HG02040.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-5261C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17930328 | ||||||
| chr8:17930402
|
C | T | 1 | a0003c0003t0002g0236 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-22-5187C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17930402 | ||||||
| chr8:17930584
|
A | G | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-22-5005A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17930584 | ||||||
| chr8:17930600
|
C | A | 1 | a0002c0002t0029g0183 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-22-4989C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17930600 | ||||||
| chr8:17930637
|
G | C | 7 | a0001c0001t0001g0012a0001c0001t0010g0010a0001c0001t0010g0011others(4): Show | 7 | HG00280.hp1 HG00642.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22-4952G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17930637 | ||||||
| chr8:17930645
|
G | C | 1 | a0001c0001t0001g0032 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-22-4944G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17930645 | ||||||
| chr8:17930748
|
C | T | 3 | a0005c0005t0015g0164a0005c0005t0015g0165a0005c0005t0015g0166 | 3 | HG02109.hp2 HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-22-4841C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17930748 | ||||||
| chr8:17930752
|
T | C | 98 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(95): Show | 98 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.-22-4837T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17930752 | ||||||
| chr8:17930817
|
T | C | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-4772T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17930817 | ||||||
| chr8:17930836
|
C | G | 1 | a0002c0002t0012g0319 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-22-4753C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17930836 | ||||||
| chr8:17930836
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-22-4753C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17930836 | ||||||
| chr8:17930880
|
CA | C | 33 | a0002c0007t0004g0004a0004c0004t0003g0113a0004c0004t0003g0114others(30): Show | 33 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.-22-4697delA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17930880 | |||||
| chr8:17930923
|
C | T | 5 | a0004c0004t0003g0336a0004c0004t0003g0351a0004c0004t0003g0352others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-4666C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17930923 | ||||||
| chr8:17930926
|
C | T | 90 | a0002c0007t0004g0278a0002c0019t0004g0337a0003c0003t0002g0003others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.-22-4663C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17930926 | ||||||
| chr8:17931002
|
C | T | 48 | a0002c0007t0004g0004a0002c0009t0016g0359a0002c0009t0016g0362others(45): Show | 48 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.-22-4587C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17931002 | ||||||
| chr8:17931065
|
A | G | 4 | a0003c0003t0009g0339a0003c0012t0002g0341a0003c0012t0009g0340others(1): Show | 4 | NA18941.hp2 NA18965.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-4524A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17931065 | ||||||
| chr8:17931072
|
A | T | 1 | a0002c0002t0012g0307 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-22-4517A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17931072 | ||||||
| chr8:17931314
|
G | A | 3 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102 | 3 | HG03209.hp1 HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-22-4275G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17931314 | ||||||
| chr8:17931350
|
G | A | 1 | a0006c0008t0007g0261 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-22-4239G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17931350 | ||||||
| chr8:17931402
|
C | T | 1 | a0001c0001t0006g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-22-4187C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17931402 | ||||||
| chr8:17931476
|
A | T | 1 | a0004c0004t0003g0126 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-22-4113A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17931476 | ||||||
| chr8:17931491
|
G | T | 4 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102others(1): Show | 4 | HG02896.hp2 HG03209.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-4098G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17931491 | ||||||
| chr8:17931622
|
C | G | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-22-3967C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17931622 | ||||||
| chr8:17931647
|
T | A | 1 | a0003c0003t0011g0329 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-22-3942T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17931647 | ||||||
| chr8:17931656
|
C | T | 1 | a0001c0001t0040g0076 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-22-3933C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17931656 | ||||||
| chr8:17931687
|
C | T | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-3902C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17931687 | ||||||
| chr8:17931688
|
G | A | 2 | a0002c0017t0031g0321a0022c0029t0045g0279 | 2 | HG01099.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-22-3901G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17931688 | ||||||
| chr8:17931711
|
A | G | 1 | a0002c0007t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-22-3878A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17931711 | ||||||
| chr8:17931745
|
T | G | 1 | a0007c0011t0001g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-22-3844T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17931745 | ||||||
| chr8:17931789
|
T | C | 271 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0017g0105others(268): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.-22-3800T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17931789 | ||||||
| chr8:17931847
|
C | T | 2 | a0002c0002t0004g0002a0002c0002t0005g0002 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-22-3742C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17931847 | ||||||
| chr8:17931900
|
C | T | 14 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(11): Show | 14 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-22-3689C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17931900 | ||||||
| chr8:17932106
|
G | C | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-22-3483G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17932106 | ||||||
| chr8:17932224
|
A | G | 4 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102others(1): Show | 4 | HG02896.hp2 HG03209.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-3365A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17932224 | ||||||
| chr8:17932232
|
C | T | 1 | a0002c0017t0003g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-22-3357C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17932232 | ||||||
| chr8:17932376
|
T | C | 1 | a0005c0005t0015g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-22-3213T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17932376 | ||||||
| chr8:17932412
|
C | G | 15 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(12): Show | 15 | HG01884.hp2 HG02145.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.-22-3177C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17932412 | ||||||
| chr8:17932550
|
A | G | 1 | a0002c0017t0031g0321 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-22-3039A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17932550 | ||||||
| chr8:17932560
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | HG02683.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-22-3029G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17932560 | ||||||
| chr8:17932561
|
G | T | 1 | a0003c0003t0002g0242 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-22-3028G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17932561 | ||||||
| chr8:17932565
|
T | C | 1 | a0002c0021t0027g0102 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-22-3024T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17932565 | ||||||
| chr8:17932587
|
T | C | 1 | a0005c0005t0014g0163 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-22-3002T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17932587 | ||||||
| chr8:17932592
|
A | G | 2 | a0003c0012t0002g0341a0003c0012t0009g0340 | 2 | NA18965.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.-22-2997A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17932592 | ||||||
| chr8:17932706
|
A | T | 1 | a0003c0012t0009g0349 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-22-2883A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17932706 | ||||||
| chr8:17932823
|
C | A | 27 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(24): Show | 28 | HG00597.hp2 NA18944.hp2 NA18948.hp1 others(25): Show |
intron_variant | MODIFIER | c.-22-2766C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17932823 | ||||||
| chr8:17932827
|
G | C | 7 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(4): Show | 7 | HG00597.hp2 NA18966.hp1 NA19001.hp2 others(4): Show |
intron_variant | MODIFIER | c.-22-2762G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17932827 | ||||||
| chr8:17932928
|
T | C | 88 | a0001c0001t0001g0147a0002c0002t0004g0002a0002c0002t0004g0180others(85): Show | 88 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.-22-2661T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17932928 | ||||||
| chr8:17933042
|
TAAGG | T | 7 | a0004c0004t0003g0132a0004c0004t0003g0133a0004c0004t0003g0137others(4): Show | 7 | HG00140.hp1 HG00323.hp2 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.-22-2543_-22-2540d others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17933042 | |||||
| chr8:17933142
|
T | C | 7 | a0001c0001t0001g0012a0001c0001t0010g0010a0001c0001t0010g0011others(4): Show | 7 | HG00280.hp1 HG00642.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22-2447T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17933142 | ||||||
| chr8:17933189
|
G | A | 1 | a0002c0002t0004g0184 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-22-2400G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17933189 | ||||||
| chr8:17933224
|
T | A | 2 | a0013c0023t0001g0153a0013c0023t0001g0154 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-22-2365T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17933224 | ||||||
| chr8:17933429
|
A | G | 2 | a0006c0008t0007g0261a0006c0008t0007g0272 | 2 | NA18612.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-22-2160A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17933429 | ||||||
| chr8:17933539
|
A | T | 12 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(9): Show | 12 | HG02109.hp1 HG02647.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.-22-2050A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17933539 | ||||||
| chr8:17933648
|
A | C | 96 | a0001c0001t0001g0146a0002c0007t0004g0278a0002c0019t0004g0213others(93): Show | 96 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.-22-1941A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17933648 | ||||||
| chr8:17933648
|
A | G | 12 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(9): Show | 12 | HG02109.hp1 HG02647.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.-22-1941A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17933648 | ||||||
| chr8:17933709
|
C | G | 122 | a0001c0001t0001g0147a0002c0002t0004g0002a0002c0002t0004g0180others(119): Show | 122 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-22-1880C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17933709 | ||||||
| chr8:17933715
|
C | T | 1 | a0002c0017t0031g0321 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-22-1874C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17933715 | ||||||
| chr8:17933745
|
G | A | 1 | a0002c0007t0030g0179 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-22-1844G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17933745 | ||||||
| chr8:17933771
|
G | T | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-1818G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17933771 | ||||||
| chr8:17933926
|
C | G | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-22-1663C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17933926 | ||||||
| chr8:17933959
|
A | C | 1 | a0002c0002t0005g0313 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-22-1630A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17933959 | ||||||
| chr8:17933994
|
A | T | 95 | a0001c0001t0001g0146a0002c0007t0004g0278a0002c0019t0004g0337others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.-22-1595A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17933994 | ||||||
| chr8:17934033
|
C | T | 12 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(9): Show | 12 | HG02109.hp1 HG02647.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.-22-1556C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17934033 | ||||||
| chr8:17934087
|
G | A | 6 | a0002c0017t0032g0322a0005c0005t0014g0160a0005c0005t0014g0171others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-1502G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17934087 | ||||||
| chr8:17934125
|
C | G | 86 | a0001c0001t0001g0147a0002c0002t0004g0002a0002c0002t0004g0180others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.-22-1464C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17934125 | ||||||
| chr8:17934125
|
C | T | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-22-1464C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17934125 | ||||||
| chr8:17934206
|
A | G | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0075 | 3 | HG02602.hp1 HG03491.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-22-1383A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17934206 | ||||||
| chr8:17934268
|
C | CT | 88 | a0001c0001t0001g0147a0001c0001t0024g0048a0002c0002t0004g0002others(85): Show | 88 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.-22-1309dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr8 | 17934268 | |||||
| chr8:17934321
|
G | C | 1 | a0006c0008t0033g0277 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-22-1268G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17934321 | ||||||
| chr8:17934685
|
T | C | 4 | a0004c0004t0003g0336a0004c0004t0003g0351a0004c0004t0003g0352others(1): Show | 4 | HG01884.hp1 HG03130.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-904T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17934685 | ||||||
| chr8:17934964
|
A | C | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-625A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17934964 | ||||||
| chr8:17935000
|
A | C | 1 | a0002c0017t0032g0322 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-22-589A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17935000 | ||||||
| chr8:17935206
|
A | G | 7 | a0007c0011t0001g0149a0007c0011t0001g0150a0007c0011t0003g0151others(4): Show | 7 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-22-383A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17935206 | ||||||
| chr8:17935257
|
T | G | 1 | a0005c0005t0015g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-22-332T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17935257 | ||||||
| chr8:17935259
|
G | A | 1 | a0004c0016t0008g0138 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-22-330G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17935259 | ||||||
| chr8:17935344
|
G | A | 142 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(139): Show | 142 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-22-245G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17935344 | ||||||
| chr8:17935351
|
A | G | 2 | a0006c0008t0007g0261a0006c0008t0007g0272 | 2 | NA18612.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-22-238A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17935351 | ||||||
| chr8:17935429
|
C | G | 1 | a0003c0040t0013g0249 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-22-160C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17935429 | ||||||
| chr8:17935503
|
A | G | 1 | a0005c0005t0014g0163 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-22-86A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17935503 | ||||||
| chr8:17935523
|
G | C | 1 | a0001c0001t0006g0049 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-22-66G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17935523 | ||||||
| chr8:17935565
|
C | G | 1 | a0003c0003t0002g0217 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-22-24C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17935565 | ||||||
| chr8:17935575
|
A | G | 125 | a0002c0007t0004g0278a0002c0017t0031g0321a0002c0017t0032g0322others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.-22-14A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17935575 | ||||||
| chr8:17935584
|
C | T | 36 | a0002c0017t0003g0104a0004c0004t0003g0113a0004c0004t0003g0114others(33): Show | 36 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(33): Show |
splice_region_variant&intron_variant | LOW | c.-22-5C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 2/38 | chr8 | 17935584 | ||||||
| chr8:17935752
|
A | G | 1 | a0006c0008t0033g0277 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.96+46A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 3/38 | chr8 | 17935752 | ||||||
| chr8:17935898
|
T | C | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+192T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 3/38 | chr8 | 17935898 | ||||||
| chr8:17936129
|
C | G | 138 | a0001c0001t0001g0147a0002c0002t0004g0002a0002c0002t0004g0180others(135): Show | 138 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.96+423C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 3/38 | chr8 | 17936129 | ||||||
| chr8:17936159
|
A | G | 7 | a0007c0011t0001g0149a0007c0011t0001g0150a0007c0011t0003g0151others(4): Show | 7 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+453A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 3/38 | chr8 | 17936159 | ||||||
| chr8:17936192
|
G | A | 1 | a0004c0004t0049g0356 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.96+486G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 3/38 | chr8 | 17936192 | ||||||
| chr8:17936195
|
G | C | 1 | a0005c0005t0015g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.96+489G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 3/38 | chr8 | 17936195 | ||||||
| chr8:17936223
|
T | C | 2 | a0005c0005t0014g0160a0005c0005t0027g0170 | 2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.96+517T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 3/38 | chr8 | 17936223 | ||||||
| chr8:17936433
|
T | C | 128 | a0001c0001t0001g0147a0002c0002t0004g0002a0002c0002t0004g0180others(125): Show | 128 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.97-701T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 3/38 | chr8 | 17936433 | ||||||
| chr8:17936460
|
T | A | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.97-674T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 3/38 | chr8 | 17936460 | ||||||
| chr8:17936526
|
G | A | 12 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(9): Show | 12 | HG02109.hp1 HG02647.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.97-608G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 3/38 | chr8 | 17936526 | ||||||
| chr8:17936530
|
C | T | 269 | a0001c0001t0001g0147a0001c0001t0017g0105a0001c0001t0017g0108others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.97-604C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 3/38 | chr8 | 17936530 | ||||||
| chr8:17937023
|
A | G | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-111A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 3/38 | chr8 | 17937023 | ||||||
| chr8:17937078
|
T | C | 12 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(9): Show | 12 | HG02109.hp1 HG02647.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.97-56T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 3/38 | chr8 | 17937078 | ||||||
| chr8:17937117
|
C | T | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-17C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 3/38 | chr8 | 17937117 | ||||||
| chr8:17937569
|
C | T | 1 | a0014c0020t0020g0098 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.342+190C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/38 | chr8 | 17937569 | ||||||
| chr8:17937692
|
A | G | 42 | a0002c0007t0001g0033a0002c0017t0003g0104a0004c0004t0003g0113others(39): Show | 42 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.342+313A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/38 | chr8 | 17937692 | ||||||
| chr8:17937755
|
T | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+376T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/38 | chr8 | 17937755 | ||||||
| chr8:17937829
|
A | G | 1 | a0002c0007t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.342+450A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/38 | chr8 | 17937829 | ||||||
| chr8:17937852
|
T | G | 3 | a0005c0005t0015g0162a0005c0005t0015g0164a0005c0005t0015g0165 | 3 | HG01891.hp1 HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.342+473T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/38 | chr8 | 17937852 | ||||||
| chr8:17937859
|
A | G | 127 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(124): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.342+480A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/38 | chr8 | 17937859 | ||||||
| chr8:17937865
|
C | T | 4 | a0005c0005t0008g0332a0005c0005t0008g0333a0005c0005t0008g0334others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+486C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/38 | chr8 | 17937865 | ||||||
| chr8:17937963
|
C | T | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+584C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/38 | chr8 | 17937963 | ||||||
| chr8:17937965
|
A | G | 7 | a0007c0011t0001g0149a0007c0011t0001g0150a0007c0011t0003g0151others(4): Show | 7 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.342+586A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/38 | chr8 | 17937965 | ||||||
| chr8:17937987
|
A | G | 258 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(255): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.342+608A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/38 | chr8 | 17937987 | ||||||
| chr8:17938121
|
A | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0008 | 2 | HG00738.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.343-619A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/38 | chr8 | 17938121 | ||||||
| chr8:17938124
|
C | T | 2 | a0002c0021t0020g0103a0002c0021t0027g0102 | 2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.343-616C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/38 | chr8 | 17938124 | ||||||
| chr8:17938155
|
T | C | 5 | a0008c0010t0004g0207a0008c0010t0004g0208a0008c0010t0004g0209others(2): Show | 5 | HG02135.hp1 NA18961.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-585T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/38 | chr8 | 17938155 | ||||||
| chr8:17938246
|
G | T | 1 | a0001c0001t0001g0074 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.343-494G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/38 | chr8 | 17938246 | ||||||
| chr8:17938255
|
C | CA | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-485_343-484ins others(1): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/38 | chr8 | 17938255 | ||||||
| chr8:17938425
|
A | G | 260 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(257): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.343-315A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/38 | chr8 | 17938425 | ||||||
| chr8:17938477
|
G | C | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.343-263G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/38 | chr8 | 17938477 | ||||||
| chr8:17938583
|
T | A | 20 | a0005c0005t0008g0168a0005c0005t0008g0169a0005c0005t0008g0174others(17): Show | 20 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.343-157T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/38 | chr8 | 17938583 | ||||||
| chr8:17938650
|
T | C | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.343-90T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/38 | chr8 | 17938650 | ||||||
| chr8:17938691
|
T | G | 1 | a0003c0012t0009g0349 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.343-49T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/38 | chr8 | 17938691 | ||||||
| chr8:17938696
|
A | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-44A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/38 | chr8 | 17938696 | ||||||
| chr8:17938703
|
T | A | 2 | a0003c0003t0002g0003a0003c0003t0011g0003 | 2 | HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.343-37T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/38 | chr8 | 17938703 | ||||||
| chr8:17938717
|
T | C | 88 | a0002c0019t0004g0337a0003c0003t0002g0003a0003c0003t0002g0156others(85): Show | 88 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.343-23T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 4/38 | chr8 | 17938717 | ||||||
| chr8:17939059
|
C | G | 3 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102 | 3 | HG03209.hp1 HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.612+50C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 5/38 | chr8 | 17939059 | ||||||
| chr8:17939094
|
C | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.612+85C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 5/38 | chr8 | 17939094 | ||||||
| chr8:17939252
|
T | A | 84 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.612+243T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 5/38 | chr8 | 17939252 | ||||||
| chr8:17939273
|
G | A | 1 | a0002c0007t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.612+264G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 5/38 | chr8 | 17939273 | ||||||
| chr8:17939334
|
C | G | 1 | a0003c0003t0002g0241 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.612+325C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 5/38 | chr8 | 17939334 | ||||||
| chr8:17939362
|
A | C | 210 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.613-329A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 5/38 | chr8 | 17939362 | ||||||
| chr8:17939375
|
A | ATAACAAT others(6): Show |
256 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(253): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.613-313_613-312ins others(13): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr8 | 17939375 | |||||
| chr8:17939432
|
T | G | 1 | a0002c0002t0004g0185 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.613-259T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 5/38 | chr8 | 17939432 | ||||||
| chr8:17939461
|
G | T | 213 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.613-230G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 5/38 | chr8 | 17939461 | ||||||
| chr8:17939546
|
A | G | 210 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.613-145A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 5/38 | chr8 | 17939546 | ||||||
| chr8:17939576
|
C | G | 1 | a0002c0002t0005g0284 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.613-115C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 5/38 | chr8 | 17939576 | ||||||
| chr8:17939589
|
C | T | 1 | a0007c0011t0001g0150 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.613-102C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 5/38 | chr8 | 17939589 | ||||||
| chr8:17939669
|
A | T | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.613-22A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 5/38 | chr8 | 17939669 | ||||||
| chr8:17939886
|
CAT | C | 6 | a0002c0017t0032g0322a0005c0005t0014g0160a0005c0005t0014g0171others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.783+28_783+29delAT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr8 | 17939886 | |||||
| chr8:17939900
|
A | G | 210 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.783+39A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17939900 | ||||||
| chr8:17940013
|
G | T | 1 | a0004c0016t0003g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.783+152G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17940013 | ||||||
| chr8:17940059
|
G | C | 1 | a0005c0005t0014g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.783+198G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17940059 | ||||||
| chr8:17940169
|
T | G | 1 | a0001c0001t0001g0050 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.783+308T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17940169 | ||||||
| chr8:17940240
|
G | A | 7 | a0007c0011t0001g0149a0007c0011t0001g0150a0007c0011t0003g0151others(4): Show | 7 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.783+379G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17940240 | ||||||
| chr8:17940249
|
A | T | 1 | a0001c0001t0001g0083 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.783+388A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17940249 | ||||||
| chr8:17940319
|
A | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.783+458A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17940319 | ||||||
| chr8:17940356
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.783+495T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17940356 | ||||||
| chr8:17940422
|
T | A | 214 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.783+561T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17940422 | ||||||
| chr8:17940465
|
G | C | 214 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.783+604G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17940465 | ||||||
| chr8:17940542
|
C | G | 3 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102 | 3 | HG03209.hp1 HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.783+681C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17940542 | ||||||
| chr8:17940672
|
G | A | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.783+811G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17940672 | ||||||
| chr8:17940734
|
G | A | 266 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(263): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.783+873G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17940734 | ||||||
| chr8:17940737
|
T | G | 1 | a0005c0005t0014g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.783+876T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17940737 | ||||||
| chr8:17940886
|
A | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01515.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.783+1025A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17940886 | ||||||
| chr8:17940914
|
A | T | 1 | a0002c0009t0005g0304 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.783+1053A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17940914 | ||||||
| chr8:17940931
|
C | G | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.783+1070C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17940931 | ||||||
| chr8:17940959
|
C | T | 3 | a0004c0004t0003g0124a0004c0004t0003g0125a0004c0004t0003g0143 | 3 | NA18945.hp1 NA18972.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.783+1098C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17940959 | ||||||
| chr8:17941006
|
C | G | 121 | a0002c0002t0004g0328a0002c0002t0005g0326a0002c0002t0005g0327others(118): Show | 121 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.783+1145C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17941006 | ||||||
| chr8:17941030
|
T | C | 1 | a0001c0001t0037g0087 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.783+1169T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17941030 | ||||||
| chr8:17941182
|
C | G | 1 | a0001c0001t0010g0015 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.783+1321C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17941182 | ||||||
| chr8:17941218
|
G | A | 5 | a0005c0005t0008g0168a0005c0005t0008g0169a0005c0005t0008g0174others(2): Show | 5 | HG02559.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.783+1357G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17941218 | ||||||
| chr8:17941247
|
A | G | 7 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(4): Show | 7 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.783+1386A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17941247 | ||||||
| chr8:17941282
|
T | A | 1 | a0003c0006t0002g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.783+1421T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17941282 | ||||||
| chr8:17941339
|
G | C | 267 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(264): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.783+1478G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17941339 | ||||||
| chr8:17941483
|
A | T | 124 | a0002c0002t0004g0328a0002c0002t0005g0326a0002c0002t0005g0327others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.783+1622A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17941483 | ||||||
| chr8:17941520
|
ATT | A | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.783+1663_783+1664d others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr8 | 17941520 | |||||
| chr8:17941530
|
T | G | 255 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.783+1669T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17941530 | ||||||
| chr8:17941531
|
T | G | 1 | a0003c0003t0011g0178 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.783+1670T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17941531 | ||||||
| chr8:17941542
|
A | T | 131 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(128): Show | 131 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.783+1681A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17941542 | ||||||
| chr8:17941543
|
A | T | 77 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(74): Show | 77 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.783+1682A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17941543 | ||||||
| chr8:17941546
|
AAAAG | A | 13 | a0002c0019t0004g0337a0003c0003t0009g0339a0003c0003t0009g0346others(10): Show | 13 | HG00597.hp1 HG02056.hp1 HG02683.hp2 others(10): Show |
intron_variant | MODIFIER | c.783+1686_783+1689d others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17941546 | ||||||
| chr8:17941583
|
G | A | 7 | a0007c0011t0001g0149a0007c0011t0001g0150a0007c0011t0003g0151others(4): Show | 7 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.783+1722G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17941583 | ||||||
| chr8:17941590
|
T | TAA | 13 | a0002c0019t0004g0337a0003c0003t0009g0339a0003c0003t0009g0346others(10): Show | 13 | HG00597.hp1 HG02056.hp1 HG02683.hp2 others(10): Show |
intron_variant | MODIFIER | c.783+1730_783+1731i others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr8 | 17941590 | |||||
| chr8:17941620
|
T | A | 144 | a0001c0001t0001g0077a0001c0001t0017g0105a0001c0001t0017g0108others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.783+1759T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17941620 | ||||||
| chr8:17941665
|
C | T | 1 | a0003c0040t0013g0249 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.783+1804C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17941665 | ||||||
| chr8:17941681
|
G | T | 3 | a0005c0005t0014g0160a0005c0005t0014g0171a0005c0005t0027g0170 | 3 | HG01891.hp2 HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.783+1820G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17941681 | ||||||
| chr8:17941732
|
T | C | 79 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.783+1871T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17941732 | ||||||
| chr8:17941781
|
C | G | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.783+1920C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17941781 | ||||||
| chr8:17941818
|
C | T | 1 | a0002c0007t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.783+1957C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17941818 | ||||||
| chr8:17941867
|
C | CT | 140 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.783+2007dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr8 | 17941867 | |||||
| chr8:17941889
|
C | T | 1 | a0003c0003t0007g0274 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.783+2028C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17941889 | ||||||
| chr8:17941924
|
G | C | 1 | a0001c0001t0001g0147 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.783+2063G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17941924 | ||||||
| chr8:17941927
|
A | G | 3 | a0002c0002t0005g0301a0002c0002t0005g0302a0002c0002t0005g0303 | 3 | HG00280.hp2 HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.783+2066A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17941927 | ||||||
| chr8:17942000
|
GTTTT | G | 13 | a0002c0019t0004g0337a0003c0003t0009g0339a0003c0003t0009g0346others(10): Show | 13 | HG00597.hp1 HG02056.hp1 HG02683.hp2 others(10): Show |
intron_variant | MODIFIER | c.783+2144_783+2147d others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr8 | 17942000 | |||||
| chr8:17942046
|
C | T | 1 | a0003c0003t0011g0178 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.783+2185C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942046 | ||||||
| chr8:17942127
|
C | G | 4 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102others(1): Show | 4 | HG02896.hp2 HG03209.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.783+2266C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942127 | ||||||
| chr8:17942178
|
G | T | 1 | a0002c0002t0004g0320 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.783+2317G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942178 | ||||||
| chr8:17942194
|
A | G | 4 | a0005c0005t0008g0168a0005c0005t0008g0169a0005c0005t0008g0174others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.783+2333A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942194 | ||||||
| chr8:17942205
|
C | T | 2 | a0002c0002t0004g0002a0002c0002t0005g0002 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.783+2344C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942205 | ||||||
| chr8:17942206
|
G | T | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.783+2345G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942206 | ||||||
| chr8:17942227
|
A | G | 144 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.783+2366A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942227 | ||||||
| chr8:17942271
|
A | C | 5 | a0002c0007t0004g0200a0002c0007t0004g0201a0002c0007t0004g0203others(2): Show | 5 | NA18942.hp1 NA18975.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.783+2410A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942271 | ||||||
| chr8:17942278
|
C | A | 141 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.783+2417C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942278 | ||||||
| chr8:17942283
|
A | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.783+2422A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942283 | ||||||
| chr8:17942296
|
G | T | 1 | a0002c0017t0003g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.783+2435G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942296 | ||||||
| chr8:17942329
|
C | T | 1 | a0002c0017t0032g0322 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.783+2468C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942329 | ||||||
| chr8:17942450
|
C | T | 2 | a0003c0003t0002g0240a0003c0003t0002g0243 | 2 | NA18960.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.783+2589C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942450 | ||||||
| chr8:17942467
|
A | C | 1 | a0002c0002t0005g0315 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.783+2606A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942467 | ||||||
| chr8:17942470
|
G | A | 144 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.783+2609G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942470 | ||||||
| chr8:17942529
|
T | C | 1 | a0002c0002t0029g0183 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.783+2668T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942529 | ||||||
| chr8:17942565
|
A | C | 3 | a0003c0003t0026g0271a0003c0003t0046g0259a0030c0041t0026g0270 | 3 | HG00639.hp2 HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.783+2704A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942565 | ||||||
| chr8:17942592
|
T | G | 144 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.783+2731T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942592 | ||||||
| chr8:17942651
|
A | G | 1 | a0003c0038t0067g0235 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.783+2790A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942651 | ||||||
| chr8:17942791
|
C | T | 2 | a0001c0001t0001g0047a0002c0007t0004g0004 | 2 | HG02622.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.783+2930C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942791 | ||||||
| chr8:17942878
|
T | A | 1 | a0004c0004t0003g0132 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.783+3017T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942878 | ||||||
| chr8:17942941
|
G | A | 1 | a0004c0004t0003g0144 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.783+3080G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942941 | ||||||
| chr8:17942941
|
G | C | 79 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.783+3080G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942941 | ||||||
| chr8:17942957
|
A | T | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.783+3096A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942957 | ||||||
| chr8:17942963
|
C | T | 120 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(117): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.783+3102C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942963 | ||||||
| chr8:17942965
|
C | G | 1 | a0001c0001t0038g0073 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.783+3104C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17942965 | ||||||
| chr8:17942996
|
CA | C | 78 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(75): Show | 78 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.783+3151delA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr8 | 17942996 | |||||
| chr8:17942996
|
CAA | C | 80 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(77): Show | 80 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.783+3150_783+3151d others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr8 | 17942996 | |||||
| chr8:17943021
|
A | G | 5 | a0004c0004t0003g0336a0004c0004t0003g0351a0004c0004t0003g0352others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.783+3160A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17943021 | ||||||
| chr8:17943053
|
T | C | 10 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(7): Show | 10 | HG02109.hp1 HG02258.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.783+3192T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17943053 | ||||||
| chr8:17943074
|
A | G | 3 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102 | 3 | HG03209.hp1 HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.783+3213A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17943074 | ||||||
| chr8:17943075
|
T | C | 1 | a0005c0005t0014g0160 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.783+3214T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17943075 | ||||||
| chr8:17943082
|
A | C | 3 | a0004c0004t0003g0120a0004c0004t0003g0121a0004c0004t0003g0122 | 3 | HG01361.hp1 HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.783+3221A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17943082 | ||||||
| chr8:17943082
|
A | G | 7 | a0007c0011t0001g0149a0007c0011t0001g0150a0007c0011t0003g0151others(4): Show | 7 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.783+3221A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17943082 | ||||||
| chr8:17943154
|
T | C | 4 | a0001c0001t0001g0032a0001c0001t0001g0051a0001c0001t0001g0052others(1): Show | 4 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(1): Show |
intron_variant | MODIFIER | c.783+3293T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17943154 | ||||||
| chr8:17943180
|
A | AT | 92 | a0001c0001t0001g0146a0001c0001t0006g0094a0001c0001t0017g0105others(89): Show | 92 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.783+3335dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr8 | 17943180 | |||||
| chr8:17943197
|
G | C | 2 | a0002c0017t0031g0321a0002c0017t0032g0322 | 2 | HG01099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.783+3336G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17943197 | ||||||
| chr8:17943260
|
T | G | 80 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(77): Show | 80 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.783+3399T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17943260 | ||||||
| chr8:17943387
|
A | G | 120 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(117): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.783+3526A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17943387 | ||||||
| chr8:17943397
|
G | T | 1 | a0002c0017t0032g0322 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.783+3536G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17943397 | ||||||
| chr8:17943482
|
C | G | 2 | a0002c0002t0004g0002a0002c0002t0005g0002 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.783+3621C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17943482 | ||||||
| chr8:17943536
|
G | A | 2 | a0004c0004t0003g0357a0004c0004t0049g0356 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.784-3650G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17943536 | ||||||
| chr8:17943558
|
C | T | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.784-3628C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17943558 | ||||||
| chr8:17943633
|
G | A | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-3553G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17943633 | ||||||
| chr8:17943663
|
C | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-3523C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17943663 | ||||||
| chr8:17943688
|
A | G | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.784-3498A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17943688 | ||||||
| chr8:17943741
|
C | G | 3 | a0005c0005t0014g0160a0005c0005t0014g0171a0005c0005t0027g0170 | 3 | HG01891.hp2 HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.784-3445C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17943741 | ||||||
| chr8:17943791
|
T | A | 1 | a0002c0002t0005g0315 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.784-3395T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17943791 | ||||||
| chr8:17943881
|
C | T | 1 | a0003c0003t0007g0269 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.784-3305C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17943881 | ||||||
| chr8:17944050
|
T | C | 1 | a0001c0001t0001g0005 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.784-3136T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17944050 | ||||||
| chr8:17944214
|
A | G | 1 | a0002c0002t0005g0303 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.784-2972A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17944214 | ||||||
| chr8:17944216
|
A | G | 210 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.784-2970A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17944216 | ||||||
| chr8:17944326
|
G | T | 1 | a0002c0002t0029g0183 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.784-2860G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17944326 | ||||||
| chr8:17944373
|
C | T | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.784-2813C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17944373 | ||||||
| chr8:17944625
|
A | G | 1 | a0002c0009t0051g0364 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.784-2561A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17944625 | ||||||
| chr8:17944659
|
C | T | 1 | a0001c0001t0002g0072 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.784-2527C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17944659 | ||||||
| chr8:17944683
|
A | C | 215 | a0001c0001t0001g0077a0002c0002t0004g0002a0002c0002t0004g0180others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.784-2503A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17944683 | ||||||
| chr8:17944708
|
T | C | 5 | a0002c0002t0005g0301a0010c0014t0022g0330a0010c0014t0022g0331others(2): Show | 5 | HG00280.hp2 HG02698.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-2478T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17944708 | ||||||
| chr8:17944729
|
A | G | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.784-2457A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17944729 | ||||||
| chr8:17944733
|
T | C | 7 | a0007c0011t0001g0149a0007c0011t0001g0150a0007c0011t0003g0151others(4): Show | 7 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.784-2453T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17944733 | ||||||
| chr8:17944765
|
T | C | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-2421T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17944765 | ||||||
| chr8:17944766
|
T | C | 137 | a0001c0001t0001g0077a0002c0002t0004g0328a0002c0002t0005g0326others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.784-2420T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17944766 | ||||||
| chr8:17944840
|
A | AT | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-2344dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr8 | 17944840 | |||||
| chr8:17944840
|
A | G | 102 | a0001c0001t0001g0077a0002c0002t0004g0328a0002c0002t0005g0326others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.784-2346A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17944840 | ||||||
| chr8:17944861
|
T | C | 126 | a0001c0001t0001g0077a0002c0002t0004g0328a0002c0002t0005g0318others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.784-2325T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17944861 | ||||||
| chr8:17944966
|
C | T | 9 | a0007c0011t0001g0149a0007c0011t0001g0150a0007c0011t0003g0151others(6): Show | 9 | HG01884.hp2 HG02698.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.784-2220C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17944966 | ||||||
| chr8:17945030
|
T | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0054a0001c0001t0006g0053 | 3 | HG04184.hp2 NA18993.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.784-2156T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17945030 | ||||||
| chr8:17945105
|
C | T | 2 | a0004c0004t0003g0351a0004c0004t0003g0352 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.784-2081C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17945105 | ||||||
| chr8:17945113
|
T | G | 1 | a0001c0001t0040g0076 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.784-2073T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17945113 | ||||||
| chr8:17945161
|
A | T | 1 | a0006c0008t0033g0277 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.784-2025A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17945161 | ||||||
| chr8:17945296
|
G | A | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-1890G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17945296 | ||||||
| chr8:17945358
|
A | G | 122 | a0001c0001t0001g0077a0002c0002t0004g0328a0002c0002t0005g0326others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.784-1828A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17945358 | ||||||
| chr8:17945373
|
C | T | 3 | a0002c0017t0031g0321a0002c0017t0032g0322a0022c0029t0045g0279 | 3 | HG01099.hp1 HG02257.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.784-1813C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17945373 | ||||||
| chr8:17945374
|
C | G | 133 | a0001c0001t0001g0077a0002c0002t0004g0328a0002c0002t0005g0326others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.784-1812C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17945374 | ||||||
| chr8:17945448
|
T | G | 2 | a0004c0016t0008g0134a0004c0016t0008g0138 | 2 | HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.784-1738T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17945448 | ||||||
| chr8:17945475
|
C | A | 1 | a0006c0008t0033g0277 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.784-1711C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17945475 | ||||||
| chr8:17945636
|
T | C | 1 | a0003c0003t0002g0245 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.784-1550T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17945636 | ||||||
| chr8:17945656
|
A | G | 1 | a0001c0001t0006g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.784-1530A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17945656 | ||||||
| chr8:17945894
|
T | G | 2 | a0002c0017t0031g0321a0002c0017t0032g0322 | 2 | HG01099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.784-1292T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17945894 | ||||||
| chr8:17945899
|
A | G | 1 | a0004c0004t0003g0114 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.784-1287A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17945899 | ||||||
| chr8:17945924
|
A | C | 2 | a0002c0017t0031g0321a0002c0017t0032g0322 | 2 | HG01099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.784-1262A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17945924 | ||||||
| chr8:17945965
|
G | C | 1 | a0005c0005t0014g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.784-1221G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17945965 | ||||||
| chr8:17945994
|
A | C | 1 | a0008c0010t0004g0207 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.784-1192A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17945994 | ||||||
| chr8:17946005
|
C | T | 12 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(9): Show | 12 | HG02109.hp1 HG02647.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.784-1181C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946005 | ||||||
| chr8:17946058
|
A | C | 1 | a0002c0002t0004g0185 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.784-1128A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946058 | ||||||
| chr8:17946070
|
C | T | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-1116C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946070 | ||||||
| chr8:17946087
|
A | C | 1 | a0002c0017t0032g0322 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.784-1099A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946087 | ||||||
| chr8:17946113
|
T | C | 20 | a0004c0004t0003g0113a0004c0004t0003g0114a0004c0004t0003g0115others(17): Show | 20 | HG00438.hp1 HG01257.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.784-1073T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946113 | ||||||
| chr8:17946157
|
G | T | 123 | a0001c0001t0001g0077a0002c0002t0004g0328a0002c0002t0005g0326others(120): Show | 123 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.784-1029G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946157 | ||||||
| chr8:17946201
|
C | A | 2 | a0002c0002t0004g0287a0002c0002t0012g0286 | 2 | HG01361.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.784-985C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946201 | ||||||
| chr8:17946210
|
A | G | 1 | a0002c0007t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.784-976A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946210 | ||||||
| chr8:17946215
|
C | T | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.784-971C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946215 | ||||||
| chr8:17946261
|
G | A | 1 | a0002c0019t0004g0213 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.784-925G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946261 | ||||||
| chr8:17946295
|
T | C | 1 | a0001c0001t0062g0093 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.784-891T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946295 | ||||||
| chr8:17946300
|
T | C | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.784-886T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946300 | ||||||
| chr8:17946317
|
A | T | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.784-869A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946317 | ||||||
| chr8:17946411
|
T | A | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-775T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946411 | ||||||
| chr8:17946414
|
G | A | 122 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.784-772G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946414 | ||||||
| chr8:17946440
|
C | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0054a0001c0001t0006g0053 | 3 | HG04184.hp2 NA18993.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.784-746C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946440 | ||||||
| chr8:17946469
|
A | G | 1 | a0004c0004t0003g0114 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.784-717A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946469 | ||||||
| chr8:17946553
|
A | G | 12 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(9): Show | 12 | HG02109.hp1 HG02647.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.784-633A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946553 | ||||||
| chr8:17946576
|
A | G | 1 | a0002c0007t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.784-610A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946576 | ||||||
| chr8:17946577
|
A | G | 7 | a0004c0004t0003g0132a0004c0004t0003g0133a0004c0004t0003g0137others(4): Show | 7 | HG00140.hp1 HG00323.hp2 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.784-609A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946577 | ||||||
| chr8:17946599
|
C | T | 1 | a0004c0004t0003g0141 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.784-587C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946599 | ||||||
| chr8:17946610
|
C | T | 4 | a0005c0005t0008g0332a0005c0005t0008g0333a0005c0005t0008g0334others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-576C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946610 | ||||||
| chr8:17946627
|
G | C | 11 | a0003c0003t0009g0346a0003c0003t0009g0347a0003c0003t0009g0348others(8): Show | 11 | HG00597.hp1 HG02683.hp2 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.784-559G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946627 | ||||||
| chr8:17946655
|
C | T | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-531C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946655 | ||||||
| chr8:17946733
|
A | T | 2 | a0003c0003t0002g0267a0003c0003t0002g0268 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.784-453A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946733 | ||||||
| chr8:17946745
|
C | T | 1 | a0003c0003t0002g0240 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.784-441C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946745 | ||||||
| chr8:17946761
|
T | C | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-425T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946761 | ||||||
| chr8:17946799
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.784-387T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946799 | ||||||
| chr8:17946832
|
A | AGT | 51 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(48): Show | 52 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.784-315_784-314dup others(2): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr8 | 17946832 | |||||
| chr8:17946832
|
A | AGTGT | 67 | a0001c0001t0001g0031a0001c0001t0001g0077a0001c0047t0006g0069others(64): Show | 67 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.784-317_784-314dup others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr8 | 17946832 | |||||
| chr8:17946832
|
A | AGTGTGT | 16 | a0003c0003t0002g0003a0003c0003t0002g0229a0003c0003t0002g0230others(13): Show | 16 | HG00099.hp1 HG01099.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.784-319_784-314dup others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr8 | 17946832 | |||||
| chr8:17946832
|
A | AGTGTGTG others(1): Show |
12 | a0001c0001t0001g0071a0002c0002t0004g0287a0002c0002t0005g0327others(9): Show | 12 | HG00609.hp1 HG01361.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.784-321_784-314dup others(8): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr8 | 17946832 | |||||
| chr8:17946832
|
A | AGTGTGTG others(3): Show |
5 | a0003c0044t0007g0234a0005c0005t0008g0332a0005c0005t0008g0333others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-323_784-314dup others(10): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr8 | 17946832 | |||||
| chr8:17946832
|
AGT | A | 51 | a0001c0001t0001g0042a0001c0001t0006g0056a0001c0001t0017g0105others(48): Show | 51 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.784-315_784-314del others(2): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr8 | 17946832 | |||||
| chr8:17946832
|
AGTGT | A | 21 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0055others(18): Show | 21 | HG00140.hp2 HG00741.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.784-317_784-314del others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr8 | 17946832 | |||||
| chr8:17946871
|
G | A | 1 | a0002c0017t0032g0322 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.784-315G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946871 | ||||||
| chr8:17946910
|
T | C | 1 | a0001c0001t0001g0005 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.784-276T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17946910 | ||||||
| chr8:17947015
|
C | T | 12 | a0002c0019t0004g0337a0003c0003t0009g0346a0003c0003t0009g0347others(9): Show | 12 | HG00597.hp1 HG02056.hp1 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.784-171C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17947015 | ||||||
| chr8:17947065
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.784-121C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17947065 | ||||||
| chr8:17947137
|
A | G | 2 | a0013c0023t0001g0153a0013c0023t0001g0154 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.784-49A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17947137 | ||||||
| chr8:17947156
|
G | A | 84 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.784-30G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17947156 | ||||||
| chr8:17947160
|
C | T | 1 | a0003c0003t0007g0257 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.784-26C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17947160 | ||||||
| chr8:17947168
|
G | T | 1 | a0003c0006t0002g0228 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.784-18G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 6/38 | chr8 | 17947168 | ||||||
| chr8:17947445
|
T | TA | 5 | a0007c0011t0001g0149a0007c0011t0001g0150a0007c0011t0003g0151others(2): Show | 5 | HG01884.hp2 HG03195.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.961+84dupA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr8 | 17947445 | |||||
| chr8:17947452
|
A | T | 1 | a0027c0031t0056g0139 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.961+89A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17947452 | ||||||
| chr8:17947595
|
A | G | 1 | a0001c0001t0002g0072 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.961+232A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17947595 | ||||||
| chr8:17947636
|
T | C | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.961+273T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17947636 | ||||||
| chr8:17947757
|
G | C | 1 | a0001c0001t0006g0053 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.961+394G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17947757 | ||||||
| chr8:17947774
|
A | G | 2 | a0002c0021t0020g0103a0002c0021t0027g0102 | 2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.961+411A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17947774 | ||||||
| chr8:17947871
|
G | A | 1 | a0001c0001t0062g0093 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.961+508G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17947871 | ||||||
| chr8:17947891
|
A | G | 125 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(122): Show | 125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.961+528A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17947891 | ||||||
| chr8:17947916
|
C | T | 1 | a0002c0017t0031g0321 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.961+553C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17947916 | ||||||
| chr8:17947923
|
C | G | 124 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.961+560C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17947923 | ||||||
| chr8:17947938
|
A | G | 2 | a0002c0017t0031g0321a0002c0017t0032g0322 | 2 | HG01099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.961+575A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17947938 | ||||||
| chr8:17947939
|
T | C | 124 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.961+576T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17947939 | ||||||
| chr8:17947993
|
A | T | 2 | a0002c0009t0051g0364a0002c0009t0063g0363 | 2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.961+630A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17947993 | ||||||
| chr8:17948057
|
A | G | 2 | a0002c0017t0031g0321a0002c0017t0032g0322 | 2 | HG01099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.961+694A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17948057 | ||||||
| chr8:17948136
|
G | A | 5 | a0001c0001t0001g0057a0001c0001t0001g0074a0001c0001t0001g0091others(2): Show | 5 | HG00741.hp1 HG01433.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.961+773G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17948136 | ||||||
| chr8:17948239
|
A | G | 4 | a0003c0003t0002g0156a0003c0003t0002g0157a0003c0003t0002g0158others(1): Show | 4 | HG00099.hp2 HG01243.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.961+876A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17948239 | ||||||
| chr8:17948294
|
C | CT | 36 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0031others(33): Show | 36 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.961+958dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr8 | 17948294 | |||||
| chr8:17948294
|
CT | C | 24 | a0001c0001t0001g0074a0002c0002t0004g0180a0002c0002t0004g0184others(21): Show | 24 | HG01070.hp2 HG01106.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.961+958delT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr8 | 17948294 | |||||
| chr8:17948294
|
CTT | C | 78 | a0001c0001t0001g0077a0002c0002t0004g0002a0002c0002t0004g0185others(75): Show | 78 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.961+957_961+958del others(2): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr8 | 17948294 | |||||
| chr8:17948294
|
CTTT | C | 102 | a0002c0002t0004g0181a0002c0002t0004g0328a0002c0002t0005g0326others(99): Show | 102 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.961+956_961+958del others(3): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr8 | 17948294 | |||||
| chr8:17948294
|
CTTTT | C | 10 | a0003c0003t0007g0219a0003c0003t0007g0232a0005c0005t0014g0160others(7): Show | 10 | HG00558.hp2 HG01884.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.961+955_961+958del others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr8 | 17948294 | |||||
| chr8:17948324
|
A | C | 3 | a0002c0017t0031g0321a0002c0017t0032g0322a0022c0029t0045g0279 | 3 | HG01099.hp1 HG02257.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.961+961A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17948324 | ||||||
| chr8:17948381
|
T | G | 1 | a0010c0014t0023g0355 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.961+1018T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17948381 | ||||||
| chr8:17948419
|
C | G | 3 | a0009c0013t0001g0215a0009c0013t0002g0148a0009c0013t0002g0214 | 3 | NA18943.hp1 NA18956.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.961+1056C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17948419 | ||||||
| chr8:17948452
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.961+1089G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17948452 | ||||||
| chr8:17948452
|
G | C | 2 | a0003c0003t0007g0257a0003c0003t0007g0269 | 2 | HG02132.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.961+1089G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17948452 | ||||||
| chr8:17948471
|
A | C | 88 | a0001c0001t0001g0077a0002c0019t0004g0337a0003c0003t0002g0003others(85): Show | 88 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.961+1108A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17948471 | ||||||
| chr8:17948484
|
T | C | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.961+1121T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17948484 | ||||||
| chr8:17948507
|
A | G | 1 | a0001c0001t0001g0071 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.961+1144A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17948507 | ||||||
| chr8:17948544
|
C | A | 76 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(73): Show | 76 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.961+1181C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17948544 | ||||||
| chr8:17948569
|
C | T | 1 | a0002c0007t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.961+1206C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17948569 | ||||||
| chr8:17948583
|
G | A | 2 | a0002c0017t0031g0321a0002c0017t0032g0322 | 2 | HG01099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.961+1220G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17948583 | ||||||
| chr8:17948585
|
C | G | 2 | a0002c0002t0021g0195a0015c0022t0004g0295 | 2 | HG01069.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.961+1222C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17948585 | ||||||
| chr8:17948592
|
C | T | 12 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(9): Show | 12 | HG02109.hp1 HG02647.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.961+1229C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17948592 | ||||||
| chr8:17948593
|
G | A | 9 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(6): Show | 9 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.961+1230G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17948593 | ||||||
| chr8:17948647
|
T | C | 78 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(75): Show | 78 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.961+1284T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17948647 | ||||||
| chr8:17948691
|
T | C | 8 | a0003c0003t0002g0156a0003c0003t0002g0157a0003c0003t0002g0158others(5): Show | 8 | HG00099.hp2 HG00639.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.961+1328T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17948691 | ||||||
| chr8:17948761
|
G | A | 267 | a0001c0001t0001g0077a0001c0001t0017g0105a0001c0001t0017g0108others(264): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.961+1398G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17948761 | ||||||
| chr8:17948910
|
A | C | 1 | a0001c0001t0006g0079 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.961+1547A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17948910 | ||||||
| chr8:17948935
|
T | C | 1 | a0002c0002t0004g0320 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.961+1572T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17948935 | ||||||
| chr8:17948973
|
G | A | 267 | a0001c0001t0001g0077a0001c0001t0017g0105a0001c0001t0017g0108others(264): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.961+1610G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17948973 | ||||||
| chr8:17948975
|
T | A | 7 | a0004c0004t0003g0132a0004c0004t0003g0133a0004c0004t0003g0137others(4): Show | 7 | HG00140.hp1 HG00323.hp2 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.961+1612T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17948975 | ||||||
| chr8:17949008
|
A | G | 1 | a0001c0001t0001g0027 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.962-1607A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17949008 | ||||||
| chr8:17949035
|
C | G | 3 | a0009c0013t0001g0215a0009c0013t0002g0148a0009c0013t0002g0214 | 3 | NA18943.hp1 NA18956.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.962-1580C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17949035 | ||||||
| chr8:17949142
|
C | G | 1 | a0001c0001t0006g0053 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.962-1473C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17949142 | ||||||
| chr8:17949161
|
G | T | 112 | a0001c0001t0001g0077a0002c0002t0004g0328a0002c0002t0005g0326others(109): Show | 112 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.962-1454G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17949161 | ||||||
| chr8:17949214
|
T | C | 1 | a0002c0002t0004g0199 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.962-1401T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17949214 | ||||||
| chr8:17949215
|
G | C | 2 | a0002c0021t0020g0103a0002c0021t0027g0102 | 2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.962-1400G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17949215 | ||||||
| chr8:17949225
|
G | A | 267 | a0001c0001t0001g0077a0001c0001t0017g0105a0001c0001t0017g0108others(264): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.962-1390G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17949225 | ||||||
| chr8:17949313
|
G | C | 1 | a0002c0009t0051g0364 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.962-1302G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17949313 | ||||||
| chr8:17949319
|
C | A | 1 | a0004c0016t0008g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.962-1296C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17949319 | ||||||
| chr8:17949319
|
C | G | 41 | a0002c0002t0028g0323a0004c0004t0003g0113a0004c0004t0003g0114others(38): Show | 41 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.962-1296C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17949319 | ||||||
| chr8:17949333
|
C | G | 42 | a0002c0002t0028g0323a0004c0004t0003g0113a0004c0004t0003g0114others(39): Show | 42 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.962-1282C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17949333 | ||||||
| chr8:17949397
|
T | C | 1 | a0002c0002t0005g0327 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.962-1218T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17949397 | ||||||
| chr8:17949480
|
T | C | 126 | a0001c0001t0001g0077a0002c0002t0004g0328a0002c0002t0005g0326others(123): Show | 126 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.962-1135T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17949480 | ||||||
| chr8:17949500
|
CT | C | 33 | a0001c0001t0010g0010a0002c0002t0004g0328a0002c0002t0005g0285others(30): Show | 33 | HG01099.hp1 HG01168.hp1 HG01517.hp2 others(30): Show |
intron_variant | MODIFIER | c.962-1101delT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr8 | 17949500 | |||||
| chr8:17949554
|
TG | T | 366 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(363): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.962-1058delG | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr8 | 17949554 | |||||
| chr8:17949568
|
G | A | 3 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102 | 3 | HG03209.hp1 HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.962-1047G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17949568 | ||||||
| chr8:17949573
|
C | A | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.962-1042C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17949573 | ||||||
| chr8:17949832
|
C | G | 12 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(9): Show | 12 | HG02109.hp1 HG02647.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.962-783C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17949832 | ||||||
| chr8:17949864
|
C | G | 1 | a0001c0001t0001g0147 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.962-751C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17949864 | ||||||
| chr8:17949875
|
A | G | 2 | a0013c0023t0001g0153a0013c0023t0001g0154 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.962-740A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17949875 | ||||||
| chr8:17950039
|
G | C | 12 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(9): Show | 12 | HG02109.hp1 HG02647.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.962-576G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17950039 | ||||||
| chr8:17950074
|
G | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0054a0001c0001t0006g0053 | 3 | HG04184.hp2 NA18993.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.962-541G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17950074 | ||||||
| chr8:17950153
|
A | G | 1 | a0003c0003t0002g0242 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.962-462A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17950153 | ||||||
| chr8:17950219
|
G | A | 119 | a0002c0002t0004g0328a0002c0002t0005g0326a0002c0002t0005g0327others(116): Show | 119 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.962-396G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17950219 | ||||||
| chr8:17950420
|
G | C | 256 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(253): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.962-195G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17950420 | ||||||
| chr8:17950466
|
T | G | 1 | a0001c0001t0001g0058 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.962-149T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17950466 | ||||||
| chr8:17950481
|
C | A | 12 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(9): Show | 12 | HG02109.hp1 HG02647.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.962-134C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17950481 | ||||||
| chr8:17950482
|
G | A | 3 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102 | 3 | HG03209.hp1 HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.962-133G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 7/38 | chr8 | 17950482 | ||||||
| chr8:17950832
|
G | C | 3 | a0002c0002t0004g0328a0002c0002t0005g0326a0002c0002t0029g0324 | 3 | HG03516.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1071+108G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17950832 | ||||||
| chr8:17951011
|
C | G | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1071+287C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17951011 | ||||||
| chr8:17951150
|
C | G | 1 | a0002c0007t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1071+426C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17951150 | ||||||
| chr8:17951221
|
A | G | 136 | a0002c0002t0004g0328a0002c0002t0005g0326a0002c0002t0005g0327others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1071+497A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17951221 | ||||||
| chr8:17951238
|
A | G | 5 | a0001c0001t0001g0035a0010c0014t0022g0330a0010c0014t0022g0331others(2): Show | 5 | HG02683.hp1 HG02698.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.1071+514A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17951238 | ||||||
| chr8:17951307
|
C | T | 1 | a0002c0002t0004g0184 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1071+583C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17951307 | ||||||
| chr8:17951345
|
G | A | 3 | a0002c0017t0031g0321a0002c0017t0032g0322a0022c0029t0045g0279 | 3 | HG01099.hp1 HG02257.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1071+621G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17951345 | ||||||
| chr8:17951438
|
A | G | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1071+714A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17951438 | ||||||
| chr8:17951502
|
A | T | 124 | a0002c0002t0004g0328a0002c0002t0005g0326a0002c0002t0005g0327others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.1071+778A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17951502 | ||||||
| chr8:17951768
|
T | C | 78 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(75): Show | 78 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.1071+1044T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17951768 | ||||||
| chr8:17951802
|
T | C | 8 | a0007c0011t0001g0149a0007c0011t0001g0150a0007c0011t0003g0151others(5): Show | 8 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1071+1078T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17951802 | ||||||
| chr8:17951852
|
C | T | 1 | a0001c0001t0006g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1072-1118C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17951852 | ||||||
| chr8:17951864
|
G | A | 2 | a0002c0017t0031g0321a0002c0017t0032g0322 | 2 | HG01099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1072-1106G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17951864 | ||||||
| chr8:17951904
|
C | G | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1072-1066C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17951904 | ||||||
| chr8:17951934
|
A | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1072-1036A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17951934 | ||||||
| chr8:17952112
|
G | A | 262 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(259): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1072-858G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17952112 | ||||||
| chr8:17952137
|
C | T | 5 | a0005c0005t0008g0168a0005c0005t0008g0169a0005c0005t0008g0174others(2): Show | 5 | HG02559.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1072-833C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17952137 | ||||||
| chr8:17952224
|
A | AAAAT | 158 | a0001c0001t0001g0050a0002c0007t0001g0033a0002c0009t0016g0359others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.1072-718_1072-715d others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | INFO_REALIGN_3_PRIME | chr8 | 17952224 | |||||
| chr8:17952224
|
A | AAAATAAA others(1): Show |
4 | a0003c0003t0026g0271a0003c0003t0046g0259a0007c0011t0001g0149others(1): Show | 4 | HG00639.hp2 HG01934.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1072-722_1072-715d others(10): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | INFO_REALIGN_3_PRIME | chr8 | 17952224 | |||||
| chr8:17952224
|
A | AAAATAAA others(5): Show |
6 | a0003c0003t0002g0243a0005c0005t0014g0163a0005c0005t0015g0162others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1072-726_1072-715d others(14): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | INFO_REALIGN_3_PRIME | chr8 | 17952224 | |||||
| chr8:17952224
|
A | AAAATAAA others(9): Show |
1 | a0005c0005t0015g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1072-730_1072-715d others(18): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | INFO_REALIGN_3_PRIME | chr8 | 17952224 | |||||
| chr8:17952224
|
AAAAT | A | 83 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1072-718_1072-715d others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | INFO_REALIGN_3_PRIME | chr8 | 17952224 | |||||
| chr8:17952282
|
G | A | 330 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0021others(327): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1072-688G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17952282 | ||||||
| chr8:17952301
|
T | A | 84 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1072-669T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17952301 | ||||||
| chr8:17952376
|
A | T | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1072-594A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17952376 | ||||||
| chr8:17952426
|
A | C | 2 | a0013c0023t0001g0153a0013c0023t0001g0154 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1072-544A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17952426 | ||||||
| chr8:17952538
|
G | T | 3 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354 | 3 | HG02698.hp2 HG03017.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1072-432G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17952538 | ||||||
| chr8:17952632
|
T | C | 86 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1072-338T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17952632 | ||||||
| chr8:17952644
|
C | G | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1072-326C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17952644 | ||||||
| chr8:17952684
|
A | G | 1 | a0003c0003t0002g0245 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1072-286A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17952684 | ||||||
| chr8:17952750
|
C | A | 1 | a0010c0014t0023g0355 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1072-220C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17952750 | ||||||
| chr8:17952772
|
G | C | 1 | a0002c0017t0032g0322 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1072-198G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17952772 | ||||||
| chr8:17952776
|
A | T | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1072-194A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17952776 | ||||||
| chr8:17952783
|
A | G | 3 | a0004c0004t0003g0357a0004c0004t0049g0356a0004c0016t0008g0138 | 3 | HG02615.hp2 HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1072-187A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17952783 | ||||||
| chr8:17952813
|
T | C | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1072-157T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17952813 | ||||||
| chr8:17952944
|
C | T | 1 | a0004c0016t0003g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1072-26C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17952944 | ||||||
| chr8:17952955
|
T | C | 20 | a0005c0005t0008g0168a0005c0005t0008g0169a0005c0005t0008g0174others(17): Show | 20 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1072-15T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 8/38 | chr8 | 17952955 | ||||||
| chr8:17953246
|
A | G | 4 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102others(1): Show | 4 | HG03209.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1288+60A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17953246 | ||||||
| chr8:17953474
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1288+288C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17953474 | ||||||
| chr8:17953489
|
A | G | 1 | a0002c0002t0004g0328 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1288+303A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17953489 | ||||||
| chr8:17953560
|
C | T | 5 | a0005c0005t0008g0168a0005c0005t0008g0169a0005c0005t0008g0174others(2): Show | 5 | HG02559.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1288+374C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17953560 | ||||||
| chr8:17953617
|
C | A | 1 | a0014c0020t0020g0098 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1288+431C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17953617 | ||||||
| chr8:17953713
|
A | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1288+527A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17953713 | ||||||
| chr8:17953754
|
C | G | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1288+568C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17953754 | ||||||
| chr8:17953825
|
A | G | 1 | a0002c0019t0004g0213 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1288+639A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17953825 | ||||||
| chr8:17953840
|
T | TA | 111 | a0003c0003t0002g0003a0003c0003t0002g0156a0003c0003t0002g0157others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.1288+655dupA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr8 | 17953840 | |||||
| chr8:17953901
|
T | C | 1 | a0002c0002t0053g0289 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1288+715T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17953901 | ||||||
| chr8:17953904
|
T | C | 1 | a0005c0005t0014g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1288+718T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17953904 | ||||||
| chr8:17954027
|
A | C | 168 | a0002c0009t0005g0304a0002c0009t0016g0359a0002c0009t0016g0362others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1288+841A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17954027 | ||||||
| chr8:17954100
|
C | T | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1288+914C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17954100 | ||||||
| chr8:17954225
|
C | T | 5 | a0007c0011t0001g0149a0007c0011t0001g0150a0007c0011t0003g0151others(2): Show | 5 | HG01884.hp2 HG03195.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1288+1039C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17954225 | ||||||
| chr8:17954312
|
A | G | 1 | a0005c0005t0014g0176 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1288+1126A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17954312 | ||||||
| chr8:17954326
|
C | G | 6 | a0004c0004t0003g0336a0004c0004t0003g0351a0004c0004t0003g0352others(3): Show | 6 | HG01884.hp1 HG02280.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1288+1140C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17954326 | ||||||
| chr8:17954402
|
G | T | 1 | a0001c0001t0001g0039 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1289-1068G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17954402 | ||||||
| chr8:17954417
|
A | G | 4 | a0001c0001t0001g0032a0001c0001t0001g0051a0001c0001t0001g0052others(1): Show | 4 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(1): Show |
intron_variant | MODIFIER | c.1289-1053A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17954417 | ||||||
| chr8:17954427
|
C | CA | 103 | a0001c0001t0001g0005a0003c0003t0002g0003a0003c0003t0002g0156others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1289-1028dupA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr8 | 17954427 | |||||
| chr8:17954427
|
C | CAA | 13 | a0005c0005t0014g0163a0005c0005t0015g0162a0005c0005t0015g0164others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1289-1029_1289-102 others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr8 | 17954427 | |||||
| chr8:17954427
|
CA | C | 42 | a0001c0001t0006g0026a0004c0004t0003g0113a0004c0004t0003g0114others(39): Show | 42 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.1289-1028delA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr8 | 17954427 | |||||
| chr8:17954492
|
C | G | 126 | a0002c0009t0005g0304a0002c0009t0016g0359a0002c0009t0016g0362others(123): Show | 126 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.1289-978C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17954492 | ||||||
| chr8:17954608
|
T | C | 3 | a0001c0001t0001g0025a0001c0001t0001g0043a0001c0001t0001g0095 | 3 | NA18960.hp1 NA18987.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1289-862T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17954608 | ||||||
| chr8:17954881
|
T | G | 9 | a0002c0009t0005g0304a0002c0009t0016g0359a0002c0009t0016g0362others(6): Show | 9 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1289-589T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17954881 | ||||||
| chr8:17954912
|
C | T | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1289-558C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17954912 | ||||||
| chr8:17955004
|
G | T | 110 | a0003c0003t0002g0003a0003c0003t0002g0156a0003c0003t0002g0157others(107): Show | 110 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1289-466G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17955004 | ||||||
| chr8:17955005
|
A | T | 110 | a0003c0003t0002g0003a0003c0003t0002g0156a0003c0003t0002g0157others(107): Show | 110 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1289-465A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17955005 | ||||||
| chr8:17955068
|
A | G | 86 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(83): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1289-402A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17955068 | ||||||
| chr8:17955233
|
C | T | 4 | a0005c0005t0008g0332a0005c0005t0008g0333a0005c0005t0008g0334others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1289-237C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17955233 | ||||||
| chr8:17955238
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | HG02683.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1289-232G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17955238 | ||||||
| chr8:17955288
|
T | C | 41 | a0004c0004t0003g0113a0004c0004t0003g0114a0004c0004t0003g0115others(38): Show | 41 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.1289-182T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17955288 | ||||||
| chr8:17955399
|
A | G | 1 | a0004c0004t0003g0117 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1289-71A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17955399 | ||||||
| chr8:17955417
|
G | C | 42 | a0002c0002t0028g0323a0004c0004t0003g0113a0004c0004t0003g0114others(39): Show | 42 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.1289-53G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17955417 | ||||||
| chr8:17955444
|
A | T | 1 | a0007c0011t0003g0152 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1289-26A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 9/38 | chr8 | 17955444 | ||||||
| chr8:17955708
|
GT | G | 6 | a0003c0003t0002g0280a0003c0012t0009g0340a0010c0014t0022g0330others(3): Show | 6 | HG00423.hp2 HG02698.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.1472+66delT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 10/38 | INFO_REALIGN_3_PRIME | chr8 | 17955708 | |||||
| chr8:17955719
|
T | TTA | 9 | a0002c0009t0005g0304a0002c0009t0016g0359a0002c0009t0016g0362others(6): Show | 9 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1472+66_1472+67ins others(2): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 10/38 | chr8 | 17955719 | ||||||
| chr8:17955741
|
G | A | 1 | a0003c0006t0013g0250 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1472+88G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 10/38 | chr8 | 17955741 | ||||||
| chr8:17955756
|
T | C | 5 | a0005c0005t0014g0160a0005c0005t0014g0171a0005c0005t0014g0175others(2): Show | 5 | HG01891.hp2 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1472+103T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 10/38 | chr8 | 17955756 | ||||||
| chr8:17955767
|
A | G | 7 | a0007c0011t0001g0149a0007c0011t0001g0150a0007c0011t0003g0151others(4): Show | 7 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1472+114A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 10/38 | chr8 | 17955767 | ||||||
| chr8:17956111
|
CACTT | C | 103 | a0003c0003t0002g0003a0003c0003t0002g0156a0003c0003t0002g0157others(100): Show | 103 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1472+461_1472+464d others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 10/38 | INFO_REALIGN_3_PRIME | chr8 | 17956111 | |||||
| chr8:17956118
|
A | T | 1 | a0002c0019t0004g0337 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1472+465A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 10/38 | chr8 | 17956118 | ||||||
| chr8:17956157
|
C | T | 1 | a0001c0001t0006g0094 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1473-447C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 10/38 | chr8 | 17956157 | ||||||
| chr8:17956167
|
A | G | 4 | a0003c0003t0002g0239a0003c0003t0002g0242a0003c0003t0002g0245others(1): Show | 4 | HG00544.hp2 NA18747.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.1473-437A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 10/38 | chr8 | 17956167 | ||||||
| chr8:17956275
|
T | C | 20 | a0005c0005t0008g0168a0005c0005t0008g0169a0005c0005t0008g0174others(17): Show | 20 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1473-329T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 10/38 | chr8 | 17956275 | ||||||
| chr8:17956368
|
G | A | 1 | a0002c0002t0029g0183 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1473-236G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 10/38 | chr8 | 17956368 | ||||||
| chr8:17956387
|
C | A | 1 | a0003c0003t0002g0237 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1473-217C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 10/38 | chr8 | 17956387 | ||||||
| chr8:17956495
|
C | G | 1 | a0001c0026t0001g0065 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1473-109C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 10/38 | chr8 | 17956495 | ||||||
| chr8:17956547
|
CTG | C | 4 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102others(1): Show | 4 | HG03209.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1473-55_1473-54del others(2): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 10/38 | INFO_REALIGN_3_PRIME | chr8 | 17956547 | |||||
| chr8:17956578
|
G | T | 119 | a0002c0009t0005g0304a0002c0009t0016g0359a0002c0009t0016g0362others(116): Show | 119 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.1473-26G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 10/38 | chr8 | 17956578 | ||||||
| chr8:17956855
|
C | T | 1 | a0003c0003t0007g0269 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1646+78C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 11/38 | chr8 | 17956855 | ||||||
| chr8:17956856
|
G | A | 1 | a0001c0001t0006g0020 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1646+79G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 11/38 | chr8 | 17956856 | ||||||
| chr8:17956916
|
A | G | 121 | a0002c0017t0003g0104a0002c0017t0031g0321a0002c0017t0032g0322others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1646+139A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 11/38 | chr8 | 17956916 | ||||||
| chr8:17956941
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1646+164A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 11/38 | chr8 | 17956941 | ||||||
| chr8:17956952
|
T | C | 5 | a0005c0005t0014g0160a0005c0005t0014g0171a0005c0005t0014g0175others(2): Show | 5 | HG01891.hp2 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1646+175T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 11/38 | chr8 | 17956952 | ||||||
| chr8:17957099
|
T | G | 1 | a0002c0007t0001g0033 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1647-165T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 11/38 | chr8 | 17957099 | ||||||
| chr8:17957171
|
G | C | 37 | a0002c0002t0004g0287a0002c0002t0004g0311a0002c0002t0004g0320others(34): Show | 37 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.1647-93G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 11/38 | chr8 | 17957171 | ||||||
| chr8:17957260
|
C | G | 3 | a0002c0021t0020g0103a0002c0021t0027g0102a0017c0027t0001g0061 | 3 | HG03209.hp1 HG03471.hp1 NA18522.hp2 |
splice_region_variant&intron_variant | LOW | c.1647-4C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 11/38 | chr8 | 17957260 | ||||||
| chr8:17957499
|
C | T | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1805-41C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 12/38 | chr8 | 17957499 | ||||||
| chr8:17957776
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG03491.hp1 | splice_donor_variant&intron_variant | HIGH | c.2040+1G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17957776 | ||||||
| chr8:17957803
|
C | T | 2 | a0002c0017t0031g0321a0002c0017t0032g0322 | 2 | HG01099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2040+28C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17957803 | ||||||
| chr8:17957871
|
A | G | 1 | a0002c0007t0030g0179 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2040+96A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17957871 | ||||||
| chr8:17958196
|
G | A | 110 | a0003c0003t0002g0003a0003c0003t0002g0156a0003c0003t0002g0157others(107): Show | 110 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.2040+421G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17958196 | ||||||
| chr8:17958245
|
C | A | 2 | a0002c0021t0020g0103a0002c0021t0027g0102 | 2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2040+470C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17958245 | ||||||
| chr8:17958273
|
A | G | 1 | a0002c0002t0060g0212 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2040+498A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17958273 | ||||||
| chr8:17958305
|
A | G | 1 | a0002c0002t0005g0294 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2040+530A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17958305 | ||||||
| chr8:17958314
|
A | G | 127 | a0002c0009t0005g0304a0002c0009t0016g0359a0002c0009t0016g0362others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.2040+539A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17958314 | ||||||
| chr8:17958375
|
A | G | 1 | a0002c0019t0004g0213 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2040+600A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17958375 | ||||||
| chr8:17958391
|
T | C | 1 | a0005c0005t0014g0163 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2040+616T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17958391 | ||||||
| chr8:17958444
|
A | C | 69 | a0003c0003t0002g0003a0003c0003t0002g0156a0003c0003t0002g0157others(66): Show | 69 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.2040+669A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17958444 | ||||||
| chr8:17958575
|
G | GTA | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.2040+811_2040+812d others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr8 | 17958575 | |||||
| chr8:17958588
|
A | T | 122 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(119): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.2040+813A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17958588 | ||||||
| chr8:17958657
|
A | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0006g0049 | 3 | HG00738.hp2 HG02486.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.2040+882A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17958657 | ||||||
| chr8:17958690
|
G | A | 11 | a0003c0003t0009g0346a0003c0003t0009g0347a0003c0003t0009g0348others(8): Show | 11 | HG00597.hp1 HG02683.hp2 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.2040+915G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17958690 | ||||||
| chr8:17958690
|
G | T | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2040+915G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17958690 | ||||||
| chr8:17958722
|
GTATT | G | 125 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(122): Show | 125 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.2040+957_2040+960d others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr8 | 17958722 | |||||
| chr8:17958746
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2040+971A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17958746 | ||||||
| chr8:17958812
|
C | G | 1 | a0003c0003t0007g0219 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2040+1037C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17958812 | ||||||
| chr8:17958813
|
C | T | 5 | a0005c0005t0008g0168a0005c0005t0008g0169a0005c0005t0008g0174others(2): Show | 5 | HG02559.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2040+1038C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17958813 | ||||||
| chr8:17958841
|
C | T | 1 | a0002c0021t0020g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2040+1066C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17958841 | ||||||
| chr8:17958847
|
G | A | 1 | a0001c0001t0006g0020 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2040+1072G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17958847 | ||||||
| chr8:17958869
|
G | T | 1 | a0010c0014t0022g0331 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2040+1094G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17958869 | ||||||
| chr8:17959052
|
C | A | 1 | a0003c0006t0011g0246 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2041-962C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17959052 | ||||||
| chr8:17959088
|
C | G | 259 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.2041-926C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17959088 | ||||||
| chr8:17959132
|
A | G | 6 | a0005c0005t0014g0163a0005c0005t0015g0162a0005c0005t0015g0164others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2041-882A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17959132 | ||||||
| chr8:17959172
|
A | G | 110 | a0003c0003t0002g0003a0003c0003t0002g0156a0003c0003t0002g0157others(107): Show | 110 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.2041-842A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17959172 | ||||||
| chr8:17959332
|
T | C | 1 | a0002c0007t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2041-682T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17959332 | ||||||
| chr8:17959345
|
T | TAC | 365 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(362): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.2041-668_2041-667i others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr8 | 17959345 | |||||
| chr8:17959441
|
C | T | 1 | a0002c0002t0004g0320 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2041-573C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17959441 | ||||||
| chr8:17959575
|
C | CTCTAGAA others(10): Show |
259 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.2041-433_2041-432i others(19): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr8 | 17959575 | |||||
| chr8:17959631
|
T | C | 117 | a0002c0017t0031g0321a0002c0017t0032g0322a0003c0003t0002g0003others(114): Show | 117 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.2041-383T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17959631 | ||||||
| chr8:17959662
|
A | G | 21 | a0002c0007t0001g0033a0004c0004t0003g0113a0004c0004t0003g0114others(18): Show | 21 | HG00438.hp1 HG01257.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.2041-352A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17959662 | ||||||
| chr8:17959878
|
CAT | C | 5 | a0002c0017t0031g0321a0005c0005t0008g0332a0005c0005t0008g0333others(2): Show | 5 | HG01099.hp1 HG02258.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041-135_2041-134d others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 13/38 | chr8 | 17959878 | ||||||
| chr8:17960506
|
A | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.2322+62A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17960506 | ||||||
| chr8:17960527
|
G | GTTTTTGT others(4): Show |
4 | a0003c0003t0002g0256a0003c0003t0009g0339a0003c0003t0011g0255others(1): Show | 4 | NA18972.hp2 NA18978.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.2322+88_2322+89ins others(11): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | INFO_REALIGN_3_PRIME | chr8 | 17960527 | |||||
| chr8:17960533
|
C | CTTTTTTT others(3): Show |
15 | a0002c0009t0005g0304a0002c0009t0016g0359a0002c0009t0016g0362others(12): Show | 15 | HG02109.hp1 HG02647.hp2 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.2322+98_2322+99ins others(10): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | INFO_REALIGN_3_PRIME | chr8 | 17960533 | |||||
| chr8:17960533
|
C | CTTTTTTT others(4): Show |
171 | a0002c0002t0004g0002a0002c0002t0004g0181a0002c0002t0004g0184others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.2322+98_2322+99ins others(11): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | INFO_REALIGN_3_PRIME | chr8 | 17960533 | |||||
| chr8:17960533
|
C | CTTTTTTT others(5): Show |
52 | a0002c0002t0004g0180a0002c0002t0004g0192a0002c0002t0005g0288others(49): Show | 52 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.2322+98_2322+99ins others(12): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | INFO_REALIGN_3_PRIME | chr8 | 17960533 | |||||
| chr8:17960533
|
C | CTTTTTTT others(6): Show |
1 | a0004c0004t0003g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2322+98_2322+99ins others(13): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | INFO_REALIGN_3_PRIME | chr8 | 17960533 | |||||
| chr8:17960533
|
C | T | 4 | a0003c0003t0002g0256a0003c0003t0009g0339a0003c0003t0011g0255others(1): Show | 4 | NA18972.hp2 NA18978.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.2322+89C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17960533 | ||||||
| chr8:17960625
|
C | T | 3 | a0002c0002t0004g0180a0002c0002t0004g0187a0002c0002t0004g0198 | 3 | HG01109.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2322+181C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17960625 | ||||||
| chr8:17960660
|
G | A | 1 | a0001c0001t0006g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2322+216G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17960660 | ||||||
| chr8:17960682
|
G | C | 1 | a0005c0005t0014g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2322+238G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17960682 | ||||||
| chr8:17960715
|
A | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.2322+271A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17960715 | ||||||
| chr8:17960746
|
G | C | 4 | a0002c0002t0005g0281a0011c0018t0019g0188a0011c0018t0019g0189others(1): Show | 4 | HG00621.hp1 NA18981.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.2322+302G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17960746 | ||||||
| chr8:17960794
|
G | C | 1 | a0002c0002t0005g0312 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2322+350G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17960794 | ||||||
| chr8:17960886
|
A | C | 1 | a0008c0010t0004g0207 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2322+442A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17960886 | ||||||
| chr8:17960929
|
C | T | 120 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(117): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.2322+485C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17960929 | ||||||
| chr8:17960931
|
T | C | 9 | a0002c0009t0005g0304a0002c0009t0016g0359a0002c0009t0016g0362others(6): Show | 9 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2322+487T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17960931 | ||||||
| chr8:17960958
|
T | C | 6 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(3): Show | 6 | HG02717.hp1 HG02886.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.2322+514T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17960958 | ||||||
| chr8:17960976
|
T | C | 1 | a0002c0007t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2322+532T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17960976 | ||||||
| chr8:17961004
|
G | C | 1 | a0003c0003t0002g0221 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2322+560G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17961004 | ||||||
| chr8:17961126
|
A | G | 1 | a0002c0019t0004g0337 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2322+682A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17961126 | ||||||
| chr8:17961175
|
A | G | 4 | a0003c0003t0002g0242a0003c0003t0002g0275a0003c0003t0002g0280others(1): Show | 4 | HG00423.hp2 NA18947.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.2322+731A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17961175 | ||||||
| chr8:17961234
|
A | C | 1 | a0001c0001t0002g0072 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2322+790A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17961234 | ||||||
| chr8:17961234
|
A | G | 1 | a0002c0002t0005g0327 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2322+790A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17961234 | ||||||
| chr8:17961242
|
G | T | 1 | a0002c0017t0003g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2323-792G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17961242 | ||||||
| chr8:17961245
|
A | G | 1 | a0002c0002t0004g0320 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2323-789A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17961245 | ||||||
| chr8:17961304
|
C | CT | 76 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0039others(73): Show | 76 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.2323-706dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | INFO_REALIGN_3_PRIME | chr8 | 17961304 | |||||
| chr8:17961304
|
C | CTT | 24 | a0001c0001t0001g0092a0002c0002t0004g0002a0002c0002t0004g0184others(21): Show | 24 | HG00741.hp1 HG01074.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.2323-707_2323-706d others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | INFO_REALIGN_3_PRIME | chr8 | 17961304 | |||||
| chr8:17961304
|
C | CTTT | 110 | a0002c0002t0004g0180a0002c0002t0004g0198a0002c0002t0028g0323others(107): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.2323-708_2323-706d others(5): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | INFO_REALIGN_3_PRIME | chr8 | 17961304 | |||||
| chr8:17961304
|
C | CTTTT | 38 | a0002c0017t0003g0104a0003c0003t0002g0156a0003c0003t0002g0157others(35): Show | 38 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2323-709_2323-706d others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | INFO_REALIGN_3_PRIME | chr8 | 17961304 | |||||
| chr8:17961304
|
C | CTTTTT | 6 | a0003c0003t0002g0158a0005c0005t0008g0333a0005c0005t0014g0175others(3): Show | 6 | HG01243.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2323-710_2323-706d others(7): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | INFO_REALIGN_3_PRIME | chr8 | 17961304 | |||||
| chr8:17961304
|
CT | C | 10 | a0001c0001t0001g0084a0002c0009t0005g0304a0002c0009t0016g0359others(7): Show | 10 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.2323-706delT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | INFO_REALIGN_3_PRIME | chr8 | 17961304 | |||||
| chr8:17961342
|
G | C | 6 | a0001c0001t0001g0025a0001c0001t0001g0042a0001c0001t0001g0043others(3): Show | 6 | NA18960.hp1 NA18971.hp1 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.2323-692G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17961342 | ||||||
| chr8:17961375
|
A | G | 115 | a0001c0001t0001g0016a0002c0017t0031g0321a0002c0017t0032g0322others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.2323-659A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17961375 | ||||||
| chr8:17961380
|
G | T | 1 | a0001c0001t0001g0092 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2323-654G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17961380 | ||||||
| chr8:17961459
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2323-575C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17961459 | ||||||
| chr8:17961471
|
C | T | 1 | a0002c0021t0027g0102 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2323-563C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17961471 | ||||||
| chr8:17961527
|
G | A | 3 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102 | 3 | HG03209.hp1 HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2323-507G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17961527 | ||||||
| chr8:17961543
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2323-491C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17961543 | ||||||
| chr8:17961601
|
G | A | 2 | a0005c0005t0014g0160a0005c0005t0027g0170 | 2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2323-433G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17961601 | ||||||
| chr8:17961668
|
A | G | 1 | a0003c0006t0013g0250 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2323-366A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17961668 | ||||||
| chr8:17961699
|
C | G | 2 | a0002c0021t0020g0103a0002c0021t0027g0102 | 2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2323-335C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17961699 | ||||||
| chr8:17961894
|
G | A | 6 | a0005c0005t0014g0163a0005c0005t0015g0162a0005c0005t0015g0164others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2323-140G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17961894 | ||||||
| chr8:17961970
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | HG02683.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2323-64G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 15/38 | chr8 | 17961970 | ||||||
| chr8:17962252
|
A | G | 121 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(118): Show | 121 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.2463+78A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 16/38 | chr8 | 17962252 | ||||||
| chr8:17962303
|
T | C | 80 | a0001c0001t0001g0082a0002c0002t0004g0002a0002c0002t0004g0180others(77): Show | 80 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.2463+129T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 16/38 | chr8 | 17962303 | ||||||
| chr8:17962463
|
G | A | 42 | a0002c0007t0001g0033a0004c0004t0003g0113a0004c0004t0003g0114others(39): Show | 42 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.2463+289G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 16/38 | chr8 | 17962463 | ||||||
| chr8:17962473
|
A | G | 4 | a0005c0005t0008g0332a0005c0005t0008g0333a0005c0005t0008g0334others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2463+299A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 16/38 | chr8 | 17962473 | ||||||
| chr8:17962488
|
C | T | 109 | a0002c0017t0003g0104a0002c0017t0031g0321a0002c0017t0032g0322others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.2463+314C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 16/38 | chr8 | 17962488 | ||||||
| chr8:17962610
|
C | A | 1 | a0001c0001t0001g0052 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2463+436C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 16/38 | chr8 | 17962610 | ||||||
| chr8:17962641
|
C | G | 1 | a0003c0003t0009g0347 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2464-460C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 16/38 | chr8 | 17962641 | ||||||
| chr8:17962728
|
A | G | 9 | a0002c0009t0005g0304a0002c0009t0016g0359a0002c0009t0016g0362others(6): Show | 9 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2464-373A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 16/38 | chr8 | 17962728 | ||||||
| chr8:17962801
|
G | A | 2 | a0002c0002t0004g0002a0002c0002t0005g0002 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2464-300G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 16/38 | chr8 | 17962801 | ||||||
| chr8:17962803
|
T | C | 6 | a0005c0005t0014g0163a0005c0005t0015g0162a0005c0005t0015g0164others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2464-298T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 16/38 | chr8 | 17962803 | ||||||
| chr8:17962882
|
G | A | 2 | a0003c0003t0026g0271a0003c0003t0046g0259 | 2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2464-219G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 16/38 | chr8 | 17962882 | ||||||
| chr8:17962902
|
CA | C | 82 | a0001c0001t0001g0043a0001c0001t0001g0075a0003c0003t0002g0003others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.2464-184delA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr8 | 17962902 | |||||
| chr8:17962924
|
G | A | 249 | a0001c0001t0001g0082a0002c0002t0004g0002a0002c0002t0004g0180others(246): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.2464-177G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 16/38 | chr8 | 17962924 | ||||||
| chr8:17962928
|
T | G | 1 | a0005c0005t0041g0161 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2464-173T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 16/38 | chr8 | 17962928 | ||||||
| chr8:17962966
|
T | C | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2464-135T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 16/38 | chr8 | 17962966 | ||||||
| chr8:17963420
|
C | T | 41 | a0004c0004t0003g0113a0004c0004t0003g0114a0004c0004t0003g0115others(38): Show | 41 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.2654+129C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 17/38 | chr8 | 17963420 | ||||||
| chr8:17963476
|
C | T | 1 | a0007c0011t0003g0151 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2654+185C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 17/38 | chr8 | 17963476 | ||||||
| chr8:17963719
|
C | T | 5 | a0002c0002t0005g0301a0010c0014t0022g0330a0010c0014t0022g0331others(2): Show | 5 | HG00280.hp2 HG02698.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.2654+428C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 17/38 | chr8 | 17963719 | ||||||
| chr8:17964228
|
A | T | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2655-340A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 17/38 | chr8 | 17964228 | ||||||
| chr8:17964234
|
G | T | 1 | a0001c0001t0001g0042 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2655-334G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 17/38 | chr8 | 17964234 | ||||||
| chr8:17964334
|
A | G | 2 | a0004c0004t0003g0135a0004c0004t0003g0136 | 2 | HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2655-234A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 17/38 | chr8 | 17964334 | ||||||
| chr8:17964335
|
T | A | 2 | a0004c0004t0003g0135a0004c0004t0003g0136 | 2 | HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2655-233T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 17/38 | chr8 | 17964335 | ||||||
| chr8:17964812
|
A | C | 1 | a0001c0001t0001g0099 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2855+44A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 18/38 | chr8 | 17964812 | ||||||
| chr8:17964829
|
A | T | 1 | a0008c0010t0058g0211 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2855+61A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 18/38 | chr8 | 17964829 | ||||||
| chr8:17964854
|
G | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0066a0017c0027t0001g0061 | 3 | HG03098.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2855+86G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 18/38 | chr8 | 17964854 | ||||||
| chr8:17964855
|
C | G | 3 | a0001c0001t0001g0021a0001c0001t0001g0066a0017c0027t0001g0061 | 3 | HG03098.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2855+87C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 18/38 | chr8 | 17964855 | ||||||
| chr8:17964968
|
A | C | 10 | a0002c0002t0004g0002a0002c0002t0004g0194a0002c0002t0005g0002others(7): Show | 10 | HG03490.hp2 HG03492.hp1 NA18942.hp1 others(7): Show |
intron_variant | MODIFIER | c.2855+200A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 18/38 | chr8 | 17964968 | ||||||
| chr8:17964992
|
T | C | 2 | a0003c0003t0002g0003a0003c0003t0011g0003 | 2 | HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.2855+224T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 18/38 | chr8 | 17964992 | ||||||
| chr8:17965066
|
C | G | 1 | a0002c0002t0005g0299 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2855+298C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 18/38 | chr8 | 17965066 | ||||||
| chr8:17965073
|
C | T | 20 | a0005c0005t0008g0168a0005c0005t0008g0169a0005c0005t0008g0174others(17): Show | 20 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.2855+305C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 18/38 | chr8 | 17965073 | ||||||
| chr8:17965092
|
T | TA | 9 | a0002c0009t0005g0304a0002c0009t0016g0359a0002c0009t0016g0362others(6): Show | 9 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2855+325dupA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 18/38 | INFO_REALIGN_3_PRIME | chr8 | 17965092 | |||||
| chr8:17965197
|
C | T | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2855+429C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 18/38 | chr8 | 17965197 | ||||||
| chr8:17965219
|
C | T | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.2855+451C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 18/38 | chr8 | 17965219 | ||||||
| chr8:17965311
|
T | C | 1 | a0002c0021t0020g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2855+543T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 18/38 | chr8 | 17965311 | ||||||
| chr8:17965375
|
C | T | 248 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.2855+607C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 18/38 | chr8 | 17965375 | ||||||
| chr8:17965651
|
T | C | 1 | a0002c0007t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2856-348T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 18/38 | chr8 | 17965651 | ||||||
| chr8:17965776
|
G | A | 3 | a0003c0003t0007g0219a0003c0003t0007g0232a0003c0044t0007g0234 | 3 | HG00558.hp2 NA18959.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.2856-223G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 18/38 | chr8 | 17965776 | ||||||
| chr8:17965776
|
G | C | 120 | a0001c0001t0001g0067a0002c0002t0004g0002a0002c0002t0004g0180others(117): Show | 120 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.2856-223G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 18/38 | chr8 | 17965776 | ||||||
| chr8:17965790
|
A | G | 119 | a0002c0002t0005g0301a0002c0017t0031g0321a0002c0017t0032g0322others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.2856-209A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 18/38 | chr8 | 17965790 | ||||||
| chr8:17965812
|
G | A | 2 | a0002c0021t0020g0103a0002c0021t0027g0102 | 2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2856-187G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 18/38 | chr8 | 17965812 | ||||||
| chr8:17965901
|
G | C | 1 | a0001c0001t0006g0101 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2856-98G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 18/38 | chr8 | 17965901 | ||||||
| chr8:17965973
|
A | C | 9 | a0002c0009t0005g0304a0002c0009t0016g0359a0002c0009t0016g0362others(6): Show | 9 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2856-26A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 18/38 | chr8 | 17965973 | ||||||
| chr8:17966595
|
T | C | 1 | a0002c0019t0004g0213 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.3221+122T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 20/38 | chr8 | 17966595 | ||||||
| chr8:17966770
|
G | A | 3 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102 | 3 | HG03209.hp1 HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3222-210G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 20/38 | chr8 | 17966770 | ||||||
| chr8:17966777
|
G | A | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3222-203G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 20/38 | chr8 | 17966777 | ||||||
| chr8:17966831
|
C | T | 1 | a0003c0003t0007g0257 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3222-149C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 20/38 | chr8 | 17966831 | ||||||
| chr8:17967184
|
C | T | 5 | a0005c0005t0015g0162a0005c0005t0015g0164a0005c0005t0015g0165others(2): Show | 5 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.3412+14C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17967184 | ||||||
| chr8:17967185
|
C | G | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3412+15C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17967185 | ||||||
| chr8:17967224
|
C | T | 12 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(9): Show | 12 | HG02109.hp1 HG02647.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.3412+54C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17967224 | ||||||
| chr8:17967273
|
G | A | 3 | a0006c0008t0007g0261a0006c0008t0007g0266a0006c0008t0007g0272 | 3 | NA18612.hp2 NA18983.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.3412+103G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17967273 | ||||||
| chr8:17967305
|
C | CCTT | 6 | a0007c0011t0001g0149a0007c0011t0001g0150a0007c0011t0003g0151others(3): Show | 6 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3412+135_3412+136i others(5): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17967305 | ||||||
| chr8:17967305
|
C | CT | 35 | a0001c0001t0017g0105a0001c0001t0018g0106a0001c0001t0018g0110others(32): Show | 35 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(32): Show |
intron_variant | MODIFIER | c.3412+149dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17967305 | |||||
| chr8:17967305
|
C | CTT | 69 | a0003c0003t0002g0156a0003c0003t0002g0157a0003c0003t0002g0158others(66): Show | 69 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.3412+148_3412+149d others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17967305 | |||||
| chr8:17967348
|
G | T | 1 | a0001c0024t0017g0107 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3412+178G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17967348 | ||||||
| chr8:17967445
|
A | G | 3 | a0005c0005t0014g0160a0005c0005t0014g0171a0005c0005t0027g0170 | 3 | HG01891.hp2 HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.3412+275A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17967445 | ||||||
| chr8:17967574
|
C | T | 1 | a0002c0002t0029g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3412+404C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17967574 | ||||||
| chr8:17967643
|
G | A | 5 | a0002c0002t0005g0301a0010c0014t0022g0330a0010c0014t0022g0331others(2): Show | 5 | HG00280.hp2 HG02698.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.3412+473G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17967643 | ||||||
| chr8:17967687
|
A | T | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.3412+517A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17967687 | ||||||
| chr8:17967756
|
G | A | 1 | a0002c0017t0031g0321 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3412+586G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17967756 | ||||||
| chr8:17967818
|
G | A | 256 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(253): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.3412+648G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17967818 | ||||||
| chr8:17968050
|
G | C | 258 | a0001c0001t0001g0082a0001c0001t0017g0105a0001c0001t0017g0108others(255): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.3412+880G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17968050 | ||||||
| chr8:17968055
|
C | CA | 84 | a0002c0002t0005g0301a0002c0002t0028g0323a0002c0009t0016g0359others(81): Show | 84 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.3412+899dupA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968055 | |||||
| chr8:17968109
|
C | T | 11 | a0005c0005t0014g0160a0005c0005t0014g0163a0005c0005t0014g0171others(8): Show | 11 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.3412+939C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17968109 | ||||||
| chr8:17968222
|
G | A | 42 | a0002c0002t0028g0323a0004c0004t0003g0113a0004c0004t0003g0114others(39): Show | 42 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.3412+1052G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17968222 | ||||||
| chr8:17968228
|
G | T | 1 | a0002c0017t0032g0322 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3412+1058G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17968228 | ||||||
| chr8:17968425
|
G | C | 1 | a0001c0001t0001g0042 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.3413-1152G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17968425 | ||||||
| chr8:17968437
|
A | C | 1 | a0003c0006t0002g0260 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.3413-1140A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17968437 | ||||||
| chr8:17968687
|
T | C | 125 | a0002c0002t0005g0301a0002c0009t0016g0359a0002c0009t0016g0362others(122): Show | 125 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.3413-890T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17968687 | ||||||
| chr8:17968726
|
A | G | 41 | a0002c0002t0028g0323a0004c0004t0003g0113a0004c0004t0003g0114others(38): Show | 41 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.3413-851A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17968726 | ||||||
| chr8:17968730
|
A | ATATGTGT others(3): Show |
1 | a0002c0017t0031g0321 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3413-846_3413-845i others(12): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968730 | |||||
| chr8:17968730
|
A | ATG | 37 | a0001c0001t0001g0032a0001c0001t0001g0066a0001c0001t0001g0067others(34): Show | 37 | HG00558.hp1 HG00609.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.3413-815_3413-814d others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968730 | |||||
| chr8:17968730
|
A | ATGTG | 8 | a0001c0001t0006g0080a0005c0005t0014g0160a0005c0005t0014g0175others(5): Show | 8 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.3413-817_3413-814d others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968730 | |||||
| chr8:17968730
|
A | ATGTGTG | 13 | a0002c0002t0004g0184a0002c0002t0012g0307a0004c0004t0003g0124others(10): Show | 13 | HG02083.hp1 HG02132.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.3413-819_3413-814d others(8): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968730 | |||||
| chr8:17968730
|
A | ATGTGTGT others(1): Show |
11 | a0002c0017t0032g0322a0004c0004t0003g0113a0004c0004t0003g0132others(8): Show | 11 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.3413-821_3413-814d others(10): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968730 | |||||
| chr8:17968730
|
A | ATGTGTGT others(3): Show |
12 | a0001c0001t0035g0111a0002c0002t0012g0155a0004c0004t0003g0115others(9): Show | 12 | HG01257.hp2 HG01361.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.3413-823_3413-814d others(12): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968730 | |||||
| chr8:17968730
|
A | ATGTGTGT others(5): Show |
14 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0024t0017g0107others(11): Show | 14 | HG01884.hp1 HG01952.hp2 HG02273.hp2 others(11): Show |
intron_variant | MODIFIER | c.3413-825_3413-814d others(14): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968730 | |||||
| chr8:17968730
|
A | ATGTGTGT others(7): Show |
2 | a0001c0001t0018g0106a0004c0004t0003g0116 | 2 | HG02886.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.3413-827_3413-814d others(16): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968730 | |||||
| chr8:17968730
|
A | ATGTGTGT others(9): Show |
4 | a0001c0001t0018g0112a0004c0004t0003g0135a0004c0004t0003g0136others(1): Show | 4 | HG02886.hp1 HG02895.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.3413-829_3413-814d others(18): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968730 | |||||
| chr8:17968730
|
A | ATGTGTGT others(15): Show |
1 | a0001c0001t0018g0110 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3413-835_3413-814d others(24): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968730 | |||||
| chr8:17968730
|
A | G | 7 | a0001c0001t0006g0094a0002c0002t0005g0301a0004c0004t0003g0133others(4): Show | 7 | HG00280.hp2 HG01261.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.3413-847A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17968730 | ||||||
| chr8:17968730
|
ATG | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0088others(4): Show | 7 | HG00642.hp1 HG03017.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.3413-815_3413-814d others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968730 | |||||
| chr8:17968730
|
ATGTG | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0086a0001c0001t0037g0087others(1): Show | 4 | HG01081.hp1 HG01934.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.3413-817_3413-814d others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968730 | |||||
| chr8:17968732
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3413-845G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17968732 | ||||||
| chr8:17968760
|
G | A | 3 | a0002c0002t0004g0328a0002c0002t0005g0326a0002c0002t0029g0324 | 3 | HG03516.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3413-817G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17968760 | ||||||
| chr8:17968762
|
G | A | 5 | a0001c0001t0001g0083a0001c0001t0001g0088a0002c0002t0004g0328others(2): Show | 5 | HG02559.hp1 HG03017.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.3413-815G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17968762 | ||||||
| chr8:17968762
|
G | GTA | 3 | a0002c0002t0005g0288a0002c0002t0005g0290a0002c0019t0004g0213 | 3 | HG00741.hp2 NA18966.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.3413-800_3413-799d others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968762 | |||||
| chr8:17968762
|
G | GTGTA | 4 | a0002c0002t0021g0308a0002c0002t0021g0309a0002c0002t0060g0212others(1): Show | 4 | HG00140.hp2 HG01070.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.3413-814_3413-813i others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968762 | |||||
| chr8:17968762
|
G | GTGTGTA | 47 | a0001c0001t0001g0082a0002c0002t0004g0181a0002c0002t0004g0192others(44): Show | 47 | HG00323.hp1 HG00544.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.3413-814_3413-813i others(8): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968762 | |||||
| chr8:17968762
|
G | GTGTGTAT others(1): Show |
4 | a0002c0002t0004g0180a0002c0002t0004g0187a0002c0002t0004g0191others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.3413-814_3413-813i others(10): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968762 | |||||
| chr8:17968762
|
G | GTGTGTAT others(3): Show |
1 | a0002c0021t0027g0102 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3413-814_3413-813i others(12): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968762 | |||||
| chr8:17968762
|
G | GTGTGTGT others(1): Show |
7 | a0002c0002t0005g0285a0002c0002t0005g0300a0002c0002t0005g0315others(4): Show | 7 | HG01167.hp1 HG01192.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.3413-814_3413-813i others(10): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968762 | |||||
| chr8:17968762
|
G | GTGTGTGT others(3): Show |
1 | a0002c0021t0020g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3413-814_3413-813i others(12): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968762 | |||||
| chr8:17968762
|
G | GTGTGTGT others(3): Show |
10 | a0001c0001t0004g0044a0002c0002t0004g0185a0002c0002t0005g0283others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.3413-814_3413-813i others(12): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968762 | |||||
| chr8:17968762
|
G | GTGTGTGT others(5): Show |
1 | a0002c0002t0005g0327 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3413-814_3413-813i others(14): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968762 | |||||
| chr8:17968762
|
G | GTGTGTGT others(5): Show |
1 | a0002c0002t0004g0194 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3413-814_3413-813i others(14): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968762 | |||||
| chr8:17968762
|
G | GTGTGTGT others(7): Show |
1 | a0002c0034t0057g0325 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3413-814_3413-813i others(16): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968762 | |||||
| chr8:17968762
|
G | GTGTGTGT others(7): Show |
2 | a0002c0002t0004g0002a0002c0002t0005g0002 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3413-814_3413-813i others(16): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968762 | |||||
| chr8:17968762
|
G | GTGTGTGT others(15): Show |
1 | a0002c0017t0003g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3413-814_3413-813i others(24): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968762 | |||||
| chr8:17968762
|
GTA | G | 6 | a0001c0001t0001g0064a0003c0003t0002g0240a0003c0003t0026g0271others(3): Show | 6 | HG00639.hp2 HG01934.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.3413-800_3413-799d others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr8 | 17968762 | |||||
| chr8:17968764
|
A | G | 144 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0084others(141): Show | 144 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.3413-813A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17968764 | ||||||
| chr8:17968766
|
A | G | 129 | a0001c0001t0018g0112a0002c0002t0005g0301a0002c0002t0028g0323others(126): Show | 129 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.3413-811A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17968766 | ||||||
| chr8:17968768
|
A | G | 24 | a0001c0001t0018g0112a0002c0002t0005g0301a0002c0009t0016g0359others(21): Show | 24 | HG00280.hp2 HG01099.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.3413-809A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17968768 | ||||||
| chr8:17968770
|
A | G | 15 | a0002c0002t0005g0301a0002c0009t0016g0359a0002c0009t0016g0362others(12): Show | 15 | HG00280.hp2 HG01099.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.3413-807A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17968770 | ||||||
| chr8:17968772
|
A | G | 2 | a0010c0014t0022g0330a0010c0014t0022g0331 | 2 | HG02698.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.3413-805A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17968772 | ||||||
| chr8:17968777
|
T | C | 9 | a0003c0003t0007g0274a0006c0008t0007g0261a0006c0008t0007g0263others(6): Show | 9 | HG00609.hp1 HG02027.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.3413-800T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17968777 | ||||||
| chr8:17968784
|
C | T | 109 | a0003c0003t0002g0003a0003c0003t0002g0156a0003c0003t0002g0157others(106): Show | 109 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.3413-793C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17968784 | ||||||
| chr8:17968803
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3413-774A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17968803 | ||||||
| chr8:17968824
|
T | A | 1 | a0001c0001t0040g0076 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3413-753T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17968824 | ||||||
| chr8:17969034
|
G | A | 102 | a0003c0003t0002g0003a0003c0003t0002g0156a0003c0003t0002g0157others(99): Show | 102 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.3413-543G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17969034 | ||||||
| chr8:17969065
|
T | A | 1 | a0002c0002t0004g0191 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3413-512T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17969065 | ||||||
| chr8:17969066
|
ACATAACA others(7): Show |
A | 1 | a0002c0002t0004g0191 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3413-510_3413-497d others(16): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17969066 | ||||||
| chr8:17969086
|
T | A | 2 | a0002c0002t0004g0191a0015c0022t0004g0295 | 2 | HG01069.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.3413-491T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17969086 | ||||||
| chr8:17969095
|
A | C | 1 | a0004c0004t0003g0129 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.3413-482A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17969095 | ||||||
| chr8:17969203
|
C | T | 2 | a0004c0004t0003g0114a0004c0004t0003g0144 | 2 | NA18612.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.3413-374C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17969203 | ||||||
| chr8:17969391
|
A | G | 5 | a0002c0002t0005g0301a0010c0014t0022g0330a0010c0014t0022g0331others(2): Show | 5 | HG00280.hp2 HG02698.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.3413-186A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17969391 | ||||||
| chr8:17969489
|
C | T | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.3413-88C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17969489 | ||||||
| chr8:17969501
|
A | C | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.3413-76A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 21/38 | chr8 | 17969501 | ||||||
| chr8:17969751
|
A | AC | 267 | a0001c0001t0001g0082a0001c0001t0004g0044a0001c0001t0017g0105others(264): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
splice_region_variant&intron_variant | LOW | c.3584+4dupC | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr8 | 17969751 | |||||
| chr8:17969806
|
A | G | 126 | a0002c0002t0005g0301a0002c0009t0016g0359a0002c0009t0016g0362others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.3584+58A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 22/38 | chr8 | 17969806 | ||||||
| chr8:17969867
|
T | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0054a0001c0001t0006g0053 | 3 | HG04184.hp2 NA18993.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.3584+119T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 22/38 | chr8 | 17969867 | ||||||
| chr8:17969876
|
T | G | 1 | a0007c0011t0001g0150 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3584+128T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 22/38 | chr8 | 17969876 | ||||||
| chr8:17970001
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | NA18981.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.3584+253C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 22/38 | chr8 | 17970001 | ||||||
| chr8:17970088
|
C | T | 120 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(117): Show | 120 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.3584+340C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 22/38 | chr8 | 17970088 | ||||||
| chr8:17970227
|
C | G | 20 | a0005c0005t0008g0168a0005c0005t0008g0169a0005c0005t0008g0174others(17): Show | 20 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.3584+479C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 22/38 | chr8 | 17970227 | ||||||
| chr8:17970259
|
A | G | 5 | a0002c0002t0005g0301a0010c0014t0022g0330a0010c0014t0022g0331others(2): Show | 5 | HG00280.hp2 HG02698.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.3584+511A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 22/38 | chr8 | 17970259 | ||||||
| chr8:17970347
|
T | G | 1 | a0001c0001t0006g0101 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.3584+599T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 22/38 | chr8 | 17970347 | ||||||
| chr8:17970431
|
A | AT | 118 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.3584+698dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr8 | 17970431 | |||||
| chr8:17970431
|
A | ATT | 6 | a0003c0003t0002g0275a0005c0005t0015g0166a0007c0011t0001g0150others(3): Show | 6 | HG02486.hp2 HG03516.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.3584+697_3584+698d others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr8 | 17970431 | |||||
| chr8:17970587
|
G | C | 1 | a0001c0026t0001g0065 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3584+839G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 22/38 | chr8 | 17970587 | ||||||
| chr8:17970648
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0002g0072 | 2 | NA18941.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.3584+900G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 22/38 | chr8 | 17970648 | ||||||
| chr8:17970653
|
A | G | 1 | a0014c0020t0004g0070 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3584+905A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 22/38 | chr8 | 17970653 | ||||||
| chr8:17970694
|
C | T | 3 | a0003c0003t0002g0231a0003c0003t0026g0271a0003c0003t0046g0259 | 3 | HG01934.hp2 HG02129.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.3584+946C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 22/38 | chr8 | 17970694 | ||||||
| chr8:17970722
|
C | T | 1 | a0005c0005t0015g0173 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3584+974C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 22/38 | chr8 | 17970722 | ||||||
| chr8:17970846
|
A | G | 88 | a0001c0001t0001g0082a0002c0002t0004g0002a0002c0002t0004g0180others(85): Show | 88 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.3584+1098A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 22/38 | chr8 | 17970846 | ||||||
| chr8:17970887
|
A | C | 1 | a0016c0046t0002g0244 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3584+1139A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 22/38 | chr8 | 17970887 | ||||||
| chr8:17971046
|
C | A | 8 | a0003c0003t0009g0346a0003c0003t0009g0347a0003c0003t0009g0348others(5): Show | 8 | HG00597.hp1 HG02683.hp2 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.3585-1283C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 22/38 | chr8 | 17971046 | ||||||
| chr8:17971127
|
A | C | 2 | a0002c0002t0005g0292a0002c0002t0005g0293 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3585-1202A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 22/38 | chr8 | 17971127 | ||||||
| chr8:17971326
|
C | T | 12 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(9): Show | 12 | HG02109.hp1 HG02647.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.3585-1003C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 22/38 | chr8 | 17971326 | ||||||
| chr8:17972171
|
T | C | 127 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.3585-158T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 22/38 | chr8 | 17972171 | ||||||
| chr8:17972235
|
C | A | 2 | a0003c0003t0002g0003a0003c0003t0011g0003 | 2 | HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.3585-94C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 22/38 | chr8 | 17972235 | ||||||
| chr8:17972247
|
C | CAA | 268 | a0001c0001t0001g0082a0001c0001t0004g0044a0001c0001t0010g0015others(265): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.3585-82_3585-81ins others(2): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 22/38 | chr8 | 17972247 | ||||||
| chr8:17972825
|
T | A | 1 | a0002c0021t0020g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3943+138T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17972825 | ||||||
| chr8:17972841
|
A | AT | 9 | a0002c0007t0001g0033a0002c0009t0016g0359a0002c0009t0016g0362others(6): Show | 9 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.3943+163dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr8 | 17972841 | |||||
| chr8:17972950
|
T | C | 83 | a0001c0001t0001g0082a0001c0001t0010g0015a0002c0002t0004g0002others(80): Show | 83 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.3943+263T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17972950 | ||||||
| chr8:17972965
|
A | T | 1 | a0002c0017t0031g0321 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3943+278A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17972965 | ||||||
| chr8:17972980
|
A | C | 84 | a0002c0002t0053g0289a0003c0003t0002g0003a0003c0003t0002g0156others(81): Show | 84 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.3943+293A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17972980 | ||||||
| chr8:17973048
|
C | G | 1 | a0001c0001t0001g0050 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3943+361C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17973048 | ||||||
| chr8:17973068
|
A | C | 9 | a0002c0009t0005g0304a0002c0009t0016g0359a0002c0009t0016g0362others(6): Show | 9 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.3943+381A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17973068 | ||||||
| chr8:17973221
|
A | T | 4 | a0002c0034t0057g0325a0007c0011t0003g0151a0007c0011t0003g0152others(1): Show | 4 | HG01884.hp2 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3943+534A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17973221 | ||||||
| chr8:17973231
|
T | G | 1 | a0003c0003t0002g0236 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.3943+544T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17973231 | ||||||
| chr8:17973717
|
GA | G | 12 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(9): Show | 12 | HG02109.hp1 HG02647.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.3943+1046delA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr8 | 17973717 | |||||
| chr8:17973779
|
T | A | 9 | a0002c0017t0003g0104a0002c0017t0031g0321a0002c0017t0032g0322others(6): Show | 9 | HG01099.hp1 HG02257.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.3943+1092T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17973779 | ||||||
| chr8:17973819
|
T | C | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.3943+1132T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17973819 | ||||||
| chr8:17973876
|
A | C | 1 | a0002c0007t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3943+1189A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17973876 | ||||||
| chr8:17974049
|
C | T | 1 | a0001c0001t0006g0056 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3943+1362C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17974049 | ||||||
| chr8:17974085
|
A | G | 1 | a0002c0002t0004g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3943+1398A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17974085 | ||||||
| chr8:17974112
|
A | G | 9 | a0002c0017t0003g0104a0002c0017t0031g0321a0002c0017t0032g0322others(6): Show | 9 | HG01099.hp1 HG02257.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.3943+1425A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17974112 | ||||||
| chr8:17974152
|
G | T | 17 | a0005c0005t0008g0168a0005c0005t0008g0169a0005c0005t0008g0174others(14): Show | 17 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.3943+1465G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17974152 | ||||||
| chr8:17974239
|
A | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.3943+1552A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17974239 | ||||||
| chr8:17974244
|
A | T | 79 | a0001c0001t0010g0015a0002c0002t0004g0002a0002c0002t0004g0180others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.3943+1557A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17974244 | ||||||
| chr8:17974284
|
G | A | 1 | a0003c0003t0002g0221 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3943+1597G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17974284 | ||||||
| chr8:17974371
|
A | G | 85 | a0001c0001t0002g0072a0003c0003t0002g0003a0003c0003t0002g0156others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.3943+1684A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17974371 | ||||||
| chr8:17974709
|
T | G | 5 | a0005c0005t0008g0168a0005c0005t0008g0169a0005c0005t0008g0174others(2): Show | 5 | HG02559.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.3943+2022T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17974709 | ||||||
| chr8:17974741
|
T | C | 2 | a0002c0017t0031g0321a0002c0017t0032g0322 | 2 | HG01099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3943+2054T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17974741 | ||||||
| chr8:17974751
|
C | G | 110 | a0001c0001t0002g0072a0003c0003t0002g0003a0003c0003t0002g0156others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.3943+2064C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17974751 | ||||||
| chr8:17974857
|
G | GCA | 82 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0040others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.3943+2205_3943+220 others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr8 | 17974857 | |||||
| chr8:17974857
|
G | GCACA | 24 | a0002c0002t0029g0183a0003c0003t0002g0003a0003c0003t0002g0233others(21): Show | 24 | HG00597.hp1 HG00639.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.3943+2203_3943+220 others(8): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr8 | 17974857 | |||||
| chr8:17974857
|
G | GCACACA | 5 | a0002c0002t0005g0301a0002c0017t0032g0322a0003c0003t0011g0178others(2): Show | 5 | HG00280.hp2 HG02257.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.3943+2201_3943+220 others(10): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr8 | 17974857 | |||||
| chr8:17974857
|
G | GCACACAC others(3): Show |
3 | a0010c0014t0022g0330a0013c0023t0001g0153a0013c0023t0001g0154 | 3 | HG02895.hp2 HG02897.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.3943+2197_3943+220 others(14): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr8 | 17974857 | |||||
| chr8:17974857
|
G | GCACACAC others(5): Show |
1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3943+2195_3943+220 others(16): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr8 | 17974857 | |||||
| chr8:17974857
|
GCA | G | 17 | a0001c0001t0001g0077a0001c0001t0017g0105a0001c0001t0017g0108others(14): Show | 17 | HG01884.hp2 HG02145.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.3943+2205_3943+220 others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr8 | 17974857 | |||||
| chr8:17974857
|
GCACACA | G | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.3943+2201_3943+220 others(10): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr8 | 17974857 | |||||
| chr8:17974859
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3943+2172A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17974859 | ||||||
| chr8:17974864
|
C | G | 4 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102others(1): Show | 4 | HG02896.hp2 HG03209.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3943+2177C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17974864 | ||||||
| chr8:17974915
|
A | G | 1 | a0011c0018t0019g0190 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.3943+2228A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17974915 | ||||||
| chr8:17974943
|
A | C | 1 | a0002c0002t0005g0326 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3943+2256A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17974943 | ||||||
| chr8:17974956
|
A | G | 1 | a0002c0007t0001g0033 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.3943+2269A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17974956 | ||||||
| chr8:17975036
|
T | C | 267 | a0001c0001t0002g0072a0001c0001t0004g0044a0001c0001t0006g0079others(264): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.3943+2349T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17975036 | ||||||
| chr8:17975072
|
C | G | 1 | a0002c0021t0020g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3943+2385C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17975072 | ||||||
| chr8:17975077
|
T | C | 4 | a0005c0005t0008g0332a0005c0005t0008g0333a0005c0005t0008g0334others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3943+2390T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17975077 | ||||||
| chr8:17975098
|
T | C | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.3943+2411T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17975098 | ||||||
| chr8:17975099
|
T | A | 9 | a0001c0001t0001g0064a0001c0001t0001g0071a0001c0001t0006g0026others(6): Show | 9 | HG00423.hp1 HG02083.hp2 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.3943+2412T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17975099 | ||||||
| chr8:17975165
|
G | A | 4 | a0003c0003t0002g0264a0003c0003t0002g0265a0003c0003t0002g0267others(1): Show | 4 | HG00639.hp1 HG01070.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.3943+2478G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17975165 | ||||||
| chr8:17975256
|
C | T | 1 | a0004c0004t0003g0126 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3943+2569C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17975256 | ||||||
| chr8:17975257
|
G | A | 1 | a0010c0014t0023g0355 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3943+2570G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17975257 | ||||||
| chr8:17975352
|
G | A | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3943+2665G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17975352 | ||||||
| chr8:17975445
|
G | T | 2 | a0004c0004t0003g0135a0004c0004t0003g0136 | 2 | HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3943+2758G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17975445 | ||||||
| chr8:17975453
|
G | T | 2 | a0004c0004t0003g0135a0004c0004t0003g0136 | 2 | HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3943+2766G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17975453 | ||||||
| chr8:17975458
|
C | T | 3 | a0002c0002t0004g0180a0002c0002t0004g0187a0002c0002t0004g0198 | 3 | HG01109.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.3943+2771C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17975458 | ||||||
| chr8:17975461
|
C | G | 4 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102others(1): Show | 4 | HG02896.hp2 HG03209.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3943+2774C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17975461 | ||||||
| chr8:17975484
|
G | A | 5 | a0002c0002t0005g0302a0002c0002t0005g0303a0002c0002t0021g0195others(2): Show | 5 | HG00140.hp2 HG01069.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.3943+2797G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17975484 | ||||||
| chr8:17975585
|
A | G | 4 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102others(1): Show | 4 | HG02896.hp2 HG03209.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3943+2898A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17975585 | ||||||
| chr8:17975607
|
A | T | 1 | a0001c0026t0001g0065 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3943+2920A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17975607 | ||||||
| chr8:17975863
|
T | C | 1 | a0007c0011t0001g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3943+3176T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17975863 | ||||||
| chr8:17976231
|
A | G | 9 | a0002c0009t0005g0304a0002c0009t0016g0359a0002c0009t0016g0362others(6): Show | 9 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.3943+3544A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17976231 | ||||||
| chr8:17976363
|
C | T | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.3943+3676C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17976363 | ||||||
| chr8:17976401
|
A | G | 9 | a0002c0009t0005g0304a0002c0009t0016g0359a0002c0009t0016g0362others(6): Show | 9 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.3943+3714A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17976401 | ||||||
| chr8:17976542
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3943+3855C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17976542 | ||||||
| chr8:17976579
|
C | T | 83 | a0001c0001t0002g0072a0003c0003t0002g0003a0003c0003t0002g0156others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.3943+3892C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17976579 | ||||||
| chr8:17976627
|
T | C | 1 | a0002c0002t0004g0191 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3943+3940T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17976627 | ||||||
| chr8:17976817
|
T | C | 128 | a0001c0001t0002g0072a0002c0002t0005g0301a0002c0002t0053g0289others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.3944-3774T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17976817 | ||||||
| chr8:17976868
|
G | GT | 7 | a0002c0002t0004g0192a0002c0002t0005g0281a0003c0003t0002g0236others(4): Show | 7 | HG00544.hp1 HG00621.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.3944-3711dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr8 | 17976868 | |||||
| chr8:17976868
|
GT | G | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.3944-3711delT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr8 | 17976868 | |||||
| chr8:17976976
|
A | G | 128 | a0001c0001t0002g0072a0002c0002t0005g0301a0002c0002t0053g0289others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.3944-3615A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17976976 | ||||||
| chr8:17977008
|
C | T | 1 | a0001c0026t0001g0065 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3944-3583C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17977008 | ||||||
| chr8:17977445
|
G | A | 9 | a0002c0009t0005g0304a0002c0009t0016g0359a0002c0009t0016g0362others(6): Show | 9 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.3944-3146G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17977445 | ||||||
| chr8:17977538
|
G | C | 1 | a0002c0002t0005g0316 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3944-3053G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17977538 | ||||||
| chr8:17977556
|
G | C | 82 | a0001c0001t0002g0072a0003c0003t0002g0003a0003c0003t0002g0156others(79): Show | 82 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.3944-3035G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17977556 | ||||||
| chr8:17977585
|
A | T | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.3944-3006A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17977585 | ||||||
| chr8:17977634
|
A | T | 5 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(2): Show | 5 | HG02717.hp1 HG02886.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.3944-2957A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17977634 | ||||||
| chr8:17977666
|
G | T | 1 | a0004c0004t0028g0119 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3944-2925G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17977666 | ||||||
| chr8:17977806
|
G | A | 83 | a0001c0001t0002g0072a0003c0003t0002g0003a0003c0003t0002g0156others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.3944-2785G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17977806 | ||||||
| chr8:17978139
|
T | G | 128 | a0001c0001t0002g0072a0002c0002t0005g0301a0002c0009t0005g0304others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.3944-2452T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17978139 | ||||||
| chr8:17978175
|
C | T | 14 | a0003c0003t0002g0003a0003c0003t0007g0257a0003c0003t0007g0258others(11): Show | 14 | HG00609.hp1 HG01099.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.3944-2416C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17978175 | ||||||
| chr8:17978176
|
A | G | 127 | a0001c0001t0002g0072a0002c0002t0005g0301a0002c0009t0005g0304others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.3944-2415A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17978176 | ||||||
| chr8:17978384
|
G | A | 1 | a0002c0002t0004g0191 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3944-2207G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17978384 | ||||||
| chr8:17978386
|
G | A | 2 | a0002c0002t0004g0287a0002c0002t0012g0286 | 2 | HG01361.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.3944-2205G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17978386 | ||||||
| chr8:17978494
|
C | G | 41 | a0001c0001t0006g0079a0004c0004t0003g0113a0004c0004t0003g0114others(38): Show | 41 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.3944-2097C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17978494 | ||||||
| chr8:17978603
|
C | G | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.3944-1988C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17978603 | ||||||
| chr8:17978692
|
G | A | 13 | a0002c0009t0005g0304a0002c0009t0016g0359a0002c0009t0016g0362others(10): Show | 13 | HG02109.hp1 HG02647.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.3944-1899G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17978692 | ||||||
| chr8:17978706
|
A | G | 3 | a0003c0003t0026g0271a0003c0003t0046g0259a0030c0041t0026g0270 | 3 | HG00639.hp2 HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.3944-1885A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17978706 | ||||||
| chr8:17978751
|
TAAAG | T | 41 | a0001c0001t0006g0079a0004c0004t0003g0113a0004c0004t0003g0114others(38): Show | 41 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.3944-1836_3944-183 others(8): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr8 | 17978751 | |||||
| chr8:17978840
|
A | G | 1 | a0002c0002t0005g0318 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3944-1751A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17978840 | ||||||
| chr8:17978890
|
G | T | 118 | a0001c0001t0002g0072a0002c0017t0003g0104a0002c0017t0031g0321others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.3944-1701G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17978890 | ||||||
| chr8:17978941
|
C | A | 3 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354 | 3 | HG02698.hp2 HG03017.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.3944-1650C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17978941 | ||||||
| chr8:17978992
|
G | T | 75 | a0002c0002t0004g0180a0002c0002t0004g0181a0002c0002t0004g0184others(72): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.3944-1599G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17978992 | ||||||
| chr8:17978999
|
C | G | 108 | a0001c0001t0002g0072a0003c0003t0002g0003a0003c0003t0002g0156others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.3944-1592C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17978999 | ||||||
| chr8:17979024
|
C | T | 9 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(6): Show | 9 | HG01891.hp1 HG02145.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3944-1567C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17979024 | ||||||
| chr8:17979121
|
C | G | 42 | a0001c0001t0006g0079a0002c0007t0001g0033a0004c0004t0003g0113others(39): Show | 42 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.3944-1470C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17979121 | ||||||
| chr8:17979133
|
G | GA | 11 | a0001c0001t0001g0043a0001c0001t0001g0084a0002c0002t0005g0182others(8): Show | 11 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.3944-1443dupA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr8 | 17979133 | |||||
| chr8:17979133
|
GA | G | 10 | a0004c0004t0003g0135a0004c0004t0003g0136a0004c0004t0003g0336others(7): Show | 10 | HG01884.hp1 HG02280.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.3944-1443delA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr8 | 17979133 | |||||
| chr8:17979224
|
A | G | 1 | a0004c0004t0003g0357 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3944-1367A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17979224 | ||||||
| chr8:17979315
|
T | C | 1 | a0002c0007t0030g0179 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3944-1276T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17979315 | ||||||
| chr8:17979457
|
T | C | 9 | a0002c0009t0005g0304a0002c0009t0016g0359a0002c0009t0016g0362others(6): Show | 9 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.3944-1134T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17979457 | ||||||
| chr8:17979580
|
A | G | 83 | a0001c0001t0002g0072a0003c0003t0002g0003a0003c0003t0002g0156others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.3944-1011A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17979580 | ||||||
| chr8:17979781
|
T | C | 87 | a0001c0001t0004g0044a0002c0002t0004g0002a0002c0002t0004g0180others(84): Show | 87 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.3944-810T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17979781 | ||||||
| chr8:17979787
|
T | TGAAAACA | 268 | a0001c0001t0002g0072a0001c0001t0004g0044a0001c0001t0006g0079others(265): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.3944-804_3944-803i others(9): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17979787 | ||||||
| chr8:17979875
|
C | T | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.3944-716C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17979875 | ||||||
| chr8:17980467
|
A | T | 1 | a0005c0005t0014g0176 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3944-124A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17980467 | ||||||
| chr8:17980483
|
C | T | 1 | a0007c0011t0001g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3944-108C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17980483 | ||||||
| chr8:17980547
|
G | T | 1 | a0001c0001t0001g0099 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3944-44G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 23/38 | chr8 | 17980547 | ||||||
| chr8:17980805
|
T | A | 9 | a0002c0009t0005g0304a0002c0009t0016g0359a0002c0009t0016g0362others(6): Show | 9 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.4108+50T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17980805 | ||||||
| chr8:17980815
|
TATA | T | 4 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102others(1): Show | 4 | HG02896.hp2 HG03209.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.4108+65_4108+67del others(3): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | INFO_REALIGN_3_PRIME | chr8 | 17980815 | |||||
| chr8:17980848
|
C | A | 14 | a0002c0002t0005g0301a0002c0009t0005g0304a0002c0009t0016g0359others(11): Show | 14 | HG00280.hp2 HG02109.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.4108+93C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17980848 | ||||||
| chr8:17980869
|
G | T | 1 | a0008c0010t0058g0211 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4108+114G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17980869 | ||||||
| chr8:17980994
|
C | A | 5 | a0002c0002t0005g0301a0010c0014t0022g0330a0010c0014t0022g0331others(2): Show | 5 | HG00280.hp2 HG02698.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.4108+239C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17980994 | ||||||
| chr8:17981000
|
T | C | 121 | a0001c0001t0002g0072a0002c0002t0005g0301a0002c0002t0053g0289others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.4108+245T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17981000 | ||||||
| chr8:17981028
|
T | C | 6 | a0003c0003t0002g0216a0003c0003t0002g0217a0003c0003t0002g0229others(3): Show | 6 | HG02071.hp2 HG02074.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.4108+273T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17981028 | ||||||
| chr8:17981128
|
A | G | 4 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102others(1): Show | 4 | HG02896.hp2 HG03209.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.4108+373A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17981128 | ||||||
| chr8:17981449
|
C | G | 1 | a0002c0007t0005g0202 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.4108+694C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17981449 | ||||||
| chr8:17981612
|
A | C | 1 | a0003c0003t0009g0348 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.4108+857A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17981612 | ||||||
| chr8:17981623
|
G | A | 3 | a0002c0002t0004g0002a0002c0002t0005g0002a0002c0002t0005g0281 | 3 | HG00621.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.4108+868G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17981623 | ||||||
| chr8:17981715
|
G | T | 41 | a0001c0001t0006g0079a0004c0004t0003g0113a0004c0004t0003g0114others(38): Show | 41 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.4108+960G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17981715 | ||||||
| chr8:17981809
|
A | G | 5 | a0002c0002t0005g0301a0010c0014t0022g0330a0010c0014t0022g0331others(2): Show | 5 | HG00280.hp2 HG02698.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.4108+1054A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17981809 | ||||||
| chr8:17981905
|
GA | G | 179 | a0001c0001t0002g0072a0001c0001t0006g0079a0001c0001t0017g0105others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.4108+1162delA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | INFO_REALIGN_3_PRIME | chr8 | 17981905 | |||||
| chr8:17981905
|
GAA | G | 77 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(74): Show | 77 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.4108+1161_4108+116 others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | INFO_REALIGN_3_PRIME | chr8 | 17981905 | |||||
| chr8:17981907
|
A | G | 4 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102others(1): Show | 4 | HG02896.hp2 HG03209.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.4108+1152A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17981907 | ||||||
| chr8:17981920
|
C | G | 1 | a0004c0004t0003g0114 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.4108+1165C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17981920 | ||||||
| chr8:17981949
|
T | C | 1 | a0001c0001t0006g0026 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.4108+1194T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17981949 | ||||||
| chr8:17981981
|
A | T | 256 | a0001c0001t0002g0072a0001c0001t0006g0079a0001c0001t0017g0105others(253): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.4108+1226A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17981981 | ||||||
| chr8:17982204
|
A | G | 2 | a0004c0004t0003g0357a0004c0004t0049g0356 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.4108+1449A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17982204 | ||||||
| chr8:17982246
|
A | T | 2 | a0001c0001t0018g0110a0001c0001t0018g0112 | 2 | HG02145.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.4108+1491A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17982246 | ||||||
| chr8:17982297
|
C | T | 1 | a0005c0005t0014g0176 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4108+1542C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17982297 | ||||||
| chr8:17982437
|
A | G | 2 | a0004c0004t0003g0135a0004c0004t0003g0136 | 2 | HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4108+1682A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17982437 | ||||||
| chr8:17982493
|
TA | T | 73 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(70): Show | 73 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.4108+1748delA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | INFO_REALIGN_3_PRIME | chr8 | 17982493 | |||||
| chr8:17982494
|
A | T | 1 | a0002c0002t0012g0319 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.4108+1739A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17982494 | ||||||
| chr8:17982504
|
T | A | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4108+1749T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17982504 | ||||||
| chr8:17982516
|
A | T | 9 | a0002c0009t0005g0304a0002c0009t0016g0359a0002c0009t0016g0362others(6): Show | 9 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.4108+1761A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17982516 | ||||||
| chr8:17982525
|
C | T | 7 | a0001c0001t0001g0025a0001c0001t0001g0042a0001c0001t0001g0043others(4): Show | 7 | NA18960.hp1 NA18971.hp1 NA18987.hp2 others(4): Show |
intron_variant | MODIFIER | c.4108+1770C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17982525 | ||||||
| chr8:17982557
|
C | T | 6 | a0004c0004t0003g0132a0004c0004t0003g0133a0004c0004t0003g0137others(3): Show | 6 | HG00140.hp1 HG00323.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.4108+1802C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17982557 | ||||||
| chr8:17982598
|
G | A | 1 | a0002c0002t0029g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4108+1843G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17982598 | ||||||
| chr8:17982605
|
C | G | 1 | a0007c0011t0001g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4108+1850C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17982605 | ||||||
| chr8:17982609
|
C | T | 1 | a0006c0008t0007g0263 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.4108+1854C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17982609 | ||||||
| chr8:17982641
|
C | T | 1 | a0032c0030t0005g0186 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.4108+1886C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17982641 | ||||||
| chr8:17982652
|
G | T | 74 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(71): Show | 74 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.4108+1897G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17982652 | ||||||
| chr8:17982653
|
C | G | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4108+1898C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17982653 | ||||||
| chr8:17982667
|
T | G | 1 | a0002c0007t0001g0033 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.4108+1912T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17982667 | ||||||
| chr8:17982864
|
T | C | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4108+2109T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17982864 | ||||||
| chr8:17982883
|
A | G | 1 | a0002c0034t0057g0325 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4108+2128A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17982883 | ||||||
| chr8:17982937
|
T | G | 1 | a0002c0002t0004g0199 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4108+2182T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17982937 | ||||||
| chr8:17983096
|
G | A | 1 | a0001c0001t0006g0101 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.4108+2341G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17983096 | ||||||
| chr8:17983118
|
A | G | 116 | a0001c0001t0002g0045a0001c0001t0002g0072a0002c0002t0053g0289others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.4109-2329A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17983118 | ||||||
| chr8:17983149
|
T | C | 2 | a0002c0009t0016g0359a0002c0009t0052g0358 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4109-2298T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17983149 | ||||||
| chr8:17983450
|
CCATT | C | 4 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102others(1): Show | 4 | HG02896.hp2 HG03209.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.4109-1992_4109-198 others(8): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | INFO_REALIGN_3_PRIME | chr8 | 17983450 | |||||
| chr8:17983478
|
T | G | 270 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0006g0079others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.4109-1969T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17983478 | ||||||
| chr8:17983585
|
T | G | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4109-1862T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17983585 | ||||||
| chr8:17983640
|
A | G | 5 | a0002c0002t0005g0301a0010c0014t0022g0330a0010c0014t0022g0331others(2): Show | 5 | HG00280.hp2 HG02698.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.4109-1807A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17983640 | ||||||
| chr8:17983648
|
A | T | 123 | a0001c0001t0002g0045a0001c0001t0002g0072a0002c0002t0005g0301others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.4109-1799A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17983648 | ||||||
| chr8:17983765
|
T | C | 51 | a0001c0001t0006g0079a0002c0007t0001g0033a0003c0003t0007g0274others(48): Show | 51 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.4109-1682T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17983765 | ||||||
| chr8:17983907
|
C | T | 1 | a0002c0019t0004g0213 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4109-1540C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17983907 | ||||||
| chr8:17984137
|
G | C | 1 | a0002c0002t0059g0291 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.4109-1310G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17984137 | ||||||
| chr8:17984162
|
C | G | 6 | a0002c0002t0005g0288a0002c0002t0005g0294a0002c0002t0005g0315others(3): Show | 6 | HG00741.hp2 HG01070.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.4109-1285C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17984162 | ||||||
| chr8:17984171
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0075 | 3 | HG02602.hp1 HG03491.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.4109-1276G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17984171 | ||||||
| chr8:17984373
|
A | G | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4109-1074A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17984373 | ||||||
| chr8:17984412
|
C | T | 10 | a0004c0004t0003g0135a0004c0004t0003g0136a0004c0004t0003g0336others(7): Show | 10 | HG01884.hp1 HG02280.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.4109-1035C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17984412 | ||||||
| chr8:17984641
|
C | A | 1 | a0003c0003t0002g0233 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.4109-806C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17984641 | ||||||
| chr8:17984650
|
G | A | 7 | a0007c0011t0001g0149a0007c0011t0001g0150a0007c0011t0003g0151others(4): Show | 7 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.4109-797G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17984650 | ||||||
| chr8:17984674
|
C | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.4109-773C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17984674 | ||||||
| chr8:17984687
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.4109-760A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17984687 | ||||||
| chr8:17984764
|
C | T | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.4109-683C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17984764 | ||||||
| chr8:17984769
|
T | G | 1 | a0003c0003t0036g0262 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4109-678T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17984769 | ||||||
| chr8:17984820
|
G | T | 7 | a0007c0011t0001g0149a0007c0011t0001g0150a0007c0011t0003g0151others(4): Show | 7 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.4109-627G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17984820 | ||||||
| chr8:17984842
|
A | G | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4109-605A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17984842 | ||||||
| chr8:17984871
|
A | G | 6 | a0005c0005t0014g0163a0005c0005t0015g0162a0005c0005t0015g0164others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.4109-576A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17984871 | ||||||
| chr8:17984991
|
T | C | 89 | a0001c0001t0004g0044a0002c0002t0004g0002a0002c0002t0004g0180others(86): Show | 89 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.4109-456T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17984991 | ||||||
| chr8:17984998
|
C | T | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.4109-449C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17984998 | ||||||
| chr8:17985208
|
G | A | 9 | a0004c0004t0003g0132a0004c0004t0003g0133a0004c0004t0003g0137others(6): Show | 9 | HG00140.hp1 HG00323.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.4109-239G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17985208 | ||||||
| chr8:17985218
|
G | A | 1 | a0002c0002t0004g0192 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.4109-229G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17985218 | ||||||
| chr8:17985245
|
A | G | 5 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102others(2): Show | 5 | HG02896.hp2 HG03209.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.4109-202A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17985245 | ||||||
| chr8:17985281
|
A | G | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4109-166A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17985281 | ||||||
| chr8:17985404
|
G | T | 5 | a0005c0005t0008g0168a0005c0005t0008g0169a0005c0005t0008g0174others(2): Show | 5 | HG02559.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.4109-43G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17985404 | ||||||
| chr8:17985415
|
A | G | 13 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(10): Show | 13 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.4109-32A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 24/38 | chr8 | 17985415 | ||||||
| chr8:17985657
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4281+38T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 25/38 | chr8 | 17985657 | ||||||
| chr8:17986170
|
A | AG | 5 | a0002c0017t0003g0104a0002c0021t0020g0103a0002c0021t0027g0102others(2): Show | 5 | HG02896.hp2 HG03209.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.4410+85dupG | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr8 | 17986170 | |||||
| chr8:17986243
|
G | A | 27 | a0002c0017t0031g0321a0002c0017t0032g0322a0005c0005t0008g0168others(24): Show | 27 | HG01099.hp1 HG01891.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.4410+156G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17986243 | ||||||
| chr8:17986381
|
G | A | 1 | a0027c0031t0056g0139 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4410+294G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17986381 | ||||||
| chr8:17986417
|
G | C | 81 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(78): Show | 81 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.4410+330G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17986417 | ||||||
| chr8:17986423
|
G | T | 3 | a0002c0002t0005g0294a0002c0002t0005g0315a0002c0002t0005g0318 | 3 | HG01167.hp1 HG01978.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.4410+336G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17986423 | ||||||
| chr8:17986478
|
T | TA | 11 | a0001c0001t0006g0094a0001c0047t0006g0069a0002c0002t0005g0316others(8): Show | 11 | HG01074.hp2 HG01255.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.4410+407dupA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr8 | 17986478 | |||||
| chr8:17986478
|
TA | T | 10 | a0001c0001t0001g0077a0001c0001t0001g0090a0001c0001t0037g0087others(7): Show | 10 | HG01069.hp1 HG01069.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.4410+407delA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr8 | 17986478 | |||||
| chr8:17986498
|
T | C | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.4410+411T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17986498 | ||||||
| chr8:17986502
|
C | T | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.4410+415C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17986502 | ||||||
| chr8:17986601
|
A | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.4410+514A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17986601 | ||||||
| chr8:17986670
|
C | T | 1 | a0002c0017t0003g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4410+583C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17986670 | ||||||
| chr8:17986692
|
T | C | 256 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0017g0105others(253): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.4410+605T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17986692 | ||||||
| chr8:17986696
|
G | A | 1 | a0002c0007t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4410+609G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17986696 | ||||||
| chr8:17986776
|
C | A | 1 | a0002c0007t0004g0201 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.4410+689C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17986776 | ||||||
| chr8:17986844
|
T | C | 116 | a0001c0001t0002g0045a0001c0001t0002g0072a0002c0002t0053g0289others(113): Show | 116 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.4410+757T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17986844 | ||||||
| chr8:17986861
|
A | G | 88 | a0001c0001t0002g0045a0001c0001t0002g0072a0002c0002t0053g0289others(85): Show | 88 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.4410+774A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17986861 | ||||||
| chr8:17986978
|
C | T | 12 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(9): Show | 12 | HG02109.hp1 HG02647.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.4410+891C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17986978 | ||||||
| chr8:17987012
|
T | G | 5 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(2): Show | 5 | HG02717.hp1 HG02886.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4410+925T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17987012 | ||||||
| chr8:17987024
|
C | T | 2 | a0002c0002t0047g0206a0002c0002t0048g0205 | 2 | HG01074.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.4410+937C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17987024 | ||||||
| chr8:17987221
|
G | A | 1 | a0001c0001t0006g0094 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4410+1134G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17987221 | ||||||
| chr8:17987361
|
A | C | 80 | a0002c0002t0004g0002a0002c0002t0004g0180a0002c0002t0004g0181others(77): Show | 80 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.4410+1274A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17987361 | ||||||
| chr8:17987389
|
A | G | 1 | a0002c0002t0004g0287 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.4410+1302A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17987389 | ||||||
| chr8:17987416
|
C | T | 1 | a0005c0005t0041g0161 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4410+1329C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17987416 | ||||||
| chr8:17987565
|
G | A | 1 | a0002c0002t0048g0205 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.4410+1478G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17987565 | ||||||
| chr8:17987733
|
A | C | 1 | a0001c0001t0040g0076 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.4410+1646A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17987733 | ||||||
| chr8:17987938
|
G | T | 51 | a0002c0017t0003g0104a0002c0021t0020g0103a0004c0004t0003g0113others(48): Show | 51 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.4410+1851G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17987938 | ||||||
| chr8:17987942
|
C | T | 5 | a0003c0003t0013g0248a0003c0006t0013g0247a0003c0006t0013g0250others(2): Show | 5 | HG00609.hp2 HG02040.hp2 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.4410+1855C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17987942 | ||||||
| chr8:17987967
|
T | A | 1 | a0001c0001t0001g0099 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.4410+1880T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17987967 | ||||||
| chr8:17988007
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.4411-1852A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17988007 | ||||||
| chr8:17988030
|
G | T | 2 | a0004c0004t0003g0357a0004c0004t0049g0356 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.4411-1829G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17988030 | ||||||
| chr8:17988069
|
A | C | 1 | a0001c0001t0039g0009 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4411-1790A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17988069 | ||||||
| chr8:17988076
|
A | T | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4411-1783A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17988076 | ||||||
| chr8:17988205
|
T | TA | 7 | a0005c0005t0014g0163a0005c0005t0014g0171a0005c0005t0015g0162others(4): Show | 7 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.4411-1646dupA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr8 | 17988205 | |||||
| chr8:17988209
|
A | AT | 88 | a0001c0001t0004g0044a0002c0002t0004g0002a0002c0002t0004g0180others(85): Show | 88 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.4411-1650_4411-164 others(5): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17988209 | ||||||
| chr8:17988381
|
C | G | 1 | a0005c0005t0041g0161 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4411-1478C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17988381 | ||||||
| chr8:17988413
|
A | G | 1 | a0005c0005t0041g0161 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4411-1446A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17988413 | ||||||
| chr8:17988441
|
C | T | 1 | a0004c0016t0008g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4411-1418C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17988441 | ||||||
| chr8:17988462
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4411-1397A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17988462 | ||||||
| chr8:17988627
|
A | G | 1 | a0002c0021t0027g0102 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4411-1232A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17988627 | ||||||
| chr8:17988638
|
T | C | 3 | a0011c0018t0019g0188a0011c0018t0019g0189a0011c0018t0019g0190 | 3 | NA18981.hp1 NA18982.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.4411-1221T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17988638 | ||||||
| chr8:17988680
|
A | G | 1 | a0032c0030t0005g0186 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.4411-1179A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17988680 | ||||||
| chr8:17989074
|
T | A | 2 | a0003c0003t0026g0271a0003c0003t0046g0259 | 2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.4411-785T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17989074 | ||||||
| chr8:17989117
|
A | T | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.4411-742A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17989117 | ||||||
| chr8:17989209
|
C | T | 1 | a0007c0011t0001g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4411-650C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17989209 | ||||||
| chr8:17989254
|
T | C | 1 | a0002c0002t0004g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4411-605T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17989254 | ||||||
| chr8:17989504
|
T | C | 50 | a0002c0007t0001g0033a0003c0003t0007g0274a0004c0004t0003g0113others(47): Show | 50 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.4411-355T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17989504 | ||||||
| chr8:17989584
|
C | T | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.4411-275C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17989584 | ||||||
| chr8:17989680
|
G | C | 99 | a0001c0001t0002g0045a0001c0001t0002g0072a0002c0002t0053g0289others(96): Show | 99 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.4411-179G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17989680 | ||||||
| chr8:17989742
|
CTT | C | 79 | a0001c0001t0002g0045a0001c0001t0002g0072a0002c0002t0053g0289others(76): Show | 79 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.4411-116_4411-115d others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17989742 | ||||||
| chr8:17989788
|
A | G | 1 | a0002c0002t0004g0320 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.4411-71A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17989788 | ||||||
| chr8:17989789
|
T | A | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.4411-70T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17989789 | ||||||
| chr8:17989822
|
A | G | 1 | a0021c0043t0004g0197 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.4411-37A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 26/38 | chr8 | 17989822 | ||||||
| chr8:17989996
|
A | G | 88 | a0001c0001t0002g0045a0001c0001t0002g0072a0002c0002t0053g0289others(85): Show | 88 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.4531+17A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17989996 | ||||||
| chr8:17990150
|
T | C | 2 | a0002c0002t0004g0180a0002c0002t0004g0198 | 2 | HG01109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4531+171T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17990150 | ||||||
| chr8:17990273
|
A | C | 15 | a0003c0003t0009g0226a0003c0003t0009g0339a0003c0003t0009g0346others(12): Show | 15 | HG00597.hp1 HG00639.hp2 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.4531+294A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17990273 | ||||||
| chr8:17990302
|
G | A | 1 | a0032c0030t0005g0186 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.4531+323G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17990302 | ||||||
| chr8:17990379
|
G | T | 1 | a0002c0017t0032g0322 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4531+400G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17990379 | ||||||
| chr8:17990396
|
G | C | 1 | a0017c0027t0001g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4531+417G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17990396 | ||||||
| chr8:17990485
|
G | GT | 6 | a0001c0001t0001g0041a0002c0019t0004g0337a0003c0003t0007g0232others(3): Show | 6 | HG02056.hp1 HG02258.hp1 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.4531+519dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | INFO_REALIGN_3_PRIME | chr8 | 17990485 | |||||
| chr8:17990503
|
C | T | 1 | a0005c0005t0041g0161 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4531+524C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17990503 | ||||||
| chr8:17990523
|
C | G | 7 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(4): Show | 7 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.4531+544C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17990523 | ||||||
| chr8:17990530
|
G | A | 86 | a0001c0001t0004g0044a0002c0002t0004g0002a0002c0002t0004g0180others(83): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.4531+551G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17990530 | ||||||
| chr8:17990541
|
T | G | 4 | a0001c0001t0002g0072a0003c0003t0002g0239a0003c0003t0002g0245others(1): Show | 4 | HG00544.hp2 NA18747.hp2 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.4531+562T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17990541 | ||||||
| chr8:17990568
|
C | T | 1 | a0002c0021t0020g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4531+589C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17990568 | ||||||
| chr8:17990626
|
C | T | 20 | a0002c0021t0027g0102a0005c0005t0008g0168a0005c0005t0008g0169others(17): Show | 20 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.4531+647C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17990626 | ||||||
| chr8:17990632
|
T | C | 87 | a0001c0001t0004g0044a0002c0002t0004g0002a0002c0002t0004g0180others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.4531+653T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17990632 | ||||||
| chr8:17990759
|
T | C | 3 | a0002c0002t0004g0180a0002c0002t0004g0187a0002c0002t0004g0198 | 3 | HG01109.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4531+780T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17990759 | ||||||
| chr8:17990885
|
G | C | 40 | a0004c0004t0003g0113a0004c0004t0003g0114a0004c0004t0003g0115others(37): Show | 40 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.4532-657G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17990885 | ||||||
| chr8:17990929
|
T | A | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.4532-613T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17990929 | ||||||
| chr8:17990959
|
C | T | 1 | a0008c0010t0058g0211 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4532-583C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17990959 | ||||||
| chr8:17991015
|
G | A | 3 | a0002c0017t0003g0104a0002c0021t0020g0103a0014c0020t0020g0098 | 3 | HG02896.hp2 HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4532-527G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17991015 | ||||||
| chr8:17991044
|
G | A | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.4532-498G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17991044 | ||||||
| chr8:17991044
|
G | GT | 6 | a0003c0003t0009g0346a0003c0003t0009g0347a0003c0003t0043g0345others(3): Show | 6 | NA18939.hp2 NA18977.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.4532-497dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | INFO_REALIGN_3_PRIME | chr8 | 17991044 | |||||
| chr8:17991046
|
A | AT | 89 | a0001c0001t0002g0045a0001c0001t0002g0072a0002c0002t0053g0289others(86): Show | 89 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.4532-483dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | INFO_REALIGN_3_PRIME | chr8 | 17991046 | |||||
| chr8:17991046
|
A | ATT | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.4532-484_4532-483d others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | INFO_REALIGN_3_PRIME | chr8 | 17991046 | |||||
| chr8:17991046
|
A | T | 7 | a0003c0003t0009g0346a0003c0003t0009g0347a0003c0003t0009g0348others(4): Show | 7 | HG00597.hp1 NA18939.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.4532-496A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17991046 | ||||||
| chr8:17991046
|
AT | A | 41 | a0002c0007t0004g0200a0004c0004t0003g0113a0004c0004t0003g0114others(38): Show | 41 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.4532-483delT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | INFO_REALIGN_3_PRIME | chr8 | 17991046 | |||||
| chr8:17991099
|
T | C | 1 | a0003c0003t0036g0262 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4532-443T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17991099 | ||||||
| chr8:17991263
|
T | A | 1 | a0015c0022t0004g0295 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.4532-279T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17991263 | ||||||
| chr8:17991337
|
T | C | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.4532-205T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17991337 | ||||||
| chr8:17991421
|
G | C | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.4532-121G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17991421 | ||||||
| chr8:17991424
|
C | A | 1 | a0002c0017t0031g0321 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4532-118C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17991424 | ||||||
| chr8:17991515
|
C | T | 1 | a0007c0011t0001g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4532-27C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 27/38 | chr8 | 17991515 | ||||||
| chr8:17991718
|
C | T | 1 | a0003c0003t0002g0243 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.4690+18C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17991718 | ||||||
| chr8:17991772
|
G | C | 1 | a0017c0027t0001g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4690+72G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17991772 | ||||||
| chr8:17991850
|
C | G | 1 | a0002c0002t0047g0206 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4690+150C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17991850 | ||||||
| chr8:17991898
|
T | G | 2 | a0013c0023t0001g0153a0013c0023t0001g0154 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4690+198T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17991898 | ||||||
| chr8:17991935
|
T | C | 1 | a0002c0002t0004g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4690+235T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17991935 | ||||||
| chr8:17991953
|
G | A | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.4690+253G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17991953 | ||||||
| chr8:17992053
|
G | A | 3 | a0002c0017t0003g0104a0002c0021t0020g0103a0014c0020t0020g0098 | 3 | HG02896.hp2 HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4690+353G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17992053 | ||||||
| chr8:17992078
|
A | G | 1 | a0004c0004t0003g0144 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.4690+378A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17992078 | ||||||
| chr8:17992144
|
A | G | 1 | a0005c0005t0041g0161 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4690+444A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17992144 | ||||||
| chr8:17992207
|
A | T | 3 | a0007c0011t0003g0151a0007c0011t0003g0152a0007c0011t0003g0172 | 3 | HG01884.hp2 HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.4690+507A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17992207 | ||||||
| chr8:17992228
|
A | G | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.4690+528A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17992228 | ||||||
| chr8:17992258
|
C | T | 1 | a0002c0002t0012g0310 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.4690+558C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17992258 | ||||||
| chr8:17992275
|
G | C | 1 | a0024c0033t0003g0350 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4690+575G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17992275 | ||||||
| chr8:17992410
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.4690+710A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17992410 | ||||||
| chr8:17992420
|
G | T | 2 | a0004c0016t0008g0134a0004c0016t0008g0138 | 2 | HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4690+720G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17992420 | ||||||
| chr8:17992433
|
C | T | 1 | a0003c0003t0002g0239 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.4690+733C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17992433 | ||||||
| chr8:17992610
|
C | CT | 90 | a0001c0001t0004g0044a0002c0002t0004g0002a0002c0002t0004g0180others(87): Show | 90 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.4691-853dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | INFO_REALIGN_3_PRIME | chr8 | 17992610 | |||||
| chr8:17992610
|
CT | C | 7 | a0001c0001t0001g0042a0002c0021t0027g0102a0005c0005t0014g0160others(4): Show | 7 | HG01891.hp1 HG01891.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.4691-853delT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | INFO_REALIGN_3_PRIME | chr8 | 17992610 | |||||
| chr8:17992630
|
T | A | 3 | a0002c0017t0003g0104a0002c0021t0020g0103a0014c0020t0020g0098 | 3 | HG02896.hp2 HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4691-853T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17992630 | ||||||
| chr8:17992639
|
C | T | 1 | a0006c0008t0007g0261 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.4691-844C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17992639 | ||||||
| chr8:17992718
|
G | C | 110 | a0001c0001t0002g0045a0001c0001t0002g0072a0002c0002t0053g0289others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.4691-765G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17992718 | ||||||
| chr8:17992756
|
G | A | 153 | a0001c0001t0004g0044a0001c0001t0017g0105a0001c0001t0017g0108others(150): Show | 153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.4691-727G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17992756 | ||||||
| chr8:17992878
|
A | G | 116 | a0001c0001t0002g0045a0001c0001t0002g0072a0002c0002t0053g0289others(113): Show | 116 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.4691-605A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17992878 | ||||||
| chr8:17992924
|
A | C | 1 | a0002c0002t0012g0286 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4691-559A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17992924 | ||||||
| chr8:17992935
|
G | GT | 110 | a0001c0001t0001g0023a0001c0001t0001g0038a0001c0001t0001g0090others(107): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.4691-530dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | INFO_REALIGN_3_PRIME | chr8 | 17992935 | |||||
| chr8:17992979
|
A | T | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.4691-504A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17992979 | ||||||
| chr8:17993008
|
G | A | 88 | a0001c0001t0002g0045a0001c0001t0002g0072a0002c0002t0053g0289others(85): Show | 88 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.4691-475G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17993008 | ||||||
| chr8:17993075
|
G | A | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.4691-408G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17993075 | ||||||
| chr8:17993170
|
G | A | 1 | a0002c0019t0004g0213 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4691-313G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17993170 | ||||||
| chr8:17993215
|
G | T | 1 | a0002c0002t0012g0319 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.4691-268G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17993215 | ||||||
| chr8:17993248
|
T | A | 1 | a0007c0011t0003g0152 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4691-235T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17993248 | ||||||
| chr8:17993257
|
C | G | 255 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.4691-226C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17993257 | ||||||
| chr8:17993274
|
A | T | 7 | a0003c0006t0002g0177a0003c0006t0002g0225a0003c0006t0002g0228others(4): Show | 7 | HG01928.hp2 HG01981.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.4691-209A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17993274 | ||||||
| chr8:17993316
|
T | G | 88 | a0001c0001t0002g0045a0001c0001t0002g0072a0002c0002t0053g0289others(85): Show | 88 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.4691-167T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17993316 | ||||||
| chr8:17993340
|
G | A | 1 | a0020c0045t0003g0127 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.4691-143G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17993340 | ||||||
| chr8:17993425
|
C | T | 15 | a0003c0003t0002g0003a0003c0003t0007g0257a0003c0003t0007g0258others(12): Show | 15 | HG00609.hp1 HG01099.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.4691-58C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 28/38 | chr8 | 17993425 | ||||||
| chr8:17993634
|
T | A | 1 | a0003c0003t0002g0242 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.4827+15T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17993634 | ||||||
| chr8:17993739
|
C | A | 151 | a0001c0001t0004g0044a0001c0001t0017g0105a0001c0001t0017g0108others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.4827+120C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17993739 | ||||||
| chr8:17993767
|
C | T | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.4827+148C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17993767 | ||||||
| chr8:17993803
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4827+184A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17993803 | ||||||
| chr8:17993926
|
G | A | 48 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(45): Show | 48 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.4827+307G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17993926 | ||||||
| chr8:17994052
|
A | C | 11 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(8): Show | 11 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.4827+433A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17994052 | ||||||
| chr8:17994069
|
A | T | 1 | a0002c0007t0001g0253 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.4827+450A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17994069 | ||||||
| chr8:17994124
|
G | C | 1 | a0002c0002t0005g0315 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4827+505G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17994124 | ||||||
| chr8:17994132
|
T | A | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4827+513T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17994132 | ||||||
| chr8:17994173
|
C | T | 1 | a0026c0032t0003g0118 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.4827+554C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17994173 | ||||||
| chr8:17994187
|
C | T | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.4827+568C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17994187 | ||||||
| chr8:17994193
|
A | G | 1 | a0001c0001t0010g0013 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4827+574A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17994193 | ||||||
| chr8:17994220
|
G | C | 1 | a0001c0001t0001g0058 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.4827+601G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17994220 | ||||||
| chr8:17994261
|
A | C | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.4827+642A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17994261 | ||||||
| chr8:17994274
|
A | G | 2 | a0004c0004t0003g0357a0004c0004t0049g0356 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.4827+655A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17994274 | ||||||
| chr8:17994307
|
A | C | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.4827+688A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17994307 | ||||||
| chr8:17994308
|
C | T | 1 | a0002c0002t0004g0199 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4827+689C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17994308 | ||||||
| chr8:17994363
|
C | G | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.4827+744C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17994363 | ||||||
| chr8:17994420
|
T | C | 1 | a0003c0003t0002g0256 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.4827+801T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17994420 | ||||||
| chr8:17994527
|
T | G | 88 | a0001c0001t0004g0044a0002c0002t0004g0002a0002c0002t0004g0180others(85): Show | 88 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.4827+908T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17994527 | ||||||
| chr8:17994639
|
T | G | 2 | a0003c0003t0026g0271a0003c0003t0046g0259 | 2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.4827+1020T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17994639 | ||||||
| chr8:17994640
|
A | C | 1 | a0001c0001t0040g0076 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.4827+1021A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17994640 | ||||||
| chr8:17994693
|
C | T | 21 | a0002c0021t0027g0102a0005c0005t0008g0168a0005c0005t0008g0169others(18): Show | 21 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.4827+1074C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17994693 | ||||||
| chr8:17994714
|
CTTTGGGA others(1028): Show |
C | 8 | a0005c0005t0008g0168a0005c0005t0008g0169a0005c0005t0008g0174others(5): Show | 8 | HG02258.hp1 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.4827+1098_4827+213 others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 17994714 | |||||
| chr8:17994822
|
G | C | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.4827+1203G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17994822 | ||||||
| chr8:17994877
|
A | G | 1 | a0003c0003t0011g0329 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4827+1258A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17994877 | ||||||
| chr8:17994909
|
CT | C | 3 | a0002c0017t0003g0104a0002c0021t0020g0103a0014c0020t0020g0098 | 3 | HG02896.hp2 HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4827+1293delT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 17994909 | |||||
| chr8:17994918
|
T | A | 1 | a0001c0001t0001g0016 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4827+1299T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17994918 | ||||||
| chr8:17994940
|
G | A | 131 | a0001c0001t0001g0016a0001c0001t0002g0045a0001c0001t0002g0072others(128): Show | 131 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.4827+1321G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17994940 | ||||||
| chr8:17994971
|
T | C | 1 | a0002c0002t0004g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4827+1352T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17994971 | ||||||
| chr8:17995003
|
T | C | 1 | a0002c0002t0005g0290 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.4827+1384T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17995003 | ||||||
| chr8:17995031
|
T | C | 10 | a0001c0001t0001g0012a0001c0001t0010g0010a0001c0001t0010g0011others(7): Show | 10 | HG00280.hp1 HG00642.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.4827+1412T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17995031 | ||||||
| chr8:17995033
|
T | C | 10 | a0001c0001t0001g0012a0001c0001t0010g0010a0001c0001t0010g0011others(7): Show | 10 | HG00280.hp1 HG00642.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.4827+1414T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17995033 | ||||||
| chr8:17995258
|
C | A | 3 | a0002c0002t0004g0180a0002c0002t0004g0187a0002c0002t0004g0198 | 3 | HG01109.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4827+1639C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17995258 | ||||||
| chr8:17995371
|
C | G | 3 | a0003c0003t0002g0256a0003c0003t0011g0255a0003c0003t0064g0254 | 3 | NA18972.hp2 NA18978.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.4827+1752C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17995371 | ||||||
| chr8:17995378
|
A | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.4827+1759A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17995378 | ||||||
| chr8:17995381
|
G | C | 3 | a0002c0002t0004g0180a0002c0002t0004g0187a0002c0002t0004g0198 | 3 | HG01109.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4827+1762G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17995381 | ||||||
| chr8:17995408
|
G | A | 1 | a0002c0017t0032g0322 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4827+1789G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17995408 | ||||||
| chr8:17995411
|
C | G | 1 | a0005c0005t0041g0161 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4827+1792C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17995411 | ||||||
| chr8:17995527
|
C | G | 1 | a0002c0002t0005g0281 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4827+1908C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17995527 | ||||||
| chr8:17995561
|
G | A | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.4827+1942G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17995561 | ||||||
| chr8:17995577
|
T | C | 49 | a0002c0007t0001g0033a0004c0004t0003g0113a0004c0004t0003g0114others(46): Show | 49 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.4827+1958T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17995577 | ||||||
| chr8:17995612
|
G | A | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.4827+1993G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17995612 | ||||||
| chr8:17995681
|
T | C | 1 | a0002c0002t0028g0323 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4827+2062T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17995681 | ||||||
| chr8:17995682
|
T | G | 1 | a0001c0001t0001g0146 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4827+2063T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17995682 | ||||||
| chr8:17995708
|
C | G | 4 | a0004c0004t0003g0116a0004c0004t0003g0124a0004c0004t0003g0125others(1): Show | 4 | NA18945.hp1 NA18972.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.4827+2089C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17995708 | ||||||
| chr8:17995745
|
G | C | 85 | a0001c0001t0004g0044a0002c0002t0004g0002a0002c0002t0004g0180others(82): Show | 85 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.4827+2126G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17995745 | ||||||
| chr8:17995751
|
T | C | 1 | a0003c0003t0007g0274 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.4827+2132T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17995751 | ||||||
| chr8:17995753
|
T | C | 1 | a0001c0001t0010g0015 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4827+2134T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17995753 | ||||||
| chr8:17995773
|
T | C | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.4827+2154T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17995773 | ||||||
| chr8:17995907
|
G | T | 2 | a0004c0016t0008g0134a0004c0016t0008g0138 | 2 | HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4827+2288G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17995907 | ||||||
| chr8:17995937
|
T | C | 2 | a0003c0003t0002g0003a0003c0003t0011g0003 | 2 | HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.4827+2318T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17995937 | ||||||
| chr8:17996022
|
C | G | 1 | a0004c0004t0050g0130 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4827+2403C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17996022 | ||||||
| chr8:17996050
|
A | G | 1 | a0024c0033t0003g0350 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4827+2431A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17996050 | ||||||
| chr8:17996051
|
G | GCTAGGAC others(4): Show |
1 | a0008c0010t0004g0209 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.4827+2433_4827+244 others(15): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 17996051 | |||||
| chr8:17996098
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4827+2479T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17996098 | ||||||
| chr8:17996136
|
G | C | 1 | a0001c0001t0001g0064 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.4827+2517G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17996136 | ||||||
| chr8:17996290
|
G | A | 20 | a0002c0021t0027g0102a0005c0005t0008g0168a0005c0005t0008g0169others(17): Show | 20 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.4827+2671G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17996290 | ||||||
| chr8:17996396
|
C | T | 1 | a0001c0001t0006g0049 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.4827+2777C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17996396 | ||||||
| chr8:17996416
|
G | A | 1 | a0003c0003t0065g0238 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.4827+2797G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17996416 | ||||||
| chr8:17996483
|
T | G | 1 | a0002c0009t0051g0364 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4827+2864T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17996483 | ||||||
| chr8:17996574
|
A | C | 1 | a0003c0003t0002g0240 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.4827+2955A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17996574 | ||||||
| chr8:17996646
|
T | C | 215 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.4827+3027T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17996646 | ||||||
| chr8:17996650
|
GTT | G | 40 | a0004c0004t0003g0113a0004c0004t0003g0114a0004c0004t0003g0115others(37): Show | 40 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.4827+3036_4827+303 others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 17996650 | |||||
| chr8:17996669
|
T | C | 1 | a0001c0001t0002g0072 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.4827+3050T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17996669 | ||||||
| chr8:17996837
|
TTTG | T | 6 | a0003c0003t0002g0221a0003c0003t0002g0233a0003c0003t0002g0240others(3): Show | 6 | NA18960.hp2 NA18975.hp1 NA18987.hp1 others(3): Show |
intron_variant | MODIFIER | c.4827+3224_4827+322 others(7): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 17996837 | |||||
| chr8:17996866
|
C | G | 1 | a0005c0005t0041g0161 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4827+3247C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17996866 | ||||||
| chr8:17996880
|
G | C | 30 | a0002c0002t0004g0287a0002c0002t0004g0311a0002c0002t0004g0320others(27): Show | 30 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.4827+3261G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17996880 | ||||||
| chr8:17996957
|
G | T | 4 | a0005c0005t0008g0332a0005c0005t0008g0333a0005c0005t0008g0334others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.4827+3338G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17996957 | ||||||
| chr8:17997052
|
A | G | 1 | a0005c0005t0014g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4827+3433A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17997052 | ||||||
| chr8:17997207
|
C | G | 1 | a0005c0005t0041g0161 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4827+3588C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17997207 | ||||||
| chr8:17997270
|
C | A | 96 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0017g0105others(93): Show | 96 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.4827+3651C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17997270 | ||||||
| chr8:17997270
|
C | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.4827+3651C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17997270 | ||||||
| chr8:17997411
|
G | A | 1 | a0003c0006t0013g0247 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4827+3792G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17997411 | ||||||
| chr8:17997440
|
C | T | 1 | a0002c0002t0004g0181 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.4827+3821C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17997440 | ||||||
| chr8:17997470
|
A | G | 1 | a0002c0002t0004g0199 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4827+3851A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17997470 | ||||||
| chr8:17997474
|
C | G | 6 | a0005c0005t0014g0163a0005c0005t0015g0162a0005c0005t0015g0164others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.4827+3855C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17997474 | ||||||
| chr8:17997601
|
A | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.4827+3982A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17997601 | ||||||
| chr8:17997648
|
G | T | 1 | a0003c0003t0064g0254 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.4827+4029G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17997648 | ||||||
| chr8:17997652
|
C | T | 1 | a0001c0001t0001g0055 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4827+4033C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17997652 | ||||||
| chr8:17997653
|
G | T | 1 | a0003c0003t0064g0254 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.4827+4034G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17997653 | ||||||
| chr8:17997724
|
A | G | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4827+4105A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17997724 | ||||||
| chr8:17997796
|
C | T | 1 | a0003c0044t0007g0234 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.4827+4177C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17997796 | ||||||
| chr8:17997808
|
T | G | 4 | a0005c0005t0008g0168a0005c0005t0008g0169a0005c0005t0008g0174others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.4827+4189T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17997808 | ||||||
| chr8:17997823
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.4827+4204G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17997823 | ||||||
| chr8:17997853
|
C | T | 3 | a0002c0002t0004g0181a0002c0002t0004g0192a0002c0002t0004g0196 | 3 | HG00544.hp1 HG02523.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.4827+4234C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17997853 | ||||||
| chr8:17997885
|
A | C | 3 | a0002c0002t0004g0180a0002c0002t0004g0187a0002c0002t0004g0198 | 3 | HG01109.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4827+4266A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17997885 | ||||||
| chr8:17997897
|
A | G | 6 | a0002c0002t0004g0328a0002c0002t0005g0326a0002c0002t0005g0327others(3): Show | 6 | HG02965.hp1 HG03041.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.4827+4278A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17997897 | ||||||
| chr8:17997920
|
C | T | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.4827+4301C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17997920 | ||||||
| chr8:17997972
|
G | A | 3 | a0002c0002t0004g0180a0002c0002t0004g0187a0002c0002t0004g0198 | 3 | HG01109.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4827+4353G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17997972 | ||||||
| chr8:17998035
|
G | GA | 12 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0057others(9): Show | 12 | HG01978.hp2 HG02027.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.4827+4433dupA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 17998035 | |||||
| chr8:17998035
|
GA | G | 13 | a0001c0001t0001g0021a0001c0001t0001g0066a0002c0002t0004g0194others(10): Show | 13 | HG01168.hp2 HG02109.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.4827+4433delA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 17998035 | |||||
| chr8:17998413
|
T | C | 3 | a0007c0011t0003g0151a0007c0011t0003g0152a0007c0011t0003g0172 | 3 | HG01884.hp2 HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.4827+4794T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17998413 | ||||||
| chr8:17998474
|
T | C | 222 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.4827+4855T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17998474 | ||||||
| chr8:17998488
|
C | G | 1 | a0005c0005t0015g0166 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4827+4869C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17998488 | ||||||
| chr8:17998505
|
T | C | 222 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.4827+4886T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17998505 | ||||||
| chr8:17998523
|
C | T | 1 | a0002c0007t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4827+4904C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17998523 | ||||||
| chr8:17998720
|
A | G | 11 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(8): Show | 11 | HG01099.hp1 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.4827+5101A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17998720 | ||||||
| chr8:17998736
|
G | A | 28 | a0002c0021t0027g0102a0005c0005t0008g0168a0005c0005t0008g0169others(25): Show | 28 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.4827+5117G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17998736 | ||||||
| chr8:17998834
|
A | G | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.4827+5215A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17998834 | ||||||
| chr8:17998915
|
A | G | 1 | a0001c0001t0039g0009 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4827+5296A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17998915 | ||||||
| chr8:17998992
|
T | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.4827+5373T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17998992 | ||||||
| chr8:17999068
|
G | A | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.4827+5449G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17999068 | ||||||
| chr8:17999156
|
C | G | 3 | a0007c0011t0003g0151a0007c0011t0003g0152a0007c0011t0003g0172 | 3 | HG01884.hp2 HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.4827+5537C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17999156 | ||||||
| chr8:17999438
|
T | C | 7 | a0007c0011t0001g0149a0007c0011t0001g0150a0007c0011t0003g0151others(4): Show | 7 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.4827+5819T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17999438 | ||||||
| chr8:17999502
|
C | A | 2 | a0013c0023t0001g0153a0013c0023t0001g0154 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4827+5883C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17999502 | ||||||
| chr8:17999519
|
T | C | 95 | a0001c0001t0004g0044a0002c0002t0004g0002a0002c0002t0004g0180others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.4827+5900T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17999519 | ||||||
| chr8:17999530
|
C | G | 1 | a0004c0004t0050g0130 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4827+5911C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17999530 | ||||||
| chr8:17999563
|
G | GCT | 3 | a0002c0017t0003g0104a0002c0021t0020g0103a0014c0020t0020g0098 | 3 | HG02896.hp2 HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4827+5948_4827+594 others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 17999563 | |||||
| chr8:17999578
|
A | G | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.4827+5959A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17999578 | ||||||
| chr8:17999627
|
G | A | 1 | a0002c0002t0004g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4827+6008G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17999627 | ||||||
| chr8:17999740
|
A | T | 41 | a0002c0007t0001g0033a0004c0004t0003g0113a0004c0004t0003g0114others(38): Show | 41 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.4827+6121A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17999740 | ||||||
| chr8:17999839
|
T | C | 90 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0038g0073others(87): Show | 90 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.4827+6220T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17999839 | ||||||
| chr8:17999907
|
G | C | 87 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0038g0073others(84): Show | 87 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.4827+6288G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17999907 | ||||||
| chr8:17999936
|
T | C | 104 | a0001c0001t0004g0044a0002c0002t0004g0002a0002c0002t0004g0180others(101): Show | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.4827+6317T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 17999936 | ||||||
| chr8:18000103
|
T | C | 1 | a0001c0001t0001g0042 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.4828-6160T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18000103 | ||||||
| chr8:18000159
|
G | T | 1 | a0010c0014t0023g0354 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4828-6104G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18000159 | ||||||
| chr8:18000201
|
C | T | 1 | a0001c0001t0001g0031 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.4828-6062C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18000201 | ||||||
| chr8:18000289
|
A | G | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0147 | 3 | HG02602.hp1 HG03491.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.4828-5974A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18000289 | ||||||
| chr8:18000311
|
G | C | 1 | a0005c0005t0014g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4828-5952G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18000311 | ||||||
| chr8:18000344
|
A | G | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.4828-5919A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18000344 | ||||||
| chr8:18000371
|
A | C | 104 | a0001c0001t0004g0044a0002c0002t0004g0002a0002c0002t0004g0180others(101): Show | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.4828-5892A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18000371 | ||||||
| chr8:18000428
|
T | C | 231 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(228): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.4828-5835T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18000428 | ||||||
| chr8:18000429
|
C | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.4828-5834C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18000429 | ||||||
| chr8:18000488
|
T | A | 1 | a0001c0001t0001g0042 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.4828-5775T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18000488 | ||||||
| chr8:18000614
|
G | GT | 86 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0038g0073others(83): Show | 86 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.4828-5641dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 18000614 | |||||
| chr8:18000632
|
G | T | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4828-5631G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18000632 | ||||||
| chr8:18000659
|
T | C | 1 | a0005c0005t0044g0335 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4828-5604T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18000659 | ||||||
| chr8:18000685
|
G | T | 20 | a0002c0021t0027g0102a0005c0005t0008g0168a0005c0005t0008g0169others(17): Show | 20 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.4828-5578G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18000685 | ||||||
| chr8:18000690
|
C | T | 1 | a0002c0009t0016g0362 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4828-5573C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18000690 | ||||||
| chr8:18000788
|
G | C | 87 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0038g0073others(84): Show | 87 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.4828-5475G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18000788 | ||||||
| chr8:18000823
|
A | G | 1 | a0004c0004t0049g0356 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4828-5440A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18000823 | ||||||
| chr8:18000928
|
T | G | 90 | a0001c0001t0004g0044a0002c0002t0004g0002a0002c0002t0004g0180others(87): Show | 90 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.4828-5335T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18000928 | ||||||
| chr8:18001020
|
G | C | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4828-5243G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18001020 | ||||||
| chr8:18001057
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4828-5206G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18001057 | ||||||
| chr8:18001214
|
A | C | 1 | a0004c0004t0003g0353 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4828-5049A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18001214 | ||||||
| chr8:18001225
|
C | G | 1 | a0005c0005t0041g0161 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4828-5038C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18001225 | ||||||
| chr8:18001278
|
T | G | 9 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(6): Show | 9 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.4828-4985T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18001278 | ||||||
| chr8:18001356
|
G | C | 1 | a0002c0002t0028g0323 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4828-4907G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18001356 | ||||||
| chr8:18001368
|
T | C | 3 | a0002c0017t0003g0104a0002c0021t0020g0103a0014c0020t0020g0098 | 3 | HG02896.hp2 HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4828-4895T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18001368 | ||||||
| chr8:18001484
|
C | G | 1 | a0002c0002t0005g0326 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4828-4779C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18001484 | ||||||
| chr8:18001505
|
A | G | 1 | a0002c0017t0032g0322 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4828-4758A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18001505 | ||||||
| chr8:18001646
|
A | G | 1 | a0003c0006t0013g0247 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4828-4617A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18001646 | ||||||
| chr8:18001669
|
A | G | 1 | a0004c0004t0003g0141 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.4828-4594A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18001669 | ||||||
| chr8:18001922
|
G | A | 2 | a0002c0017t0031g0321a0002c0017t0032g0322 | 2 | HG01099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.4828-4341G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18001922 | ||||||
| chr8:18001988
|
AACCTTTC others(918): Show |
A | 48 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(45): Show | 48 | HG01099.hp1 HG01891.hp1 HG01891.hp2 others(45): Show |
intron_variant | MODIFIER | c.4828-4267_4828-334 others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 18001988 | |||||
| chr8:18001995
|
C | CT | 17 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0035others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.4828-4228dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 18001995 | |||||
| chr8:18001995
|
C | CTT | 7 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0027others(4): Show | 7 | HG00738.hp2 HG02486.hp1 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.4828-4229_4828-422 others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 18001995 | |||||
| chr8:18001995
|
CTTTTTTT others(3): Show |
C | 5 | a0001c0001t0001g0059a0001c0001t0001g0067a0001c0001t0001g0092others(2): Show | 5 | HG00741.hp1 HG01106.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.4828-4237_4828-422 others(14): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 18001995 | |||||
| chr8:18001995
|
CTTTTTTT others(4): Show |
C | 25 | a0001c0001t0001g0077a0002c0002t0004g0287a0002c0002t0005g0281others(22): Show | 25 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.4828-4238_4828-422 others(15): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 18001995 | |||||
| chr8:18001995
|
CTTTTTTT others(5): Show |
C | 103 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0071others(100): Show | 103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.4828-4239_4828-422 others(16): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 18001995 | |||||
| chr8:18001995
|
CTTTTTTT others(6): Show |
C | 38 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0028others(35): Show | 39 | HG00423.hp1 HG00558.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.4828-4240_4828-422 others(17): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 18001995 | |||||
| chr8:18001995
|
CTTTTTTT others(7): Show |
C | 5 | a0001c0001t0001g0043a0002c0002t0004g0328a0002c0002t0005g0326others(2): Show | 5 | HG01515.hp2 HG03516.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.4828-4241_4828-422 others(18): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 18001995 | |||||
| chr8:18001995
|
CTTTTTTT others(8): Show |
C | 1 | a0002c0034t0057g0325 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4828-4242_4828-422 others(19): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 18001995 | |||||
| chr8:18001995
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0006g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.4828-4244_4828-422 others(21): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 18001995 | |||||
| chr8:18001995
|
CTTTTTTT others(11): Show |
C | 7 | a0007c0011t0001g0149a0007c0011t0001g0150a0007c0011t0003g0151others(4): Show | 7 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.4828-4245_4828-422 others(22): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 18001995 | |||||
| chr8:18001995
|
CTTTTTTT others(12): Show |
C | 9 | a0001c0001t0001g0058a0002c0002t0053g0289a0003c0003t0002g0156others(6): Show | 9 | HG00099.hp2 HG01070.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.4828-4246_4828-422 others(23): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 18001995 | |||||
| chr8:18001995
|
CTTTTTTT others(13): Show |
C | 24 | a0003c0003t0002g0003a0003c0003t0002g0264a0003c0003t0007g0219others(21): Show | 24 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.4828-4247_4828-422 others(24): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 18001995 | |||||
| chr8:18001995
|
CTTTTTTT others(14): Show |
C | 43 | a0001c0001t0002g0045a0001c0001t0002g0072a0003c0003t0002g0216others(40): Show | 43 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.4828-4248_4828-422 others(25): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 18001995 | |||||
| chr8:18001995
|
CTTTTTTT others(15): Show |
C | 2 | a0003c0003t0002g0243a0003c0003t0011g0178 | 2 | NA18960.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.4828-4249_4828-422 others(26): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 18001995 | |||||
| chr8:18002013
|
T | C | 1 | a0002c0002t0005g0316 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.4828-4250T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18002013 | ||||||
| chr8:18002025
|
TTTTTTTT others(46): Show |
T | 1 | a0001c0001t0001g0083 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4828-4229_4828-417 others(57): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 18002025 | |||||
| chr8:18002064
|
C | CT | 18 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0075others(15): Show | 18 | HG00621.hp1 HG01069.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.4828-4186dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 18002064 | |||||
| chr8:18002064
|
C | CTT | 66 | a0001c0001t0004g0044a0002c0002t0004g0002a0002c0002t0004g0180others(63): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.4828-4187_4828-418 others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 18002064 | |||||
| chr8:18002068
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4828-4195T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18002068 | ||||||
| chr8:18002069
|
T | C | 2 | a0013c0023t0001g0153a0013c0023t0001g0154 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4828-4194T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18002069 | ||||||
| chr8:18002071
|
T | C | 50 | a0002c0002t0028g0323a0003c0003t0007g0274a0004c0004t0003g0113others(47): Show | 50 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.4828-4192T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18002071 | ||||||
| chr8:18002075
|
TTTC | T | 72 | a0001c0001t0002g0045a0001c0001t0002g0072a0002c0002t0053g0289others(69): Show | 72 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.4828-4185_4828-418 others(7): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 18002075 | |||||
| chr8:18002077
|
TC | T | 58 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0006g0080others(55): Show | 58 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.4828-4185delC | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18002077 | ||||||
| chr8:18002078
|
C | T | 180 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(177): Show | 181 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.4828-4185C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18002078 | ||||||
| chr8:18002086
|
T | A | 1 | a0001c0047t0006g0069 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.4828-4177T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18002086 | ||||||
| chr8:18002102
|
A | T | 1 | a0004c0004t0003g0142 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4828-4161A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18002102 | ||||||
| chr8:18002245
|
C | T | 10 | a0003c0003t0002g0003a0003c0003t0007g0219a0003c0003t0007g0232others(7): Show | 10 | HG00558.hp2 HG01099.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.4828-4018C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18002245 | ||||||
| chr8:18002529
|
A | C | 1 | a0003c0003t0002g0221 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.4828-3734A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18002529 | ||||||
| chr8:18002596
|
G | A | 86 | a0001c0001t0004g0044a0002c0002t0004g0002a0002c0002t0004g0180others(83): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.4828-3667G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18002596 | ||||||
| chr8:18002678
|
G | T | 212 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.4828-3585G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18002678 | ||||||
| chr8:18002710
|
A | C | 2 | a0002c0002t0005g0299a0002c0002t0005g0313 | 2 | HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.4828-3553A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18002710 | ||||||
| chr8:18002718
|
G | A | 11 | a0002c0002t0004g0191a0002c0002t0047g0206a0002c0002t0048g0205others(8): Show | 11 | HG00140.hp1 HG00323.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.4828-3545G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18002718 | ||||||
| chr8:18002718
|
G | T | 1 | a0001c0001t0001g0096 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.4828-3545G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18002718 | ||||||
| chr8:18002739
|
G | A | 1 | a0004c0004t0003g0121 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.4828-3524G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18002739 | ||||||
| chr8:18002901
|
C | T | 2 | a0001c0001t0001g0023a0002c0002t0012g0310 | 2 | HG01257.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.4828-3362C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18002901 | ||||||
| chr8:18002968
|
T | C | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4828-3295T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18002968 | ||||||
| chr8:18002978
|
G | C | 2 | a0010c0014t0022g0330a0010c0014t0022g0331 | 2 | HG02698.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.4828-3285G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18002978 | ||||||
| chr8:18003030
|
C | T | 48 | a0002c0002t0028g0323a0004c0004t0003g0113a0004c0004t0003g0114others(45): Show | 48 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.4828-3233C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18003030 | ||||||
| chr8:18003060
|
C | T | 1 | a0003c0003t0007g0258 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.4828-3203C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18003060 | ||||||
| chr8:18003255
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4828-3008A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18003255 | ||||||
| chr8:18003302
|
A | G | 2 | a0002c0021t0020g0103a0014c0020t0020g0098 | 2 | HG02896.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.4828-2961A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18003302 | ||||||
| chr8:18003354
|
T | C | 130 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0017g0105others(127): Show | 130 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.4828-2909T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18003354 | ||||||
| chr8:18003457
|
T | G | 90 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0038g0073others(87): Show | 90 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.4828-2806T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18003457 | ||||||
| chr8:18003472
|
G | T | 4 | a0004c0004t0003g0116a0004c0004t0003g0124a0004c0004t0003g0125others(1): Show | 4 | NA18945.hp1 NA18972.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.4828-2791G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18003472 | ||||||
| chr8:18003473
|
T | C | 4 | a0004c0004t0003g0116a0004c0004t0003g0124a0004c0004t0003g0125others(1): Show | 4 | NA18945.hp1 NA18972.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.4828-2790T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18003473 | ||||||
| chr8:18003766
|
T | C | 1 | a0002c0019t0004g0213 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4828-2497T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18003766 | ||||||
| chr8:18003797
|
T | C | 1 | a0003c0006t0013g0247 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4828-2466T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18003797 | ||||||
| chr8:18003875
|
A | C | 1 | a0002c0017t0032g0322 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4828-2388A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18003875 | ||||||
| chr8:18003888
|
A | C | 1 | a0017c0027t0001g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4828-2375A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18003888 | ||||||
| chr8:18003950
|
A | G | 11 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(8): Show | 11 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.4828-2313A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18003950 | ||||||
| chr8:18004049
|
T | TA | 28 | a0002c0017t0031g0321a0002c0017t0032g0322a0002c0021t0027g0102others(25): Show | 28 | HG01099.hp1 HG01891.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.4828-2205dupA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 18004049 | |||||
| chr8:18004126
|
T | G | 1 | a0003c0003t0007g0219 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.4828-2137T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18004126 | ||||||
| chr8:18004243
|
T | C | 1 | a0023c0042t0016g0361 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4828-2020T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18004243 | ||||||
| chr8:18004261
|
T | C | 3 | a0002c0002t0004g0180a0002c0002t0004g0187a0002c0002t0004g0198 | 3 | HG01109.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4828-2002T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18004261 | ||||||
| chr8:18004286
|
T | C | 2 | a0003c0003t0009g0226a0003c0012t0009g0340 | 2 | NA18965.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.4828-1977T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18004286 | ||||||
| chr8:18004493
|
T | A | 8 | a0005c0005t0008g0168a0005c0005t0008g0169a0005c0005t0008g0174others(5): Show | 8 | HG02258.hp1 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.4828-1770T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18004493 | ||||||
| chr8:18004521
|
AAAT | A | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.4828-1736_4828-173 others(7): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 18004521 | |||||
| chr8:18004531
|
T | A | 2 | a0002c0017t0031g0321a0002c0017t0032g0322 | 2 | HG01099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.4828-1732T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18004531 | ||||||
| chr8:18004589
|
G | C | 1 | a0002c0007t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4828-1674G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18004589 | ||||||
| chr8:18004627
|
C | T | 3 | a0006c0008t0007g0263a0006c0008t0033g0277a0006c0008t0034g0282 | 3 | HG00609.hp1 HG02523.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.4828-1636C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18004627 | ||||||
| chr8:18004647
|
T | C | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4828-1616T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18004647 | ||||||
| chr8:18004944
|
A | G | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.4828-1319A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18004944 | ||||||
| chr8:18004971
|
T | G | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 6 | NA18944.hp2 NA18948.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.4828-1292T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18004971 | ||||||
| chr8:18005019
|
T | G | 1 | a0032c0030t0005g0186 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.4828-1244T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18005019 | ||||||
| chr8:18005048
|
C | G | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4828-1215C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18005048 | ||||||
| chr8:18005122
|
G | T | 1 | a0004c0004t0003g0133 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4828-1141G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18005122 | ||||||
| chr8:18005192
|
T | C | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4828-1071T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18005192 | ||||||
| chr8:18005357
|
G | GT | 117 | a0001c0001t0001g0027a0001c0001t0004g0044a0002c0002t0004g0002others(114): Show | 117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.4828-891dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr8 | 18005357 | |||||
| chr8:18005360
|
T | G | 21 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(18): Show | 21 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.4828-903T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18005360 | ||||||
| chr8:18005516
|
A | G | 1 | a0014c0020t0020g0098 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4828-747A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18005516 | ||||||
| chr8:18005581
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4828-682C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18005581 | ||||||
| chr8:18005833
|
A | G | 5 | a0004c0004t0003g0336a0004c0004t0003g0351a0004c0004t0003g0352others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.4828-430A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18005833 | ||||||
| chr8:18005945
|
A | C | 1 | a0001c0001t0035g0111 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4828-318A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18005945 | ||||||
| chr8:18005951
|
A | C | 1 | a0002c0002t0005g0327 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4828-312A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18005951 | ||||||
| chr8:18006025
|
G | C | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4828-238G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18006025 | ||||||
| chr8:18006180
|
T | G | 2 | a0002c0017t0031g0321a0002c0017t0032g0322 | 2 | HG01099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.4828-83T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 29/38 | chr8 | 18006180 | ||||||
| chr8:18006443
|
A | G | 1 | a0002c0021t0027g0102 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4962+46A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18006443 | ||||||
| chr8:18006511
|
A | G | 1 | a0032c0030t0005g0186 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.4962+114A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18006511 | ||||||
| chr8:18006686
|
G | A | 1 | a0027c0031t0056g0139 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4962+289G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18006686 | ||||||
| chr8:18006751
|
G | A | 1 | a0002c0007t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4962+354G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18006751 | ||||||
| chr8:18006763
|
A | G | 2 | a0003c0003t0007g0257a0003c0003t0007g0269 | 2 | HG02132.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.4962+366A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18006763 | ||||||
| chr8:18007043
|
A | C | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4962+646A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18007043 | ||||||
| chr8:18007113
|
T | C | 1 | a0002c0002t0005g0281 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4962+716T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18007113 | ||||||
| chr8:18007323
|
A | G | 67 | a0002c0007t0001g0033a0002c0017t0003g0104a0002c0017t0031g0321others(64): Show | 67 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.4962+926A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18007323 | ||||||
| chr8:18007377
|
G | T | 7 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(4): Show | 7 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.4962+980G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18007377 | ||||||
| chr8:18007392
|
A | G | 7 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(4): Show | 7 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.4962+995A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18007392 | ||||||
| chr8:18007476
|
G | A | 240 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0017g0105others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.4962+1079G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18007476 | ||||||
| chr8:18007544
|
A | G | 7 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(4): Show | 7 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.4962+1147A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18007544 | ||||||
| chr8:18007558
|
C | G | 6 | a0005c0005t0014g0163a0005c0005t0015g0162a0005c0005t0015g0164others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.4962+1161C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18007558 | ||||||
| chr8:18007575
|
A | T | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4962+1178A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18007575 | ||||||
| chr8:18007631
|
C | G | 7 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(4): Show | 7 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.4962+1234C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18007631 | ||||||
| chr8:18007739
|
T | G | 7 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(4): Show | 7 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.4962+1342T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18007739 | ||||||
| chr8:18007805
|
G | A | 1 | a0002c0002t0004g0320 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.4962+1408G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18007805 | ||||||
| chr8:18007814
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.4962+1417A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18007814 | ||||||
| chr8:18007834
|
A | T | 7 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(4): Show | 7 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.4962+1437A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18007834 | ||||||
| chr8:18007885
|
T | G | 1 | a0001c0001t0001g0058 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.4962+1488T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18007885 | ||||||
| chr8:18008091
|
A | G | 7 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(4): Show | 7 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.4963-1456A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18008091 | ||||||
| chr8:18008147
|
G | A | 2 | a0002c0002t0005g0296a0002c0002t0005g0297 | 2 | HG01243.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.4963-1400G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18008147 | ||||||
| chr8:18008187
|
C | T | 240 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0017g0105others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.4963-1360C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18008187 | ||||||
| chr8:18008188
|
G | A | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.4963-1359G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18008188 | ||||||
| chr8:18008197
|
T | A | 1 | a0003c0003t0007g0257 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.4963-1350T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18008197 | ||||||
| chr8:18008367
|
T | C | 1 | a0002c0017t0032g0322 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4963-1180T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18008367 | ||||||
| chr8:18008401
|
C | G | 1 | a0001c0001t0001g0059 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4963-1146C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18008401 | ||||||
| chr8:18008469
|
A | G | 1 | a0014c0020t0020g0098 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4963-1078A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18008469 | ||||||
| chr8:18008510
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4963-1037A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18008510 | ||||||
| chr8:18008617
|
G | T | 1 | a0002c0002t0004g0199 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4963-930G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18008617 | ||||||
| chr8:18008871
|
A | G | 365 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(362): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.4963-676A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18008871 | ||||||
| chr8:18008884
|
C | T | 7 | a0003c0003t0009g0346a0003c0003t0009g0347a0003c0003t0009g0348others(4): Show | 7 | HG00597.hp1 NA18939.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.4963-663C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18008884 | ||||||
| chr8:18009020
|
A | T | 1 | a0006c0008t0068g0273 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.4963-527A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18009020 | ||||||
| chr8:18009024
|
T | C | 89 | a0001c0001t0004g0044a0001c0024t0017g0107a0002c0002t0004g0002others(86): Show | 89 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.4963-523T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18009024 | ||||||
| chr8:18009043
|
AGGAAGCT others(90): Show |
A | 1 | a0002c0017t0032g0322 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4963-491_4963-395d others(99): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr8 | 18009043 | |||||
| chr8:18009140
|
T | A | 265 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.4963-407T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18009140 | ||||||
| chr8:18009205
|
G | C | 7 | a0007c0011t0001g0149a0007c0011t0001g0150a0007c0011t0003g0151others(4): Show | 7 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.4963-342G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18009205 | ||||||
| chr8:18009378
|
A | G | 1 | a0002c0007t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4963-169A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 30/38 | chr8 | 18009378 | ||||||
| chr8:18009766
|
T | G | 52 | a0002c0002t0028g0323a0002c0007t0001g0033a0003c0003t0007g0274others(49): Show | 52 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.5160+22T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 31/38 | chr8 | 18009766 | ||||||
| chr8:18009802
|
C | G | 1 | a0002c0002t0004g0199 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.5160+58C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 31/38 | chr8 | 18009802 | ||||||
| chr8:18009838
|
A | G | 1 | a0014c0020t0004g0070 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.5160+94A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 31/38 | chr8 | 18009838 | ||||||
| chr8:18009909
|
T | C | 28 | a0002c0017t0031g0321a0002c0017t0032g0322a0002c0021t0027g0102others(25): Show | 28 | HG01099.hp1 HG01891.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.5160+165T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 31/38 | chr8 | 18009909 | ||||||
| chr8:18010314
|
C | G | 2 | a0004c0004t0003g0135a0004c0004t0003g0136 | 2 | HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.5161-295C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 31/38 | chr8 | 18010314 | ||||||
| chr8:18010320
|
A | G | 1 | a0002c0002t0004g0191 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.5161-289A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 31/38 | chr8 | 18010320 | ||||||
| chr8:18010461
|
A | C | 1 | a0002c0009t0016g0365 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.5161-148A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 31/38 | chr8 | 18010461 | ||||||
| chr8:18010469
|
A | G | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5161-140A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 31/38 | chr8 | 18010469 | ||||||
| chr8:18010520
|
C | A | 244 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(241): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.5161-89C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 31/38 | chr8 | 18010520 | ||||||
| chr8:18010557
|
A | ATTATGTA others(22): Show |
6 | a0002c0021t0027g0102a0005c0005t0014g0160a0005c0005t0014g0171others(3): Show | 6 | HG01891.hp2 HG02258.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.5161-51_5161-23dup others(29): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr8 | 18010557 | |||||
| chr8:18010561
|
T | C | 7 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(4): Show | 7 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.5161-48T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 31/38 | chr8 | 18010561 | ||||||
| chr8:18010579
|
T | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.5161-30T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 31/38 | chr8 | 18010579 | ||||||
| chr8:18010710
|
C | T | 54 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(51): Show | 54 | HG00597.hp1 HG00639.hp2 HG01099.hp1 others(51): Show |
intron_variant | MODIFIER | c.5220+42C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 32/38 | chr8 | 18010710 | ||||||
| chr8:18010736
|
C | A | 242 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.5220+68C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 32/38 | chr8 | 18010736 | ||||||
| chr8:18010754
|
G | T | 1 | a0004c0004t0050g0130 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5220+86G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 32/38 | chr8 | 18010754 | ||||||
| chr8:18010797
|
A | G | 5 | a0001c0001t0002g0072a0003c0003t0002g0239a0003c0003t0002g0242others(2): Show | 5 | HG00544.hp2 NA18747.hp2 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.5220+129A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 32/38 | chr8 | 18010797 | ||||||
| chr8:18010814
|
A | G | 1 | a0002c0007t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5220+146A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 32/38 | chr8 | 18010814 | ||||||
| chr8:18010828
|
A | C | 6 | a0005c0005t0014g0163a0005c0005t0015g0162a0005c0005t0015g0164others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.5220+160A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 32/38 | chr8 | 18010828 | ||||||
| chr8:18010841
|
C | T | 1 | a0002c0021t0027g0102 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5220+173C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 32/38 | chr8 | 18010841 | ||||||
| chr8:18010993
|
A | C | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5221-244A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 32/38 | chr8 | 18010993 | ||||||
| chr8:18011012
|
T | C | 198 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.5221-225T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 32/38 | chr8 | 18011012 | ||||||
| chr8:18011129
|
C | A | 1 | a0003c0003t0013g0248 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.5221-108C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 32/38 | chr8 | 18011129 | ||||||
| chr8:18011386
|
A | ACTAT | 65 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(62): Show | 65 | HG00597.hp1 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.5350+23_5350+26dup others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr8 | 18011386 | |||||
| chr8:18011849
|
CACTTCCA others(23): Show |
C | 21 | a0002c0021t0027g0102a0005c0005t0008g0168a0005c0005t0008g0169others(18): Show | 21 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.5511+54_5511+83del others(30): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr8 | 18011849 | |||||
| chr8:18012097
|
C | T | 6 | a0003c0003t0002g0003a0003c0003t0007g0257a0003c0003t0007g0258others(3): Show | 6 | HG01099.hp2 HG01192.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.5511+270C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 34/38 | chr8 | 18012097 | ||||||
| chr8:18012326
|
T | C | 206 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.5511+499T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 34/38 | chr8 | 18012326 | ||||||
| chr8:18012434
|
C | T | 18 | a0002c0017t0003g0104a0002c0021t0020g0103a0003c0003t0009g0226others(15): Show | 18 | HG00597.hp1 HG00639.hp2 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.5511+607C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 34/38 | chr8 | 18012434 | ||||||
| chr8:18012702
|
C | T | 1 | a0005c0005t0041g0161 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5511+875C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 34/38 | chr8 | 18012702 | ||||||
| chr8:18012704
|
G | A | 1 | a0002c0007t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5511+877G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 34/38 | chr8 | 18012704 | ||||||
| chr8:18012784
|
C | G | 1 | a0006c0008t0068g0273 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.5511+957C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 34/38 | chr8 | 18012784 | ||||||
| chr8:18012952
|
C | T | 233 | a0001c0001t0001g0032a0001c0001t0002g0045a0001c0001t0002g0072others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.5512-1012C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 34/38 | chr8 | 18012952 | ||||||
| chr8:18012977
|
G | A | 1 | a0004c0004t0003g0116 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.5512-987G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 34/38 | chr8 | 18012977 | ||||||
| chr8:18013019
|
G | A | 1 | a0002c0021t0027g0102 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5512-945G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 34/38 | chr8 | 18013019 | ||||||
| chr8:18013291
|
A | G | 9 | a0002c0009t0005g0304a0002c0009t0016g0359a0002c0009t0016g0362others(6): Show | 9 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.5512-673A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 34/38 | chr8 | 18013291 | ||||||
| chr8:18013374
|
C | T | 1 | a0005c0005t0041g0161 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5512-590C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 34/38 | chr8 | 18013374 | ||||||
| chr8:18013377
|
C | G | 19 | a0001c0001t0038g0073a0002c0017t0003g0104a0002c0021t0020g0103others(16): Show | 19 | HG00597.hp1 HG00639.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.5512-587C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 34/38 | chr8 | 18013377 | ||||||
| chr8:18013637
|
TC | T | 4 | a0007c0011t0001g0149a0007c0011t0001g0150a0013c0023t0001g0153others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.5512-326delC | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 34/38 | chr8 | 18013637 | ||||||
| chr8:18013682
|
A | G | 2 | a0002c0017t0031g0321a0002c0017t0032g0322 | 2 | HG01099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5512-282A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 34/38 | chr8 | 18013682 | ||||||
| chr8:18013706
|
A | G | 1 | a0002c0017t0003g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.5512-258A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 34/38 | chr8 | 18013706 | ||||||
| chr8:18013747
|
A | T | 89 | a0001c0001t0004g0044a0001c0024t0017g0107a0002c0002t0004g0002others(86): Show | 89 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.5512-217A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 34/38 | chr8 | 18013747 | ||||||
| chr8:18014054
|
G | C | 41 | a0004c0004t0003g0113a0004c0004t0003g0114a0004c0004t0003g0115others(38): Show | 41 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.5584+18G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 35/38 | chr8 | 18014054 | ||||||
| chr8:18014089
|
T | A | 144 | a0001c0001t0004g0044a0001c0024t0017g0107a0002c0002t0004g0002others(141): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.5584+53T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 35/38 | chr8 | 18014089 | ||||||
| chr8:18014095
|
T | TA | 9 | a0001c0001t0001g0052a0001c0001t0001g0095a0001c0001t0006g0101others(6): Show | 9 | HG00621.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.5584+75dupA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr8 | 18014095 | |||||
| chr8:18014095
|
T | TAA | 11 | a0002c0021t0027g0102a0005c0005t0014g0160a0005c0005t0014g0163others(8): Show | 11 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.5584+74_5584+75dup others(2): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr8 | 18014095 | |||||
| chr8:18014095
|
T | TAAA | 9 | a0005c0005t0008g0168a0005c0005t0008g0169a0005c0005t0008g0174others(6): Show | 9 | HG02258.hp1 HG02559.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.5584+73_5584+75dup others(3): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr8 | 18014095 | |||||
| chr8:18014095
|
TA | T | 45 | a0001c0001t0006g0019a0001c0047t0006g0069a0004c0004t0003g0113others(42): Show | 45 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.5584+75delA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr8 | 18014095 | |||||
| chr8:18014108
|
A | AC | 3 | a0002c0002t0005g0299a0002c0002t0005g0313a0002c0002t0012g0155 | 3 | HG02300.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.5584+72_5584+73ins others(1): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 35/38 | chr8 | 18014108 | ||||||
| chr8:18014110
|
A | AC | 17 | a0002c0021t0020g0103a0003c0003t0009g0226a0003c0003t0009g0339others(14): Show | 17 | HG00597.hp1 HG00639.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.5584+74_5584+75ins others(1): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 35/38 | chr8 | 18014110 | ||||||
| chr8:18014110
|
A | C | 90 | a0001c0001t0004g0044a0001c0024t0017g0107a0002c0002t0004g0002others(87): Show | 90 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.5584+74A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 35/38 | chr8 | 18014110 | ||||||
| chr8:18014111
|
A | AG | 68 | a0001c0001t0002g0045a0001c0001t0002g0072a0002c0002t0053g0289others(65): Show | 68 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.5584+75_5584+76ins others(1): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 35/38 | chr8 | 18014111 | ||||||
| chr8:18014111
|
A | G | 1 | a0003c0003t0007g0257 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.5584+75A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 35/38 | chr8 | 18014111 | ||||||
| chr8:18014318
|
A | T | 1 | a0004c0004t0003g0132 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.5585-266A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 35/38 | chr8 | 18014318 | ||||||
| chr8:18014320
|
A | AT | 17 | a0002c0021t0020g0103a0003c0003t0009g0226a0003c0003t0009g0339others(14): Show | 17 | HG00597.hp1 HG00639.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.5585-264_5585-263i others(3): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 35/38 | chr8 | 18014320 | ||||||
| chr8:18014320
|
A | T | 242 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.5585-264A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 35/38 | chr8 | 18014320 | ||||||
| chr8:18014323
|
C | T | 1 | a0006c0008t0068g0273 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.5585-261C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 35/38 | chr8 | 18014323 | ||||||
| chr8:18014393
|
T | TA | 94 | a0001c0001t0004g0044a0001c0024t0017g0107a0002c0002t0004g0002others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.5585-187dupA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr8 | 18014393 | |||||
| chr8:18014492
|
C | G | 1 | a0005c0005t0041g0161 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5585-92C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 35/38 | chr8 | 18014492 | ||||||
| chr8:18014515
|
T | C | 16 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(13): Show | 16 | HG02109.hp1 HG02145.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.5585-69T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 35/38 | chr8 | 18014515 | ||||||
| chr8:18014911
|
G | A | 1 | a0012c0015t0025g0343 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.5841+71G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18014911 | ||||||
| chr8:18015149
|
C | G | 1 | a0002c0002t0066g0317 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.5841+309C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18015149 | ||||||
| chr8:18015241
|
C | T | 2 | a0001c0001t0038g0073a0003c0012t0009g0349 | 2 | HG01934.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.5841+401C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18015241 | ||||||
| chr8:18015251
|
T | TA | 159 | a0001c0001t0001g0016a0001c0001t0001g0090a0001c0001t0004g0044others(156): Show | 159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.5841+425dupA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18015251 | |||||
| chr8:18015263
|
A | C | 18 | a0002c0007t0030g0179a0002c0021t0020g0103a0003c0003t0009g0226others(15): Show | 18 | HG00597.hp1 HG00639.hp2 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.5841+423A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18015263 | ||||||
| chr8:18015346
|
G | A | 1 | a0005c0005t0008g0168 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.5841+506G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18015346 | ||||||
| chr8:18015362
|
A | G | 1 | a0001c0001t0006g0053 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.5841+522A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18015362 | ||||||
| chr8:18015395
|
A | C | 19 | a0001c0001t0038g0073a0002c0007t0030g0179a0002c0021t0020g0103others(16): Show | 19 | HG00597.hp1 HG00639.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.5841+555A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18015395 | ||||||
| chr8:18015453
|
C | A | 61 | a0002c0007t0001g0033a0002c0009t0005g0304a0002c0009t0016g0359others(58): Show | 61 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.5841+613C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18015453 | ||||||
| chr8:18015523
|
A | AT | 62 | a0002c0007t0001g0033a0002c0009t0005g0304a0002c0009t0016g0359others(59): Show | 62 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.5841+683_5841+684i others(3): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18015523 | ||||||
| chr8:18015524
|
A | C | 62 | a0002c0007t0001g0033a0002c0009t0005g0304a0002c0009t0016g0359others(59): Show | 62 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.5841+684A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18015524 | ||||||
| chr8:18015678
|
T | TC | 7 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(4): Show | 7 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.5841+838_5841+839i others(3): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18015678 | ||||||
| chr8:18015679
|
G | C | 267 | a0001c0001t0001g0021a0001c0001t0001g0059a0001c0001t0001g0066others(264): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.5841+839G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18015679 | ||||||
| chr8:18015876
|
C | G | 1 | a0002c0002t0005g0284 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.5841+1036C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18015876 | ||||||
| chr8:18015958
|
G | A | 1 | a0003c0040t0013g0249 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.5841+1118G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18015958 | ||||||
| chr8:18015962
|
C | T | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5841+1122C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18015962 | ||||||
| chr8:18016000
|
T | G | 1 | a0003c0003t0009g0347 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.5841+1160T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18016000 | ||||||
| chr8:18016014
|
G | A | 5 | a0005c0005t0014g0163a0005c0005t0015g0164a0005c0005t0015g0165others(2): Show | 5 | HG02109.hp2 HG02486.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.5841+1174G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18016014 | ||||||
| chr8:18016075
|
A | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.5841+1235A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18016075 | ||||||
| chr8:18016163
|
C | T | 1 | a0002c0002t0004g0196 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.5841+1323C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18016163 | ||||||
| chr8:18016173
|
C | T | 1 | a0006c0008t0068g0273 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.5841+1333C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18016173 | ||||||
| chr8:18016286
|
A | AAGAT | 93 | a0001c0001t0004g0044a0001c0024t0017g0107a0002c0002t0004g0002others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.5841+1449_5841+145 others(8): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18016286 | |||||
| chr8:18016316
|
T | G | 6 | a0002c0021t0027g0102a0005c0005t0014g0160a0005c0005t0014g0171others(3): Show | 6 | HG01891.hp2 HG02258.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.5841+1476T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18016316 | ||||||
| chr8:18016342
|
G | C | 1 | a0001c0047t0006g0069 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.5841+1502G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18016342 | ||||||
| chr8:18016408
|
G | A | 1 | a0002c0002t0005g0326 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5841+1568G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18016408 | ||||||
| chr8:18016415
|
T | G | 1 | a0001c0001t0001g0043 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.5841+1575T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18016415 | ||||||
| chr8:18016429
|
C | CAGAGAAG others(9): Show |
61 | a0001c0001t0002g0045a0001c0001t0002g0072a0002c0002t0053g0289others(58): Show | 61 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.5841+1591_5841+160 others(20): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18016429 | |||||
| chr8:18016429
|
CAGAGA | C | 92 | a0001c0001t0004g0044a0001c0024t0017g0107a0002c0002t0004g0002others(89): Show | 92 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.5841+1599_5841+160 others(9): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18016429 | |||||
| chr8:18016602
|
A | T | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.5841+1762A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18016602 | ||||||
| chr8:18016624
|
G | T | 1 | a0001c0001t0006g0094 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5841+1784G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18016624 | ||||||
| chr8:18016637
|
C | T | 4 | a0007c0011t0001g0149a0007c0011t0001g0150a0013c0023t0001g0153others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.5841+1797C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18016637 | ||||||
| chr8:18016779
|
A | G | 1 | a0002c0007t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5841+1939A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18016779 | ||||||
| chr8:18016821
|
G | A | 60 | a0001c0001t0002g0045a0001c0001t0002g0072a0002c0002t0053g0289others(57): Show | 60 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.5841+1981G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18016821 | ||||||
| chr8:18016939
|
C | T | 1 | a0002c0002t0005g0182 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5841+2099C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18016939 | ||||||
| chr8:18016965
|
A | C | 1 | a0002c0017t0003g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.5841+2125A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18016965 | ||||||
| chr8:18016967
|
G | C | 7 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(4): Show | 7 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.5841+2127G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18016967 | ||||||
| chr8:18016971
|
G | T | 52 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(49): Show | 52 | HG00597.hp1 HG00639.hp2 HG01099.hp1 others(49): Show |
intron_variant | MODIFIER | c.5841+2131G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18016971 | ||||||
| chr8:18017017
|
C | T | 1 | a0002c0007t0004g0278 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.5841+2177C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18017017 | ||||||
| chr8:18017095
|
A | C | 201 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.5841+2255A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18017095 | ||||||
| chr8:18017168
|
TC | T | 200 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.5841+2332delC | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18017168 | |||||
| chr8:18017183
|
C | T | 51 | a0003c0003t0007g0219a0003c0003t0013g0248a0004c0004t0003g0113others(48): Show | 51 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.5841+2343C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18017183 | ||||||
| chr8:18017297
|
G | A | 9 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(6): Show | 9 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.5841+2457G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18017297 | ||||||
| chr8:18017373
|
A | C | 91 | a0001c0001t0004g0044a0001c0024t0017g0107a0002c0002t0004g0002others(88): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.5841+2533A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18017373 | ||||||
| chr8:18017416
|
T | A | 7 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(4): Show | 7 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.5841+2576T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18017416 | ||||||
| chr8:18017426
|
T | A | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5841+2586T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18017426 | ||||||
| chr8:18017448
|
G | GA | 7 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(4): Show | 7 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.5841+2615dupA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18017448 | |||||
| chr8:18017457
|
C | T | 24 | a0002c0017t0031g0321a0002c0017t0032g0322a0002c0021t0027g0102others(21): Show | 24 | HG01099.hp1 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.5841+2617C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18017457 | ||||||
| chr8:18017496
|
C | T | 1 | a0001c0001t0006g0080 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.5841+2656C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18017496 | ||||||
| chr8:18017509
|
C | T | 7 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(4): Show | 7 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.5841+2669C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18017509 | ||||||
| chr8:18017530
|
TG | T | 6 | a0003c0003t0002g0003a0003c0003t0007g0257a0003c0003t0007g0258others(3): Show | 6 | HG01099.hp2 HG01192.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.5841+2693delG | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18017530 | |||||
| chr8:18017565
|
A | T | 1 | a0001c0001t0010g0015 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.5841+2725A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18017565 | ||||||
| chr8:18017603
|
C | T | 7 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(4): Show | 7 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.5841+2763C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18017603 | ||||||
| chr8:18017672
|
G | C | 2 | a0004c0004t0003g0135a0004c0004t0003g0136 | 2 | HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.5841+2832G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18017672 | ||||||
| chr8:18017681
|
C | G | 1 | a0001c0001t0001g0012 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.5841+2841C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18017681 | ||||||
| chr8:18017713
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.5841+2873C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18017713 | ||||||
| chr8:18017734
|
A | T | 265 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.5841+2894A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18017734 | ||||||
| chr8:18017769
|
T | C | 264 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.5841+2929T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18017769 | ||||||
| chr8:18017784
|
T | C | 269 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.5841+2944T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18017784 | ||||||
| chr8:18017792
|
G | T | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.5841+2952G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18017792 | ||||||
| chr8:18017794
|
C | T | 55 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(52): Show | 55 | HG00597.hp1 HG00639.hp2 HG01099.hp1 others(52): Show |
intron_variant | MODIFIER | c.5841+2954C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18017794 | ||||||
| chr8:18017822
|
C | T | 1 | a0002c0009t0016g0362 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5841+2982C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18017822 | ||||||
| chr8:18017847
|
C | CCAT | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.5841+3009_5841+301 others(7): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18017847 | |||||
| chr8:18018016
|
A | G | 1 | a0002c0002t0004g0192 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.5841+3176A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018016 | ||||||
| chr8:18018039
|
G | C | 86 | a0001c0001t0004g0044a0001c0024t0017g0107a0002c0002t0004g0002others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.5841+3199G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018039 | ||||||
| chr8:18018090
|
A | G | 3 | a0002c0002t0005g0299a0002c0002t0005g0313a0002c0009t0005g0304 | 3 | HG02809.hp1 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.5841+3250A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018090 | ||||||
| chr8:18018181
|
G | C | 1 | a0004c0004t0003g0357 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5841+3341G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018181 | ||||||
| chr8:18018197
|
T | A | 8 | a0003c0003t0002g0003a0003c0003t0007g0219a0003c0003t0007g0232others(5): Show | 8 | HG00558.hp2 HG01099.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.5841+3357T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018197 | ||||||
| chr8:18018311
|
G | C | 1 | a0003c0003t0002g0231 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.5841+3471G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018311 | ||||||
| chr8:18018573
|
G | C | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5841+3733G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018573 | ||||||
| chr8:18018636
|
C | A | 25 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(22): Show | 25 | HG00597.hp1 HG00639.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.5841+3796C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018636 | ||||||
| chr8:18018665
|
G | A | 1 | a0002c0007t0030g0179 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.5841+3825G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018665 | ||||||
| chr8:18018681
|
T | C | 257 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(254): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.5841+3841T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018681 | ||||||
| chr8:18018695
|
T | C | 253 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.5841+3855T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018695 | ||||||
| chr8:18018749
|
T | G | 1 | a0003c0003t0007g0257 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.5841+3909T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018749 | ||||||
| chr8:18018753
|
G | C | 1 | a0001c0001t0010g0015 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.5841+3913G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018753 | ||||||
| chr8:18018765
|
C | T | 1 | a0001c0001t0040g0076 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.5841+3925C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018765 | ||||||
| chr8:18018804
|
C | T | 1 | a0003c0003t0002g0157 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.5841+3964C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018804 | ||||||
| chr8:18018809
|
C | CA | 10 | a0002c0009t0016g0362a0003c0003t0002g0224a0003c0006t0002g0252others(7): Show | 10 | HG01884.hp1 HG01981.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.5841+3982dupA | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018809 | |||||
| chr8:18018815
|
A | T | 1 | a0001c0001t0038g0073 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.5841+3975A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018815 | ||||||
| chr8:18018826
|
G | GTA | 31 | a0002c0002t0053g0289a0002c0009t0016g0359a0002c0009t0016g0362others(28): Show | 31 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.5841+3998_5841+399 others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018826 | |||||
| chr8:18018838
|
ATG | A | 12 | a0001c0001t0001g0042a0001c0001t0001g0071a0001c0001t0001g0082others(9): Show | 12 | HG00597.hp1 HG01891.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.5841+4012_5841+401 others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018838 | |||||
| chr8:18018838
|
ATGTG | A | 3 | a0004c0004t0028g0119a0004c0016t0008g0134a0004c0016t0008g0138 | 3 | HG01952.hp2 HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.5841+4010_5841+401 others(8): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018838 | |||||
| chr8:18018840
|
G | A | 83 | a0001c0001t0002g0045a0002c0002t0005g0294a0002c0002t0005g0315others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.5841+4000G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018840 | ||||||
| chr8:18018842
|
G | A | 2 | a0001c0001t0002g0072a0003c0006t0011g0246 | 2 | NA18941.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.5841+4002G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018842 | ||||||
| chr8:18018844
|
G | A | 3 | a0004c0004t0028g0119a0004c0016t0008g0134a0004c0016t0008g0138 | 3 | HG01952.hp2 HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.5841+4004G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018844 | ||||||
| chr8:18018848
|
G | A | 34 | a0001c0001t0038g0073a0003c0003t0002g0216a0003c0003t0002g0220others(31): Show | 34 | HG00323.hp2 HG00558.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.5841+4008G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018848 | ||||||
| chr8:18018848
|
G | GTATA | 10 | a0003c0003t0002g0241a0003c0003t0007g0274a0003c0006t0002g0225others(7): Show | 10 | HG00609.hp1 HG02027.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.5841+4009_5841+401 others(8): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018848 | |||||
| chr8:18018848
|
G | GTATATA | 5 | a0003c0003t0002g0157a0003c0003t0002g0229a0003c0003t0002g0265others(2): Show | 5 | HG01070.hp1 HG02071.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.5841+4009_5841+401 others(10): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018848 | |||||
| chr8:18018848
|
G | GTATATAT others(3): Show |
1 | a0003c0003t0002g0230 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.5841+4009_5841+401 others(14): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018848 | |||||
| chr8:18018848
|
GTGTGTA | G | 12 | a0002c0002t0004g0328a0002c0002t0005g0306a0002c0002t0005g0326others(9): Show | 12 | HG01261.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.5841+4010_5841+401 others(10): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018848 | |||||
| chr8:18018848
|
GTGTGTAT others(1): Show |
G | 78 | a0001c0001t0004g0044a0001c0024t0017g0107a0002c0002t0004g0002others(75): Show | 78 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.5841+4010_5841+401 others(12): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018848 | |||||
| chr8:18018848
|
GTGTGTAT others(3): Show |
G | 7 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(4): Show | 7 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.5841+4010_5841+401 others(14): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018848 | |||||
| chr8:18018848
|
GTGTGTAT others(5): Show |
G | 3 | a0002c0002t0004g0311a0002c0002t0005g0316a0002c0002t0066g0317 | 3 | HG00323.hp1 HG01074.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.5841+4010_5841+402 others(16): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018848 | |||||
| chr8:18018848
|
GTGTGTAT others(9): Show |
G | 1 | a0002c0002t0005g0302 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5841+4010_5841+402 others(20): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018848 | |||||
| chr8:18018850
|
G | A | 112 | a0001c0001t0038g0073a0002c0002t0053g0289a0003c0003t0002g0156others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.5841+4010G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018850 | ||||||
| chr8:18018850
|
G | GTA | 6 | a0001c0001t0001g0022a0001c0001t0001g0047a0001c0001t0001g0068others(3): Show | 6 | HG02559.hp1 HG03491.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.5841+4011_5841+401 others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018850 | |||||
| chr8:18018850
|
GTGTA | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0043a0001c0001t0001g0095others(1): Show | 4 | HG03453.hp1 NA18960.hp1 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.5841+4012_5841+401 others(8): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018850 | |||||
| chr8:18018850
|
GTGTATAT others(3): Show |
G | 1 | a0001c0001t0062g0093 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5841+4012_5841+402 others(14): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018850 | |||||
| chr8:18018852
|
G | A | 171 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0021others(168): Show | 172 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.5841+4012G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018852 | ||||||
| chr8:18018852
|
G | GTA | 8 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0046others(5): Show | 8 | HG01433.hp1 HG01928.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.5841+4039_5841+404 others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018852 | |||||
| chr8:18018852
|
G | GTATA | 3 | a0009c0013t0002g0214a0013c0023t0001g0153a0013c0023t0001g0154 | 3 | HG02895.hp2 HG02897.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.5841+4037_5841+404 others(8): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018852 | |||||
| chr8:18018852
|
GTATA | G | 3 | a0001c0001t0001g0050a0001c0001t0001g0089a0001c0001t0001g0099 | 3 | HG01981.hp2 HG01993.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.5841+4037_5841+404 others(8): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018852 | |||||
| chr8:18018854
|
A | G | 9 | a0001c0001t0001g0147a0002c0009t0016g0359a0002c0009t0016g0362others(6): Show | 9 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.5841+4014A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018854 | ||||||
| chr8:18018855
|
T | C | 3 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0355 | 3 | HG02698.hp2 HG03017.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.5841+4015T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018855 | ||||||
| chr8:18018856
|
A | G | 1 | a0002c0009t0063g0363 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5841+4016A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018856 | ||||||
| chr8:18018857
|
T | C | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.5841+4017T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018857 | ||||||
| chr8:18018859
|
T | C | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.5841+4019T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018859 | ||||||
| chr8:18018861
|
T | C | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.5841+4021T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018861 | ||||||
| chr8:18018861
|
T | TATATATA others(29): Show |
3 | a0003c0003t0026g0271a0003c0003t0046g0259a0030c0041t0026g0270 | 3 | HG00639.hp2 HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.5841+4038_5841+403 others(40): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018861 | |||||
| chr8:18018863
|
T | C | 1 | a0010c0014t0023g0354 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.5841+4023T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018863 | ||||||
| chr8:18018873
|
T | C | 5 | a0003c0003t0002g0003a0003c0003t0007g0257a0003c0003t0007g0258others(2): Show | 5 | HG01099.hp2 HG01192.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.5841+4033T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018873 | ||||||
| chr8:18018873
|
TATATATA others(5): Show |
T | 4 | a0005c0005t0008g0168a0005c0005t0008g0169a0005c0005t0008g0174others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.5841+4035_5841+404 others(16): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018873 | |||||
| chr8:18018875
|
T | C | 15 | a0001c0001t0038g0073a0002c0021t0027g0102a0003c0003t0009g0226others(12): Show | 15 | HG00597.hp1 HG01934.hp1 HG02683.hp2 others(12): Show |
intron_variant | MODIFIER | c.5841+4035T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018875 | ||||||
| chr8:18018875
|
TATATACA others(3): Show |
T | 3 | a0005c0005t0008g0332a0005c0005t0008g0333a0005c0005t0044g0335 | 3 | HG02258.hp1 HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.5841+4037_5841+404 others(14): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018875 | |||||
| chr8:18018877
|
TATACACA others(1): Show |
T | 6 | a0003c0003t0002g0003a0003c0003t0007g0257a0003c0003t0007g0258others(3): Show | 6 | HG01099.hp2 HG01192.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.5841+4039_5841+404 others(12): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018877 | |||||
| chr8:18018878
|
A | G | 2 | a0010c0014t0022g0330a0010c0014t0022g0331 | 2 | HG02698.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.5841+4038A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018878 | ||||||
| chr8:18018879
|
T | C | 86 | a0001c0001t0004g0044a0001c0024t0017g0107a0002c0002t0004g0002others(83): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.5841+4039T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018879 | ||||||
| chr8:18018879
|
TACAC | T | 6 | a0005c0005t0014g0163a0005c0005t0015g0162a0005c0005t0015g0164others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.5841+4045_5841+404 others(8): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018879 | |||||
| chr8:18018880
|
A | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.5841+4040A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018880 | ||||||
| chr8:18018881
|
C | T | 108 | a0001c0001t0002g0045a0002c0002t0029g0183a0002c0002t0053g0289others(105): Show | 108 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.5841+4041C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018881 | ||||||
| chr8:18018882
|
A | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.5841+4042A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018882 | ||||||
| chr8:18018883
|
C | T | 230 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(227): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.5841+4043C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018883 | ||||||
| chr8:18018884
|
A | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.5841+4044A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018884 | ||||||
| chr8:18018885
|
C | T | 203 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.5841+4045C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018885 | ||||||
| chr8:18018886
|
A | G | 2 | a0010c0014t0023g0354a0010c0014t0023g0355 | 2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.5841+4046A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018886 | ||||||
| chr8:18018887
|
C | T | 32 | a0002c0002t0004g0311a0002c0002t0005g0316a0002c0002t0028g0323others(29): Show | 32 | HG00323.hp1 HG00544.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.5841+4047C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018887 | ||||||
| chr8:18018891
|
T | C | 28 | a0002c0002t0004g0311a0002c0002t0005g0316a0002c0002t0028g0323others(25): Show | 28 | HG00323.hp1 HG00544.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.5841+4051T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018891 | ||||||
| chr8:18018893
|
C | T | 30 | a0002c0002t0004g0311a0002c0002t0005g0316a0002c0002t0028g0323others(27): Show | 30 | HG00323.hp1 HG00544.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.5841+4053C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018893 | ||||||
| chr8:18018895
|
T | C | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.5841+4055T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018895 | ||||||
| chr8:18018895
|
TAC | T | 8 | a0001c0001t0002g0072a0003c0003t0002g0243a0004c0004t0028g0119others(5): Show | 8 | HG01884.hp2 HG01952.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.5841+4059_5841+406 others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018895 | |||||
| chr8:18018895
|
TACAC | T | 97 | a0001c0001t0004g0044a0001c0024t0017g0107a0002c0002t0004g0002others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.5841+4057_5841+406 others(8): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018895 | |||||
| chr8:18018897
|
C | T | 120 | a0001c0001t0002g0045a0001c0001t0017g0105a0001c0001t0017g0108others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.5841+4057C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018897 | ||||||
| chr8:18018899
|
C | T | 36 | a0001c0001t0002g0072a0002c0002t0004g0311a0002c0002t0005g0316others(33): Show | 36 | HG00323.hp1 HG00544.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.5841+4059C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018899 | ||||||
| chr8:18018901
|
T | C | 2 | a0010c0014t0023g0354a0010c0014t0023g0355 | 2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.5841+4061T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018901 | ||||||
| chr8:18018902
|
A | G | 2 | a0010c0014t0022g0330a0010c0014t0022g0331 | 2 | HG02698.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.5841+4062A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018902 | ||||||
| chr8:18018903
|
T | C | 6 | a0003c0003t0002g0003a0003c0003t0007g0257a0003c0003t0007g0258others(3): Show | 6 | HG01099.hp2 HG01192.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.5841+4063T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018903 | ||||||
| chr8:18018904
|
A | C | 1 | a0002c0002t0012g0310 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.5841+4064A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018904 | ||||||
| chr8:18018904
|
A | G | 2 | a0010c0014t0023g0354a0010c0014t0023g0355 | 2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.5841+4064A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018904 | ||||||
| chr8:18018911
|
T | A | 9 | a0001c0001t0002g0072a0002c0007t0001g0033a0003c0003t0002g0243others(6): Show | 9 | HG01884.hp2 HG01952.hp2 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.5841+4071T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018911 | ||||||
| chr8:18018911
|
T | TAA | 18 | a0003c0003t0002g0217a0003c0003t0002g0224a0003c0003t0002g0233others(15): Show | 18 | HG00544.hp2 HG02074.hp1 HG02886.hp1 others(15): Show |
intron_variant | MODIFIER | c.5841+4073_5841+407 others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018911 | |||||
| chr8:18018911
|
T | TATAA | 81 | a0001c0001t0002g0045a0002c0002t0053g0289a0003c0003t0002g0156others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.5841+4072_5841+407 others(8): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018911 | |||||
| chr8:18018913
|
A | T | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.5841+4073A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18018913 | ||||||
| chr8:18018922
|
CATATA | C | 30 | a0002c0017t0031g0321a0002c0017t0032g0322a0002c0021t0027g0102others(27): Show | 30 | HG01099.hp1 HG01099.hp2 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.5841+4088_5841+409 others(9): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018922 | |||||
| chr8:18018961
|
TAA | T | 257 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(254): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.5841+4123_5841+412 others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18018961 | |||||
| chr8:18019017
|
T | G | 4 | a0005c0005t0008g0168a0005c0005t0008g0169a0005c0005t0008g0174others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.5841+4177T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18019017 | ||||||
| chr8:18019033
|
C | G | 2 | a0002c0002t0005g0326a0002c0002t0029g0324 | 2 | HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.5841+4193C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18019033 | ||||||
| chr8:18019060
|
A | G | 91 | a0001c0001t0004g0044a0001c0024t0017g0107a0002c0002t0004g0002others(88): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.5841+4220A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18019060 | ||||||
| chr8:18019064
|
T | G | 91 | a0001c0001t0004g0044a0001c0024t0017g0107a0002c0002t0004g0002others(88): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.5841+4224T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18019064 | ||||||
| chr8:18019065
|
T | A | 91 | a0001c0001t0004g0044a0001c0024t0017g0107a0002c0002t0004g0002others(88): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.5841+4225T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18019065 | ||||||
| chr8:18019074
|
C | T | 1 | a0002c0002t0005g0182 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5841+4234C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18019074 | ||||||
| chr8:18019112
|
G | A | 1 | a0010c0014t0023g0355 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.5841+4272G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18019112 | ||||||
| chr8:18019153
|
G | C | 1 | a0005c0005t0041g0161 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5841+4313G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18019153 | ||||||
| chr8:18019298
|
A | G | 1 | a0002c0002t0005g0299 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.5841+4458A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18019298 | ||||||
| chr8:18019324
|
G | T | 253 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.5841+4484G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18019324 | ||||||
| chr8:18019361
|
C | T | 1 | a0006c0008t0068g0273 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.5841+4521C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18019361 | ||||||
| chr8:18019380
|
A | G | 1 | a0001c0001t0006g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.5841+4540A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18019380 | ||||||
| chr8:18019585
|
T | A | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5841+4745T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18019585 | ||||||
| chr8:18019594
|
C | T | 7 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(4): Show | 7 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.5841+4754C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18019594 | ||||||
| chr8:18019638
|
A | G | 7 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(4): Show | 7 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.5841+4798A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18019638 | ||||||
| chr8:18019644
|
T | G | 1 | a0007c0011t0003g0152 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.5841+4804T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18019644 | ||||||
| chr8:18019791
|
G | A | 6 | a0003c0003t0002g0003a0003c0003t0007g0257a0003c0003t0007g0258others(3): Show | 6 | HG01099.hp2 HG01192.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.5841+4951G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18019791 | ||||||
| chr8:18020240
|
C | G | 87 | a0001c0001t0004g0044a0001c0024t0017g0107a0002c0002t0004g0002others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.5842-5121C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18020240 | ||||||
| chr8:18020315
|
G | A | 273 | a0001c0001t0001g0021a0001c0001t0001g0059a0001c0001t0001g0066others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.5842-5046G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18020315 | ||||||
| chr8:18020371
|
G | A | 265 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.5842-4990G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18020371 | ||||||
| chr8:18020413
|
A | T | 15 | a0003c0003t0009g0226a0003c0003t0009g0339a0003c0003t0009g0346others(12): Show | 15 | HG00597.hp1 HG00639.hp2 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.5842-4948A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18020413 | ||||||
| chr8:18020447
|
T | C | 1 | a0002c0002t0005g0284 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.5842-4914T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18020447 | ||||||
| chr8:18020539
|
G | A | 1 | a0002c0002t0005g0316 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.5842-4822G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18020539 | ||||||
| chr8:18020593
|
A | G | 2 | a0002c0021t0020g0103a0014c0020t0020g0098 | 2 | HG02896.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5842-4768A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18020593 | ||||||
| chr8:18020646
|
A | G | 251 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.5842-4715A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18020646 | ||||||
| chr8:18020661
|
A | C | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.5842-4700A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18020661 | ||||||
| chr8:18020661
|
A | G | 247 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.5842-4700A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18020661 | ||||||
| chr8:18020679
|
C | G | 1 | a0006c0008t0007g0266 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.5842-4682C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18020679 | ||||||
| chr8:18020744
|
T | A | 1 | a0002c0017t0003g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.5842-4617T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18020744 | ||||||
| chr8:18020761
|
A | G | 3 | a0001c0001t0001g0046a0001c0001t0001g0077a0001c0001t0001g0090 | 3 | NA18950.hp1 NA18956.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.5842-4600A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18020761 | ||||||
| chr8:18020864
|
G | A | 1 | a0002c0002t0005g0281 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.5842-4497G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18020864 | ||||||
| chr8:18021053
|
C | T | 7 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(4): Show | 7 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.5842-4308C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18021053 | ||||||
| chr8:18021057
|
A | G | 1 | a0003c0003t0002g0231 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.5842-4304A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18021057 | ||||||
| chr8:18021063
|
T | C | 87 | a0001c0001t0004g0044a0001c0024t0017g0107a0002c0002t0004g0002others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.5842-4298T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18021063 | ||||||
| chr8:18021206
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.5842-4155C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18021206 | ||||||
| chr8:18021218
|
T | C | 173 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0017g0105others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.5842-4143T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18021218 | ||||||
| chr8:18021253
|
T | C | 5 | a0004c0004t0003g0336a0004c0004t0003g0351a0004c0004t0003g0352others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.5842-4108T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18021253 | ||||||
| chr8:18021373
|
G | A | 236 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(233): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.5842-3988G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18021373 | ||||||
| chr8:18021519
|
T | G | 119 | a0001c0001t0002g0045a0001c0001t0002g0072a0002c0002t0028g0323others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.5842-3842T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18021519 | ||||||
| chr8:18021645
|
A | T | 1 | a0001c0001t0006g0094 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5842-3716A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18021645 | ||||||
| chr8:18021883
|
A | C | 110 | a0001c0001t0001g0089a0001c0001t0002g0045a0001c0001t0002g0072others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.5842-3478A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18021883 | ||||||
| chr8:18021928
|
A | G | 17 | a0002c0021t0020g0103a0003c0003t0009g0226a0003c0003t0009g0339others(14): Show | 17 | HG00597.hp1 HG00639.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.5842-3433A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18021928 | ||||||
| chr8:18021968
|
C | A | 10 | a0004c0016t0008g0134a0004c0016t0008g0138a0005c0005t0008g0168others(7): Show | 10 | HG02258.hp1 HG02559.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.5842-3393C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18021968 | ||||||
| chr8:18022022
|
T | C | 2 | a0001c0001t0001g0082a0009c0013t0001g0215 | 2 | NA18998.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.5842-3339T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18022022 | ||||||
| chr8:18022163
|
G | C | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.5842-3198G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18022163 | ||||||
| chr8:18022184
|
A | G | 1 | a0002c0007t0004g0201 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.5842-3177A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18022184 | ||||||
| chr8:18022468
|
C | A | 2 | a0002c0002t0004g0002a0002c0002t0005g0002 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.5842-2893C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18022468 | ||||||
| chr8:18022477
|
A | G | 1 | a0003c0003t0002g0220 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.5842-2884A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18022477 | ||||||
| chr8:18022502
|
A | G | 1 | a0003c0006t0054g0227 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.5842-2859A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18022502 | ||||||
| chr8:18022534
|
C | T | 1 | a0001c0001t0024g0048 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.5842-2827C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18022534 | ||||||
| chr8:18022571
|
C | T | 3 | a0005c0005t0014g0160a0005c0005t0014g0171a0005c0005t0027g0170 | 3 | HG01891.hp2 HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.5842-2790C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18022571 | ||||||
| chr8:18022619
|
T | C | 1 | a0002c0002t0012g0310 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.5842-2742T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18022619 | ||||||
| chr8:18022734
|
C | A | 182 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.5842-2627C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18022734 | ||||||
| chr8:18022737
|
T | C | 1 | a0002c0017t0031g0321 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.5842-2624T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18022737 | ||||||
| chr8:18022751
|
C | G | 83 | a0001c0001t0004g0044a0001c0024t0017g0107a0002c0002t0004g0002others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.5842-2610C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18022751 | ||||||
| chr8:18022872
|
C | G | 4 | a0002c0002t0028g0323a0002c0017t0003g0104a0004c0004t0003g0357others(1): Show | 4 | HG02615.hp2 HG02630.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.5842-2489C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18022872 | ||||||
| chr8:18022927
|
T | A | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.5842-2434T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18022927 | ||||||
| chr8:18022939
|
C | T | 2 | a0002c0002t0005g0296a0002c0002t0005g0297 | 2 | HG01243.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.5842-2422C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18022939 | ||||||
| chr8:18022958
|
G | A | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5842-2403G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18022958 | ||||||
| chr8:18022980
|
T | A | 7 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(4): Show | 7 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.5842-2381T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18022980 | ||||||
| chr8:18023088
|
A | G | 1 | a0001c0001t0006g0053 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.5842-2273A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18023088 | ||||||
| chr8:18023107
|
T | C | 83 | a0001c0001t0004g0044a0001c0024t0017g0107a0002c0002t0004g0002others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.5842-2254T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18023107 | ||||||
| chr8:18023116
|
C | T | 83 | a0001c0001t0004g0044a0001c0024t0017g0107a0002c0002t0004g0002others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.5842-2245C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18023116 | ||||||
| chr8:18023189
|
C | G | 1 | a0002c0007t0004g0201 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.5842-2172C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18023189 | ||||||
| chr8:18023248
|
G | C | 2 | a0003c0003t0002g0224a0003c0012t0002g0341 | 2 | NA18970.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.5842-2113G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18023248 | ||||||
| chr8:18023271
|
G | A | 1 | a0003c0006t0013g0251 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.5842-2090G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18023271 | ||||||
| chr8:18023298
|
C | T | 7 | a0001c0001t0004g0044a0002c0007t0004g0200a0002c0007t0004g0201others(4): Show | 7 | NA18942.hp1 NA18961.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.5842-2063C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18023298 | ||||||
| chr8:18023360
|
T | A | 83 | a0001c0001t0004g0044a0001c0024t0017g0107a0002c0002t0004g0002others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.5842-2001T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18023360 | ||||||
| chr8:18023369
|
C | T | 1 | a0002c0002t0012g0307 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5842-1992C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18023369 | ||||||
| chr8:18023408
|
G | A | 42 | a0002c0002t0028g0323a0002c0017t0003g0104a0004c0004t0003g0113others(39): Show | 42 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.5842-1953G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18023408 | ||||||
| chr8:18023449
|
T | G | 1 | a0003c0003t0002g0217 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.5842-1912T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18023449 | ||||||
| chr8:18023458
|
C | T | 1 | a0002c0002t0005g0315 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.5842-1903C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18023458 | ||||||
| chr8:18023523
|
T | A | 5 | a0008c0010t0004g0207a0008c0010t0004g0208a0008c0010t0004g0209others(2): Show | 5 | HG02135.hp1 NA18961.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.5842-1838T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18023523 | ||||||
| chr8:18023559
|
A | ATTGTT | 3 | a0002c0002t0005g0299a0002c0002t0005g0313a0002c0009t0005g0304 | 3 | HG02809.hp1 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.5842-1799_5842-179 others(9): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18023559 | |||||
| chr8:18023666
|
T | G | 4 | a0002c0017t0031g0321a0002c0017t0032g0322a0022c0029t0045g0279others(1): Show | 4 | HG01099.hp1 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.5842-1695T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18023666 | ||||||
| chr8:18023744
|
T | C | 266 | a0001c0001t0001g0089a0001c0001t0002g0045a0001c0001t0002g0072others(263): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.5842-1617T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18023744 | ||||||
| chr8:18024062
|
C | T | 1 | a0027c0031t0056g0139 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5842-1299C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18024062 | ||||||
| chr8:18024074
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.5842-1287C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18024074 | ||||||
| chr8:18024099
|
A | T | 2 | a0013c0023t0001g0153a0013c0023t0001g0154 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.5842-1262A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18024099 | ||||||
| chr8:18024146
|
A | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.5842-1215A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18024146 | ||||||
| chr8:18024192
|
C | A | 2 | a0002c0017t0031g0321a0002c0017t0032g0322 | 2 | HG01099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5842-1169C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18024192 | ||||||
| chr8:18024227
|
G | A | 1 | a0017c0027t0001g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.5842-1134G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18024227 | ||||||
| chr8:18024272
|
G | T | 1 | a0002c0017t0031g0321 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.5842-1089G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18024272 | ||||||
| chr8:18024326
|
T | C | 245 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.5842-1035T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18024326 | ||||||
| chr8:18024383
|
A | C | 1 | a0002c0002t0004g0185 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.5842-978A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18024383 | ||||||
| chr8:18024497
|
A | G | 1 | a0003c0003t0002g0245 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.5842-864A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18024497 | ||||||
| chr8:18024528
|
T | C | 263 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.5842-833T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18024528 | ||||||
| chr8:18024567
|
A | G | 23 | a0002c0021t0027g0102a0004c0016t0008g0134a0004c0016t0008g0138others(20): Show | 23 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.5842-794A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18024567 | ||||||
| chr8:18024572
|
A | C | 1 | a0001c0048t0006g0081 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.5842-789A>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18024572 | ||||||
| chr8:18024604
|
T | G | 1 | a0027c0031t0056g0139 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5842-757T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18024604 | ||||||
| chr8:18024638
|
G | A | 23 | a0002c0021t0027g0102a0004c0016t0008g0134a0004c0016t0008g0138others(20): Show | 23 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.5842-723G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18024638 | ||||||
| chr8:18024676
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.5842-685T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18024676 | ||||||
| chr8:18024712
|
A | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.5842-649A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18024712 | ||||||
| chr8:18024795
|
C | T | 263 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.5842-566C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18024795 | ||||||
| chr8:18024852
|
T | C | 27 | a0002c0021t0027g0102a0004c0016t0008g0134a0004c0016t0008g0138others(24): Show | 27 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.5842-509T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18024852 | ||||||
| chr8:18024974
|
C | T | 72 | a0001c0001t0002g0045a0001c0001t0002g0072a0002c0002t0053g0289others(69): Show | 72 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.5842-387C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18024974 | ||||||
| chr8:18025017
|
C | T | 3 | a0002c0002t0005g0296a0002c0002t0005g0297a0028c0035t0005g0298 | 3 | HG01243.hp2 HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.5842-344C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18025017 | ||||||
| chr8:18025118
|
G | A | 8 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.5842-243G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18025118 | ||||||
| chr8:18025133
|
C | CT | 110 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0043others(107): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.5842-209dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18025133 | |||||
| chr8:18025133
|
C | CTT | 31 | a0001c0001t0001g0083a0002c0021t0027g0102a0003c0038t0067g0235others(28): Show | 31 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.5842-210_5842-209d others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18025133 | |||||
| chr8:18025133
|
CT | C | 65 | a0001c0001t0001g0084a0001c0001t0002g0072a0001c0001t0010g0011others(62): Show | 65 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.5842-209delT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18025133 | |||||
| chr8:18025133
|
CTT | C | 10 | a0001c0001t0002g0045a0003c0003t0002g0216a0003c0003t0002g0217others(7): Show | 10 | HG02071.hp2 HG02074.hp1 NA18943.hp1 others(7): Show |
intron_variant | MODIFIER | c.5842-210_5842-209d others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18025133 | |||||
| chr8:18025171
|
C | T | 23 | a0002c0021t0027g0102a0004c0016t0008g0134a0004c0016t0008g0138others(20): Show | 23 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.5842-190C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18025171 | ||||||
| chr8:18025197
|
T | TA | 254 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.5842-164_5842-163i others(3): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18025197 | ||||||
| chr8:18025203
|
C | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.5842-158C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18025203 | ||||||
| chr8:18025305
|
C | T | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.5842-56C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18025305 | ||||||
| chr8:18025336
|
A | AT | 10 | a0002c0007t0005g0202a0002c0009t0016g0359a0002c0009t0016g0362others(7): Show | 10 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.5842-14dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr8 | 18025336 | |||||
| chr8:18025336
|
A | T | 3 | a0001c0001t0002g0045a0009c0013t0002g0148a0009c0013t0002g0214 | 3 | NA18943.hp1 NA18956.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.5842-25A>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 36/38 | chr8 | 18025336 | ||||||
| chr8:18025730
|
T | C | 1 | a0001c0001t0006g0094 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.6049+72T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18025730 | ||||||
| chr8:18025787
|
G | A | 254 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.6049+129G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18025787 | ||||||
| chr8:18025889
|
G | A | 1 | a0005c0005t0014g0160 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6049+231G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18025889 | ||||||
| chr8:18025891
|
G | A | 83 | a0001c0001t0004g0044a0002c0002t0004g0002a0002c0002t0004g0180others(80): Show | 83 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.6049+233G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18025891 | ||||||
| chr8:18025892
|
C | T | 1 | a0004c0004t0003g0143 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.6049+234C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18025892 | ||||||
| chr8:18025893
|
G | A | 2 | a0005c0005t0014g0160a0022c0029t0045g0279 | 2 | HG02809.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.6049+235G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18025893 | ||||||
| chr8:18025894
|
G | C | 1 | a0005c0005t0014g0160 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6049+236G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18025894 | ||||||
| chr8:18025896
|
G | C | 1 | a0005c0005t0014g0160 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6049+238G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18025896 | ||||||
| chr8:18025897
|
G | T | 1 | a0005c0005t0014g0160 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6049+239G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18025897 | ||||||
| chr8:18025898
|
C | A | 1 | a0005c0005t0014g0160 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6049+240C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18025898 | ||||||
| chr8:18025902
|
C | A | 1 | a0005c0005t0014g0160 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6049+244C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18025902 | ||||||
| chr8:18025903
|
G | T | 1 | a0005c0005t0014g0160 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6049+245G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18025903 | ||||||
| chr8:18025904
|
C | T | 1 | a0005c0005t0014g0160 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6049+246C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18025904 | ||||||
| chr8:18025914
|
C | T | 72 | a0001c0001t0002g0045a0001c0001t0002g0072a0002c0002t0053g0289others(69): Show | 72 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.6049+256C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18025914 | ||||||
| chr8:18025946
|
C | T | 1 | a0005c0005t0014g0171 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6049+288C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18025946 | ||||||
| chr8:18025960
|
G | A | 1 | a0005c0005t0008g0332 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6049+302G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18025960 | ||||||
| chr8:18025979
|
A | G | 23 | a0002c0021t0027g0102a0004c0016t0008g0134a0004c0016t0008g0138others(20): Show | 23 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.6049+321A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18025979 | ||||||
| chr8:18026025
|
G | A | 2 | a0002c0017t0031g0321a0002c0017t0032g0322 | 2 | HG01099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6049+367G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026025 | ||||||
| chr8:18026032
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.6049+374C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026032 | ||||||
| chr8:18026064
|
T | C | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.6049+406T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026064 | ||||||
| chr8:18026076
|
A | G | 2 | a0006c0008t0007g0276a0006c0008t0068g0273 | 2 | HG02135.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.6049+418A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026076 | ||||||
| chr8:18026081
|
G | A | 72 | a0001c0001t0002g0045a0001c0001t0002g0072a0002c0002t0053g0289others(69): Show | 72 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.6049+423G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026081 | ||||||
| chr8:18026112
|
T | C | 3 | a0003c0003t0026g0271a0003c0003t0046g0259a0030c0041t0026g0270 | 3 | HG00639.hp2 HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.6049+454T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026112 | ||||||
| chr8:18026121
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0040g0076 | 2 | NA18948.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.6049+463G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026121 | ||||||
| chr8:18026148
|
A | G | 254 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.6049+490A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026148 | ||||||
| chr8:18026151
|
G | A | 77 | a0001c0001t0004g0044a0002c0002t0004g0002a0002c0002t0004g0181others(74): Show | 77 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.6049+493G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026151 | ||||||
| chr8:18026159
|
C | A | 366 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(363): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.6049+501C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026159 | ||||||
| chr8:18026162
|
TCTGAAA | T | 71 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(68): Show | 72 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.6049+506_6049+511d others(8): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr8 | 18026162 | |||||
| chr8:18026163
|
C | CA | 3 | a0004c0004t0003g0123a0004c0004t0003g0128a0020c0045t0003g0127 | 3 | NA18949.hp2 NA19057.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.6049+505_6049+506i others(3): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026163 | ||||||
| chr8:18026163
|
CT | C | 12 | a0002c0009t0052g0358a0002c0009t0063g0363a0004c0004t0003g0117others(9): Show | 12 | HG01257.hp2 HG01496.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.6049+506delT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026163 | ||||||
| chr8:18026163
|
CTG | C | 8 | a0004c0004t0003g0352a0004c0004t0003g0357a0004c0016t0003g0131others(5): Show | 8 | HG01891.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.6049+506_6049+507d others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026163 | ||||||
| chr8:18026163
|
CTGA | C | 14 | a0001c0001t0001g0043a0001c0001t0001g0064a0001c0001t0001g0095others(11): Show | 14 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.6049+506_6049+508d others(5): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026163 | ||||||
| chr8:18026163
|
CTGAA | C | 18 | a0001c0001t0001g0025a0001c0001t0001g0042a0001c0001t0001g0054others(15): Show | 18 | HG00423.hp1 HG00621.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.6049+506_6049+509d others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026163 | ||||||
| chr8:18026163
|
CTGAAA | C | 16 | a0001c0001t0001g0096a0001c0001t0001g0099a0001c0001t0006g0019others(13): Show | 16 | HG00140.hp1 HG00323.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.6049+506_6049+510d others(7): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026163 | ||||||
| chr8:18026163
|
CTGAAACA | C | 98 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0016others(95): Show | 98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.6049+506_6049+512d others(9): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026163 | ||||||
| chr8:18026163
|
CTGAAACA others(1): Show |
C | 43 | a0001c0001t0001g0035a0001c0001t0001g0046a0001c0001t0018g0106others(40): Show | 43 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.6049+506_6049+513d others(10): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026163 | ||||||
| chr8:18026163
|
CTGAAACA others(2): Show |
C | 57 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0017g0105others(54): Show | 57 | HG00544.hp2 HG00558.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.6049+506_6049+514d others(11): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026163 | ||||||
| chr8:18026163
|
CTGAAACA others(3): Show |
C | 3 | a0003c0003t0002g0231a0003c0003t0009g0226a0010c0014t0023g0355 | 3 | HG02129.hp1 HG04228.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.6049+506_6049+515d others(12): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026163 | ||||||
| chr8:18026163
|
CTGAAACA others(4): Show |
C | 3 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354 | 3 | HG02698.hp2 HG03017.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.6049+506_6049+516d others(13): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026163 | ||||||
| chr8:18026164
|
T | A | 23 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(20): Show | 23 | HG00438.hp1 HG01361.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.6049+506T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026164 | ||||||
| chr8:18026165
|
G | A | 35 | a0002c0009t0016g0359a0002c0009t0016g0362a0002c0009t0016g0365others(32): Show | 35 | HG00438.hp1 HG01257.hp2 HG01361.hp1 others(32): Show |
intron_variant | MODIFIER | c.6049+507G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026165 | ||||||
| chr8:18026169
|
C | A | 91 | a0001c0001t0001g0025a0001c0001t0001g0042a0001c0001t0001g0043others(88): Show | 91 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.6049+511C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026169 | ||||||
| chr8:18026218
|
G | T | 254 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.6049+560G>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026218 | ||||||
| chr8:18026243
|
T | C | 72 | a0001c0001t0002g0045a0001c0001t0002g0072a0002c0002t0053g0289others(69): Show | 72 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.6049+585T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026243 | ||||||
| chr8:18026250
|
C | T | 1 | a0003c0003t0007g0258 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.6049+592C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026250 | ||||||
| chr8:18026260
|
C | CT | 102 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(99): Show | 103 | HG00280.hp1 HG00423.hp1 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.6049+618dupT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr8 | 18026260 | |||||
| chr8:18026260
|
C | CTT | 17 | a0001c0001t0001g0027a0001c0001t0001g0032a0001c0001t0001g0036others(14): Show | 17 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.6049+617_6049+618d others(4): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr8 | 18026260 | |||||
| chr8:18026260
|
CT | C | 82 | a0001c0001t0004g0044a0002c0002t0004g0002a0002c0002t0004g0180others(79): Show | 82 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.6049+618delT | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr8 | 18026260 | |||||
| chr8:18026375
|
A | G | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.6049+717A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026375 | ||||||
| chr8:18026625
|
C | T | 1 | a0002c0002t0004g0184 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.6049+967C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026625 | ||||||
| chr8:18026629
|
G | C | 1 | a0027c0031t0056g0139 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.6049+971G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026629 | ||||||
| chr8:18026664
|
G | C | 1 | a0027c0031t0056g0139 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.6050-973G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026664 | ||||||
| chr8:18026694
|
C | G | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.6050-943C>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026694 | ||||||
| chr8:18026739
|
T | A | 1 | a0027c0031t0056g0139 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.6050-898T>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026739 | ||||||
| chr8:18026924
|
C | A | 1 | a0003c0003t0002g0240 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.6050-713C>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026924 | ||||||
| chr8:18026973
|
C | T | 2 | a0004c0004t0003g0113a0004c0004t0050g0130 | 2 | HG00438.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.6050-664C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026973 | ||||||
| chr8:18026982
|
C | T | 1 | a0004c0004t0003g0126 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.6050-655C>T | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18026982 | ||||||
| chr8:18027031
|
T | C | 1 | a0022c0029t0045g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.6050-606T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18027031 | ||||||
| chr8:18027097
|
T | C | 133 | a0001c0001t0004g0044a0002c0002t0004g0002a0002c0002t0004g0180others(130): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.6050-540T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18027097 | ||||||
| chr8:18027177
|
G | C | 2 | a0005c0005t0014g0175a0005c0005t0014g0176 | 2 | HG02258.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.6050-460G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18027177 | ||||||
| chr8:18027187
|
G | C | 1 | a0027c0031t0056g0139 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.6050-450G>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18027187 | ||||||
| chr8:18027256
|
A | G | 261 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.6050-381A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18027256 | ||||||
| chr8:18027273
|
T | TGTCA | 86 | a0001c0001t0004g0044a0002c0002t0004g0002a0002c0002t0004g0180others(83): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.6050-363_6050-360d others(6): Show |
PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr8 | 18027273 | |||||
| chr8:18027275
|
T | C | 1 | a0005c0005t0014g0163 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.6050-362T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18027275 | ||||||
| chr8:18027362
|
G | A | 1 | a0003c0003t0002g0242 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.6050-275G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18027362 | ||||||
| chr8:18027382
|
A | G | 8 | a0001c0001t0017g0105a0001c0001t0017g0108a0001c0001t0018g0106others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.6050-255A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18027382 | ||||||
| chr8:18027392
|
T | G | 2 | a0001c0001t0038g0073a0003c0012t0009g0349 | 2 | HG01934.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.6050-245T>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18027392 | ||||||
| chr8:18027462
|
G | A | 258 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0004g0044others(255): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.6050-175G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18027462 | ||||||
| chr8:18027487
|
G | A | 1 | a0003c0003t0002g0156 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.6050-150G>A | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18027487 | ||||||
| chr8:18027582
|
T | C | 83 | a0001c0001t0004g0044a0002c0002t0004g0002a0002c0002t0004g0180others(80): Show | 83 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.6050-55T>C | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18027582 | ||||||
| chr8:18027610
|
A | G | 4 | a0010c0014t0022g0330a0010c0014t0022g0331a0010c0014t0023g0354others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.6050-27A>G | PCM1 | ENSG00000078674.20 | transcript | ENST00000325083.13 | protein_coding | 38/38 | chr8 | 18027610 |